Departamento de Parasitologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brasil.
Transbound Emerg Dis. 2012 Aug;59(4):353-60. doi: 10.1111/j.1865-1682.2011.01278.x. Epub 2011 Dec 4.
Deer are important natural reservoir hosts of Anaplasmataceae. The present study used nested PCR and nucleotide sequencing to evaluate the occurrence of Anaplasmataceae species in 23 free-living and six captive specimens of the cervids Mazama gouazoubira and Blastocerus dichotomus in Minas Gerais State, Brazil. Blood samples were tested for the presence of Ehrlichia and Anaplasma spp. using nPCR assays and sequencing of the msp4, msp1 and 16S rRNA genes. The identity of each sequence was confirmed by comparison with sequences available from GenBank using BLAST software. Of the animals investigated, 93.1% (27/29) were infected with haemoparasites including Anaplasma marginale (79.3%), Ehrlichia chaffeensis (3.4%), Anaplasma bovis (3.4%) and Anaplasma spp. (assigned to A. platys and A. phagocytophilum) (17.2%). Co-infection occurred in 20% (6/29) of the deer examined. Four (13.8%) were infected with A. marginale and Anaplasma sp., one (3.4%) was infected with A. marginale and E. chaffeensis, and one (3.4%) was infected with A. marginale and A. bovis. The results of the present study suggest that cross-protection does not occur in these deer. Immunological cross-reaction occurs when sera are tested diagnostically because these bacteria are closely related taxonomically, reinforcing the importance of molecular diagnosis followed by nucleotide sequencing.
鹿是安巴氏菌科的重要自然储主。本研究采用巢式 PCR 和核苷酸测序评估了巴西米纳斯吉拉斯州 23 只自由生活和 6 只圈养的马泽马·古泽比拉鹿和白尾鹿中安巴氏菌科物种的发生情况。使用 nPCR 检测和 msp4、msp1 和 16S rRNA 基因测序检测血样中是否存在埃立克体和安巴氏体。通过使用 BLAST 软件将每个序列与 GenBank 中可用的序列进行比较,确认每个序列的身份。在所研究的动物中,93.1%(27/29)感染了血液寄生虫,包括边缘无浆体(79.3%)、恰菲埃立克体(3.4%)、牛无浆体(3.4%)和安巴氏体(归为 A. platys 和 A. phagocytophilum)(17.2%)。20%(6/29)检查的鹿发生了共感染。4 只(13.8%)感染了边缘无浆体和安巴氏体,1 只(3.4%)感染了边缘无浆体和恰菲埃立克体,1 只(3.4%)感染了边缘无浆体和牛无浆体。本研究结果表明,这些鹿不会发生交叉保护。当血清进行诊断性检测时会发生免疫交叉反应,因为这些细菌在分类上密切相关,这强化了分子诊断后进行核苷酸测序的重要性。