Centers for Disease Control and Prevention, Fort Collins, CO, USA.
Am J Trop Med Hyg. 2012 Aug;87(2):319-26. doi: 10.4269/ajtmh.2012.11-0555.
Small mammals from the Democratic Republic (DR) of the Congo and Tanzania were tested to determine the prevalence and genetic diversity of Bartonella species. The presence of Bartonella DNA was assessed in spleen samples of the animals by rpoB- and gltA-polymerase chain reactions (PCRs). By rpoB-PCR, Bartonella was detected in 8 of 59 animals of DR Congo and in 16 of 39 Tanzanian animals. By gltA-PCR, Bartonella was detected in 5 and 15 animals of DR Congo and Tanzania, respectively. The gene sequences from Arvicanthis neumanni were closely related to Bartonella elizabethae. The genotypes from Lophuromys spp. and from Praomys delectorum were close to Bartonella tribocorum. Five genogroups were not genetically related to any known Bartonella species. These results suggest the need to conduct further studies to establish the zoonotic risks linked with those Bartonella species and, in particular, to verify whether these agents might be responsible for human cases of febrile illness of unknown etiology in Africa.
来自刚果民主共和国和坦桑尼亚的小型哺乳动物被检测,以确定巴尔通体物种的流行率和遗传多样性。通过 rpoB-和 gltA-聚合酶链反应(PCR)评估动物脾脏样本中巴尔通体 DNA 的存在情况。通过 rpoB-PCR,在刚果民主共和国的 59 只动物中有 8 只和坦桑尼亚的 39 只动物中有 16 只检测到巴尔通体。通过 gltA-PCR,在刚果民主共和国和坦桑尼亚的 5 只和 15 只动物中分别检测到了巴尔通体。来自 Arvicanthis neumanni 的基因序列与 Bartonella elizabethae 密切相关。来自 Lophuromys spp. 和 Praomys delectorum 的基因型与 Bartonella tribocorum 接近。有 5 个基因型组与任何已知的巴尔通体物种没有遗传关系。这些结果表明需要进一步研究,以确定与这些巴尔通体物种相关的动物源性风险,特别是要验证这些病原体是否可能导致非洲不明病因的发热性疾病的人类病例。