URMITE, Aix Marseille Université, UM63, CNRS 7278, IRD 198, INSERM 1095, IHU - Méditerranée Infection, 19-21 Boulevard Jean Moulin, 13385, Marseille Cedex 05, France.
Eur J Clin Microbiol Infect Dis. 2017 Nov;36(11):2207-2213. doi: 10.1007/s10096-017-3047-z. Epub 2017 Jul 2.
Bartonella henselae, the agent of cat scratch disease (CSD), appears to be a common organism responsible for lymphadenitis in both adults and children. There is a very low isolation rate for B. henselae from lymph nodes of patients with CSD. Our objective was to evaluate B. henselae viability in a large series of lymph nodes from patients with CSD. From January to November 2016, we analyzed lymph node biopsy samples from patients diagnosed with CSD. We used reverse transcription-quantitative polymerase chain reaction (RT-qPCR) to detect B. henselae RNA, as well as cultures, histological analyses, and fluorescence in situ hybridization (FISH). We tested 87 lymph nodes positive for B. henselae DNA but only 8 (9%) presented with B. henselae RNA. We did not find a significant difference for the pap threshold cycle (C) values between RNA-positive and RNA-negative lymph nodes (p = 0.5). Cultures, histological analyses, and FISH were negative for all the tested samples. We provide evidence that B. henselae are not or are rarely viable in most cases in the lymph nodes of patients with CSD.
汉赛巴尔通体,即猫抓病的病原体,似乎是一种常见的病原体,可引起成人和儿童的淋巴结炎。从猫抓病患者的淋巴结中分离汉赛巴尔通体的分离率非常低。我们的目的是评估大量猫抓病患者淋巴结中汉赛巴尔通体的活力。2016 年 1 月至 11 月,我们分析了诊断为猫抓病的患者的淋巴结活检样本。我们使用逆转录定量聚合酶链反应(RT-qPCR)检测汉赛巴尔通体 RNA,以及培养、组织学分析和荧光原位杂交(FISH)。我们检测了 87 个汉赛巴尔通体 DNA 阳性的淋巴结,但只有 8 个(9%)有汉赛巴尔通体 RNA。我们没有发现 RNA 阳性和 RNA 阴性淋巴结的 pap 阈值循环(C)值有显著差异(p=0.5)。所有检测样本的培养、组织学分析和 FISH 均为阴性。我们提供的证据表明,在大多数情况下,猫抓病患者淋巴结中的汉赛巴尔通体是无活力或很少有活力的。