Mahan S M, Simbi B H, Burridge M J
UF/USAID/SADC Heartwater Research Project, Central Veterinary Research and Diagnostic Laboratory, P.O. Box CY 551, Causeway, Harare, Zimbabwe.
Onderstepoort J Vet Res. 2004 Jun;71(2):99-105. doi: 10.4102/ojvr.v71i2.271.
White-tailed deer are susceptible to heartwater (Ehrlichia [Cowdria] ruminantium infection) and are likely to suffer high mortality if the disease spreads to the United States. It is vital, therefore, to validate a highly specific and sensitive detection method for E. ruminantium infection that can be reliably used in testing white-tailed deer, which are reservoirs of antigenically or genetically related agents such as Ehrlichia chaffeensis, Anaplasma (Ehrlichia) phagocytophilum (HGE agent) and Ehrlichia ewingii. Recently, a novel but as yet unnamed ehrlichial species, the white-tailed deer ehrlichia (WTDE), has been discovered in deer populations in the United States. Although the significance of WTDE as a pathogen is unknown at present, it can be distinguished from other Ehrlichia spp. based on 16S rRNA gene sequence analysis. In this study it was differentiated from E. ruminantium by the use of the pCS20 PCR assay which has high specificity and sensitivity for the detection of E. ruminantium. This assay did not amplify DNA from the WTDE DNA samples isolated from deer resident in Florida, Georgia and Missouri, but amplified the specific 279 bp fragment from E. ruminantium DNA. The specificity of the pCS20 PCR assay for E. ruminantium was confirmed by Southern hybridization. Similarly, the 16S PCR primers (nested) that amplify a specific 405-412 bp fragment from the WTDE DNA samples, did not amplify any product from E. ruminantium DNA. This result demonstrates that it would be possible to differentiate between E. ruminantium and the novel WTDE agent found in white tailed deer by applying the two respective PCR assays followed by Southern hybridizations. Since the pCS20 PCR assay also does not amplify any DNA products from E. chaffeensis or Ehrlichia canis DNA, it is therefore the method of choice for the detection of E. ruminantium in these deer and other animal hosts.
白尾鹿易感染心水病(反刍动物埃立克体[考德里体]感染),如果该病传播到美国,它们很可能会遭受高死亡率。因此,至关重要的是要验证一种高度特异性和敏感性的反刍动物埃立克体感染检测方法,该方法能够可靠地用于检测白尾鹿,白尾鹿是诸如恰菲埃立克体、嗜吞噬细胞无形体(人粒细胞埃立克体病病原体)和尤因埃立克体等抗原或基因相关病原体的储存宿主。最近,在美国的鹿群中发现了一种新的但尚未命名的埃立克体物种,即白尾鹿埃立克体(WTDE)。尽管目前WTDE作为病原体的重要性尚不清楚,但基于16S rRNA基因序列分析,它可以与其他埃立克体属物种区分开来。在本研究中,通过使用对反刍动物埃立克体检测具有高特异性和敏感性的pCS20 PCR检测法,将其与反刍动物埃立克体区分开来。该检测法未扩增从佛罗里达州、佐治亚州和密苏里州的鹿中分离的WTDE DNA样本中的DNA,但从反刍动物埃立克体DNA中扩增出了特定的279 bp片段。通过Southern杂交证实了pCS20 PCR检测法对反刍动物埃立克体的特异性。同样,从WTDE DNA样本中扩增出特定405 - 412 bp片段的16S PCR引物(巢式),未从反刍动物埃立克体DNA中扩增出任何产物。这一结果表明,通过应用两种各自的PCR检测法并随后进行Southern杂交,有可能区分反刍动物埃立克体和在白尾鹿中发现的新型WTDE病原体。由于pCS20 PCR检测法也未从恰菲埃立克体或犬埃立克体DNA中扩增出任何DNA产物,因此它是在这些鹿和其他动物宿主中检测反刍动物埃立克体的首选方法。