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首页> 外文期刊>Journal of Equine Veterinary Science >A Multiplex Polymerase Chain Reaction Assay for Direct Detection and Differentiation of beta-Hemolytic Streptococci in Clinical Samples from Horses
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A Multiplex Polymerase Chain Reaction Assay for Direct Detection and Differentiation of beta-Hemolytic Streptococci in Clinical Samples from Horses

机译:多重聚合酶链反应法可直接检测和鉴别马临床样品中的β-溶血性链球菌

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摘要

Streptococcus equi subspecies equi. S equi subspecies zooepidemicus, and S dysgalactiae subspecies equisimilis are beta-hemolytic Streptococci, often isolated from horses with respiratory or genital diseases. The aim of this study was (i) defining and validating a multiplex polymerase chain reaction (PCR) protocol for identifying these Streptococci in bacterial cultures and for detecting them directly in equine clinical specimens, and (ii) defining and validating a cheap DNA extraction protocol for clinical specimens. When respiratory and genital samples from symptomatic and asymptomatic horses were tested by bacterial culture and by multiplex PCR, all the 150 samples culture-positive for S equi, S zooepidemicus, or S equisimilis were also positive by PCR. Of 150 culture-negative samples, 143 were negative by PCR. Seven samples were positive by PCR but negative by bacteriology. The multiplex PCR protocol described in this study is proven suitable for a sensitive, specific, and rapid detection and identification of S equi, S zooepidemicus, and S equisimilis in cultured bacterial colonies, as well as in clinical specimens from symptomatic or asymptomatic horses. The inclusion of internal control primers in the PCR protocol excludes false-negative results. A cheap DNA extraction method has been also validated for swabs, tracheal aspirates, bronchoalveolar lavage, and guttural pouches lavage samples
机译:马链球菌马亚种马。 S equi兽疫亚种和S dysgalactiae兽亚种是β溶血性链球菌,通常从患有呼吸道或生殖器疾病的马中分离出来。这项研究的目的是(i)定义和验证用于在细菌培养物中鉴定这些链球菌并直接在马的临床标本中检测它们的多重聚合酶链反应(PCR)方案,以及(ii)定义和验证一种廉价的DNA提取方案用于临床标本。当通过细菌培养和多重PCR检测来自有症状和无症状马的呼吸道和生殖器样本时,对S equi,S zooepidemicus或S equisimilis培养阳性的150个样本均通过PCR呈阳性。在150个培养阴性样品中,有143个通过PCR阴性。 PCR检测阳性7份,细菌学检测阴性。事实证明,该研究中描述的多重PCR方案适用于敏感,特异性和快速检测和鉴定培养的细菌菌落以及有症状或无症状马的临床标本中的S equi,S兽疫和S equisimilis。 PCR方案中包含内部对照引物可排除假阴性结果。还已经验证了一种廉价的DNA提取方法可用于拭子,气管抽吸物,支气管肺泡灌洗和咽喉囊灌洗样本

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