Iqbal Z, Rikihisa Y
Department of Veterinary Pathobiology, Ohio State University, Columbus 43210.
Vet Microbiol. 1994 Dec;42(4):281-7. doi: 10.1016/0378-1135(94)90059-0.
Doxycycline treatment resulted in a carrier status in 3 dogs and complete clearance of Ehrlichia canis in 2 dogs (Iqbal and Rikihisa, 1994). Using specimens obtained during that study applicability of polymerase chain reactions (PCRs) in detecting E. canis DNA in tissue specimens and correlation of PCR results with our previous cell culture isolation results were evaluated. PCRs using a pair of primers specific to E. canis 16SrRNA gene sequence were used to detect DNA of E. canis in tissues of 5 experimentally-infected dogs 2 months after doxycycline treatment. An approximately 600 bp product defined by the specific primers was amplified in blood, kidney, lymph nodes, liver, and/or spleen of 3 dogs from which E. canis was reisolated in cell culture. In contrast, E. canis DNA was not detected in tissue or blood specimens of the 2 dogs from which E. canis was not reisolated after doxycycline treatment or in 2 control uninfected dogs. The findings indicate PCR is effective in detecting E. canis in tissues.
强力霉素治疗使3只犬呈携带状态,2只犬的犬埃立克体被完全清除(伊克巴尔和里基希萨,1994年)。利用该研究期间获得的标本,评估了聚合酶链反应(PCR)在检测组织标本中犬埃立克体DNA的适用性以及PCR结果与我们之前细胞培养分离结果的相关性。使用一对针对犬埃立克体16SrRNA基因序列的特异性引物进行PCR,以检测5只经强力霉素治疗2个月后的实验感染犬组织中的犬埃立克体DNA。在3只犬的血液、肾脏、淋巴结、肝脏和/或脾脏中扩增出由特异性引物界定的约600 bp产物,这3只犬的犬埃立克体在细胞培养中被重新分离出来。相比之下,在2只经强力霉素治疗后未重新分离出犬埃立克体的犬的组织或血液标本中,以及在2只未感染的对照犬中,均未检测到犬埃立克体DNA。这些发现表明PCR在检测组织中的犬埃立克体方面是有效的。