首页> 外文期刊>Journal of dairy science >Differentiation of Staphylococcus aureus and Staphylococcus epidermidis by PCR for the fibrinogen binding protein gene
【24h】

Differentiation of Staphylococcus aureus and Staphylococcus epidermidis by PCR for the fibrinogen binding protein gene

机译:金黄色葡萄球菌和表皮葡萄球菌的纤维蛋白原结合蛋白基因PCR鉴定。

获取原文
获取原文并翻译 | 示例
       

摘要

Mastitis is one of the most common and burdensome diseases afflicting dairy animals. Among other causes of mastitis, staphylococci are frequently associated with clinical and subclinical mastitis. Although Staphylococcus aureus is the predominant species involved, Staphylococcus epidermidis and other coagulase-negative staphylococci are increasingly being isolated from cases of bovine mastitis. Although Staph. aureus and Staph. epidermidis can be easily differentiated based on their biochemical properties, such phenotypic identification is time consuming and laborious. This study aimed to rapidly identify Staph. aureus and Staph. epidermidis. Accordingly, a multiplex PCR was developed and we found that a single gene encoding the adhesin fibrinogen binding protein could be used to identify and differentiate the two species. Consequently, a multiplex reaction combining a triplex PCR for Staph. aureus and a duplex PCR for Staph. epidermidis was standardized, first using bacterial cultures and then with pasteurized milk spiked with live organisms or DNA extracted from the organisms. The test could specifically detect Staph. aureus and Staph. epidermidis even in the presence of a dozen other organisms. The limit of detection for detecting Staph. aureus and Staph. epidermidis separately was 10 to 100 cfu/mL for simplex PCR and 10~4 cfu/mL for multiplex PCR. Conversely, the limit was 10~6 cfu/ mL by multiplex PCR for simultaneous detection of both the organisms when spiked into culture medium or pasteurized milk. Overnight enrichment enhanced the assay sensitivity 100-fold. The assay had a high diagnostic sensitivity and specificity. The application of the test was verified on 602 field isolates of staphylococci that had been characterized earlier by phenotypic methods. Importantly, 25 coagulase-negative isolates were identified as Staph. aureus by the multiplex PCR. The test could be adapted for use in clinical diagnostic laboratories.
机译:乳腺炎是困扰奶牛的最常见和最繁重的疾病之一。在乳腺炎的其他原因中,葡萄球菌经常与临床和亚临床乳腺炎相关。尽管金黄色葡萄球菌是最主要的物种,但从牛乳腺炎病例中越来越多地分离到表皮葡萄球菌和其他凝固酶阴性葡萄球菌。虽然葡萄球菌。金黄色葡萄球菌和葡萄球菌。根据表皮的生化特性可以轻松区分它们,这种表型鉴定既费时又费力。这项研究旨在快速鉴定葡萄球菌。金黄色葡萄球菌和葡萄球菌。表皮因此,开发了多重PCR,我们发现编码粘附素纤维蛋白原结合蛋白的单个基因可用于鉴定和区分这两个物种。因此,多重反应结合了针对葡萄球菌的三重PCR。金黄色葡萄球菌和金黄色葡萄球菌的双重PCR。表皮是标准化的,首先使用细菌培养物,然后使用加有活生物体或从生物体中提取的DNA的巴氏灭菌牛奶。该测试可以特异性检测葡萄球菌。金黄色葡萄球菌和葡萄球菌。甚至在其他十几种生物体的存在下也存在表皮。用于检测葡萄球菌的检测极限。金黄色葡萄球菌和葡萄球菌。对于单纯PCR,表皮分别为10〜100 cfu / mL,对于多重PCR,表皮为10〜4 cfu / mL。相反,当加标到培养基或巴氏灭菌的牛奶中时,通过同时检测两种生物的多重PCR的极限是10〜6 cfu / mL。过夜浓缩可将测定灵敏度提高100倍。该测定法具有很高的诊断敏感性和特异性。该测试的应用已在先前已通过表型方法表征的602株葡萄球菌中进行了验证。重要的是,已鉴定出25个凝固酶阴性分离株为葡萄球菌。金黄色葡萄球菌通过多重PCR。该测试可适合在临床诊断实验室中使用。

著录项

  • 来源
    《Journal of dairy science》 |2013年第5期|2857-2865|共9页
  • 作者单位

    Ella Foundation, Genome Valley, Turkapally, Shameerpet Mandal, Hyderabad 500078, India;

    Ella Foundation, Genome Valley, Turkapally, Shameerpet Mandal, Hyderabad 500078, India;

    Veterinary College, Karnataka Veterinary, Animal and Fisheries Sciences University, Bengaluru 560024, India;

    Veterinary College, Karnataka Veterinary, Animal and Fisheries Sciences University, Bengaluru 560024, India;

    Veterinary College, Karnataka Veterinary, Animal and Fisheries Sciences University, Bengaluru 560024, India;

    Veterinary College, Karnataka Veterinary, Animal and Fisheries Sciences University, Bengaluru 560024, India;

    Ella Foundation, Genome Valley, Turkapally, Shameerpet Mandal, Hyderabad 500078, India;

    CAR Research Complex for Goa, Ela, Old Goa 403402, India;

    Veterinary College, Anand Agricultural University, Anand 388001, India;

    KNP College of Veterinary Sciences, Maharashtra Animal and Fishery Sciences University, Shirval, India;

    Bombay Veterinary College, Maharashtra Animal and Fishery Sciences University, Mumbai, India;

    College of Veterinary Science, Sri Venkateswara Veterinary University, Hyderabad, India;

    College of Veterinary Science, Sri Venkateswara Veterinary University, Hyderabad, India;

    College of Veterinary Science, Sri Venkateswara Veterinary University, Hyderabad, India;

    Ella Foundation, Genome Valley, Turkapally, Shameerpet Mandal, Hyderabad 500078, India;

    School of Biomedical Sciences, Curtin Health Innovation Research Institute, Curtin University, Perth, Australia;

    School of Biomedical Sciences, Curtin Health Innovation Research Institute, Curtin University, Perth, Australia;

    School of Biomedical Sciences, Curtin Health Innovation Research Institute, Curtin University, Perth, Australia;

    School of Biomedical Sciences, Curtin Health Innovation Research Institute, Curtin University, Perth, Australia;

    School of Biomedical Sciences, Curtin Health Innovation Research Institute, Curtin University, Perth, Australia;

    Veterinary College, Karnataka Veterinary, Animal and Fisheries Sciences University, Bengaluru 560024, India;

    Ella Foundation, Genome Valley, Turkapally, Shameerpet Mandal, Hyderabad 500078, India;

  • 收录信息 美国《科学引文索引》(SCI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    bovine mastitis; staphylococci; detection and differentiation; multiplex PCR;

    机译:牛乳腺炎葡萄球菌检测和区分;多重PCR;
  • 入库时间 2022-08-17 23:24:10

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号