Loading…
The gene for toxic shock toxin is carried by a family of mobile pathogenicity islands in Staphylococcus aureus
Tst, the gene for toxic shock syndrome toxin‐1 (TSST‐1), is part of a 15.2 kb genetic element in Staphylococcus aureus that is absent in TSST‐1‐negative strains. The prototype, in RN4282, is flanked by a 17 nucleotide direct repeat and contains genes for a second possible superantigen toxin, a Diche...
Saved in:
Published in: | Molecular microbiology 1998-07, Vol.29 (2), p.527-543 |
---|---|
Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c5377-8bd2175174754676ac861721ca9013265a11df6db88abc5a763f4a6670445db13 |
---|---|
cites | cdi_FETCH-LOGICAL-c5377-8bd2175174754676ac861721ca9013265a11df6db88abc5a763f4a6670445db13 |
container_end_page | 543 |
container_issue | 2 |
container_start_page | 527 |
container_title | Molecular microbiology |
container_volume | 29 |
creator | Lindsay, Jodi A. Ruzin, Alexey Ross, Hope F. Kurepina, Natasha Novick, Richard P. |
description | Tst, the gene for toxic shock syndrome toxin‐1 (TSST‐1), is part of a 15.2 kb genetic element in Staphylococcus aureus that is absent in TSST‐1‐negative strains. The prototype, in RN4282, is flanked by a 17 nucleotide direct repeat and contains genes for a second possible superantigen toxin, a Dichelobacter nodosus VapE homologue and a putative integrase. It is readily transferred to a recA− recipient, and it always inserts into a unique chromosomal copy of the 17 nucleotide sequence in the same orientation. It is excised and circularized by staphylococcal phages φ13 and 80α and replicates during the growth of the latter, which transduces it at very high frequency. Because of its site and orientation specificity and because it lacks other identifiable phage‐like genes, we consider it to be a pathogenicity island (PI) rather than a transposon or a defective phage. The tst element in RN4282, near tyrB, is designated SaPI1. That in RN3984 in the trp region is only partially homologous to SaPI1 and is excised by phage 80 but not by 80α. It is designated SaPI2. These PIs are the first in any Gram‐positive species and the first for which mobility has been demonstrated. Their mobility may be responsible for the spread of TSST‐1 production among S. aureus strains. |
doi_str_mv | 10.1046/j.1365-2958.1998.00947.x |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_16489153</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>32661215</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5377-8bd2175174754676ac861721ca9013265a11df6db88abc5a763f4a6670445db13</originalsourceid><addsrcrecordid>eNqNUctO4zAUtRAIOh0-YSSLBbsEO45fEpsRAgapaBYUaXaW4zhTlyTu2Ilo_h6XVl2wmtW90nno3nMAgBjlGJXsZp1jwmhWSCpyLKXIEZIlz7cnYHYETsEMSYoyIoo_F-BbjGuEMEGMnINzyQskOJqBfrmy8K_tLWx8gIPfOgPjypu3z72HLkKjQ3C2htUENWx059oJ-gZ2vnKthRs9rHwycMYNU6K3uq8jTMqXQW9WU-uNN2aMUI_BjvE7OGt0G-3lYc7B68P98u5Xtvj9-HT3c5EZSjjPRFUXmFPMS05Lxpk2gmFeYKNleqFgVGNcN6yuhNCVoZoz0pSaMY7KktYVJnNwvffdBP9vtHFQnYvGtuk668eoMCuFxJQk4tUX4tqPoU-3KSwZTWEylkhiTzLBxxhsozbBdTpMCiO160Ot1S52tYtd7fpQn32obZL-OPiPVWfro_BQQMJv9_h7CnP6b1_1_PyUFvIBPZ6Y8Q</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>196513666</pqid></control><display><type>article</type><title>The gene for toxic shock toxin is carried by a family of mobile pathogenicity islands in Staphylococcus aureus</title><source>Wiley-Blackwell Read & Publish Collection</source><creator>Lindsay, Jodi A. ; Ruzin, Alexey ; Ross, Hope F. ; Kurepina, Natasha ; Novick, Richard P.</creator><creatorcontrib>Lindsay, Jodi A. ; Ruzin, Alexey ; Ross, Hope F. ; Kurepina, Natasha ; Novick, Richard P.</creatorcontrib><description>Tst, the gene for toxic shock syndrome toxin‐1 (TSST‐1), is part of a 15.2 kb genetic element in Staphylococcus aureus that is absent in TSST‐1‐negative strains. The prototype, in RN4282, is flanked by a 17 nucleotide direct repeat and contains genes for a second possible superantigen toxin, a Dichelobacter nodosus VapE homologue and a putative integrase. It is readily transferred to a recA− recipient, and it always inserts into a unique chromosomal copy of the 17 nucleotide sequence in the same orientation. It is excised and circularized by staphylococcal phages φ13 and 80α and replicates during the growth of the latter, which transduces it at very high frequency. Because of its site and orientation specificity and because it lacks other identifiable phage‐like genes, we consider it to be a pathogenicity island (PI) rather than a transposon or a defective phage. The tst element in RN4282, near tyrB, is designated SaPI1. That in RN3984 in the trp region is only partially homologous to SaPI1 and is excised by phage 80 but not by 80α. It is designated SaPI2. These PIs are the first in any Gram‐positive species and the first for which mobility has been demonstrated. Their mobility may be responsible for the spread of TSST‐1 production among S. aureus strains.</description><identifier>ISSN: 0950-382X</identifier><identifier>EISSN: 1365-2958</identifier><identifier>DOI: 10.1046/j.1365-2958.1998.00947.x</identifier><identifier>PMID: 9720870</identifier><language>eng</language><publisher>Oxford BSL: Blackwell Science Ltd, UK</publisher><subject>Amino Acid Sequence ; Bacterial Toxins ; Base Sequence ; DNA Transposable Elements ; Enterotoxins - genetics ; Genetic Variation ; Molecular Sequence Data ; Rec A Recombinases - genetics ; Sequence Analysis, DNA ; Sequence Deletion ; Species Specificity ; Staphylococcus aureus - genetics ; Staphylococcus aureus - pathogenicity ; Staphylococcus Phages - genetics ; Superantigens ; Transduction, Genetic</subject><ispartof>Molecular microbiology, 1998-07, Vol.29 (2), p.527-543</ispartof><rights>Blackwell Science Ltd, Oxford</rights><rights>Copyright Blackwell Scientific Publications Ltd. Jul 1998</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5377-8bd2175174754676ac861721ca9013265a11df6db88abc5a763f4a6670445db13</citedby><cites>FETCH-LOGICAL-c5377-8bd2175174754676ac861721ca9013265a11df6db88abc5a763f4a6670445db13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9720870$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lindsay, Jodi A.</creatorcontrib><creatorcontrib>Ruzin, Alexey</creatorcontrib><creatorcontrib>Ross, Hope F.</creatorcontrib><creatorcontrib>Kurepina, Natasha</creatorcontrib><creatorcontrib>Novick, Richard P.</creatorcontrib><title>The gene for toxic shock toxin is carried by a family of mobile pathogenicity islands in Staphylococcus aureus</title><title>Molecular microbiology</title><addtitle>Mol Microbiol</addtitle><description>Tst, the gene for toxic shock syndrome toxin‐1 (TSST‐1), is part of a 15.2 kb genetic element in Staphylococcus aureus that is absent in TSST‐1‐negative strains. The prototype, in RN4282, is flanked by a 17 nucleotide direct repeat and contains genes for a second possible superantigen toxin, a Dichelobacter nodosus VapE homologue and a putative integrase. It is readily transferred to a recA− recipient, and it always inserts into a unique chromosomal copy of the 17 nucleotide sequence in the same orientation. It is excised and circularized by staphylococcal phages φ13 and 80α and replicates during the growth of the latter, which transduces it at very high frequency. Because of its site and orientation specificity and because it lacks other identifiable phage‐like genes, we consider it to be a pathogenicity island (PI) rather than a transposon or a defective phage. The tst element in RN4282, near tyrB, is designated SaPI1. That in RN3984 in the trp region is only partially homologous to SaPI1 and is excised by phage 80 but not by 80α. It is designated SaPI2. These PIs are the first in any Gram‐positive species and the first for which mobility has been demonstrated. Their mobility may be responsible for the spread of TSST‐1 production among S. aureus strains.</description><subject>Amino Acid Sequence</subject><subject>Bacterial Toxins</subject><subject>Base Sequence</subject><subject>DNA Transposable Elements</subject><subject>Enterotoxins - genetics</subject><subject>Genetic Variation</subject><subject>Molecular Sequence Data</subject><subject>Rec A Recombinases - genetics</subject><subject>Sequence Analysis, DNA</subject><subject>Sequence Deletion</subject><subject>Species Specificity</subject><subject>Staphylococcus aureus - genetics</subject><subject>Staphylococcus aureus - pathogenicity</subject><subject>Staphylococcus Phages - genetics</subject><subject>Superantigens</subject><subject>Transduction, Genetic</subject><issn>0950-382X</issn><issn>1365-2958</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNqNUctO4zAUtRAIOh0-YSSLBbsEO45fEpsRAgapaBYUaXaW4zhTlyTu2Ilo_h6XVl2wmtW90nno3nMAgBjlGJXsZp1jwmhWSCpyLKXIEZIlz7cnYHYETsEMSYoyIoo_F-BbjGuEMEGMnINzyQskOJqBfrmy8K_tLWx8gIPfOgPjypu3z72HLkKjQ3C2htUENWx059oJ-gZ2vnKthRs9rHwycMYNU6K3uq8jTMqXQW9WU-uNN2aMUI_BjvE7OGt0G-3lYc7B68P98u5Xtvj9-HT3c5EZSjjPRFUXmFPMS05Lxpk2gmFeYKNleqFgVGNcN6yuhNCVoZoz0pSaMY7KktYVJnNwvffdBP9vtHFQnYvGtuk668eoMCuFxJQk4tUX4tqPoU-3KSwZTWEylkhiTzLBxxhsozbBdTpMCiO160Ot1S52tYtd7fpQn32obZL-OPiPVWfro_BQQMJv9_h7CnP6b1_1_PyUFvIBPZ6Y8Q</recordid><startdate>199807</startdate><enddate>199807</enddate><creator>Lindsay, Jodi A.</creator><creator>Ruzin, Alexey</creator><creator>Ross, Hope F.</creator><creator>Kurepina, Natasha</creator><creator>Novick, Richard P.</creator><general>Blackwell Science Ltd, UK</general><general>Blackwell Publishing Ltd</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>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>199807</creationdate><title>The gene for toxic shock toxin is carried by a family of mobile pathogenicity islands in Staphylococcus aureus</title><author>Lindsay, Jodi A. ; Ruzin, Alexey ; Ross, Hope F. ; Kurepina, Natasha ; Novick, Richard P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5377-8bd2175174754676ac861721ca9013265a11df6db88abc5a763f4a6670445db13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Amino Acid Sequence</topic><topic>Bacterial Toxins</topic><topic>Base Sequence</topic><topic>DNA Transposable Elements</topic><topic>Enterotoxins - genetics</topic><topic>Genetic Variation</topic><topic>Molecular Sequence Data</topic><topic>Rec A Recombinases - genetics</topic><topic>Sequence Analysis, DNA</topic><topic>Sequence Deletion</topic><topic>Species Specificity</topic><topic>Staphylococcus aureus - genetics</topic><topic>Staphylococcus aureus - pathogenicity</topic><topic>Staphylococcus Phages - genetics</topic><topic>Superantigens</topic><topic>Transduction, Genetic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lindsay, Jodi A.</creatorcontrib><creatorcontrib>Ruzin, Alexey</creatorcontrib><creatorcontrib>Ross, Hope F.</creatorcontrib><creatorcontrib>Kurepina, Natasha</creatorcontrib><creatorcontrib>Novick, Richard P.</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>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Molecular microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lindsay, Jodi A.</au><au>Ruzin, Alexey</au><au>Ross, Hope F.</au><au>Kurepina, Natasha</au><au>Novick, Richard P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The gene for toxic shock toxin is carried by a family of mobile pathogenicity islands in Staphylococcus aureus</atitle><jtitle>Molecular microbiology</jtitle><addtitle>Mol Microbiol</addtitle><date>1998-07</date><risdate>1998</risdate><volume>29</volume><issue>2</issue><spage>527</spage><epage>543</epage><pages>527-543</pages><issn>0950-382X</issn><eissn>1365-2958</eissn><abstract>Tst, the gene for toxic shock syndrome toxin‐1 (TSST‐1), is part of a 15.2 kb genetic element in Staphylococcus aureus that is absent in TSST‐1‐negative strains. The prototype, in RN4282, is flanked by a 17 nucleotide direct repeat and contains genes for a second possible superantigen toxin, a Dichelobacter nodosus VapE homologue and a putative integrase. It is readily transferred to a recA− recipient, and it always inserts into a unique chromosomal copy of the 17 nucleotide sequence in the same orientation. It is excised and circularized by staphylococcal phages φ13 and 80α and replicates during the growth of the latter, which transduces it at very high frequency. Because of its site and orientation specificity and because it lacks other identifiable phage‐like genes, we consider it to be a pathogenicity island (PI) rather than a transposon or a defective phage. The tst element in RN4282, near tyrB, is designated SaPI1. That in RN3984 in the trp region is only partially homologous to SaPI1 and is excised by phage 80 but not by 80α. It is designated SaPI2. These PIs are the first in any Gram‐positive species and the first for which mobility has been demonstrated. Their mobility may be responsible for the spread of TSST‐1 production among S. aureus strains.</abstract><cop>Oxford BSL</cop><pub>Blackwell Science Ltd, UK</pub><pmid>9720870</pmid><doi>10.1046/j.1365-2958.1998.00947.x</doi><tpages>17</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0950-382X |
ispartof | Molecular microbiology, 1998-07, Vol.29 (2), p.527-543 |
issn | 0950-382X 1365-2958 |
language | eng |
recordid | cdi_proquest_miscellaneous_16489153 |
source | Wiley-Blackwell Read & Publish Collection |
subjects | Amino Acid Sequence Bacterial Toxins Base Sequence DNA Transposable Elements Enterotoxins - genetics Genetic Variation Molecular Sequence Data Rec A Recombinases - genetics Sequence Analysis, DNA Sequence Deletion Species Specificity Staphylococcus aureus - genetics Staphylococcus aureus - pathogenicity Staphylococcus Phages - genetics Superantigens Transduction, Genetic |
title | The gene for toxic shock toxin is carried by a family of mobile pathogenicity islands in Staphylococcus aureus |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-03T19%3A25%3A23IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20gene%20for%20toxic%20shock%20toxin%20is%20carried%20by%20a%20family%20of%20mobile%20pathogenicity%20islands%20in%20Staphylococcus%20aureus&rft.jtitle=Molecular%20microbiology&rft.au=Lindsay,%20Jodi%20A.&rft.date=1998-07&rft.volume=29&rft.issue=2&rft.spage=527&rft.epage=543&rft.pages=527-543&rft.issn=0950-382X&rft.eissn=1365-2958&rft_id=info:doi/10.1046/j.1365-2958.1998.00947.x&rft_dat=%3Cproquest_cross%3E32661215%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c5377-8bd2175174754676ac861721ca9013265a11df6db88abc5a763f4a6670445db13%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=196513666&rft_id=info:pmid/9720870&rfr_iscdi=true |