Expression of the sarA family of genes in different strains of Staphylococcus aureus.
Identifieur interne : 000747 ( PubMed/Corpus ); précédent : 000746; suivant : 000748Expression of the sarA family of genes in different strains of Staphylococcus aureus.
Auteurs : Anand Ballal ; Adhar C. MannaSource :
- Microbiology (Reading, England) [ 1350-0872 ] ; 2009.
English descriptors
- KwdEn :
- Bacterial Proteins (biosynthesis), Bacterial Proteins (genetics), Blotting, Western, DNA-Binding Proteins (biosynthesis), DNA-Binding Proteins (genetics), Gene Expression Profiling, Gene Expression Regulation, Bacterial, Humans, Multigene Family, RNA, Bacterial (analysis), RNA, Bacterial (genetics), Repressor Proteins (biosynthesis), Repressor Proteins (genetics), Staphylococcal Infections (microbiology), Staphylococcus aureus (genetics), Staphylococcus aureus (metabolism), Trans-Activators (biosynthesis), Trans-Activators (genetics), Transcription Factors (biosynthesis), Transcription Factors (genetics), Transcription, Genetic.
- MESH :
- chemical , analysis : RNA, Bacterial.
- chemical , biosynthesis : Bacterial Proteins, DNA-Binding Proteins, Repressor Proteins, Trans-Activators, Transcription Factors.
- chemical , genetics : Bacterial Proteins, DNA-Binding Proteins, RNA, Bacterial, Repressor Proteins, Trans-Activators, Transcription Factors.
- genetics : Staphylococcus aureus.
- metabolism : Staphylococcus aureus.
- microbiology : Staphylococcal Infections.
- Blotting, Western, Gene Expression Profiling, Gene Expression Regulation, Bacterial, Humans, Multigene Family, Transcription, Genetic.
Abstract
Expression of genes involved in the pathogenesis of Staphylococcus aureus is controlled by global regulatory loci, including two-component regulatory systems and transcriptional regulators. The staphylococcal-specific SarA family of transcription regulators control large numbers of target genes involved in virulence, autolysis, biofilm formation, stress responses and metabolic processes, and are recognized as potential therapeutic targets. Expression of some of these important regulators has been examined, mostly in laboratory strains, while the pattern of expression of these genes in other strains, especially clinical isolates, is largely unknown. In this report, a comparative analysis of 10 sarA-family genes was conducted in six different S. aureus strains, including two laboratory (RN6390, SH1000) and four clinical (MW2, Newman, COL and UAMS-1) strains, by Northern and Western blot analyses. Transcription of most of the sarA-family genes showed a strong growth phase-dependence in all strains tested. Among these genes, no difference was observed in expression of the sarA, sarV, sarT and sarU genes, while a major difference was observed in expression of the sarX gene only in strain RN6390. Expression of mgrA, rot, sarZ, sarR and sarS was observed in all strains, but the level of expression varied from strain to strain.
DOI: 10.1099/mic.0.027417-0
PubMed: 19389785
Links to Exploration step
pubmed:19389785Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Expression of the sarA family of genes in different strains of Staphylococcus aureus.</title><author><name sortKey="Ballal, Anand" sort="Ballal, Anand" uniqKey="Ballal A" first="Anand" last="Ballal">Anand Ballal</name><affiliation><nlm:affiliation>Center for Infectious Disease Research and Vaccinology, South Dakota State University, Brookings, SD 57007, USA.</nlm:affiliation></affiliation></author><author><name sortKey="Manna, Adhar C" sort="Manna, Adhar C" uniqKey="Manna A" first="Adhar C" last="Manna">Adhar C. Manna</name><affiliation><nlm:affiliation>Center for Infectious Disease Research and Vaccinology, South Dakota State University, Brookings, SD 57007, USA.</nlm:affiliation></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2009">2009</date><idno type="RBID">pubmed:19389785</idno><idno type="pmid">19389785</idno><idno type="doi">10.1099/mic.0.027417-0</idno><idno type="wicri:Area/PubMed/Corpus">000747</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">000747</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Expression of the sarA family of genes in different strains of Staphylococcus aureus.</title><author><name sortKey="Ballal, Anand" sort="Ballal, Anand" uniqKey="Ballal A" first="Anand" last="Ballal">Anand Ballal</name><affiliation><nlm:affiliation>Center for Infectious Disease Research and Vaccinology, South Dakota State University, Brookings, SD 57007, USA.</nlm:affiliation></affiliation></author><author><name sortKey="Manna, Adhar C" sort="Manna, Adhar C" uniqKey="Manna A" first="Adhar C" last="Manna">Adhar C. Manna</name><affiliation><nlm:affiliation>Center for Infectious Disease Research and Vaccinology, South Dakota State University, Brookings, SD 57007, USA.</nlm:affiliation></affiliation></author></analytic><series><title level="j">Microbiology (Reading, England)</title><idno type="ISSN">1350-0872</idno><imprint><date when="2009" type="published">2009</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Bacterial Proteins (biosynthesis)</term><term>Bacterial Proteins (genetics)</term><term>Blotting, Western</term><term>DNA-Binding Proteins (biosynthesis)</term><term>DNA-Binding Proteins (genetics)</term><term>Gene Expression Profiling</term><term>Gene Expression Regulation, Bacterial</term><term>Humans</term><term>Multigene Family</term><term>RNA, Bacterial (analysis)</term><term>RNA, Bacterial (genetics)</term><term>Repressor Proteins (biosynthesis)</term><term>Repressor Proteins (genetics)</term><term>Staphylococcal Infections (microbiology)</term><term>Staphylococcus aureus (genetics)</term><term>Staphylococcus aureus (metabolism)</term><term>Trans-Activators (biosynthesis)</term><term>Trans-Activators (genetics)</term><term>Transcription Factors (biosynthesis)</term><term>Transcription Factors (genetics)</term><term>Transcription, Genetic</term></keywords><keywords scheme="MESH" type="chemical" qualifier="analysis" xml:lang="en"><term>RNA, Bacterial</term></keywords><keywords scheme="MESH" type="chemical" qualifier="biosynthesis" xml:lang="en"><term>Bacterial Proteins</term><term>DNA-Binding Proteins</term><term>Repressor Proteins</term><term>Trans-Activators</term><term>Transcription Factors</term></keywords><keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Bacterial Proteins</term><term>DNA-Binding Proteins</term><term>RNA, Bacterial</term><term>Repressor Proteins</term><term>Trans-Activators</term><term>Transcription Factors</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Staphylococcus aureus</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Staphylococcus aureus</term></keywords><keywords scheme="MESH" qualifier="microbiology" xml:lang="en"><term>Staphylococcal Infections</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Blotting, Western</term><term>Gene Expression Profiling</term><term>Gene Expression Regulation, Bacterial</term><term>Humans</term><term>Multigene Family</term><term>Transcription, Genetic</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Expression of genes involved in the pathogenesis of Staphylococcus aureus is controlled by global regulatory loci, including two-component regulatory systems and transcriptional regulators. The staphylococcal-specific SarA family of transcription regulators control large numbers of target genes involved in virulence, autolysis, biofilm formation, stress responses and metabolic processes, and are recognized as potential therapeutic targets. Expression of some of these important regulators has been examined, mostly in laboratory strains, while the pattern of expression of these genes in other strains, especially clinical isolates, is largely unknown. In this report, a comparative analysis of 10 sarA-family genes was conducted in six different S. aureus strains, including two laboratory (RN6390, SH1000) and four clinical (MW2, Newman, COL and UAMS-1) strains, by Northern and Western blot analyses. Transcription of most of the sarA-family genes showed a strong growth phase-dependence in all strains tested. Among these genes, no difference was observed in expression of the sarA, sarV, sarT and sarU genes, while a major difference was observed in expression of the sarX gene only in strain RN6390. Expression of mgrA, rot, sarZ, sarR and sarS was observed in all strains, but the level of expression varied from strain to strain.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">19389785</PMID><DateCompleted><Year>2009</Year><Month>10</Month><Day>01</Day></DateCompleted><DateRevised><Year>2020</Year><Month>01</Month><Day>27</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Print">1350-0872</ISSN><JournalIssue CitedMedium="Print"><Volume>155</Volume><Issue>Pt 7</Issue><PubDate><Year>2009</Year><Month>Jul</Month></PubDate></JournalIssue><Title>Microbiology (Reading, England)</Title><ISOAbbreviation>Microbiology (Reading, Engl.)</ISOAbbreviation></Journal><ArticleTitle>Expression of the sarA family of genes in different strains of Staphylococcus aureus.</ArticleTitle><Pagination><MedlinePgn>2342-2352</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1099/mic.0.027417-0</ELocationID><Abstract><AbstractText>Expression of genes involved in the pathogenesis of Staphylococcus aureus is controlled by global regulatory loci, including two-component regulatory systems and transcriptional regulators. The staphylococcal-specific SarA family of transcription regulators control large numbers of target genes involved in virulence, autolysis, biofilm formation, stress responses and metabolic processes, and are recognized as potential therapeutic targets. Expression of some of these important regulators has been examined, mostly in laboratory strains, while the pattern of expression of these genes in other strains, especially clinical isolates, is largely unknown. In this report, a comparative analysis of 10 sarA-family genes was conducted in six different S. aureus strains, including two laboratory (RN6390, SH1000) and four clinical (MW2, Newman, COL and UAMS-1) strains, by Northern and Western blot analyses. Transcription of most of the sarA-family genes showed a strong growth phase-dependence in all strains tested. Among these genes, no difference was observed in expression of the sarA, sarV, sarT and sarU genes, while a major difference was observed in expression of the sarX gene only in strain RN6390. Expression of mgrA, rot, sarZ, sarR and sarS was observed in all strains, but the level of expression varied from strain to strain.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Ballal</LastName><ForeName>Anand</ForeName><Initials>A</Initials><AffiliationInfo><Affiliation>Center for Infectious Disease Research and Vaccinology, South Dakota State University, Brookings, SD 57007, USA.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>Division of Basic Biomedical Sciences, University of South Dakota, Vermillion, SD 57069, USA.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Manna</LastName><ForeName>Adhar C</ForeName><Initials>AC</Initials><AffiliationInfo><Affiliation>Center for Infectious Disease Research and Vaccinology, South Dakota State University, Brookings, SD 57007, USA.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>Division of Basic Biomedical Sciences, University of South Dakota, Vermillion, SD 57069, USA.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><GrantList CompleteYN="Y"><Grant><GrantID>P20 RR016479</GrantID><Acronym>RR</Acronym><Agency>NCRR NIH HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>2P20 RR016479</GrantID><Acronym>RR</Acronym><Agency>NCRR NIH HHS</Agency><Country>United States</Country></Grant></GrantList><PublicationTypeList><PublicationType UI="D003160">Comparative Study</PublicationType><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D052061">Research Support, N.I.H., Extramural</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2009</Year><Month>04</Month><Day>23</Day></ArticleDate></Article><MedlineJournalInfo><Country>England</Country><MedlineTA>Microbiology</MedlineTA><NlmUniqueID>9430468</NlmUniqueID><ISSNLinking>1350-0872</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D001426">Bacterial Proteins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D004268">DNA-Binding Proteins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D012329">RNA, Bacterial</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D012097">Repressor Proteins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="C088021">SarA protein, bacterial</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="C433204">SarH3 protein, Staphylococcus aureus</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="C476149">SarS protein, Staphylococcus aureus</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="C470922">SarU protein, Staphylococcus aureus</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="C489658">Sarv protein, Staphylococcus aureus</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D015534">Trans-Activators</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D014157">Transcription Factors</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="C408643">rot protein, Staphylococcus aureus</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D001426" MajorTopicYN="N">Bacterial Proteins</DescriptorName><QualifierName UI="Q000096" MajorTopicYN="Y">biosynthesis</QualifierName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D015153" MajorTopicYN="N">Blotting, Western</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D004268" MajorTopicYN="N">DNA-Binding Proteins</DescriptorName><QualifierName UI="Q000096" MajorTopicYN="N">biosynthesis</QualifierName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D020869" MajorTopicYN="N">Gene Expression Profiling</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D015964" MajorTopicYN="N">Gene Expression Regulation, Bacterial</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005810" MajorTopicYN="Y">Multigene Family</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D012329" MajorTopicYN="N">RNA, Bacterial</DescriptorName><QualifierName UI="Q000032" MajorTopicYN="N">analysis</QualifierName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D012097" MajorTopicYN="N">Repressor Proteins</DescriptorName><QualifierName UI="Q000096" MajorTopicYN="N">biosynthesis</QualifierName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D013203" MajorTopicYN="N">Staphylococcal Infections</DescriptorName><QualifierName UI="Q000382" MajorTopicYN="Y">microbiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D013211" MajorTopicYN="Y">Staphylococcus aureus</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D015534" MajorTopicYN="N">Trans-Activators</DescriptorName><QualifierName UI="Q000096" MajorTopicYN="Y">biosynthesis</QualifierName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D014157" MajorTopicYN="N">Transcription Factors</DescriptorName><QualifierName UI="Q000096" MajorTopicYN="N">biosynthesis</QualifierName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D014158" MajorTopicYN="N">Transcription, Genetic</DescriptorName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="entrez"><Year>2009</Year><Month>4</Month><Day>25</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2009</Year><Month>4</Month><Day>25</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2009</Year><Month>10</Month><Day>2</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">19389785</ArticleId><ArticleId IdType="doi">10.1099/mic.0.027417-0</ArticleId><ArticleId IdType="pmc">PMC2888119</ArticleId></ArticleIdList><ReferenceList><Reference><Citation>Mol Microbiol. 1999 Jul;33(2):307-16</Citation><ArticleIdList><ArticleId IdType="pubmed">10411747</ArticleId></ArticleIdList></Reference><Reference><Citation>J Biol Chem. 1999 Dec 24;274(52):37169-76</Citation><ArticleIdList><ArticleId IdType="pubmed">10601279</ArticleId></ArticleIdList></Reference><Reference><Citation>J Bacteriol. 2000 Jun;182(11):3197-203</Citation><ArticleIdList><ArticleId IdType="pubmed">10809700</ArticleId></ArticleIdList></Reference><Reference><Citation>Mol Microbiol. 2000 Jul;37(2):398-409</Citation><ArticleIdList><ArticleId IdType="pubmed">10931334</ArticleId></ArticleIdList></Reference><Reference><Citation>Infect Immun. 2001 Feb;69(2):885-96</Citation><ArticleIdList><ArticleId IdType="pubmed">11159982</ArticleId></ArticleIdList></Reference><Reference><Citation>J Bacteriol. 2001 Mar;183(6):1843-52</Citation><ArticleIdList><ArticleId IdType="pubmed">11222581</ArticleId></ArticleIdList></Reference><Reference><Citation>Infect Immun. 2001 Apr;69(4):2448-55</Citation><ArticleIdList><ArticleId IdType="pubmed">11254606</ArticleId></ArticleIdList></Reference><Reference><Citation>Proc Natl Acad Sci U S A. 2001 Jun 5;98(12):6877-82</Citation><ArticleIdList><ArticleId IdType="pubmed">11381122</ArticleId></ArticleIdList></Reference><Reference><Citation>Lancet. 2001 Apr 21;357(9264):1225-40</Citation><ArticleIdList><ArticleId IdType="pubmed">11418146</ArticleId></ArticleIdList></Reference><Reference><Citation>Infect Immun. 2001 Aug;69(8):4749-58</Citation><ArticleIdList><ArticleId IdType="pubmed">11447147</ArticleId></ArticleIdList></Reference><Reference><Citation>Nat Struct Biol. 2001 Aug;8(8):710-4</Citation><ArticleIdList><ArticleId IdType="pubmed">11473263</ArticleId></ArticleIdList></Reference><Reference><Citation>J Bacteriol. 2001 Dec;183(24):7341-53</Citation><ArticleIdList><ArticleId IdType="pubmed">11717293</ArticleId></ArticleIdList></Reference><Reference><Citation>Infect Immun. 2002 Feb;70(2):470-80</Citation><ArticleIdList><ArticleId IdType="pubmed">11796572</ArticleId></ArticleIdList></Reference><Reference><Citation>Lancet. 2002 May 25;359(9320):1819-27</Citation><ArticleIdList><ArticleId IdType="pubmed">12044378</ArticleId></ArticleIdList></Reference><Reference><Citation>J Bacteriol. 2002 Oct;184(19):5457-67</Citation><ArticleIdList><ArticleId IdType="pubmed">12218034</ArticleId></ArticleIdList></Reference><Reference><Citation>Infect Immun. 2003 Jan;71(1):343-53</Citation><ArticleIdList><ArticleId IdType="pubmed">12496184</ArticleId></ArticleIdList></Reference><Reference><Citation>J Bacteriol. 2003 Jan;185(2):610-9</Citation><ArticleIdList><ArticleId IdType="pubmed">12511508</ArticleId></ArticleIdList></Reference><Reference><Citation>J Bacteriol. 2003 May;185(10):3127-38</Citation><ArticleIdList><ArticleId IdType="pubmed">12730173</ArticleId></ArticleIdList></Reference><Reference><Citation>Mol Microbiol. 2003 Jun;48(6):1429-49</Citation><ArticleIdList><ArticleId IdType="pubmed">12791129</ArticleId></ArticleIdList></Reference><Reference><Citation>Mol Microbiol. 2003 Jun;48(6):1451-66</Citation><ArticleIdList><ArticleId IdType="pubmed">12791130</ArticleId></ArticleIdList></Reference><Reference><Citation>J Bacteriol. 2003 Jul;185(13):3703-10</Citation><ArticleIdList><ArticleId IdType="pubmed">12813062</ArticleId></ArticleIdList></Reference><Reference><Citation>J Bacteriol. 2003 Jul;185(14):4219-25</Citation><ArticleIdList><ArticleId IdType="pubmed">12837797</ArticleId></ArticleIdList></Reference><Reference><Citation>Infect Immun. 2003 Sep;71(9):5139-48</Citation><ArticleIdList><ArticleId IdType="pubmed">12933857</ArticleId></ArticleIdList></Reference><Reference><Citation>Proc Natl Acad Sci U S A. 1992 Jul 15;89(14):6462-6</Citation><ArticleIdList><ArticleId IdType="pubmed">1321441</ArticleId></ArticleIdList></Reference><Reference><Citation>FEMS Immunol Med Microbiol. 2004 Jan 15;40(1):1-9</Citation><ArticleIdList><ArticleId IdType="pubmed">14734180</ArticleId></ArticleIdList></Reference><Reference><Citation>FEMS Microbiol Rev. 2004 May;28(2):183-200</Citation><ArticleIdList><ArticleId IdType="pubmed">15109784</ArticleId></ArticleIdList></Reference><Reference><Citation>J Bacteriol. 2004 Aug;186(16):5267-80</Citation><ArticleIdList><ArticleId IdType="pubmed">15292128</ArticleId></ArticleIdList></Reference><Reference><Citation>Proc Natl Acad Sci U S A. 2004 Aug 17;101(33):12312-7</Citation><ArticleIdList><ArticleId IdType="pubmed">15304642</ArticleId></ArticleIdList></Reference><Reference><Citation>J Bacteriol. 2005 Jan;187(2):576-92</Citation><ArticleIdList><ArticleId IdType="pubmed">15629929</ArticleId></ArticleIdList></Reference><Reference><Citation>Infect Immun. 2005 Jun;73(6):3806-9</Citation><ArticleIdList><ArticleId IdType="pubmed">15908418</ArticleId></ArticleIdList></Reference><Reference><Citation>Infect Immun. 2005 Jul;73(7):4391-4</Citation><ArticleIdList><ArticleId IdType="pubmed">15972535</ArticleId></ArticleIdList></Reference><Reference><Citation>J Bacteriol. 2006 Jan;188(2):669-76</Citation><ArticleIdList><ArticleId IdType="pubmed">16385056</ArticleId></ArticleIdList></Reference><Reference><Citation>Proc Natl Acad Sci U S A. 2006 Feb 14;103(7):2392-7</Citation><ArticleIdList><ArticleId IdType="pubmed">16455801</ArticleId></ArticleIdList></Reference><Reference><Citation>J Bacteriol. 2006 Mar;188(5):1899-910</Citation><ArticleIdList><ArticleId IdType="pubmed">16484201</ArticleId></ArticleIdList></Reference><Reference><Citation>Mol Microbiol. 2006 Jun;60(5):1289-301</Citation><ArticleIdList><ArticleId IdType="pubmed">16689803</ArticleId></ArticleIdList></Reference><Reference><Citation>J Bacteriol. 2006 Jun;188(12):4288-99</Citation><ArticleIdList><ArticleId IdType="pubmed">16740935</ArticleId></ArticleIdList></Reference><Reference><Citation>Mol Microbiol. 2006 Aug;61(4):1038-48</Citation><ArticleIdList><ArticleId IdType="pubmed">16879652</ArticleId></ArticleIdList></Reference><Reference><Citation>Nat Chem Biol. 2006 Nov;2(11):591-5</Citation><ArticleIdList><ArticleId IdType="pubmed">16980961</ArticleId></ArticleIdList></Reference><Reference><Citation>Microbiology. 2006 Oct;152(Pt 10):3075-90</Citation><ArticleIdList><ArticleId IdType="pubmed">17005987</ArticleId></ArticleIdList></Reference><Reference><Citation>Mol Microbiol. 2006 Dec;62(6):1601-17</Citation><ArticleIdList><ArticleId IdType="pubmed">17087772</ArticleId></ArticleIdList></Reference><Reference><Citation>Microbiology. 2007 May;153(Pt 5):1538-45</Citation><ArticleIdList><ArticleId IdType="pubmed">17464068</ArticleId></ArticleIdList></Reference><Reference><Citation>JAMA. 2007 Oct 17;298(15):1763-71</Citation><ArticleIdList><ArticleId IdType="pubmed">17940231</ArticleId></ArticleIdList></Reference><Reference><Citation>Int J Biochem Cell Biol. 2008;40(3):355-61</Citation><ArticleIdList><ArticleId IdType="pubmed">18083623</ArticleId></ArticleIdList></Reference><Reference><Citation>J Infect Dis. 2008 May 1;197(9):1254-62</Citation><ArticleIdList><ArticleId IdType="pubmed">18422437</ArticleId></ArticleIdList></Reference><Reference><Citation>Clin Infect Dis. 2008 Jun 1;46 Suppl 5:S350-9</Citation><ArticleIdList><ArticleId IdType="pubmed">18462090</ArticleId></ArticleIdList></Reference><Reference><Citation>Infect Immun. 2009 Jan;77(1):419-28</Citation><ArticleIdList><ArticleId IdType="pubmed">18955469</ArticleId></ArticleIdList></Reference><Reference><Citation>Mol Microbiol. 2009 Jan;71(1):198-211</Citation><ArticleIdList><ArticleId IdType="pubmed">19007410</ArticleId></ArticleIdList></Reference><Reference><Citation>J Bacteriol. 2009 Mar;191(5):1656-65</Citation><ArticleIdList><ArticleId IdType="pubmed">19103928</ArticleId></ArticleIdList></Reference><Reference><Citation>EMBO J. 1993 Oct;12(10):3967-75</Citation><ArticleIdList><ArticleId IdType="pubmed">7691599</ArticleId></ArticleIdList></Reference><Reference><Citation>Mol Microbiol. 1994 Jan;11(2):237-48</Citation><ArticleIdList><ArticleId IdType="pubmed">8170386</ArticleId></ArticleIdList></Reference><Reference><Citation>J Bacteriol. 1996 Aug;178(15):4563-70</Citation><ArticleIdList><ArticleId IdType="pubmed">8755885</ArticleId></ArticleIdList></Reference><Reference><Citation>J Bacteriol. 1998 Aug;180(15):3828-36</Citation><ArticleIdList><ArticleId IdType="pubmed">9683479</ArticleId></ArticleIdList></Reference><Reference><Citation>N Engl J Med. 1998 Aug 20;339(8):520-32</Citation><ArticleIdList><ArticleId IdType="pubmed">9709046</ArticleId></ArticleIdList></Reference></ReferenceList></PubmedData></pubmed></record>Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Sante/explor/StressCovidV1/Data/PubMed/Corpus
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000747 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/PubMed/Corpus/biblio.hfd -nk 000747 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= Sante
|area= StressCovidV1
|flux= PubMed
|étape= Corpus
|type= RBID
|clé= pubmed:19389785
|texte= Expression of the sarA family of genes in different strains of Staphylococcus aureus.
}}
Pour générer des pages wiki
HfdIndexSelect -h $EXPLOR_AREA/Data/PubMed/Corpus/RBID.i -Sk "pubmed:19389785" \
| HfdSelect -Kh $EXPLOR_AREA/Data/PubMed/Corpus/biblio.hfd \
| NlmPubMed2Wicri -a StressCovidV1
| This area was generated with Dilib version V0.6.33. |  |