Comparison of the Common Immunogenic Protein Components of Pasteurella multocida Serotypes B:2 and B: 3,4
Pasteurella multocida B serotipi Güney Asya'daki sığır ve mandalarda yaygın olarak görülen ve kanda septisemi ile seyreden hemorajik septisemi (HS)'nin en önemli nedenidir. Hastalık için günümüzde kullanılan aşılar yeteri kadar etkili değildir ve sadece sınırlı bir sürede etkisini göstermektedir. Canlı/subunit aşılarda kullanılmak üzere Pasteurella multocida'nın immunojenik komponentlerinin belirlenmesi için yapılan çalışmamızda, B:2 ve B:3,4 serotiplerinin dış membran proteinleri (OMP) izole edilmiş ve bunların profilleri karşılaştırılmıştır. İmmunbloting sonucunda 39.0, 33.5 ve 31.0 kDa moleküler ağırlıklarında 3 adet ortak immunojenik polipeptit belirlenmiştir. İdentifiye edilen dış membran proteinlerinin immunojenitesi ayrıca bunlardan elde edilen antiserumlar ile doğrulanmıştır. Bu çalışmada identifiye edilen antijenik OMP'ler uzun süre etki gösteren yeni, güvenli ve etkin aşıların formülasyonlarının geliştirilmesine katkı sağlayacaktır.
Pasteurella multocida B:2 ve B:3,4 Serotiplerinin Ortak İmmunojenik Protein Komponentlerinin Karşılaştırılması
Serotype B of Pasteurella multocida is a major agent of haemorrhagic septicaemia (HS), a form of blood poisoning widespread in cattle and buffalo from Southern Asia. The vaccines currently used against the disease are not potent enough, being effective only for a limited duration only. In an attempt to identify immunogenic components of P. multocida for use as live/subunit vaccines, the outer membrane proteins (OMPs) of B:2 and B:3,4 serotypes were isolated and their profiles compared. Three common immunogenic components; polypeptides of molecular weight (MW) 39.0, 33.5, 31.0 kDa, were identified by immunoblotting. The immunogenicity of identified OMPs was also confirmed using antisera generated against them. The antigenic OMPs identified in current research could be explored in the formulation of new, safe and effective vaccines for indigenous buffalo and cattle breeds with a prolonged efficacy.
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- Dabo SM, Taylor JD, Confer AW: Pasteurella multocida and bovine respiratory disease. Anim Health Res Rev, 8, 129-150, 2007. DOI: 10.1017/ S1466252307001399
- Al-Hasani K, Boyce J, McCarl VP, Bottomley S, Wilkie I, Adler B: Identification of novel immunogens in Pasteurella multocida. Microbial Cell Fact, 6, 1-5, 2007. DOI: 10.1186/1475-2859-6-3
- Munir R, Shahwar D, Farooq U, Nawaz I, Shahzad I, Khanum A: Outer membrane protein profiling of Pasteurella Multocida. Pakistan Vet J, 27 (1): 1-4, 2007
- Harper M, Boyce JD, Adler B: Pasteurella multocida pathogenesis: years after Pasteur. FEMS Microbiol Lett, 265, 1-10, 2006. DOI: 1111/j.1574-6968.2006.00442.x
- Kamran M, Ahmad MD, Anjum AA, Maqbool A, Muhammad K, Khan HM, Hudda N, Nawaz M, Ali MA: Antigenic variation among Pasteurella multocida isolates from diseased buffaloes by protein profiling and cluster analysis. J Animal Plant Sci, 24 (4): 1101-1109, 2014.
- Prasannavadhana A, Kumar S, Thomas P, Sarangi LN, Gupta SK, Priyadarshini A, Nagaleekar VK, Singh VP: Outer membrane proteome analysis of Indian strain of Pasteurella multocida serotype B:2 by MALDI- TOF/MS analysis. Sci World J, 2014 (2014): 1-10, Article ID 617034, 2014. DOI: 10.1155/ 2014/617034
- Joshi S, Tewari K, Singh R: Comparative immunogenicity and protective efficacy of different preparations of outer membrane proteins of Pasteurella multocida (B:2) in a mouse model. Vet Arhiv, 83 (6): 665-676, 2013.
- Kevin LM, Paul AR: Purification of P. multocida antigens by ultra- centrifugation and isoelectronic focusing. Can J Microbiol, 28 (5): 511- ,1982.
- Katsuda K, Hoshinoo K, Ueno Y, Kohmoto M, Mikami O: Virulence genes and antimicrobial susceptibility in Pasteurella multocida isolates from calves. Vet Microbiol, 167, 737-41, 2013. DOI: 10.1016/j.vetmic.2013.09.029
- Taylor JD, Fulton RW, Dabo SM, Lehenbauer TW, Confer AW. Comparison of genotypic and phenotypic characterization methods for Pasteurella multocida isolates from fatal cases of bovine respiratory disease. J Vet Diagn Invest, 22, 366-375, 2010. DOI: 10.1177/104063871002200304
- Verma S, Sharma M, Katoch S, Verma L, Kumar S, Dogra V, Chahota R, Dhar P, Singh G: Profiling of virulence associated genes of Pasteurella multocida isolated from cattle. Vet Res Commun, 37, 83-89, DOI: 10.1007/s11259-012-9539-5
- Rimler RB: Restriction endonuclease analysis using HhaI and HpaII to discriminate among group B Pasteurella multocida associated with haemorrhagic septicaemia. J Med Microbiol, 49, 81-87, 2000. DOI: 1099/0022-1317-49-1-81
- Ahmad TA, Rammah SS, Sheweita SA, Haroun M, El-Sayed LH: Development of immunization trials against Pasteurella multocida. Vaccine, 32, 909-917, 2014. DOI: 10.1016/j.vaccine.2013.11.068
- Jamali H, Rezagholipour M, Fallah S, Dadrasnia A, Chelliah S, Velappan RD, Wei KS, Ismail S: Prevalence, characterization and antibiotic resistance of Pasteurella multocida isolated from bovine respiratory infection. Vet J, 202, 381-383, 2014. DOI: 10.1016/j.tvjl.2014.07.024
- Laemmli UK: Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature, 227, 680-685, 1970. DOI: 10.1038/ a0
- Myint A, Carter GR, Jones TO: Prevention of experimental haemorrhagic septicaemia with a live vaccine. Vet Rec, 120 (21): 500-501, Choi KH, Maheshwaran SK, Felice LJ: Characterization of outer membrane protein enriched extracts from P. multocida isolated from turkeys. Am J Vet Res, 50, 676-686, 1989.
- Cary CJ, Peter GK, Chrisp CE, Keren DF: Serological analysis of five serotypes of Pasteurella multocida of rabbit origin by use of an enzyme linked immune sorbent assay with lipopoly saccharide as antigen. J Clin Microbiol, 20 (2): 191-194, 1984.
- Mahmood T, Yang PC: Western Blot: Technique, theory and troubleshooting. North Am J med Sci, 4, 429-434, 2012. DOI: 10.4103/1947- 100998
- Fomsgaard A, Freudenberg MA, Galanos C: Modification of the silver staining technique to detect lipopolysaccharide in poly acrylamide gels. J Clin Microbiol, 28 (12): 2627-2631. 1990.
- Bastuji BG, Bauden RA, Dubray G, Limet JN: Sodium dodecyl sulphate polyacrylamide gel electrophoresis and immunoblotting analysis of smooth lipopolysaccharide heterogeneity among Brucella biovars related to A and M specificities. J ClinMicrobiol, 28 (10): 2169-2174, 1990.
- Towbin H, Staehelin T, Gordon J: Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: Procedure and some applications. Proc Natl Acad Sci USA, 76 (9): 4350-4354, 1979.
- Ptai US, Srivastava SK, Roy SC, More T: Immunogenecity of outer membrane protein of P. multocida in buffalo calves. Vet Microbiol, 52, 301- , 1996. DOI: 10.1016/S0378-1135(96)00066-1
- Jain A, Roy A, Rank DN, Joshi CG, Purohit JH: Characterization of the Pasteurella multocida isolates by their outer membrane protein profiles. Indian J Comp Microbiol Immunol Infect Dis, 26 (1): 63-65, 2005.
- Kedrak A, Opacka BB: Analysis of protein patterns of P. multocida strains isolated from poultry. Bull Vet Inst Pulawy, 46, 150-155, 2002.
- Johnson RB, Dawkins HJS, Spencer TL: Electrophoretic profiles of the Pasteurella multocida isolates from animals with hemorrhagic septicemia. Am J Vet Res, 52, 1644-1648, 1991.
- Tomer P, Chaturvedi GC, Malik MP, Monga D: Comparative analysis of the outer membrane protein profiles isolates of the Pasteurella multocida (B:2) associated with haemorrhagic septicaemia. Vet Res Commun, 26, 513- , 2002. DOI: 10.1023/A:1020212430041
- Opacka BB: Expression of iron-regulated outer membrane proteins (IROMPs) by Pasteurella multocida strains isolated from cattle. Bull Vet Inst Pulawy, 46, 157-164, 2002.