全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

A Novel Lactococcal Vaccine Expressing a Peptide from the M2 Antigen of H5N2 Highly Pathogenic Avian Influenza A Virus Prolongs Survival of Vaccinated Chickens

DOI: 10.1155/2013/316926

Full-Text   Cite this paper   Add to My Lib

Abstract:

A cost-effective and efficacious influenza vaccine for use in commercial poultry farms would help protect against avian influenza outbreaks. Current influenza vaccines for poultry are expensive and subtype specific, and therefore there is an urgent need to develop a universal avian influenza vaccine. We have constructed a live bacterial vaccine against avian influenza by expressing a conserved peptide from the ectodomain of M2 antigen (M2e) on the surface of Lactococcus lactis (LL). Chickens were vaccinated intranasally with the lactococcal vaccine (LL-M2e) or subcutaneously with keyhole-limpet-hemocyanin conjugated M2e (KLH-M2e). Vaccinated and nonvaccinated birds were challenged with high pathogenic avian influenza virus A subtype H5N2. Birds vaccinated with LL-M2e or KLH-M2e had median survival times of 5.5 and 6.0 days, respectively, which were significantly longer than non-vaccinated birds (3.5 days). Birds vaccinated subcutaneously with KLH-M2e had a lower mean viral burden than either of the other two groups. However, there was a significant correlation between the time of survival and M2e-specific serum IgG. The results of these trials show that birds in both vaccinated groups had significantly ( ) higher median survival times than non-vaccinated birds and that this protection could be due to M2e-specific serum IgG. 1. Introduction The US Poultry industry annually produces over 43 billion pounds of high-quality broiler chickens and turkeys and over 90 billion eggs, which in 2010 had a market value of $34.7 billion [1, 2]. Avian diseases are a constant threat to the industry. Viruses are of particular concern because antibiotics cannot control them, although vaccines can control some avian viral infections. Avian vaccines are an important component of protecting the value of commercial poultry. However, many commercial birds are not vaccinated because of the cost, labor, and difficulty in differentiating infected from vaccinated animals. Avian influenza virus is an important concern to the poultry industry both in the USA and worldwide. It is highly contagious and causes two levels of disease [3]. Low pathogenic strains cause a disease that is seldom fatal but results in slower growth and lower egg production. The highly pathogenic form of the disease results in systemic morbidity and a high mortality rate (90–100%). Highly pathogenic avian influenza (HPAI) is a significant public health concern because of recent highly pathogenic H5N1 avian influenza outbreaks causing human deaths in Asia, Europe, Middle East, and Africa. According to the world

References

[1]  USDA Economic Research Service, 2012, http://www.ers.usda.gov/.
[2]  US Poultry and Egg Association, 2012, http://www.uspoultry.org/economic_data/.
[3]  B. Z. Londt, J. Banks, and D. J. Alexander, “Highly pathogenic avian influenza viruses with low virulence for chickens in in vivo tests,” Avian Pathology, vol. 36, no. 5, pp. 347–350, 2007.
[4]  L. G. Bermúdez-Humarán, N. G. Cortes-Perez, F. Lefèvre et al., “A novel mucosal vaccine based on live lactococci expressing E7 antigen and IL-12 induces systemic and mucosal immune responses and protects mice against human papillomavirus type 16-induced tumors,” Journal of Immunology, vol. 175, no. 11, pp. 7297–7302, 2005.
[5]  L. Chamberlain, J. M. Wells, K. Robinson, K. Schofield, and R. LePage, “Mucosal immunization with recombinant Lactococcus lactis,” in Gram-Positive Bacteria as Vaccine Vehicles for Mucosal Immunization, G. Pozzi and J. M. Wells, Eds., pp. 83–106, Landes Bioscience, Austin, Tex, USA, 1997.
[6]  Y. Dieye, A. J. W. Hoekman, F. Clier, V. Juillard, H. J. Boot, and J. C. Piard, “Ability of Lactococcus lactis to export viral capsid antigens: a crucial step for development of live vaccines,” Applied and Environmental Microbiology, vol. 69, no. 12, pp. 7281–7288, 2003.
[7]  V. Enouf, P. Langella, J. Commissaire, J. Cohen, and G. Corthier, “Bovine rotavirus nonstructural protein 4 produced by Lactococcus lactis is antigenic and immunogenic,” Applied and Environmental Microbiology, vol. 67, no. 4, pp. 1423–1428, 2001.
[8]  B. L. Geller, N. Wade, T. D. Gilberts, D. E. Hruby, R. Johanson, and L. Topisirovic, “Surface expression of the conserved C repeat region of streptococcal M6 protein within the Pip bacteriophage receptor of Lactococcus lactis,” Applied and Environmental Microbiology, vol. 67, no. 12, pp. 5370–5376, 2001.
[9]  M. H. Lee, Y. Roussel, M. Wilks, and S. Tabaqchali, “Expression of Helicobacter pylori urease subunit B gene in Lactococcus lactis MG1363 and its use as a vaccine delivery system against H. pylori infection in mice,” Vaccine, vol. 19, no. 28-29, pp. 3927–3935, 2001.
[10]  H. Pei, J. Liu, Y. Cheng et al., “Expression of SARS-coronavirus nucleocapsid protein in Escherichia coli and Lactococcus lactis for serodiagnosis and mucosal vaccination,” Applied Microbiology and Biotechnology, vol. 68, no. 2, pp. 220–227, 2005.
[11]  C. A. Perez, C. Eichwald, O. Burrone, and D. de Mendoza, “Rotavirus vp7 antigen produced by Lactococcus lactis induces neutralizing antibodies in mice,” Journal of Applied Microbiology, vol. 99, no. 5, pp. 1158–1164, 2005.
[12]  K. Q. Xin, Y. Hoshino, Y. Toda et al., “Immunogenicity and protective efficacy of orally administered recombinant Lactococcus lactis expressing surface-bound HIV Env,” Blood, vol. 102, no. 1, pp. 223–228, 2003.
[13]  H. Lei, Y. Xu, J. Chen, X. Wei, and D. M. K. Lam, “Immunoprotection against influenza H5N1 virus by oral administration of enteric-coated recombinant Lactococcus lactis mini-capsules,” Virology, vol. 407, no. 2, pp. 319–324, 2010.
[14]  P. Mannam, K. F. Jones, and B. L. Geller, “Mucosal vaccine made from live, recombinant Lactococcus lactis protects mice against pharyngeal infection with Streptococcus pyogenes,” Infection and Immunity, vol. 72, no. 6, pp. 3444–3450, 2004.
[15]  P. Zou, W. Liu, and Y. H. Chen, “The epitope recognized by a monoclonal antibody in influenza A virus M2 protein is immunogenic and confers immune protection,” International Immunopharmacology, vol. 5, no. 4, pp. 631–635, 2005.
[16]  G. Corthier, C. Delorme, S. D. Ehrlich, and P. Renault, “Use of luciferase genes as biosensors to study bacterial physiology in the digestive tract,” Applied and Environmental Microbiology, vol. 64, no. 7, pp. 2721–2722, 1998.
[17]  S. Drouault, G. Corthier, S. D. Ehrlich, and P. Renault, “Survival, physiology, and lysis of Lactococcus lactis in the digestive tract,” Applied and Environmental Microbiology, vol. 65, no. 11, pp. 4881–4886, 1999.
[18]  N. Klijn, A. H. Weerkamp, and W. M. de Vos, “Genetic marking of Lactococcus lactis shows its survival in the human gastrointestinal tract,” Applied and Environmental Microbiology, vol. 61, no. 7, pp. 2771–2774, 1995.
[19]  T. Vesa, P. Pochart, and P. Marteau, “Pharmacokinetics of Lactobacillus plantarum NCIMB 8826, Lactobacillus fermentum KLD, and Lactococcus lactis MG 1363 in the human gastrointestinal tract,” Alimentary Pharmacology and Therapeutics, vol. 14, no. 6, pp. 823–828, 2000.
[20]  L. G. Bermúdez-Humarán, P. Langella, A. Miyoshi et al., “Production of human papillomavirus type 16 E7 protein in Lactococcus lactis,” Applied and Environmental Microbiology, vol. 68, no. 2, pp. 917–922, 2002.
[21]  J. Czerwiński, O. H?jberg, S. Smulikowska, R. M. Engberg, and A. Mieczkowska, “Influence of dietary peas and organic acids and probiotic supplementation on performance and caecal microbial ecology of broiler chickens,” British Poultry Science, vol. 51, no. 2, pp. 258–269, 2010.
[22]  K. N. Olsen, M. Henriksen, M. Bisgaard, O. L. Nielsen, and H. Christensen, “Investigation of chicken intestinal bacterial communities by 16S rRNA targeted fluorescence in situ hybridization,” Antonie van Leeuwenhoek, vol. 94, no. 3, pp. 423–437, 2008.
[23]  J. Feng, M. Zhang, K. Mozdzanowska et al., “Influenza A virus infection engenders a poor antibody response against the ectodomain of matrix protein 2,” Virology Journal, vol. 3, pp. 102–113, 2006.
[24]  B. E. Johansson, T. M. Moran, C. A. Bona, S. W. Popple, and E. D. Kilbourne, “Immunologic response to influenza virus neuraminidase is influenced by prior experience with the associated viral hemagglutinin: II. Sequential infection of mice simulates human experience,” Journal of Immunology, vol. 139, no. 6, pp. 2010–2014, 1987.
[25]  W. Liu, H. Li, and Y. H. Chen, “N-terminus of M2 protein could induce antibodies with inhibitory activity against influenza virus replication,” FEMS Immunology and Medical Microbiology, vol. 35, no. 2, pp. 141–146, 2003.
[26]  M. Schotsaert, M. de Filette, W. Fiers, and X. Saelens, “Universal M2 ectodomain-based influenza A vaccines: preclinical and clinical developments,” Expert Review of Vaccines, vol. 8, no. 4, pp. 499–508, 2009.
[27]  S. Babapoor, T. Neef, C. Mittelholzer et al., “A novel vaccine using nanoparticle platform to present immunogenic M2e against avian influenza infection,” Influenza Research and Treatment, vol. 2011, Article ID 126794, 12 pages, 2011.
[28]  M. de Filette, W. M. Jou, A. Birkett et al., “Universal influenza A vaccine: optimization of M2-based constructs,” Virology, vol. 337, no. 1, pp. 149–161, 2005.
[29]  J. Fan, X. Liang, M. S. Horton et al., “Preclinical study of influenza virus a M2 peptide conjugate vaccines in mice, ferrets, and rhesus monkeys,” Vaccine, vol. 22, no. 23-24, pp. 2993–3003, 2004.
[30]  A. M. Frace, A. I. Klimov, T. Rowe, R. A. Black, and J. M. Katz, “Modified M2 proteins produce heterotypic immunity against influenza A virus,” Vaccine, vol. 17, no. 18, pp. 2237–2244, 1999.
[31]  K. Mozdzanowska, J. Feng, M. Eid et al., “Induction of influenza type A virus-specific resistance by immunization of mice with a synthetic multiple antigenic peptide vaccine that contains ectodomains of matrix protein 2,” Vaccine, vol. 21, no. 19-20, pp. 2616–2626, 2003.
[32]  S. Neirynck, T. Deroo, X. Saelens, P. Vanlandschoot, W. M. Jou, and W. Fiers, “A universal influenza A vaccine based on the extracellular domain of the M2 protein,” Nature Medicine, vol. 5, no. 10, pp. 1157–1163, 1999.
[33]  H. Holo and I. F. Nes, “High-frequency transformation, by electroporation, of Lactococcus lactis subsp. cremoris grown with glycine in osmotically stabilized media,” Applied and Environmental Microbiology, vol. 55, no. 12, pp. 3119–3123, 1989.
[34]  P. M. Walsh and L. L. McKay, “Recombinant plasmid associated with cell aggregation and high-frequency conjugation of Streptococcus lactis ML3,” Journal of Bacteriology, vol. 146, no. 3, pp. 937–944, 1981.
[35]  F. M. Ausubel, R. Brent, R. E. Kingston et al., Current Protocols in Molecular Biology, John Wiley & Sons, New York, NY, USA, 1998.
[36]  H. B. Donald and A. Isaacs, “Counts of influenza virus particles,” Journal of General Microbiology, vol. 10, no. 3, pp. 457–464, 1954.
[37]  D. E. Swayne, D. A. Senne, and C. W. Beard, A Laboratory Manual for the Isolation and Identification of Avian Pathogens, American Association of Avian Pathologists, Kennett Square, Pa, USA, 1998.
[38]  K. Sitz and D. Birx, “Lymphocyte proliferation assay,” Methods in Molecular Medicine, vol. 17, pp. 343–353, 1999.
[39]  A. G. Grandea III, O. A. Olsen, T. C. Cox et al., “Human antibodies reveal a protective epitope that is highly conserved among human and nonhuman influenza A viruses,” Proceedings of the National Academy of Sciences of the United States of America, vol. 107, no. 28, pp. 12658–12663, 2010.
[40]  D. Zharikova, K. Mozdzanowska, J. Feng, M. Zhang, and W. Gerhard, “Influenza type A virus escape mutants emerge in vivo in the presence of antibodies to the ectodomain of matrix protein 2,” Journal of Virology, vol. 79, no. 11, pp. 6644–6654, 2005.
[41]  W. Gerhard, K. Mozdzanowska, and D. Zharikova, “Prospects for universal influenza virus vaccine,” Emerging Infectious Diseases, vol. 12, no. 4, pp. 569–574, 2006.
[42]  H. Lei, Z. Sheng, Q. Ding et al., “Evaluation of oral immunization with recombinant avian influenza virus HA1 displayed on the Lactococcus lactis surface and combined with the mucosal adjuvant cholera toxin subunit B,” Clinical and Vaccine Immunology, vol. 18, no. 7, pp. 1046–1051, 2011.
[43]  Y. J. Li, G. P. Ma, G. W. Li et al., “Oral vaccination with the porcine rotavirus VP4 outer capsid protein expressed by Lactococcus lactis induces specific antibody production,” Journal of Biomedicine and Biotechnology, vol. 2010, Article ID 708460, 9 pages, 2010.
[44]  J. Bessa, N. Schmitz, H. J. Hinton, K. Schwarz, A. Jegerlehner, and M. F. Bachmann, “Efficient induction of mucosal and systemic immune responses by virus-like particles administered intranasally: implications for vaccine design,” European Journal of Immunology, vol. 38, no. 1, pp. 114–126, 2008.
[45]  J. Denis, E. Acosta-Ramirez, Y. Zhao et al., “Development of a universal influenza A vaccine based on the M2e peptide fused to the papaya mosaic virus (PapMV) vaccine platform,” Vaccine, vol. 26, no. 27-28, pp. 3395–3403, 2008.
[46]  K. Mozdzanowska, D. Zharikova, M. Cudic, L. Otvos, and W. Gerhard, “Roles of adjuvant and route of vaccination in antibody response and protection engendered by a synthetic matrix protein 2-based influenza A virus vaccine in the mouse,” Virology Journal, vol. 4, pp. 118–131, 2007.
[47]  D. G. Eliasson, K. El Bakkouri, K. Sch?n et al., “CTA1-M2e-DD: a novel mucosal adjuvant targeted influenza vaccine,” Vaccine, vol. 26, no. 9, pp. 1243–1252, 2008.
[48]  K. Mozdzanowska, M. Furchner, D. Zharikova, J. Feng, and W. Gerhard, “Roles of CD4+ T-cell-independent and -dependent antibody responses in the control of influenza virus infection: evidence for noncognate CD4+ T-cell activities that enhance the therapeutic activity of antiviral antibodies,” Journal of Virology, vol. 79, no. 10, pp. 5943–5951, 2005.
[49]  A. Jegerlehner, N. Schmitz, T. Storni, and M. F. Bachmann, “Influenza A vaccine based on the extracellular domain of M2: weak protection mediated via antibody-dependent NK cell activity,” Journal of Immunology, vol. 172, no. 9, pp. 5598–5605, 2004.
[50]  S. M. Tompkins, Z. S. Zhao, C. Y. Lo et al., “Matrix protein 2 vaccination and protection against influenza viruses, including subtype H5N1,” Emerging Infectious Diseases, vol. 13, no. 3, pp. 426–435, 2007.
[51]  R. Wang, A. Song, J. Levin et al., “Therapeutic potential of a fully human monoclonal antibody against influenza A virus M2 protein,” Antiviral Research, vol. 80, no. 2, pp. 168–177, 2008.
[52]  K. El Bakkouri, F. Descamps, M. de Filette et al., “Universal vaccine based on ectodomain of matrix protein 2 of influenza A: Fc receptors and alveolar macrophages mediate protection,” Journal of Immunology, vol. 186, no. 2, pp. 1022–1031, 2011.

Full-Text

comments powered by Disqus

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133

WeChat 1538708413