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Molecular characterization of virulence and resistance features in Staphylococcus aureus clinical strains isolated from cutaneous lesions in patients with drug adverse reactions

机译:从药物不良反应患者的皮肤病变中分离出的金黄色葡萄球菌临床菌株的毒力和耐药特性的分子表征

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Patients treated with epidermal growth factor inhibitors often experience cutaneous adverse reactions that could be complicated by infections driven by specific pathogens such as the community emergent methicillin resistant Staphylococcus aureus. This study was conducted on a total of 42 S. aureus clinical strains isolated in 2016 from acneiform reactions pustule and periungual lesions in patients with cutaneous drug adverse reactions. Multiplex PCR was performed on genomic DNA from isolates in order to identify the SCCmec central elements and the virulence genes: bbp (bone bound sialoprotein), ebpS (elastin-binding protein), fnbB, fnbA (fibronectin-binding proteins), fib, clfA, clfB (clumping factors A and B), cna (collagen-binding protein), luk-PV (Panton-Valentine leukocidin), hlg (gamma-haemolysin), tst (toxic shock syndrome toxin). The obtained results confirmed the increased virulence potential and the high prevalence of SSCmec type VIII, followed by type IV and II in cutaneous isolates from patients with dermatologic toxic effects.
机译:用表皮生长因子抑制剂治疗的患者经常会发生皮肤不良反应,这些不良反应可能由特定病原体(如社区出现的耐甲氧西林的金黄色葡萄球菌)驱动感染并发。这项研究针对2016年从皮肤药物不良反应患者的痤疮样反应脓疱和唇周病变中分离出的总共42株金黄色葡萄球菌临床菌株进行。为了对分离株的基因组DNA进行多重PCR,以鉴定SCCmec中心元件和毒力基因:bbp(骨结合唾液蛋白),ebpS(弹性蛋白结合蛋白),fnbB,fnbA(纤连蛋白结合蛋白),fib,clfA ,clfB(聚集因子A和B),cna(胶原结合蛋白),luk-PV(潘顿-华伦白蛋白),hlg(γ-溶血素),tst(中毒性休克综合征毒素)。获得的结果证实,在具有皮肤病学毒性作用的患者的皮肤分离物中,VIII型SSCmec的致病力增强且发病率较高,其次是IV型和II型。

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