Molecular Characterization of Mycoplasma gallisepticum Isolates from Jordan
Two groups of Mycoplasma gallisepticum (MG) isolates (n = 24) from Jordan were analyzed by molecular methods and compared with other Middle Eastern isolates, related international isolates, and reference strains. The first group (n = 19) was isolated from July 2004 to January 2005 (isolation per...
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description | Two groups of Mycoplasma gallisepticum (MG) isolates (n = 24) from Jordan were analyzed by molecular methods and compared with other Middle Eastern isolates, related international isolates, and reference strains. The first group (n = 19) was isolated from July 2004 to January 2005 (isolation period A), and the newer group (n = 5) from June 2007 to April 2008 (isolation period B). The groups of isolates are from chicken flocks from northern Jordan, but are not from the same farms. None of the flocks were vaccinated for MG. Random amplified polymorphic DNA analysis, targeted sequencing of the partial MG cytadhesin 2 (mgc2), and the MG 16S–23S rRNA intergenic spacer region (IGSR) divided the Jordanian isolates into two groups. All of the 19 isolates from time period A, in addition to two isolates from time period B, were indistinguishable from the F strain. Three of five isolates from time period B were characterized as wild types and were indistinguishable from each other. The wild-type field strain was readily distinguished from the F strain. It was 91% and 96.4% similar to the F strain based on Clustal-W alignments of sequences of mgc2 and IGSR, respectively. Sequence similarity of mgc2 gene of the Jordan wild-type strain to isolates from Israel and Egypt ranged from 96.5% to 100%, whereas for IGSR it was 99.4%–100%. We theorize that the F-strain live MG vaccine, commonly used in Jordan prior to 2007, was transmitted to nonvaccinated poultry in the region and was a predominant genotype during time period A. |
doi_str_mv | 10.1637/9526-091510-Reg.1 |
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The first group (n = 19) was isolated from July 2004 to January 2005 (isolation period A), and the newer group (n = 5) from June 2007 to April 2008 (isolation period B). The groups of isolates are from chicken flocks from northern Jordan, but are not from the same farms. None of the flocks were vaccinated for MG. Random amplified polymorphic DNA analysis, targeted sequencing of the partial MG cytadhesin 2 (mgc2), and the MG 16S–23S rRNA intergenic spacer region (IGSR) divided the Jordanian isolates into two groups. All of the 19 isolates from time period A, in addition to two isolates from time period B, were indistinguishable from the F strain. Three of five isolates from time period B were characterized as wild types and were indistinguishable from each other. The wild-type field strain was readily distinguished from the F strain. It was 91% and 96.4% similar to the F strain based on Clustal-W alignments of sequences of mgc2 and IGSR, respectively. Sequence similarity of mgc2 gene of the Jordan wild-type strain to isolates from Israel and Egypt ranged from 96.5% to 100%, whereas for IGSR it was 99.4%–100%. We theorize that the F-strain live MG vaccine, commonly used in Jordan prior to 2007, was transmitted to nonvaccinated poultry in the region and was a predominant genotype during time period A.</description><identifier>ISSN: 0005-2086</identifier><identifier>EISSN: 1938-4351</identifier><identifier>DOI: 10.1637/9526-091510-Reg.1</identifier><identifier>PMID: 21793435</identifier><language>eng</language><publisher>953 College Station Road, Athens, GA 30602-4875: American Association of Avian Pathologists</publisher><subject>Animal diseases ; Animals ; Chickens ; Flocks ; Genetic polymorphism ; IGSR ; Infections ; Intergenic DNA ; Jordan ; Jordan - epidemiology ; MG ; mgc2 ; Middle East ; Mycoplasma gallisepticum ; Mycoplasma gallisepticum - genetics ; Mycoplasma Infections - epidemiology ; Mycoplasma Infections - microbiology ; Mycoplasma Infections - veterinary ; Phylogeny ; Polymerase chain reaction ; Poultry Diseases - epidemiology ; Poultry Diseases - microbiology ; RAPD ; Regular s ; Sequencing ; Vaccination</subject><ispartof>Avian diseases, 2011-06, Vol.55 (2), p.212-216</ispartof><rights>American Association of Avian Pathologists</rights><rights>Copyright 2011 American Association of Avian Pathologists, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b394t-2607e93bb3e6f699796ae81c05896962b23c83380cb825b690df2fcb298af7c73</citedby><cites>FETCH-LOGICAL-b394t-2607e93bb3e6f699796ae81c05896962b23c83380cb825b690df2fcb298af7c73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://bioone.org/doi/pdf/10.1637/9526-091510-Reg.1$$EPDF$$P50$$Gbioone$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/41319323$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,780,784,803,26977,27923,27924,52362,58016,58249</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21793435$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gharaibeh, Saad</creatorcontrib><creatorcontrib>Laibinis, Victoria</creatorcontrib><creatorcontrib>Wooten, Ruth</creatorcontrib><creatorcontrib>Stabler, Lisa</creatorcontrib><creatorcontrib>Ferguson-Noel, Naola</creatorcontrib><title>Molecular Characterization of Mycoplasma gallisepticum Isolates from Jordan</title><title>Avian diseases</title><addtitle>Avian Dis</addtitle><description>Two groups of Mycoplasma gallisepticum (MG) isolates (n = 24) from Jordan were analyzed by molecular methods and compared with other Middle Eastern isolates, related international isolates, and reference strains. The first group (n = 19) was isolated from July 2004 to January 2005 (isolation period A), and the newer group (n = 5) from June 2007 to April 2008 (isolation period B). The groups of isolates are from chicken flocks from northern Jordan, but are not from the same farms. None of the flocks were vaccinated for MG. Random amplified polymorphic DNA analysis, targeted sequencing of the partial MG cytadhesin 2 (mgc2), and the MG 16S–23S rRNA intergenic spacer region (IGSR) divided the Jordanian isolates into two groups. All of the 19 isolates from time period A, in addition to two isolates from time period B, were indistinguishable from the F strain. Three of five isolates from time period B were characterized as wild types and were indistinguishable from each other. The wild-type field strain was readily distinguished from the F strain. It was 91% and 96.4% similar to the F strain based on Clustal-W alignments of sequences of mgc2 and IGSR, respectively. Sequence similarity of mgc2 gene of the Jordan wild-type strain to isolates from Israel and Egypt ranged from 96.5% to 100%, whereas for IGSR it was 99.4%–100%. We theorize that the F-strain live MG vaccine, commonly used in Jordan prior to 2007, was transmitted to nonvaccinated poultry in the region and was a predominant genotype during time period A.</description><subject>Animal diseases</subject><subject>Animals</subject><subject>Chickens</subject><subject>Flocks</subject><subject>Genetic polymorphism</subject><subject>IGSR</subject><subject>Infections</subject><subject>Intergenic DNA</subject><subject>Jordan</subject><subject>Jordan - epidemiology</subject><subject>MG</subject><subject>mgc2</subject><subject>Middle East</subject><subject>Mycoplasma gallisepticum</subject><subject>Mycoplasma gallisepticum - genetics</subject><subject>Mycoplasma Infections - epidemiology</subject><subject>Mycoplasma Infections - microbiology</subject><subject>Mycoplasma Infections - veterinary</subject><subject>Phylogeny</subject><subject>Polymerase chain reaction</subject><subject>Poultry Diseases - epidemiology</subject><subject>Poultry Diseases - microbiology</subject><subject>RAPD</subject><subject>Regular s</subject><subject>Sequencing</subject><subject>Vaccination</subject><issn>0005-2086</issn><issn>1938-4351</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU1PwyAYx4nR6Jx-AA-a3jx1e4CWwtEsvm8xMXomwOisoWNCe5ifXpZOz54ekv_veckPhC4wTDCj1VSUhOUgcIkhf7WrCT5AIywozwta4kM0AoAyJ8DZCTqN8RMAV4LBMToh6UETNELPC--s6Z0K2exDBWU6G5pv1TV-nfk6W2yN3zgVW5WtlHNNtJuuMX2bPUbvVGdjVgffZk8-LNX6DB3VykV7vq9j9H53-zZ7yOcv94-zm3muqSi6nDCorKBaU8tqJkS6SVmODZRcMMGIJtRwSjkYzUmpmYBlTWqjieCqrkxFx-h6mLsJ_qu3sZNtE411Tq2t76PkQuCCFewfJAdMeUEhkXggTfAxBlvLTWhaFbYSg9zJljvZcpAtk2yJU8_VfnqvW7v86_i1m4DLAfiMnQ9_eYFp-iVCUz4dct14v7b_WPkDrAaSrg</recordid><startdate>201106</startdate><enddate>201106</enddate><creator>Gharaibeh, Saad</creator><creator>Laibinis, Victoria</creator><creator>Wooten, Ruth</creator><creator>Stabler, Lisa</creator><creator>Ferguson-Noel, Naola</creator><general>American Association of Avian Pathologists</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><scope>7QL</scope><scope>7U9</scope><scope>C1K</scope><scope>H94</scope></search><sort><creationdate>201106</creationdate><title>Molecular Characterization of Mycoplasma gallisepticum Isolates from Jordan</title><author>Gharaibeh, Saad ; Laibinis, Victoria ; Wooten, Ruth ; Stabler, Lisa ; Ferguson-Noel, Naola</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b394t-2607e93bb3e6f699796ae81c05896962b23c83380cb825b690df2fcb298af7c73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Animal diseases</topic><topic>Animals</topic><topic>Chickens</topic><topic>Flocks</topic><topic>Genetic polymorphism</topic><topic>IGSR</topic><topic>Infections</topic><topic>Intergenic DNA</topic><topic>Jordan</topic><topic>Jordan - epidemiology</topic><topic>MG</topic><topic>mgc2</topic><topic>Middle East</topic><topic>Mycoplasma gallisepticum</topic><topic>Mycoplasma gallisepticum - genetics</topic><topic>Mycoplasma Infections - epidemiology</topic><topic>Mycoplasma Infections - microbiology</topic><topic>Mycoplasma Infections - veterinary</topic><topic>Phylogeny</topic><topic>Polymerase chain reaction</topic><topic>Poultry Diseases - epidemiology</topic><topic>Poultry Diseases - microbiology</topic><topic>RAPD</topic><topic>Regular s</topic><topic>Sequencing</topic><topic>Vaccination</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gharaibeh, Saad</creatorcontrib><creatorcontrib>Laibinis, Victoria</creatorcontrib><creatorcontrib>Wooten, Ruth</creatorcontrib><creatorcontrib>Stabler, Lisa</creatorcontrib><creatorcontrib>Ferguson-Noel, Naola</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><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Virology and AIDS Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Avian diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gharaibeh, Saad</au><au>Laibinis, Victoria</au><au>Wooten, Ruth</au><au>Stabler, Lisa</au><au>Ferguson-Noel, Naola</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular Characterization of Mycoplasma gallisepticum Isolates from Jordan</atitle><jtitle>Avian diseases</jtitle><addtitle>Avian Dis</addtitle><date>2011-06</date><risdate>2011</risdate><volume>55</volume><issue>2</issue><spage>212</spage><epage>216</epage><pages>212-216</pages><issn>0005-2086</issn><eissn>1938-4351</eissn><abstract>Two groups of Mycoplasma gallisepticum (MG) isolates (n = 24) from Jordan were analyzed by molecular methods and compared with other Middle Eastern isolates, related international isolates, and reference strains. The first group (n = 19) was isolated from July 2004 to January 2005 (isolation period A), and the newer group (n = 5) from June 2007 to April 2008 (isolation period B). The groups of isolates are from chicken flocks from northern Jordan, but are not from the same farms. None of the flocks were vaccinated for MG. Random amplified polymorphic DNA analysis, targeted sequencing of the partial MG cytadhesin 2 (mgc2), and the MG 16S–23S rRNA intergenic spacer region (IGSR) divided the Jordanian isolates into two groups. All of the 19 isolates from time period A, in addition to two isolates from time period B, were indistinguishable from the F strain. Three of five isolates from time period B were characterized as wild types and were indistinguishable from each other. The wild-type field strain was readily distinguished from the F strain. It was 91% and 96.4% similar to the F strain based on Clustal-W alignments of sequences of mgc2 and IGSR, respectively. Sequence similarity of mgc2 gene of the Jordan wild-type strain to isolates from Israel and Egypt ranged from 96.5% to 100%, whereas for IGSR it was 99.4%–100%. We theorize that the F-strain live MG vaccine, commonly used in Jordan prior to 2007, was transmitted to nonvaccinated poultry in the region and was a predominant genotype during time period A.</abstract><cop>953 College Station Road, Athens, GA 30602-4875</cop><pub>American Association of Avian Pathologists</pub><pmid>21793435</pmid><doi>10.1637/9526-091510-Reg.1</doi><tpages>5</tpages></addata></record> |
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subjects | Animal diseases Animals Chickens Flocks Genetic polymorphism IGSR Infections Intergenic DNA Jordan Jordan - epidemiology MG mgc2 Middle East Mycoplasma gallisepticum Mycoplasma gallisepticum - genetics Mycoplasma Infections - epidemiology Mycoplasma Infections - microbiology Mycoplasma Infections - veterinary Phylogeny Polymerase chain reaction Poultry Diseases - epidemiology Poultry Diseases - microbiology RAPD Regular s Sequencing Vaccination |
title | Molecular Characterization of Mycoplasma gallisepticum Isolates from Jordan |
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