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Detection of the intercellular adhesion gene cluster (ica) in clinical Staphylococcus aureus isolates

机译:临床金黄色葡萄球菌分离株中细胞间黏附基因簇的检测

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摘要

Staphylococcus aureus is a major hospital and community pathogen having the aptitude to cause a wide variety of infections in men. The ability of microorganisms to produce biofilm facilitates them to withstand the host immune response and is recognized as one factor contributing to chronic or persistent infections. It was demonstrated that the ica-encoded genes lead to the biosynthesis of polysaccharide intercellular adhesion (PIA) molecules, and may be involved in the accumulation phase of biofilm formation. Different studies have shown the decisive role of the ica gene as virulence factors in staphylococcal infections. This study was carried out to demonstrate the relationship between ica gene and production of slime layer in S. aureus strains. Sixty S. aureus strains were isolated from patients. The isolates were identified morphologically and biochemically following standard laboratory methods. After identification, the staphylococcal isolates were maintained in trypticase soy broth (TSB), to which 15% glycerol was added, and stored at –20°C. Slime formation and biofilm assay was monitored. A PCR assay was developed to identify the presence of icaD (intercellular adhesion gene) gene in all isolates. Thirty-nine slime producing colonies with CRA plates (65%) formed black colors, the remaining 21 isolates were pink (35%). In the quantitative biofilm assay 35 (58%) produced biofilm while 25 (42%) isolates did not exhibit this property. All isolates were positive for detection of icaD gene by PCR method. The interaction of icaA and icaD in the investigated isolates may be important in slime layer formation and biofilm phenomena.We propose PCR detection of the ica gene locus as a rapid and effective method to be used for discrimination between potentially virulent and nonvirulent isolates, with implications for therapeutic and preventive measures pertainin to the management of colonized indwelling catheters.
机译:金黄色葡萄球菌是主要的医院和社区病原体,具有引起男性多种感染的倾向。微生物产生生物膜的能力使它们能够抵抗宿主的免疫反应,并被认为是导致慢性或持续感染的因素之一。事实证明,ICA编码的基因导致多糖细胞间粘附(PIA)分子的生物合成,并可能参与生物膜形成的积累阶段。不同的研究表明,ica基因作为葡萄球菌感染中的致病因子具有决定性作用。进行该研究以证明ica基因与金黄色葡萄球菌菌株中的粘液层产生之间的关系。从患者中分离出六十株金黄色葡萄球菌。按照标准实验室方法在形态和生化上鉴定出分离物。鉴定后,将葡萄球菌分离株保存在胰蛋白酶大豆肉汤(TSB)中,向其中加入15%甘油,并保存在–20°C下。监测粘液形成和生物膜测定。已开发出一种PCR检测方法来鉴定所有分离物中icaD(细胞间粘附基因)基因的存在。带有CRA板的39个产生粘液的菌落(65%)形成黑色,其余21个分离株为粉红色(35%)。在定量生物膜测定中,有35个(58%)产生了生物膜,而25个(42%)分离株没有表现出这种特性。所有分离株通过PCR方法检测icaD基因均为阳性。 icaA和icaD在被研究菌株中的相互作用可能对粘液层形成和生物膜现象很重要。我们建议对ica基因位点进行PCR检测,作为一种快速有效的方法,用于区分潜在的有毒力和无毒力的菌株,具有重要意义。用于治疗和预防措施的有关定居留置导管的管理。

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