Correlation Engine 2.0
Clear Search sequence regions


  • bacteria (1)
  • case reports (1)
  • cell death (1)
  • cytokines (4)
  • exhibits (4)
  • humans (1)
  • IL 10 (1)
  • IL 12p40 (1)
  • IL 6 (1)
  • infect (1)
  • macrophages (5)
  • marrow (1)
  • mice (1)
  • mycobacterium (14)
  • oxygen (1)
  • pathogenesis (1)
  • rough (4)
  • sepsis (1)
  • strain (3)
  • TNF α (1)
  • Sizes of these terms reflect their relevance to your search.

    Mycobacterium mucogenicum (Mmuc), a rapidly growing nontuberculous mycobacterium (NTM), can infect humans (posttraumatic wound infections and catheter-related sepsis). Similar to other NTM species, Mmuc exhibits colony morphologies of rough (Mmuc-R) and smooth (Mmuc-S) types. Although there are several case reports on Mmuc infection, no experimental evidence supports that the R-type is more virulent. In addition, the immune response and metabolic reprogramming of Mmuc have not been studied on the basis of morphological characteristics. Thus, a standard ATCC Mmuc strain and two clinical strains were analyzed, and macrophages were generated from mouse bone marrow. Cytokines and cell death were measured by ELISA and FACS, respectively. Mitochondrial respiration and glycolytic changes were measured by XF seahorse. Higher numbers of intracellular bacteria were found in Mmuc-R-infected macrophages than in Mmuc-S-infected macrophages. Additionally, Mmuc-R induced higher levels of the cytokines TNF-α, IL-6, IL-12p40, and IL-10 and induced more BMDM necrotic death. Furthermore, our metabolic data showed marked glycolytic and respiratory differences between the control and each type of Mmuc infection, and changes in these parameters significantly promoted glucose metabolism, extracellular acidification, and oxygen consumption in BMDMs. In conclusion, at least in the strains we tested, Mmuc-R is more virulent, induces a stronger immune response, and shifts bioenergetic metabolism more extensively than the S-type. This study is the first to report differential immune responses and metabolic reprogramming after Mmuc infection and might provide a fundamental basis for additional studies on Mmuc pathogenesis.

    Citation

    Minji Kang, Ho Won Kim, A-Reum Yu, Jeong Seong Yang, Seung Heon Lee, Ji Won Lee, Hoe Sun Yoon, Byung Soo Lee, Hwan-Woo Park, Sung Ki Lee, Seungwan Lee, Jake Whang, Jong-Seok Kim. Comparison of Macrophage Immune Responses and Metabolic Reprogramming in Smooth and Rough Variant Infections of Mycobacterium mucogenicum. International journal of molecular sciences. 2022 Feb 24;23(5)

    Expand section icon Mesh Tags

    Expand section icon Substances


    PMID: 35269631

    View Full Text