Cell state transition analysis identifies interventions that improve control of Mycobacterium tuberculosis infection by susceptible macrophages

被引:2
|
作者
Yabaji, Shivraj M. [1 ]
Rukhlenko, Oleksii S. [2 ]
Chatterjee, Sujoy [1 ]
Bhattacharya, Bidisha [1 ]
Wood, Emily [2 ]
Kasaikina, Marina [1 ]
Kholodenko, Boris N. [2 ,3 ,4 ]
Gimelbrant, Alexander A. [5 ]
Kramnik, Igor [1 ,6 ,7 ]
机构
[1] Boston Univ, Natl Emerging Infect Dis Labs NEIDL, Boston, MA 02215 USA
[2] Univ Coll Dublin, Sch Med & Med Sci, Syst Biol Ireland, Belfield Dublin 4, Ireland
[3] Univ Coll Dublin, Conway Inst Biomol & Biomed Res, Belfield Dublin 4, Ireland
[4] Yale Univ, Sch Med, Dept Pharmacol, New Haven, CT 06510 USA
[5] Altius Inst Biomed Sci, Seattle, WA USA
[6] Boston Univ, Sch Med, Dept Med, Pulm Ctr, Boston, MA 02118 USA
[7] Boston Univ, Sch Med, Dept Microbiol, Boston, MA 02118 USA
来源
SCIENCE ADVANCES | 2023年 / 9卷 / 39期
基金
美国国家卫生研究院;
关键词
PATHOGENESIS; RESISTANT;
D O I
10.1126/sciadv.adh4119
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Understanding cell state transitions and purposefully controlling them to improve therapies is a longstanding challenge in biological research and medicine. Here, we identify a transcriptional signature that distinguishes activated macrophages from the tuberculosis (TB) susceptible and resistant mice. We then apply the cSTAR (cell state transition assessment and regulation) approach to data from screening-by-RNA sequencing to identify chemical perturbations that shift the transcriptional state of tumor necrosis factor (TNF)-activated TB-susceptible macrophages toward that of TB-resistant cells, i.e., prevents their aberrant activation without suppressing beneficial TNF responses. Last, we demonstrate that the compounds identified with this approach enhance the resistance of the TB-susceptible mouse macrophages to virulent Mycobacterium tuberculosis.
引用
收藏
页数:14
相关论文
共 50 条
  • [1] Human Alveolar Macrophages Adopt Aerobic Glycolysis To Control Mycobacterium Tuberculosis Infection
    Gleeson, L. E.
    Sheedy, F. J.
    O'Leary, S.
    O'Sullivan, M. P.
    O'Neill, L. A.
    Keane, J. M.
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2015, 191
  • [2] Observational study of the use of infection control interventions for Mycobacterium tuberculosis in pediatric facilities
    Kellerman, SE
    Saiman, L
    San Gabriel, P
    Besser, R
    Jarvis, WR
    PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2001, 20 (06) : 566 - 570
  • [3] Transcriptome profiling of human alveolar macrophages to probe phenotypic heterogeneity and control of Mycobacterium tuberculosis infection
    Mhango, D.
    EUROPEAN JOURNAL OF IMMUNOLOGY, 2019, 49 : 530 - 530
  • [4] Mycobacterium tuberculosis Infection-Driven Foamy Macrophages and Their Implications in Tuberculosis Control as Targets for Host-Directed Therapy
    Shim, Dahee
    Kim, Hagyu
    Shin, Sung Jae
    FRONTIERS IN IMMUNOLOGY, 2020, 11
  • [5] Comparative proteome analysis revealed the differences in response to both Mycobacterium tuberculosis and Mycobacterium bovis infection of bovine alveolar macrophages
    Cai, Yurong
    Gao, Weifeng
    Wang, Pu
    Zhang, Gang
    Wang, Xiaoping
    Jiang, Lingling
    Zeng, Jin
    Wang, Yujiong
    Wu, Zhiwei
    Li, Yong
    FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY, 2023, 13
  • [6] TOLLIP inhibits lipid accumulation and the integrated stress response in alveolar macrophages to control Mycobacterium tuberculosis infection
    Venkatasubramanian, Sambasivan
    Plumlee, Courtney R.
    Dill-McFarland, Kimberly A.
    Cohen, Sara B.
    Gern, Benjamin H.
    Rane, Divya A.
    Meyer, Mackenzie K.
    Saha, Aparajita
    Hinderstein, Sarah A.
    Pearson, Gemma L.
    Lietzke, Anne C.
    Pacheco, Amanda
    Chow, Yu-Hua
    Hung, Chi F.
    Soleimanpour, Scott A.
    Altman, Matthew
    Urdahl, Kevin B.
    Shah, Javeed A.
    NATURE MICROBIOLOGY, 2024, 9 (04) : 949 - 963
  • [7] TOLLIP inhibits lipid accumulation and the integrated stress response in alveolar macrophages to control Mycobacterium tuberculosis infection
    Sambasivan Venkatasubramanian
    Courtney R. Plumlee
    Kimberly A. Dill-McFarland
    Sara B. Cohen
    Benjamin H. Gern
    Divya A. Rane
    Mackenzie K. Meyer
    Aparajita Saha
    Sarah A. Hinderstein
    Gemma L. Pearson
    Anne C. Lietzke
    Amanda Pacheco
    Yu-Hua Chow
    Chi F. Hung
    Scott A. Soleimanpour
    Matthew Altman
    Kevin B. Urdahl
    Javeed A. Shah
    Nature Microbiology, 2024, 9 : 949 - 963
  • [8] The role of memory T cell response in resistant and susceptible mice following an aerosol infection with mycobacterium tuberculosis.
    Kamath, AB
    Alt, J
    Donovan, M
    Debbabi, H
    Chackerian, A
    Behar, SM
    CLINICAL IMMUNOLOGY, 2002, 103 (03) : S32 - S32
  • [9] MEMORY T-CELL-MEDIATED RESISTANCE TO MYCOBACTERIUM-TUBERCULOSIS INFECTION IN INNATELY SUSCEPTIBLE AND RESISTANT MICE
    HUBBARD, RD
    FLORY, CM
    COLLINS, FM
    INFECTION AND IMMUNITY, 1991, 59 (06) : 2012 - 2016
  • [10] In-depth analysis of a mixed Mycobacterium tuberculosis infection involving a multidrug-resistant strain and a susceptible strain
    Abascal, Estefania
    Herranz, Marta
    Serrano, Maria Jesus Ruiz
    Fernandez-Gonzalez, Francisco
    Munoz, Patricia
    Gotuzzo, Eduardo
    de Viedma, Dario Garcia
    CLINICAL MICROBIOLOGY AND INFECTION, 2021, 27 (04) : 641 - 643