Aix-Marseille Université, CNRS, EIPL IMM FR3479Marseille, France.
Aix Marseille Université, URMITE, UMR CNRS 7278, IRD 198, INSERM 1095, IHU Méditerranée InfectionMarseille, France.
Front Cell Infect Microbiol. 2017 May 17;7:189. doi: 10.3389/fcimb.2017.00189. eCollection 2017.
Adipose tissues were shown to host which is persisting inside mature adipocytes. It remains unknown whether this holds true for , a rare representative of the complex responsible for lymphatic and pulmonary tuberculosis. Here, we infected primary murine white and brown pre-adipocytes and murine 3T3-L1 pre-adipocytes and mature adipocytes with and as a positive control. Both mycobacteria were able to infect 18-22% of challenged primary murine pre-adipocytes; and to replicate within these cells during a 7-day experiment with the intracellular inoculums being significantly higher in brown than in white pre-adipocytes for ( = 0.02) and ( = 0.03). Further infection of 3T3-L1 mature adipocytes yielded 9% of infected cells by and 17% of infected cells by ( = 0.001). Interestingly, replicated and accumulated intra-cytosolic lipid inclusions within mature adipocytes over a 12-day experiment; while stopped replicating at day 3 post-infection. These results indicate that brown pre-adipocytes could be one of the potential targets for complex mycobacteria; and illustrate differential outcome of complex mycobacteria into adipose tissues. While white adipose tissue is an unlikely sanctuary for , it is still an open question whether and could persist in brown adipose tissues.
脂肪组织被证明是一种持续性存在于成熟脂肪细胞内的微生物。目前尚不清楚这是否适用于 ,一种罕见的淋巴结核和肺外结核复杂分枝杆菌的代表。在这里,我们用 和 作为阳性对照感染原代鼠白色和棕色前脂肪细胞以及鼠 3T3-L1 前脂肪细胞和成熟脂肪细胞。两种分枝杆菌都能够感染 18-22%的受挑战的原代鼠前脂肪细胞;并在 7 天的实验中在这些细胞内复制,其中棕色前脂肪细胞中的胞内接种物显著高于白色前脂肪细胞,分别为 (=0.02)和 (=0.03)。进一步感染 3T3-L1 成熟脂肪细胞, 感染细胞的比例为 9%, 感染细胞的比例为 17%(=0.001)。有趣的是,在 12 天的实验中, 复制并在成熟脂肪细胞内积累细胞内脂滴包涵体;而 在感染后第 3 天停止复制。这些结果表明,棕色前脂肪细胞可能是 复杂分枝杆菌的潜在靶细胞之一;并说明了 复杂分枝杆菌进入脂肪组织的不同结果。虽然白色脂肪组织不太可能是 的避难所,但 和 是否能在棕色脂肪组织中持续存在仍然是一个悬而未决的问题。