2015
DOI: 10.1292/jvms.14-0532
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Protectivity conferred by immunization with intranasal recombinant outer membrane protein H from <i>Pasteurella multocida</i> serovar A:1 in chickens

Abstract: Recombinant outer membrane protein H (rOmpH) is a potential fowl cholera vaccine candidate. The present study was aimed at developing rOmpH formulations for intranasal administration. The rOmpH was purified and formulated with either Escherichia coli enterotoxin B (LTB) or CpG oligodeoxynucleotides (ODN) as an adjuvant. Antibody responses in chickens intranasally immunized with rOmpH in combination with 2 different adjuvants were significantly increased (P<0.05) post immunization. Chicken survival rates showed… Show more

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Cited by 22 publications
(27 citation statements)
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“…Bacterial strains, media and growth conditions P. multocida strains X-73 (serovar A:1, ATCC15742), P-1059 (serovar A:3, ATCC11039) and P-1662 (serovar A:4, provided by Prof. Dr Takuo Sawada, Nippon Veterinary and Life Science University, Tokyo, Japan) were grown in Tryptose broth (Difco Laboratories, Franklin Lakes, NJ, USA) at 37°C for 6 h and then subcultured on dextrose starch agar (Difco) at 37°C for 18 h. E. coli strain PQE-ompH (Thanasarasakulpong et al, 2015) was grown at 37°C in Luria-Bertani (LB) broth or on agar supplemented with 100 µg/ml ampicillin and 25 µg/ml kanamycin (Sigma-Aldrich, St. Louis, MO, USA).…”
Section: Methodsmentioning
confidence: 99%
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“…Bacterial strains, media and growth conditions P. multocida strains X-73 (serovar A:1, ATCC15742), P-1059 (serovar A:3, ATCC11039) and P-1662 (serovar A:4, provided by Prof. Dr Takuo Sawada, Nippon Veterinary and Life Science University, Tokyo, Japan) were grown in Tryptose broth (Difco Laboratories, Franklin Lakes, NJ, USA) at 37°C for 6 h and then subcultured on dextrose starch agar (Difco) at 37°C for 18 h. E. coli strain PQE-ompH (Thanasarasakulpong et al, 2015) was grown at 37°C in Luria-Bertani (LB) broth or on agar supplemented with 100 µg/ml ampicillin and 25 µg/ml kanamycin (Sigma-Aldrich, St. Louis, MO, USA).…”
Section: Methodsmentioning
confidence: 99%
“…The nasal vaccine is theoretically capable of enhancing the release of immunoglobulin A (IgA) at the mucosal surface, as well as serum immunoglobulin G or Y (IgG or IgY). In addition, the vaccination method can be conducted via nasal droplets or spraying (Woodrow et al, 2012); this is more convenient for use in a mass population or in farm bird flocks (Thanasarasakulpong et al, 2015). Induction of the immune response following mucosal vaccines usually depends upon the use of appropriate adjuvants that can initiate and support the transition from innate to adaptive immunity (Freytag & Clements, 2005).…”
Section: Introductionmentioning
confidence: 99%
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