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Host Factors in the Infection Cycle of Bamboo mosaic virus
To complete the infection cycle efficiently, the virus must hijack the host systems in order to benefit for all the steps and has to face all the defense mechanisms from the host. This review involves a discussion of how these positive and negative factors regulate the viral RNA accumulation identif...
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Published in: | Frontiers in microbiology 2017-03, Vol.8, p.437-437 |
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description | To complete the infection cycle efficiently, the virus must hijack the host systems in order to benefit for all the steps and has to face all the defense mechanisms from the host. This review involves a discussion of how these positive and negative factors regulate the viral RNA accumulation identified for the
(BaMV), a single-stranded RNA virus. The genome of BaMV is approximately 6.4 kb in length, encoding five functional polypeptides. To reveal the host factors involved in the infection cycle of BaMV, a few different approaches were taken to screen the candidates. One of the approaches is isolating the viral replicase-associated proteins by co-immunoprecipitation with the transiently expressed tagged viral replicase in plants. Another approach is using the cDNA-amplified fragment length polymorphism technique to screen the differentially expressed genes derived from
plants after infection. The candidates are examined by knocking down the expression in plants using the
-based virus-induced gene silencing technique following BaMV inoculation. The positive or negative regulators could be described as reducing or enhancing the accumulation of BaMV in plants when the expression levels of these proteins are knocked down. The possible roles of these host factors acting on the accumulation of BaMV will be discussed. |
doi_str_mv | 10.3389/fmicb.2017.00437 |
format | article |
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(BaMV), a single-stranded RNA virus. The genome of BaMV is approximately 6.4 kb in length, encoding five functional polypeptides. To reveal the host factors involved in the infection cycle of BaMV, a few different approaches were taken to screen the candidates. One of the approaches is isolating the viral replicase-associated proteins by co-immunoprecipitation with the transiently expressed tagged viral replicase in plants. Another approach is using the cDNA-amplified fragment length polymorphism technique to screen the differentially expressed genes derived from
plants after infection. The candidates are examined by knocking down the expression in plants using the
-based virus-induced gene silencing technique following BaMV inoculation. The positive or negative regulators could be described as reducing or enhancing the accumulation of BaMV in plants when the expression levels of these proteins are knocked down. The possible roles of these host factors acting on the accumulation of BaMV will be discussed.</description><identifier>ISSN: 1664-302X</identifier><identifier>EISSN: 1664-302X</identifier><identifier>DOI: 10.3389/fmicb.2017.00437</identifier><identifier>PMID: 28360904</identifier><language>eng</language><publisher>Switzerland: Frontiers Media S.A</publisher><subject>Microbiology</subject><ispartof>Frontiers in microbiology, 2017-03, Vol.8, p.437-437</ispartof><rights>Copyright © 2017 Huang, Chen and Tsai. 2017 Huang, Chen and Tsai</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c462t-88a1f38d50cb891d1135b99e6edf63c877e0cb1669a0ca2d59f0213754f792603</citedby><cites>FETCH-LOGICAL-c462t-88a1f38d50cb891d1135b99e6edf63c877e0cb1669a0ca2d59f0213754f792603</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5350103/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5350103/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,733,786,790,891,27957,27958,53827,53829</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28360904$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Huang, Ying-Ping</creatorcontrib><creatorcontrib>Chen, I-Hsuan</creatorcontrib><creatorcontrib>Tsai, Ching-Hsiu</creatorcontrib><title>Host Factors in the Infection Cycle of Bamboo mosaic virus</title><title>Frontiers in microbiology</title><addtitle>Front Microbiol</addtitle><description>To complete the infection cycle efficiently, the virus must hijack the host systems in order to benefit for all the steps and has to face all the defense mechanisms from the host. This review involves a discussion of how these positive and negative factors regulate the viral RNA accumulation identified for the
(BaMV), a single-stranded RNA virus. The genome of BaMV is approximately 6.4 kb in length, encoding five functional polypeptides. To reveal the host factors involved in the infection cycle of BaMV, a few different approaches were taken to screen the candidates. One of the approaches is isolating the viral replicase-associated proteins by co-immunoprecipitation with the transiently expressed tagged viral replicase in plants. Another approach is using the cDNA-amplified fragment length polymorphism technique to screen the differentially expressed genes derived from
plants after infection. The candidates are examined by knocking down the expression in plants using the
-based virus-induced gene silencing technique following BaMV inoculation. The positive or negative regulators could be described as reducing or enhancing the accumulation of BaMV in plants when the expression levels of these proteins are knocked down. The possible roles of these host factors acting on the accumulation of BaMV will be discussed.</description><subject>Microbiology</subject><issn>1664-302X</issn><issn>1664-302X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNpVkE1LAzEQhoMottTePUmOXrZOkv1IPAharC0UvCh4C9lsYiO7m7rZLfTfu2211DnMDMzMOy8PQtcEJoxxcWcrp_MJBZJNAGKWnaEhSdM4YkA_zk_6ARqH8AV9xED7fIkGlLMUBMRDdD_3ocUzpVvfBOxq3K4MXtTW6Nb5Gk-3ujTYW_ykqtx7XPmgnMYb13ThCl1YVQYz_q0j9D57fpvOo-Xry2L6uIx0nNI24lwRy3iRgM65IAUhLMmFMKkpbMo0zzLTT3q3QoFWtEiEBUpYlsQ2EzQFNkIPB911l1em0KZuG1XKdeMq1WylV07-n9RuJT_9RiYsAQKsF7j9FWj8d2dCKysXtClLVRvfBUk4ZyRLaSL6VTis6saH0Bh7fENA7qjLPXW5oy731PuTm1N7x4M_xuwHe3h9wQ</recordid><startdate>20170315</startdate><enddate>20170315</enddate><creator>Huang, Ying-Ping</creator><creator>Chen, I-Hsuan</creator><creator>Tsai, Ching-Hsiu</creator><general>Frontiers Media S.A</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20170315</creationdate><title>Host Factors in the Infection Cycle of Bamboo mosaic virus</title><author>Huang, Ying-Ping ; Chen, I-Hsuan ; Tsai, Ching-Hsiu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c462t-88a1f38d50cb891d1135b99e6edf63c877e0cb1669a0ca2d59f0213754f792603</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Microbiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Huang, Ying-Ping</creatorcontrib><creatorcontrib>Chen, I-Hsuan</creatorcontrib><creatorcontrib>Tsai, Ching-Hsiu</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Frontiers in microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Huang, Ying-Ping</au><au>Chen, I-Hsuan</au><au>Tsai, Ching-Hsiu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Host Factors in the Infection Cycle of Bamboo mosaic virus</atitle><jtitle>Frontiers in microbiology</jtitle><addtitle>Front Microbiol</addtitle><date>2017-03-15</date><risdate>2017</risdate><volume>8</volume><spage>437</spage><epage>437</epage><pages>437-437</pages><issn>1664-302X</issn><eissn>1664-302X</eissn><notes>ObjectType-Article-2</notes><notes>SourceType-Scholarly Journals-1</notes><notes>ObjectType-Feature-3</notes><notes>content type line 23</notes><notes>ObjectType-Review-1</notes><notes>This article was submitted to Virology, a section of the journal Frontiers in Microbiology</notes><notes>Edited by: Jean-François Laliberté, Institut National de la Recherche Scientifique, Canada</notes><notes>Reviewed by: Sergey Morozov, Moscow State University, Russia; Jianwei Wang, China Academy of Chinese Medical Sciences, China</notes><abstract>To complete the infection cycle efficiently, the virus must hijack the host systems in order to benefit for all the steps and has to face all the defense mechanisms from the host. This review involves a discussion of how these positive and negative factors regulate the viral RNA accumulation identified for the
(BaMV), a single-stranded RNA virus. The genome of BaMV is approximately 6.4 kb in length, encoding five functional polypeptides. To reveal the host factors involved in the infection cycle of BaMV, a few different approaches were taken to screen the candidates. One of the approaches is isolating the viral replicase-associated proteins by co-immunoprecipitation with the transiently expressed tagged viral replicase in plants. Another approach is using the cDNA-amplified fragment length polymorphism technique to screen the differentially expressed genes derived from
plants after infection. The candidates are examined by knocking down the expression in plants using the
-based virus-induced gene silencing technique following BaMV inoculation. The positive or negative regulators could be described as reducing or enhancing the accumulation of BaMV in plants when the expression levels of these proteins are knocked down. The possible roles of these host factors acting on the accumulation of BaMV will be discussed.</abstract><cop>Switzerland</cop><pub>Frontiers Media S.A</pub><pmid>28360904</pmid><doi>10.3389/fmicb.2017.00437</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Microbiology |
title | Host Factors in the Infection Cycle of Bamboo mosaic virus |
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