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首页> 外文期刊>The Indian Journal of Animal Sciences >Multiplex PCR for rapid detection of Streptococcus agalactiae, Streptococcus uberis and Streptococcus dysgalactiae in subclinical mastitis milk
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Multiplex PCR for rapid detection of Streptococcus agalactiae, Streptococcus uberis and Streptococcus dysgalactiae in subclinical mastitis milk

机译:多重PCR快速检测亚临床乳腺炎乳中的无乳链球菌,乳房链球菌和乳链球菌乳汁少症。

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摘要

To improve mastitis diagnosis and achieve rapid, specific, reliable and cost effective test, a multiplex PCR for simultaneous detection and differentiation of major streptococcal species, viz. Streptococcus agalactiae, Streptococcus uberis and Streptococcus dysgalactiae was developed. Evaluation with 24 ATCC strains and 606 strains comprising streptococci (84) and staphylococci (522) showed the assay to be highly accurate. The threshold of detection of the mPCR assay was lOfg of genomic DNA and < 10~2 CFU ml ~ (-1). Assessment of 115 milk samples collected from subclinically infected herd, showed mPCR assay to be more efficacious than culture method. Identification of Streptococcus species using this assay will be crucial to determine prevalence ofStreptococcus in a herd. This will facilitate early diagnosis, treatment and control of the rate of infection at farm level. The assay can be implemented for routine monitoring of herd health and can be of great value for promoting prevention of streptococcal mastitis.
机译:为了改善乳腺炎的诊断并实现快速,特异性,可靠和具有成本效益的测试,多重PCR可同时检测和区分主要链球菌种,即。开发了无乳链球菌,乳房链球菌和痢疾链球菌。用24株ATCC菌株和606株包含链球菌(84)和葡萄球菌(522)的菌株进行评估,结果表明该测定方法非常准确。 mPCR测定的检测阈值是基因组DNA的10g和<10〜2 CFU ml〜(-1)。对从亚临床感染牛群中采集的115份牛奶样品的评估显示,mPCR分析比培养方法更有效。使用该测定法鉴定链球菌种类对于确定牛群中链球菌的流行至关重要。这将有助于农场一级的感染率的早期诊断,治疗和控制。该方法可用于常规监测牛群健康,对促进预防链球菌性乳腺炎具有重要价值。

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