Characterization of a highly virulent Avibacterium paragallinarum isolate.
Avibacterium paragallinarum
HMTp210 hypervariable region
characterization
Journal
Journal of animal science
ISSN: 1525-3163
Titre abrégé: J Anim Sci
Pays: United States
ID NLM: 8003002
Informations de publication
Date de publication:
03 Jan 2023
03 Jan 2023
Historique:
received:
14
03
2023
accepted:
25
10
2023
pmc-release:
26
10
2024
medline:
13
11
2023
pubmed:
26
10
2023
entrez:
26
10
2023
Statut:
ppublish
Résumé
Infectious coryza (IC) is an important respiratory infectious disease in chickens. In this study, an Avibacterium paragallinarum Page serovar C strain, named ZJ-C, was isolated from a local layer flock that was routinely vaccinated with an inactivated trivalent vaccine, using reference strain Modesto as the serovar C immunogen. The pathogenicity, immunogenicity, and genetic characteristics of ZJ-C were studied. The minimum pathogenic dose of the isolate was 100 CFU, which was 1/1,000 of the dose of the serovar C reference strain Modesto. The vaccination-challenge trial in specific pathogen-free (SPF) chickens showed that the ZJ-C bacterin could provide 100% protection against challenge from both ZJ-C and Modesto strains, whereas Modesto provided 100% protection against challenge from itself, but only 70% protection against ZJ-C. Sequence analysis of the HMTp210 hypervariable region (region 2) showed that the homology of region 2 between ZJ-C and Modesto was 96.14%, whereas the homology between ZJ-C and the Kume serovar C-4 reference strain HP60 was 99.83%. Phylogenetic analysis of region 2 showed that ZJ-C was most closely related to cluster C-4, represented by HP60. The experimental data obtained in this study will help the selection of optimal vaccine strains and assist serotyping studies of Av. paragallinarum. Vaccination with inactivated multivalent vaccines is a primary strategy to control Infectious coryza. Avibacterium paragallinarum serotyping is important for effective protection as inactivated whole-cell vaccines provide protection against only the serogroup or serovar from which the vaccine was derived. In this study, a novel serovar within the serogroup C Avibacterium paragallinarum isolate ZJ-C has been characterized first time in China. It was highly virulent and induced 100% cross-protection to Modesto bacterin vaccinated chickens, but not the other way around.
Autres résumés
Type: plain-language-summary
(eng)
Vaccination with inactivated multivalent vaccines is a primary strategy to control Infectious coryza. Avibacterium paragallinarum serotyping is important for effective protection as inactivated whole-cell vaccines provide protection against only the serogroup or serovar from which the vaccine was derived. In this study, a novel serovar within the serogroup C Avibacterium paragallinarum isolate ZJ-C has been characterized first time in China. It was highly virulent and induced 100% cross-protection to Modesto bacterin vaccinated chickens, but not the other way around.
Identifiants
pubmed: 37882211
pii: 7330242
doi: 10.1093/jas/skad365
pmc: PMC10638103
pii:
doi:
Substances chimiques
Bacterial Vaccines
0
Vaccines, Inactivated
0
Types de publication
Journal Article
Randomized Controlled Trial, Veterinary
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : the Beijing Natural Science Foundation
ID : 6212009
Organisme : Reform and Development Project of Beijing Academy of Agricultural and Forestry Sciences
ID : XMS202302
Informations de copyright
© The Author(s) 2023. Published by Oxford University Press on behalf of the American Society of Animal Science. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.
Références
Avian Dis. 1990 Jul-Sep;34(3):643-5
pubmed: 2241694
Avian Dis. 2020 Jun;64(2):197-202
pubmed: 32550620
Vet Immunol Immunopathol. 2018 May;199:77-80
pubmed: 29678233
Avian Pathol. 2008 Apr;37(2):183-6
pubmed: 18393097
J Clin Microbiol. 1983 Jun;17(6):958-64
pubmed: 6874914
Avian Dis. 2020 Jun;64(2):157-165
pubmed: 32550616
Avian Dis. 1996 Apr-Jun;40(2):398-407
pubmed: 8790892
Vet Sci. 2022 Jan 12;9(1):
pubmed: 35051111
Poult Sci. 2020 Dec;99(12):6525-6532
pubmed: 33248567
Clin Microbiol Rev. 1999 Oct;12(4):627-32
pubmed: 10515906
Vet Microbiol. 2014 Dec 5;174(3-4):474-482
pubmed: 25465664
Avian Dis. 2019 Sep 1;63(3):486-494
pubmed: 31967433
Onderstepoort J Vet Res. 1996 Sep;63(3):217-26
pubmed: 8917859
Avian Pathol. 2004 Oct;33(5):506-11
pubmed: 15545030
J Vet Diagn Invest. 2016 Sep;28(5):555-60
pubmed: 27423732
Am J Vet Res. 1962 Jan;23:85-95
pubmed: 14483162
J Clin Microbiol. 1989 Jul;27(7):1510-3
pubmed: 2768440
Avian Dis. 2004 Dec;48(4):886-9
pubmed: 15666870
Onderstepoort J Vet Res. 2004 Mar;71(1):1-8
pubmed: 15185569
Res Vet Sci. 2013 Jun;94(3):504-9
pubmed: 23178044
Microbiology (Reading). 2002 Jul;148(Pt 7):2171-2179
pubmed: 12101304
Avian Pathol. 2003 Jun;32(3):265-9
pubmed: 12850915
J Vet Med Sci. 2017 Jul 19;79(7):1210-1214
pubmed: 28552860
Avian Dis. 2021 Sep;65(3):329-334
pubmed: 34427403
Onderstepoort J Vet Res. 2002 Jun;69(2):163-9
pubmed: 12234003
Avian Pathol. 2019 Dec;48(6):549-556
pubmed: 31280592
J Vet Diagn Invest. 2014 Mar;26(2):272-6
pubmed: 24590665
Vaccine. 2011 Jan 17;29(4):660-7
pubmed: 21115052
Aust Vet J. 2003 Jan-Feb;81(1-2):96-7
pubmed: 15084021
J Vet Med Sci. 2012 Feb;74(2):271-3
pubmed: 21979456