Department of Microbiology, College of Medicine, Chungnam National University, Daejeon 301-747, South Korea; Department of Medical Science, College of Medicine, Chungnam National University, Daejeon 301-747, South Korea.
Department of Molecular and Life Science, Hanyang University, Ansan 426-791, South Korea.
Microbes Infect. 2017 Jan;19(1):5-17. doi: 10.1016/j.micinf.2016.09.001. Epub 2016 Sep 13.
Mycobacterial ESX systems are often related to pathogenesis during infection. However, little is known about the function of ESX systems of Mycobacterium abscessus (Mab). This study focuses on the Mab ESX-3 cluster, which contains major genes such as esxH (Rv0288, low molecular weight protein antigen 7; CFP-7) and esxG (Rv0287, ESAT-6 like protein). An esx-3 (MAB 2224c-2234c)-deletional mutant of Mab (Δesx) was constructed and used to infect murine and human macrophages. We then investigated whether Mab Δesx modulated innate host immune responses in macrophages. Mab Δesx infection resulted in less pathological and inflammatory responses. Additionally, Δesx resulted in significantly decreased activation of inflammatory signaling and cytokine production in macrophages compared to WT. Moreover, recombinant EsxG·EsxH (rEsxGH) proteins encoded by the ESX-3 region showed synergistic enhancement of inflammatory cytokine generation in macrophages infected with Δesx. Taken together, our data suggest that Mab ESX-3 plays an important role in inflammatory and pathological responses during Mab infection.
分枝杆菌 ESX 系统通常与感染过程中的发病机制有关。然而,对于脓肿分枝杆菌 (Mab) ESX 系统的功能知之甚少。本研究集中于 Mab ESX-3 簇,该簇包含 esxH (Rv0288,低分子量蛋白抗原 7; CFP-7) 和 esxG (Rv0287,ESAT-6 样蛋白) 等主要基因。构建了 Mab (Δesx) 的 esx-3 (MAB 2224c-2234c)-缺失突变体,并用于感染鼠和人巨噬细胞。然后我们研究了 Mab Δesx 是否调节巨噬细胞中的固有宿主免疫反应。Mab Δesx 感染导致较少的病理和炎症反应。此外,与 WT 相比,Δesx 导致巨噬细胞中炎症信号和细胞因子产生的激活显著降低。此外,由 ESX-3 区域编码的重组 EsxG·EsxH (rEsxGH) 蛋白显示出在感染 Δesx 的巨噬细胞中炎症细胞因子生成的协同增强作用。总之,我们的数据表明 Mab ESX-3 在 Mab 感染期间的炎症和病理反应中起重要作用。