International Journal of MicrobiologyVolume 2012 (2012), Article ID 268123, 5 pagesdoi:10.1155/2012/268123

Review Article

Histoplasma Virulence and Host Responses

Mircea Radu Mihu¹ and Joshua Daniel Nosanchuk²

¹Department of Medicine, Sound Shore Medical Center of Westchester, New Rochelle, NY 10802, USA²Division of Infectious Diseases, Departments of Medicine and Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY 10461, USA

Received 12 July 2011; Accepted 9 August 2011

Academic Editor: Julian R. Naglik

Copyright © 2012 Mircea Radu Mihu and Joshua Daniel Nosanchuk. 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.

Histoplasma capsulatum is the most prevalent cause of fungal respiratory disease. The disease extent and outcomes are the result of the complex interaction between the pathogen and a host's immune system. The focus of our paper consists in presenting the current knowledge regarding the multiple facets of the dynamic host-pathogen relationship in the context of the virulence arsenal displayed by the fungus and the innate and adaptive immune responses of the host.

1. Introduction

Histoplasmosis was first described in 1906 by Darling among the workers of the Panama Canal [1], and it is currently the most common cause of fungal respiratory disease with almost 500,000 individuals acquiring the fungus each year [2]. The etiologic agent responsible for histoplasmosis is Histoplasma capsulatum, a thermally dimorphic fungus with worldwide distribution. The fungus is primarily found in soil, where it exists in a mycelia form. In the United States, highly endemic areas include regions along the Mississippi and Ohio River valleys, where seroprevalence studies have shown that up to 80% of individuals are skin test positive for histoplasmin [3].

The entry portal of H. capsulatum is through inhalation of aerosolized of 2–4 μm diameter microconidia [4]. Morphogenesis is initiated after infection with the conidia developing into a 2–4 μm oval yeast form. The fungus is rapidly ingested by macrophages and neutrophils, but manages to avoid intracellular destruction. Intracellular yeast can be transported diffusely via the lymphatics and into the bloodstream. Nevertheless, initial infection is typically contained by innate and adaptive host responses. In immunocompetent individuals, the pulmonary disease is usually subclinical to limited, typically with flu-like symptoms, including fever, cough, headaches, and myalgias. However, lethal disease can occur in otherwise healthy individuals who acquire a large inoculum infection. Additionally, severe primary infection is more common and reactivation of latent infection occurs in immunocompromised persons, particularly in HIV-infected population and transplant recipients. Disseminated disease occurs in a small fraction of infected individuals, but this form of histoplasmosis continues to carry a high fatality rate even in patients receiving appropriate medical treatment [5]. More recently, treatments with inhibitors of tumor necrosis factor-α have been shown to place patients at high risk for developing histoplasmosis [6].

2. H. capsulatum Virulence Factors

The characterized virulence determinants of H. capsulatum are mainly surface expressed molecules that mediate the interaction between the fungus and the host’s immune cells allowing the pathogen to evade destruction by innate immune response and facilitate the replication of the yeast in its new environment.

Heat shock protein 60 (HSP60), which has important roles in chaperoning intracellular proteins and supervising adequate protein folding, has also recently been described as an essential surface molecule, mediating the recognition and phagocytosis of the yeast by macrophages [7]. It acts as a ligand for CD11/CD18 macrophage receptor and, despite low number of antigenic sites, the coupling with the CR3 receptor is followed by rapid ingestion of the yeast. The interaction between Histoplasma and macrophage through HSP60 binding to CR3 results only in a mild host immune reaction, as it does not lead to a significant activation of phagocytes in the absence of other costimulatory signals [8]. This process allows the microorganism to survive and replicate inside the host cells [9, 10].

Heat shock protein 82 (HSP82) is another important molecule in normal development of H. capsulatum that also participates in the response to cellular stresses; it binds to a variety of cellular proteins, keeping them inactive until they have reached their proper intracellular location or have received the proper activation signal [11]. The role of HSP82 is further complicated by the thermal dimorphism displayed by Histoplasma, since changes in temperature represent both a stress inducer and a signal for yeast phase transformation. Recently, Edwards et al. demonstrated that a reduction in HSP82 decreases Histoplasma virulence in macrophages and severely impairs the fungus’ ability to infect lungs in a murine infection model [12]. This suggests that a low basal level of HSP82 expression is sufficient only to preserve cellular functions at mammalian body temperature, but not to withstand other stresses encountered during infection. The temperature values during febrile episodes in the host, for example, represent one stress that requires HSP82 function, and defective mutant strains show a decreased ability to recover from transient in vitro incubation at 40°C. However, even at 37°C these defective mutants showed decreased virulence within macrophages, despite having identical growth in culture at similar temperature; this implies that HSP82 extends its role to enduring additional, nonthermal stresses during host infection. One example is the ability to survive oxidative stress, as shown by peroxide challenge studies [12].

YPS3 is a yeast phase-specific gene encountered in a subset of H. capsulatum strains. The encoded protein is found both as a fungal cell wall constituent and as a secreted molecule [13]. The exact function of this gene remains to be determined, but its importance in virulence is a certainty, since YPS3 mutants are attenuated in vivo [14].

The production of cell wall melanin is associated with virulence for diverse fungi; H. capsulatum conidia and yeast produce melanin or melanin-like pigments in vitro and yeast cells are melanized during mammalian infections [15]. The melanization process decreases the susceptibility of the fungus to amphotericin B and caspofungin and melanin can abrogate the potency of certain host defense mechanisms, such as free radicals and microbicidal peptides [16, 17].

Calcium-binding protein (CBP) represents another important factor in Histoplasma pathogenicity. CBP is secreted by the fungal cells during the yeast-phase of intracellular growth within the macrophage [18], and its importance for the virulence of the fungus was demonstrated both in vitro and in vivo. For example, CBP1 gene deletion yeast cells were rapidly cleared from the lungs of infected mice. Additionally, H. capsulatum growth is inhibited in limiting calcium conditions [19]. One of the hypotheses is that calcium acquisition represents an important factor for intracellular survival of the microorganism; another hypothesis targets the modulating effect of CBP in binding calcium to facilitate optimal phagolysosomal conditions for yeast growth.

Many H. capsulatum strains express α-(1,3)-glucan on their yeast cell surface. This polysaccharide forms a layer that conceals cell surface β glucans, which have antigenic properties, eluding the identification by the host phagocytic cells. The β glucan found in the cell wall of Histoplasma and other fungi is recognized by the Dectin-1 receptor on macrophages resulting in the triggered formation of reactive oxygen species and secretion of proinflammatory cytokines [20]. Confirmatory evidence for the role of the α-glucan was obtained using Ags-1-deficient Histoplasma mutant strains, where yeasts lacking the cell wall α-(1,3)-glucan were attenuated for virulence [21].

Histone 2B (H2B) has also been found to play a role in pathogenesis [22]. Histones are mainly intracellular components, but a study investigating passive immunity through administration of monoclonal antibodies from mice immunized with Histoplasma revealed antibody recognition of H2B present on the cell wall. The means by which historically intracellular-based molecules, as HSP60 or H2B, reach the yeast cell wall where they can interact with host cells was unclear until recently when macromolecular transport to the extracellular space was demonstrated to occur via vesicular secretion and active vesicular transport [23, 24].

Hydroxamate siderophores production by Histoplasma is another newly characterized virulence factor. Strains defective for the gene coding for siderophore production display impaired intracellular growth in both human and murine macrophages, which can be reversed by either exogenous iron addition or restoration of SID1 expression [25, 26].

3. Host Defense Mechanisms

After being exposed to Histoplasma, the host relies on both innate and adaptive immune response mechanisms to neutralize the pathogen and withstand infection. Macrophages and dendritic cells have major roles in the activation of cellular pathways, and the numerous cytokines, especially IFN-γ and TNF-α, significantly impact host responses.

Macrophages have a central role in the interaction between the fungus and the host, although their contribution has a dual nature. They represent the first line of defense during infection with H. capsulatum, as they rapidly phagocytose the inhaled conidia and transforming yeast cells, and the infected macrophage subsequently activate effector T cells and enhance the release of Th1-associated proinflammatory cytokines (IL-12, IFN-γ, and TNF-α) [27, 28]. Deprivation of zinc and iron is amongst the means used by macrophages to neutralize the intruding pathogen [29], along with production of superoxide, nitric oxide, and lysosomal hydrolysis. However, the fungus displays various mechanisms to elude destruction after phagocytosis. For example, H. capsulatum yeast cells are able to regulate the pH of the phagolysosomes at a neutral pH (approximately pH 6.5), where lysosomal hydrolases have decreased activity. Hence, the H. capsulatum yeast cells manage to survive and even replicate inside macrophages [30].

Dendritic cells are also an important effector of the innate immunity. They are able to phagocytose and degrade the fungal cells with higher efficacy than macrophages, which might be due to recognition of the pathogen via a different type of receptor (fibronectin receptor on dendritic cells versus CD18 on macrophages) [31]. Dendritic cells also are extremely efficient at processing and presenting antigens to specific CD8 T cells, either following ingestion of the yeast, or through “cross presentation” of fungal antigens engulfed from infected apoptotic macrophages [32]. In a recent study, the addition of antigen-presenting dendritic cells was found to suppress excessive production of IL-4 by CD4 T cells in lungs of CCR2-deficient mice infected with H. capsulatum, demonstrating the importance of these cells in the regulation of immune responses [33].

Cellular immunity is crucial in the host defense against intracellular pathogens; therefore, T cells, as the central effectors of the cellular immunity, have a substantial role in neutralizing H. capsulatum yeast cells. Mice depleted of both CD4 and CD8 T cells have accelerated time to death after challenge with H. capsulatum yeast cells, especially in a primary histoplasmosis model, which underlines the importance of the interaction between the two cell subsets in withstanding Histoplasma infection by eliciting a Th1 response [34]. CD4 cell depletion is associated with survival during primary infection, as a result of impaired IFN-γ production. The elimination of CD8 T cells results in decreased clearance of yeast cells in primary but not secondary infection. One particular subpopulation of T cells, Vβ4⁺ T cells, is preferentially expended during infection with H. capsulatum, and elimination of these cells from mice impairs their ability to resolve infection [35]. Th17 T cells and their interaction with regulatory T cells have recently been linked via the chemoattractant mediator CCR5 to the host’s ability to effectively combat H. capsulatum infection; increases in Th17 cytokines and reductions in the number of regulatory T cells were associated with accelerated fungal clearance in CCR5-deficient animals [36].

Although cytokine responses are complex in histoplasmosis and alter over the course of disease, the main cytokines involved in Histoplasma clearance from the host are IL-12, IFN-γ, and TNF-α [34]. IL-12 through its ability to regulate IFN-γ production is critical in inducing a protective immune response in primary infection with the pathogen. IFN-γ is pivotal for the host's innate resistance to systemic infection with H. capsulatum. Survival of mice is significantly reduced in IFN-γ-deficient mice as well as in wild-type mice treated with neutralizing antibody to IFN-γ [37]. Patients with impaired IFN-γ signaling due to genetic defects are at increased risk for severe disease forms and administration of the cytokine can be therapeutic. For example, a report of recurrent disseminated H. capsulatum osteomyelitis in a patient with genetic IFN-γ receptor 1 deficiency describes progressive clearing of all bone lesions and normalization of inflammatory markers following subcutaneous therapy with IFN-γ [38]. Although IFN-γ is critical in primary infection, survival in secondary infection can be achieved in the absence of IFN-γ, as immunization of IFN-γ-deficient mice with an initial sublethal inoculum can prolong the survival of these mice when subsequently challenged with a high concentration of H. capsulatum yeast cells [39]. The major mechanism by which these mice were able to control secondary infection was through increased production of TNF-α.

TNF-α is a key modulator of disease in both primary and secondary histoplasmosis, though different protective mechanisms are involved in these conditions [34, 40]. In primary infection, decreased survival of TNF-α-deficient mice has been attributed to an impaired ability to generate reactive nitrogen intermediates in the alveolar macrophages, although inducible nitric oxide synthase expression in lung tissue is preserved. During secondary infection, the increased mortality is largely due to a biased host reaction to a Th2-type response that is associated with elevated levels of both IL-4 and IL-10. These findings parallel the clinical data that clearly demonstrates that therapy with TNF-α inhibitors poses a significant increased risk for reactivation of latent histoplasmosis with a greater likelihood of severe, disseminated disease [8].

Humoral immune responses generally have a limited role in the clearance of intracellular pathogens; however, the protective role of antibodies against surface molecules of H. capsulatum has been described. Administration of monoclonal antibodies to Histoplasma H2B reduces fungal burden, decreases pulmonary inflammation, and prolongs survival in murine infection models [22]. The protective response was associated with increased levels of IL-4, IL-6, and IFN-γ. Similarly, antibodies to H. capsulatum HSP60 prolong the survival of the lethally infected animals [41, 42].

4. Discussion

Histoplasmosis is the most common endemic dimorphic fungal pathogen of man. The continuously expanding population of immunocompromised patients, secondary to the ongoing HIV epidemic, the increasing use of immunosuppressant therapies and rising number of transplant recipients, represents a high risk cohort for histoplasmosis. The mortality rate associated with invasive histoplasmosis is still unacceptably high, despite the use of broad spectrum antifungal agents, which emphasizes the need for developing novel therapies and effective preventive strategies.

As outlined in this paper, targeting virulence determinants of H. capsulatum and attempts to modify the capacity of the host to respond to the fungal invader are actively being pursued by researchers. Recent studies investigating the capacity of H. capsulatum to release a large number of proteins and other immunologically active compounds [23, 24, 43, 44] demonstrate the breadth of the fungus’ ability to modify host responses. The high frequency of disease in the endemic areas and the increasing prevalence of the disseminated disease forms justify the development of adequate immunization strategies. Most recently, data has shown that vaccine-induced fungus-specific Th17 cells can confer protection against pulmonary histoplasmosis by recruiting and activating neutrophils and macrophages to the alveolar space [45]. Harnessing the host’s existing armamentarium or supplementing the host’s capacity, such as with the administration of cytokines or antibody to H. capsulatum, will be rich areas of study for the future.

References

S. T. Darling, “The morphology of the parasite (Histoplasma capsulatum) and the lesions of histoplasmosis, a fatal disease of tropical America,” Journal of Experimental Medicine, vol. 11, no. 4, pp. 515–531, 1909.

L. J. Wheat and C. A. Kauffman, “Histoplasmosis,” Infectious Disease Clinics of North America, vol. 17, no. 1, pp. 1–19, 2003.

http://www.cdc.gov/nczved/divisions/dfbmd/diseases/histoplasmosis

R. A. Goodwin, J. E. Loyd, and R. M. Des Prez, “Histoplasmosis in normal hosts,” Medicine, vol. 60, no. 4, pp. 231–266, 1981.

G. S. Deepe Jr., “The immune response to Histoplasma capsulatum: unearthing its secrets,” Journal of Laboratory and Clinical Medicine, vol. 123, no. 2, pp. 201–205, 1994.

G. S. Deepe Jr., “Modulation of infection with Histoplasma capsulatum by inhibition of tumor necrosis factor-α activity,” Clinical Infectious Diseases, vol. 41, no. 3, pp. S204–S207, 2005.

K. H. Long, F. J. Gomez, R. E. Morris, and S. L. Newman, “Identification of heat shock protein 60 as the ligand on Histoplasma capsulatum that mediates binding to CD18 receptors on human macrophages,” Journal of Immunology, vol. 170, no. 1, pp. 487–494, 2003.

M. R. W. Ehlers, “CR3: a general purpose adhesion-recognition receptor essential for innate immunity,” Microbes and Infection, vol. 2, no. 3, pp. 289–294, 2000.

L. G. Eissenberg and W. E. Goldman, “Histoplasma capsulatum fails to trigger release of superoxide from macrophages,” Infection and Immunity, vol. 55, no. 1, pp. 29–34, 1987.

J. E. Wolf, V. Kerchberger, G. S. Kobayashi, and J. R. Little, “Modulation of the macrophage oxidative burst by Histoplasma capsulatum,” Journal of Immunology, vol. 138, no. 2, pp. 582–586, 1987.

K. A. Borkovich, F. W. Farrelly, D. B. Finkelstein, J. Taulien, and S. Lindquist, “Hsp82 Is an essential protein that is required in higher concentrations for growth of cells at higher temperatures,” Molecular and Cellular Biology, vol. 9, no. 9, pp. 3919–3930, 1989.

J. A. Edwards, O. Zemska, and C. A. Rappleye, “Discovery of a role for Hsp82 in Histoplasma virulence through a quantitative screen for macrophage lethality,” Infection and Immunity, vol. 79, no. 8, pp. 3348–3357, 2011.

C. H. Weaver, K. C. F. Sheehan, and E. J. Keath, “Localization of a yeast-phase-specific gene product to the cell wall in Histoplasma capsulatum,” Infection and Immunity, vol. 64, no. 8, pp. 3048–3054, 1996.

M. L. Bohse and J. P. Woods, “RNA interference-mediated silencing of the YPS3 gene of Histoplasma capsulatum reveals virulence defects,” Infection and Immunity, vol. 75, no. 6, pp. 2811–2817, 2007.

J. D. Nosanchuk, B. L. Gómez, S. Youngchim et al., “Histoplasma capsulatum synthesizes melanin-like pigments in vitro and during mammalian infection,” Infection and Immunity, vol. 70, no. 9, pp. 5124–5131, 2002.

D. Van Duin, A. Casadevall, and J. D. Nosanchuk, “Melanization of Cryptococcus neoformans and Histoplasma capsulatum reduces their susceptibilities to amphotericin B and caspofungin,” Antimicrobial Agents and Chemotherapy, vol. 46, no. 11, pp. 3394–3400, 2002.

J. D. Nosanchuk and A. Casadevall, “Impact of melanin on microbial virulence and clinical resistance to antimicrobial compounds,” Antimicrobial Agents and Chemotherapy, vol. 50, no. 11, pp. 3519–3528, 2006.

J. W. Batanghari, G. S. Deepe Jr., E. Di Cera, and W. E. Goldman, “Histoplasma acquisition of calcium and expression of CBP1 during intracellular parasitism,” Molecular Microbiology, vol. 27, no. 3, pp. 531–539, 1998.

T. S. Sebghati, J. T. Engle, and W. E. Goldman, “Intracellular parasitism by Histoplasma capsulatum: fungal virulence and calcium dependence,” Science, vol. 290, no. 5495, pp. 1368–1372, 2000.

C. A. Rappleye, L. G. Eissenberg, and W. E. Goldman, “Histoplasma capsulatumα-(1,3)-glucan blocks innate immune recognition by the β-glucan receptor,” Proceedings of the National Academy of Sciences of the United States of America, vol. 104, no. 4, pp. 1366–1370, 2007.

C. A. Rappleye, J. T. Engle, and W. E. Goldman, “RNA interference in Histoplasma capsulatum demonstrates a role for α-(1,3)-glucan in virulence,” Molecular Microbiology, vol. 53, no. 1, pp. 153–165, 2004.

J. D. Nosanchuk, J. N. Steenbergen, L. Shi, G. S. Deepe Jr., and A. Casadevall, “Antibodies to a cell surface histone-like protein protect against Histoplasma capsulatum,” Journal of Clinical Investigation, vol. 112, no. 8, pp. 1164–1175, 2003.

J. D. Nosanchuk, L. Nimrichter, A. Casadevall, and M. L. Rodrigues, “A role for vesicular transport of macromolecules across cell walls in fungal pathogenesis,” Communicative and Integrative Biology, vol. 1, no. 1, pp. 37–39, 2008.

P. C. Albuquerque, E. S. Nakayasu, M. L. Rodrigues et al., “Vesicular transport in Histoplasma capsulatum: an effective mechanism for trans-cell wall transfer of proteins and lipids in ascomycetes,” Cellular Microbiology, vol. 10, no. 8, pp. 1695–1710, 2008.

J. Hilty, A. George Smulian, and S. L. Newman, “Histoplasma capsulatum utilizes siderophores for intracellular iron acquisition in macrophages,” Medical Mycology, vol. 49, no. 6, pp. 633–642, 2011.

L. H. Hwang, J. A. Mayfield, J. Rine, and A. Sil, “Histoplasma requires SID1, a member of an iron-regulated siderophore gene cluster, for host colonization,” PLoS Pathogens, vol. 4, no. 4, Article ID e1000044, 2008.

E. Lázár-Molnár, A. Gácser, G. J. Freeman, S. C. Almo, S. G. Nathenson, and J. D. Nosanchuk, “The PD-1/PD-L costimulatory pathway critically affects host resistance to the pathogenic fungus Histoplasma capsulatum,” Proceedings of the National Academy of Sciences of the United States of America, vol. 105, no. 7, pp. 2658–2663, 2008.

P. Zhou, M. C. Sieve, J. Bennett et al., “IL-12 prevents mortality in mice infected with Histoplasma capsulatum through induction of IFN-γ,” Journal of Immunology, vol. 155, no. 2, pp. 785–795, 1995.

M. S. Winters, Q. Chan, J. A. Caruso, and G. S. Deepe Jr., “Metallomic analysis of macrophages infected with Histoplasma capsulatum reveals a fundamental role for zinc in host defenses,” Journal of Infectious Diseases, vol. 202, no. 7, pp. 1136–1145, 2010.

K. Seider, A. Heyken, A. Lüttich, P. Miramón, and B. Hube, “Interaction of pathogenic yeasts with phagocytes: survival, persistence and escape,” Current Opinion in Microbiology, vol. 13, no. 4, pp. 392–400, 2010.

L. A. Gildea, R. E. Morris, and S. L. Newman, “Histoplasma capsulatum yeasts are phagocytosed via very late antigen-5, killed, and processed for antigen presentation by human dendritic cells,” Journal of Immunology, vol. 166, no. 2, pp. 1049–1056, 2001.

J. S. Lin, C. W. Yang, D. W. Wang, and B. A. Wu-Hsieh, “Dendritic cells cross-present exogenous fungal antigens to stimulate a protective CD8 T cell response in infection by Histoplasma capsulatum,” Journal of Immunology, vol. 174, no. 10, pp. 6282–6291, 2005.

W. A. Szymczak and G. S. Deepe Jr., “Antigen-presenting dendritic cells rescue CD4-depleted CCR2-/- mice from lethal Histoplasma capsulatum infection,” Infection and Immunity, vol. 78, no. 5, pp. 2125–2137, 2010.

R. Allendörfer, G. D. Brunner, and G. S. Deepe Jr., “Complex requirements for nascent and memory immunity in pulmonary histoplasmosis,” Journal of Immunology, vol. 162, no. 12, pp. 7389–7396, 1999.

F. J. Gomez, J. A. Cain, R. Gibbons, R. Allendoerfer, and G. S. Deepe Jr., “Vβ4+ T cells promote clearance of infection in murine pulmonary histoplasmosis,” Journal of Clinical Investigation, vol. 102, no. 5, pp. 984–995, 1998.

D. N. Kroetz and G. S. Deepe Jr., “CCR5 dictates the equilibrium of proinflammatory IL-17+and regulatory Foxp3+ T cells in fungal infection,” Journal of Immunology, vol. 184, no. 9, pp. 5224–5231, 2010.

K. V. Clemons, W. C. Darbonne, J. T. Curnutte, R. A. Sobel, and D. A. Stevens, “Experimental histoplasmosis in mice treated with anti-murine interferon- γ antibody and in interferon-γ gene knockout mice,” Microbes and Infection, vol. 2, no. 9, pp. 997–1001, 2000.

C. S. Zerbe and S. M. Holland, “Disseminated histoplasmosis in persons with interferon-gamma receptor 1 deficiency,” Clinical Infectious Diseases, vol. 41, no. 4, pp. e38–41, 2005.

P. Zhou, G. Miller, and R. A. Seder, “Factors involved in regulating primary and secondary immunity to infection with Histoplasma capsulatum: TNF-α plays a critical role in maintaining secondary immunity in the absence of IFN-γ,” Journal of Immunology, vol. 160, no. 3, pp. 1359–1368, 1998.

R. Allendoerfer and G. S. Deepe Jr., “Blockade of endogenous TNF-α exacerbates primary and secondary pulmonary histoplasmosis by differential mechanisms,” Journal of Immunology, vol. 160, no. 12, pp. 6072–6082, 1998.

A. J. Guimaraes, S. Frases, F. J. Gomez, R. M. Zancope-Oliveira, and J. D. Nosanchuk, “Monoclonal antibodies to heat shock protein 60 alter the pathogenesis of Histoplasma capsulatum,” Infection and Immunity, vol. 77, no. 4, pp. 1357–1367, 2009.

A. J. Guimarães, S. Frases, B. Pontes et al., “Agglutination of Histoplasma capsulatum by IgG monoclonal antibodies against Hsp60 impacts macrophage effector functions,” Infection and Immunity, vol. 79, no. 2, pp. 918–927, 2011.

A. J. Guimarães, E. S. Nakayasu, T. J. P. Sobreira et al., “Histoplasma capsulatum heat-shock 60 orchestrates the adaptation of the fungus to temperature stress,” PLoS ONE, vol. 6, no. 2, article e14660, 2011.

E. D. Holbrook, J. A. Edwards, B. H. Youseff, and C. A. Rappleye, “Definition of the extracellular proteome of pathogenic-phase Histoplasma capsulatum,” Journal of Proteome Research, vol. 10, no. 4, pp. 1929–1943, 2011.

M. Wüthrich, B. Gern, C. Y. Hung et al., “Vaccine-induced protection against 3 systemic mycoses endemic to North America requires Th17 cells in mice,” Journal of Clinical Investigation, vol. 121, no. 2, pp. 554–568, 2011.