A mosquito small RNA genomics resource reveals dynamic evolution and host responses to viruses and transposons
Although mosquitoes are major transmission vectors for pathogenic arboviruses, viral infection has little impact on mosquito health. This immunity is caused in part by mosquito RNA interference (RNAi) pathways that generate antiviral small interfering RNAs (siRNAs) and Piwi-interacting RNAs (piRNAs)...
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Veröffentlicht in: | Genome research 2021-03, Vol.31 (3), p.512-528 |
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creator | Ma, Qicheng Srivastav, Satyam P Gamez, Stephanie Dayama, Gargi Feitosa-Suntheimer, Fabiana Patterson, Edward I Johnson, Rebecca M Matson, Erik M Gold, Alexander S Brackney, Douglas E Connor, John H Colpitts, Tonya M Hughes, Grant L Rasgon, Jason L Nolan, Tony Akbari, Omar S Lau, Nelson C |
description | Although mosquitoes are major transmission vectors for pathogenic arboviruses, viral infection has little impact on mosquito health. This immunity is caused in part by mosquito RNA interference (RNAi) pathways that generate antiviral small interfering RNAs (siRNAs) and Piwi-interacting RNAs (piRNAs). RNAi also maintains genome integrity by potently repressing mosquito transposon activity in the germline and soma. However, viral and transposon small RNA regulatory pathways have not been systematically examined together in mosquitoes. Therefore, we developed an integrated mosquito small RNA genomics (MSRG) resource that analyzes the transposon and virus small RNA profiles in mosquito cell cultures and somatic and gonadal tissues across four medically important mosquito species. Our resource captures both somatic and gonadal small RNA expression profiles within mosquito cell cultures, and we report the evolutionary dynamics of a novel Mosquito-Conserved piRNA Cluster Locus (MCpiRCL) made up of satellite DNA repeats. In the larger culicine mosquito genomes we detected highly regular periodicity in piRNA biogenesis patterns coinciding with the expansion of Piwi pathway genes. Finally, our resource enables detection of cross talk between piRNA and siRNA populations in mosquito cells during a response to virus infection. The MSRG resource will aid efforts to dissect and combat the capacity of mosquitoes to tolerate and spread arboviruses. |
doi_str_mv | 10.1101/gr.265157.120 |
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This immunity is caused in part by mosquito RNA interference (RNAi) pathways that generate antiviral small interfering RNAs (siRNAs) and Piwi-interacting RNAs (piRNAs). RNAi also maintains genome integrity by potently repressing mosquito transposon activity in the germline and soma. However, viral and transposon small RNA regulatory pathways have not been systematically examined together in mosquitoes. Therefore, we developed an integrated mosquito small RNA genomics (MSRG) resource that analyzes the transposon and virus small RNA profiles in mosquito cell cultures and somatic and gonadal tissues across four medically important mosquito species. Our resource captures both somatic and gonadal small RNA expression profiles within mosquito cell cultures, and we report the evolutionary dynamics of a novel Mosquito-Conserved piRNA Cluster Locus (MCpiRCL) made up of satellite DNA repeats. In the larger culicine mosquito genomes we detected highly regular periodicity in piRNA biogenesis patterns coinciding with the expansion of Piwi pathway genes. Finally, our resource enables detection of cross talk between piRNA and siRNA populations in mosquito cells during a response to virus infection. The MSRG resource will aid efforts to dissect and combat the capacity of mosquitoes to tolerate and spread arboviruses.</description><identifier>ISSN: 1088-9051</identifier><identifier>ISSN: 1549-5469</identifier><identifier>EISSN: 1549-5469</identifier><identifier>DOI: 10.1101/gr.265157.120</identifier><identifier>PMID: 33419731</identifier><language>eng</language><publisher>United States: Cold Spring Harbor Laboratory Press</publisher><subject>Animals ; Cell culture ; Culicidae ; Culicidae - genetics ; Culicidae - virology ; DNA Transposable Elements - genetics ; Genomics ; Mosquitoes ; Periodicity ; Resource ; RNA viruses ; RNA, Small Interfering - genetics ; RNA-mediated interference ; Satellite DNA ; siRNA ; Transposons ; Vectors ; Viral infections ; Viruses</subject><ispartof>Genome research, 2021-03, Vol.31 (3), p.512-528</ispartof><rights>2021 Ma et al.; Published by Cold Spring Harbor Laboratory Press.</rights><rights>Copyright Cold Spring Harbor Laboratory Press Mar 2021</rights><rights>2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c415t-9767ac00daab6142fa1f8ff7706f22b130754b7afdd9ddaf0f3ebe122578ef43</citedby><cites>FETCH-LOGICAL-c415t-9767ac00daab6142fa1f8ff7706f22b130754b7afdd9ddaf0f3ebe122578ef43</cites><orcidid>0000-0001-5380-991X ; 0000-0001-9907-1404 ; 0000-0002-6853-9884 ; 0000-0002-4050-8429 ; 0000-0002-7567-7185</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/PMC7919454/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7919454/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33419731$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ma, Qicheng</creatorcontrib><creatorcontrib>Srivastav, Satyam P</creatorcontrib><creatorcontrib>Gamez, Stephanie</creatorcontrib><creatorcontrib>Dayama, Gargi</creatorcontrib><creatorcontrib>Feitosa-Suntheimer, Fabiana</creatorcontrib><creatorcontrib>Patterson, Edward I</creatorcontrib><creatorcontrib>Johnson, Rebecca M</creatorcontrib><creatorcontrib>Matson, Erik M</creatorcontrib><creatorcontrib>Gold, Alexander S</creatorcontrib><creatorcontrib>Brackney, Douglas E</creatorcontrib><creatorcontrib>Connor, John H</creatorcontrib><creatorcontrib>Colpitts, Tonya M</creatorcontrib><creatorcontrib>Hughes, Grant L</creatorcontrib><creatorcontrib>Rasgon, Jason L</creatorcontrib><creatorcontrib>Nolan, Tony</creatorcontrib><creatorcontrib>Akbari, Omar S</creatorcontrib><creatorcontrib>Lau, Nelson C</creatorcontrib><title>A mosquito small RNA genomics resource reveals dynamic evolution and host responses to viruses and transposons</title><title>Genome research</title><addtitle>Genome Res</addtitle><description>Although mosquitoes are major transmission vectors for pathogenic arboviruses, viral infection has little impact on mosquito health. This immunity is caused in part by mosquito RNA interference (RNAi) pathways that generate antiviral small interfering RNAs (siRNAs) and Piwi-interacting RNAs (piRNAs). RNAi also maintains genome integrity by potently repressing mosquito transposon activity in the germline and soma. However, viral and transposon small RNA regulatory pathways have not been systematically examined together in mosquitoes. Therefore, we developed an integrated mosquito small RNA genomics (MSRG) resource that analyzes the transposon and virus small RNA profiles in mosquito cell cultures and somatic and gonadal tissues across four medically important mosquito species. Our resource captures both somatic and gonadal small RNA expression profiles within mosquito cell cultures, and we report the evolutionary dynamics of a novel Mosquito-Conserved piRNA Cluster Locus (MCpiRCL) made up of satellite DNA repeats. In the larger culicine mosquito genomes we detected highly regular periodicity in piRNA biogenesis patterns coinciding with the expansion of Piwi pathway genes. Finally, our resource enables detection of cross talk between piRNA and siRNA populations in mosquito cells during a response to virus infection. 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Srivastav, Satyam P ; Gamez, Stephanie ; Dayama, Gargi ; Feitosa-Suntheimer, Fabiana ; Patterson, Edward I ; Johnson, Rebecca M ; Matson, Erik M ; Gold, Alexander S ; Brackney, Douglas E ; Connor, John H ; Colpitts, Tonya M ; Hughes, Grant L ; Rasgon, Jason L ; Nolan, Tony ; Akbari, Omar S ; Lau, Nelson C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c415t-9767ac00daab6142fa1f8ff7706f22b130754b7afdd9ddaf0f3ebe122578ef43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Animals</topic><topic>Cell culture</topic><topic>Culicidae</topic><topic>Culicidae - genetics</topic><topic>Culicidae - virology</topic><topic>DNA Transposable Elements - genetics</topic><topic>Genomics</topic><topic>Mosquitoes</topic><topic>Periodicity</topic><topic>Resource</topic><topic>RNA viruses</topic><topic>RNA, Small Interfering - genetics</topic><topic>RNA-mediated interference</topic><topic>Satellite DNA</topic><topic>siRNA</topic><topic>Transposons</topic><topic>Vectors</topic><topic>Viral infections</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ma, Qicheng</creatorcontrib><creatorcontrib>Srivastav, Satyam P</creatorcontrib><creatorcontrib>Gamez, Stephanie</creatorcontrib><creatorcontrib>Dayama, Gargi</creatorcontrib><creatorcontrib>Feitosa-Suntheimer, Fabiana</creatorcontrib><creatorcontrib>Patterson, Edward I</creatorcontrib><creatorcontrib>Johnson, Rebecca M</creatorcontrib><creatorcontrib>Matson, Erik M</creatorcontrib><creatorcontrib>Gold, Alexander S</creatorcontrib><creatorcontrib>Brackney, Douglas E</creatorcontrib><creatorcontrib>Connor, John H</creatorcontrib><creatorcontrib>Colpitts, Tonya M</creatorcontrib><creatorcontrib>Hughes, Grant L</creatorcontrib><creatorcontrib>Rasgon, Jason L</creatorcontrib><creatorcontrib>Nolan, Tony</creatorcontrib><creatorcontrib>Akbari, Omar S</creatorcontrib><creatorcontrib>Lau, Nelson C</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Genome research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ma, Qicheng</au><au>Srivastav, Satyam P</au><au>Gamez, Stephanie</au><au>Dayama, Gargi</au><au>Feitosa-Suntheimer, Fabiana</au><au>Patterson, Edward I</au><au>Johnson, Rebecca M</au><au>Matson, Erik M</au><au>Gold, Alexander S</au><au>Brackney, Douglas E</au><au>Connor, John H</au><au>Colpitts, Tonya M</au><au>Hughes, Grant L</au><au>Rasgon, Jason L</au><au>Nolan, Tony</au><au>Akbari, Omar S</au><au>Lau, Nelson C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A mosquito small RNA genomics resource reveals dynamic evolution and host responses to viruses and transposons</atitle><jtitle>Genome research</jtitle><addtitle>Genome Res</addtitle><date>2021-03-01</date><risdate>2021</risdate><volume>31</volume><issue>3</issue><spage>512</spage><epage>528</epage><pages>512-528</pages><issn>1088-9051</issn><issn>1549-5469</issn><eissn>1549-5469</eissn><abstract>Although mosquitoes are major transmission vectors for pathogenic arboviruses, viral infection has little impact on mosquito health. This immunity is caused in part by mosquito RNA interference (RNAi) pathways that generate antiviral small interfering RNAs (siRNAs) and Piwi-interacting RNAs (piRNAs). RNAi also maintains genome integrity by potently repressing mosquito transposon activity in the germline and soma. However, viral and transposon small RNA regulatory pathways have not been systematically examined together in mosquitoes. Therefore, we developed an integrated mosquito small RNA genomics (MSRG) resource that analyzes the transposon and virus small RNA profiles in mosquito cell cultures and somatic and gonadal tissues across four medically important mosquito species. Our resource captures both somatic and gonadal small RNA expression profiles within mosquito cell cultures, and we report the evolutionary dynamics of a novel Mosquito-Conserved piRNA Cluster Locus (MCpiRCL) made up of satellite DNA repeats. In the larger culicine mosquito genomes we detected highly regular periodicity in piRNA biogenesis patterns coinciding with the expansion of Piwi pathway genes. Finally, our resource enables detection of cross talk between piRNA and siRNA populations in mosquito cells during a response to virus infection. The MSRG resource will aid efforts to dissect and combat the capacity of mosquitoes to tolerate and spread arboviruses.</abstract><cop>United States</cop><pub>Cold Spring Harbor Laboratory Press</pub><pmid>33419731</pmid><doi>10.1101/gr.265157.120</doi><tpages>17</tpages><orcidid>https://orcid.org/0000-0001-5380-991X</orcidid><orcidid>https://orcid.org/0000-0001-9907-1404</orcidid><orcidid>https://orcid.org/0000-0002-6853-9884</orcidid><orcidid>https://orcid.org/0000-0002-4050-8429</orcidid><orcidid>https://orcid.org/0000-0002-7567-7185</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals Cell culture Culicidae Culicidae - genetics Culicidae - virology DNA Transposable Elements - genetics Genomics Mosquitoes Periodicity Resource RNA viruses RNA, Small Interfering - genetics RNA-mediated interference Satellite DNA siRNA Transposons Vectors Viral infections Viruses |
title | A mosquito small RNA genomics resource reveals dynamic evolution and host responses to viruses and transposons |
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