Laboratório de Imunoparasitologia, Departamento de Patologia, Reprodução e Saúde Única, Faculdade de Ciências Agrárias e Veterinárias, Universidade Estadual "Júlio de Mesquita Filho" (FCAV/UNESP), Jaboticabal, Brazil.
Department of Veterinary Surgery, School of Veterinary Medicine, Federal University of Uberlândia, Uberlândia, Minas Gerais, Brazil.
Acta Trop. 2021 Oct;222:106037. doi: 10.1016/j.actatropica.2021.106037. Epub 2021 Jul 3.
Bartonella henselae is the causative agent for the infectious disease Cat Scratch Disease (CSD), which can be fatal. Domestic and wild felines are known to be its main mammal reservoirs. The present study aimed to investigate the occurrence and genetic diversity of Bartonella spp. in cats sampled in São Paulo (SP) and Minas Gerais (MG) States, Southeastern Brazil. Based on a quantitative real-time PCR (qPCR) assay, a Bartonella sp. nuoG gene fragment was detected in 39.9% (122/306) of the blood samples (46/151 cats of SP; 76/155 cats of MG). The blood samples were submitted to a pre-enrichment culture technique that allowed the detection of 12 additional positive samples, which showed to be negative in the qPCR using DNA blood samples as templates. Furthermore, five B. henselae isolates were obtained from qPCR-negative samples for both blood and pre-enrichment culture. Seven out of 24 Ctenocephalides felis fleas were positive for Bartonella spp. in the qPCR assay; 4/7 positive fleas were collected from Bartonella-negative cats. Twenty-three rpoB B. henselae cloned sequences were obtained from nine cats' blood samples, showing the occurrence of 13 different genotypes. Median-joining network and SplitsTree distance analysis showed that the obtained sequences represented distinct B. henselae genotypes when compared to those previously deposited in GenBank. Intra-host diversity was found, since different rpoB genotypes of B. henselae were detected in individual single cats. Bartonella henselae isolates showed two allelic profiles (ST37 in cats from MG state and ST9 in SP state) by MLST (Multilocus Sequence Typing) based on sequencing of eight molecular markers. The present study is the first molecular report of Bartonella sp. in cats from Minas Gerais State. In summary, this body of work showed the occurrence of different B. henselae rpoB genotypes at an intra-reservoir host level. Based on qPCR from blood samples and pre-enrichment liquid culture and isolation, occurrence of 33.1% (50/151) and 56.8% (88/155) for Bartonella sp. was found in cats from SP and MG states, respectively. Two different allelic profiles of B. henselae were found in cats from the states of São Paulo (ST9) and Minas Gerais (ST37), suggesting a clonal evolution of Bartonellae in a certain geographical region.
汉赛巴尔通体是猫抓病(CSD)这一传染性疾病的病原体,该病可能致命。家养和野生猫科动物被认为是其主要哺乳动物宿主。本研究旨在调查巴通体在巴西东南部圣保罗州(SP)和米纳斯吉拉斯州(MG)猫群中的发生情况和遗传多样性。基于实时荧光定量 PCR(qPCR)检测,在 306 份血液样本(SP 地区 151 只猫中 46 份;MG 地区 155 只猫中 76 份)中检测到巴通体 nuoG 基因片段。对这些血液样本进行预增菌培养技术处理,检测到另外 12 个阳性样本,而这些样本使用 DNA 血液样本作为模板进行 qPCR 时呈阴性。此外,从 qPCR 阴性的血液和预增菌培养样本中获得了 5 株汉赛巴尔通体分离株。在 qPCR 检测中,24 只猫栉首蚤中有 7 只跳蚤呈巴通体阳性;7 只阳性跳蚤均采集自巴通体阴性的猫。从 9 只猫的血液样本中获得了 23 个汉赛巴尔通体 rpoB 克隆序列,显示出 13 种不同基因型。中值连接网络和 SplitsTree 距离分析显示,与先前在 GenBank 中登记的序列相比,获得的序列代表了不同的汉赛巴尔通体基因型。由于在单个猫体内检测到不同的汉赛巴尔通体 rpoB 基因型,因此存在宿主内多样性。汉赛巴尔通体分离株通过基于 8 个分子标记的 MLST(多位点序列分型)显示出两种等位基因谱(MG 州的猫为 ST37,SP 州的猫为 ST9)。本研究首次报道了米纳斯吉拉斯州猫中存在巴通体。总之,本研究在宿主水平上显示了不同汉赛巴尔通体 rpoB 基因型的存在。基于血液样本的 qPCR、预增菌液体培养和分离,分别在 SP 州和 MG 州的猫中发现巴通体的检出率为 33.1%(50/151)和 56.8%(88/155)。在来自圣保罗州(ST9)和米纳斯吉拉斯州(ST37)的猫中发现了两种不同的汉赛巴尔通体等位基因谱,这表明在特定地理区域内巴通体发生了克隆进化。