Cross-protection conferred by immunization with an rOmpH-based intranasal fowl cholera vaccine

© 2017 Houghton Trust Ltd. A previous study demonstrated that a recombinant outer membrane protein H (rOmpH)-based intranasal fowl cholera vaccine elicited efficient homologous protection against the Pasteurella multocida strain X-73 (A:1) in chickens. The present study aimed to determine the cross-...

Full description

Saved in:
Bibliographic Details
Main Authors: Varinrak T., Poolperm P., Sawada T., Sthitmatee N.
Format: Journal
Published: 2017
Online Access:https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85019733415&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/40123
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Chiang Mai University
id th-cmuir.6653943832-40123
record_format dspace
spelling th-cmuir.6653943832-401232017-09-28T04:06:43Z Cross-protection conferred by immunization with an rOmpH-based intranasal fowl cholera vaccine Varinrak T. Poolperm P. Sawada T. Sthitmatee N. © 2017 Houghton Trust Ltd. A previous study demonstrated that a recombinant outer membrane protein H (rOmpH)-based intranasal fowl cholera vaccine elicited efficient homologous protection against the Pasteurella multocida strain X-73 (A:1) in chickens. The present study aimed to determine the cross-protectivity against heterologous P. multocida strains. The rOmpH was purified via electroelution and formulated with two kinds of adjuvants. The vaccine formulations in a total volume of 100 µl were 100 µg rOmpH with 3 µg of Escherichia coli enterotoxin B or 10 µg of CpG ODN2007. Chickens were assigned to three experimental groups depending on bacterial strain challenge exposure as well as three control groups. The chickens were immunized intranasally three times at three-week intervals. Challenge exposures were conducted by inoculation with homologous strain X-73 or heterologous strains P-1059 (A:3) or P-1662 (A:4) at four weeks after the final immunization. The specific antibody against rOmpH was produced in vaccinated birds. Sera IgY and secretory IgA antibody titres were significantly increased (P < 0.05) post-immunization. The stimulation index values of the vaccinated groups were significantly different from stimulation index values of the non-vaccinated groups (P < 0.05). Chicken survival rates after exposure to avian P. multocida strains ranged from 70% to 100%. There was no significant difference in protection between two kinds of adjuvants in vaccine formulations. Statistical analysis indicated no significant differences in protection among avian P. multocida strains challenge exposure. We conclude that an in-house rOmpH-based intranasal fowl cholera vaccine produced efficient cross-protectivity against heterologous strains of P. multocida. 2017-09-28T04:06:43Z 2017-09-28T04:06:43Z 5 Journal 03079457 2-s2.0-85019733415 10.1080/03079457.2017.1321105 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85019733415&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/40123
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
description © 2017 Houghton Trust Ltd. A previous study demonstrated that a recombinant outer membrane protein H (rOmpH)-based intranasal fowl cholera vaccine elicited efficient homologous protection against the Pasteurella multocida strain X-73 (A:1) in chickens. The present study aimed to determine the cross-protectivity against heterologous P. multocida strains. The rOmpH was purified via electroelution and formulated with two kinds of adjuvants. The vaccine formulations in a total volume of 100 µl were 100 µg rOmpH with 3 µg of Escherichia coli enterotoxin B or 10 µg of CpG ODN2007. Chickens were assigned to three experimental groups depending on bacterial strain challenge exposure as well as three control groups. The chickens were immunized intranasally three times at three-week intervals. Challenge exposures were conducted by inoculation with homologous strain X-73 or heterologous strains P-1059 (A:3) or P-1662 (A:4) at four weeks after the final immunization. The specific antibody against rOmpH was produced in vaccinated birds. Sera IgY and secretory IgA antibody titres were significantly increased (P < 0.05) post-immunization. The stimulation index values of the vaccinated groups were significantly different from stimulation index values of the non-vaccinated groups (P < 0.05). Chicken survival rates after exposure to avian P. multocida strains ranged from 70% to 100%. There was no significant difference in protection between two kinds of adjuvants in vaccine formulations. Statistical analysis indicated no significant differences in protection among avian P. multocida strains challenge exposure. We conclude that an in-house rOmpH-based intranasal fowl cholera vaccine produced efficient cross-protectivity against heterologous strains of P. multocida.
format Journal
author Varinrak T.
Poolperm P.
Sawada T.
Sthitmatee N.
spellingShingle Varinrak T.
Poolperm P.
Sawada T.
Sthitmatee N.
Cross-protection conferred by immunization with an rOmpH-based intranasal fowl cholera vaccine
author_facet Varinrak T.
Poolperm P.
Sawada T.
Sthitmatee N.
author_sort Varinrak T.
title Cross-protection conferred by immunization with an rOmpH-based intranasal fowl cholera vaccine
title_short Cross-protection conferred by immunization with an rOmpH-based intranasal fowl cholera vaccine
title_full Cross-protection conferred by immunization with an rOmpH-based intranasal fowl cholera vaccine
title_fullStr Cross-protection conferred by immunization with an rOmpH-based intranasal fowl cholera vaccine
title_full_unstemmed Cross-protection conferred by immunization with an rOmpH-based intranasal fowl cholera vaccine
title_sort cross-protection conferred by immunization with an romph-based intranasal fowl cholera vaccine
publishDate 2017
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85019733415&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/40123
_version_ 1681421751818387456