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Staphylococcus aureus clinical isolates: Antibiotic susceptibility, molecular characteristics, and ability to form biofilm

dc.contributor.authorN. Indrawattanaen_US
dc.contributor.authorO. Sungkhachaten_US
dc.contributor.authorN. Sookrungen_US
dc.contributor.authorM. Chongsa-Nguanen_US
dc.contributor.authorA. Tungtrongchitren_US
dc.contributor.authorS. P. Voravuthikunchaien_US
dc.contributor.authorT. Kong-Ngoenen_US
dc.contributor.authorH. Kurazonoen_US
dc.contributor.authorW. Chaicumpaen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherPrince of Songkla Universityen_US
dc.contributor.otherObihiro University of Agriculture and Veterinary Medicineen_US
dc.date.accessioned2018-10-19T04:35:57Z
dc.date.available2018-10-19T04:35:57Z
dc.date.issued2013-09-23en_US
dc.description.abstractPeriodic monitoring of Staphylococcus aureus characteristics in a locality is imperative as their drug-resistant variants cause treatment problem. In this study, antibiograms, prevalence of toxin genes (sea-see, seg-ser, seu, tsst-1, eta, etb, and etd), PFGE types, accessory gene regulator (agr) groups, and ability to form biofilm of 92 S. aureus Thailand clinical isolates were investigated. They were classified into 10 drug groups: groups 1-7 (56 isolates) were methicillin resistant (MRSA) and 8-10 (36 isolates) were methicillin sensitive (MSSA). One isolate did not have any toxin gene, 4 isolates carried one toxin gene (seq), and 87 isolates had two or more toxin genes. No isolate had see, etb, or tsst-1; six isolates had eta or etd. Combined seg-sei-sem-sen-seo of the highly prevalent egc locus was 26.1%. The seb, sec, sel, seu, and eta associated significantly with MSSA; sek was more in MRSA. The sek-seq association was 52.17% while combined sed-sej was not found. Twenty-three PFGE types were revealed, no association of toxin genes with PFGE types. All four agr groups were present; agr group 1 was predominant (58.70%) but agr group 2 strains carried more toxin genes and were more frequent toxin producers. Biofilm formation was found in 72.83% of the isolates but there was no association with antibiograms. This study provides insight information on molecular and phenotypic markers of Thailand S. aureus clinical isolates which should be useful for future active surveillance that aimed to control a spread of existing antimicrobial resistant bacteria and early recognition of a newly emerged variant. © 2013 N. Indrawattana et al.en_US
dc.identifier.citationBioMed Research International. Vol.2013, (2013)en_US
dc.identifier.doi10.1155/2013/314654en_US
dc.identifier.issn23146141en_US
dc.identifier.issn23146133en_US
dc.identifier.other2-s2.0-84884240870en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/31212
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84884240870&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectImmunology and Microbiologyen_US
dc.titleStaphylococcus aureus clinical isolates: Antibiotic susceptibility, molecular characteristics, and ability to form biofilmen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84884240870&origin=inwarden_US

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