Huggins Lucas G, Michaels Christopher J, Cruickshank Sheena M, Preziosi Richard F, Else Kathryn J
Faculty of Biology, Medicine and Health, University of Manchester, MAHSC, Manchester, United Kingdom.
Herpetology Section, ZSL London Zoo, London, United Kingdom.
PLoS One. 2017 Sep 21;12(9):e0185151. doi: 10.1371/journal.pone.0185151. eCollection 2017.
Anthropogenic disturbance via resource acquisition, habitat fragmentation and climate change, amongst other factors, has led to catastrophic global biodiversity losses and species extinctions at an accelerating rate. Amphibians are currently one of the worst affected classes with at least a third of species categorised as being threatened with extinction. At the same time, they are also critically important for many habitats and provide man with a powerful proxy for ecosystem health by acting as a bioindicator group. Whilst the causes of synchronised amphibian losses are varied recent research has begun to highlight a growing role that macroparasites are playing in amphibian declines. However, diagnosing parasite infection in the field can be problematic, principally relying on collection and euthanasia of hosts, followed by necropsy and morphological identification of parasites in situ. The current study developed a non-invasive PCR-based methodology for sensitive detection and identification of parasitic nematode DNA released in the faeces of infected amphibians as egg or tissue fragments (environmental DNA). A DNA extraction protocol optimised for liberation of DNA from resilient parasite eggs was developed alongside the design of a novel, nematode universal, degenerate primer pair, thus avoiding the difficulties of using species specific primers in situations where common parasite species are unknown. Used in conjunction this protocol and primer pair was tested on a wide range of faecal samples from captive and wild amphibians. The primers and protocol were validated and detected infections, including a Railletnema nematode infection in poison dart frogs from ZSL London Zoo and Mantella cowani frogs in the wild. Furthermore, we demonstrate the efficacy of our PCR-based protocol for detecting nematode infection in other hosts, such as the presence of pinworm (Aspiculuris) in two tortoise species and whipworm (Trichuris muris) in mice. Our environmental DNA approach mitigates problems associated with microscopic identification and can be applied to detect nematode parasitoses in wild and captive hosts for infection surveillance and maintenance of healthy populations.
通过资源获取、栖息地破碎化和气候变化等因素造成的人为干扰,以及其他因素,已导致全球生物多样性灾难性丧失,物种灭绝速度不断加快。两栖动物是目前受影响最严重的类群之一,至少三分之一的物种被归类为面临灭绝威胁。与此同时,它们对许多栖息地也至关重要,并且通过作为生物指示物种群体,为人类提供了一个衡量生态系统健康状况的有力指标。虽然两栖动物同步减少的原因多种多样,但最近的研究开始凸显大型寄生虫在两栖动物数量减少中所起的日益重要的作用。然而,在野外诊断寄生虫感染可能存在问题,主要依赖于宿主的采集和安乐死,随后进行尸体剖检并在原地对寄生虫进行形态学鉴定。本研究开发了一种基于非侵入性聚合酶链反应(PCR)的方法,用于灵敏检测和鉴定受感染两栖动物粪便中以卵或组织片段形式释放的寄生线虫DNA(环境DNA)。在设计一种新型的线虫通用简并引物对的同时,还开发了一种针对从有弹性的寄生虫卵中释放DNA进行优化的DNA提取方案,从而避免了在常见寄生虫种类未知的情况下使用物种特异性引物的困难。结合使用该方案和引物对,对来自圈养和野生两栖动物的各种粪便样本进行了测试。对引物和方案进行了验证,并检测到了感染情况,包括伦敦动物学会伦敦动物园的箭毒蛙和野生的曼氏彩蛙感染了雷氏线虫。此外,我们还证明了基于PCR的方案在检测其他宿主中的线虫感染方面的有效性,例如两种陆龟感染蛲虫(Aspiculuris)以及小鼠感染鞭虫(Trichuris muris)。我们的环境DNA方法减轻了与显微镜鉴定相关的问题,可用于检测野生和圈养宿主中的线虫寄生虫感染,以进行感染监测和维持健康种群。