Polymerase chain reaction-based genetic typing of Japanese porcine reproductive and respiratory syndrome viruses
National Institute of Animal Health, Kannondai, Tsukuba, Ibaraki, Japan. Porcine reproductive and respiratory syndrome viruses (PRRSVs) are classified into 2 distinct genotypes: the North American type and the European type. The Japanese PRRSVs were genotyped by reverse transcriptase-polymerase chai...
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Veröffentlicht in: | Journal of veterinary diagnostic investigation 2004-07, Vol.16 (4), p.342-347 |
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creator | Yoshii, M Kaku, Y Murakami, Y Shimizu, M Kato, K Ikeda, H |
description | National Institute of Animal Health, Kannondai, Tsukuba, Ibaraki, Japan.
Porcine reproductive and respiratory syndrome viruses (PRRSVs) are classified into 2 distinct genotypes: the North American type and the European type. The Japanese PRRSVs were genotyped by reverse transcriptase-polymerase chain reaction using the reported primer pairs that were either reactive to both types, specific to the North American type or specific to the European type. All the PRRSV genomes from 66 tissue homogenates or sera and 55 infectious viruses were of the North American type, whereas no European-type viral genome was detected. Two PCR primers specific to the North American type showed different detection efficiency. Half of the tissue samples and 15% of the infectious viruses were not detected with one primer pair, although all of them were detected with the other primer pair. Nucleotide sequencing analysis of the forward-and reverse primer-binding sites of the nonreactive viruses indicated that all these viruses had nucleotide mismatches within the 4 bases corresponding to the 3' end of the reverse primer. These mismatches appeared to be responsible for the nonreactivity of the former primers to these viruses. |
doi_str_mv | 10.1177/104063870401600417 |
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Porcine reproductive and respiratory syndrome viruses (PRRSVs) are classified into 2 distinct genotypes: the North American type and the European type. The Japanese PRRSVs were genotyped by reverse transcriptase-polymerase chain reaction using the reported primer pairs that were either reactive to both types, specific to the North American type or specific to the European type. All the PRRSV genomes from 66 tissue homogenates or sera and 55 infectious viruses were of the North American type, whereas no European-type viral genome was detected. Two PCR primers specific to the North American type showed different detection efficiency. Half of the tissue samples and 15% of the infectious viruses were not detected with one primer pair, although all of them were detected with the other primer pair. Nucleotide sequencing analysis of the forward-and reverse primer-binding sites of the nonreactive viruses indicated that all these viruses had nucleotide mismatches within the 4 bases corresponding to the 3' end of the reverse primer. These mismatches appeared to be responsible for the nonreactivity of the former primers to these viruses.</description><identifier>ISSN: 1040-6387</identifier><identifier>EISSN: 1943-4936</identifier><identifier>DOI: 10.1177/104063870401600417</identifier><identifier>PMID: 15305750</identifier><language>eng</language><publisher>Los Angeles, CA: J Vet Diagn Invest</publisher><subject>Animals ; Base Sequence ; Genotype ; Japan ; Molecular Sequence Data ; North America ; Porcine Reproductive and Respiratory Syndrome ; Porcine respiratory and reproductive syndrome virus - genetics ; Reverse Transcriptase Polymerase Chain Reaction - veterinary ; Sequence Analysis, DNA ; Swine</subject><ispartof>Journal of veterinary diagnostic investigation, 2004-07, Vol.16 (4), p.342-347</ispartof><rights>2004 American Association of Veterinary Laboratory Diagnosticians</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c436t-9c65ebdccc5ca48891db37463d80d23f6d9dc0b6eaf6af7f875ca9f8ee1f1e033</citedby><cites>FETCH-LOGICAL-c436t-9c65ebdccc5ca48891db37463d80d23f6d9dc0b6eaf6af7f875ca9f8ee1f1e033</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/104063870401600417$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/104063870401600417$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>315,781,785,21823,27928,27929,43625,43626</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15305750$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yoshii, M</creatorcontrib><creatorcontrib>Kaku, Y</creatorcontrib><creatorcontrib>Murakami, Y</creatorcontrib><creatorcontrib>Shimizu, M</creatorcontrib><creatorcontrib>Kato, K</creatorcontrib><creatorcontrib>Ikeda, H</creatorcontrib><title>Polymerase chain reaction-based genetic typing of Japanese porcine reproductive and respiratory syndrome viruses</title><title>Journal of veterinary diagnostic investigation</title><addtitle>J Vet Diagn Invest</addtitle><description>National Institute of Animal Health, Kannondai, Tsukuba, Ibaraki, Japan.
Porcine reproductive and respiratory syndrome viruses (PRRSVs) are classified into 2 distinct genotypes: the North American type and the European type. The Japanese PRRSVs were genotyped by reverse transcriptase-polymerase chain reaction using the reported primer pairs that were either reactive to both types, specific to the North American type or specific to the European type. All the PRRSV genomes from 66 tissue homogenates or sera and 55 infectious viruses were of the North American type, whereas no European-type viral genome was detected. Two PCR primers specific to the North American type showed different detection efficiency. Half of the tissue samples and 15% of the infectious viruses were not detected with one primer pair, although all of them were detected with the other primer pair. Nucleotide sequencing analysis of the forward-and reverse primer-binding sites of the nonreactive viruses indicated that all these viruses had nucleotide mismatches within the 4 bases corresponding to the 3' end of the reverse primer. These mismatches appeared to be responsible for the nonreactivity of the former primers to these viruses.</description><subject>Animals</subject><subject>Base Sequence</subject><subject>Genotype</subject><subject>Japan</subject><subject>Molecular Sequence Data</subject><subject>North America</subject><subject>Porcine Reproductive and Respiratory Syndrome</subject><subject>Porcine respiratory and reproductive syndrome virus - genetics</subject><subject>Reverse Transcriptase Polymerase Chain Reaction - veterinary</subject><subject>Sequence Analysis, DNA</subject><subject>Swine</subject><issn>1040-6387</issn><issn>1943-4936</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEtv3CAUhVGVqnn1D3RRscrOCRgM9jKK2jwUqV00a4ThMsPIBhfsifzvSzQjZVEpq4su3zkcDkLfKLmmVMobSjgRrJVlUEEIp_ITOqMdZxXvmDgp53JTvRGn6DznHSFN3Uj6BZ3ShpFGNuQMTb_jsI6QdAZsttoHnECb2cdQ9WVn8QYCzN7geZ182ODo8JOedIDCTzEZH6AophTtUlR7wDrYssiTT3qOacV5DTbFEfDepyVDvkSfnR4yfD3OC_Ty88efu4fq-df9493tc2U4E3PVGdFAb40xjdG8bTtqeya5YLYltmZO2M4a0gvQTmgnXSsL17kWgDoKhLELdHXwLdn-LpBnNfpsYBhK9rhkJYSUgrGugPUBNCnmnMCpKflRp1VRot56Vv_3XETfj-5LP4J9lxyLLcDNAch6A2oXlxTKbz-2PAbe-s321SdQedTDUB6o1W5vPRWKK8Zr9g-4D5aE</recordid><startdate>20040701</startdate><enddate>20040701</enddate><creator>Yoshii, M</creator><creator>Kaku, Y</creator><creator>Murakami, Y</creator><creator>Shimizu, M</creator><creator>Kato, K</creator><creator>Ikeda, H</creator><general>J Vet Diagn Invest</general><general>SAGE Publications</general><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>7X8</scope></search><sort><creationdate>20040701</creationdate><title>Polymerase chain reaction-based genetic typing of Japanese porcine reproductive and respiratory syndrome viruses</title><author>Yoshii, M ; Kaku, Y ; Murakami, Y ; Shimizu, M ; Kato, K ; Ikeda, H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c436t-9c65ebdccc5ca48891db37463d80d23f6d9dc0b6eaf6af7f875ca9f8ee1f1e033</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Animals</topic><topic>Base Sequence</topic><topic>Genotype</topic><topic>Japan</topic><topic>Molecular Sequence Data</topic><topic>North America</topic><topic>Porcine Reproductive and Respiratory Syndrome</topic><topic>Porcine respiratory and reproductive syndrome virus - genetics</topic><topic>Reverse Transcriptase Polymerase Chain Reaction - veterinary</topic><topic>Sequence Analysis, DNA</topic><topic>Swine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yoshii, M</creatorcontrib><creatorcontrib>Kaku, Y</creatorcontrib><creatorcontrib>Murakami, Y</creatorcontrib><creatorcontrib>Shimizu, M</creatorcontrib><creatorcontrib>Kato, K</creatorcontrib><creatorcontrib>Ikeda, H</creatorcontrib><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>Journal of veterinary diagnostic investigation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yoshii, M</au><au>Kaku, Y</au><au>Murakami, Y</au><au>Shimizu, M</au><au>Kato, K</au><au>Ikeda, H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Polymerase chain reaction-based genetic typing of Japanese porcine reproductive and respiratory syndrome viruses</atitle><jtitle>Journal of veterinary diagnostic investigation</jtitle><addtitle>J Vet Diagn Invest</addtitle><date>2004-07-01</date><risdate>2004</risdate><volume>16</volume><issue>4</issue><spage>342</spage><epage>347</epage><pages>342-347</pages><issn>1040-6387</issn><eissn>1943-4936</eissn><abstract>National Institute of Animal Health, Kannondai, Tsukuba, Ibaraki, Japan.
Porcine reproductive and respiratory syndrome viruses (PRRSVs) are classified into 2 distinct genotypes: the North American type and the European type. The Japanese PRRSVs were genotyped by reverse transcriptase-polymerase chain reaction using the reported primer pairs that were either reactive to both types, specific to the North American type or specific to the European type. All the PRRSV genomes from 66 tissue homogenates or sera and 55 infectious viruses were of the North American type, whereas no European-type viral genome was detected. Two PCR primers specific to the North American type showed different detection efficiency. Half of the tissue samples and 15% of the infectious viruses were not detected with one primer pair, although all of them were detected with the other primer pair. Nucleotide sequencing analysis of the forward-and reverse primer-binding sites of the nonreactive viruses indicated that all these viruses had nucleotide mismatches within the 4 bases corresponding to the 3' end of the reverse primer. These mismatches appeared to be responsible for the nonreactivity of the former primers to these viruses.</abstract><cop>Los Angeles, CA</cop><pub>J Vet Diagn Invest</pub><pmid>15305750</pmid><doi>10.1177/104063870401600417</doi><tpages>6</tpages></addata></record> |
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subjects | Animals Base Sequence Genotype Japan Molecular Sequence Data North America Porcine Reproductive and Respiratory Syndrome Porcine respiratory and reproductive syndrome virus - genetics Reverse Transcriptase Polymerase Chain Reaction - veterinary Sequence Analysis, DNA Swine |
title | Polymerase chain reaction-based genetic typing of Japanese porcine reproductive and respiratory syndrome viruses |
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