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

Author:

Yabaji Shivraj M.1ORCID,Rukhlenko Oleksii S.2ORCID,Chatterjee Sujoy1,Bhattacharya Bidisha1,Wood Emily2,Kasaikina Marina1,Kholodenko Boris N.234ORCID,Gimelbrant Alexander A.5ORCID,Kramnik Igor167ORCID

Affiliation:

1. The National Emerging Infectious Diseases Laboratories (NEIDL), Boston University, Boston, MA, USA.

2. Systems Biology Ireland, School of Medicine and Medical Science, University College Dublin, Belfield Dublin 4, Ireland.

3. Conway Institute of Biomolecular and Biomedical Research, University College Dublin, Belfield Dublin 4, Ireland.

4. Department of Pharmacology, Yale University School of Medicine, New Haven, CT, USA.

5. Altius Institute for Biomedical Sciences, Seattle, WA, USA.

6. Pulmonary Center, The Department of Medicine, Boston University School of Medicine, Boston, MA, USA.

7. Department of Microbiology, Boston University School of Medicine, Boston, MA, USA.

Abstract

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 .

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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