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Genetic characterization of an isolate of canine distemper virus from a Tibetan Mastiff in China

Canine distemper (CD) is a highly contagious, often fatal, multisystemic, and incurable disease in dogs and other carnivores, which is caused by canine distemper virus (CDV). Although vaccines have been used as the principal means of controlling the disease, CD has been reported in vaccinated animal...

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Autores principales: Li, Weike, Li, Tiansong, Liu, Yuxiu, Gao, Yuwei, Yang, Songtao, Feng, Na, Sun, Heting, Wang, Shengle, Wang, Lei, Bu, Zhigao, Xia, Xianzhu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7089258/
https://www.ncbi.nlm.nih.gov/pubmed/24691820
http://dx.doi.org/10.1007/s11262-014-1062-z
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author Li, Weike
Li, Tiansong
Liu, Yuxiu
Gao, Yuwei
Yang, Songtao
Feng, Na
Sun, Heting
Wang, Shengle
Wang, Lei
Bu, Zhigao
Xia, Xianzhu
author_facet Li, Weike
Li, Tiansong
Liu, Yuxiu
Gao, Yuwei
Yang, Songtao
Feng, Na
Sun, Heting
Wang, Shengle
Wang, Lei
Bu, Zhigao
Xia, Xianzhu
author_sort Li, Weike
collection PubMed
description Canine distemper (CD) is a highly contagious, often fatal, multisystemic, and incurable disease in dogs and other carnivores, which is caused by canine distemper virus (CDV). Although vaccines have been used as the principal means of controlling the disease, CD has been reported in vaccinated animals. The hemoagglutinin (H) protein is one of the most important antigens for inducing protective immunity against CD, and antigenic variation of recent CDV strains may explain vaccination failure. In this study, a new CDV isolate (TM-CC) was obtained from a Tibetan Mastiff that died of distemper, and its genome was characterized. Phylogenetic analysis of the H gene revealed that the CDV-TM-CC strain is unique among 20 other CDV strains and can be classified into the Asia-1 group with the Chinese strains, Hebei and HLJ1-06, and the Japanese strain, CYN07-hV. The H gene of CDV-TM-CC shows low identity (90.4 % nt and 88.9 % aa) with the H gene of the classical Onderstepoort vaccine strain, which may explain the inability of the Tibetan Mastiff to mount a protective immune response. We also performed a comprehensive phylogenetic analysis of the N, P, and F protein sequences, as well as potential N-glycosylation sites and cysteine residues. This analysis shows that an N-glycosylation site at aa 108-110 within the F protein of CDV-TM-CC is specific for the wild-type strains (5804P, A75/17, and 164071) and the Asia-1 group strains, and may be another important factor for the poor immune response. These results provide important information for the design of CD vaccines in the China region and elsewhere.
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spelling pubmed-70892582020-03-23 Genetic characterization of an isolate of canine distemper virus from a Tibetan Mastiff in China Li, Weike Li, Tiansong Liu, Yuxiu Gao, Yuwei Yang, Songtao Feng, Na Sun, Heting Wang, Shengle Wang, Lei Bu, Zhigao Xia, Xianzhu Virus Genes Article Canine distemper (CD) is a highly contagious, often fatal, multisystemic, and incurable disease in dogs and other carnivores, which is caused by canine distemper virus (CDV). Although vaccines have been used as the principal means of controlling the disease, CD has been reported in vaccinated animals. The hemoagglutinin (H) protein is one of the most important antigens for inducing protective immunity against CD, and antigenic variation of recent CDV strains may explain vaccination failure. In this study, a new CDV isolate (TM-CC) was obtained from a Tibetan Mastiff that died of distemper, and its genome was characterized. Phylogenetic analysis of the H gene revealed that the CDV-TM-CC strain is unique among 20 other CDV strains and can be classified into the Asia-1 group with the Chinese strains, Hebei and HLJ1-06, and the Japanese strain, CYN07-hV. The H gene of CDV-TM-CC shows low identity (90.4 % nt and 88.9 % aa) with the H gene of the classical Onderstepoort vaccine strain, which may explain the inability of the Tibetan Mastiff to mount a protective immune response. We also performed a comprehensive phylogenetic analysis of the N, P, and F protein sequences, as well as potential N-glycosylation sites and cysteine residues. This analysis shows that an N-glycosylation site at aa 108-110 within the F protein of CDV-TM-CC is specific for the wild-type strains (5804P, A75/17, and 164071) and the Asia-1 group strains, and may be another important factor for the poor immune response. These results provide important information for the design of CD vaccines in the China region and elsewhere. Springer US 2014-04-02 2014 /pmc/articles/PMC7089258/ /pubmed/24691820 http://dx.doi.org/10.1007/s11262-014-1062-z Text en © Springer Science+Business Media New York 2014 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Article
Li, Weike
Li, Tiansong
Liu, Yuxiu
Gao, Yuwei
Yang, Songtao
Feng, Na
Sun, Heting
Wang, Shengle
Wang, Lei
Bu, Zhigao
Xia, Xianzhu
Genetic characterization of an isolate of canine distemper virus from a Tibetan Mastiff in China
title Genetic characterization of an isolate of canine distemper virus from a Tibetan Mastiff in China
title_full Genetic characterization of an isolate of canine distemper virus from a Tibetan Mastiff in China
title_fullStr Genetic characterization of an isolate of canine distemper virus from a Tibetan Mastiff in China
title_full_unstemmed Genetic characterization of an isolate of canine distemper virus from a Tibetan Mastiff in China
title_short Genetic characterization of an isolate of canine distemper virus from a Tibetan Mastiff in China
title_sort genetic characterization of an isolate of canine distemper virus from a tibetan mastiff in china
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7089258/
https://www.ncbi.nlm.nih.gov/pubmed/24691820
http://dx.doi.org/10.1007/s11262-014-1062-z
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