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线虫感染的微孢子虫的分离与鉴定。

Isolation and Identification of Nematode-Infecting Microsporidia.

机构信息

Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada.

出版信息

Curr Protoc. 2024 May;4(5):e1035. doi: 10.1002/cpz1.1035.

DOI:10.1002/cpz1.1035
PMID:38727641
Abstract

Nematodes are naturally infected by the fungal-related pathogen microsporidia. These ubiquitous eukaryotic parasites are poorly understood, despite infecting most types of animals. Identifying novel species of microsporidia and studying them in an animal model can expedite our understanding of their infection biology and evolution. Nematodes present an excellent avenue for pursuing such work, as they are abundant in the environment and many species are easily culturable in the laboratory. The protocols presented here describe how to isolate bacterivorous nematodes from rotting substrates, screen them for microsporidia infection, and molecularly identify the nematode and microsporidia species. Additionally, we detail how to remove environmental contaminants and generate a spore preparation of microsporidia from infected samples. We also discuss potential pitfalls and provide suggestions on how to mitigate them. These protocols allow for the identification of novel microsporidia species, which can serve as an excellent starting point for genomic analysis, determination of host specificity, and infection characterization. © 2024 The Authors. Current Protocols published by Wiley Periodicals LLC. Basic Protocol 1: Gathering samples Support Protocol 1: Generating 10× and 40× Escherichia coli OP50 and seeding NGM plates Basic Protocol 2: Microsporidia screening, testing for Caenorhabditis elegans susceptibility, and sample freezing Basic Protocol 3: DNA extraction, PCR amplification, and sequencing to identify nematode and microsporidia species Basic Protocol 4: Removal of contaminating microbes and preparation of microsporidia spores Support Protocol 2: Bleach-synchronizing nematodes.

摘要

线虫自然感染真菌相关病原体微孢子虫。这些无处不在的真核寄生虫尽管感染了大多数类型的动物,但仍未被充分了解。鉴定新的微孢子虫物种并在动物模型中研究它们,可以加速我们对其感染生物学和进化的理解。线虫提供了一个很好的研究途径,因为它们在环境中非常丰富,而且许多物种在实验室中很容易培养。这里介绍的方案描述了如何从腐烂的基质中分离食细菌线虫,筛选它们是否感染微孢子虫,并通过分子鉴定线虫和微孢子虫的物种。此外,我们详细介绍了如何去除环境污染物,并从感染样本中生成微孢子虫的孢子制备物。我们还讨论了潜在的陷阱,并提供了如何减轻这些陷阱的建议。这些方案可用于鉴定新的微孢子虫物种,这可以作为基因组分析、宿主特异性确定和感染特征描述的良好起点。© 2024 作者。Wiley Periodicals LLC 出版的《当代协议》。基本方案 1:收集样本支持方案 1:生成 10×和 40×大肠杆菌 OP50 并接种 NGM 平板基本方案 2:微孢子虫筛选、测试秀丽隐杆线虫的敏感性以及样本冷冻基本方案 3:DNA 提取、PCR 扩增和测序以鉴定线虫和微孢子虫的物种基本方案 4:去除污染微生物和制备微孢子虫孢子支持方案 2:漂白同步线虫。

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