Genetic analysis of foot-and-mouth disease virus serotype A of Indian origin and detection of positive selection and recombination in leader protease- and capsid-coding regions
The leader protease (L pro ) and capsid-coding sequences (P1) constitute approximately 3 kb of the foot-and-mouth disease virus (FMDV). We studied the phylogenetic relationship of 46 FMDV serotype A isolates of Indian origin collected during the period 1968–2005 and also eight vaccine strains using...
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creator | Nagendrakumar, S. B. Madhanmohan, M. Rangarajan, P. N. Srinivasan, V. A. |
description | The leader protease (L
pro
) and capsid-coding sequences (P1) constitute approximately 3 kb of the foot-and-mouth disease virus (FMDV). We studied the phylogenetic relationship of 46 FMDV serotype A isolates of Indian origin collected during the period 1968–2005 and also eight vaccine strains using the neighbour-joining tree and Bayesian tree methods. The viruses were categorized under three major groups — Asian, Euro-South American and European. The Indian isolates formed a distinct genetic group among the Asian isolates. The Indian isolates were further classified into different genetic subgroups ( |
doi_str_mv | 10.1007/s12038-009-0011-9 |
format | Article |
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pro
) and capsid-coding sequences (P1) constitute approximately 3 kb of the foot-and-mouth disease virus (FMDV). We studied the phylogenetic relationship of 46 FMDV serotype A isolates of Indian origin collected during the period 1968–2005 and also eight vaccine strains using the neighbour-joining tree and Bayesian tree methods. The viruses were categorized under three major groups — Asian, Euro-South American and European. The Indian isolates formed a distinct genetic group among the Asian isolates. The Indian isolates were further classified into different genetic subgroups (<5% divergence). Post-1995 isolates were divided into two subgroups while a few isolates which originated in the year 2005 from Andhra Pradesh formed a separate group. These isolates were closely related to the isolates of the 1970s. The FMDV isolates seem to undergo reverse mutation or convergent evolution wherein sequences identical to the ancestors are present in the isolates in circulation. The eight vaccine strains included in the study were not related to each other and belonged to different genetic groups. Recombination was detected in the L
pro
region in one isolate (A IND 20/82) and in the VP1 coding 1D region in another isolate (A RAJ 21/96). Positive selection was identified at aa positions 23 in the L
pro
(
P
<0.05; 0.046*) and at aa 171 in the capsid protein VP1 (
P
<0.01; 0.003**).</description><identifier>ISSN: 0250-5991</identifier><identifier>EISSN: 0973-7138</identifier><identifier>DOI: 10.1007/s12038-009-0011-9</identifier><identifier>PMID: 19430121</identifier><language>eng</language><publisher>New Delhi: Springer India</publisher><subject>Biomedical and Life Sciences ; Biomedicine ; Capsid Proteins - genetics ; Cell Biology ; Endopeptidases - genetics ; Evolution, Molecular ; Foot & mouth disease ; Foot-and-mouth disease virus ; Foot-and-Mouth Disease Virus - genetics ; Foot-and-Mouth Disease Virus - isolation & purification ; Genetics ; Immunology ; India ; Life Sciences ; Microbiology ; Phylogeny ; Plant Sciences ; Proteases ; Recombination, Genetic ; Selection, Genetic ; Sequence Analysis, RNA ; Serotyping ; Vaccines ; Zoology</subject><ispartof>Journal of biosciences, 2009-03, Vol.34 (1), p.85-101</ispartof><rights>Indian Academy of Sciences 2009</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c498t-948e415227d5b9128f54b2fa5cdbcf5cd4925038f120eba74cf7715aef0443803</citedby><cites>FETCH-LOGICAL-c498t-948e415227d5b9128f54b2fa5cdbcf5cd4925038f120eba74cf7715aef0443803</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s12038-009-0011-9$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s12038-009-0011-9$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,780,784,885,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19430121$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nagendrakumar, S. B.</creatorcontrib><creatorcontrib>Madhanmohan, M.</creatorcontrib><creatorcontrib>Rangarajan, P. N.</creatorcontrib><creatorcontrib>Srinivasan, V. A.</creatorcontrib><title>Genetic analysis of foot-and-mouth disease virus serotype A of Indian origin and detection of positive selection and recombination in leader protease- and capsid-coding regions</title><title>Journal of biosciences</title><addtitle>J Biosci</addtitle><addtitle>J Biosci</addtitle><description>The leader protease (L
pro
) and capsid-coding sequences (P1) constitute approximately 3 kb of the foot-and-mouth disease virus (FMDV). We studied the phylogenetic relationship of 46 FMDV serotype A isolates of Indian origin collected during the period 1968–2005 and also eight vaccine strains using the neighbour-joining tree and Bayesian tree methods. The viruses were categorized under three major groups — Asian, Euro-South American and European. The Indian isolates formed a distinct genetic group among the Asian isolates. The Indian isolates were further classified into different genetic subgroups (<5% divergence). Post-1995 isolates were divided into two subgroups while a few isolates which originated in the year 2005 from Andhra Pradesh formed a separate group. These isolates were closely related to the isolates of the 1970s. The FMDV isolates seem to undergo reverse mutation or convergent evolution wherein sequences identical to the ancestors are present in the isolates in circulation. The eight vaccine strains included in the study were not related to each other and belonged to different genetic groups. Recombination was detected in the L
pro
region in one isolate (A IND 20/82) and in the VP1 coding 1D region in another isolate (A RAJ 21/96). Positive selection was identified at aa positions 23 in the L
pro
(
P
<0.05; 0.046*) and at aa 171 in the capsid protein VP1 (
P
<0.01; 0.003**).</description><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Capsid Proteins - genetics</subject><subject>Cell Biology</subject><subject>Endopeptidases - genetics</subject><subject>Evolution, Molecular</subject><subject>Foot & mouth disease</subject><subject>Foot-and-mouth disease virus</subject><subject>Foot-and-Mouth Disease Virus - genetics</subject><subject>Foot-and-Mouth Disease Virus - isolation & purification</subject><subject>Genetics</subject><subject>Immunology</subject><subject>India</subject><subject>Life Sciences</subject><subject>Microbiology</subject><subject>Phylogeny</subject><subject>Plant Sciences</subject><subject>Proteases</subject><subject>Recombination, Genetic</subject><subject>Selection, Genetic</subject><subject>Sequence Analysis, RNA</subject><subject>Serotyping</subject><subject>Vaccines</subject><subject>Zoology</subject><issn>0250-5991</issn><issn>0973-7138</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqFksGO1SAUhhujccbRB3BjiAt3KFB6KRuTyUTHSSZxo2tC4dBh0gsV6E3uW80jSu-9cdTEuKA053z_f1r4m-Y1Je8pIeJDpoy0PSZE1kUplk-acyJFiwVt-6f1nXUEd1LSs-ZFzveVkbwlz5uzw04ZPW8eriFA8QbpoKd99hlFh1yMBetg8TYu5Q5Zn0FnQDuflowypFj2M6DLFb0J1uuAYvKjD9XEIgsFTPExrO05Zl_8DqpqOlVXJoGJ28EHfahU4QTaQkJztV5H4QNl9Jy9xSZaH8aqGSucXzbPnJ4yvDrtF833z5--XX3Bt1-vb64ub7Hhsi9Y8h447RgTthskZb3r-MCc7owdjKtPLuvhtL2rRwiDFtw4IWinwRHO2560F83Ho--8DFuwBkJJelJz8lud9ipqr_7sBH-nxrhTgkjSc1kN3p0MUvyxQC5q67OBadIB4pLVRjDKNh37L8hoSxjnooJv_wLv45LqvVWm3TDGRbeOpUfIpJhzAvfrkylRa2rUMTWqpkatqVGr5s3v__qoOMWkAuwI5NoKI6THyf92_Qn4qNEV</recordid><startdate>20090301</startdate><enddate>20090301</enddate><creator>Nagendrakumar, S. 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B.</au><au>Madhanmohan, M.</au><au>Rangarajan, P. N.</au><au>Srinivasan, V. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genetic analysis of foot-and-mouth disease virus serotype A of Indian origin and detection of positive selection and recombination in leader protease- and capsid-coding regions</atitle><jtitle>Journal of biosciences</jtitle><stitle>J Biosci</stitle><addtitle>J Biosci</addtitle><date>2009-03-01</date><risdate>2009</risdate><volume>34</volume><issue>1</issue><spage>85</spage><epage>101</epage><pages>85-101</pages><issn>0250-5991</issn><eissn>0973-7138</eissn><abstract>The leader protease (L
pro
) and capsid-coding sequences (P1) constitute approximately 3 kb of the foot-and-mouth disease virus (FMDV). We studied the phylogenetic relationship of 46 FMDV serotype A isolates of Indian origin collected during the period 1968–2005 and also eight vaccine strains using the neighbour-joining tree and Bayesian tree methods. The viruses were categorized under three major groups — Asian, Euro-South American and European. The Indian isolates formed a distinct genetic group among the Asian isolates. The Indian isolates were further classified into different genetic subgroups (<5% divergence). Post-1995 isolates were divided into two subgroups while a few isolates which originated in the year 2005 from Andhra Pradesh formed a separate group. These isolates were closely related to the isolates of the 1970s. The FMDV isolates seem to undergo reverse mutation or convergent evolution wherein sequences identical to the ancestors are present in the isolates in circulation. The eight vaccine strains included in the study were not related to each other and belonged to different genetic groups. Recombination was detected in the L
pro
region in one isolate (A IND 20/82) and in the VP1 coding 1D region in another isolate (A RAJ 21/96). Positive selection was identified at aa positions 23 in the L
pro
(
P
<0.05; 0.046*) and at aa 171 in the capsid protein VP1 (
P
<0.01; 0.003**).</abstract><cop>New Delhi</cop><pub>Springer India</pub><pmid>19430121</pmid><doi>10.1007/s12038-009-0011-9</doi><tpages>17</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biomedical and Life Sciences Biomedicine Capsid Proteins - genetics Cell Biology Endopeptidases - genetics Evolution, Molecular Foot & mouth disease Foot-and-mouth disease virus Foot-and-Mouth Disease Virus - genetics Foot-and-Mouth Disease Virus - isolation & purification Genetics Immunology India Life Sciences Microbiology Phylogeny Plant Sciences Proteases Recombination, Genetic Selection, Genetic Sequence Analysis, RNA Serotyping Vaccines Zoology |
title | Genetic analysis of foot-and-mouth disease virus serotype A of Indian origin and detection of positive selection and recombination in leader protease- and capsid-coding regions |
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