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Validation of a sensitive PCR assay for the detection of Chelonid fibropapilloma-associated herpesvirus in latent turtle infections

机译:灵敏PCR检测法在潜伏龟感染中检测与螯合性纤维乳头瘤相关的疱疹病毒的验证

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The Chelonid fibropapilloma-associated herpesvirus (CFPHV) is hypothesized to be the causative agent of fibropapillomatosis, a neoplastic disease in sea turtles, given its consistent detection by PCR in fibropapilloma tumours. CFPHV has also been detected recently by PCR in tissue samples from clinically healthy (non exhibiting fibropapilloma tumours) turtles, thus representing presumably latent infections of the pathogen. Given that template copy numbers of viruses in latent infections can be very low, extremely sensitive PCR assays are needed to optimize detection efficiency. In this study, efficiency of several PCR assays designed for CFPHV detection is explored and compared to a method published previously. The results show that adoption of a triplet set of singleplex PCR assays outperforms other methods, with an approximately 3-fold increase in detection success in comparison to the standard assay. Thus, a new assay for the detection of CFPHV DNA markers is presented, and adoption of its methodology is recommended in future CFPHV screens among sea turtles
机译:假使与螯合型纤维乳头瘤相关的疱疹病毒(CFPHV)是海龟中一种赘生性疾病-纤维乳头状瘤病的病原体,因为它通过PCR在纤维乳头状瘤瘤中得到了一致的检测。最近还通过PCR在临床健康的(未表现出纤维乳头瘤肿瘤)乌龟的组织样本中检测到CFPHV,因此推测是潜在的病原体感染。鉴于潜在感染中病毒的模板拷贝数可能非常低,因此需要极度敏感的PCR分析来优化检测效率。在这项研究中,探索了几种用于CFPHV检测的PCR检测方法的效率,并将其与以前发表的方法进行了比较。结果表明,采用三元组的单重PCR检测优于其他方法,与标准检测相比,检测成功率提高了约3倍。因此,提出了一种检测CFPHV DNA标记的新方法,并建议在海龟今后的CFPHV筛查中采用该方法。

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