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格氏棘阿米巴内杀伤溃疡分枝杆菌:共培养模型。

Intra-amoebal killing of Mycobacterium ulcerans by Acanthamoeba griffini: A co-culture model.

机构信息

Aix Marseille Université, URMITE, UMR CNRS 7278, IRD 198, INSERM 1095, IHU Méditerranée Infection, Marseille 13005, France.

Aix Marseille Université, URMITE, UMR CNRS 7278, IRD 198, INSERM 1095, IHU Méditerranée Infection, Marseille 13005, France.

出版信息

Microb Pathog. 2018 Jan;114:1-7. doi: 10.1016/j.micpath.2017.11.022. Epub 2017 Nov 20.

DOI:10.1016/j.micpath.2017.11.022
PMID:29155010
Abstract

Mycobacterium ulcerans, a decaying Mycobacterium marinum derivative is responsible for Buruli ulcer, a notifiable non-contagious disabling infection highly prevalent in some West African countries. Aquatic environments are suspected to host M. ulcerans, however, the exact reservoirs remain unknown. While M. marinum was found to resist amoebal microbicidal activities, this remains unknown for M. ulcerans. In this study M. ulcerans was co-cultured with the moderately halophile Acanthamoeba griffini at 30 °C to probe this tropical amoeba as a potential reservoir for M. ulcerans. In triplicate experiments, we observed engulfment of M. ulcerans by A. griffini trophozoites, followed by an unexpected significant difference of 98.4% (day 1), 99.5% (day 2), 99.5% (day 3) and 99.9% (day 7) between the number of intra-amoebal mycobacteria detected by PCR and the number of viable intra-amoebal mycobacteria measured by 10-week culture. Further encystment revealed only one Mycobacterium organism for 150 A. griffini cysts observed by electron microscopy and the culture of excysted amoebae remained sterile. In conclusion, these data install M. ulcerans as susceptible to A. griffini microbicidal activities rendering this amoeba species an unlikely host of M. ulcerans in natural environments.

摘要

溃疡分枝杆菌,一种腐烂的海分枝杆菌衍生物,是导致布鲁里溃疡的病原体,这是一种在一些西非国家流行的传染性非致残性感染。水生环境被怀疑是溃疡分枝杆菌的宿主,但确切的储存宿主仍然未知。虽然已经发现海分枝杆菌能够抵抗阿米巴的杀菌活性,但溃疡分枝杆菌是否如此尚不清楚。在这项研究中,溃疡分枝杆菌与中嗜盐性棘阿米巴在 30°C 下共培养,以探究这种热带阿米巴是否可能是溃疡分枝杆菌的储存宿主。在重复的实验中,我们观察到阿米巴滋养体吞噬了溃疡分枝杆菌,随后令人惊讶的是,在第 1、2、3 和 7 天,PCR 检测到的细胞内分枝杆菌数量与 10 周培养法测量的活细胞内分枝杆菌数量之间的差异分别为 98.4%、99.5%、99.5%和 99.9%。进一步囊化后,通过电子显微镜观察到的 150 个棘阿米巴囊泡中仅发现一个分枝杆菌,而孵育出的阿米巴的培养仍然无菌。总之,这些数据表明溃疡分枝杆菌易受棘阿米巴的杀菌活性影响,这使得这种阿米巴物种不太可能成为自然环境中溃疡分枝杆菌的宿主。

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