dc.creatorDabul, Andrei Nicoli Gebieluca
dc.creatorCamargo, Ilana Lopes Baratella da Cunha
dc.date.accessioned2017-06-02T14:25:49Z
dc.date.accessioned2018-07-04T17:13:12Z
dc.date.available2017-06-02T14:25:49Z
dc.date.available2018-07-04T17:13:12Z
dc.date.created2017-06-02T14:25:49Z
dc.date.issued2014-02
dc.identifierFEMS Microbiology Letters,Chichester : Wiley-Blackwell,v. 321, n. 1, p. 7-8, Feb. 2014
dc.identifier0378-1097
dc.identifierhttp://www.producao.usp.br/handle/BDPI/51302
dc.identifier10.1111/1574-6968.12358
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1646293
dc.description.abstractIn this manuscript, we show that the most important clonal complexes of Staphylococcus aureus, CC1, CC5, CC8, CC15 and CC97, are now all connected by EBURST when run on the Multi-locus sequence typing (MLST) database. The seven loci suggested for the MLST scheme of S. aureus are not enough to separate the most important clones such as New York/Japan and Brazilian Epidemic Clone (BEC). They now all belong to the same clonal complex and this may be the time to think about a new way to discriminate them.
dc.languageeng
dc.publisherWiley-Blackwell
dc.publisherChichester
dc.relationFEMS Microbiology Letters
dc.rightsCopyright Wiley-Blackwell
dc.rightsrestrictedAccess
dc.subjectTyping method
dc.subjectMolecular epidemiology
dc.subjectSequence typing
dc.titleClonal complexes of Staphylococcus aureus: all mixed and together
dc.typeArtículos de revistas


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