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Deciphering the biology of porcine epidemic diarrhea virus in the era of reverse genetics

Emergence of the porcine epidemic diarrhea virus (PEDV) as a global threat to the swine industry underlies the urgent need for deeper understanding of this virus. To date, we have yet to identify functions for all the major gene products, much less grasp their implications for the viral life cycle a...

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Autores principales: Teeravechyan, Samaporn, Frantz, Phanramphoei Namprachan, Wongthida, Phonphimon, Chailangkarn, Thanathom, Jaru-ampornpan, Peera, Koonpaew, Surapong, Jongkaewwattana, Anan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114553/
https://www.ncbi.nlm.nih.gov/pubmed/27212685
http://dx.doi.org/10.1016/j.virusres.2016.05.003
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author Teeravechyan, Samaporn
Frantz, Phanramphoei Namprachan
Wongthida, Phonphimon
Chailangkarn, Thanathom
Jaru-ampornpan, Peera
Koonpaew, Surapong
Jongkaewwattana, Anan
author_facet Teeravechyan, Samaporn
Frantz, Phanramphoei Namprachan
Wongthida, Phonphimon
Chailangkarn, Thanathom
Jaru-ampornpan, Peera
Koonpaew, Surapong
Jongkaewwattana, Anan
author_sort Teeravechyan, Samaporn
collection PubMed
description Emergence of the porcine epidemic diarrhea virus (PEDV) as a global threat to the swine industry underlies the urgent need for deeper understanding of this virus. To date, we have yet to identify functions for all the major gene products, much less grasp their implications for the viral life cycle and pathogenic mechanisms. A major reason is the lack of genetic tools for studying PEDV. In this review, we discuss the reverse genetics approaches that have been successfully used to engineer infectious clones of PEDV as well as other potential and complementary methods that have yet to be applied to PEDV. The importance of proper cell culture for successful PEDV propagation and maintenance of disease phenotype are addressed in our survey of permissive cell lines. We also highlight areas of particular relevance to PEDV pathogenesis and disease that have benefited from reverse genetics studies and pressing questions that await resolution by such studies. In particular, we examine the spike protein as a determinant of viral tropism, entry and virulence, ORF3 and its association with cell culture adaptation, and the nucleocapsid protein and its potential role in modulating PEDV pathogenicity. Finally, we conclude with an exploration of how reverse genetics can help mitigate the global impact of PEDV by addressing the challenges of vaccine development.
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spelling pubmed-71145532020-04-02 Deciphering the biology of porcine epidemic diarrhea virus in the era of reverse genetics Teeravechyan, Samaporn Frantz, Phanramphoei Namprachan Wongthida, Phonphimon Chailangkarn, Thanathom Jaru-ampornpan, Peera Koonpaew, Surapong Jongkaewwattana, Anan Virus Res Article Emergence of the porcine epidemic diarrhea virus (PEDV) as a global threat to the swine industry underlies the urgent need for deeper understanding of this virus. To date, we have yet to identify functions for all the major gene products, much less grasp their implications for the viral life cycle and pathogenic mechanisms. A major reason is the lack of genetic tools for studying PEDV. In this review, we discuss the reverse genetics approaches that have been successfully used to engineer infectious clones of PEDV as well as other potential and complementary methods that have yet to be applied to PEDV. The importance of proper cell culture for successful PEDV propagation and maintenance of disease phenotype are addressed in our survey of permissive cell lines. We also highlight areas of particular relevance to PEDV pathogenesis and disease that have benefited from reverse genetics studies and pressing questions that await resolution by such studies. In particular, we examine the spike protein as a determinant of viral tropism, entry and virulence, ORF3 and its association with cell culture adaptation, and the nucleocapsid protein and its potential role in modulating PEDV pathogenicity. Finally, we conclude with an exploration of how reverse genetics can help mitigate the global impact of PEDV by addressing the challenges of vaccine development. Elsevier B.V. 2016-12-02 2016-05-20 /pmc/articles/PMC7114553/ /pubmed/27212685 http://dx.doi.org/10.1016/j.virusres.2016.05.003 Text en © 2016 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Teeravechyan, Samaporn
Frantz, Phanramphoei Namprachan
Wongthida, Phonphimon
Chailangkarn, Thanathom
Jaru-ampornpan, Peera
Koonpaew, Surapong
Jongkaewwattana, Anan
Deciphering the biology of porcine epidemic diarrhea virus in the era of reverse genetics
title Deciphering the biology of porcine epidemic diarrhea virus in the era of reverse genetics
title_full Deciphering the biology of porcine epidemic diarrhea virus in the era of reverse genetics
title_fullStr Deciphering the biology of porcine epidemic diarrhea virus in the era of reverse genetics
title_full_unstemmed Deciphering the biology of porcine epidemic diarrhea virus in the era of reverse genetics
title_short Deciphering the biology of porcine epidemic diarrhea virus in the era of reverse genetics
title_sort deciphering the biology of porcine epidemic diarrhea virus in the era of reverse genetics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114553/
https://www.ncbi.nlm.nih.gov/pubmed/27212685
http://dx.doi.org/10.1016/j.virusres.2016.05.003
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