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首页> 外文期刊>Reports of Biochemistry and Molecular Biology >Determining the Biofilm Forming Gene Profile of Staphylococcus aureus Clinical Isolates via Multiplex Colony PCR Method
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Determining the Biofilm Forming Gene Profile of Staphylococcus aureus Clinical Isolates via Multiplex Colony PCR Method

机译:通过多重菌落PCR方法确定金黄色葡萄球菌临床分离物的生物膜形成基因谱

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Background:Among hospitalized patients, Staphylococcus aureus (S. aureus) infections pose a serious healththreat. The present study investigated the frequency of biofilm forming genes among clinical isolates S. aureusand their susceptibility to antibiotics.Methods: The clinical samples were analyzed via standard biochemical assays for identifying differentbacterium, which was then confirmed using the multiplex colony PCR method. Those samples identified as S.aureus were examined for the presence of the cna, fnbA, fnbB and pvl genes. The antibiotic susceptibility of theS. aureusisolates was then tested.Results:Using the standard biochemical assay approach, 54 S. aureus strains were identified. However, whenusing the multiplex PCR method 50 S. aureus strains were identified among the clinical samples. The in vitrobiofilm formation assays determined 3 (6%) strains of S. aureus to be strong biofilm forming, 15 (30%) of theisolates were determined to be moderate biofilm forming and, 32 (64%) were determined to be weak biofilmforming. Among the isolated strains, the specific frequencies of the biofilm forming genes were determined tobe 31 (62%) for cna, 35 (70%) for fnbA, 13 (26%) for fnbB and 1 (2%) for pvl. In 11 (22%) of the isolatedstrains fnbA, fnbB and cna genes were all present. All strains were determined to be penicillin, amoxicillin andclavulanic acid resistant.Conclusions: Due to the increase of the antibiotic resistance in biofilm producing S. aureus strains, rapididentification of antibiotic resistance can help to eliminate the infection effectively.
机译:背景:住院患者中,金黄色葡萄球菌(金黄色葡萄球菌)感染造成严重的健康。本研究研究了临床分离物中生物膜形成基因的频率S. aureus和它们对抗生素的易感性。方法:通过标准生化测定来分析临床样品,用于鉴定不同的分布,然后使用多重菌落PCR方法确认。检查鉴定为S.aureus的样品是否存在CNA,FNBA,FNBB和PVL基因。这些抗生素易感性。然后测试了天花糖液。结果:使用标准生化测定方法,鉴定了54秒的金黄色葡萄球菌株。然而,当临床样品中鉴定了多重PCR方法50s.Sureus菌株。在vittobiofilm形成测定中确定的3(6%)的S.UUREUS菌株为强生物膜形成,将15个(30%)的分离物测定为中等的生物膜成型,并测定32(64%)弱生物晶体。在分离的菌株中,将生物膜形成基因的特定频率测定为CNA,35(70%)的FNBA,35(70%)的FNBB,13(26%),用于PV1的1(2%)。在11(22%)的孤立的孤立FNBA中,全部存在FNBB和CNA基因。所有菌株都被确定为青霉素,阿莫西林和蛋白酸耐酸性。结论:由于生物膜产生的抗生素抗性的增加,抗生素抗性的抗生素抗性可以有助于有效消除感染。

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