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基于聚合酶链反应检测来自牛亚临床乳腺炎病例的金黄色葡萄球菌中编码毒力决定因素的基因

PCR-based detection of genes encoding virulence determinants in Staphylococcus aureus from bovine subclinical mastitis cases.

作者信息

Kalorey Dewanand Rajaram, Shanmugam Yuvaraj, Kurkure Nitin Vasantrao, Chousalkar Kapil Kamalakarrao, Barbuddhe Sukhadeo Baliram

机构信息

Department of Microbiology, Nagpur Veterinary College, Maharashtra Animal and Fishery Sciences University, Nagpur, Maharashtra, India.

出版信息

J Vet Sci. 2007 Jun;8(2):151-4. doi: 10.4142/jvs.2007.8.2.151.

Abstract

The present study was carried out to genotypically characterize Staphylococcus aureus (S. aureus) isolated from bovine mastitis cases. A total of 37 strains of S. aureus were isolated during processing of 552 milk samples from 140 cows. The S. aureus strains were characterized phenotypically, and were further characterized genotypically by polymerase chain reaction using oligonucleotide primers that amplified genes encoding coagulase (coa), clumping factor (clfA), thermonuclease (nuc), enterotoxin A (entA), and the gene segments encoding the immunoglobulin G binding region and the X region of protein A gene spa. All of the isolates yielded an amplicon with a size of approximately 1,042 bp of the clfA gene. The amplification of the polymorphic spa gene segment encoding the immunoglobulin G binding region was observed in 34 isolates and X-region binding was detected in 26 isolates. Amplification of the coa gene yielded three different products in 20, 10, and 7 isolates. The amplification of the thermonuclease gene, nuc, was observed in 36 out of 37 isolates. All of the samples were negative for the entA gene. The phenotypic and genotypic findings of the present strategies might provide an understanding of the distribution of the prevalent S. aureus clones among bovine mastitis isolates, and might aid in the development of steps to control S. aureus infections in dairy herds.

摘要

本研究旨在对从牛乳腺炎病例中分离出的金黄色葡萄球菌进行基因分型鉴定。在对来自140头奶牛的552份牛奶样本进行处理的过程中,共分离出37株金黄色葡萄球菌。对金黄色葡萄球菌菌株进行了表型鉴定,并通过聚合酶链反应进一步进行基因分型鉴定,使用的寡核苷酸引物可扩增编码凝固酶(coa)、凝聚因子(clfA)、耐热核酸酶(nuc)、肠毒素A(entA)的基因,以及编码免疫球蛋白G结合区域和蛋白A基因spa的X区域的基因片段。所有分离株均产生了大小约为1042 bp的clfA基因扩增子。在34株分离株中观察到编码免疫球蛋白G结合区域的多态性spa基因片段的扩增,在26株分离株中检测到X区域结合。coa基因的扩增在20株、10株和7株分离株中产生了三种不同的产物。37株分离株中有36株观察到耐热核酸酶基因nuc的扩增。所有样本的entA基因均为阴性。本研究策略的表型和基因型研究结果可能有助于了解牛乳腺炎分离株中流行的金黄色葡萄球菌克隆的分布情况,并可能有助于制定控制奶牛群中金黄色葡萄球菌感染的措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff62/2872713/0e9143a78c76/jvs-8-151-g001.jpg

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