Rotavirus A genotype P[4]G2: Genetic diversity and reassortment events among strains circulating in Brazil between 2005 and 2009
Group A rotaviruses (RV‐A) are the leading cause of severe gastroenteritis in infants and young children worldwide. Due to the epidemiologic complexity of RV‐A, especially in developing countries, it is important to determine which genotypes are circulating, principally after the introduction in Mar...
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creator | Gómez, Mariela Martínez de Mendonça, Marcos César Lima Volotão, Eduardo de Mello Tort, Luis Fernando López da Silva, Marcelle Figueira Marques Cristina, Juan Leite, Jose Paulo Gagliardi |
description | Group A rotaviruses (RV‐A) are the leading cause of severe gastroenteritis in infants and young children worldwide. Due to the epidemiologic complexity of RV‐A, especially in developing countries, it is important to determine which genotypes are circulating, principally after the introduction in March 2006 of the monovalent (P[8]G1) Rotarix® vaccine in Brazil by the National Immunization Program. In Phase III trials with Rotarix®, the prevalence of genotype P[4]G2 was extremely low, and therefore, evaluation of heterotypic immunization against this genotype was performed by meta‐analysis statistics tests. Different studies have shown the re‐emergence of genotype P[4]G2 in Brazil, since 2005, as well as in other countries, suggesting that it could be a continental phenomenon related to the temporal variability in the genotype's naturally occurring distribution. It is important to note that genotype P[4]G2 does not share VP4 or VP7 antigens with the vaccine strain. Therefore, we performed a phylogenetic analysis based on VP4 (VP8*), VP7, VP6, and NSP4 genes of RV‐A genotype P[4]G2 samples isolated from the five regions of Brazil between 2005 and 2009. This study revealed that different genetic variants of RV‐A genotype P[4]G2 circulated in Brazil between 2005 and 2009, and that this variability is determined mainly by: occurrence of point mutations; reassortment events; and widespread global gene flow. The results obtained in this study are important to our understanding of the epidemiology and evolution of RV‐A genotype P[4]G2 and demonstrate the importance of continuous monitoring and molecular characterization of RV‐A strains circulating in human and animal populations. J. Med. Virol. 83:1093–1106, 2011. © 2011 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/jmv.22071 |
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Due to the epidemiologic complexity of RV‐A, especially in developing countries, it is important to determine which genotypes are circulating, principally after the introduction in March 2006 of the monovalent (P[8]G1) Rotarix® vaccine in Brazil by the National Immunization Program. In Phase III trials with Rotarix®, the prevalence of genotype P[4]G2 was extremely low, and therefore, evaluation of heterotypic immunization against this genotype was performed by meta‐analysis statistics tests. Different studies have shown the re‐emergence of genotype P[4]G2 in Brazil, since 2005, as well as in other countries, suggesting that it could be a continental phenomenon related to the temporal variability in the genotype's naturally occurring distribution. It is important to note that genotype P[4]G2 does not share VP4 or VP7 antigens with the vaccine strain. Therefore, we performed a phylogenetic analysis based on VP4 (VP8*), VP7, VP6, and NSP4 genes of RV‐A genotype P[4]G2 samples isolated from the five regions of Brazil between 2005 and 2009. This study revealed that different genetic variants of RV‐A genotype P[4]G2 circulated in Brazil between 2005 and 2009, and that this variability is determined mainly by: occurrence of point mutations; reassortment events; and widespread global gene flow. The results obtained in this study are important to our understanding of the epidemiology and evolution of RV‐A genotype P[4]G2 and demonstrate the importance of continuous monitoring and molecular characterization of RV‐A strains circulating in human and animal populations. J. Med. Virol. 83:1093–1106, 2011. © 2011 Wiley‐Liss, Inc.</description><identifier>ISSN: 0146-6615</identifier><identifier>EISSN: 1096-9071</identifier><identifier>DOI: 10.1002/jmv.22071</identifier><identifier>PMID: 21503926</identifier><identifier>CODEN: JMVIDB</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Amino Acid Sequence ; Amino Acid Substitution ; Base Sequence ; Biological and medical sciences ; Brazil - epidemiology ; Child, Preschool ; Fundamental and applied biological sciences. Psychology ; Gastroenteritis - epidemiology ; Gastroenteritis - virology ; Gene Flow ; genetic variability ; Genetic Variation ; Genotype ; Human viral diseases ; Humans ; Infant ; Infectious diseases ; Medical sciences ; Microbiology ; Miscellaneous ; Molecular Sequence Data ; PG2 genotype ; phylogenetic analysis ; Phylogeny ; Reassortant Viruses - classification ; Reassortant Viruses - genetics ; Reassortant Viruses - isolation & purification ; reassortment ; Reverse Transcriptase Polymerase Chain Reaction ; RNA, Viral - genetics ; RNA, Viral - isolation & purification ; Rotavirus - classification ; Rotavirus - genetics ; Rotavirus - isolation & purification ; rotavirus A ; Rotavirus Infections - epidemiology ; Rotavirus Infections - virology ; Sequence Alignment ; Sequence Analysis, DNA ; Viral diseases ; Viral Proteins - genetics ; Virology</subject><ispartof>Journal of medical virology, 2011-06, Vol.83 (6), p.1093-1106</ispartof><rights>Copyright © 2011 Wiley‐Liss, Inc.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2011 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4861-3678358d35554779bb5fe791e6dd1e6bc598a08148ee2923d28773941147cf333</citedby><cites>FETCH-LOGICAL-c4861-3678358d35554779bb5fe791e6dd1e6bc598a08148ee2923d28773941147cf333</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjmv.22071$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjmv.22071$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24134587$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21503926$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gómez, Mariela Martínez</creatorcontrib><creatorcontrib>de Mendonça, Marcos César Lima</creatorcontrib><creatorcontrib>Volotão, Eduardo de Mello</creatorcontrib><creatorcontrib>Tort, Luis Fernando López</creatorcontrib><creatorcontrib>da Silva, Marcelle Figueira Marques</creatorcontrib><creatorcontrib>Cristina, Juan</creatorcontrib><creatorcontrib>Leite, Jose Paulo Gagliardi</creatorcontrib><title>Rotavirus A genotype P[4]G2: Genetic diversity and reassortment events among strains circulating in Brazil between 2005 and 2009</title><title>Journal of medical virology</title><addtitle>J. Med. Virol</addtitle><description>Group A rotaviruses (RV‐A) are the leading cause of severe gastroenteritis in infants and young children worldwide. Due to the epidemiologic complexity of RV‐A, especially in developing countries, it is important to determine which genotypes are circulating, principally after the introduction in March 2006 of the monovalent (P[8]G1) Rotarix® vaccine in Brazil by the National Immunization Program. In Phase III trials with Rotarix®, the prevalence of genotype P[4]G2 was extremely low, and therefore, evaluation of heterotypic immunization against this genotype was performed by meta‐analysis statistics tests. Different studies have shown the re‐emergence of genotype P[4]G2 in Brazil, since 2005, as well as in other countries, suggesting that it could be a continental phenomenon related to the temporal variability in the genotype's naturally occurring distribution. It is important to note that genotype P[4]G2 does not share VP4 or VP7 antigens with the vaccine strain. Therefore, we performed a phylogenetic analysis based on VP4 (VP8*), VP7, VP6, and NSP4 genes of RV‐A genotype P[4]G2 samples isolated from the five regions of Brazil between 2005 and 2009. This study revealed that different genetic variants of RV‐A genotype P[4]G2 circulated in Brazil between 2005 and 2009, and that this variability is determined mainly by: occurrence of point mutations; reassortment events; and widespread global gene flow. The results obtained in this study are important to our understanding of the epidemiology and evolution of RV‐A genotype P[4]G2 and demonstrate the importance of continuous monitoring and molecular characterization of RV‐A strains circulating in human and animal populations. J. Med. Virol. 83:1093–1106, 2011. © 2011 Wiley‐Liss, Inc.</description><subject>Amino Acid Sequence</subject><subject>Amino Acid Substitution</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Brazil - epidemiology</subject><subject>Child, Preschool</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gastroenteritis - epidemiology</subject><subject>Gastroenteritis - virology</subject><subject>Gene Flow</subject><subject>genetic variability</subject><subject>Genetic Variation</subject><subject>Genotype</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Infant</subject><subject>Infectious diseases</subject><subject>Medical sciences</subject><subject>Microbiology</subject><subject>Miscellaneous</subject><subject>Molecular Sequence Data</subject><subject>PG2 genotype</subject><subject>phylogenetic analysis</subject><subject>Phylogeny</subject><subject>Reassortant Viruses - classification</subject><subject>Reassortant Viruses - genetics</subject><subject>Reassortant Viruses - isolation & purification</subject><subject>reassortment</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>RNA, Viral - genetics</subject><subject>RNA, Viral - isolation & purification</subject><subject>Rotavirus - classification</subject><subject>Rotavirus - genetics</subject><subject>Rotavirus - isolation & purification</subject><subject>rotavirus A</subject><subject>Rotavirus Infections - epidemiology</subject><subject>Rotavirus Infections - virology</subject><subject>Sequence Alignment</subject><subject>Sequence Analysis, DNA</subject><subject>Viral diseases</subject><subject>Viral Proteins - genetics</subject><subject>Virology</subject><issn>0146-6615</issn><issn>1096-9071</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kVtrFEEQhQdRzBp98A9Ig4j4MEnfL77F1WwMcQ3i5UGk6ZmpDb2Z6Vm7ZzauT_502-wmguBLVVF8dU7BKYrHBB8QjOnhslsfUIoVuVNMCDayNHm-W0ww4bKUkoi94kFKS4yxNpTeL_YoEZgZKifFrw_94NY-jgkdoQsI_bBZATr_yr_N6Es0gwCDr1Hj1xCTHzbIhQZFcCn1ceggDAjWuSbkuj5coDRE50NCtY_12LrB550P6FV0P32LKhiuAAKiGItroTyYh8W9hWsTPNr1_eLT8ZuP05Py7P3s7fTorKy5lqRkUmkmdMOEEFwpU1ViAcoQkE2TS1ULox3WhGsAaihrqFaKGU4IV_WCMbZfPN_qrmL_fYQ02M6nGtrWBejHZLWkWU4ynsmn_5DLfowhP2eJ4AJryYTJ1IstVcc-pQgLu4q-c3FjCbZ_UrE5FXudSmaf7BTHqoPmlryJIQPPdoBLtWsX0YXap78cJ4wLrTJ3uOWufAub_zva03efb6zL7YVPA_y4vXDx0krFlLBf5jM7Pz4_mdLT13bOfgPa_7AQ</recordid><startdate>201106</startdate><enddate>201106</enddate><creator>Gómez, Mariela Martínez</creator><creator>de Mendonça, Marcos César Lima</creator><creator>Volotão, Eduardo de Mello</creator><creator>Tort, Luis Fernando López</creator><creator>da Silva, Marcelle Figueira Marques</creator><creator>Cristina, Juan</creator><creator>Leite, Jose Paulo Gagliardi</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</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>7QL</scope><scope>7TK</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>201106</creationdate><title>Rotavirus A genotype P[4]G2: Genetic diversity and reassortment events among strains circulating in Brazil between 2005 and 2009</title><author>Gómez, Mariela Martínez ; de Mendonça, Marcos César Lima ; Volotão, Eduardo de Mello ; Tort, Luis Fernando López ; da Silva, Marcelle Figueira Marques ; Cristina, Juan ; Leite, Jose Paulo Gagliardi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4861-3678358d35554779bb5fe791e6dd1e6bc598a08148ee2923d28773941147cf333</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Amino Acid Sequence</topic><topic>Amino Acid Substitution</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Brazil - epidemiology</topic><topic>Child, Preschool</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gastroenteritis - epidemiology</topic><topic>Gastroenteritis - virology</topic><topic>Gene Flow</topic><topic>genetic variability</topic><topic>Genetic Variation</topic><topic>Genotype</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Infant</topic><topic>Infectious diseases</topic><topic>Medical sciences</topic><topic>Microbiology</topic><topic>Miscellaneous</topic><topic>Molecular Sequence Data</topic><topic>PG2 genotype</topic><topic>phylogenetic analysis</topic><topic>Phylogeny</topic><topic>Reassortant Viruses - classification</topic><topic>Reassortant Viruses - genetics</topic><topic>Reassortant Viruses - isolation & purification</topic><topic>reassortment</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>RNA, Viral - genetics</topic><topic>RNA, Viral - isolation & purification</topic><topic>Rotavirus - classification</topic><topic>Rotavirus - genetics</topic><topic>Rotavirus - isolation & purification</topic><topic>rotavirus A</topic><topic>Rotavirus Infections - epidemiology</topic><topic>Rotavirus Infections - virology</topic><topic>Sequence Alignment</topic><topic>Sequence Analysis, DNA</topic><topic>Viral diseases</topic><topic>Viral Proteins - genetics</topic><topic>Virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gómez, Mariela Martínez</creatorcontrib><creatorcontrib>de Mendonça, Marcos César Lima</creatorcontrib><creatorcontrib>Volotão, Eduardo de Mello</creatorcontrib><creatorcontrib>Tort, Luis Fernando López</creatorcontrib><creatorcontrib>da Silva, Marcelle Figueira Marques</creatorcontrib><creatorcontrib>Cristina, Juan</creatorcontrib><creatorcontrib>Leite, Jose Paulo Gagliardi</creatorcontrib><collection>Istex</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>Bacteriology Abstracts (Microbiology B)</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of medical virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gómez, Mariela Martínez</au><au>de Mendonça, Marcos César Lima</au><au>Volotão, Eduardo de Mello</au><au>Tort, Luis Fernando López</au><au>da Silva, Marcelle Figueira Marques</au><au>Cristina, Juan</au><au>Leite, Jose Paulo Gagliardi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rotavirus A genotype P[4]G2: Genetic diversity and reassortment events among strains circulating in Brazil between 2005 and 2009</atitle><jtitle>Journal of medical virology</jtitle><addtitle>J. Med. Virol</addtitle><date>2011-06</date><risdate>2011</risdate><volume>83</volume><issue>6</issue><spage>1093</spage><epage>1106</epage><pages>1093-1106</pages><issn>0146-6615</issn><eissn>1096-9071</eissn><coden>JMVIDB</coden><abstract>Group A rotaviruses (RV‐A) are the leading cause of severe gastroenteritis in infants and young children worldwide. Due to the epidemiologic complexity of RV‐A, especially in developing countries, it is important to determine which genotypes are circulating, principally after the introduction in March 2006 of the monovalent (P[8]G1) Rotarix® vaccine in Brazil by the National Immunization Program. In Phase III trials with Rotarix®, the prevalence of genotype P[4]G2 was extremely low, and therefore, evaluation of heterotypic immunization against this genotype was performed by meta‐analysis statistics tests. Different studies have shown the re‐emergence of genotype P[4]G2 in Brazil, since 2005, as well as in other countries, suggesting that it could be a continental phenomenon related to the temporal variability in the genotype's naturally occurring distribution. It is important to note that genotype P[4]G2 does not share VP4 or VP7 antigens with the vaccine strain. Therefore, we performed a phylogenetic analysis based on VP4 (VP8*), VP7, VP6, and NSP4 genes of RV‐A genotype P[4]G2 samples isolated from the five regions of Brazil between 2005 and 2009. This study revealed that different genetic variants of RV‐A genotype P[4]G2 circulated in Brazil between 2005 and 2009, and that this variability is determined mainly by: occurrence of point mutations; reassortment events; and widespread global gene flow. The results obtained in this study are important to our understanding of the epidemiology and evolution of RV‐A genotype P[4]G2 and demonstrate the importance of continuous monitoring and molecular characterization of RV‐A strains circulating in human and animal populations. J. Med. Virol. 83:1093–1106, 2011. © 2011 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>21503926</pmid><doi>10.1002/jmv.22071</doi><tpages>14</tpages></addata></record> |
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subjects | Amino Acid Sequence Amino Acid Substitution Base Sequence Biological and medical sciences Brazil - epidemiology Child, Preschool Fundamental and applied biological sciences. Psychology Gastroenteritis - epidemiology Gastroenteritis - virology Gene Flow genetic variability Genetic Variation Genotype Human viral diseases Humans Infant Infectious diseases Medical sciences Microbiology Miscellaneous Molecular Sequence Data PG2 genotype phylogenetic analysis Phylogeny Reassortant Viruses - classification Reassortant Viruses - genetics Reassortant Viruses - isolation & purification reassortment Reverse Transcriptase Polymerase Chain Reaction RNA, Viral - genetics RNA, Viral - isolation & purification Rotavirus - classification Rotavirus - genetics Rotavirus - isolation & purification rotavirus A Rotavirus Infections - epidemiology Rotavirus Infections - virology Sequence Alignment Sequence Analysis, DNA Viral diseases Viral Proteins - genetics Virology |
title | Rotavirus A genotype P[4]G2: Genetic diversity and reassortment events among strains circulating in Brazil between 2005 and 2009 |
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