University of Edinburgh, Royal (Dick) School of Veterinary Studies, Easter Bush Veterinary Centre, Roslin, Midlothian EH25 9RG, United Kingdom.
Department of Comparative Biology and Experimental Medicine, Faculty of Veterinary Medicine, University of Calgary, Calgary, Alberta T2N 4N1, Canada.
Int J Parasitol. 2018 Feb;48(2):159-165. doi: 10.1016/j.ijpara.2017.08.010. Epub 2017 Oct 27.
Parasitic nematode species have extremely high levels of genetic diversity, presenting a number of experimental challenges for genomic and genetic work. Consequently, there is a need to develop inbred laboratory strains with reduced levels of polymorphism. The most efficient approach to inbred line development is single pair mating, but this is challenging for obligate parasites where the adult sexual reproductive stages are inside the host, and thus difficult to experimentally manipulate. This paper describes a successful approach to single pair mating of a parasitic nematode, Haemonchus contortus. The method allows for polyandrous mating behaviour and involves the surgical transplantation of a single adult male worm with multiple immature adult females directly into the sheep abomasum. We used a panel of microsatellite markers to monitor and validate the single pair mating crosses and to ensure that the genotypes of progeny and subsequent filial generations were consistent with those expected from a mating between a single female parent of known genotype and a single male parent of unknown genotype. We have established two inbred lines that both show a significant overall reduction in genetic diversity based on microsatellite genotyping and genome-wide single nucleotide polymorphism. There was an approximately 50% reduction in heterozygous SNP sites across the genome in the MHco3.N1 line compared with the MoHco3(ISE) parental strain. The MHco3.N1 inbred line has subsequently been used to provide DNA template for whole genome sequencing of H. contortus. This work provides proof of concept and methodologies for forward genetic analysis of obligate parasitic nematodes.
寄生线虫物种具有极高的遗传多样性,这给基因组学和遗传学研究带来了许多实验挑战。因此,需要开发遗传背景一致、多态性降低的近交系实验室品系。最有效的近交系培育方法是单对交配,但对于成年性生殖阶段在宿主体内的专性寄生虫来说,这种方法具有挑战性,难以进行实验操作。本文描述了一种成功的单对交配方法,用于寄生线虫旋毛虫。该方法允许多雄交配行为,并涉及将单个成年雄性蠕虫与多个未成熟的成年雌性蠕虫直接移植到绵羊皱胃中。我们使用了一组微卫星标记来监测和验证单对交配,并确保后代和随后的后代的基因型与已知基因型的单个雌性亲本与未知基因型的单个雄性亲本之间的交配所预期的基因型一致。我们已经建立了两个近交系,它们的遗传多样性都显著降低,这是基于微卫星基因分型和全基因组单核苷酸多态性。与亲本菌株 MoHco3(ISE)相比,MHco3.N1 系基因组中杂合 SNP 位点减少了约 50%。随后,MHco3.N1 近交系被用于提供旋毛虫全基因组测序的 DNA 模板。这项工作为专性寄生线虫的正向遗传分析提供了概念证明和方法。