Liddell Allison M, Stockham Steven L, Scott Michael A, Sumner John W, Paddock Christopher D, Gaudreault-Keener Monique, Arens Max Q, Storch Gregory A
Department of Internal Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
J Clin Microbiol. 2003 Oct;41(10):4617-22. doi: 10.1128/JCM.41.10.4617-4622.2003.
To investigate the species distribution of Ehrlichia present in Missouri dogs, we tested 78 dogs suspected of having acute ehrlichiosis and 10 healthy dogs. Blood from each dog was screened with a broad-range 16S rRNA gene PCR assay that detects known pathogenic species of Ehrlichia and ANAPLASMA: The species was determined by using species-specific PCR assays and nucleotide sequencing. Ehrlichia antibody testing was performed by using an indirect immunofluorescence assay with Ehrlichia chaffeensis as the antigenic substrate. The broad-range assay detected Ehrlichia or Anaplasma DNA in 20 (26%) of the symptomatic dogs and 2 (20%) of the asymptomatic dogs. E. ewingii accounted for 20 (91%), and E. chaffeensis accounted for 1 (5%) of the positives. Anaplasma phagocytophilum DNA was detected in one dog, and the sequences of regions of the 16S rRNA gene and the groESL operon amplified from the blood of this dog matched the published sequences of this organism. Antibodies reactive with E. chaffeensis were detected in 14 (67%) of the 21 PCR-positive dogs and in 12 (19%) of the 64 PCR-negative dogs. Combining the results of PCR and serology indicated that 33 (39%) of 85 evaluable dogs had evidence of past or current Ehrlichia infection. We conclude that E. ewingii is the predominant etiologic agent of canine ehrlichiosis in the areas of Missouri included in this survey. E. canis, a widely recognized agent of canine ehrlichiosis, was not detected in any animal. The finding of E. ewingii in asymptomatic dogs suggests that dogs could be a reservoir for this Ehrlichia species.
为调查密苏里州犬只中埃立克体的种类分布,我们检测了78只疑似患有急性埃立克体病的犬只和10只健康犬只。每只犬的血液通过一种检测埃立克体和无形体已知致病种类的广谱16S rRNA基因PCR检测法进行筛查:通过使用种特异性PCR检测法和核苷酸测序来确定种类。采用以恰菲埃立克体作为抗原底物的间接免疫荧光检测法进行埃立克体抗体检测。广谱检测法在20只(26%)有症状犬只和2只(20%)无症状犬只中检测到了埃立克体或无形体DNA。尤因埃立克体占阳性的20只(91%),恰菲埃立克体占1只(5%)。在一只犬中检测到嗜吞噬细胞无形体DNA,从这只犬血液中扩增的16S rRNA基因区域和groESL操纵子的序列与该生物体已发表的序列匹配。在21只PCR阳性犬中的14只(67%)以及64只PCR阴性犬中的12只(19%)检测到了与恰菲埃立克体反应的抗体。将PCR和血清学结果相结合表明,85只可评估犬中有33只(39%)有既往或当前埃立克体感染的证据。我们得出结论,在本次调查涵盖的密苏里州地区,尤因埃立克体是犬埃立克体病的主要病原体。犬埃立克体病一种广泛认可的病原体犬埃立克体,在任何动物中均未检测到。在无症状犬中发现尤因埃立克体表明犬可能是这种埃立克体的宿主。