Gajadhar A, Steeves-Gurnsey T, Kendall J, Lankester M, Stéen M
Centre for Animal Parasitology, Health of Animals Laboratory, Canadian Food Inspection Agency, Saskatoon, Saskatchewan.
J Wildl Dis. 2000 Oct;36(4):713-22. doi: 10.7589/0090-3558-36.4.713.
Molecular genetics was used to devise the first reliable diagnostic tool for differentiating morphologically indistinguishable dorsal-spined, first-stage larvae (L1's) and other stages of the nematode protostrongylid subfamily Elaphostrongylinae. A polymerase chain reaction (PCR) assay employing specifically designed primers was developed to selectively amplify DNA of the ITS-2 region of the ribosomal gene. Amplification of the entire ITS-2 region differentiated between larvae of the genera Elaphostrongylus and Parelaphostrongylus, based on the lengths of fragments produced. Three sets of primers were designed and used successfully to distinguish larvae at the species level. Although it was demonstrated that one primer set in a single PCR assay was capable of distinguishing each of the three Parelaphostrongylus spp., a second primer set would be required for confirmation in routine diagnostic use. Two of the three primer sets were capable of amplifying DNA from all six elaphostrongyline species and of identifying Elaphostrongylus alces and Parelaphostrongylus odocoilei. Although two separate fragments were produced from each Elaphostrongylus cervi and Elaphostrongylus rangiferi, it was not possible to distinguish these two parasites from each other based on the fragment size. The use of various nematodes, hosts, and fecal controls demonstrated the reliability of the primers for all developmental stages including L1's, third-stage larvae, and adult worms. These primers also have potential for identifying other lungworms as was shown by the amplification of Umingmakstrongylus pallikuukensis, the muskox protostrongylid, and Dictyocaulus sp. from white-tailed deer. Although this assay may benefit from further refinement, its present design provides researchers, wildlife managers, clinicians, and animal health regulators with a practical tool for the control, management, and study of meningeal and tissue worms and their close relatives.
分子遗传学被用于设计首个可靠的诊断工具,以区分形态上难以辨别的具背刺第一期幼虫(L1)和线虫原圆科后圆亚科其他阶段的幼虫。开发了一种使用专门设计引物的聚合酶链反应(PCR)检测方法,以选择性扩增核糖体基因ITS-2区域的DNA。基于产生的片段长度,整个ITS-2区域的扩增区分了后圆属和拟后圆属的幼虫。设计了三组引物并成功用于在种水平上区分幼虫。尽管已证明在单个PCR检测中一组引物能够区分三种拟后圆属物种中的每一种,但在常规诊断应用中仍需要第二组引物进行确认。三组引物中的两组能够扩增所有六种后圆线虫物种的DNA,并识别出麂后圆线虫和驯鹿拟后圆线虫。虽然从每只鹿后圆线虫和驯鹿后圆线虫都产生了两个单独的片段,但基于片段大小无法区分这两种寄生虫。使用各种线虫、宿主和粪便对照证明了这些引物对包括L1、第三期幼虫和成虫在内的所有发育阶段的可靠性。这些引物也有识别其他肺线虫的潜力,如从白尾鹿中扩增出的麝牛原圆线虫和网尾线虫属所示。尽管该检测方法可能需要进一步完善,但其目前的设计为研究人员、野生动物管理者、临床医生和动物健康监管者提供了一个用于控制、管理和研究脑膜虫和组织虫及其近缘种的实用工具。