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Full genome analysis of a novel type II feline coronavirus NTU156
Infections by type II feline coronaviruses (FCoVs) have been shown to be significantly correlated with fatal feline infectious peritonitis (FIP). Despite nearly six decades having passed since its first emergence, different studies have shown that type II FCoV represents only a small portion of the...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7089305/ https://www.ncbi.nlm.nih.gov/pubmed/23239278 http://dx.doi.org/10.1007/s11262-012-0864-0 |
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author | Lin, Chao-Nan Chang, Ruey-Yi Su, Bi-Ling Chueh, Ling-Ling |
author_facet | Lin, Chao-Nan Chang, Ruey-Yi Su, Bi-Ling Chueh, Ling-Ling |
author_sort | Lin, Chao-Nan |
collection | PubMed |
description | Infections by type II feline coronaviruses (FCoVs) have been shown to be significantly correlated with fatal feline infectious peritonitis (FIP). Despite nearly six decades having passed since its first emergence, different studies have shown that type II FCoV represents only a small portion of the total FCoV seropositivity in cats; hence, there is very limited knowledge of the evolution of type II FCoV. To elucidate the correlation between viral emergence and FIP, a local isolate (NTU156) that was derived from a FIP cat was analyzed along with other worldwide strains. Containing an in-frame deletion of 442 nucleotides in open reading frame 3c, the complete genome size of NTU156 (28,897 nucleotides) appears to be the smallest among the known type II feline coronaviruses. Bootscan analysis revealed that NTU156 evolved from two crossover events between type I FCoV and canine coronavirus, with recombination sites located in the RNA-dependent RNA polymerase and M genes. With an exchange of nearly one-third of the genome with other members of alphacoronaviruses, the new emerging virus could gain new antigenicity, posing a threat to cats that either have been infected with a type I virus before or never have been infected with FCoV. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11262-012-0864-0) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7089305 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-70893052020-03-23 Full genome analysis of a novel type II feline coronavirus NTU156 Lin, Chao-Nan Chang, Ruey-Yi Su, Bi-Ling Chueh, Ling-Ling Virus Genes Article Infections by type II feline coronaviruses (FCoVs) have been shown to be significantly correlated with fatal feline infectious peritonitis (FIP). Despite nearly six decades having passed since its first emergence, different studies have shown that type II FCoV represents only a small portion of the total FCoV seropositivity in cats; hence, there is very limited knowledge of the evolution of type II FCoV. To elucidate the correlation between viral emergence and FIP, a local isolate (NTU156) that was derived from a FIP cat was analyzed along with other worldwide strains. Containing an in-frame deletion of 442 nucleotides in open reading frame 3c, the complete genome size of NTU156 (28,897 nucleotides) appears to be the smallest among the known type II feline coronaviruses. Bootscan analysis revealed that NTU156 evolved from two crossover events between type I FCoV and canine coronavirus, with recombination sites located in the RNA-dependent RNA polymerase and M genes. With an exchange of nearly one-third of the genome with other members of alphacoronaviruses, the new emerging virus could gain new antigenicity, posing a threat to cats that either have been infected with a type I virus before or never have been infected with FCoV. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11262-012-0864-0) contains supplementary material, which is available to authorized users. Springer US 2012-12-14 2013 /pmc/articles/PMC7089305/ /pubmed/23239278 http://dx.doi.org/10.1007/s11262-012-0864-0 Text en © Springer Science+Business Media New York 2012 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 Lin, Chao-Nan Chang, Ruey-Yi Su, Bi-Ling Chueh, Ling-Ling Full genome analysis of a novel type II feline coronavirus NTU156 |
title | Full genome analysis of a novel type II feline coronavirus NTU156 |
title_full | Full genome analysis of a novel type II feline coronavirus NTU156 |
title_fullStr | Full genome analysis of a novel type II feline coronavirus NTU156 |
title_full_unstemmed | Full genome analysis of a novel type II feline coronavirus NTU156 |
title_short | Full genome analysis of a novel type II feline coronavirus NTU156 |
title_sort | full genome analysis of a novel type ii feline coronavirus ntu156 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7089305/ https://www.ncbi.nlm.nih.gov/pubmed/23239278 http://dx.doi.org/10.1007/s11262-012-0864-0 |
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