Journal of Immunology Research

Volume 2014 (2014), Article ID 237043, 17 pages

http://dx.doi.org/10.1155/2014/237043

Review Article

The Impact of “Omic” and Imaging Technologies on Assessing the Host Immune Response to Biodefence Agents

Julia A. Tree,¹ Helen Flick-Smith,² Michael J. Elmore,¹ and Caroline A. Rowland²

¹Biodefence and PreClinical Evaluation Group, Public Health England (PHE), Porton Down, Salisbury, Wiltshire, SP5 3NU, UK

²Biomedical Sciences Department, Defence Science and Technology Laboratory (Dstl), Porton Down, Salisbury, Wiltshire, SP4 0JQ, UK

Received 15 April 2014; Revised 23 July 2014; Accepted 5 August 2014; Published 16 September 2014

Academic Editor: Louise Pitt

Copyright © 2014 British Crown Copyright. Published with the permission of the controller of Her Majesty’s Stationery Office. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Understanding the interactions between host and pathogen is important for the development and assessment of medical countermeasures to infectious agents, including potential biodefence pathogens such as Bacillus anthracis, Ebola virus, and Francisella tularensis. This review focuses on technological advances which allow this interaction to be studied in much greater detail. Namely, the use of “omic” technologies (next generation sequencing, DNA, and protein microarrays) for dissecting the underlying host response to infection at the molecular level; optical imaging techniques (flow cytometry and fluorescence microscopy) for assessing cellular responses to infection; and biophotonic imaging for visualising the infectious disease process. All of these technologies hold great promise for important breakthroughs in the rational development of vaccines and therapeutics for biodefence agents.

1. Introduction

Understanding host-pathogen interactions is important for the development and assessment of medical countermeasures to infectious agents. The advent of new imaging and “omic” technologies has provided the ability to follow these interactions from whole animal to cellular and molecular levels, enabling a greater understanding of the mechanisms involved; this facilitates the development and refinement of new and existing vaccines and therapeutics. For example, advances in bioimaging provide a noninvasive means of identifying the internal systemic spread of infection in animal models and the impact of a prophylaxis or a therapy on the disease process. This can be combined with the analysis of responses at a cellular level using flow cytometry and microscopy techniques. The use of microarrays has also enhanced our understanding of the host response to infection and provides supportive information to help elucidate the innate and adaptive immune mechanisms essential for protection against pathogens, as well as the virulence mechanisms deployed by the pathogen. Although in its infancy, next generation sequencing also holds great potential for defining host-pathogen interactions. This review will assess the impact of these technologies on the ability to assess the host response and how this has been applied to help progress the development of vaccines and immunotherapies against biodefence agents described in the Centers for Disease Control and prevention (CDC) Select Agent list (http://www.selectagents.gov/). Biodefence agents are dangerous pathogens that require high levels of biocontainment and are relatively less-studied (compared with the majority of public health pathogens) and cases are relatively rare. Therefore, studies to test the efficacy of therapeutics in a healthy population from an endemic area are often not feasible and the use of animal models is essential. This review focuses on the use of these new techniques to help us understand host responses in animal models as well as humans. In this context, both “omic” and imaging technologies hold great promise for important breakthroughs in the rational development of vaccines and therapies.

2. “Omic” Technologies

Traditionally, many immunological studies have focused on examining single immune parameters, such as cytokines, using techniques like ELISA and ELISpot. This approach does not highlight interconnecting pathways that control the immune response when the host encounters an infectious agent. With the emergence of transcriptomic technologies, such as microarray and next-generation sequencing, thousands of parameters of the immune system can be measured at the same time at a genome-wide scale. This allows a systematic, unbiased approach to understand how transcript changes correlate with diverse states of the immune system [1]. This section aims to review the use of microarrays and next-generation sequencing in relation to defining the host response against biodefence agents, vaccines, and therapies.

2.1. Microarrays

2.1.1. DNA Microarrays

A DNA microarray consists of a solid surface, usually a glass microscope slide onto which DNA molecules (probes), in picomolar concentrations, are chemically bonded. The purpose of a microarray is to detect the presence and abundance of labelled nucleic acids (targets) in a biological sample, which will hybridise to the DNA on the array. The level of binding between a probe and its target is quantified by measuring the fluorescence emitted by the hybridized targets when scanned. In the majority of microarray experiments the labelled nucleic acids are derived from the mRNA of a sample or tissue, and so the microarray measures gene expression [2].

Most microarrays are prepared so that they cover the whole genome of a species; however, in the absence of a fully sequenced organism, researchers have used smaller focused arrays designed from publically available gene sequences [3, 4]. Alternatively, whole genome microarrays have been used from related animals to predict immune profiles [5] or new arrays have been constructed using cross-species hybridisation bioinformatics to create probes to unsequenced genes [6]. These kinds of approaches are currently being superseded by the use of next-generation sequence analysis which can generate new sequence information rapidly and accurately. On occasion this information has been used to build new microarray platforms; a successful example of this has been applied to the ferret model of influenza [7]. Today, DNA microarrays have been constructed for studying gene expression changes in a number of different species including the mouse, rat, cow, dog, cat, chicken, horse, pig, rabbit, sheep, guinea pig, ferret, chimpanzee, marmoset, rhesus, and cynomolgus macaque.

DNA microarrays have revolutionized our understanding of the host gene expression changes in response to infection with various pathogens. This information has largely been obtained from in vitro infection experiments. Primary cells taken from naïve human volunteers [8–15] or continuous cell lines [16–22] have been infected and incubated with a pathogen for different time periods (ranging from 1 to 48 hours) and host gene signatures generated (Table 1). Microarray studies performed in this way provide insights into the cellular response following infection with, for instance, Monkeypox virus. Alkhalil et al. (2010) showed that many genes (89.08%) in MK2 cells underwent downregulation by 1.5-fold changes or more [21] following infection with Monkeypox virus. Bourquain et al. (2013) also found major unresponsiveness of HeLa cells after exposure [16]. Rubins et al. (2011) concluded, from studies on different human cell types, that Monkeypox virus selectively inhibited the expression of genes with critical roles in cell-signalling pathways that activate innate immune responses (such as TNF-α, IL-1 α and β, CCL5, and IL-6) [14]. Thus it would appear that Monkeypox virus downregulates or silences genes so that the host is less responsive to infection.

Table 1: Microarray studies performed with various Biodefence Agents.

Pathogen
Purpose of study
Arrays used
Material tested
Reference

Response to infection

Burkholderia pseudomallei
Profile human antibody responses in healthy and recovered patients.
Protein array containing 154 B.  pseudomallei proteins.
Human plasma from healthy and recovered melioidosis patients.
[33]

Burkholderia pseudomallei
Gene expression changes following intravenous infection with bacteria in BALB/c mice.
Sentrix MouseRef-8 cDNA array (Illumina).
Liver and spleen from BALB/c mice.
[24]

Burkholderia pseudomallei
Differences in gene expression after 2 hour exposure to B.  pseudomallei and B.  thailandensis in vitro.
GeneChip human genome U133 (Affymetrix).
A549 human lung epithelial cells.
[22]

Bacillus anthracis
Gene expression changes in cells exposed to Edema toxin.
GeneChip murine genome (Affymetrix).
RAW 264.7 murine macrophages.
[17]

Bacillus anthracis
Gene expression changes in cells exposed to lethal toxin.
GeneChip human genome U133 plus 2.0 (Affymetrix).
Human monocytes from the blood of naïve volunteers.
[8]

Bacillus anthracis
Murine macrophage gene expression changes following exposure to protective antigen and lethal factor from B.  anthracis.
PCR product DNA array.
RAW 264.7 murine macrophages.
[18]

Bacillus anthracis spores
Gene expression profiling of human macrophages following infection in vitro.
GeneChip human genome U133 Plus 2.0 (Affymetrix).
Human alveolar macrophages following bronchoscopy.
[9]

Brucella melitensis
Gene expression analysis of mucosal epithelial cells following infection in vitro.
10K human ESTs microarray (Microarray centre, Ontario, Canada).
Epithelial-like human HeLa cell line.
[19]

Brucella melitensis
Kinetics of human antibody responses to acute and chronic brucellosis.
Brucella melitensis protein array.
Sera from brucellosis patients.
[34]

Brucella melitensis
Investigate host gene changes in vivo following infection with Brucella in a calf ligated ileal loop model.
Custom-made 13K bovine 70 mer oligo array.
Infected Peyer’s patch from calf ligated ileal loop.
[31]

Brucella melitensis
Full proteome-wide serological analysis of B.  melitensis in humans.
Protein microarray containing 3046 proteins from B.  melitensis.
Sera from brucellosis patients.
[35]

Coxiella burnetii
Profile humoral immune response of naïve and acute Q-fever patients.
Protein microarray containing 84% of C.  burnetii.
Human sera from Q-fever patients.
[36]

Coxiella burnetii
Comparison of the antibody profiles from acute and chronic Q-fever patients.
Protein microarray containing 93% of C.  burnetii.
Human sera from Q-fever patients.
[37]

Coxiella burnetii
Define the humoral immune profile using Q-fever patient sera.
Custom-made protein microarray containing 19 proteins from C.  burnetii.
Human sera from Q-fever patients.
[38]

Ebola and Marburg viruses
Gene signatures following infection in vitro with Ebola virus, Marburg virus.
Human cDNA array (Agilent).
Human hepatoblastoma (Huh7) cells.
[20]

Ebola virus
Entry into human macrophages. Infection studies in vitro.
GeneChip human genome HG-U95Av2 array (Affymetrix).
Primary human macrophages.
[10]

Francisella tularensis live vaccine strain (LVS)
Human neutrophil gene expression, in vitro infection studies.
GeneChip human genome U133 plus 2.0 (Affymetrix).
Polymorphonuclear leukocytes (PMNs) from human blood.
[11]

Francisella tularensis  LVS
In vitro infection studies using Human PBMCs.
Human gene array (Affymetrix).
Human peripheral blood mononuclear cells (PBMCs).
[12]

Francisella tularensis (SchuS4)
Gene expression following inhalation of F.  tularensis in BALB/c mice.
Mouse array covering 1500 genes. (Ocimumbio).
Lung tissue taken from infected BALB/c mice.
[27]

Francisella tularensis (FSC033/snMF)
Gene expression following aerosol exposure with F.  tularensis in C57BL/6 mice.
Custom-made mouse cDNA array.
Lung tissue taken from infected C57BL/6 mice.
[30]

Francisella tularensis (SchuS4)
Gene expression of human monocytes infected in vitro with F.  tularensis.
GeneChip human genome U133 plus 2 (Affymetrix).
Naïve human peripheral blood monocytes.
[13]

Francisella tularensis (SchuS4)
Comparison of mouse global transcriptional responses to F. tularensis, Yersinia pestis, Pseudomonas aeruginosa and  Legionella pneumophila.
Mouse whole genome 44K arrays (Agilent).
Lung tissue from infected BALB/c mice.
[29]

Monkeypox and Vaccinia virus
Comparison of gene expression profiles following infection in vitro with Monkeypox or Vaccinia virus.
Human cDNA arrays with 406 Variola and Vaccinia virus genes.
Primary human macrophages, primary human fibroblasts and HeLa cells.
[14]

Monkeypox and Vaccinia virus
Comparison of gene expression profiles, in vitro infection studies.
Whole human genome oligo microarray (Agilent).
HeLa cells.
[16]

Monkeypox virus
Gene expression changes in vitro 3 and 7 hours post-challenge with Monkeypox virus.
Rhesus macaque genome microarrays (Affymetrix).
Macaca mulatta kidney cells (MK2).
[21]

Monkeypox virus
Comparison of antibody responses to monkeypox virus infection and human smallpox vaccination.
Protein array covering 92–95% of representative proteins from Monkeypox and Vaccinia virus.
Blood from humans with smallpox vaccination and cyno macaques infected with Monkeypox virus.
[39]

Variola virus
Host gene expression changes in Variola virus infected cynomolgus macaques.
Human cDNA microarrays.
PBMC’s sampled from infected monkeys.
[5]

Yersinia pestis
Gene expression changes following infection in vitro.
Human nylon blots (1185 cDNA spots) (Clontech).
Primary human monocytes and/or mixed with lymphocytes (PBMCs).
[15]

Venezuelan equine encephalitis virus (VEEV)
Gene expression of VEEV infected mice.
Oligo array mouse 70 mer. (Operon) & GEArray, focused mouse Toll-like receptor signaling microarray.
VEEV infected mouse brain CD-1 mice.
[25, 26]

Vaccines

Anthrax vaccine adjuvant CpG ODN
Measure gene expression changes in mice and splenocytes treated with CpG ODN.
Murine oligonucleotide array (custom-made).
Spleens and splenocytes from various breds of mice.
[40–42]

Francisella tularensis LVS
Assess the memory response of PBMCs taken from LVS vaccinated and naïve humans.
GeneChip human genome U133 (Affymetrix).
Re-stimulated PBMCs from LVS vaccinated and naïve humans.
[43]

Killed Francisella tularensis (LVS) adjuvanted with ISCOMS admixed with CpG
Define antibody profiles of vaccinated mice.
Whole proteome microarray custom-made.
BALB/c mice vaccinated with LVS.
[44]

Q-fever vaccine
Assess antibody immune profiles of Q-Vax vaccinated humans.
C.  burnetii protein microarray (custom-made).
Sera from vaccinated humans.
[45]

Smallpox vaccines
Assess antibody profiles generated to MVA, Acam2000 and/or Dryvax smallpox vaccines.
Protein array containing Vaccinia virus proteins [46].
Mouse, rabbit, macaque, black-tailed prairie dog and human sera.
[47–51]

Therapies

Anti-coagulant treatments for Ebola virus infection
Comparison of NHP host genome responses responding to candidate therapeutics following infection with Ebola virus.
Human genome cDNA microarray.
PBMC’s from rhesus macaques infected with ZEBOV and treated shortly after exposure with rNAPc2 or rhAPC.
[32]

Omission from this table does not constitute absence of data.

DNA microarray analysis has been used to improve our understanding of the host response following exposure to the bacterium [18], spores [9], edema toxin [17], and lethal toxin [8] of Bacillus anthracis, the causative agent of anthrax. Studies on human peripheral monocytes revealed that anthrax lethal toxin targets multiple normal immune-regulatory pathways that would be expected to protect the host against anthrax infection. They hypothesised that the increase in RGS14 levels and decrease in CCR5, along with IL-1R2, impairs monocyte function and facilitates bacterial survival [8].

Despite the ready availability of DNA microarrays for use with different animal species, relatively few in vivo transcription studies have been published using models of infection with biodefence infectious agents compared with public health pathogens such as tuberculosis (TB) or human immunodeficiency virus (HIV). Using the mouse model, gene signatures have been determined in different organs following infection with Burkholderia pseudomallei [23, 24], Venezuelan equine encephalitis virus (VEEV) [25, 26], and Francisella tularensis [27–30]. Very recently a bovine model has been used for investigating host mRNA expression changes to Brucella melitensis by examining the infected Peyer’s patch from a calf ligated ileal loop. This study showed that the early infectious process of Brucella was primarily accomplished by compromising the mucosal immune barrier and subverting critical immune response mechanisms [31].

Some microarray studies have been performed using nonhuman primates (NHPs) infected with Ebola virus [32] and Variola virus [5]. In studies at Public Health England the mRNA profiles of NHPs infected with Monkeypox virus and B. anthracis are currently underway (personal communication, Karen Kempsell). There is scope for many more informative microarray studies to be performed in various animal models of biodefence agents.

2.1.2. Protein Microarrays

Protein microarray is a more recent technology, providing a platform for high-throughput proteomics. Construction is similar to DNA microarrays, except that the immobilised species is a protein or a peptide, and the array aims to represent partially or wholly the entire proteome [52]. Two methods of protein generation are used: (1) the “standard” method where the gene for each protein is amplified, cloned, produced in an in vitro expression system (typically in Escherichia coli), and printed directly onto glass slides [46]; (2) an alternative method where the encoding DNA is printed onto the slide and expressed in situ at the time required (NAPPA, nucleic acid programmable array) [53].

One of the most powerful applications of protein microarrays is in the study of the humoral immune response to infection. Arrays have been used to assess host antibody profiles (or “immunosignature”) in response to infection with B. melitensis [34, 35], B. pseudomallei [33, 54], Vaccinia/Variola virus [47], Monkeypox virus [39], and Coxiella burnetii [36–38] (Table 1). Studies on C. burnetii, the etiological agent of Q-fever, have helped to identify new diagnostic antigens [36, 38, 45]. Seven C. burnetii proteins (GroEL, YbgF, RplL, Mip, OmpH, Com1, and Dnak) were identified (from protein arrays studies) and then fabricated on a small array and tested with sera from patients with other diseases (Rickettsial spotted fever, Legionella pneumonia, or Streptococcal pneumonia) as well as Q-fever, in order to develop a diagnostic assay. The selected antigens demonstrated moderate specificity for recognizing Q-fever in patient sera [38]. The use of protein microarrays has also aided the identification of different IgG and IgM profiles for differentiating acute and chronic Q-fever [37] and a proof-of-concept diagnostic assay (immunostrip) to distinguish the two disease states [37]. In addition to identifying antigens for diagnostic tools, antibody profiling, using protein arrays, also provides candidate antigens for subunit vaccine development [37].

2.1.3. Use of Microarrays for the Evaluation of Vaccines and Therapies

Microarray technology has been used to help understand the cell-mediated and humoral immune responses following infection with infectious agents; furthermore it has also improved our understanding of the mechanism of action of therapeutics and biodefence vaccines. For instance a transcriptomic approach, using DNA microarrays, was used to assess the host response to treatment with therapeutic agents (rNAPc2 or rhAPC) designed to block the coagulation pathway during Ebola virus infection in NHPs [32]. Coagulation abnormalities in Ebola hemorrhagic fever have been previously reported [55] suggesting that blocking the development of coagulopathies during Ebola virus infection might limit pathogenesis. Microarray analysis showed that the overall circulating immune response in NHPs was similar both in the presence and absence of coagulation inhibitors; however, the profiles of the surviving NHPs in the treated groups clustered together [32]. Only small numbers (2/8 and 2/11) of animals survived in each treatment group but the study did reveal that several differentially expressed genes correlated with survival, namely, chemokine ligand 8 (CCL8/MCP-2) and coagulation-associated genes TFPI and PDPN [32]. Further work is clearly needed in this area as these genes may provide possible targets for early-stage diagnostics or future therapeutics.

A limited number of studies have been performed using DNA microarrays to understand the underlying protective mechanisms of licensed or novel biodefence vaccines. DNA arrays have been used to examine the immunostimulatory properties of CpG motifs [40–42] which when used as an adjuvant have been shown to significantly prolong the protection induced by anthrax vaccine adsorbed (AVA) [56, 57]. Recently, Paranavitana and colleagues examined the transcriptional profile of human volunteers who had received the live vaccine strain (LVS), an attenuated strain of F. tularensis [43]. PBMCs from individuals were restimulated with LVS in vitro and memory responses were evaluated. The microarray results revealed that both dendritic cells and macrophages played significant roles in antigen presentation. Significantly differentially expressed genes including IL-15, GM-CSF, IL-9, and IL-10 as well as genes associated with T-cell, B-cell, and natural killer cell activities were identified. Paranavitana et al. concluded that the manipulation of the dendritic cell maturation pathway, with stimuli to promote efficient antigen presentation, may be a way forward for future vaccine development against Francisella [43].

The antibody profile evoked by smallpox vaccines has been examined in detail following the development of a Vaccinia proteome microarray by Davies et al. in 2005 [46]. Since then, the immunosignature evoked by three different vaccines (Acam2000, Dryvax, and MVA) in the mouse, rabbit, macaque, prairie dog, and humans have been defined [47–50]. Follow-up studies using protein arrays involved examining the sera from more than 2000 smallpox-vaccinated humans. Six dominant antigens were identified comprising 3 membrane and 3 nonmembrane antigens from the intracellular mature virion [51]. These antigens were then evaluated in an ELISA format with sera from MVA and DryVax vaccinees. Overall, these ELISAs should aid in monitoring the human immune response to MVA in both vaccinia naïve and previously vaccinated individuals, thus assisting with vaccine development in the future.

Protein arrays have also been used to examine the immunosignature of mice vaccinated with killed F. tularensis LVS adjuvanted with immune stimulating complexes (ISCOMS) and CpG [44]. Similarly, protein arrays were used to assess the immunosignature of Q-Vax (Q-fever) vaccine [45]. Both studies identified protective proteins which should aid the design of new or improved vaccines.

Advances in “omic” technology have also assisted with the identification of candidate T-cell antigens. An ORFeome flexible cloning approach was developed by Jing and colleagues whilst analysing the CD4 T-cell response to vaccinia virus using PBMCs from Smallpox vaccinated individuals in 2009 [58]. This method has since been used to identify candidate T-cell antigens for herpes simplex virus type 1 (HSV-1) [59]. This could be applied to the identification of T-cell antigens for Biodefence vaccines.

2.2. Next Generation Sequencing

Next generation sequencing (NGS; also known as high-throughput, short-read, or deep sequencing) has revolutionised sequence-based analyses over the last decade. The underlying principle is that it uses micro-/nanotechnologies to run millions of parallel sequencing reactions, generating millions or billions of bases per run (which is up to 6 logs greater than the output using the Sanger method). Read lengths are typically comparatively short, a result of which is that any particular base is sequenced many times (known as coverage or read depth). There are a number of competing platforms, with Illumina, ABI SOLiD, Roche 454, and Ion Torrent technologies being widely used, each having different characteristics with regard to average read length, total bases sequenced per run, and cost-per-base [60–62]. Other more specialized NGS technologies are PacBio Single Molecule Real Time (SMRT) and Oxford Nanopore [63, 64].

NGS technology can be applied to both DNA (DNA-seq), and RNA (after conversion to cDNA-RNA-seq). RNA-seq analysis aims to identify the transcriptome (the complete set of transcripts of the cell, which includes mRNA, noncoding RNAs, and small RNAs). RNA-seq is increasingly being used as an alternative to microarray as a method of measuring gene expression [65, 66] and uses the sequence read depth of the RNA species as a measure of the absolute level in the sample. The two methods have a high degree of correspondence [67, 68], and similar analytical statistical techniques can be used, although data preprocessing and sample normalization require different bioinformatic techniques [69]. RNA-seq is reported to have significant advantages over microarray, such as less bias/variation, lower background signal, and a larger dynamic range (up to 100-fold greater). Importantly, it does not depend on prior knowledge of a reference transcriptome and therefore can lead to discovery of previously unknown RNA species and of “edited” RNA species such as splice variants [70]. However, certain disadvantages do exist, such as nonuniform read coverage, inability to detect a rare transcript (unless high read depth is obtained), and discrepancy in read depth or library sizes between samples [65].

2.2.1. Use of RNA-Seq to Study Host Response to Pathogens

Upon infection of a host with a pathogen, changes in the expression of both organisms occur. These are usually investigated separately due to the low pathogen:host transcript ratio (up to 200-fold); thus enrichment of the pathogen transcripts is often required [71]. Pathogen expression profiling examples include analysis of the F. tularensis transcriptome during infection of mouse macrophages [72] and sRNA expression of Yersinia pestis grown in vitro and in the mouse lung [73].

RNA-seq has been used to investigate the host response to different virulent strains of B. melitensis in mouse peritoneal macrophages [74]. Compared with previous microarray studies, deep sequencing provided a more sensitive and comprehensive unbiased coverage of the host transcriptome, with many alternative and novel transcripts being discovered. In particular, it was shown that a live attenuated vaccine strain (M5-90) had a reduced ability to avoid phagosome-lysosome fusion and activate MAPK pathways when compared with the virulent strain M28. This may account for the difference in the ability of the two strains to survive in the host [74]. A second study examining the microRNA (miRNA) profile of RAW264.7 cells in response to B. melitensis infection also used a high throughput sequencing approach [75]. Zheng and colleagues concluded that Brucella may establish a chronic infection by regulating the host miRNA profile [75].

The human host response to Dengue virus infection has also been reported using RNA-Seq [76]. A significant amount of previously uncharacterised gene isoforms and alternative transcripts over a range of pathways were shown, and particularly there was a greater number of host differentially regulated transcripts upon infection by an attenuated DENV strain than by the wild-type, suggesting that there may be a previously uncharacterised innate immune response which is largely evaded in wild-type strains [76].

2.2.2. Dual RNA-Seq

Ideally it would be preferable to monitor the gene expression profiles of the pathogen and host simultaneously. This “dual RNA-seq” approach is technically and bioinformatically more challenging [77, 78] but may well become the established method. However, recent examples do exist for the simultaneous profiling of the host and viral [79] or bacterial [29, 80] species. For instance, Walter and colleagues exposed mice to virulent F. tularensis and discovered that, while acute infection at four hours was associated with marked suppression of multiple aspects of the innate immune response (relative to other pathogens examined), a subset of immune-related transcripts was uniquely induced by Francisella. They also showed that a classical inflammatory response was activated in the lungs of mice, 24 hours after infection and this simultaneously correlated with a dramatic change in bacterial gene expression patterns [29]. These results should help to identify potential virulence factors which target host inflammatory pathways, in the future.

Dual RNA-seq has also been used to evaluate the immune response following smallpox vaccination. PBMCs taken from Dryvax vaccinated individuals were either stimulated with or without live Vaccinia virus for 8 hours [81]. Results showed detection of all annotated Vaccinia genes, with those genes classified as “early” in the viral life cycle expressed at significantly higher levels. On the host side numerous innate genes and pathways were activated upon vaccinia infection. A number of chemokines, cytokines, interferons, and macrophage-associated genes exhibited downregulation upon infection whilst there was an upregulation of histones, IFNβ, IFNγ, and heat shock proteins [81].

2.2.3. Other Uses of NGS Sequencing

T and B Cell Repertoire Diversity. The immunological repertoire is a term defining the collection of surface-expressed B-cell (BCRs) and T-cell receptors (TCRs). Receptor diversity is generated dynamically by sequence rearrangement of specific loci in the germline genome, leading to a vast diversity of differing clones [82]. Classically, studies on the immune repertoire have used techniques that either provide a limited description or sample a limited number of sequences (e.g., CDR3 spectratyping, targeted sequencing [83]). The high-throughput nature of NGS technology allows simultaneous analysis of potentially the entire immune repertoire in a single experiment (using DNA-Seq or RNA-Seq) [84–86]. Recent applications have included studying the changes in the antibody responses to Dengue virus infection [87] and Influenza vaccination [88] and there is clearly scope to apply this technique to monitor the immune repertoire in response to other infectious diseases, vaccines, or therapeutics.

3. Optical Imaging of Host-Pathogen Interactions

Imaging infection using optical sources relies on the detection of specific targets using fluorescence or bioluminescence. Fluorescent light is emitted with a characteristic emission spectrum following excitation at specific wavelengths. Fluorescent molecules may be used to tag specific molecules of interest. Very often the molecule of interest will be an antibody which in turn will be directed to specific targets (e.g., surface receptors on host cells). Alternatively, endogenous proteins can be made to fluoresce, for example, in genetically modified animals or pathogens, or fluorescent dyes can be used to label pathogens or cells. Bioluminescence is produced by the reaction of a luciferase enzyme with its substrate and requires energy and oxygen to occur. Unlike fluorescence imaging, where the signal is still detectable for some hours after the host has died, bioluminescent imaging requires living cells. This section aims to review how our understanding of biodefence pathogens, vaccines, and immunotherapies and their interactions with the host has been greatly aided by imaging techniques such as flow cytometry, fluorescence microscopy and real time in vivo biophotonic imaging.

3.1. Flow Cytometry

This technique is routinely used as an important tool for assessing cellular responses to infection and vaccination in both human patients and animal models of infection. It is used for cellular phenotyping and functional assays including fluorescence-based proliferation assays. Bead-based assays are also available to assess levels of soluble factors including cytokines in samples from in vitro and ex vivo tissues. Intracellular cytokine responses can also be measured by intracellular staining, with fluorochrome labelled antibodies, to determine cellular phenotypes generated following vaccination or therapeutic treatment with specific antigens. Antibodies for specific cell targets are generally available for a number of animal species particularly the mouse and rat, but cell target ranges are limited for less commonly used species such as the marmoset, which in turn can limit the analysis of cellular responses in these models. In order to understand host-responses, fluorescently labelled pathogen-specific antibodies allow the presence of intracellular bacteria to be identified within host cells [89]. Alternatively bacteria expressing fluorescent molecules, for example, green fluorescent protein (GFP) [90], m-cherry red [91] or other fluorescent markers may be used. In combination with specific antibody staining of host cells, fluorescent labelling of pathogens has allowed the location of pathogens within host cells to be identified in both in vitro and in vivo infection studies using flow cytometry and immunofluorescence microscopy.

3.1.1. Pathogenesis and Assessment of Immunotherapies

Flow cytometry has highlighted a key role for various cell types in murine infection models of Y. pestis, the causative agent of plague. The importance of neutrophils in respiratory Y. pestis was demonstrated in two early studies [92, 93]. Furthermore, flow cytometry was used to identify the target host cells of Y. pestis in a murine pneumonic infection model where alveolar macrophages (CD11c⁺CD11b⁺F4/80⁺) were identified as the initial cell type to uptake the bacterium followed by neutrophils [94]. An additional study investigating intratracheal inoculation of Y. pestis showed the interaction of this bacterium with CD11c⁺DEC205⁺CD11b- cells in the airways and lung. Depletion of this cell type suggested an important role for it in the initial replication and dissemination of Y. pestis from the lung [95]. It is speculated that the difference in cellular tropism of Y. pestis described in these respiratory studies maybe due to the difference between aerosol and intratracheal dosing and differing strains of the organism. In an intradermal model of infection, Y. pestis was also found to reduce the activation of inflammatory cells, particularly neutrophils, at the site of infection. Using bacterial mutants, the Y. pestis virulence plasmid pYV was shown to be involved in this evasion of early inflammatory responses in the skin [96].

Neutrophil inflammatory responses have been characterised following infection in mouse models with both B. pseudomallei [97] and Burkholderia mallei [98] by flow cytometry where neutrophils were found to be crucial for protection in both respiratory and intraperitoneal forms of these related infections. The role of neutrophils in Burkholderia infection in the murine host also aligns with human ex vivo studies where phagocytosis and apoptosis of B. pseudomallei by human blood neutrophils were impaired in neutrophils from diabetic patients. This impaired neutrophil function may contribute to the increased susceptibility to Burkholderia infection observed in diabetic patients [99].

Using flow cytometry to understand host-pathogen interactions has the potential to enable an association between host immune markers with protective effects following treatment with therapeutics and vaccines. A number of studies have assessed the immune response to immunotherapeutic approaches for treatment of infection to further understand potentially protective immune responses in in vivo models of infection using immunostimulants including CpG motifs [100]. One study using phosphoantigens as an immunotherapy in a marmoset model of B. pseudomallei infection [101] showed that, although there was no effect on survival, strong cell-mediated immune responses were detected which could inform future treatment strategies. In another study, decreased bacterial numbers and increased survival to a novel immunotherapeutic strategy using Acai polysaccharides against pulmonary F. tularensis or B. pseudomallei infection in vivo [102] were associated with IFN-γ production by NK cells in the lung.

Flow cytometry bead-based assays have the potential to aid our understanding of potential protective mechanisms of novel immunotherapeutics by assessing cytokine responses. These assays have been used in studies investigating the effects of IFN-γ therapy in mice during B. pseudomallei infection [103] and to understand changes occurring as a result of treatment with an HMGB1-antibody antibiotic combination therapy [104]. This study showed that treated mice had significantly higher IFN-γ levels which correlated with survival. They have also been used to further our understanding of the protective immune responses involved following a combination of preexposure vaccination and postexposure CpG immunotherapy against B. pseudomallei infection in vivo [105] where both intranasal and intraperitoneal vaccinations with 2D2 attenuated vaccine strain were found to generate antigen-specific IFN-γ CD4⁺ T cell responses. A greater pulmonary T cell response was observed following vaccination via the intranasal route which corresponded with increased protection against pulmonary infection.

3.1.2. Vaccine Studies

Immune responses elicited in vivo following immunization and ex vivo cellular restimulation with specific antigens from vaccinated or infected animals have been used to determine specific, memory-type responses to vaccines. This has broadened our understanding of a number of vaccination strategies for biodefence pathogens including live vaccines for B. pseudomallei [106] and F. tularensis [107], novel live vaccine strategies against F. tularensis infection [108], and heat-killed vaccines to B. mallei [109]. Potential immune correlates of protection have also been identified in studies by comparing profiles of lymphocyte populations following vaccination (prior to infection) and their responses during infection with Monkeypox virus [110]. In depth assessment of T-cell signatures in vaccines or individuals with naturally acquired F. tularensis infection suggested that these signatures could be used to identify protective correlates of immunity to F. tularensis [111]. Additionally, the identification of putative vaccine candidates [112] and the longevity of immune responses to vaccines have also been greatly aided by flow cytometry in follow-on studies of F. tularensis live vaccine strain (LVS) vaccination [111, 113]. Immune responses to vaccination have also been used in preclinical animal models (murine and primate) and in Phase I clinical trials to assess host responses to a recombinant plague vaccine. Although a number of memory cell phenotypes were investigated, flow cytometry lacked the sensitivity to detect changes in immune profiles between vaccinated and placebo groups [114]. Understanding immune responses generated by novel vaccines can facilitate the rational development of vaccines which induce the most appropriate immune responses to protect against infection, for example, by engineering the known protective F1-antigen against Y. pestis to include B-cell and T-cell epitopes [115].

3.1.3. Other Uses of Flow Cytometric Techniques

In addition to examining lymphocyte responses, the role of antigen-presenting cells in generating protective immunity during vaccination to B. pseudomallei (e.g., dendritic cells (DCs) [116]) and F. tularensis LVS [107] has also been aided by the use of flow cytometry techniques. The use of a GFP strain (BP82-GFP) of an intradermally delivered live, attenuated B. pseudomallei vaccine [117] and specific cell staining demonstrated that the most efficient cell type at uptake and transport of bacteria to the draining lymph node was the neutrophil.

Fluorescent-activated cell sorting and cDNA technologies have recently been used together to generate antigen-specific monoclonal antibodies [118]. The overall aim of this is the provision of antibody treatments for infectious diseases and an example of this has already been applied to emerging coronavirus species including severe acute respiratory syndrome (SARS) [119]. This technology may well be used for developing therapeutics for biodefence agents in the future. Other potential applications of flow cytometry in biosecurity research, outside the area of investigation of host-pathogen interactions, are reviewed in Marrone, 2009 [120].

3.2. Fluorescence Microscopy

A number of recent advances in fluorescent microscopy techniques such as confocal microscopy, intravital 2-photon microscopy, dynamic live cell imaging, and super resolution microscopy have been used to interrogate host-pathogen interactions, based on detection of specific fluorescent signals to provide detailed images of pathogens colocalised with or within host cells. Fluorescence microscopy is also being investigated for its utility in the diagnosis of infections including B. pseudomallei. In comparison with flow cytometry, fluorescence microscopy can provide a much more detailed assessment of how pathogens interact with individual host cells. These studies are aided through the use of a range of fluorescent dyes for both the pathogen and cellular structures/organelles including DNA dyes such as DRAQ5 or DAPI which are important for nuclear identification.

3.2.1. In Vitro Infection Models

Fluorescence microscopy has enabled us to understand the intracellular nature and niches of pathogens and their ability to evade immune pathways to enable their survival within host cells. For example, identifying the lysosomal escape mechanism of F. tularensis into the cytosol provided an understanding of its ability to survive within host macrophages [121]. Fluorescence microscopy has also been used to investigate the role of complement in uptake of F. tularensis into cells [122] and the immune evasion of this pathway by F. tularensis [123]. It has also been used to understand the effect of modulators on macrophage function and phagosomal escape of F. tularensis LVS [124] and the interaction of B. mallei with macrophages in vitro to assess which bacterial components are important in the pathogenesis of disease [125]. Understanding the effects of F. tularensis LVS strains and their altered interactions with host cells [126] has potential implications for future licensing of these vaccines. Our understanding of the interaction of F. tularensis and other bacteria with host cells and its intracellular nature has contributed to development of treatment regimens including delivery of antibiotic therapies suitable for treating intracellular infection. Fluorescence microscopy also has the potential to elucidate host pathway targets which could be therapeutically manipulated to prevent evasion of the host response by bacteria and aid in intracellular clearance. For example, the interaction of F. tularensis and B. pseudomallei with pathways of autophagic digestion has been assessed using fluorescence microscopy in in vitro studies. The interaction of B. pseudomallei with autophagosomes using GFP-LC3-expressing RAW 264.7 cells and fluorescently labelled bacteria (both wildtype and mutants) elucidated mechanisms of evasion of the autophagic pathway by B. pseudomallei [127]. F. tularensis was also found to utilize one autophagic pathway for its survival [111]. Further studies identified potential new therapeutic compounds to target the autophagic pathway [128, 129]. It was demonstrated that inducing alternative autophagic pathways using the novel inducer AR-12 reduced bacterial growth in F. tularensis infection [112]. Confocal scanning microscopy has enhanced our understanding of the interaction of C. burnetii with host-cells and intracellular vacuoles [130]. The dynamics between vacuoles, lysosomes, and the processes which regulate actin dynamics in formation of vacuoles, including GTPases and associated proteins, have been investigated in detail using C. burnetii mutants [107]. This has led to identification of host targets with the potential for therapeutic targeting. Confocal microscopy has also been utilised to develop a high content imaging assay to understand the formation of multinucleated giant cells (MNGCs) during B. pseudomallei infection which is a unique mechanism used by Burkholderia spp. and is thought to allow spread of the infection without detection by the immune system [131]. This quantitative method allowed the effect of bacterial mutants, thought to subvert the formation of MNGCs, to be assessed. Importantly, this method was also used to investigate the effect of small molecule inhibitors on MNGC formation and thus has the potential to be used as a screening tool for novel therapeutics. Confocal microscopy has also been used to investigate the interaction of viral pathogens including filoviruses such as Ebola virus with host cells [132, 133] and by mapping the interaction between the viral proteins polymerase L and its cofactor VP-35. In this model in vitro system, immunofluorescence analysis demonstrated that this interaction was disrupted by mutants containing the VP-35 binding site which led to reduced Ebola virus replication, thus identifying a potential target for development as a novel antiviral therapy [134].

3.2.2. In Vivo Infection Models

F. tularensis was detected by phase-contrast and fluorescence microscopy using in situ hybridization [135] and an m-cherry red strain of B. melitensis identified bacteria associated with host cells in tissue sections from in vivo infection models [91]. This study showed the in situ colocalisation of B. melitensis with a number of different cellular phenotypes within granulomas in the spleen and liver. Understanding these immune-pathological lesions using complex immunohistochemistry and fluorescent bacterial strains has the potential to allow identification of new treatments for bacteria which so effectively evade and manipulate host responses to enable their survival. The binding of monoclonal antibody therapies to the Y. pestis bacterium using immunofluorescence demonstrated the specificity of potential therapies for bubonic plague. This prior testing of monoclonal antibody therapies was important to determine the specificity of any protection observed in in vivo studies [136]. Intravital microscopy, which adds an additional parameter of time to microscopy studies, was used to identify the rapidity of the neutrophil response in situ during intradermal infection with ds-red expressing Y. pestis strain in a GFP-expressing neutrophil transgenic mouse model [137]. The dynamic interactions between ds-red Y. pestis and GFP-neutrophils following intradermal infection and the association between Y. pestis and neutrophils were confirmed by confocal microscopy which specifically demonstrated that, within 4 hours, Y. pestis had been phagocytosed by neutrophils and was intracellular and not just associated with cells. This led the authors to investigate the role of neutrophils in dissemination of plague to the lymph nodes using antibody depletion which suggested that Y. pestis subverted the host response very early in infection to prevent dissemination to the lymph nodes.

3.3. Biphotonic Imaging: Real-Time In Vivo Imaging

Visualising the infectious disease process as it occurs inside a living animal is of major benefit to the development of medical countermeasures. This can be achieved using biphotonic imaging (BPI), a sensitive and noninvasive method of detecting light emitted either as a bioluminescent (BL) or fluorescent (FL) signal, using photon detectors such as those based on a charge coupled device (CCD) camera. BPI has enabled new insights into pathogen dissemination, host responses to infection, interactions between host and pathogen, and the effects of antimicrobials and vaccines. This technique can also be used to refine animal experiments with each animal acting as its own control, therefore, increasing the power of these studies. The creation of BL or FL strains of pathogenic organisms has enabled this field to progress and description of the processes involved in BPI and creation of these strains are comprehensively reviewed in Andreu et al. [138].

Using BPI different patterns of pathogen dissemination can be readily observed allowing discrimination of the growth and spread of different forms of the pathogen or target organs depending on route of infection. For example, BL expressing variants of B. anthracis Sterne strain that only produced a BL signal during either spore germination or vegetative growth of the bacterium have permitted identification of sites of germination and spread during the early stages of anthrax infection [139]. BPI studies helped determine the site of anthrax spore germination after inhalational infection [140] where light emitting bacteria in the upper respiratory tract and lung were observed within 30 min of inhalational infection [140, 141].

BPI studies showed that dissemination of Y. pestis was found to vary depending on route of infection [142, 143]. Subcutaneous (s.c.) administration in the abdominal linea alba region resulted in pathogen spread from the inguinal lymph node (LN) to axillary LN, then to liver and spleen whereas s.c. infection in the more traditional cervical “scruff” region, base of the tail, in the footpad [144] or ear pinna [143] resulted in a different pattern of signal intensity originating at the site of injection. Intranasal (i.n.) challenge with BL Y. pestis leads to a detectable BL signal [143, 145] in the upper abdominal region which was confirmed to originate from the lung by ex vivo imaging of tissues. BPI has also been used to investigate the dissemination of BL strains of F. tularensis type A (SCHU S4) and type B (LVS) [146]. Visualising areas of BL LVS infection and bacterial spread [147] provided important information on the effects of instillation volume and anaesthesia in delivery of i.n. bacterial challenge with the potential to impact on the wider development of in vivo pulmonary infection models.

The pattern of dissemination of BL B. pseudomallei following inhalational challenge has been investigated [148, 149]. The spread of both wild type and capsule mutant strains of B. pseudomallei has been compared in the BALB/c mouse model with an immunocompentent, hairless SKH-1 mouse strain, that is, particularly useful for FL imaging studies due to low autofluorescent background usually generated by fur. Infection studies with a BL strain of B. mallei have also been reported [150, 151] with a BL signal detectable in the lung after i.n. challenge from 48 h after infection (p.i.), before progressing to the liver and spleen.

These pathogen dissemination models have subsequently been used to assess the effect of antibiotics and immunotherapies. A substantial reduction of bacterial signal was found in B. mallei-infected mice treated with the antibiotic levofloxacin compared to untreated mice [150]; however, when the antibiotic was discontinued at 96 h p.i., reemergence of the BL bacterial signal was observed. This mouse model of B. mallei infection has been further used to investigate the effects of CpG treatment alone, previously shown to provide protection against B. mallei infection when given preexposure to mice [152]. Mott et al. (2013) [151] used dual signal imaging to elucidate the role of CpGs on neutrophil activation using a neutrophil-specific fluorescent probe. This cyanine 7-conjugate, PEG modified hexapeptide reagent specifically binds to the formylpeptide receptor of neutrophils [136]. This has allowed real-time colocalisation of BL bacterial spread with FL neutrophil responses in the lung during the course of infection.

The effects of immunisation with protective antigen (PA) vaccine demonstrated that, in immunised mice, dissemination of BL B. anthracis beyond the nasopharynx region was prevented. The effect of PA vaccine immunisation on anthrax spore germination and bacterial spread has also been assessed [141]. This work clearly demonstrated that although spore germination and bacterial growth occur at the same rate in both immunised and unimmunised mice, bacterial growth was quickly neutralised in the immunised mice whereas BL bacteria spread rapidly in unimmunised controls. BL expressing B. anthracis strains modified to express only one of the anthrax toxins stimulated different patterns of early immune response after cutaneous infection of the ear pinna [153]. In this study, draining LN were removed following BPI and immune cell populations were analysed by flow cytometry. The Lethal toxin-expressing strain stimulated increases in the total cell populations of neutrophils, CD4⁺ and CD8⁺ T-cells whereas the immunosuppressive edema toxin-expressing strain stimulated only an increase in CD8⁺ T-cells.

3.4. Emerging Technologies

3.4.1. Imaging Flow Cytometry

Recent developments in flow cytometry include the development of imaging flow cytometers including the ImagestreamX. Imaging flow cytometry adds another dimension to flow cytometric applications with images of each cell being produced in addition to fluorescence readouts and has the ability to further advance our understanding of host-pathogen interactions. It is particularly suitable for assessing the colocalisation of pathogens within host cells and for examining cellular processes for uptake and processing of pathogens, for example, phagocytosis, autophagy, and apoptosis. The number of publications which incorporate use of ImagestreamX for investigating host-pathogen interactions is growing each year with a limited number of publications on a wide range of public health related pathogens including Yersinia enterocolitica [154], Plasmodium falciparum [155, 156], and Neisseria meningitidis [157]. As yet, no studies for biodefence pathogens have been published. However, pathogens which have been used to model biodefence pathogens, such as Yersinia pseudotuberculosis as a model for Yersinia pestis, have been documented [158] demonstrating the potential of this technology. At Defense Science and Technology Laboratory, we are currently using the ImagestreamX to examine the interactions of B. pseudomallei, F. tularensis, and other pathogens with cellular targets in samples from both in vivo and in vitro studies (Figure 1). This technique has the potential of providing a high-throughput imaging technique for the analysis of host-pathogen interactions and assessment of immunotherapeutics for biodefence pathogens.

Figure 1: ImageStreamX Mk1 imaging depicting intracellular infection of ex vivo and in vitro cells. (a) Infected and (b) uninfected ex vivo lung cells stained with fluorescently labelled antibodies specific for Burkholderia pseudomallei (Bps) and the neutrophil marker Ly6G. A composite (overlayed) fluorescence image shows intracellular Bps inside neutrophils (Ly6G/Bps). Mouse macrophage cell line (P388D.1) infected (c) in vitro with F. tularensis SCHU S4 (Ft) or uninfected controls (d). Each Image series shows 6 representative cells from one sample. SSC = Side Scatter; BF = Brightfield; FITC = Fluorescein Isothiocyanate; BV = Brilliant Violet.

3.4.2. Other Imaging Technologies

Ultrasound magnetic resonance imaging (MRI) and radiography are all technologies which have been used clinically in the diagnosis of infectious diseases including anthrax and tuberculosis. Some of these technologies have been used in biodefence research, for example, positron emission tomography (PET)/computer tomography (CT) imaging was used to examine inflammation patterns in Monkeypox virus infection of primates [159]. The use of these imaging technologies in high containment, alongside optical imaging technologies, has the potential to provide a multi-faceted approach to imaging to further enhance our understanding of the pathogenesis of infection with Biodefence agents in the future. The use of other imaging technologies and their potential application to biodefence disease in the clinic is reviewed in [160].

4. Conclusions

Biodefence agents are dangerous pathogens that pose unique challenges for researchers. Human cases of these diseases are relatively rare and therefore animal models play a key role in helping to understand pathogenesis. Imaging and “omic” technologies have greatly aided our ability to study the host response during the course of an infection and have thus provided important insights. Also since it is neither ethical nor feasible to conduct conventional phase III efficacy trials, using biodefence agents in human volunteers, these key technologies can play an important role in the evaluation of vaccines and therapies. They provide evidence to support the concepts defined by the Food and Drug Agency (FDA) Animal Rule [161] for licensing new medical countermeasures.

Currently the majority of studies using the “omic” and imaging techniques, described in this review, have examined the host response independently from pathogen virulence. In the future, however, due to rapid advances in NGS platform technologies and imaging technologies, it is anticipated that examining pathogen virulence whilst simultaneously interrogating host responses will be achieved. Overall, this should reduce and refine animal experiments and thus allow the identification of both host and pathogen markers during infection at the same time. This will further enhance our knowledge of host-pathogen interactions and aid in the development of vaccines and therapeutics for these dangerous pathogens.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgment

The authors would like to acknowledge Dominic Jenner (Dstl) for his contribution to this review.

References

B. A. Kidd, L. A. Peters, E. E. Schadt, and J. T. Dudley, “Unifying immunology with informatics and multiscale biology,” Nature Immunology, vol. 15, no. 2, pp. 118–127, 2014.

D. Stekel, Microarray Bioinformatics, Cambridge University Press, Cambridge, UK, 2003.

J. A. Tree, M. J. Elmore, S. Javed, A. Williams, and P. D. Marsh, “Development of a guinea pig immune response-related microarray and its use to define the host response following Mycobacterium bovis BCG vaccination,” Infection and Immunity, vol. 74, no. 2, pp. 1436–1441, 2006.

N. A. Datson, M. C. Morsink, S. Atanasova et al., “Development of the first marmoset-specific DNA microarray (EUMAMA): a new genetic tool for large-scale expression profiling in a non-human primate,” BMC Genomics, vol. 8, article 190, 2007.

K. H. Rubins, L. E. Hensley, P. B. Jahrling et al., “The host response to smallpox: analysis of the gene expression program in peripheral blood cells in a nonhuman primate model,” Proceedings of the National Academy of Sciences of the United States of America, vol. 101, no. 42, pp. 15190–15195, 2004.

R. Jain, B. Dey, and A. K. Tyagi, “Development of the first oligonucleotide microarray for global gene expression profiling in guinea pigs: defining the transcription signature of infectious diseases,” BMC Genomics, vol. 13, no. 1, article 520, 2012.

C. E. Bruder, S. Yao, F. Larson et al., “Transcriptome sequencing and development of an expression microarray platform for the domestic ferret,” BMC Genomics, vol. 11, article 251, no. 1, 2010.

K. M. Chauncey, M. C. Lopez, G. Sidhu et al., “Bacillus anthracis' lethal toxin induces broad transcriptional responses in human peripheral monocytes,” BMC Immunology, vol. 13, article 33, 2012.

M. Dozmorov, W. Wu, K. Chakrabarty et al., “Gene expression profiling of human alveolar macrophages infected by B. anthracis spores demonstrates TNF-α and NF-κb are key components of the innate immune response to the pathogen,” BMC Infectious Diseases, vol. 9, article 152, 2009.

V. Wahl-Jensen, S. Kurz, F. Feldmann et al., “Ebola virion attachment and entry into human macrophages profoundly effects early cellular gene expression,” PLoS Neglected Tropical Diseases, vol. 5, no. 10, Article ID e1359, 2011.

J. T. Schwartz, S. Bandyopadhyay, S. D. Kobayashi et al., “Francisella tularensis alters human neutrophil gene expression: insights into the molecular basis of delayed neutrophil apoptosis,” Journal of Innate Immunity, vol. 5, no. 2, pp. 124–136, 2013.

C. Paranavitana, P. R. Pittman, M. Velauthapillai, E. Zelazowska, and L. DaSilva, “Transcriptional profiling of Francisella tularensis infected peripheral blood mononuclear cells: a predictive tool for tularemia,” FEMS Immunology and Medical Microbiology, vol. 54, no. 1, pp. 92–103, 2008.

J. P. Butchar, T. J. Cremer, C. D. Clay et al., “Microarray analysis of human monocytes infected with Francisella tularensis identifies new targets of host response subversion,” PLoS ONE, vol. 3, no. 8, Article ID e2924, 2008.

K. H. Rubins, L. E. Hensley, D. A. Relman, and P. O. Brown, “Stunned silence: gene expression programs in human cells infected with monkeypox or vaccinia virus,” PLoS ONE, vol. 6, no. 1, Article ID e15615, 2011.

R. Das, A. Dhokalia, X.-Z. Huang et al., “Study of proinflammatory responses induced by Yersinia pestis in human monocytes using cDNA arrays,” Genes and Immunity, vol. 8, no. 4, pp. 308–319, 2007.

D. Bourquain, P. W. Dabrowski, and A. Nitsche, “Comparison of host cell gene expression in cowpox, monkeypox or vaccinia virus-infected cells reveals virus-specific regulation of immune response genes,” Virology Journal, vol. 10, article 61, 2013.

J. E. Comer, C. L. Galindo, F. Zhang et al., “Murine macrophage transcriptional and functional responses to Bacillus anthracis edema toxin,” Microbial Pathogenesis, vol. 41, no. 2-3, pp. 96–110, 2006.

N. H. Bergman, K. D. Passalacqua, R. Gaspard, L. M. Shetron-Rama, J. Quackenbush, and P. C. Hanna, “Murine macrophage transcriptional responses to Bacillus anthracis infection and intoxication,” Infection and Immunity, vol. 73, no. 2, pp. 1069–1080, 2005.

C. A. Rossetti, K. L. Drake, and L. G. Adams, “Transcriptome analysis of HeLa cells response to Brucella melitensis infection: a molecular approach to understand the role of the mucosal epithelium in the onset of the Brucella pathogenesis,” Microbes and Infection, vol. 14, no. 9, pp. 756–767, 2012.

J. C. Kash, E. Mühlberger, V. Carter et al., “Global suppression of the host antiviral response by Ebola- and Marburgviruses: increased antagonism of the type I interferon response is associated with enhanced virulence,” Journal of Virology, vol. 80, no. 6, pp. 3009–3020, 2006.

A. Alkhalil, R. Hammamieh, J. Hardick, M. A. Ichou, M. Jett, and S. Ibrahim, “Gene expression profiling of monkeypox virus-infected cells reveals novel interfaces for host-virus interactions,” Virology Journal, vol. 7, article 173, 2010.

P. Wongprompitak, S. Sirisinha, and S. C. Chaiyaroj, “Differential gene expression profiles of lung epithelial cells exposed to Burkholderia pseudomallei and Burkholderia thailandensis during the initial phase of infection,” Asian Pacific Journal of Allergy and Immunology, vol. 27, no. 1, pp. 59–70, 2009.

C.-Y. Chin, D. M. Monack, and S. Nathan, “Delayed activation of host innate immune pathways in streptozotocin-induced diabetic hosts leads to more severe disease during infection with Burkholderia pseudomallei,” Immunology, vol. 135, no. 4, pp. 312–332, 2012.

C.-Y. Chin, D. M. Monack, and S. Nathan, “Genome wide transcriptome profiling of a murine acute melioidosis model reveals new insights into how Burkholderia pseudomallei overcomes host innate immunity,” BMC Genomics, vol. 11, no. 1, article 672, 2010.

A. Sharma and R. K. Maheshwari, “Oligonucleotide array analysis of Toll-like receptors and associated signalling genes in Venezuelan equine encephalitis virus-infected mouse brain,” Journal of General Virology, vol. 90, no. 8, pp. 1836–1847, 2009.

A. Sharma, B. Bhattacharya, R. K. Puri, and R. K. Maheshwari, “Venezuelan equine encephalitis virus infection causes modulation of inflammatory and immune response genes in mouse brain,” BMC Genomics, vol. 9, article 289, 2008.

J. David, A. J. Gates, G. D. Griffiths, and R. A. Lukaszewski, “Gene expression following low dose inhalational Francisella tularensis (SchuS4) exposure in Balb/c mice and the potential role of the epithelium and cell adhesion,” Microbes and Infection, vol. 14, no. 4, pp. 369–379, 2012.

H. Andersson, B. Hartmanová, P. Rydén, L. Noppa, L. Näslund, and A. Sjöstedt, “A microarray analysis of the murine macrophage response to infection with Francisella tularensis LVS,” Journal of Medical Microbiology, vol. 55, no. 8, pp. 1023–1033, 2006.

K.-A. Walters, R. Olsufka, R. E. Kuestner et al., “Francisella tularensis subsp. tularensis induces a unique pulmonary inflammatory response: role of bacterial gene expression in temporal regulation of host defense responses,” PLoS ONE, vol. 8, no. 5, Article ID e62412, 2013.

H. Andersson, B. Hartmanová, R. KuoLee et al., “Transcriptional profiling of host responses in mouse lungs following aerosol infection with type A Francisella tularensis,” Journal of Medical Microbiology, vol. 55, no. 3, pp. 263–271, 2006.

C. A. Rossetti, K. L. Drake, P. Siddavatam, et al., “Systems biology analysis of brucella infected peyer's patch reveals rapid invasion with modest transient perturbations of the host transcriptome,” PLoS ONE, vol. 8, no. 12, Article ID e81719, 2013.

J. Y. Yen, S. Garamszegi, J. B. Geisbert et al., “Therapeutics of Ebola hemorrhagic fever: whole-genome transcriptional analysis of successful disease mitigation,” Journal of Infectious Diseases, vol. 204, supplement 3, pp. S1043–S1052, 2011.

D. Suwannasaen, J. Mahawantung, W. Chaowagul et al., “Human immune responses to Burkholderia pseudomallei characterized by protein microarray analysis,” Journal of Infectious Diseases, vol. 203, no. 7, pp. 1002–1011, 2011.

A. P. Cannella, J. C. Lin, L. Liang et al., “Serial kinetics of the antibody response against the complete Brucella melitensis ORFeome in focal vertebral brucellosis,” Journal of Clinical Microbiology, vol. 50, no. 3, pp. 922–926, 2012.

L. Liang, X. Tan, S. Juarez et al., “Systems biology approach predicts antibody signature associated with Brucella melitensis infection in humans,” Journal of Proteome Research, vol. 10, no. 10, pp. 4813–4824, 2011.

A. Vigil, R. Ortega, R. Nakajima-Sasaki et al., “Genome-wide profiling of humoral immune response to Coxiella burnetii infection by protein microarray,” Proteomics, vol. 10, no. 12, pp. 2259–2269, 2010.

A. Vigil, C. Chen, A. Jain et al., “Profiling the humoral immune response of acute and chronic Q fever by protein microarray,” Molecular & Cellular Proteomics, vol. 10, no. 10, 2011.

X. Xiong, X. Wang, B. Wen, S. Graves, and J. Stenos, “Potential serodiagnostic markers for Q fever identified in Coxiella burnetii by immunoproteomic and protein microarray approaches,” BMC Microbiology, vol. 12, article 35, 2012.

S. Keasey, C. Pugh, A. Tikhonov et al., “Proteomic basis of the antibody response to monkeypox virus infection examined in cynomolgus macaques and a comparison to human smallpox vaccination,” PLoS ONE, vol. 5, no. 12, Article ID e15547, 2010.

D. M. Klinman, S. Klaschik, K. Tomaru, H. Shirota, D. Tross, and H. Ikeuchi, “Immunostimulatory CpG oligonucleotides: effect on gene expression and utility as vaccine adjuvants,” Vaccine, vol. 28, no. 8, pp. 1919–1923, 2010.

S. Klaschik, I. Gursel, and D. M. Klinman, “CpG-mediated changes in gene expression in murine spleen cells identified by microarray analysis,” Molecular Immunology, vol. 44, no. 6, pp. 1095–1104, 2007.

S. Klaschik, D. Tross, and D. M. Klinman, “Inductive and suppressive networks regulate TLR9-dependent gene expression in vivo,” Journal of Leukocyte Biology, vol. 85, no. 5, pp. 788–795, 2009.

C. Paranavitana, L. DaSilva, A. Vladimirova, P. R. Pittman, M. Velauthapillai, and M. Nikolich, “Transcriptional profiling of recall responses to Francisella live vaccine strain,” Pathogens and Disease, vol. 70, no. 2, pp. 141–152, 2014.

J. E. Eyles, B. Unal, M. G. Hartley et al., “Immunodominant Francisella tularensis antigens identified using proteome microarray,” Proteomics, vol. 7, no. 13, pp. 2172–2183, 2007.

P. A. Beare, C. Chen, T. Bouman et al., “Candidate antigens for Q fever serodiagnosis revealed by immunoscreening of a Coxiella burnetii protein microarray,” Clinical and Vaccine Immunology, vol. 15, no. 12, pp. 1771–1779, 2008.

D. H. Davies, X. Liang, J. E. Hernandez et al., “Profiling the humoral immune response to infection by using proteome microarrays: high-throughput vaccine and diagnostic antigen discovery,” Proceedings of the National Academy of Sciences of the United States of America, vol. 102, no. 3, pp. 547–552, 2005.

D. H. Davies, D. M. Molina, J. Wrammert et al., “Proteome-wide analysis of the serological response to vaccinia and smallpox,” Proteomics, vol. 7, no. 10, pp. 1678–1686, 2007.

D. H. Davies, L. S. Wyatt, F. K. Newman et al., “Antibody profiling by proteome microarray reveals the immunogenicity of the attenuated smallpox vaccine modified vaccinia virus Ankara is comparable to that of Dryvax,” Journal of Virology, vol. 82, no. 2, pp. 652–663, 2008.

D. H. Davies, M. M. McCausland, C. Valdez et al., “Vaccinia virus H3L envelope protein is a major target of neutralizing antibodies in humans and elicits protection against lethal challenge in mice,” Journal of Virology, vol. 79, no. 18, pp. 11724–11733, 2005.

M. B. Townsend, M. S. Keckler, N. Patel et al., “Humoral immunity to smallpox vaccines and monkeypox virus challenge: proteomic assessment and clinical correlations,” Journal of Virology, vol. 87, no. 2, pp. 900–911, 2013.

G. Hermanson, S. Chun, J. Felgner et al., “Measurement of antibody responses to Modified Vaccinia virus Ankara (MVA) and Dryvax using proteome microarrays and development of recombinant protein ELISAs,” Vaccine, vol. 30, no. 3, pp. 614–625, 2012.

F. X. Sutandy, J. Qian, C. S. Chen, and H. Zhu, “Overview of protein microarrays,” in Current Protocols in Protein Science, chapter 27, unit 27.1, 2013.

N. Ramachandran, J. V. Raphael, E. Hainsworth et al., “Next-generation high-density self-assembling functional protein arrays,” Nature Methods, vol. 5, no. 6, pp. 535–538, 2008.

P. L. Felgner, M. A. Kayala, A. Vigil et al., “A Burkholderia pseudomallei protein microarray reveals serodiagnostic and cross-reactive antigens,” Proceedings of the National Academy of Sciences of the United States of America, vol. 106, no. 32, pp. 13499–13504, 2009.

T. W. Geisbert, H. A. Young, P. B. Jahrling, K. J. Davis, E. Kagan, and L. E. Hensley, “Mechanisms underlying coagulation abnormalities in ebola hemorrhagic fever: overexpression of tissue factor in primate monocytes/macrophages is a key event,” Journal of Infectious Diseases, vol. 188, no. 11, pp. 1618–1629, 2003.

H. Xie, I. Gursel, B. E. Ivins et al., “CpG oligodeoxynucleotides adsorbed onto polylactide-co-glycolide microparticles improve the immunogenicity and protective activity of the licensed anthrax vaccine,” Infection and Immunity, vol. 73, no. 2, pp. 828–833, 2005.

D. M. Klinman, H. Xie, and B. E. Ivins, “CpG oligonucleotides improve the protective immune response induced by the licensed anthrax vaccine,” Annals of the New York Academy of Sciences, vol. 1082, pp. 137–150, 2006.

L. Jing, S. M. McCaughey, D. H. Davies et al., “ORFeome approach to the clonal, HLA allele-specific CD4 T-cell response to a complex pathogen in humans,” Journal of Immunological Methods, vol. 347, no. 1-2, pp. 36–45, 2009.

L. Jing, J. Haas, T. M. Chong et al., “Cross-presentation and genome-wide screening reveal candidate T cells antigens for a herpes simplex virus type 1 vaccine,” Journal of Clinical Investigation, vol. 122, no. 8, p. 3024, 2012.

M. A. Quail, M. Smith, P. Coupland et al., “A tale of three next generation sequencing platforms: comparison of Ion Torrent, Pacific Biosciences and Illumina MiSeq sequencers,” BMC Genomics, vol. 13, no. 1, article 341, 2012.

M. L. Metzker, “Sequencing technologies—the next generation,” Nature Reviews Genetics, vol. 11, no. 1, pp. 31–46, 2010.

N. J. Loman, R. V. Misra, T. J. Dallman et al., “Performance comparison of benchtop high-throughput sequencing platforms,” Nature Biotechnology, vol. 30, no. 5, pp. 434–439, 2012.

R. J. Roberts, M. O. Carneiro, and M. C. Schatz, “The advantages of SMRT sequencing,” Genome Biology, vol. 14, no. 6, p. 405, 2013.

G. F. Schneider and C. Dekker, “DNA sequencing with nanopores,” Nature Biotechnology, vol. 30, no. 4, pp. 326–328, 2012.

Z. Wang, M. Gerstein, and M. Snyder, “RNA-Seq: a revolutionary tool for transcriptomics,” Nature Reviews Genetics, vol. 10, no. 1, pp. 57–63, 2009.

A. Oshlack, M. D. Robinson, and M. D. Young, “From RNA-seq reads to differential expression results,” Genome Biology, vol. 11, no. 12, article 220, 2010.

J. R. Bradford, Y. Hey, T. Yates, Y. Li, S. D. Pepper, and C. J. Miller, “A comparison of massively parallel nucleotide sequencing with oligonucleotide microarrays for global transcription profiling,” BMC Genomics, vol. 11, article 282, no. 1, 2010.

S. Kogenaru, Y. Qing, Y. Guo, and N. Wang, “RNA-seq and microarray complement each other in transcriptome profiling,” BMC Genomics, vol. 13, no. 1, article 629, 2012.

C. Soneson and M. Delorenzi, “A comparison of methods for differential expression analysis of RNA-seq data,” BMC Bioinformatics, vol. 14, article 91, 2013.

S. Zhao, W. P. Fung-Leung, A. Bittner, K. Ngo, and X. Liu, “Comparison of RNA-Seq and microarray in transcriptome profiling of activated T cells,” PLoS ONE, vol. 9, no. 1, Article ID e78644, 2014.

Z. W. Bent, M. B. Tran-Gyamfi, S. A. Langevin et al., “Enriching pathogen transcripts from infected samples: a capture-based approach to enhanced host-pathogen RNA sequencing,” Analytical Biochemistry, vol. 438, no. 1, pp. 90–96, 2013.

Z. W. Bent, D. M. Brazel, M. B. Tran-Gyamfi, R. Y. Hamblin, V. A. VanderNoot, and S. S. Branda, “Use of a capture-based pathogen transcript enrichment strategy for RNA-Seq analysis of the Francisella Tularensis LVS transcriptome during infection of murine macrophages,” PLoS ONE, vol. 8, no. 10, Article ID e77834, 2013.

Y. Yan, S. Su, X. Meng, et al., “Determination of sRNA expressions by RNA-seq in Yersinia pestis grown in vitro and during infection,” PLoS ONE, vol. 8, no. 9, Article ID e74495, 2013.

F. Wang, S. Hu, W. Liu, Z. Qiao, Y. Gao, and Z. Bu, “Deep-sequencing analysis of the mouse transcriptome response to infection with brucella melitensis strains of differing virulence,” PLoS ONE, vol. 6, no. 12, Article ID e28485, 2011.

K. Zheng, D.-S. Chen, Y.-Q. Wu et al., “MicroRNA expression profile in RAW264.7 cells in response to Brucella melitensis infection,” International Journal of Biological Sciences, vol. 8, no. 7, pp. 1013–1022, 2012.

O. M. Sessions, Y. Tan, K. C. Goh et al., “Host cell transcriptome profile during wild-type and attenuated dengue virus infection,” PLoS Neglected Tropical Diseases, vol. 7, no. 3, Article ID e2107, 2013.

A. J. Westermann, S. A. Gorski, and J. Vogel, “Dual RNA-seq of pathogen and host,” Nature Reviews Microbiology, vol. 10, no. 9, pp. 618–630, 2012.

G. Xu, E. K. Flemington, C. M. Taylor, et al., “RNA CoMPASS: a dual approach for pathogen and host transcriptome analysis of RNA-seq datasets,” PLoS ONE, vol. 9, no. 2, Article ID e89445, 2014.

Z. Yang, D. P. Bruno, C. A. Martens, S. F. Porcella, and B. Moss, “Simultaneous high-resolution analysis of vaccinia virus and host cell transcriptomes by deep RNA sequencing,” Proceedings of the National Academy of Sciences of the United States of America, vol. 107, no. 25, pp. 11513–11518, 2010.

M. S. Humphrys, T. Creasy, Y. Sun, et al., “Simultaneous transcriptional profiling of bacteria and their host cells,” PLoS ONE, vol. 8, Article ID e80597, 2013.

R. B. Kennedy, A. L. Oberg, I. G. Ovsyannikova, I. H. Haralambieva, D. Grill, and G. A. Poland, “Transcriptomic profiles of high and low antibody responders to smallpox vaccine,” Genes and Immunity, vol. 14, no. 5, pp. 277–285, 2013.

H. Robins, “Immunosequencing: applications of immune repertoire deep sequencing,” Current Opinion in Immunology, vol. 25, no. 5, pp. 646–652, 2013.

A. Six, M. E. Mariotti-Ferrandiz, W. Chaara, et al., “The past, present, and future of immune repertoire biology—the rise of next-generation repertoire analysis,” Frontiers in Immunology, vol. 4, p. 413, 2013.

G. Georgiou, G. C. Ippolito, J. Beausang, et al., “The promise and challenge of high-throughput sequencing of the antibody repertoire,” Nature Biotechnology, vol. 32, no. 2, pp. 158–168, 2014.

P. D. Baum, V. Venturi, and D. A. Price, “Wrestling with the repertoire: The promise and perils of next generation sequencing for antigen receptors,” European Journal of Immunology, vol. 42, no. 11, pp. 2834–2839, 2012.

J. Benichou, R. Ben-Hamo, Y. Louzoun, and S. Efroni, “Rep-Seq:uncovering the immunological repertoire through next-generation sequencing,” Immunology, vol. 135, no. 3, pp. 183–191, 2012.

P. Parameswaran, Y. Liu, K. M. Roskin et al., “Convergent antibody signatures in human dengue,” Cell Host & Microbe, vol. 13, no. 6, pp. 691–700, 2013.

J. D. Galson, A. J. Pollardemail, J. Trück, and D. F. Kelly, “Studying the antibody repertoire after vaccination: practical applications,” Trends in Immunology, vol. 35, no. 7, pp. 319–331, 2014.

J. A. Edwards, D. Rockx-Brouwer, V. Nair, and J. Celli, “Restricted cytosolic growth of Francisella tularensis subsp. tularensis by IFN-γ activation of macrophages,” Microbiology, vol. 156, no. 2, pp. 327–339, 2010.

A. M. Balagopal, A. S. MacFarlane, N. Mohapatra, S. Soni, J. S. Gunn, and L. S. Schlesinger, “Characterization of the receptor-ligand pathways important for entry and survival of Francisella tularensis in human macrophages,” Infection and Immunity, vol. 74, no. 9, pp. 5114–5125, 2006.

R. Copin, M. A. Vitry, D. Hanot Mambres et al., “In situ microscopy analysis reveals local innate immune response developed around Brucella infected cells in resistant and susceptible mice,” PLoS Pathogens, vol. 8, no. 3, Article ID e1002575, 2012.

R. A. Lukaszewski, D. J. Kenny, R. Taylor, D. G. C. Rees, M. G. Hartley, and P. C. F. Oyston, “Pathogenesis of Yersinia pestis infection in BALB/c mice: effects on host macrophages and neutrophils,” Infection and Immunity, vol. 73, no. 11, pp. 7142–7150, 2005.

T. R. Laws, M. S. Davey, R. W. Titball, and R. Lukaszewski, “Neutrophils are important in early control of lung infection by Yersinia pestis,” Microbes and Infection, vol. 12, no. 4, pp. 331–335, 2010.

R. D. Pechous, V. Sivaraman, P. A. Price, N. M. Stasulli, and W. E. Goldman, “Early host cell targets of Yersinia pestis during primary pneumonic plague,” PLoS Pathogens, vol. 9, no. 10, Article ID e1003679, 2013.

C. M. G. Bosio, A. W. Goodyear, and S. W. Dow, “Early interaction of Yersinia pestis with APCs in the lung,” The Journal of Immunology, vol. 175, no. 10, pp. 6750–6756, 2005.

C. F. Bosio, C. O. Jarrett, D. Gardner, and B. J. Hinnebusch, “Kinetics of innate immune response to Yersinia pestis after intradermal infection in a mouse model,” Infection and Immunity, vol. 80, no. 11, pp. 4034–4045, 2012.

T. R. Laws, S. J. Smither, R. A. Lukaszewski, and H. S. Atkins, “Neutrophils are the predominant cell-type to associate with Burkholderia pseudomallei in a BALB/c mouse model of respiratory melioidosis,” Microbial Pathogenesis, vol. 51, no. 6, pp. 471–475, 2011.

C. A. Rowland, M. S. Lever, K. F. Griffin, G. J. Bancroft, and R. A. Lukaszewski, “Protective cellular responses to Burkholderia mallei infection,” Microbes and Infection, vol. 12, no. 11, pp. 846–853, 2010.

S. Chanchamroen, C. Kewcharoenwong, W. Susaengrat, M. Ato, and G. Lertmemongkolchai, “Human polymorphonuclear neutrophil responses to Burkholderia pseudomallei in healthy and diabetic subjects,” Infection and Immunity, vol. 77, no. 1, pp. 456–463, 2009.

B. M. Judy, K. Taylor, A. Deeraksa et al., “Prophylactic application of CpG oligonucleotides augments the early host response and confers protection in acute melioidosis,” PLoS ONE, vol. 7, no. 3, Article ID e34176, 2012.

T. R. Laws, “In vivo Manipulation of γ9⁺ T cells in the common marmoset (Callithrix Jacchus) with phosphoantigen and effect on the progression of respiratory melioidosis,” PLoS ONE, vol. 8, no. 9, Article ID e74789, 2013.

J. A. Skyberg, M. F. Rollins, J. S. Holderness et al., “Nasal acai polysaccharides potentiate innate immunity to protect against pulmonary Francisella tularensis and Burkholderia pseudomallei infections,” PLoS Pathogens, vol. 8, no. 3, Article ID e1002587, 2012.

K. L. Propst, R. M. Troyer, L. M. Kellihan, H. P. Schweizer, and S. W. Dow, “Immunotherapy markedly increases the effectiveness of antimicrobial therapy for treatment of Burkholderia pseudomallei infection,” Antimicrobial Agents and Chemotherapy, vol. 54, no. 5, pp. 1785–1792, 2010.

R. V. D'Elia, T. R. Laws, A. Carter, R. Lukaszewski, and G. C. Clark, “Targeting the “rising DAMP” during a Francisella tularensis infection,” Antimicrobial Agents and Chemotherapy, vol. 57, no. 9, pp. 4222–4228, 2013.

A. Easton, K. Chu, N. Patel et al., “Combining vaccination and postexposure CpG therapy provides optimal protection against lethal sepsis in a biodefense model of human melioidosis,” Journal of Infectious Diseases, vol. 204, no. 4, pp. 636–644, 2011.

A. Haque, K. Chu, A. Easton et al., “A live experimental vaccine against Burkholderia pseudomallei elicits CD4+ T cell-mediated immunity, priming T cells specific for 2 type III secretion system proteins,” Journal of Infectious Diseases, vol. 194, no. 9, pp. 1241–1248, 2006.

D. M. Schmitt, D. M. O'Dee, J. Horzempa et al., “A Francisella tularensis live vaccine strain that improves stimulation of antigen-presenting cells does not enhance vaccine efficacy,” PLoS ONE, vol. 7, no. 2, Article ID e31172, 2012.

Q. Jia, R. Bowen, J. Sahakian, B. J. Dillon, and M. A. Horwitz, “A heterologous prime-boost vaccination strategy comprising the Francisella tularensis live vaccine strain capB mutant and recombinant attenuated Listeria monocytogenes expressing F. tularensis IglC induces potent protective immunity in mice against virulent F. tularensis aerosol challenge,” Infection and Immunity, vol. 81, no. 5, pp. 1550–1561, 2013.

G. C. Whitlock, R. A. Lukaszewski, B. M. Judy, S. Paessler, A. G. Torres, and D. M. Estes, “Host immunity in the protective response to vaccination with heat-killed Burkholderia mallei,” BMC Immunology, vol. 9, article 55, 2008.

G. J. Hatch, V. A. Graham, K. R. Bewley et al., “Assessment of the protective effect of imvamune and Acam2000 vaccines against aerosolized monkeypox virus in cynomolgus macaques,” Journal of Virology, vol. 87, no. 14, pp. 7805–7815, 2013.

K. Eneslätt, M. Normark, R. Björk et al., “Signatures of T cells as correlates of immunity to Francisella tularensis,” PLoS ONE, vol. 7, no. 3, Article ID e32367, 2012.

A. Sjöstedt, M. Eriksson, G. Sandström, and A. Tärnvik, “Various membrane proteins of Francisella tularensis induce interferon-γ production in both CD4+ and CD8+ T cells of primed humans,” Immunology, vol. 76, no. 4, pp. 584–592, 1992.

A. Tarnvik, M. L. Lofgren, S. Lofgren, G. Sandström, and H. Wolf-Watz, “Long-lasting cell-mediated immunity induced by a live Francisella tularensis vaccine,” Journal of Clinical Microbiology, vol. 22, no. 4, pp. 527–530, 1985.

E. D. Williamson, H. C. Flick-Smith, C. LeButt et al., “Human immune response to a plague vaccine comprising recombinant F1 and V antigens,” Infection and Immunity, vol. 73, no. 6, pp. 3598–3608, 2005.

R. Ali, R. A. Naqvi, S. Kumar, A. A. Bhat, and D. N. Rao, “Multiple Antigen Peptide Containing B and T Cell Epitopes of F1 Antigen of Yersinia pestis Showed Enhanced Th1 Immune Response in Murine Model,” Scandinavian Journal of Immunology, vol. 77, no. 5, pp. 361–371, 2013.

P. P. Tippayawat, M. Pinsiri, D. Rinchai et al., “Burkholderia pseudomallei proteins presented by monocyte-derived dendritic cells stimulate human memory T cells in vitro,” Infection and Immunity, vol. 79, no. 1, pp. 305–313, 2011.

E. B. Silva, A. Goodyear, M. D. Sutherland, et al., “Correlates of immune protection following cutaneous immunization with an attenuated Burkholderia pseudomallei vaccine,” Infection and Immunity, vol. 81, no. 12, pp. 4626–4634, 2013.

N. Kurosawa, M. Yoshioka, R. Fujimoto, F. Yamagishi, and M. Isobe, “Rapid production of antigen-specific monoclonal antibodies from a variety of animals,” BMC Biology, vol. 10, p. 80, 2012.

M. M. Coughlin and B. S. Prabhakar, “Neutralizing human monoclonal antibodies to severe acute respiratory syndrome coronavirus: target, mechanism of action, and therapeutic potential,” Reviews in Medical Virology, vol. 22, no. 1, pp. 2–17, 2012.

B. L. Marrone, “Flow cytometry: a multipurpose technology for a wide spectrum of global biosecurity applications,” Journal of the Association for Laboratory Automation, vol. 14, no. 3, pp. 148–156, 2009.

M. Santic, R. Asare, I. Skrobonja, S. Jones, and Y. A. Kwaik, “Acquisition of the vacuolar ATPase proton pump and phagosome acidification are essential for escape of Francisella tularensis into the macrophage cytosol,” Infection and Immunity, vol. 76, no. 6, pp. 2671–2677, 2008.

J. T. Schwartz, J. H. Barker, M. E. Long, J. Kaufman, J. McCracken, and L.-A. H. Allen, “Natural IgM mediates complement-dependent uptake of Francisella tularensis by human neutrophils via complement receptors 1 and 3 in nonimmune serum,” The Journal of Immunology, vol. 189, no. 6, pp. 3064–3077, 2012.

S. Dai, M. V. S. Rajaram, H. M. Curry, R. Leander, and L. S. Schlesinger, “Fine Tuning Inflammation at the Front Door: Macrophage Complement Receptor 3-mediates Phagocytosis and Immune Suppression for Francisella tularensis,” PLoS Pathogens, vol. 9, no. 1, Article ID e1003114, 2013.

D. L. Clemens, B.-Y. Lee, and M. A. Horwitz, “Francisella tularensis phagosomal escape does not require acidification of the phagosome,” Infection and Immunity, vol. 77, no. 5, pp. 1757–1773, 2009.

M. N. Burtnick, D. DeShazer, V. Nair, F. C. Gherardini, and P. J. Brett, “Burkholderia mallei cluster 1 type VI secretion mutants exhibit growth and actin polymerization defects in RAW 264.7 murine macrophages,” Infection and Immunity, vol. 78, no. 1, pp. 88–99, 2010.

D. L. Clemens, B.-Y. Lee, and M. A. Horwitz, “O-antigen-deficient francisella tularensis live vaccine strain mutants are ingested via an aberrant form of looping phagocytosis and show altered kinetics of intracellular trafficking in human macrophages,” Infection and Immunity, vol. 80, no. 3, pp. 952–967, 2012.

M. Cullinane, L. Gong, X. Li et al., “Stimulation of autophagy suppresses the intracellular survival of Burkholderia pseudomallei in mammalian cell lines,” Autophagy, vol. 4, no. 6, pp. 744–753, 2008.

S. Steele, J. Brunton, B. Ziehr, S. Taft-Benz, N. Moorman, and T. Kawula, “Francisella tularensis Harvests Nutrients Derived via ATG5-Independent Autophagy to Support Intracellular Growth,” PLoS Pathogens, vol. 9, no. 8, Article ID e1003562, 2013.

H.-C. Chiu, S. Soni, S. K. Kulp et al., “Eradication of intracellular Francisella tularensis in THP-1 human macrophages with a novel autophagy inducing agent,” Journal of Biomedical Science, vol. 16, article 110, no. 1, 2009.

M. Aguilera, R. Salinas, E. Rosales, S. Carminati, M. I. Colombo, and W. Berón, “Actin dynamics and Rho GTPases regulate the size and formation of parasitophorous vacuoles containing Coxiella burnetii,” Infection and Immunity, vol. 77, no. 10, pp. 4609–4620, 2009.

G. Pegoraro, B. P. Eaton, R. L. Ulrich, et al., “A high-content imaging assay for the quantification of the Burkholderia pseudomallei induced multinucleated giant cell (MNGC) phenotype in murine macrophages,” BMC Microbiology, vol. 14, p. 98, 2014.

C. J. Empig and M. A. Goldsmith, “Association of the caveola vesicular system with cellular entry by filoviruses,” Journal of Virology, vol. 76, no. 10, pp. 5266–5270, 2002.

E. Adu-Gyamfi, M. A. Digman, E. Gratton, and R. V. Stahelin, “Investigation of Ebola VP40 assembly and oligomerization in live cells using number and brightness analysis,” Biophysical Journal, vol. 102, no. 11, pp. 2517–2525, 2012.

M. Trunschke, D. Conrad, S. Enterlein, J. Olejnik, K. Brauburger, and E. Mühlberger, “The L-VP35 and L-L interaction domains reside in the amino terminus of the Ebola virus L protein and are potential targets for antivirals,” Virology, vol. 441, no. 2, pp. 135–145, 2013.

W. D. Splettstoesser, E. Seibold, E. Zeman, K. Trebesius, and A. Podbielski, “Rapid differentiation of Francisella species and subspecies by fluorescent in situ hybridization targeting the 23S rRNA,” BMC Microbiology, vol. 10, article 72, 2010.

X. Xiao, Z. Zhu, J. L. Dankmeyer et al., “Human anti-plague monoclonal antibodies protect mice from Yersinia pestis in a bubonic plague model,” PLoS ONE, vol. 5, no. 10, Article ID e13047, 2010.

J. G. H. Shannon, A. M. Dorward, D. W. Nair, V. Carmody, A. B. Hinnebusch, and B. J. Yersinia pestis, “Yersinia pestis subverts the dermal neutrophil response in a mouse model of bubonic plague,” mBio, vol. 4, no. 5, p. e00170, 2013.

N. Andreu, A. Zelmer, and S. Wiles, “Noninvasive biophotonic imaging for studies of infectious disease,” FEMS Microbiology Reviews, vol. 35, no. 2, pp. 360–394, 2011.

P. Sanz, L. D. Teel, F. Alem, H. M. Carvalho, S. C. Darnell, and A. D. O'Brien, “Detection of Bacillus anthracis spore germination in vivo by bioluminescence imaging,” Infection and Immunity, vol. 76, no. 3, pp. 1036–1047, 2008.

I. J. Glomski, F. Dumetz, G. Jouvion, M. R. Huerre, M. Mock, and P. L. Goossens, “Inhaled non-capsulated Bacillus anthracis in A/J mice: nasopharynx and alveolar space as dual portals of entry, delayed dissemination, and specific organ targeting,” Microbes and Infection, vol. 10, no. 12-13, pp. 1398–1404, 2008.

I. J. Glomski, J.-P. Corre, M. Mock, and P. L. Goossens, “Noncapsulated toxinogenic Bacillus anthracis presents a specific growth and dissemination pattern in naive and protective antigen-immune mice,” Infection and Immunity, vol. 75, no. 10, pp. 4754–4761, 2007.

T. Nham, S. Filali, C. Danne, A. Derbise, and E. Carniel, “Imaging of bubonic plague dynamics by in vivo tracking of bioluminescent yersinia pestis,” PLoS ONE, vol. 7, no. 4, Article ID e34714, 2012.

R. J. Gonzalez, E. H. Weening, R. Frothingham, G. D. Sempowski, and V. L. Miller, “Bioluminescence imaging to track bacterial dissemination of Yersinia pestis using different routes of infection in mice,” BMC Microbiology, vol. 12, article 147, 2012.

Y. Sun, M. G. Connor, J. M. Pennington, and M. B. Lawrenz, “Development of bioluminescent bioreporters for in vitro and in vivo tracking of Yersinia pestis,” PLoS ONE, vol. 7, no. 10, Article ID e47123, 2012.

J. Sha, J. A. Rosenzweig, M. L. Kirtley et al., “A non-invasive in vivo imaging system to study dissemination of bioluminescent Yersinia pestis CO92 in a mouse model of pneumonic plague,” Microbial Pathogenesis, vol. 55, no. 1, pp. 39–50, 2013.

X. R. Bina, M. A. Miller, and J. E. Bina, “Construction of a bioluminescence reporter plasmid for Francisella tularensis,” Plasmid, vol. 64, no. 3, pp. 156–161, 2010.

M. A. Miller, J. M. Stabenow, J. Parvathareddy et al., “Visualization of murine intranasal dosing efficiency using luminescent Francisella tularensis: effect of instillation volume and form of anesthesia,” PLoS ONE, vol. 7, no. 2, Article ID e31359, 2012.

J. M. Warawa, D. Long, R. Rosenke, D. Gardner, and F. C. Gherardini, “Bioluminescent diagnostic imaging to characterize altered respiratory tract colonization by the Burkholderia pseudomallei capsule mutant,” Frontiers in Microbiology, vol. 2, article 133, 2011.

S. J. Owen, M. Batzloff, F. Chehrehasa et al., “Nasal-associated lymphoid tissue and olfactory epithelium as portals of entry for burkholderia pseudomallei in murine melioidosis,” Journal of Infectious Diseases, vol. 199, no. 12, pp. 1761–1770, 2009.

S. Massey, K. Johnston, T. M. Mott et al., “In vivo bioluminescence imaging of burkholderia mallei respiratory infection and treatment in the mouse model,” Frontiers in Microbiology, vol. 2, article 174, 2011.

T. M. Mott, R. Katie Johnston, S. Vijayakumar et al., “Monitoring therapeutic treatments against infections using imaging techniques,” Pathogens, vol. 2, no. 2, pp. 383–401, 2013.

D. M. Waag, M. J. McCluskie, N. Zhang, and A. M. Krieg, “A CpG oligonucleotide can protect mice from a low aerosol challenge dose of Burkholderia mallei,” Infection and Immunity, vol. 74, no. 3, pp. 1944–1948, 2006.

F. Dumetz, G. Jouvion, H. Khun et al., “Noninvasive imaging technologies reveal edema toxin as a key virulence factor in anthrax,” The American Journal of Pathology, vol. 178, no. 6, pp. 2523–2535, 2011.

S. E. Autenrieth, P. Warnke, G. H. Wabnitz et al., “Depletion of dendritic cells enhances innate anti-bacterial host defense through modulation of phagocyte homeostasis,” PLoS Pathogens, vol. 8, no. 2, Article ID e1002552, 2012.

I. Safeukui, P. A. Buffet, S. Perrot et al., “Surface area loss and increased sphericity account for the splenic entrapment of subpopulations of Plasmodium falciparum ring-infected erythrocytes,” PLoS ONE, vol. 8, no. 3, Article ID e60150, 2013.

P.-Y. Mantel, A. N. Hoang, I. Goldowitz et al., “Malaria-infected erythrocyte-derived microvesicles mediate cellular communication within the parasite population and with the host immune system,” Cell Host & Microbe, vol. 13, no. 5, pp. 521–534, 2013.

S. N. Bartley, Y.-L. Tzeng, K. Heel et al., “Attachment and invasion of neisseria meningitidis to host cells is related to surface hydrophobicity, bacterial cell size and capsule,” PLoS ONE, vol. 8, no. 2, Article ID e55798, 2013.

E. A. Durand, F. J. Maldonado-Arocho, C. Castillo, R. L. Walsh, and J. Mecsas, “The presence of professional phagocytes dictates the number of host cells targeted for Yop translocation during infection,” Cellular Microbiology, vol. 12, no. 8, pp. 1064–1082, 2010.

J. Dyall, R. F. Johnson, D.-Y. Chen et al., “Evaluation of monkeypox disease progression by molecular imaging,” Journal of Infectious Diseases, vol. 204, no. 12, pp. 1902–1911, 2011.

K. Li, D. Thomasson, L. Ketai et al., “Potential applications of conventional and molecular imaging to biodefense research,” Clinical Infectious Diseases, vol. 40, no. 10, pp. 1471–1480, 2005.

H. H. S. Food and Drug Administration, “New drug and biological drug products; evidence needed to demonstrate effectiveness of new drugs when human efficacy studies are not ethical or feasible. Final rule,” Federal Register, vol. 67, no. 105, pp. 37988–37998, 2002.