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Comparative study of virulence factors among methicillin resistant Staphylococcus aureus clinical isolates

机译:耐药因子在甲氧西林金黄色葡萄球菌临床分离株中的比较研究

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Methicillin resistant Staphylococcus aureus (MRSA) is recognized worldwide as a leading cause of hospital and community infections. Biofilm formation by MRSA is an extremely important virulence factor to be understood. Our aim was to establish phenotypic and genotypic characterization of virulence factors among 43 MRSA clinical isolates in a Tunisian hospital. We investigated enzymatic profiles, biofilm production and prevalences of genes encoding intracellular adhesion molecules (icaA and icaD), Microbial Surface Components Recognizing Adhesive Matrix Molecules genes (fnbA, fnbB and cna) and exoenzymes genes (geh, sspA and sspB). Our findings revealed that caseinase, gelatinase, lipase and lecithinase activities were detected in 100%, 100%, 76.6% and 93.3% of cases respectively. This study showed that 23 strains (76.7%) were slime producers on Congo red medium. Furthermore, 46.5% and 53.5% of isolates were respectively highly and moderately biofilm-forming on polystyrene. Significant association was found between both biofilm tests. PCR detection showed that 74.4%, 18.6%, 69.8%, 65.1% and 74.4% of isolates harbored fnbA, fnbB, icaA, icaD and cna genes respectively. In addition, 34.9%, 18.6% and 30.2% of MRSA strains were found positive for sspA, sspB and geh genes respectively. Further, statistical data showed that the presence of the fnbA and fnbB genes was significantly associated with a high biofilm production on polystyrene. However, no statistical association was observed for the icaA, icaD and cna genes. This study indicates that the detection of fnbA and fnbB contributing to the first step of biofilm formation has been predictable of high biofilm production. As studied factors contribute to MRSA virulence, this research could be of value in orienting towards the development of new preventive and therapeutic measures.
机译:耐素抗性金黄色葡萄球菌(MRSA)在全球范围内被认为是医院和社区感染的主要原因。 MRSA的生物膜形成是要理解的极其重要的毒力因素。我们的目的是建立43例MRSA临床分离株中的毒力因子的表型和基因型表征在突尼斯医院的43例临床孤立株中。我们研究了编码细胞内粘附分子(ICAA和ICAD)的生物膜生产和普遍的基因的酶促曲线,微生物表面组分识别粘合剂基质分子基因(FNBA,FNBB和CNA)和外酶基因(GEH,SSPA和SSPB)。我们的研究结果表明,分别以100%,100%,76.6%和93.3%的病例检测到酪蛋白酶,明胶酶,脂肪酶和卵磷脂酶活性。该研究表明,23株(76.7%)是刚果红培养基上的粘液生产商。此外,46.5%和53.5%的分离物在聚苯乙烯上分别高度和中度生物膜形成。在Biofilm测试之间发现了重要的关联。 PCR检测表明,分别为74.4%,18.6%,69.8%,65.1%和74.4%分别分离酸盐,分别是患有FNBA,FNBB,ICAA,ICAD和CNA基因的分离物。此外,对于SSPA,SSPB和GEH基因,发现34.9%,18.6%和30.2%的MRSA菌株。此外,统计数据显示FNBA和FNBB基因的存在与聚苯乙烯的高生物膜产生显着相关。然而,对于ICAA,ICAD和CNA基因没有观察到统计关联。该研究表明,对生物膜形成第一步的FNBA和FNBB的检测已经预测了高生物膜生产。随着研究的因素有助于MRSA毒力,这项研究可能具有朝向发展新的预防和治疗措施的价值。

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