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使用实时Taqman PCR检测法对两栖动物样本中的蛙壶菌病(蛙壶菌)进行快速定量检测。

Rapid quantitative detection of chytridiomycosis (Batrachochytrium dendrobatidis) in amphibian samples using real-time Taqman PCR assay.

作者信息

Boyle D G, Boyle D B, Olsen V, Morgan J A T, Hyatt A D

机构信息

Australian Animal Health Laboratory, CSIRO Livestock Industries, Private Bag 24, Geelong, Victoria 3220, Australia.

出版信息

Dis Aquat Organ. 2004 Aug 9;60(2):141-8. doi: 10.3354/dao060141.

Abstract

Batrachochytrium dendrobatidis is a major pathogen of frogs worldwide, associated with declines in amphibian populations. Diagnosis of chytridiomycosis to date has largely relied upon histological and immunohistochemical examination of toe clips. This technique is invasive and insensitive particularly at early stages of infection when treatment may be possible. We have developed a real-time PCR Taqman assay that can accurately detect and quantify one zoospore in a diagnostic sample. This assay will assist the early detection of B. dendrobatidis in both captive and wild populations, with a high degree of sensitivity and specificity, thus facilitating treatment and protection of endangered populations, monitoring of pristine environments and preventing further global spread via amphibian trade.

摘要

蛙壶菌是全球青蛙的主要病原体,与两栖动物数量减少有关。迄今为止,蛙壶菌病的诊断主要依赖于对趾尖组织进行组织学和免疫组织化学检查。这种技术具有侵入性且不敏感,尤其是在感染早期(此时可能进行治疗)。我们开发了一种实时荧光定量PCR Taqman检测方法,该方法能够在诊断样本中准确检测和定量一个游动孢子。该检测方法将有助于在圈养和野生种群中早期检测蛙壶菌,具有高度的敏感性和特异性,从而便于对濒危种群进行治疗和保护、监测原始环境,并防止通过两栖动物贸易在全球范围内进一步传播。

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