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首页> 外文期刊>Advances in Microbiology >Inter-Laboratory Ring Trial to Evaluate Reverse Transcription Polymerase Chain Reaction Methods Used for &i&Dolphin Morbillivirus&/i& Detection in Italy
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Inter-Laboratory Ring Trial to Evaluate Reverse Transcription Polymerase Chain Reaction Methods Used for &i&Dolphin Morbillivirus&/i& Detection in Italy

机译:实验室间环试验,以评估用于海豚莫比利病毒的反转录聚合酶链反应方法。在意大利检测

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Dolphin Morbillivirus (DMV) is one of the most frequently detected pathogens in stranded cetacean specimens worldwide as well as in Italy. Due to the persistence of DMV in the Mediterranean Sea and to the lack of information about the efficiency of the available diagnostic techniques, the Italian National Reference Centre for diagnostic activities on dead stranded marine mammals (C.Re.Di.Ma) performed the first inter-laboratory ring trial with the aim to standardize a diagnostic biomolecular approach for DMV in Italy. Viral isolation is usually considered the “gold standard” for the definitive diagnosis of most pathogens, but it is not often feasible in DMV diagnosis, due to the poor preservation of virus-targeted tissues in stranded cetacean carcasses, as well as to the lack of appropriate sensitivity of cell lines towards DMV variability. Therefore direct viral detection on tissues by means of reverse transcription-PCR (RT-PCR) represents a valuable option for DMV infection’s diagnosis. For detecting DMV in cetacean die-offs occurred in the Mediterranean basin since 2013, C.Re.Di.Ma developed an RT-PCR based method targeting to a 287 bp fragment of DMV nucleoprotein (N) gene. With the purpose to evaluate its performances in terms of accuracy (Se = sensitivity and Sp = specificity) and precision (reproducibility), it was submitted to a ring trial. So, 12 Public Laboratories belonging to the Italian dead stranded marine mammals diagnostic network were asked to analyze a panel of 40 samples (positive and negative for DMV, using different dilutions of a viral suspension obtained from a cell culture supernatant of a DMV strain) with the aforementioned technique. Furthermore, we also aimed at comparing the accuracy of other 7 molecular methods routinely applied for DMV detection in Italy. For this purpose, the second panel of identical 40 DMV +ve and -ve samples was provided to Laboratories that routinely used DMV detection methods other than those developed by C.Re.Di.Ma, in order to be analyzed simultaneously with the method they usually applied. The C.Re.Di.Ma technique showed high accuracy [mean Se = 97.8% (95% CI 84.2% - 99.3%), mean Sp = 98.1% (95% CI 72.5% - 99.9%)] and very good precision [k combined equal to 0.91 (95% CI 0.87 - 0.95)]. In conclusion, this study highlighted a satisfactory reliability of most of the molecular methods used in Italy for DMV detection.
机译:海豚杯状病毒(DMV)是全世界以及意大利在滞留的鲸类标本中最常发现的病原体之一。由于DMV在地中海地区的持续存在以及缺乏有关可用诊断技术效率的信息,意大利国家死海滞留哺乳动物诊断活动参考中心(C.Re.Di.Ma)进行了首次实验室间环试验,旨在标准化意大利DMV的诊断性生物分子方法。病毒分离通常被认为是大多数病原体明确诊断的“黄金标准”,但是由于在以束缚方式捕食的鲸类动物尸体中以病毒为目标的组织保存不佳,因此在DMV诊断中通常不可行。细胞株对DMV变异性的适当敏感性。因此,通过逆转录PCR(RT-PCR)对组织进行直接病毒检测代表了DMV感染诊断的宝贵选择。为了检测自2013年以来地中海盆地鲸鱼死亡中的DMV,C.Re.Di.Ma开发了一种基于RT-PCR的方法,靶向DMV核蛋白(N)基因的287 bp片段。为了评估其准确度(Se =灵敏度,Sp =特异性)和精密度(可再现性)的性能,将其提交给了环试验。因此,要求属于意大利死海海洋哺乳动物诊断网络的12个公共实验室分析一组40个样品(DMV阳性和阴性,使用从DMV菌株细胞培养上清液中获得的不同稀释度的病毒悬液),上述技术。此外,我们还旨在比较意大利常规用于DMV检测的其他7种分子方法的准确性。为此,将第二组相同的40个DMV + ve和-ve样品提供给实验室,这些实验室通常使用C.Re.Di.Ma开发的DMV检测方法以外的方法,以便与它们同时进行分析。通常适用。 C.Re.Di.Ma技术显示出很高的准确度[平均值Se = 97.8%(95%CI 84.2%-99.3%),平均Sp = 98.1%(95%CI 72.5%-99.9%)]和非常好的精确度[ k的总和等于0.91(95%CI 0.87-0.95)。总之,这项研究突出了意大利用于DMV检测的大多数分子方法的令人满意的可靠性。

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