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首页> 外文期刊>Letters in Applied Microbiology >Simultaneous identification by multiplex PCR of major Prototheca spp. isolated from bovine and buffalo intramammary infection and bulk tank
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Simultaneous identification by multiplex PCR of major Prototheca spp. isolated from bovine and buffalo intramammary infection and bulk tank

机译:通过多重PCR同时鉴定主要的Prototheca spp。从牛和水牛乳房内感染和散装储罐中分离

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Bovine mastitis caused by Prototheca spp. infection is increasing worldwide, therefore becoming more relevant to the dairy industry. Almost all Prototheca isolates from bovine mammary protothecosis came from P.zopfii genotype 2, with a lower prevalence of infection due to P.blaschkeae and rarely to P.wickerhamii. In this study, we report the development of two multiplex PCR assays able to discriminate among the three species responsible for bovine intramammary infection (IMI). Our assay is based on the specific amplification of new DNA target from mitochondria and chloroplasts partial sequences, of different Prototheca isolates. Both methods were set up using reference strains belonging to all Prototheca species and validated by the analysis of 93 isolates from bovine and buffalo IMI and bulk tank milk samples. The investigation involves 70 isolates from North, 13 from Central and 10 from South Italian regions. Isolates from bovine were most commonly identified as P.zopfii genotype 2, and only in one case as P.blaschkeae, whereas isolates from buffaloes belonged both to P.zopfii genotype 2 and P.wickerhamii. These findings proved the suitability of our multiplex PCRs as a rapid test to discriminate among pathogenic Prototheca strains.
机译:由Prototheca spp引起的牛乳腺炎。感染在世界范围内正在增加,因此与乳制品行业越来越相关。牛乳原虫病的所有原生动物分离株几乎都来自P.zopfii基因型2,其由败血假单胞菌引起的感染率较低,而很少出现柳条氏假单胞菌。在这项研究中,我们报告了两个多重PCR分析方法的发展,该方法能够区分造成牛乳内感染(IMI)的三个物种。我们的检测方法基于不同原生动物分离物的线粒体和叶绿体部分序列中新的DNA靶标的特异性扩增。两种方法均使用属于所有Prototheca物种的参考菌株建立,并通过分析来自牛和水牛IMI和散装罐装牛奶样品的93种分离株进行了验证。调查涉及来自北部的70株隔离株,来自中部的13株和来自意大利南部地区的10株。来自牛的分离株最常被鉴定为P.zopfii基因型2,仅在一种情况下被鉴定为P.blaschkeae,而来自水牛的分离株则同时属于P.zopfii基因型2和P.wickerhamii。这些发现证明了我们的多重PCR作为区分致病性Prototheca菌株的快速测试方法的适用性。

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