Sreedharan Gayathri, Singh Panwar Yashwant, Murthy Saketh, Klop-Toker Kaya, Ibáñez Roberto, Illueca Estefany E, Webb Rebecca, Govindappa Venu, Subba Barkha, Segu Harika, Kumar Komanduri Krishna Pavan, Vasudevan Karthikeyan
CSIR-Centre for Cellular and Molecular Biology, Hyderabad, India.
School of Environmental and Life Sciences, University of Newcastle, Australia.
Transbound Emerg Dis. 2023 Apr 30;2023:9980566. doi: 10.1155/2023/9980566. eCollection 2023.
Chytridiomycosis is an infectious disease in amphibians caused by two chytrid fungi, () and (), and is the worst infectious disease known in wildlife so far. Worldwide spread of the disease has caused unprecedented loss of global amphibian diversity. Although some lineages of are enzootic and are not as deadly as the pandemic lineage, nearly 40% of amphibian species are still declining globally due to chytridiomycosis. Efficient surveillance and monitoring of chytridiomycosis are the immediate safeguard against rapid declines or extinctions of amphibian populations. Previous studies showed that existing diagnostic assays were not sensitive to certain haplotypes like those from Korea, China, India, Japan, and Brazil and thereby, there is a need for a universal, sensitive, specific, reproducible, and affordable diagnostic assay. We designed a one-step SYBR green-based quantitative polymerase chain reaction (nSYBR qPCR) for robust detection of It amplifies an 82 base-pair segment between the 5.8S rRNA and ITS2 of the genome. The primer pair was tested on 40 isolates from four known lineages. Using skin swab samples of wild amphibians and cultured zoospores from Australia and Panama, we compared the clinical specificity and sensitivity of the newly described primers to the existing TaqMan-based qPCR assay. From India, we used samples which had been previously tested with Nested PCR to validate the new primer pairs. The newly described primer pair was then tested on swab samples from Anura, Caudata and Gymnophiona from India. We report widespread chytridiomycosis with varying infection loads on them. The new assay showed comparable efficiency to the TaqMan-based qPCR assay. This diagnostic assay can facilitate widespread surveillance of chytridiomycosis where it has been previously absent, which may reveal several reservoirs of the pathogen and can improve our understanding of this important wildlife disease.
蛙壶菌病是一种由两种壶菌真菌,即蛙壶菌(Batrachochytrium dendrobatidis,Bd)和新几内亚蛙壶菌(Batrachochytrium salamandrivorans,Bsal)引起的两栖动物传染病,是迄今为止已知的野生动物中最严重的传染病。该疾病在全球范围内的传播已导致全球两栖动物多样性遭受前所未有的损失。尽管蛙壶菌的一些谱系是地方性的,不像大流行谱系那样致命,但由于蛙壶菌病,全球近40%的两栖动物物种仍在减少。对蛙壶菌病进行有效的监测是防止两栖动物种群迅速减少或灭绝的当务之急。先前的研究表明,现有的诊断检测方法对某些蛙壶菌单倍型不敏感,如来自韩国、中国、印度、日本和巴西的单倍型,因此,需要一种通用、灵敏、特异、可重复且经济实惠的诊断检测方法。我们设计了一种基于SYBR Green的一步法定量聚合酶链反应(nSYBR qPCR),用于可靠地检测蛙壶菌。它扩增蛙壶菌基因组5.8S rRNA和ITS2之间的一个82个碱基对的片段。该引物对在来自四个已知蛙壶菌谱系的40个分离株上进行了测试。我们使用来自澳大利亚和巴拿马的野生两栖动物的皮肤拭子样本以及培养的游动孢子,将新描述的引物的临床特异性和灵敏度与现有的基于TaqMan的qPCR检测方法进行了比较。我们使用了之前用巢式PCR检测过的来自印度的样本,以验证新的引物对。然后,在来自印度的无尾目、有尾目和蚓螈目的拭子样本上对新描述的引物对进行了测试。我们报告了这些样本上存在感染负荷不同的广泛的蛙壶菌病。新检测方法显示出与基于TaqMan的qPCR检测方法相当的效率。这种诊断检测方法可以促进在以前没有蛙壶菌病的地区进行广泛监测,这可能会揭示该病原体的几个储存宿主,并能增进我们对这种重要的野生动物疾病的了解。