Baculovirus IAP1 induces caspase-dependent apoptosis in insect cells
Baculoviruses encode inhibitors of apoptosis (IAPs), which are classified into five groups, IAP1–5, based on their sequence homology. Most of the baculovirus IAPs with anti-apoptotic functions belong to the IAP3 group, with certain exceptions. The functional roles of IAPs from other groups during vi...
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description | Baculoviruses encode inhibitors of apoptosis (IAPs), which are classified into five groups, IAP1–5, based on their sequence homology. Most of the baculovirus IAPs with anti-apoptotic functions belong to the IAP3 group, with certain exceptions. The functional roles of IAPs from other groups during virus infection have not been well established. We have previously shown that Hyphantria cunea multiple nucleopolyhedrovirus (HycuMNPV) encodes three iap genes, hycu-iap1, hycu-iap2 and hycu-iap3, and that only Hycu-IAP3 has anti-apoptotic activity against actinomycin D-induced apoptosis of Spodoptera frugiperda Sf9 cells. In the present study, we demonstrate that transient expression of Hycu-IAP1 is capable of inducing apoptosis and/or stimulating caspase-3-like protease activity in various lepidopteran and dipteran cell lines. Transient-expression assay analysis also demonstrates that not only Hycu-IAP1 but also IAP1s from Autographa californica MNPV, Bombyx mori NPV and Orgyia pseudotsugata MNPV (OpMNPV) are capable of inducing apoptosis, and that apoptosis induced by Hycu-IAP1 is precluded by the functional anti-apoptotic baculovirus protein Hycu-IAP3. In HycuMNPV-infected Spilosoma imparilis (SpIm) cells and OpMNPV-infected Ld652Y cells, caspase-3-like protease activity is markedly stimulated during the late stages of infection, and the caspase-3-like protease activity stimulated in HycuMNPV-infected SpIm cells is repressed by RNA interference-mediated silencing of hycu-iap1. In addition, initiator caspase Bm-Dronc, the B. mori homologue of Dronc, is cleaved upon transfection of BM-N cells with a plasmid expressing Hycu-IAP1. These results provide the first evidence that baculovirus IAP1s act to induce caspase-dependent apoptosis, possibly by replacing the cellular IAP1 that prevents Dronc activation. |
doi_str_mv | 10.1099/vir.0.033332-0 |
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Most of the baculovirus IAPs with anti-apoptotic functions belong to the IAP3 group, with certain exceptions. The functional roles of IAPs from other groups during virus infection have not been well established. We have previously shown that Hyphantria cunea multiple nucleopolyhedrovirus (HycuMNPV) encodes three iap genes, hycu-iap1, hycu-iap2 and hycu-iap3, and that only Hycu-IAP3 has anti-apoptotic activity against actinomycin D-induced apoptosis of Spodoptera frugiperda Sf9 cells. In the present study, we demonstrate that transient expression of Hycu-IAP1 is capable of inducing apoptosis and/or stimulating caspase-3-like protease activity in various lepidopteran and dipteran cell lines. Transient-expression assay analysis also demonstrates that not only Hycu-IAP1 but also IAP1s from Autographa californica MNPV, Bombyx mori NPV and Orgyia pseudotsugata MNPV (OpMNPV) are capable of inducing apoptosis, and that apoptosis induced by Hycu-IAP1 is precluded by the functional anti-apoptotic baculovirus protein Hycu-IAP3. In HycuMNPV-infected Spilosoma imparilis (SpIm) cells and OpMNPV-infected Ld652Y cells, caspase-3-like protease activity is markedly stimulated during the late stages of infection, and the caspase-3-like protease activity stimulated in HycuMNPV-infected SpIm cells is repressed by RNA interference-mediated silencing of hycu-iap1. In addition, initiator caspase Bm-Dronc, the B. mori homologue of Dronc, is cleaved upon transfection of BM-N cells with a plasmid expressing Hycu-IAP1. These results provide the first evidence that baculovirus IAP1s act to induce caspase-dependent apoptosis, possibly by replacing the cellular IAP1 that prevents Dronc activation.</description><identifier>ISSN: 1465-2099</identifier><identifier>ISSN: 0022-1317</identifier><identifier>EISSN: 1465-2099</identifier><identifier>DOI: 10.1099/vir.0.033332-0</identifier><identifier>PMID: 21795471</identifier><identifier>CODEN: JGVIAY</identifier><language>eng</language><publisher>Reading: Society for General Microbiology</publisher><subject>Animals ; Apoptosis ; Autographa californica multiple nucleopolyhedrovirus ; Baculovirus ; Biological and medical sciences ; Bombyx mori nucleopolyhedrovirus ; Caspase 3 - metabolism ; caspases ; Cell Line ; Diptera ; enzyme activity ; Fundamental and applied biological sciences. Psychology ; genes ; Host-Pathogen Interactions ; Hyphantria cunea ; Inhibitor of Apoptosis Proteins - metabolism ; insects ; Lepidoptera - virology ; Microbiology ; Miscellaneous ; Nucleopolyhedroviruses - pathogenicity ; Orgyia pseudotsugata multiple nucleopolyhedrovirus ; plasmids ; RNA ; RNA interference ; sequence homology ; Spilosoma ; Spodoptera frugiperda ; transfection ; Viral Proteins - metabolism ; Virology ; viruses</subject><ispartof>Journal of general virology, 2011-11, Vol.92 (Pt 11), p.2654-2663</ispartof><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c454t-c03f99d18f05c218c2210b712037fc557fa89e3106f83bb51905d93b2f1d495e3</citedby><cites>FETCH-LOGICAL-c454t-c03f99d18f05c218c2210b712037fc557fa89e3106f83bb51905d93b2f1d495e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3733,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24698426$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21795471$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ikeda, Motoko</creatorcontrib><creatorcontrib>Yamada, Hayato</creatorcontrib><creatorcontrib>Ito, Hiroyuki</creatorcontrib><creatorcontrib>Kobayashi, Michihiro</creatorcontrib><title>Baculovirus IAP1 induces caspase-dependent apoptosis in insect cells</title><title>Journal of general virology</title><addtitle>J Gen Virol</addtitle><description>Baculoviruses encode inhibitors of apoptosis (IAPs), which are classified into five groups, IAP1–5, based on their sequence homology. Most of the baculovirus IAPs with anti-apoptotic functions belong to the IAP3 group, with certain exceptions. The functional roles of IAPs from other groups during virus infection have not been well established. We have previously shown that Hyphantria cunea multiple nucleopolyhedrovirus (HycuMNPV) encodes three iap genes, hycu-iap1, hycu-iap2 and hycu-iap3, and that only Hycu-IAP3 has anti-apoptotic activity against actinomycin D-induced apoptosis of Spodoptera frugiperda Sf9 cells. In the present study, we demonstrate that transient expression of Hycu-IAP1 is capable of inducing apoptosis and/or stimulating caspase-3-like protease activity in various lepidopteran and dipteran cell lines. Transient-expression assay analysis also demonstrates that not only Hycu-IAP1 but also IAP1s from Autographa californica MNPV, Bombyx mori NPV and Orgyia pseudotsugata MNPV (OpMNPV) are capable of inducing apoptosis, and that apoptosis induced by Hycu-IAP1 is precluded by the functional anti-apoptotic baculovirus protein Hycu-IAP3. In HycuMNPV-infected Spilosoma imparilis (SpIm) cells and OpMNPV-infected Ld652Y cells, caspase-3-like protease activity is markedly stimulated during the late stages of infection, and the caspase-3-like protease activity stimulated in HycuMNPV-infected SpIm cells is repressed by RNA interference-mediated silencing of hycu-iap1. In addition, initiator caspase Bm-Dronc, the B. mori homologue of Dronc, is cleaved upon transfection of BM-N cells with a plasmid expressing Hycu-IAP1. These results provide the first evidence that baculovirus IAP1s act to induce caspase-dependent apoptosis, possibly by replacing the cellular IAP1 that prevents Dronc activation.</description><subject>Animals</subject><subject>Apoptosis</subject><subject>Autographa californica multiple nucleopolyhedrovirus</subject><subject>Baculovirus</subject><subject>Biological and medical sciences</subject><subject>Bombyx mori nucleopolyhedrovirus</subject><subject>Caspase 3 - metabolism</subject><subject>caspases</subject><subject>Cell Line</subject><subject>Diptera</subject><subject>enzyme activity</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>genes</subject><subject>Host-Pathogen Interactions</subject><subject>Hyphantria cunea</subject><subject>Inhibitor of Apoptosis Proteins - metabolism</subject><subject>insects</subject><subject>Lepidoptera - virology</subject><subject>Microbiology</subject><subject>Miscellaneous</subject><subject>Nucleopolyhedroviruses - pathogenicity</subject><subject>Orgyia pseudotsugata multiple nucleopolyhedrovirus</subject><subject>plasmids</subject><subject>RNA</subject><subject>RNA interference</subject><subject>sequence homology</subject><subject>Spilosoma</subject><subject>Spodoptera frugiperda</subject><subject>transfection</subject><subject>Viral Proteins - metabolism</subject><subject>Virology</subject><subject>viruses</subject><issn>1465-2099</issn><issn>0022-1317</issn><issn>1465-2099</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpN0EtLxDAQB_Agio_Vq0ftRTx1nUmTtjnq-lpYUFDPIU0TqXTb2mkFv72Rro8hMIH8GCZ_xo4R5ghKXXxU_RzmkITiMWyxfRSpjHl42v5332MHRG8AKITMdtkex0xJkeE-u74ydqzbMGakaHn5iFHVlKN1FFlDnSEXl65zTemaITJd2w0tVRRMOOTsEFlX13TIdrypyR1t-oy93N48L-7j1cPdcnG5iq2QYogtJF6pEnMP0nLMLecIRYYcksxbKTNvcuUShNTnSVFIVCBLlRTcYymUdMmMnU9zu759Hx0Nel3R9wamce1IOle5REwwD3I-Sdu3RL3zuuurtek_NYL-Dk6HH2vQU3ChzdjJZvRYrF35y3-SCuBsAwxZU_veNLaiPydSlQueBnc6OW9abV77YF6eOGAKoRSG9b4AehF-MQ</recordid><startdate>20111101</startdate><enddate>20111101</enddate><creator>Ikeda, Motoko</creator><creator>Yamada, Hayato</creator><creator>Ito, Hiroyuki</creator><creator>Kobayashi, Michihiro</creator><general>Society for General Microbiology</general><scope>FBQ</scope><scope>IQODW</scope><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></search><sort><creationdate>20111101</creationdate><title>Baculovirus IAP1 induces caspase-dependent apoptosis in insect cells</title><author>Ikeda, Motoko ; Yamada, Hayato ; Ito, Hiroyuki ; Kobayashi, Michihiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c454t-c03f99d18f05c218c2210b712037fc557fa89e3106f83bb51905d93b2f1d495e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Animals</topic><topic>Apoptosis</topic><topic>Autographa californica multiple nucleopolyhedrovirus</topic><topic>Baculovirus</topic><topic>Biological and medical sciences</topic><topic>Bombyx mori nucleopolyhedrovirus</topic><topic>Caspase 3 - metabolism</topic><topic>caspases</topic><topic>Cell Line</topic><topic>Diptera</topic><topic>enzyme activity</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>genes</topic><topic>Host-Pathogen Interactions</topic><topic>Hyphantria cunea</topic><topic>Inhibitor of Apoptosis Proteins - metabolism</topic><topic>insects</topic><topic>Lepidoptera - virology</topic><topic>Microbiology</topic><topic>Miscellaneous</topic><topic>Nucleopolyhedroviruses - pathogenicity</topic><topic>Orgyia pseudotsugata multiple nucleopolyhedrovirus</topic><topic>plasmids</topic><topic>RNA</topic><topic>RNA interference</topic><topic>sequence homology</topic><topic>Spilosoma</topic><topic>Spodoptera frugiperda</topic><topic>transfection</topic><topic>Viral Proteins - metabolism</topic><topic>Virology</topic><topic>viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ikeda, Motoko</creatorcontrib><creatorcontrib>Yamada, Hayato</creatorcontrib><creatorcontrib>Ito, Hiroyuki</creatorcontrib><creatorcontrib>Kobayashi, Michihiro</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of general virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ikeda, Motoko</au><au>Yamada, Hayato</au><au>Ito, Hiroyuki</au><au>Kobayashi, Michihiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Baculovirus IAP1 induces caspase-dependent apoptosis in insect cells</atitle><jtitle>Journal of general virology</jtitle><addtitle>J Gen Virol</addtitle><date>2011-11-01</date><risdate>2011</risdate><volume>92</volume><issue>Pt 11</issue><spage>2654</spage><epage>2663</epage><pages>2654-2663</pages><issn>1465-2099</issn><issn>0022-1317</issn><eissn>1465-2099</eissn><coden>JGVIAY</coden><abstract>Baculoviruses encode inhibitors of apoptosis (IAPs), which are classified into five groups, IAP1–5, based on their sequence homology. Most of the baculovirus IAPs with anti-apoptotic functions belong to the IAP3 group, with certain exceptions. The functional roles of IAPs from other groups during virus infection have not been well established. We have previously shown that Hyphantria cunea multiple nucleopolyhedrovirus (HycuMNPV) encodes three iap genes, hycu-iap1, hycu-iap2 and hycu-iap3, and that only Hycu-IAP3 has anti-apoptotic activity against actinomycin D-induced apoptosis of Spodoptera frugiperda Sf9 cells. In the present study, we demonstrate that transient expression of Hycu-IAP1 is capable of inducing apoptosis and/or stimulating caspase-3-like protease activity in various lepidopteran and dipteran cell lines. Transient-expression assay analysis also demonstrates that not only Hycu-IAP1 but also IAP1s from Autographa californica MNPV, Bombyx mori NPV and Orgyia pseudotsugata MNPV (OpMNPV) are capable of inducing apoptosis, and that apoptosis induced by Hycu-IAP1 is precluded by the functional anti-apoptotic baculovirus protein Hycu-IAP3. In HycuMNPV-infected Spilosoma imparilis (SpIm) cells and OpMNPV-infected Ld652Y cells, caspase-3-like protease activity is markedly stimulated during the late stages of infection, and the caspase-3-like protease activity stimulated in HycuMNPV-infected SpIm cells is repressed by RNA interference-mediated silencing of hycu-iap1. In addition, initiator caspase Bm-Dronc, the B. mori homologue of Dronc, is cleaved upon transfection of BM-N cells with a plasmid expressing Hycu-IAP1. These results provide the first evidence that baculovirus IAP1s act to induce caspase-dependent apoptosis, possibly by replacing the cellular IAP1 that prevents Dronc activation.</abstract><cop>Reading</cop><pub>Society for General Microbiology</pub><pmid>21795471</pmid><doi>10.1099/vir.0.033332-0</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Apoptosis Autographa californica multiple nucleopolyhedrovirus Baculovirus Biological and medical sciences Bombyx mori nucleopolyhedrovirus Caspase 3 - metabolism caspases Cell Line Diptera enzyme activity Fundamental and applied biological sciences. Psychology genes Host-Pathogen Interactions Hyphantria cunea Inhibitor of Apoptosis Proteins - metabolism insects Lepidoptera - virology Microbiology Miscellaneous Nucleopolyhedroviruses - pathogenicity Orgyia pseudotsugata multiple nucleopolyhedrovirus plasmids RNA RNA interference sequence homology Spilosoma Spodoptera frugiperda transfection Viral Proteins - metabolism Virology viruses |
title | Baculovirus IAP1 induces caspase-dependent apoptosis in insect cells |
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