Bohuski Elizabeth, Lorch Jeffrey M, Griffin Kathryn M, Blehert David S
United States Geological Survey, National Wildlife Health Center, Madison, WI, USA.
Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, WI, USA.
BMC Vet Res. 2015 Apr 15;11:95. doi: 10.1186/s12917-015-0407-8.
Fungal skin infections associated with Ophidiomyces ophiodiicola, a member of the Chrysosporium anamorph of Nannizziopsis vriesii (CANV) complex, have been linked to an increasing number of cases of snake fungal disease (SFD) in captive snakes around the world and in wild snake populations in eastern North America. The emergence of SFD in both captive and wild situations has led to an increased need for tools to better diagnose and study the disease.
We developed two TaqMan real-time polymerase chain reaction (PCR) assays to rapidly detect O. ophiodiicola in clinical samples. One assay targets the internal transcribed spacer region (ITS) of the fungal genome while the other targets the more variable intergenic spacer region (IGS). The PCR assays were qualified using skin samples collected from 50 snakes for which O. ophiodiicola had been previously detected by culture, 20 snakes with gross skin lesions suggestive of SFD but which were culture-negative for O. ophiodiicola, and 16 snakes with no clinical signs of infection. Both assays performed equivalently and proved to be more sensitive than traditional culture methods, detecting O. ophiodiicola in 98% of the culture-positive samples and in 40% of the culture-negative snakes that had clinical signs of SFD. In addition, the assays did not cross-react with a panel of 28 fungal species that are closely related to O. ophiodiicola or that commonly occur on the skin of snakes. The assays did, however, indicate that some asymptomatic snakes (~6%) may harbor low levels of the fungus, and that PCR should be paired with histology when a definitive diagnosis is required.
These assays represent the first published methods to detect O. ophiodiicola by real-time PCR. The ITS assay has great utility for assisting with SFD diagnoses whereas the IGS assay offers a valuable tool for research-based applications.
与奥氏蛇菌(Ophidiomyces ophiodiicola)相关的皮肤真菌感染,奥氏蛇菌是弗里西拟南芥金黄变种(Nannizziopsis vriesii)无性型(CANV)复合体的成员,与世界各地圈养蛇以及北美东部野生蛇种群中越来越多的蛇真菌病(SFD)病例有关。圈养和野生环境中SFD的出现导致对更好地诊断和研究该疾病的工具的需求增加。
我们开发了两种TaqMan实时聚合酶链反应(PCR)检测方法,以快速检测临床样本中的奥氏蛇菌。一种检测方法针对真菌基因组的内部转录间隔区(ITS),而另一种针对变化更大的基因间隔区(IGS)。使用从50条蛇采集的皮肤样本对PCR检测方法进行验证,这些蛇之前通过培养检测出奥氏蛇菌;20条蛇有明显的皮肤病变提示患有SFD,但奥氏蛇菌培养呈阴性;以及16条没有感染临床症状的蛇。两种检测方法表现相当,且比传统培养方法更敏感,在98%的培养阳性样本以及40%有SFD临床症状但培养阴性的蛇中检测到奥氏蛇菌。此外,这些检测方法与一组28种与奥氏蛇菌密切相关或常见于蛇皮肤的真菌物种没有交叉反应。然而,这些检测方法表明一些无症状的蛇(约6%)可能携带低水平的真菌,并且在需要明确诊断时,PCR应与组织学检查相结合。
这些检测方法是首次发表的通过实时PCR检测奥氏蛇菌的方法。ITS检测方法在辅助SFD诊断方面有很大用途,而IGS检测方法为基于研究的应用提供了有价值的工具。