首页> 外文期刊>Veterinary Parasitology >Development of a quantitative PCR for rapid and sensitive diagnosis of an intranuclear coccidian parasite in Testudines (TINC), and detection in the critically endangered Arakan forest turtle (Heosemys depressa)
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Development of a quantitative PCR for rapid and sensitive diagnosis of an intranuclear coccidian parasite in Testudines (TINC), and detection in the critically endangered Arakan forest turtle (Heosemys depressa)

机译:定量PCR的开发,用于快速,灵敏地诊断睾丸中的球虫内球虫,并在极度濒危的若开森林龟(Heosemys depressa)中进行检测

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摘要

The intranuclear coccidian parasite of Testudines (TINC) is responsible for significant disease in turtles and tortoises causing high mortality and affecting several threatened species. Diagnostic testing has been limited to relatively labor intensiveand expensive pan-coccidial PCR and sequencing techniques. A qPCR assay targeting a specific and conserved region of TINC 18S rRNA was designed. The qPCR reaction was run on samples known to be TINC positive and the results were consistent and analytically specific. The assay was able to detect as little as 10 copies of target DNA in a sample. Testing of soil and invertebrates was negative and did not provide any further insights into life cycles. This assay was used to identify TINC in a novel host species, the critically endangered Arakan forest turtle (Heosemys depressa).
机译:睾丸内核球虫的寄生虫(TINC)导致乌龟和乌龟中的重大疾病,导致高死亡率,并影响了几种濒危物种。诊断测试仅限于相对劳动强度大且昂贵的泛球虫PCR和测序技术。设计了针对TINC 18S rRNA特定且保守区域的qPCR分析。对已知为TINC阳性的样品进行qPCR反应,结果一致且分析特异性。该测定法能够检测到样品中少至10个拷贝的目标DNA。对土壤和无脊椎动物的检测是阴性的,没有提供对生命周期的任何进一步了解。该测定法用于鉴定新型寄主物种(极度濒危的若开森林龟(Heosemys depressa))中的TINC。

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