Multi-peaked adaptive landscape for chikungunya virus evolution predicts continued fitness optimization in Aedes albopictus mosquitoes
Host species-specific fitness landscapes largely determine the outcome of host switching during pathogen emergence. Using chikungunya virus (CHIKV) to study adaptation to a mosquito vector, we evaluated mutations associated with recently evolved sub-lineages. Multiple Aedes albopictu s-adaptive fitn...
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Veröffentlicht in: | Nature communications 2014-06, Vol.5 (1), p.4084-4084, Article 4084 |
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creator | Tsetsarkin, Konstantin A. Chen, Rubing Yun, Ruimei Rossi, Shannan L. Plante, Kenneth S. Guerbois, Mathilde Forrester, Naomi Perng, Guey Chuen Sreekumar, Easwaran Leal, Grace Huang, Jing Mukhopadhyay, Suchetana Weaver, Scott C. |
description | Host species-specific fitness landscapes largely determine the outcome of host switching during pathogen emergence. Using chikungunya virus (CHIKV) to study adaptation to a mosquito vector, we evaluated mutations associated with recently evolved sub-lineages. Multiple
Aedes albopictu
s-adaptive fitness peaks became available after CHIKV acquired an initial adaptive (E1-A226V) substitution, permitting rapid lineage diversification observed in nature. All second-step mutations involved replacements by glutamine or glutamic acid of E2 glycoprotein amino acids in the acid-sensitive region, providing a framework to anticipate additional
A. albopictus
-adaptive mutations. The combination of second-step adaptive mutations into a single, ‘super-adaptive’ fitness peak also predicted the future emergence of CHIKV strains with even greater transmission efficiency in some current regions of endemic circulation, followed by their likely global spread.
The ability of a pathogen to adapt to new hosts affects its ability to spread in new environments. Here, Tsetsarkin
et al.
analysed mutations that enabled the chikungunya virus to adapt to a mosquito vector and predict that specific mutations will result in greater transmission efficiency. |
doi_str_mv | 10.1038/ncomms5084 |
format | Article |
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Aedes albopictu
s-adaptive fitness peaks became available after CHIKV acquired an initial adaptive (E1-A226V) substitution, permitting rapid lineage diversification observed in nature. All second-step mutations involved replacements by glutamine or glutamic acid of E2 glycoprotein amino acids in the acid-sensitive region, providing a framework to anticipate additional
A. albopictus
-adaptive mutations. The combination of second-step adaptive mutations into a single, ‘super-adaptive’ fitness peak also predicted the future emergence of CHIKV strains with even greater transmission efficiency in some current regions of endemic circulation, followed by their likely global spread.
The ability of a pathogen to adapt to new hosts affects its ability to spread in new environments. Here, Tsetsarkin
et al.
analysed mutations that enabled the chikungunya virus to adapt to a mosquito vector and predict that specific mutations will result in greater transmission efficiency.</description><identifier>ISSN: 2041-1723</identifier><identifier>EISSN: 2041-1723</identifier><identifier>DOI: 10.1038/ncomms5084</identifier><identifier>PMID: 24933611</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>13/109 ; 631/181/2474 ; 631/326/596/2562 ; 64/60 ; Aedes - virology ; Animals ; Chikungunya Fever - transmission ; Chikungunya Fever - virology ; Chikungunya virus ; Chikungunya virus - classification ; Chikungunya virus - genetics ; Chikungunya virus - physiology ; Evolution, Molecular ; Female ; Humanities and Social Sciences ; Humans ; Insect Vectors - virology ; Mice ; Molecular Sequence Data ; multidisciplinary ; Phylogeny ; Science ; Science (multidisciplinary) ; Viral Envelope Proteins - genetics</subject><ispartof>Nature communications, 2014-06, Vol.5 (1), p.4084-4084, Article 4084</ispartof><rights>Springer Nature Limited 2014</rights><rights>Copyright Nature Publishing Group Jun 2014</rights><rights>Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c442t-941c76b61e0a074ed1becad4bbeb05676fc587a2bb7ea53aa16856a3ea1581c63</citedby><cites>FETCH-LOGICAL-c442t-941c76b61e0a074ed1becad4bbeb05676fc587a2bb7ea53aa16856a3ea1581c63</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/PMC7091890/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7091890/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,41120,42189,51576,53791,53793</link.rule.ids><linktorsrc>$$Uhttps://doi.org/10.1038/ncomms5084$$EView_record_in_Springer_Nature$$FView_record_in_$$GSpringer_Nature</linktorsrc><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24933611$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tsetsarkin, Konstantin A.</creatorcontrib><creatorcontrib>Chen, Rubing</creatorcontrib><creatorcontrib>Yun, Ruimei</creatorcontrib><creatorcontrib>Rossi, Shannan L.</creatorcontrib><creatorcontrib>Plante, Kenneth S.</creatorcontrib><creatorcontrib>Guerbois, Mathilde</creatorcontrib><creatorcontrib>Forrester, Naomi</creatorcontrib><creatorcontrib>Perng, Guey Chuen</creatorcontrib><creatorcontrib>Sreekumar, Easwaran</creatorcontrib><creatorcontrib>Leal, Grace</creatorcontrib><creatorcontrib>Huang, Jing</creatorcontrib><creatorcontrib>Mukhopadhyay, Suchetana</creatorcontrib><creatorcontrib>Weaver, Scott C.</creatorcontrib><title>Multi-peaked adaptive landscape for chikungunya virus evolution predicts continued fitness optimization in Aedes albopictus mosquitoes</title><title>Nature communications</title><addtitle>Nat Commun</addtitle><addtitle>Nat Commun</addtitle><description>Host species-specific fitness landscapes largely determine the outcome of host switching during pathogen emergence. Using chikungunya virus (CHIKV) to study adaptation to a mosquito vector, we evaluated mutations associated with recently evolved sub-lineages. Multiple
Aedes albopictu
s-adaptive fitness peaks became available after CHIKV acquired an initial adaptive (E1-A226V) substitution, permitting rapid lineage diversification observed in nature. All second-step mutations involved replacements by glutamine or glutamic acid of E2 glycoprotein amino acids in the acid-sensitive region, providing a framework to anticipate additional
A. albopictus
-adaptive mutations. The combination of second-step adaptive mutations into a single, ‘super-adaptive’ fitness peak also predicted the future emergence of CHIKV strains with even greater transmission efficiency in some current regions of endemic circulation, followed by their likely global spread.
The ability of a pathogen to adapt to new hosts affects its ability to spread in new environments. Here, Tsetsarkin
et al.
analysed mutations that enabled the chikungunya virus to adapt to a mosquito vector and predict that specific mutations will result in greater transmission efficiency.</description><subject>13/109</subject><subject>631/181/2474</subject><subject>631/326/596/2562</subject><subject>64/60</subject><subject>Aedes - virology</subject><subject>Animals</subject><subject>Chikungunya Fever - transmission</subject><subject>Chikungunya Fever - virology</subject><subject>Chikungunya virus</subject><subject>Chikungunya virus - classification</subject><subject>Chikungunya virus - genetics</subject><subject>Chikungunya virus - physiology</subject><subject>Evolution, Molecular</subject><subject>Female</subject><subject>Humanities and Social Sciences</subject><subject>Humans</subject><subject>Insect Vectors - virology</subject><subject>Mice</subject><subject>Molecular Sequence Data</subject><subject>multidisciplinary</subject><subject>Phylogeny</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Viral Envelope Proteins - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Nature communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Tsetsarkin, Konstantin A.</au><au>Chen, Rubing</au><au>Yun, Ruimei</au><au>Rossi, Shannan L.</au><au>Plante, Kenneth S.</au><au>Guerbois, Mathilde</au><au>Forrester, Naomi</au><au>Perng, Guey Chuen</au><au>Sreekumar, Easwaran</au><au>Leal, Grace</au><au>Huang, Jing</au><au>Mukhopadhyay, Suchetana</au><au>Weaver, Scott C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Multi-peaked adaptive landscape for chikungunya virus evolution predicts continued fitness optimization in Aedes albopictus mosquitoes</atitle><jtitle>Nature communications</jtitle><stitle>Nat Commun</stitle><addtitle>Nat Commun</addtitle><date>2014-06-16</date><risdate>2014</risdate><volume>5</volume><issue>1</issue><spage>4084</spage><epage>4084</epage><pages>4084-4084</pages><artnum>4084</artnum><issn>2041-1723</issn><eissn>2041-1723</eissn><abstract>Host species-specific fitness landscapes largely determine the outcome of host switching during pathogen emergence. Using chikungunya virus (CHIKV) to study adaptation to a mosquito vector, we evaluated mutations associated with recently evolved sub-lineages. Multiple
Aedes albopictu
s-adaptive fitness peaks became available after CHIKV acquired an initial adaptive (E1-A226V) substitution, permitting rapid lineage diversification observed in nature. All second-step mutations involved replacements by glutamine or glutamic acid of E2 glycoprotein amino acids in the acid-sensitive region, providing a framework to anticipate additional
A. albopictus
-adaptive mutations. The combination of second-step adaptive mutations into a single, ‘super-adaptive’ fitness peak also predicted the future emergence of CHIKV strains with even greater transmission efficiency in some current regions of endemic circulation, followed by their likely global spread.
The ability of a pathogen to adapt to new hosts affects its ability to spread in new environments. Here, Tsetsarkin
et al.
analysed mutations that enabled the chikungunya virus to adapt to a mosquito vector and predict that specific mutations will result in greater transmission efficiency.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>24933611</pmid><doi>10.1038/ncomms5084</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 13/109 631/181/2474 631/326/596/2562 64/60 Aedes - virology Animals Chikungunya Fever - transmission Chikungunya Fever - virology Chikungunya virus Chikungunya virus - classification Chikungunya virus - genetics Chikungunya virus - physiology Evolution, Molecular Female Humanities and Social Sciences Humans Insect Vectors - virology Mice Molecular Sequence Data multidisciplinary Phylogeny Science Science (multidisciplinary) Viral Envelope Proteins - genetics |
title | Multi-peaked adaptive landscape for chikungunya virus evolution predicts continued fitness optimization in Aedes albopictus mosquitoes |
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