Wildlife Epidemiology Lab, College of Veterinary Medicine, University of Illinois at Urbana-Champaign, 2001 S Lincoln Ave., Urbana, Illinois 61802, USA.
Franz Theodore Stone Laboratory, Ohio State University, 878 Bayview Ave., Put-in-Bay, Ohio 43456, USA.
J Wildl Dis. 2021 Apr 1;57(2):380-385. doi: 10.7589/JWD-D-20-00013.
Ophidiomycosis, commonly called snake fungal disease, has been linked to significant morbidity of free-ranging snakes in North America and Europe. Diagnosis of ophidiomycosis currently requires detection of skin lesions via physical exam or characteristic histopathology as well as detection of the causative agent, Ophidiomyces ophidiicola, through quantitative (q)PCR or fungal culture of a skin swab or tissue sample. While reliable, these methods require specialized training, invasive procedures (e.g., biopsy), and several days or weeks to receive results. Additionally, screening entire populations can quickly become costly. A fast, easy-to-use, cost-efficient, and sensitive screening tool is needed to optimize conservation strategies and treatment intervention. Our objective was to investigate the association between skin fluorescence under long-wave ultraviolet (UV) light (365 nm) and the detection of Ophidiomyces ophidiicola DNA using qPCR. Fifty-eight Lake Erie watersnakes (Nerodia sipedon insularum) collected in June of 2018 and 2019 from islands in western Lake Erie, Ottawa County, Ohio, US were visually inspected for skin lesions, photographed under natural light and UV light, and swabbed for qPCR analysis. Fluorescence was highly associated with the presence of skin lesions, and the presence of at least one fluorescent skin lesion was 86% sensitive and 100% specific for identifying animals with apparent ophidiomycosis, with a positive predictive value of 100%. While we recommend performing standard diagnostics along with fluorescence, our study supports the use of visual UV fluorescence identification as a preliminary, affordable, noninvasive, and field-applicable method to screen populations for ophidiomycosis.
蛇真菌病,俗称蛇曲霉病,与北美的自由放养蛇的高发病率有关。目前,蛇曲霉病的诊断需要通过体格检查或特征性组织病理学检查来检测皮肤损伤,以及通过定量(q)PCR 或皮肤拭子或组织样本的真菌培养来检测病原体蛇曲霉。虽然可靠,但这些方法需要专门的培训、侵入性程序(例如活检),并且需要数天或数周才能得到结果。此外,对整个群体进行筛查很快就会变得昂贵。需要一种快速、易于使用、具有成本效益且敏感的筛选工具,以优化保护策略和治疗干预措施。我们的目标是研究长波紫外线(UV)下皮肤荧光(365nm)与 qPCR 检测蛇曲霉 DNA 之间的关联。2018 年和 2019 年 6 月,从美国俄亥俄州奥塔瓦县西部伊利湖的岛屿上收集了 58 条伊利湖水蛇(Nerodia sipedon insularum),对它们进行了皮肤病变的目视检查、自然光和紫外线下的拍照,并进行了 qPCR 分析。荧光与皮肤病变的存在高度相关,至少有一个荧光皮肤病变的存在对识别明显患有蛇曲霉病的动物的敏感性为 86%,特异性为 100%,阳性预测值为 100%。虽然我们建议同时进行标准诊断,但我们的研究支持将视觉 UV 荧光识别作为一种初步的、经济实惠的、非侵入性的和适用于现场的方法,用于筛查蛇曲霉病的人群。