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Comprehensive interactome analysis of the spike protein of swine acute diarrhea syndrome coronavirus
Swine acute diarrhea syndrome coronavirus (SADS-CoV) is a recently discovered coronavirus that causes severe and acute diarrhea and rapid weight loss in piglets. SADS-CoV was reported to be capable of infecting cell lines derived from diverse species, including bats, mice, hamsters, rats, chickens,...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Chinese Medical Association Publishing House. Published by Elsevier BV.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8127515/ https://www.ncbi.nlm.nih.gov/pubmed/34027383 http://dx.doi.org/10.1016/j.bsheal.2021.05.002 |
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author | Wang, Qingxing Luo, Yun Shang, Weijuan Shi, Zhengli Xiao, Gengfu Zhang, Leike |
author_facet | Wang, Qingxing Luo, Yun Shang, Weijuan Shi, Zhengli Xiao, Gengfu Zhang, Leike |
author_sort | Wang, Qingxing |
collection | PubMed |
description | Swine acute diarrhea syndrome coronavirus (SADS-CoV) is a recently discovered coronavirus that causes severe and acute diarrhea and rapid weight loss in piglets. SADS-CoV was reported to be capable of infecting cell lines derived from diverse species, including bats, mice, hamsters, rats, chickens, pigs, nonhuman primates, and humans, implying its high risk of cross-species infection. However, its receptor is still unknown. In this study, the receptor-binding domain of the SADS-CoV spike (S) protein was purified and then subjected to affinity purification (AP)-coupled mass spectrometry (MS)-based proteomic analysis to identify the interactors of the SADS-CoV S protein. Forty-three host proteins were identified, and a Gene Ontology analysis indicated that these interactors can be grouped into categories such as “cell-cell adhesion”, “translation” “viral transcription”, suggesting that these processes may participate in the SADS-CoV life cycles. RNA interference-based screening of these interactors indicated that PPIB and vimentin can affect SADS-CoV replication. Our study provides an overarching view into the host interactome of the SADS-CoV S protein and highlights potential targets for the development of therapeutics against SADS-CoV. |
format | Online Article Text |
id | pubmed-8127515 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Chinese Medical Association Publishing House. Published by Elsevier BV. |
record_format | MEDLINE/PubMed |
spelling | pubmed-81275152021-05-18 Comprehensive interactome analysis of the spike protein of swine acute diarrhea syndrome coronavirus Wang, Qingxing Luo, Yun Shang, Weijuan Shi, Zhengli Xiao, Gengfu Zhang, Leike Biosaf Health Article Swine acute diarrhea syndrome coronavirus (SADS-CoV) is a recently discovered coronavirus that causes severe and acute diarrhea and rapid weight loss in piglets. SADS-CoV was reported to be capable of infecting cell lines derived from diverse species, including bats, mice, hamsters, rats, chickens, pigs, nonhuman primates, and humans, implying its high risk of cross-species infection. However, its receptor is still unknown. In this study, the receptor-binding domain of the SADS-CoV spike (S) protein was purified and then subjected to affinity purification (AP)-coupled mass spectrometry (MS)-based proteomic analysis to identify the interactors of the SADS-CoV S protein. Forty-three host proteins were identified, and a Gene Ontology analysis indicated that these interactors can be grouped into categories such as “cell-cell adhesion”, “translation” “viral transcription”, suggesting that these processes may participate in the SADS-CoV life cycles. RNA interference-based screening of these interactors indicated that PPIB and vimentin can affect SADS-CoV replication. Our study provides an overarching view into the host interactome of the SADS-CoV S protein and highlights potential targets for the development of therapeutics against SADS-CoV. Chinese Medical Association Publishing House. Published by Elsevier BV. 2021-06 2021-05-17 /pmc/articles/PMC8127515/ /pubmed/34027383 http://dx.doi.org/10.1016/j.bsheal.2021.05.002 Text en © 2021 Chinese Medical Association Publishing House. Published by Elsevier BV. 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 Wang, Qingxing Luo, Yun Shang, Weijuan Shi, Zhengli Xiao, Gengfu Zhang, Leike Comprehensive interactome analysis of the spike protein of swine acute diarrhea syndrome coronavirus |
title | Comprehensive interactome analysis of the spike protein of swine acute diarrhea syndrome coronavirus |
title_full | Comprehensive interactome analysis of the spike protein of swine acute diarrhea syndrome coronavirus |
title_fullStr | Comprehensive interactome analysis of the spike protein of swine acute diarrhea syndrome coronavirus |
title_full_unstemmed | Comprehensive interactome analysis of the spike protein of swine acute diarrhea syndrome coronavirus |
title_short | Comprehensive interactome analysis of the spike protein of swine acute diarrhea syndrome coronavirus |
title_sort | comprehensive interactome analysis of the spike protein of swine acute diarrhea syndrome coronavirus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8127515/ https://www.ncbi.nlm.nih.gov/pubmed/34027383 http://dx.doi.org/10.1016/j.bsheal.2021.05.002 |
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