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Genomic characterization and pathogenicity of porcine deltacoronavirus strain CHN-HG-2017 from China

Porcine deltacoronavirus (PDCoV) was first detected in Hong Kong and has recently spread to many countries around the world. PDCoV causes acute diarrhea and vomiting in pigs, resulting in significant economic losses in the global pork industry. In this study, a Chinese PDCoV strain, designated CHN-H...

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Autores principales: Zhang, Meng-Jia, Liu, De-Jian, Liu, Xiao-Li, Ge, Xing-Yi, Jongkaewwattana, Anan, He, Qi-Gai, Luo, Rui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Vienna 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7087286/
https://www.ncbi.nlm.nih.gov/pubmed/30377826
http://dx.doi.org/10.1007/s00705-018-4081-6
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author Zhang, Meng-Jia
Liu, De-Jian
Liu, Xiao-Li
Ge, Xing-Yi
Jongkaewwattana, Anan
He, Qi-Gai
Luo, Rui
author_facet Zhang, Meng-Jia
Liu, De-Jian
Liu, Xiao-Li
Ge, Xing-Yi
Jongkaewwattana, Anan
He, Qi-Gai
Luo, Rui
author_sort Zhang, Meng-Jia
collection PubMed
description Porcine deltacoronavirus (PDCoV) was first detected in Hong Kong and has recently spread to many countries around the world. PDCoV causes acute diarrhea and vomiting in pigs, resulting in significant economic losses in the global pork industry. In this study, a Chinese PDCoV strain, designated CHN-HG-2017, was isolated from feces of a suckling piglet with severe watery diarrhea on a farm located in central China. Subsequently, the virus was identified by an indirect immunofluorescence assay and electron microscopy. A nucleotide sequence alignment showed that the whole genome of CHN-HG-2017 is 97.6%-99.1% identical to other PDCoV strains. Analysis of potential recombination sites showed that CHN-HG-2017 is a possible recombinant originating from the strains CH/SXD1/2015 and Vietnam/HaNoi6/2015. Furthermore, the pathogenicity of this recombinant PDCoV strain was investigated in 5-day-old piglets by oral inoculation. The challenged piglets developed typical symptoms, such as vomiting, anorexia, diarrhea and lethargy, from 1 to 7 days post-inoculation (DPI). Viral shedding was detected in rectal swabs until 14 DPI in the challenged piglets. Interestingly, high titers of virus-neutralizing antibodies in sera were detected at 21 DPI. Tissues of small intestines from CHN-HG-2017-infected piglets at 4 DPI displayed significant macroscopic and microscopic lesions with clear viral antigen expression. Our analysis of the full genome sequence of a recombinant PDCoV and its virulence in suckling piglets might provide new insights into the pathogenesis of PDCoV and facilitate further investigation of this newly emerged pathogen.
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spelling pubmed-70872862020-03-23 Genomic characterization and pathogenicity of porcine deltacoronavirus strain CHN-HG-2017 from China Zhang, Meng-Jia Liu, De-Jian Liu, Xiao-Li Ge, Xing-Yi Jongkaewwattana, Anan He, Qi-Gai Luo, Rui Arch Virol Original Article Porcine deltacoronavirus (PDCoV) was first detected in Hong Kong and has recently spread to many countries around the world. PDCoV causes acute diarrhea and vomiting in pigs, resulting in significant economic losses in the global pork industry. In this study, a Chinese PDCoV strain, designated CHN-HG-2017, was isolated from feces of a suckling piglet with severe watery diarrhea on a farm located in central China. Subsequently, the virus was identified by an indirect immunofluorescence assay and electron microscopy. A nucleotide sequence alignment showed that the whole genome of CHN-HG-2017 is 97.6%-99.1% identical to other PDCoV strains. Analysis of potential recombination sites showed that CHN-HG-2017 is a possible recombinant originating from the strains CH/SXD1/2015 and Vietnam/HaNoi6/2015. Furthermore, the pathogenicity of this recombinant PDCoV strain was investigated in 5-day-old piglets by oral inoculation. The challenged piglets developed typical symptoms, such as vomiting, anorexia, diarrhea and lethargy, from 1 to 7 days post-inoculation (DPI). Viral shedding was detected in rectal swabs until 14 DPI in the challenged piglets. Interestingly, high titers of virus-neutralizing antibodies in sera were detected at 21 DPI. Tissues of small intestines from CHN-HG-2017-infected piglets at 4 DPI displayed significant macroscopic and microscopic lesions with clear viral antigen expression. Our analysis of the full genome sequence of a recombinant PDCoV and its virulence in suckling piglets might provide new insights into the pathogenesis of PDCoV and facilitate further investigation of this newly emerged pathogen. Springer Vienna 2018-10-30 2019 /pmc/articles/PMC7087286/ /pubmed/30377826 http://dx.doi.org/10.1007/s00705-018-4081-6 Text en © Springer-Verlag GmbH Austria, part of Springer Nature 2018 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 Original Article
Zhang, Meng-Jia
Liu, De-Jian
Liu, Xiao-Li
Ge, Xing-Yi
Jongkaewwattana, Anan
He, Qi-Gai
Luo, Rui
Genomic characterization and pathogenicity of porcine deltacoronavirus strain CHN-HG-2017 from China
title Genomic characterization and pathogenicity of porcine deltacoronavirus strain CHN-HG-2017 from China
title_full Genomic characterization and pathogenicity of porcine deltacoronavirus strain CHN-HG-2017 from China
title_fullStr Genomic characterization and pathogenicity of porcine deltacoronavirus strain CHN-HG-2017 from China
title_full_unstemmed Genomic characterization and pathogenicity of porcine deltacoronavirus strain CHN-HG-2017 from China
title_short Genomic characterization and pathogenicity of porcine deltacoronavirus strain CHN-HG-2017 from China
title_sort genomic characterization and pathogenicity of porcine deltacoronavirus strain chn-hg-2017 from china
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7087286/
https://www.ncbi.nlm.nih.gov/pubmed/30377826
http://dx.doi.org/10.1007/s00705-018-4081-6
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