Patrelle Cécile, Jouet Damien, Lehrter Véronique, Ferté Hubert
EA4688 "Vecpar", UFR de Pharmacie, Université de Reims Champagne-Ardenne, 51 rue Cognacq-Jay, 51096 Reims Cedex, France.
EA4688 "Vecpar", UFR de Pharmacie, Université de Reims Champagne-Ardenne, 51 rue Cognacq-Jay, 51096 Reims Cedex, France.
Mol Biochem Parasitol. 2014 Sep;196(2):122-5. doi: 10.1016/j.molbiopara.2014.09.004. Epub 2014 Sep 26.
Twelve novel polymorphic microsatellite markers were produced and characterized for Spiculopteragia spiculoptera (Nematoda, Trichostrongyloidae) a common parasite of abomasum of Roe and Red deer, using next generation sequencing approach, and two multiplexes PCR were developed with these markers. Polymorphism of each locus was tested in 40 individuals of this species from diverse wild populations of cervids, and was tested for crossed-amplification on four other species of nematodes, close to S. spiculoptera among the Trichostrongyloidea: 20 Spiculopteragia houdemeri, 34 Ostertagia leptospicularis, 16 Ashworthius sidemi, and 25 Trichostrongylus spp. Our new microsatellite markers seem to be specific to Spiculopteragia spiculoptera since no amplifications were obtained for the four other species. The number of alleles per locus ranged from 2 to 12, the average observed and expected heterozygosity per locus ranged from 0.025 to 0.641 and from 0.049 to 0.664, respectively. Four of the 12 microsatellite loci showed significant deviations from Hardy-Weinberg equilibrium (which two slightly significant). One locus pair showed significant linkage disequilibrium (Sspi4 vs. Sspi8). Neither evidence of scoring error due to stuttering nor evidence of large allele dropout was found at all of the 12 loci, but evidence of null alleles was indicated at three loci because of general excess of homozygotes for most allele size classes. These polymorphic loci will be useful markers to study population genetics structure of Spiculopteragia spiculoptera in order to understand transfer and to explain the relationships between deer populations.
利用下一代测序方法,为梅花鹿和马鹿皱胃常见寄生虫——尖刺细颈线虫(线虫纲,毛圆科)开发并鉴定了12个新的多态性微卫星标记,并利用这些标记开发了两个多重PCR。在来自不同野生鹿类种群的40个该物种个体中测试了每个位点的多态性,并在毛圆总科中与尖刺细颈线虫亲缘关系较近的其他四种线虫上测试了交叉扩增情况:20条霍氏细颈线虫、34条细颈奥斯特线虫、16条西德艾氏线虫和25条毛圆属线虫。我们新的微卫星标记似乎对尖刺细颈线虫具有特异性,因为其他四种线虫均未获得扩增产物。每个位点的等位基因数量在2到12个之间,每个位点的平均观察杂合度和期望杂合度分别在0.025到0.641之间和0.049到0.664之间。12个微卫星位点中有4个显示出显著偏离哈迪 - 温伯格平衡(其中两个略有显著)。一对位点显示出显著的连锁不平衡(Sspi4与Sspi8)。在所有12个位点均未发现由于结巴导致的评分错误证据,也未发现大等位基因缺失的证据,但由于大多数等位基因大小类别的纯合子普遍过量,在三个位点表明存在无效等位基因的证据。这些多态性位点将成为研究尖刺细颈线虫种群遗传结构的有用标记,以便了解其传播并解释鹿群之间的关系。