Porcine Deltacoronavirus Engages the Transmissible Gastroenteritis Virus Functional Receptor Porcine Aminopeptidase N for Infectious Cellular Entry

Identification of cellular receptors used by coronavirus (CoV) entry into the host cells is critical to an understanding of pathogenesis and to development of intervention strategies. The fourth CoV genus, , evolutionarily related to the , has just been defined recently. In the current study, we dem...

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Veröffentlicht in:Journal of virology 2018-06, Vol.92 (12)
Hauptverfasser: Wang, Bin, Liu, Yan, Ji, Chun-Miao, Yang, Yong-Le, Liang, Qi-Zhang, Zhao, Pengwei, Xu, Ling-Dong, Lei, Xi-Mei, Luo, Wen-Ting, Qin, Pan, Zhou, Jiyong, Huang, Yao-Wei
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container_issue 12
container_start_page
container_title Journal of virology
container_volume 92
creator Wang, Bin
Liu, Yan
Ji, Chun-Miao
Yang, Yong-Le
Liang, Qi-Zhang
Zhao, Pengwei
Xu, Ling-Dong
Lei, Xi-Mei
Luo, Wen-Ting
Qin, Pan
Zhou, Jiyong
Huang, Yao-Wei
description Identification of cellular receptors used by coronavirus (CoV) entry into the host cells is critical to an understanding of pathogenesis and to development of intervention strategies. The fourth CoV genus, , evolutionarily related to the , has just been defined recently. In the current study, we demonstrate that porcine aminopeptidase N (pAPN) acts as a cross-genus CoV functional receptor for both enteropathogenic porcine deltacoronovirus (PDCoV) and alphacoronovirus (AlphaCoV) (transmissible gastroenteritis virus [TGEV]) based upon three lines of evidence. First, the soluble S1 protein of PDCoV bound to the surface of target porcine cell lines known to express pAPN as efficiently as TGEV-S1, which could be blocked by soluble pAPN pretreatment. Second, both PDCoV-S1 and TGEV-S1 physically recognized and interacted with pAPN by coimmunoprecipitation in pAPN cDNA-transfected cells and by dot blot hybridization assay. Finally, exogenous expression of pAPN in refractory cells conferred susceptibility to PDCoV-S1 binding and to PDCoV entry and productive infection. PDCoV-S1 appeared to have a lower pAPN-binding affinity and likely consequent lower infection efficiency in pAPN-expressing refractory cells than TGEV-S1, suggesting that there may be differences between these two viruses in the virus-binding regions in pAPN. This study paves the way for dissecting the molecular mechanisms of PDCoV-host interactions and pathogenesis as well as facilitates future vaccine development and intervention strategies against PDCoV infection. The emergence of new human and animal coronaviruses is believed to have occurred through interspecies transmission that is mainly mediated by a species-specific receptor of the host. Among the four genera of the , a couple of functional receptors for the representative members in the genera and have been identified, whereas receptors for and , which are believed to originate from birds, are still unknown. Porcine coronaviruses, including the newly discovered porcine deltacoronavirus (PDCoV) associated with diarrhea in newborn piglets, have posed a serious threat to the pork industry in Asia and North America. Here, we report that PDCoV employs the alphacoronavirus TGEV functional receptor porcine aminopeptidase N (pAPN) for cellular entry, demonstrating the usage of pAPN as a cross-genus CoV functional receptor. The identification of the PDCoV receptor provides another example of the expanded host range of CoV and paves the way for furth
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The fourth CoV genus, , evolutionarily related to the , has just been defined recently. In the current study, we demonstrate that porcine aminopeptidase N (pAPN) acts as a cross-genus CoV functional receptor for both enteropathogenic porcine deltacoronovirus (PDCoV) and alphacoronovirus (AlphaCoV) (transmissible gastroenteritis virus [TGEV]) based upon three lines of evidence. First, the soluble S1 protein of PDCoV bound to the surface of target porcine cell lines known to express pAPN as efficiently as TGEV-S1, which could be blocked by soluble pAPN pretreatment. Second, both PDCoV-S1 and TGEV-S1 physically recognized and interacted with pAPN by coimmunoprecipitation in pAPN cDNA-transfected cells and by dot blot hybridization assay. Finally, exogenous expression of pAPN in refractory cells conferred susceptibility to PDCoV-S1 binding and to PDCoV entry and productive infection. PDCoV-S1 appeared to have a lower pAPN-binding affinity and likely consequent lower infection efficiency in pAPN-expressing refractory cells than TGEV-S1, suggesting that there may be differences between these two viruses in the virus-binding regions in pAPN. This study paves the way for dissecting the molecular mechanisms of PDCoV-host interactions and pathogenesis as well as facilitates future vaccine development and intervention strategies against PDCoV infection. The emergence of new human and animal coronaviruses is believed to have occurred through interspecies transmission that is mainly mediated by a species-specific receptor of the host. Among the four genera of the , a couple of functional receptors for the representative members in the genera and have been identified, whereas receptors for and , which are believed to originate from birds, are still unknown. Porcine coronaviruses, including the newly discovered porcine deltacoronavirus (PDCoV) associated with diarrhea in newborn piglets, have posed a serious threat to the pork industry in Asia and North America. Here, we report that PDCoV employs the alphacoronavirus TGEV functional receptor porcine aminopeptidase N (pAPN) for cellular entry, demonstrating the usage of pAPN as a cross-genus CoV functional receptor. The identification of the PDCoV receptor provides another example of the expanded host range of CoV and paves the way for further investigation of PDCoV-host interaction and pathogenesis.</description><identifier>ISSN: 0022-538X</identifier><identifier>EISSN: 1098-5514</identifier><identifier>DOI: 10.1128/JVI.00318-18</identifier><identifier>PMID: 29618640</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Animals ; CD13 Antigens - metabolism ; Cell Line ; Chlorocebus aethiops ; Coronavirus - metabolism ; Coronavirus Infections - pathology ; Coronavirus Infections - virology ; Cricetinae ; Host Specificity - genetics ; Receptors, Virus - genetics ; Receptors, Virus - metabolism ; Swine ; Swine Diseases - pathology ; Swine Diseases - virology ; Transmissible gastroenteritis virus - metabolism ; Vero Cells ; Virus Attachment ; Virus Internalization ; Virus-Cell Interactions</subject><ispartof>Journal of virology, 2018-06, Vol.92 (12)</ispartof><rights>Copyright © 2018 American Society for Microbiology.</rights><rights>Copyright © 2018 American Society for Microbiology. 2018 American Society for Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c384t-86b2c114a43bb2c1510a1f991cf23198be508d65ff3c716aa3e4918434d8be8b3</citedby><cites>FETCH-LOGICAL-c384t-86b2c114a43bb2c1510a1f991cf23198be508d65ff3c716aa3e4918434d8be8b3</cites><orcidid>0000-0001-9755-8411</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974500/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974500/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29618640$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Bin</creatorcontrib><creatorcontrib>Liu, Yan</creatorcontrib><creatorcontrib>Ji, Chun-Miao</creatorcontrib><creatorcontrib>Yang, Yong-Le</creatorcontrib><creatorcontrib>Liang, Qi-Zhang</creatorcontrib><creatorcontrib>Zhao, Pengwei</creatorcontrib><creatorcontrib>Xu, Ling-Dong</creatorcontrib><creatorcontrib>Lei, Xi-Mei</creatorcontrib><creatorcontrib>Luo, Wen-Ting</creatorcontrib><creatorcontrib>Qin, Pan</creatorcontrib><creatorcontrib>Zhou, Jiyong</creatorcontrib><creatorcontrib>Huang, Yao-Wei</creatorcontrib><title>Porcine Deltacoronavirus Engages the Transmissible Gastroenteritis Virus Functional Receptor Porcine Aminopeptidase N for Infectious Cellular Entry</title><title>Journal of virology</title><addtitle>J Virol</addtitle><description>Identification of cellular receptors used by coronavirus (CoV) entry into the host cells is critical to an understanding of pathogenesis and to development of intervention strategies. The fourth CoV genus, , evolutionarily related to the , has just been defined recently. In the current study, we demonstrate that porcine aminopeptidase N (pAPN) acts as a cross-genus CoV functional receptor for both enteropathogenic porcine deltacoronovirus (PDCoV) and alphacoronovirus (AlphaCoV) (transmissible gastroenteritis virus [TGEV]) based upon three lines of evidence. First, the soluble S1 protein of PDCoV bound to the surface of target porcine cell lines known to express pAPN as efficiently as TGEV-S1, which could be blocked by soluble pAPN pretreatment. Second, both PDCoV-S1 and TGEV-S1 physically recognized and interacted with pAPN by coimmunoprecipitation in pAPN cDNA-transfected cells and by dot blot hybridization assay. Finally, exogenous expression of pAPN in refractory cells conferred susceptibility to PDCoV-S1 binding and to PDCoV entry and productive infection. PDCoV-S1 appeared to have a lower pAPN-binding affinity and likely consequent lower infection efficiency in pAPN-expressing refractory cells than TGEV-S1, suggesting that there may be differences between these two viruses in the virus-binding regions in pAPN. This study paves the way for dissecting the molecular mechanisms of PDCoV-host interactions and pathogenesis as well as facilitates future vaccine development and intervention strategies against PDCoV infection. The emergence of new human and animal coronaviruses is believed to have occurred through interspecies transmission that is mainly mediated by a species-specific receptor of the host. Among the four genera of the , a couple of functional receptors for the representative members in the genera and have been identified, whereas receptors for and , which are believed to originate from birds, are still unknown. 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The identification of the PDCoV receptor provides another example of the expanded host range of CoV and paves the way for further investigation of PDCoV-host interaction and pathogenesis.</description><subject>Animals</subject><subject>CD13 Antigens - metabolism</subject><subject>Cell Line</subject><subject>Chlorocebus aethiops</subject><subject>Coronavirus - metabolism</subject><subject>Coronavirus Infections - pathology</subject><subject>Coronavirus Infections - virology</subject><subject>Cricetinae</subject><subject>Host Specificity - genetics</subject><subject>Receptors, Virus - genetics</subject><subject>Receptors, Virus - metabolism</subject><subject>Swine</subject><subject>Swine Diseases - pathology</subject><subject>Swine Diseases - virology</subject><subject>Transmissible gastroenteritis virus - metabolism</subject><subject>Vero Cells</subject><subject>Virus Attachment</subject><subject>Virus Internalization</subject><subject>Virus-Cell Interactions</subject><issn>0022-538X</issn><issn>1098-5514</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUU1vGyEURFWjxnV767ni2EM34S3sGi6RIjcfjqKkqtKoN8Titw7RGlxgI-V35A8H50vtCcSbmcfMEPIF2B5ALffPrhd7jHGQFch3ZAJMyappQLwnE8bqumq4_LNLPqZ0yxgI0YoPZLdWLchWsAl5-BmidR7pDxyysSEGb-5cHBM98iuzwkTzDdKraHxau5RcNyA9MSnHgD5jdNklev2EPx69za7QB_oLLW5yiPRV_HDtfNiUN7c0CekF7ctw4XvcMgp3jsMwDiaWpTnefyI7vRkSfn45p-T38dHV_LQ6vzxZzA_PK8ulyJVsu9oCCCN4t701wAz0SoHtaw5KdtgwuWybvud2Bq0xHIUCKbhYlpns-JQcPOtuxm6NS1scRTPoTXRrE-91ME7_P_HuRq_CnW7UTDQl8yn59iIQw98RU9YlI1u8GI_Flq5L_lCrmVQF-v0ZamNIKWL_tgaY3vaoS4_6qUcNssC__vu1N_BrcfwRpO2dgg</recordid><startdate>20180615</startdate><enddate>20180615</enddate><creator>Wang, Bin</creator><creator>Liu, Yan</creator><creator>Ji, Chun-Miao</creator><creator>Yang, Yong-Le</creator><creator>Liang, Qi-Zhang</creator><creator>Zhao, Pengwei</creator><creator>Xu, Ling-Dong</creator><creator>Lei, Xi-Mei</creator><creator>Luo, Wen-Ting</creator><creator>Qin, Pan</creator><creator>Zhou, Jiyong</creator><creator>Huang, Yao-Wei</creator><general>American Society for Microbiology</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-9755-8411</orcidid></search><sort><creationdate>20180615</creationdate><title>Porcine Deltacoronavirus Engages the Transmissible Gastroenteritis Virus Functional Receptor Porcine Aminopeptidase N for Infectious Cellular Entry</title><author>Wang, Bin ; 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The fourth CoV genus, , evolutionarily related to the , has just been defined recently. In the current study, we demonstrate that porcine aminopeptidase N (pAPN) acts as a cross-genus CoV functional receptor for both enteropathogenic porcine deltacoronovirus (PDCoV) and alphacoronovirus (AlphaCoV) (transmissible gastroenteritis virus [TGEV]) based upon three lines of evidence. First, the soluble S1 protein of PDCoV bound to the surface of target porcine cell lines known to express pAPN as efficiently as TGEV-S1, which could be blocked by soluble pAPN pretreatment. Second, both PDCoV-S1 and TGEV-S1 physically recognized and interacted with pAPN by coimmunoprecipitation in pAPN cDNA-transfected cells and by dot blot hybridization assay. Finally, exogenous expression of pAPN in refractory cells conferred susceptibility to PDCoV-S1 binding and to PDCoV entry and productive infection. PDCoV-S1 appeared to have a lower pAPN-binding affinity and likely consequent lower infection efficiency in pAPN-expressing refractory cells than TGEV-S1, suggesting that there may be differences between these two viruses in the virus-binding regions in pAPN. This study paves the way for dissecting the molecular mechanisms of PDCoV-host interactions and pathogenesis as well as facilitates future vaccine development and intervention strategies against PDCoV infection. The emergence of new human and animal coronaviruses is believed to have occurred through interspecies transmission that is mainly mediated by a species-specific receptor of the host. Among the four genera of the , a couple of functional receptors for the representative members in the genera and have been identified, whereas receptors for and , which are believed to originate from birds, are still unknown. Porcine coronaviruses, including the newly discovered porcine deltacoronavirus (PDCoV) associated with diarrhea in newborn piglets, have posed a serious threat to the pork industry in Asia and North America. Here, we report that PDCoV employs the alphacoronavirus TGEV functional receptor porcine aminopeptidase N (pAPN) for cellular entry, demonstrating the usage of pAPN as a cross-genus CoV functional receptor. The identification of the PDCoV receptor provides another example of the expanded host range of CoV and paves the way for further investigation of PDCoV-host interaction and pathogenesis.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>29618640</pmid><doi>10.1128/JVI.00318-18</doi><orcidid>https://orcid.org/0000-0001-9755-8411</orcidid><oa>free_for_read</oa></addata></record>
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source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central
subjects Animals
CD13 Antigens - metabolism
Cell Line
Chlorocebus aethiops
Coronavirus - metabolism
Coronavirus Infections - pathology
Coronavirus Infections - virology
Cricetinae
Host Specificity - genetics
Receptors, Virus - genetics
Receptors, Virus - metabolism
Swine
Swine Diseases - pathology
Swine Diseases - virology
Transmissible gastroenteritis virus - metabolism
Vero Cells
Virus Attachment
Virus Internalization
Virus-Cell Interactions
title Porcine Deltacoronavirus Engages the Transmissible Gastroenteritis Virus Functional Receptor Porcine Aminopeptidase N for Infectious Cellular Entry
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