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Genotypic and phenotypic characterization of Staphylococcus aureus isolates from human and animal origin in Portugal.

dc.contributor.authorSalgueiro, Vanessa
dc.contributor.authorManageiro, Vera
dc.contributor.authorClemente, Lurdes
dc.contributor.authorFerreira, Eugénia
dc.contributor.authorCaniça, Manuela
dc.date.accessioned2017-02-16T16:36:32Z
dc.date.available2017-02-16T16:36:32Z
dc.date.issued2016
dc.description.abstractBackground: Different methicillin-susceptible (MSSA) and methicillin-resistant (MRSA) Staphylococcus aureus clones have been encountered in isolates of human and animal origins. The objective of this study was to identify and characterize S. aureus from humans, and to compare their phenotypic and genotypic characteristics with animal isolates. Material/methods: Fifty-eight S. aureus isolates recovered from different specimens of patients admitted at Portuguese hospitals, comprising community-acquired and nosocomial infections, were studied. Seventeen S. aureus strains isolated from animals were also studied. Antibiotic susceptibility testing was performed to all S. aureus isolates by disk diffusion and E-test, according to EUCAST guidelines. Different antibiotic resistant genes were searched by PCR. MLST, spa and agr typing methods were applied to evaluate diversity and genetic relatedness. Results: The majority of the 58 clinical S. aureus was MRSA (70.7%), with reduced susceptibility to cefoxitin due to expression of the mecA gene; no mecC gene was detected. Additionally, 82.8% had decreased susceptibility to ciprofloxacin. Two (3.4%) linezolid-resistant S. aureus strains (CC5-ST105-t1094-agr 2 and CC8-ST239-t1223-agr 1) harboured mutations in the domain V of the 23S rRNA and/or in the rlmN gene, which explained the resistance phenotype. Decreased susceptibility to daptomycin (17.2%) was related with hospital environment clones, such as CC22-ST22-t032 and CC8-ST239-t037. Eleven (19%) S. aureus had a phenotype of multidrug resistance, with one (1.7%) characterized as hGISA (clone ST5/ST105-t002-agr 2). Among clinical strains, the most frequent spa types were t032 (ST22), followed closely by t002 (ST5/ST105); 2 new spa types (t14878 and t14933) were detected. Contrarily, all S. aureus isolated from animals were MSSA, showing susceptibility profiles to almost all antibiotics tested; four strains isolated from rabbits showed decreased susceptibility to ciprofloxacin. Furthermore, among S. aureus from animals we also identified CC398-ST398-t571 and CC130-t84 that have been described both in humans and animal infections, a new spa type (t15307), and three new ST (ST3254, ST3269 and ST3270). Globally, ST5 and ST34 were found in both reservoirs, while ST22/ST105 and ST121 were the most frequently identified among human and animal isolates, respectively. Conclusions: The identification of the same ST and spa types in S. aureus from humans and animals suggests a potential dissemination of strains between these two environments. In countries with high MRSA rates like Portugal, it is necessary to implement strategies in hospitals and also in veterinary areas in order to reduce the spread of this bacterium, which is a public health problem today.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationSalgueiro, V., Manageiro, V., Clemente, L., Ferreira, E., Caniça, M. 2016. Genotypic and phenotypic characterization of Staphylococcus aureus isolates from human and animal origin in Portugal. 26th European Congress of Clinical Microbiology and Infectious Diseases, Amsterdam, Netherlands. P0222.pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.18/4221
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.subjectStaphylococcus aureuspt_PT
dc.subjectAntibiotic Resistancept_PT
dc.subjectCC398-ST398-t571pt_PT
dc.subjectResistência aos Antimicrobianospt_PT
dc.titleGenotypic and phenotypic characterization of Staphylococcus aureus isolates from human and animal origin in Portugal.pt_PT
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlaceAmsterdam, Netherlandspt_PT
oaire.citation.title26th European Congress of Clinical Microbiology and Infectious Diseases (ECCMID), 9-12 April 2016pt_PT
rcaap.rightsclosedAccesspt_PT
rcaap.typeconferenceObjectpt_PT

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