| Literature DB >> 27637463 |
Yi Sak Kim1, Chul-Su Yang2, Loi T Nguyen3, Jin Kyung Kim1, Hyo Sun Jin1, Jin Ho Choe1, Soo Yeon Kim1, Hye-Mi Lee1, Mingyu Jung4, Jin-Man Kim4, Myung Hee Kim3, Eun-Kyeong Jo1, Ji-Chan Jang5.
Abstract
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.Entities:
Keywords: ESX-3; Host inflammation; Mycobacterium abscessus
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Year: 2016 PMID: 27637463 DOI: 10.1016/j.micinf.2016.09.001
Source DB: PubMed Journal: Microbes Infect ISSN: 1286-4579 Impact factor: 2.700