Transcriptional analysis of the major antigenic protein 1 multigene family of Cowdria ruminantium
The major antigenic protein 1 (MAP1) of the tick-borne rickettsial pathogen Cowdria ruminantium is encoded by a multigene family containing conserved and variable genes. The part of a locus containing the map1 multigene family that was characterized contained three homologous, but non-identical map1...
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creator | Bekker, Cornelis P.J Bell-Sakyi, Lesley Paxton, Edith A Martinez, Dominique Bensaid, Albert Jongejan, Frans |
description | The major antigenic protein 1 (MAP1) of the tick-borne rickettsial pathogen
Cowdria ruminantium is encoded by a multigene family containing conserved and variable genes. The part of a locus containing the
map1 multigene family that was characterized contained three homologous, but non-identical
map1 genes, designated
map1-2,
map1-1, and
map1. Reverse transcriptase-polymerase chain reaction was used to study the transcriptional activity of these genes in isolates of
C. ruminantium grown in bovine endothelial cells, in two different tick cell lines, and in
Amblyomma
variegatum ticks. The
map1 gene was always transcribed, whereas transcription of
map1-2 was not detected under any of the tested conditions. The
map1-1 gene transcript was detected in
A. variegatum ticks, but was not found in virulent
C. ruminantium Senegal grown in bovine endothelial cells at 30 or 37°C. Interestingly, transcripts of
map1-1 were also found in different passages of the in vitro attenuated Senegal isolate grown in bovine endothelial cells, as well as in the Gardel isolate grown in two tick cell lines. When transcribed,
map1-1 was present on a polycistronic messenger together with
map1. |
doi_str_mv | 10.1016/S0378-1119(02)00408-0 |
format | Article |
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Cowdria ruminantium is encoded by a multigene family containing conserved and variable genes. The part of a locus containing the
map1 multigene family that was characterized contained three homologous, but non-identical
map1 genes, designated
map1-2,
map1-1, and
map1. Reverse transcriptase-polymerase chain reaction was used to study the transcriptional activity of these genes in isolates of
C. ruminantium grown in bovine endothelial cells, in two different tick cell lines, and in
Amblyomma
variegatum ticks. The
map1 gene was always transcribed, whereas transcription of
map1-2 was not detected under any of the tested conditions. The
map1-1 gene transcript was detected in
A. variegatum ticks, but was not found in virulent
C. ruminantium Senegal grown in bovine endothelial cells at 30 or 37°C. Interestingly, transcripts of
map1-1 were also found in different passages of the in vitro attenuated Senegal isolate grown in bovine endothelial cells, as well as in the Gardel isolate grown in two tick cell lines. When transcribed,
map1-1 was present on a polycistronic messenger together with
map1.</description><identifier>ISSN: 0378-1119</identifier><identifier>EISSN: 1879-0038</identifier><identifier>DOI: 10.1016/S0378-1119(02)00408-0</identifier><identifier>PMID: 12039046</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Amblyomma variegatum ; Amino Acid Sequence ; Animals ; Antigens, Bacterial ; Bacterial Outer Membrane Proteins - genetics ; Cattle ; Cell Line ; Cells, Cultured ; Cloning, Molecular ; Cowdria ruminantium ; Differential transcription ; DNA, Bacterial - chemistry ; DNA, Bacterial - genetics ; Ehrlichia ruminantium - genetics ; Endothelium, Vascular - cytology ; Endothelium, Vascular - microbiology ; major antigenic protein 1 ; Molecular Sequence Data ; Multigene Family - genetics ; RNA, Bacterial - genetics ; RNA, Bacterial - metabolism ; Sequence Alignment ; Sequence Analysis, DNA ; Sequence Homology, Amino Acid ; Tick cell lines ; Ticks ; Ticks - cytology ; Ticks - microbiology ; Transcription, Genetic</subject><ispartof>Gene, 2002-02, Vol.285 (1), p.193-201</ispartof><rights>2002</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c425t-5129b0affc1250f23e104f5fc0f5ea434e4495215bd0554b649ddcacf9fd59663</citedby><cites>FETCH-LOGICAL-c425t-5129b0affc1250f23e104f5fc0f5ea434e4495215bd0554b649ddcacf9fd59663</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0378-1119(02)00408-0$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12039046$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bekker, Cornelis P.J</creatorcontrib><creatorcontrib>Bell-Sakyi, Lesley</creatorcontrib><creatorcontrib>Paxton, Edith A</creatorcontrib><creatorcontrib>Martinez, Dominique</creatorcontrib><creatorcontrib>Bensaid, Albert</creatorcontrib><creatorcontrib>Jongejan, Frans</creatorcontrib><title>Transcriptional analysis of the major antigenic protein 1 multigene family of Cowdria ruminantium</title><title>Gene</title><addtitle>Gene</addtitle><description>The major antigenic protein 1 (MAP1) of the tick-borne rickettsial pathogen
Cowdria ruminantium is encoded by a multigene family containing conserved and variable genes. The part of a locus containing the
map1 multigene family that was characterized contained three homologous, but non-identical
map1 genes, designated
map1-2,
map1-1, and
map1. Reverse transcriptase-polymerase chain reaction was used to study the transcriptional activity of these genes in isolates of
C. ruminantium grown in bovine endothelial cells, in two different tick cell lines, and in
Amblyomma
variegatum ticks. The
map1 gene was always transcribed, whereas transcription of
map1-2 was not detected under any of the tested conditions. The
map1-1 gene transcript was detected in
A. variegatum ticks, but was not found in virulent
C. ruminantium Senegal grown in bovine endothelial cells at 30 or 37°C. Interestingly, transcripts of
map1-1 were also found in different passages of the in vitro attenuated Senegal isolate grown in bovine endothelial cells, as well as in the Gardel isolate grown in two tick cell lines. When transcribed,
map1-1 was present on a polycistronic messenger together with
map1.</description><subject>Amblyomma variegatum</subject><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Antigens, Bacterial</subject><subject>Bacterial Outer Membrane Proteins - genetics</subject><subject>Cattle</subject><subject>Cell Line</subject><subject>Cells, Cultured</subject><subject>Cloning, Molecular</subject><subject>Cowdria ruminantium</subject><subject>Differential transcription</subject><subject>DNA, Bacterial - chemistry</subject><subject>DNA, Bacterial - genetics</subject><subject>Ehrlichia ruminantium - genetics</subject><subject>Endothelium, Vascular - cytology</subject><subject>Endothelium, Vascular - microbiology</subject><subject>major antigenic protein 1</subject><subject>Molecular Sequence Data</subject><subject>Multigene Family - genetics</subject><subject>RNA, Bacterial - genetics</subject><subject>RNA, Bacterial - metabolism</subject><subject>Sequence Alignment</subject><subject>Sequence Analysis, DNA</subject><subject>Sequence Homology, Amino Acid</subject><subject>Tick cell lines</subject><subject>Ticks</subject><subject>Ticks - cytology</subject><subject>Ticks - microbiology</subject><subject>Transcription, Genetic</subject><issn>0378-1119</issn><issn>1879-0038</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkctOwzAQRS0EouXxCSCvECwCY8dO4hVCFS8JiQVlbbnOGIzyKHYC6t-TtBUs8cKWRufOjO8l5ITBJQOWXb1AmhcJY0ydA78AEFAksEOmrMhVApAWu2T6i0zIQYwfMBwp-T6ZMA6pApFNiZkH00Qb_LLzbWMqaoZrFX2kraPdO9LafLRhqHb-DRtv6TK0HfqGMlr31bqI1JnaV6tRMWu_y-ANDX3tm1HU10dkz5kq4vH2PSSvd7fz2UPy9Hz_OLt5Sqzgsksk42oBxjnLuATHU2QgnHQWnEQjUoFCKMmZXJTDJ8QiE6osrbFOuVKqLEsPydmm77DhZ4-x07WPFqvKNNj2UecszwuQ6b8gK1Lgqhg7yg1oQxtjQKeXwdcmrDQDPYag1yHo0WENXK9D0DDoTrcD-kWN5Z9q6_oAXG8AHPz48hh0tB4bi6UPaDtdtv6fET_dnZeP</recordid><startdate>20020220</startdate><enddate>20020220</enddate><creator>Bekker, Cornelis P.J</creator><creator>Bell-Sakyi, Lesley</creator><creator>Paxton, Edith A</creator><creator>Martinez, Dominique</creator><creator>Bensaid, Albert</creator><creator>Jongejan, Frans</creator><general>Elsevier B.V</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>7QL</scope><scope>7TM</scope><scope>C1K</scope><scope>7X8</scope></search><sort><creationdate>20020220</creationdate><title>Transcriptional analysis of the major antigenic protein 1 multigene family of Cowdria ruminantium</title><author>Bekker, Cornelis P.J ; Bell-Sakyi, Lesley ; Paxton, Edith A ; Martinez, Dominique ; Bensaid, Albert ; Jongejan, Frans</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c425t-5129b0affc1250f23e104f5fc0f5ea434e4495215bd0554b649ddcacf9fd59663</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Amblyomma variegatum</topic><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Antigens, Bacterial</topic><topic>Bacterial Outer Membrane Proteins - genetics</topic><topic>Cattle</topic><topic>Cell Line</topic><topic>Cells, Cultured</topic><topic>Cloning, Molecular</topic><topic>Cowdria ruminantium</topic><topic>Differential transcription</topic><topic>DNA, Bacterial - chemistry</topic><topic>DNA, Bacterial - genetics</topic><topic>Ehrlichia ruminantium - genetics</topic><topic>Endothelium, Vascular - cytology</topic><topic>Endothelium, Vascular - microbiology</topic><topic>major antigenic protein 1</topic><topic>Molecular Sequence Data</topic><topic>Multigene Family - genetics</topic><topic>RNA, Bacterial - genetics</topic><topic>RNA, Bacterial - metabolism</topic><topic>Sequence Alignment</topic><topic>Sequence Analysis, DNA</topic><topic>Sequence Homology, Amino Acid</topic><topic>Tick cell lines</topic><topic>Ticks</topic><topic>Ticks - cytology</topic><topic>Ticks - microbiology</topic><topic>Transcription, Genetic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bekker, Cornelis P.J</creatorcontrib><creatorcontrib>Bell-Sakyi, Lesley</creatorcontrib><creatorcontrib>Paxton, Edith A</creatorcontrib><creatorcontrib>Martinez, Dominique</creatorcontrib><creatorcontrib>Bensaid, Albert</creatorcontrib><creatorcontrib>Jongejan, Frans</creatorcontrib><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>Nucleic Acids Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><jtitle>Gene</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bekker, Cornelis P.J</au><au>Bell-Sakyi, Lesley</au><au>Paxton, Edith A</au><au>Martinez, Dominique</au><au>Bensaid, Albert</au><au>Jongejan, Frans</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Transcriptional analysis of the major antigenic protein 1 multigene family of Cowdria ruminantium</atitle><jtitle>Gene</jtitle><addtitle>Gene</addtitle><date>2002-02-20</date><risdate>2002</risdate><volume>285</volume><issue>1</issue><spage>193</spage><epage>201</epage><pages>193-201</pages><issn>0378-1119</issn><eissn>1879-0038</eissn><abstract>The major antigenic protein 1 (MAP1) of the tick-borne rickettsial pathogen
Cowdria ruminantium is encoded by a multigene family containing conserved and variable genes. The part of a locus containing the
map1 multigene family that was characterized contained three homologous, but non-identical
map1 genes, designated
map1-2,
map1-1, and
map1. Reverse transcriptase-polymerase chain reaction was used to study the transcriptional activity of these genes in isolates of
C. ruminantium grown in bovine endothelial cells, in two different tick cell lines, and in
Amblyomma
variegatum ticks. The
map1 gene was always transcribed, whereas transcription of
map1-2 was not detected under any of the tested conditions. The
map1-1 gene transcript was detected in
A. variegatum ticks, but was not found in virulent
C. ruminantium Senegal grown in bovine endothelial cells at 30 or 37°C. Interestingly, transcripts of
map1-1 were also found in different passages of the in vitro attenuated Senegal isolate grown in bovine endothelial cells, as well as in the Gardel isolate grown in two tick cell lines. When transcribed,
map1-1 was present on a polycistronic messenger together with
map1.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>12039046</pmid><doi>10.1016/S0378-1119(02)00408-0</doi><tpages>9</tpages></addata></record> |
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subjects | Amblyomma variegatum Amino Acid Sequence Animals Antigens, Bacterial Bacterial Outer Membrane Proteins - genetics Cattle Cell Line Cells, Cultured Cloning, Molecular Cowdria ruminantium Differential transcription DNA, Bacterial - chemistry DNA, Bacterial - genetics Ehrlichia ruminantium - genetics Endothelium, Vascular - cytology Endothelium, Vascular - microbiology major antigenic protein 1 Molecular Sequence Data Multigene Family - genetics RNA, Bacterial - genetics RNA, Bacterial - metabolism Sequence Alignment Sequence Analysis, DNA Sequence Homology, Amino Acid Tick cell lines Ticks Ticks - cytology Ticks - microbiology Transcription, Genetic |
title | Transcriptional analysis of the major antigenic protein 1 multigene family of Cowdria ruminantium |
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