Karmakar Amit, Jana Debarati, Dutta Kunal, Dua Parimal, Ghosh Chandradipa
Microbiology Laboratory, Department of Human Physiology with Community Health, Vidyasagar University, Paschim Medinipur, West Bengal 721102, India.
J Pathog. 2018 Sep 2;2018:4518541. doi: 10.1155/2018/4518541. eCollection 2018.
Panton-Valentine leukocidin () is a cytotoxin that causes leukocyte destruction and tissue necrosis. The aim of this study was to determine the prevalence of the , , and genes in isolates obtained from anterior nares and superficial infection sites of skin in a slum population of West Bengal, India. Expression level of gene was also analysed. Twenty-two strains were isolated, and phenotype and genotype specific examinations for isolates were carried out. Molecular identification was done by PCR using species-specific 16S rRNA primer pairs and finally 22 isolates were found to be positive as . The antibiotic responsiveness of all these isolates and the minimum inhibitory concentration (MIC) of MRSA isolates were determined using the broth dilution method with vancomycin. Antibiogram analysis of isolated strains with respect to different antimicrobial agents revealed antibiotic resistance ranging from 27 to 91%. The results of MIC for vancomycin showed 95% of strains to be VSSA and 5% to be VISA. 68% isolates were resistant to methicillin. All the isolates were subjected to detection of A, and genes, and 9%, 68%, and 27% were found to harbour A, and genes, respectively. All the MRSA strains produced high to moderate levels of biofilm. gene expression was carried out by Real-Time PCR. The low ∆Ct value (0.493) was indicative of high expression of in one strain. Thus, detection of gene in community acquired indicates the emergence of pathogenic in community setup in the studied region. The existing exploration is extremely imperative and informative for the high level multi-drug resistant infections inclusive of MRSA.
潘顿-瓦伦丁杀白细胞素(PVL)是一种导致白细胞破坏和组织坏死的细胞毒素。本研究的目的是确定从印度西孟加拉邦一个贫民窟人群的前鼻孔和皮肤浅表感染部位分离出的葡萄球菌分离株中PVL、PVL-A和PVL-B基因的流行情况。还分析了lukS-PV基因的表达水平。分离出22株金黄色葡萄球菌菌株,并对这些分离株进行了表型和基因型特异性检测。通过使用物种特异性16S rRNA引物对的PCR进行分子鉴定,最终发现22株分离株均为金黄色葡萄球菌阳性。使用万古霉素肉汤稀释法测定所有这些分离株的抗生素反应性以及耐甲氧西林金黄色葡萄球菌(MRSA)分离株的最低抑菌浓度(MIC)。对分离出的金黄色葡萄球菌菌株针对不同抗菌剂的抗菌谱分析显示,抗生素耐药率在27%至91%之间。万古霉素的MIC结果显示,95%的菌株为万古霉素敏感金黄色葡萄球菌(VSSA),5%为万古霉素中介金黄色葡萄球菌(VISA)。68%的分离株对甲氧西林耐药。所有分离株均进行了PVL-A、PVL-B和lukS-PV基因检测,分别发现9%、68%和27%的分离株携带PVL-A、PVL-B和lukS-PV基因。所有MRSA菌株均产生高水平至中等水平的生物膜。通过实时PCR进行lukS-PV基因表达分析。低∆Ct值(0.493)表明一株金黄色葡萄球菌菌株中lukS-PV表达水平高。因此,在社区获得性金黄色葡萄球菌中检测到lukS-PV基因表明在所研究地区的社区环境中出现了致病性金黄色葡萄球菌。现有的探索对于包括MRSA在内的高水平多药耐药金黄色葡萄球菌感染极为重要且信息丰富。