Full genomic analysis of a simian SA11-like G3P[2] rotavirus strain isolated from an asymptomatic infant: Identification of novel VP1, VP6 and NSP4 genotypes

▶ Full genomic analysis of a simian SA11-like human G3P[2] rotavirus strain, B10. ▶ Eight out of the 11 gene segments of strain B10 were of simian origin.▶ Identification of novel VP1, VP6 and NSP4 genotypes.▶ Evidence for interspecies transmission of rotaviruses from wild animals to humans. We repo...

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Veröffentlicht in:Infection, genetics and evolution genetics and evolution, 2011, Vol.11 (1), p.57-63
Hauptverfasser: Ghosh, Souvik, Gatheru, Zipporah, Nyangao, James, Adachi, Noriaki, Urushibara, Noriko, Kobayashi, Nobumichi
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container_issue 1
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container_title Infection, genetics and evolution
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creator Ghosh, Souvik
Gatheru, Zipporah
Nyangao, James
Adachi, Noriaki
Urushibara, Noriko
Kobayashi, Nobumichi
description ▶ Full genomic analysis of a simian SA11-like human G3P[2] rotavirus strain, B10. ▶ Eight out of the 11 gene segments of strain B10 were of simian origin.▶ Identification of novel VP1, VP6 and NSP4 genotypes.▶ Evidence for interspecies transmission of rotaviruses from wild animals to humans. We report here the full genomic analysis of a simian SA11-like G3P[2] group A rotavirus (GAR) strain, B10, isolated from an asymptomatic infant in Kenya in 1987. By nucleotide sequence identities and phylogenetic analyses, the VP7–VP4–VP2–VP3–NSP1–NSP2–NSP3–NSP5 genes of strain B10 exhibited maximum genetic relatedness to those of the different isolates of simian strain SA11, and were assigned to the G3–P[2]–C5–M5–A5–N5–T5–H5 genotypes, respectively. On the other hand, the VP1, VP6 and NSP4 genes of strain B10 did not belong to any of the established GAR genotypes, and therefore, were assigned to new genotype numbers R8, I16 and E13, respectively, by the Rotavirus Classification Working Group. These observations suggested that strain B10 might have originated from reassortment event/s involving simian SA11-like strains and GAR strains from unknown animal host species (possibly other wild animals) preceding transmission to humans. Alternatively, considering the lack of data on simian GARs, it might be also possible that the VP1, VP6 and NSP4 genes of strain B10 are those of unknown simian strains, and that strain B10 might be a typical simian strain that was directly transmitted to humans. Therefore, either hypothesis pointed towards a rare instance of possible direct transmission of GARs from an animal host (possibly a monkey or some other wild animal) to humans. This was corroborated by the presence of different species of wild animals including non-human primates, and unhygienic conditions at the sampling site. To our knowledge, the present study is the first report on the detection of a simian SA11-like G3P[2] GAR strain in humans.
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We report here the full genomic analysis of a simian SA11-like G3P[2] group A rotavirus (GAR) strain, B10, isolated from an asymptomatic infant in Kenya in 1987. By nucleotide sequence identities and phylogenetic analyses, the VP7–VP4–VP2–VP3–NSP1–NSP2–NSP3–NSP5 genes of strain B10 exhibited maximum genetic relatedness to those of the different isolates of simian strain SA11, and were assigned to the G3–P[2]–C5–M5–A5–N5–T5–H5 genotypes, respectively. On the other hand, the VP1, VP6 and NSP4 genes of strain B10 did not belong to any of the established GAR genotypes, and therefore, were assigned to new genotype numbers R8, I16 and E13, respectively, by the Rotavirus Classification Working Group. These observations suggested that strain B10 might have originated from reassortment event/s involving simian SA11-like strains and GAR strains from unknown animal host species (possibly other wild animals) preceding transmission to humans. Alternatively, considering the lack of data on simian GARs, it might be also possible that the VP1, VP6 and NSP4 genes of strain B10 are those of unknown simian strains, and that strain B10 might be a typical simian strain that was directly transmitted to humans. Therefore, either hypothesis pointed towards a rare instance of possible direct transmission of GARs from an animal host (possibly a monkey or some other wild animal) to humans. This was corroborated by the presence of different species of wild animals including non-human primates, and unhygienic conditions at the sampling site. 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We report here the full genomic analysis of a simian SA11-like G3P[2] group A rotavirus (GAR) strain, B10, isolated from an asymptomatic infant in Kenya in 1987. By nucleotide sequence identities and phylogenetic analyses, the VP7–VP4–VP2–VP3–NSP1–NSP2–NSP3–NSP5 genes of strain B10 exhibited maximum genetic relatedness to those of the different isolates of simian strain SA11, and were assigned to the G3–P[2]–C5–M5–A5–N5–T5–H5 genotypes, respectively. On the other hand, the VP1, VP6 and NSP4 genes of strain B10 did not belong to any of the established GAR genotypes, and therefore, were assigned to new genotype numbers R8, I16 and E13, respectively, by the Rotavirus Classification Working Group. These observations suggested that strain B10 might have originated from reassortment event/s involving simian SA11-like strains and GAR strains from unknown animal host species (possibly other wild animals) preceding transmission to humans. Alternatively, considering the lack of data on simian GARs, it might be also possible that the VP1, VP6 and NSP4 genes of strain B10 are those of unknown simian strains, and that strain B10 might be a typical simian strain that was directly transmitted to humans. Therefore, either hypothesis pointed towards a rare instance of possible direct transmission of GARs from an animal host (possibly a monkey or some other wild animal) to humans. This was corroborated by the presence of different species of wild animals including non-human primates, and unhygienic conditions at the sampling site. To our knowledge, the present study is the first report on the detection of a simian SA11-like G3P[2] GAR strain in humans.</description><subject>Antigens, Viral - genetics</subject><subject>Biological and medical sciences</subject><subject>Capsid Proteins - genetics</subject><subject>Epidemiology. 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Vaccinations</topic><topic>General aspects</topic><topic>genes</topic><topic>Genes, Viral</topic><topic>genetic relationships</topic><topic>Genome, Viral</topic><topic>genomics</topic><topic>Genotype</topic><topic>Glycoproteins - genetics</topic><topic>Group A rotavirus</topic><topic>Human</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Infant</topic><topic>Infectious diseases</topic><topic>Medical sciences</topic><topic>monkeys</topic><topic>Novel genotypes</topic><topic>nucleotide sequences</topic><topic>Phylogeny</topic><topic>Primates</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>Rotavirus - genetics</topic><topic>Rotavirus - isolation &amp; purification</topic><topic>Rotavirus A</topic><topic>Simian</topic><topic>Toxins, Biological - genetics</topic><topic>Viral Core Proteins - genetics</topic><topic>Viral diseases</topic><topic>Viral diseases of the digestive system</topic><topic>Viral Nonstructural Proteins - genetics</topic><topic>wild animals</topic><topic>Zoonosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ghosh, Souvik</creatorcontrib><creatorcontrib>Gatheru, Zipporah</creatorcontrib><creatorcontrib>Nyangao, James</creatorcontrib><creatorcontrib>Adachi, Noriaki</creatorcontrib><creatorcontrib>Urushibara, Noriko</creatorcontrib><creatorcontrib>Kobayashi, Nobumichi</creatorcontrib><collection>AGRIS</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>MEDLINE - Academic</collection><jtitle>Infection, genetics and evolution</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ghosh, Souvik</au><au>Gatheru, Zipporah</au><au>Nyangao, James</au><au>Adachi, Noriaki</au><au>Urushibara, Noriko</au><au>Kobayashi, Nobumichi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Full genomic analysis of a simian SA11-like G3P[2] rotavirus strain isolated from an asymptomatic infant: Identification of novel VP1, VP6 and NSP4 genotypes</atitle><jtitle>Infection, genetics and evolution</jtitle><addtitle>Infect Genet Evol</addtitle><date>2011</date><risdate>2011</risdate><volume>11</volume><issue>1</issue><spage>57</spage><epage>63</epage><pages>57-63</pages><issn>1567-1348</issn><eissn>1567-7257</eissn><abstract>▶ Full genomic analysis of a simian SA11-like human G3P[2] rotavirus strain, B10. ▶ Eight out of the 11 gene segments of strain B10 were of simian origin.▶ Identification of novel VP1, VP6 and NSP4 genotypes.▶ Evidence for interspecies transmission of rotaviruses from wild animals to humans. We report here the full genomic analysis of a simian SA11-like G3P[2] group A rotavirus (GAR) strain, B10, isolated from an asymptomatic infant in Kenya in 1987. By nucleotide sequence identities and phylogenetic analyses, the VP7–VP4–VP2–VP3–NSP1–NSP2–NSP3–NSP5 genes of strain B10 exhibited maximum genetic relatedness to those of the different isolates of simian strain SA11, and were assigned to the G3–P[2]–C5–M5–A5–N5–T5–H5 genotypes, respectively. On the other hand, the VP1, VP6 and NSP4 genes of strain B10 did not belong to any of the established GAR genotypes, and therefore, were assigned to new genotype numbers R8, I16 and E13, respectively, by the Rotavirus Classification Working Group. These observations suggested that strain B10 might have originated from reassortment event/s involving simian SA11-like strains and GAR strains from unknown animal host species (possibly other wild animals) preceding transmission to humans. Alternatively, considering the lack of data on simian GARs, it might be also possible that the VP1, VP6 and NSP4 genes of strain B10 are those of unknown simian strains, and that strain B10 might be a typical simian strain that was directly transmitted to humans. Therefore, either hypothesis pointed towards a rare instance of possible direct transmission of GARs from an animal host (possibly a monkey or some other wild animal) to humans. This was corroborated by the presence of different species of wild animals including non-human primates, and unhygienic conditions at the sampling site. To our knowledge, the present study is the first report on the detection of a simian SA11-like G3P[2] GAR strain in humans.</abstract><cop>Kidlington</cop><pub>Elsevier B.V</pub><pmid>21035567</pmid><doi>10.1016/j.meegid.2010.10.010</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; ScienceDirect Journals (5 years ago - present)
subjects Antigens, Viral - genetics
Biological and medical sciences
Capsid Proteins - genetics
Epidemiology. Vaccinations
General aspects
genes
Genes, Viral
genetic relationships
Genome, Viral
genomics
Genotype
Glycoproteins - genetics
Group A rotavirus
Human
Human viral diseases
Humans
Infant
Infectious diseases
Medical sciences
monkeys
Novel genotypes
nucleotide sequences
Phylogeny
Primates
Reverse Transcriptase Polymerase Chain Reaction
Rotavirus - genetics
Rotavirus - isolation & purification
Rotavirus A
Simian
Toxins, Biological - genetics
Viral Core Proteins - genetics
Viral diseases
Viral diseases of the digestive system
Viral Nonstructural Proteins - genetics
wild animals
Zoonosis
title Full genomic analysis of a simian SA11-like G3P[2] rotavirus strain isolated from an asymptomatic infant: Identification of novel VP1, VP6 and NSP4 genotypes
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