DNA fingerprinting of plasmid-containing serotype A: 3,4 Pasteurella multocida isolated from cases of fowl cholera in chickens and turkeys
The live, attenuated vaccine strains of Pasteurella multocida have been hypothesized to be responsible for homologous serotype outbreaks of fowl cholera on farms that use the commercial vaccines. We have further hypothesized that the naturally occurring Clemson University (CU) vaccine strain may be...
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Veröffentlicht in: | Avian diseases 2000, Vol.44 (1), p.201-204 |
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description | The live, attenuated vaccine strains of Pasteurella multocida have been hypothesized to be responsible for homologous serotype outbreaks of fowl cholera on farms that use the commercial vaccines. We have further hypothesized that the naturally occurring Clemson University (CU) vaccine strain may be transformed to virulence by the acquisition of plasmid DNA. To test this hypothesis, we obtained seven homologous serotype (A:3,4) P. multocida isolates, all plasmid bearing, that were cultured from fowl cholera cases in vaccinated flocks and compared the isolates with the CU reference vaccine by molecular methods. Restriction fragment length polymorphisms (RFLPs) were detected by DNA/DNA hybridization with labeled probes specific for the cya, aroA, and rrn genes of P. multocida. The RFLPs obtained from BglII-digested genomic DNA probed with cya demonstrated no differences among the isolates. Although three isolates probed with aroA showed a RFLP identical to the vaccine strain, five isolates were distinctly difference. Isolates probed with rrn grouped into three different restriction patterns that were dissimilar from that of the vaccine strain. Therefore, we have shown that these fowl cholera isolates are different from the CU vaccine strain and that these outbreaks were not vaccine related. |
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We have further hypothesized that the naturally occurring Clemson University (CU) vaccine strain may be transformed to virulence by the acquisition of plasmid DNA. To test this hypothesis, we obtained seven homologous serotype (A:3,4) P. multocida isolates, all plasmid bearing, that were cultured from fowl cholera cases in vaccinated flocks and compared the isolates with the CU reference vaccine by molecular methods. Restriction fragment length polymorphisms (RFLPs) were detected by DNA/DNA hybridization with labeled probes specific for the cya, aroA, and rrn genes of P. multocida. The RFLPs obtained from BglII-digested genomic DNA probed with cya demonstrated no differences among the isolates. Although three isolates probed with aroA showed a RFLP identical to the vaccine strain, five isolates were distinctly difference. Isolates probed with rrn grouped into three different restriction patterns that were dissimilar from that of the vaccine strain. Therefore, we have shown that these fowl cholera isolates are different from the CU vaccine strain and that these outbreaks were not vaccine related.</description><identifier>ISSN: 0005-2086</identifier><identifier>EISSN: 1938-4351</identifier><identifier>DOI: 10.2307/1592526</identifier><identifier>PMID: 10737663</identifier><language>eng</language><publisher>United States: American Association of Avian Pathologists, Inc</publisher><subject>Animals ; Chickens ; Cholera ; DNA ; DNA fingerprinting ; DNA Fingerprinting - veterinary ; Electrophoresis, Polyacrylamide Gel - veterinary ; genetic variation ; Genomics ; Nucleic Acid Hybridization ; outbreaks ; Pasteurella Infections - genetics ; Pasteurella Infections - microbiology ; Pasteurella Infections - veterinary ; Pasteurella multocida ; Pasteurella multocida - genetics ; Pasteurella multocida - isolation & purification ; Plasmids ; Polymerase Chain Reaction - veterinary ; Polymorphism, Restriction Fragment Length ; Poultry Diseases - genetics ; Poultry Diseases - microbiology ; Research Notes ; restriction fragment length polymorphism ; Turkeys ; Vaccination ; Virulence</subject><ispartof>Avian diseases, 2000, Vol.44 (1), p.201-204</ispartof><rights>Copyright 2000 The American Association of Avian Pathologists, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c330t-c2c9d68f1d49dfdd833454bc67fcaecc977b588c3f23d08314dbf6f07f87a9ae3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/1592526$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/1592526$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,780,784,803,4023,27922,27923,27924,58016,58249</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10737663$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, M.D</creatorcontrib><creatorcontrib>Burch, F.T</creatorcontrib><creatorcontrib>Maurer, J.J</creatorcontrib><creatorcontrib>Henk, A</creatorcontrib><creatorcontrib>Thayer, S</creatorcontrib><title>DNA fingerprinting of plasmid-containing serotype A: 3,4 Pasteurella multocida isolated from cases of fowl cholera in chickens and turkeys</title><title>Avian diseases</title><addtitle>Avian Dis</addtitle><description>The live, attenuated vaccine strains of Pasteurella multocida have been hypothesized to be responsible for homologous serotype outbreaks of fowl cholera on farms that use the commercial vaccines. We have further hypothesized that the naturally occurring Clemson University (CU) vaccine strain may be transformed to virulence by the acquisition of plasmid DNA. To test this hypothesis, we obtained seven homologous serotype (A:3,4) P. multocida isolates, all plasmid bearing, that were cultured from fowl cholera cases in vaccinated flocks and compared the isolates with the CU reference vaccine by molecular methods. Restriction fragment length polymorphisms (RFLPs) were detected by DNA/DNA hybridization with labeled probes specific for the cya, aroA, and rrn genes of P. multocida. The RFLPs obtained from BglII-digested genomic DNA probed with cya demonstrated no differences among the isolates. Although three isolates probed with aroA showed a RFLP identical to the vaccine strain, five isolates were distinctly difference. Isolates probed with rrn grouped into three different restriction patterns that were dissimilar from that of the vaccine strain. Therefore, we have shown that these fowl cholera isolates are different from the CU vaccine strain and that these outbreaks were not vaccine related.</description><subject>Animals</subject><subject>Chickens</subject><subject>Cholera</subject><subject>DNA</subject><subject>DNA fingerprinting</subject><subject>DNA Fingerprinting - veterinary</subject><subject>Electrophoresis, Polyacrylamide Gel - veterinary</subject><subject>genetic variation</subject><subject>Genomics</subject><subject>Nucleic Acid Hybridization</subject><subject>outbreaks</subject><subject>Pasteurella Infections - genetics</subject><subject>Pasteurella Infections - microbiology</subject><subject>Pasteurella Infections - veterinary</subject><subject>Pasteurella multocida</subject><subject>Pasteurella multocida - genetics</subject><subject>Pasteurella multocida - isolation & purification</subject><subject>Plasmids</subject><subject>Polymerase Chain Reaction - veterinary</subject><subject>Polymorphism, Restriction Fragment Length</subject><subject>Poultry Diseases - genetics</subject><subject>Poultry Diseases - microbiology</subject><subject>Research Notes</subject><subject>restriction fragment length polymorphism</subject><subject>Turkeys</subject><subject>Vaccination</subject><subject>Virulence</subject><issn>0005-2086</issn><issn>1938-4351</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1v1DAQQC0EoktB_APwAcGFwNiTxHFvq_IpVYAEPUdefxS3Sbx4HKH9C_xqssoeOHGa0ejpSfMYeyrgjURQb0WjZSPbe2wjNHZVjY24zzYA0FQSuvaMPSK6BRBKt_CQnQlQqNoWN-zPuy9bHuJ04_M-x6ksG0-B7wdDY3SVTVMxcTpeyedUDnvPtxccX9f8m6Hi5-yHwfBxHkqy0RkeKQ2meMdDTiO3hjwdfSH9Hrj9mQafF2Za1mjv_ETcTI6XOd_5Az1mD4IZyD85zXN2_eH9j8tP1dXXj58vt1eVRYRSWWm1a7sgXK1dcK5DrJt6Z1sVrPHWaqV2TddZDBIddChqtwttABU6ZbTxeM5ert59Tr9mT6UfI9njH5NPM_VKANZCtgv4agVtTkTZh35JNJp86AX0x-z9KftCPjsp593o3T_c2nkBXqzALZWU_-N5vmLBpN7c5Ej99XcJAkFqiRpq_AuTBpMo</recordid><startdate>2000</startdate><enddate>2000</enddate><creator>Lee, M.D</creator><creator>Burch, F.T</creator><creator>Maurer, J.J</creator><creator>Henk, A</creator><creator>Thayer, S</creator><general>American Association of Avian Pathologists, Inc</general><scope>FBQ</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>7X8</scope></search><sort><creationdate>2000</creationdate><title>DNA fingerprinting of plasmid-containing serotype A: 3,4 Pasteurella multocida isolated from cases of fowl cholera in chickens and turkeys</title><author>Lee, M.D ; Burch, F.T ; Maurer, J.J ; Henk, A ; Thayer, S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c330t-c2c9d68f1d49dfdd833454bc67fcaecc977b588c3f23d08314dbf6f07f87a9ae3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Animals</topic><topic>Chickens</topic><topic>Cholera</topic><topic>DNA</topic><topic>DNA fingerprinting</topic><topic>DNA Fingerprinting - veterinary</topic><topic>Electrophoresis, Polyacrylamide Gel - veterinary</topic><topic>genetic variation</topic><topic>Genomics</topic><topic>Nucleic Acid Hybridization</topic><topic>outbreaks</topic><topic>Pasteurella Infections - genetics</topic><topic>Pasteurella Infections - microbiology</topic><topic>Pasteurella Infections - veterinary</topic><topic>Pasteurella multocida</topic><topic>Pasteurella multocida - genetics</topic><topic>Pasteurella multocida - isolation & purification</topic><topic>Plasmids</topic><topic>Polymerase Chain Reaction - veterinary</topic><topic>Polymorphism, Restriction Fragment Length</topic><topic>Poultry Diseases - genetics</topic><topic>Poultry Diseases - microbiology</topic><topic>Research Notes</topic><topic>restriction fragment length polymorphism</topic><topic>Turkeys</topic><topic>Vaccination</topic><topic>Virulence</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, M.D</creatorcontrib><creatorcontrib>Burch, F.T</creatorcontrib><creatorcontrib>Maurer, J.J</creatorcontrib><creatorcontrib>Henk, A</creatorcontrib><creatorcontrib>Thayer, S</creatorcontrib><collection>AGRIS</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>Avian diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, M.D</au><au>Burch, F.T</au><au>Maurer, J.J</au><au>Henk, A</au><au>Thayer, S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>DNA fingerprinting of plasmid-containing serotype A: 3,4 Pasteurella multocida isolated from cases of fowl cholera in chickens and turkeys</atitle><jtitle>Avian diseases</jtitle><addtitle>Avian Dis</addtitle><date>2000</date><risdate>2000</risdate><volume>44</volume><issue>1</issue><spage>201</spage><epage>204</epage><pages>201-204</pages><issn>0005-2086</issn><eissn>1938-4351</eissn><abstract>The live, attenuated vaccine strains of Pasteurella multocida have been hypothesized to be responsible for homologous serotype outbreaks of fowl cholera on farms that use the commercial vaccines. We have further hypothesized that the naturally occurring Clemson University (CU) vaccine strain may be transformed to virulence by the acquisition of plasmid DNA. To test this hypothesis, we obtained seven homologous serotype (A:3,4) P. multocida isolates, all plasmid bearing, that were cultured from fowl cholera cases in vaccinated flocks and compared the isolates with the CU reference vaccine by molecular methods. Restriction fragment length polymorphisms (RFLPs) were detected by DNA/DNA hybridization with labeled probes specific for the cya, aroA, and rrn genes of P. multocida. The RFLPs obtained from BglII-digested genomic DNA probed with cya demonstrated no differences among the isolates. Although three isolates probed with aroA showed a RFLP identical to the vaccine strain, five isolates were distinctly difference. Isolates probed with rrn grouped into three different restriction patterns that were dissimilar from that of the vaccine strain. Therefore, we have shown that these fowl cholera isolates are different from the CU vaccine strain and that these outbreaks were not vaccine related.</abstract><cop>United States</cop><pub>American Association of Avian Pathologists, Inc</pub><pmid>10737663</pmid><doi>10.2307/1592526</doi><tpages>4</tpages></addata></record> |
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subjects | Animals Chickens Cholera DNA DNA fingerprinting DNA Fingerprinting - veterinary Electrophoresis, Polyacrylamide Gel - veterinary genetic variation Genomics Nucleic Acid Hybridization outbreaks Pasteurella Infections - genetics Pasteurella Infections - microbiology Pasteurella Infections - veterinary Pasteurella multocida Pasteurella multocida - genetics Pasteurella multocida - isolation & purification Plasmids Polymerase Chain Reaction - veterinary Polymorphism, Restriction Fragment Length Poultry Diseases - genetics Poultry Diseases - microbiology Research Notes restriction fragment length polymorphism Turkeys Vaccination Virulence |
title | DNA fingerprinting of plasmid-containing serotype A: 3,4 Pasteurella multocida isolated from cases of fowl cholera in chickens and turkeys |
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