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Molecular Characterization and Cross-Reactivity of Feline Calicivirus Circulating in Southwestern China
Feline calicivirus (FCV) is an important pathogen of cats that has two genogroups (GI and GII). To investigate the prevalence and molecular characteristics of FCVs in southwestern China, 162 nasal swab samples were collected from cats in animal shelters and pet hospitals. In total, 38 of the clinica...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8473038/ https://www.ncbi.nlm.nih.gov/pubmed/34578393 http://dx.doi.org/10.3390/v13091812 |
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author | Zhou, Long Fu, Nengsheng Ding, Lu Li, Yan Huang, Jian Sha, Xue Zhou, Qun Song, Xin Zhang, Bin |
author_facet | Zhou, Long Fu, Nengsheng Ding, Lu Li, Yan Huang, Jian Sha, Xue Zhou, Qun Song, Xin Zhang, Bin |
author_sort | Zhou, Long |
collection | PubMed |
description | Feline calicivirus (FCV) is an important pathogen of cats that has two genogroups (GI and GII). To investigate the prevalence and molecular characteristics of FCVs in southwestern China, 162 nasal swab samples were collected from cats in animal shelters and pet hospitals. In total, 38 of the clinical samples (23.46%) were identified as FCV positive using nested RT-PCR. Phylogenetic analyses using 10 capsid protein VP1 sequences revealed that 8 GI and 2 GII strains formed two independent clusters. Additionally, three separated FCVs that were not clustered phylogenetically (two GI and one GII strains) were successfully isolated from clinical samples and their full-length genomes were obtained. Phylogenetic and recombinant analyses of a GI FCV revealed genomic breakpoints in ORF1 and ORF2 regions with evidence for recombinant events between GI sub-genogroups, which is reported in China for the first time. Furthermore, sera obtained from mice immunized independently with the three FCV isolates and a commercial vaccine were used to evaluate the cross-reactivity of neutralizing antibodies. The three separate FCVs were neutralized by each other at a 1:19 to 1:775 titer range, whereas the triple-inactivated vaccine was at a titer of 1:16, which suggested that different genogroup/sub-genogroup FCV strains exhibit significantly different titers of neutralizing antibodies, including the commercial FCV vaccine. Thus, our study revealed the genetic diversity and complex cross-reactivity levels of FCVs in southwestern China, which provides new insights for application in vaccination strategies. |
format | Online Article Text |
id | pubmed-8473038 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-84730382021-09-28 Molecular Characterization and Cross-Reactivity of Feline Calicivirus Circulating in Southwestern China Zhou, Long Fu, Nengsheng Ding, Lu Li, Yan Huang, Jian Sha, Xue Zhou, Qun Song, Xin Zhang, Bin Viruses Article Feline calicivirus (FCV) is an important pathogen of cats that has two genogroups (GI and GII). To investigate the prevalence and molecular characteristics of FCVs in southwestern China, 162 nasal swab samples were collected from cats in animal shelters and pet hospitals. In total, 38 of the clinical samples (23.46%) were identified as FCV positive using nested RT-PCR. Phylogenetic analyses using 10 capsid protein VP1 sequences revealed that 8 GI and 2 GII strains formed two independent clusters. Additionally, three separated FCVs that were not clustered phylogenetically (two GI and one GII strains) were successfully isolated from clinical samples and their full-length genomes were obtained. Phylogenetic and recombinant analyses of a GI FCV revealed genomic breakpoints in ORF1 and ORF2 regions with evidence for recombinant events between GI sub-genogroups, which is reported in China for the first time. Furthermore, sera obtained from mice immunized independently with the three FCV isolates and a commercial vaccine were used to evaluate the cross-reactivity of neutralizing antibodies. The three separate FCVs were neutralized by each other at a 1:19 to 1:775 titer range, whereas the triple-inactivated vaccine was at a titer of 1:16, which suggested that different genogroup/sub-genogroup FCV strains exhibit significantly different titers of neutralizing antibodies, including the commercial FCV vaccine. Thus, our study revealed the genetic diversity and complex cross-reactivity levels of FCVs in southwestern China, which provides new insights for application in vaccination strategies. MDPI 2021-09-12 /pmc/articles/PMC8473038/ /pubmed/34578393 http://dx.doi.org/10.3390/v13091812 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Zhou, Long Fu, Nengsheng Ding, Lu Li, Yan Huang, Jian Sha, Xue Zhou, Qun Song, Xin Zhang, Bin Molecular Characterization and Cross-Reactivity of Feline Calicivirus Circulating in Southwestern China |
title | Molecular Characterization and Cross-Reactivity of Feline Calicivirus Circulating in Southwestern China |
title_full | Molecular Characterization and Cross-Reactivity of Feline Calicivirus Circulating in Southwestern China |
title_fullStr | Molecular Characterization and Cross-Reactivity of Feline Calicivirus Circulating in Southwestern China |
title_full_unstemmed | Molecular Characterization and Cross-Reactivity of Feline Calicivirus Circulating in Southwestern China |
title_short | Molecular Characterization and Cross-Reactivity of Feline Calicivirus Circulating in Southwestern China |
title_sort | molecular characterization and cross-reactivity of feline calicivirus circulating in southwestern china |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8473038/ https://www.ncbi.nlm.nih.gov/pubmed/34578393 http://dx.doi.org/10.3390/v13091812 |
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