Journal of Nanomaterials
Volume 2015 (2015), Article ID 101464, 4 pages
http://dx.doi.org/10.1155/2015/101464

Research Article

Experimental Study on the Components in Polyvalent “Ghost” Salmonella Vaccine for Veterinary Use

Daniela Vasileva Pencheva,¹ Elena Ilieva Velichkova,¹ Denis Zdravkov Sandarov,² Adrian Draganov Cardoso,² Maria Hristova Mileva,³ Petia Dinkova Genova-Kalou,⁴ and Rayna Bryaskova⁵

¹BB-NCIPD, 26 Yanko Sakazov Boulevard, 1504 Sofia, Bulgaria
²Faculty of Biology, Sofia University “St. Kliment Ohridski”, 8 Dragan Tsankov Boulevard, 1164 Sofia, Bulgaria
³Veterinary Clinic “Zoocenter”, 1799 Sofia, Bulgaria
⁴National Centre of Infectious and Parasitic Diseases, 26 Yanko Sakazov Boulevard, 1504 Sofia, Bulgaria
⁵UCTM, 8 “St. Kliment Ohridski” Boulevard, 1756 Sofia, Bulgaria

Received 19 March 2015; Revised 26 June 2015; Accepted 28 June 2015

Academic Editor: Abdelwahab Omri

Copyright © 2015 Daniela Vasileva Pencheva et al. 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.

Development of “ghost” Salmonella vaccines, inactivated by using a hybrid nanomaterial based on silver nanoparticles (AgNps) stabilized via polyvinyl alcohol (PVA), is an innovative approach in vaccine production. For this purpose, a series of attempts to establish the components of the polyvalent “ghost” Salmonella vaccine and the most suitable methods for its preparation were performed. The following strains S. Enteritidis, S. Newport-Puerto Rico, and S. Typhimurium were chosen as appropriate candidates for their incorporation in order to create polyvalent Salmonella “ghost” vaccine for veterinary use.

1. Introduction

Obtaining of “ghost” vaccine by inactivating bacteria with hybrid material based on silver nanoparticles stabilized by polyvinyl alcohol (PVA/AgNps) is an innovative new approach to the application of whole cell inactivated vaccines [1]. There are many advantages of using vaccines treated by this way such as keeping the antigenic range and creating complex protective immunity. Annually in many European countries and the United States are reported a large number of cases of Salmonella gastroenteritis. Approximately 80 deaths are recorded each year in the UK [2]. There are also known data caused by a significant number of nontyphoidal Salmonella systemic and nonenteric forms of human infections. In a study performed for five-year period in Bulgaria it was found that 21% of them are resistant to ampicillin and gentamicin, 17.64% are resistant to tetracycline, 14.28% are resistant to nalidixic acid, and 10% of them are resistant to chloramphenicol [3]. About half of the Salmonella outbreaks are due to contaminated poultry and poultry products. The route to poultry infection is the colonization of the hen house and its pets, such as rodents, insects, and wild birds. Salmonella in the feces of laying eggs contaminate surface or penetrate through the cracks of light shells. Concerning hens with ovarian microorganism infection it was established that S. Enteritidis can reach the egg by internal vertical transmission via the reproductive tract to the yolk or albumin [4]. Historically S. Typhimurium is the most commonly reported serotype. In 2001, the three most common Salmonella serotypes (more than 50% of all isolates) were S. Typhimurium (22%), S. Enteritidis (18%), and S. Newport (10%) [5]. S. Newport is one of the Salmonella serotypes causing diseases in cattle [6]. The emergence of multidrug-resistant Salmonella strains raises the question of strengthening the measures related to the prevention and protection at poultry. An inactivated Salmonella vaccine is available on the market for the active immunization of chickens, hens, and their parents [7]. It contains formalin-inactivated cells of S. Enteritidis PT4: 1  ×  10⁹ cells and S. Typhimurium DT104: 1 × 10⁹ cells. This type of inactivated Salmonella vaccines cannot offer 100% protection due to the destruction of bacterial cells as a result of treatment with formalin. An alternative to this vaccine could be a vaccine derived from ghost cells resulting from treatment with the hybrid material.

The aim of the present investigation is to establish the components of the polyvalent “ghost” Salmonella vaccine with preserved integrity of the cell surface by inactivation of different Salmonella strains with AgNps stabilized by PVA.

2. Materials and Methods

PVA/AgNps hybrid materials were prepared by adding a silver salt (AgNO₃), the precursor for silver ions, to the PVA solution thus leading to coordination of silver ions with hydroxyl groups (-OH) from PVA. Boiling the PVA solution at 100°C for 60 min in the presence of AgNO₃ results in the formation of silver nanoparticles stabilized in PVA, which protects the silver nanoparticles from agglomeration and ensures the homogeneous distribution of silver nanoparticles. The formation of silver nanoparticles was proven by UV-Vis spectroscopy and transmission electron microscopy (TEM) [8]. The silver concentration in PVA/AgNps solution was 174 mg/L as determined by ICP analysis.

To determine the Minimal Bactericidal Concentration (MBC) of the synthesized samples, the following control strains from the collection of “Laboratory for Control of In Vitro Diagnostic Medical Devices” by “BB-NCIPD” S. Typhi London, S. Paratyphi B, S. Nairobi, S. Typhimurium, 79a S. Newport-Puerto Rico, S. Enteritidis, and S. Enteritidis ATCC 13076 were used. The PVA/AgNps solution (174 mg/L) is diluted initially with injection water at ratio 1 : 6 thus leading to starting concentration of 29 mg/L. In five sterile tubes, successively falling twofold dilutions starting from a working dilution of PVA/AgNps in a volume of 1 mL with water for injection to a concentration of 0.45 mg/L were performed. To each tube was added a quantity of the bacterial suspension (by validated patented methodology) to provide from 10⁵ to 10⁶ CFU (Colonies Forming Units) of them. From a suspension the related positive control was seeded by the same amount using surface method on agar plates with Soybean Casein Agar (SCA). Tubes and plates were placed for 24 hours at °C. Each tube was plated by agar surface plate method on plate with SCA, which was cultured in a thermostat at °C in order to confirm inactivation of the bacterial suspension.

From working cultures of 4 control Salmonella strains, S. Typhimurium, S. Newport-Puerto Rico, S. Enteritidis, and S. Enteritidis ATCC 13076, were prepared as antigens for immunization “ghost” Salmonella vaccines. To obtain the required bacterial mass of pure culture, the strain was inoculated on plain agar slant layer. A standardized bacterial suspension from each strain was separately treated with the hybrid material PVA/AgNps, added in an amount that is in a silver concentration of 30 mg/L in the final volume of the antigen. Confirmed inactivated bacterial suspension standardized in densitometer to 3 MF was used as an antigen for immunization of rabbits. Intravenous immunizations were carried out with increasing antigenic load of 0.5 to 2 mL as established in the “BB-NCIPD” scheme on Californian rabbits: immunization in vena marginalis in intervals of 3 to 4 days.

The resulting serum was titrated in reaction stage agglutination to establish the specific titer. The presence of cross-agglutinines in different hyperimmune sera was established by slide agglutination reaction (Table 1).

Table 1: Content of cross-agglutinins diluted to 1 : 50 anti-Salmonella sera.

Strains
S. enterica serovar Enteritidis ATCC 13076
1,9,12; gm;—
S. enterica serovar Enteritidis
1,9,12; gm;—
79 a S. enterica serovar Newport-Puerto Rico 6,8 20;—;1,2
S. enterica serovar Typhimurium
1,4,5,12;i;1,5

Anti-S.Enteritidis ATCC 13076 serum
++++
+
−
++

Anti-S. Enteritidis serum
−
++++
−
+++

Anti-S.Newport-Puerto Rico serum
−
−
++++
++

Anti-S. Typhimurium serum
−
−
+++
++++

++++: very good visible agglutinates in clear liquid; +++: good visible agglutinates in almost clear liquid; ++: visible agglutinates in turbid liquid; +: slightly visible agglutinates in turbid liquid.

Cell viability after the cytotoxicity analysis of the material was determined by a modification of the MTT [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] [9] analysis on the cell line of mouse fibroblast cells (L20B). It gives information about the possibilities of application of the hybrid material that will perform bactericidal effect without affecting the metabolism of host cells.

3. Results and Discussion

Initially, the Minimal Bactericidal Concentration (MBC) of PVA/AgNps hybrid materials for the organisms Salmonella enterica serovar Typhi London, Salmonella enterica serovar Paratyphi B, and Salmonella enterica serovar Nairobi, which were added to the reaction mixture at a concentration of 10⁵ to 10⁶ CFU via a validated methodology, was determined according to the requirements of CLSI M 26-A [10]. It was established that the MBC was defined at 0.054 mg/L silver concentration in all cases.

MBC for the strains provided for involvement in the experimental “ghost” Salmonella vaccine, Salmonella enterica serovar Typhimurium, Salmonella enterica serovar Newport-Puerto Rico, Salmonella enterica serovar Enteritidis, and Salmonella enterica serovar Enteritidis ATCC 13076, was additionally determined. Before performing the test, the MBC for both strains S. enterica serovar Enteritidis and S. enterica serovar Typhimurium was established as lower than 0.027 mg/L. Only for S. Newport-Puerto Rico was the MBC 0.108 mg/L (≈0.11 mg/L) (Figure 1). Therefore, it was assumed that the tested Salmonella strains were sensitive to silver, as tests with the same hybrid material showed that MBC values equal to or more than 1.1 mg/L are sign for silver resistance [11]. Evidence of widespread resistance of Salmonella to silver has long been cited in the literature, resulting in a plasmid encoding the genes for resistance to heavy metals [12].

(a)

(b)

(c)

(d)

Figure 1: MBC of PVA/AgNps determined by macrodilution method for (a) S. Newport-Puerto Rico, (b) S. Enteritidis ATCC 13076, (c) S. Enteritidis, and (d) S. Typhimurium.

Maximal nontoxic concentration (MNC) was defined as 0.007 mg/L, while the concentration required to inhibit cell viability by 50% (CD₅₀) was determined as 0.53 mg/L in a dose-dependent manner (Figure 2). As the MBC from the respective strains was determined at 10⁵ to 10⁶ CFU bacterial load, therefore, to inactivate one billionth bacterial suspension, silver concentration of 30 mg/L suspension was applied.

Figure 2: Cytotoxic effect of PVA/AgNps on the viability of mouse fibroblast (L20B) cell line at 24 h and 48 h.

Sera were tested in the reaction slide agglutination at a dilution with TRIS saline buffer as 1 : 50 for presence of cross-agglutinins from other strains used in the experiment (Table 1). With reference to the scheme of White-Kaufmann [13] common H1 antigens in the second phase of S. enterica serovar Newport-Puerto Rico and S. enterica serovar Typhimurium were found. This explains the coagglutination in anti-S. Newport-Puerto Rico and anti-S. Typhimurium sera. Having common O1 antigens explains coagglutination in sera: anti-S. Enteritidis and anti-S. Typhimurium serum.

The specific titer of all obtained after immunization rabbit antisera was determined in a Gruber’s reaction stage agglutination. Anti-S. Enteritidis ATCC 13076, anti-S. Newport-Puerto Rico, and anti-S. Typhimurium sera were with O-titer 1 : 6400. Only anti-S. Enteritidis serum has O titer 1 : 1600. A significant difference in the activity of sera obtained from both strains S. Enteritidis was found; therefore it was considered as appropriate to incorporate both of them in the ongoing prospective studies on the composition of polyvalent Salmonella “ghost” vaccine for veterinary use.

TEM analysis a month after completion of the immunization was performed (Figure 3) to one of those used in attempts antigens. It was found that the presence of the PVA/AgNps for longer period in the antigen for the immunization results in complete lysis of the bacterial cells after apoptosis. Therefore, an additional step consisting in washing of the antigen with saline after inactivation with PVA/AgNps, in order to preserve the inactivated bacterial cells in the form of “ghost” cells, is necessary.

Figure 3: TEM analysis of the Salmonella antigen, inactivated with PVA/AgNp.

4. Conclusions

PVA/AgNps hybrid material was applied to obtain “ghost” cells with preserved integrity of the cell surface by inactivation of different Salmonella strains. Initially, MBC for different Salmonella strains was determined by macrodilution method. Minimal nontoxic concentration of PVA/AgNp and CD₅₀ were established as well. The specific titer of all obtained after immunization rabbit antisera was determined in a Gruber’s reaction stage agglutination, as strains S. Enteritidis, S. Newport-Puerto Rico, and S. Typhimurium were chosen as appropriate candidates for their incorporation in order to create polyvalent Salmonella “ghost” vaccine for veterinary use.

The addition of more strains to the vaccine will expand its range of possible causes, and their inactivation by PVA/AgNps will allow retention of a full range of antigenic determinants thus providing complete protection.

Conflict of Interests

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

Acknowledgments

The authors thank their colleagues from the “BB-NCIPD,” “Laboratory for Control of In Vitro Diagnostic Medical Devices,” and Dr. Ivanov, veterinarian, Head of “Vivarium,” for assistance in carrying out experiments on laboratory animals.

References

D. Pencheva, R. Bryaskova, and P. Genova-Kalou, “Properties and possibilities for application of the hybrid material with silver nanoparticles (PVA/AgNps),” in Proceedings of the 9th Workshop on Biological Activity of Metals, Synthetic Compounds and Natural Products, pp. 38–54, Institute of Experimental Morphology, Pathology and Anthropology, IEPAM, Bulgarian Academy of Sciences, November 2014.

Salmonella Gastroenteritis, http://patient.info/doctor/Salmonella-gastroenteritis

G. Asseva, P. Petrov, K. Ivanova, and T. Kantardjiev, “Systemic and extraintestinal forms of human infection due to non-typhoid salmonellae in Bulgaria, 2005–2010,” European Journal of Clinical Microbiology and Infectious Diseases, vol. 31, no. 11, pp. 3217–3221, 2012.

J. Guard-Petter, “The chicken, the egg and Salmonella enteritidis,” Environmental Microbiology, vol. 3, no. 7, pp. 421–430, 2001.

W. Winn Jr., S. Allen, W. Janda et al., Koneman's Color atlas and Textbook of Diagnostic Microbiology, 2006.

S. Clark, Salmonella Newport: An Emerging Disease in Dairy Cattle, 2004, https://www.addl.purdue.edu/newsletters/2004/summer/summer2004.pdf.

E. N. T. Meeusen, J. Walker, A. Peters, P.-P. Pastoret, and G. Jungersen, “Current status of veterinary vaccines,” Clinical Microbiology Reviews, vol. 20, no. 3, pp. 489–510, 2007.

R. Bryaskova, D. Pencheva, G. M. Kale, U. Lad, and T. Kantardjiev, “Synthesis, characterisation and antibacterial activity of PVA/TEOS/Ag-Np hybrid thin films,” Journal of Colloid and Interface Science, vol. 349, no. 1, pp. 77–85, 2010.

T. Mosmann, “Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays,” Journal of Immunological Methods, vol. 65, no. 1-2, pp. 55–63, 1983.

CLSI, “Methods for determining bactericidal activity of antimicrobial agents: approved guideline,” CLSI M26-A, Clinical & Laboratory Standards Institute, 1999, (vol.19, no. 18).

M. Iliev, “Antimicrobials' resistant salmonella strains tested for susceptibility to hybrid material with included silver nanoparticles,” Problems of Infectious and Parasitic Diseases, vol. 41, no. 1, pp. 9–13, 2013.

I. Chopra, “The increasing use of silver-based products as antimicrobial agents: a useful development or a cause for concern?” Journal of Antimicrobial Chemotherapy, vol. 59, no. 4, pp. 587–590, 2007.

A. D. G. Patrick and F.-X. Weill, Antigenic Formulae of the Salmonella Serovars, WHO Collaborating Centre for Reference and Research on Salmonella, Paris, France, 2007.