Kalia 2023 Cell Rep: Difference between revisions

Latest revision as of 14:53, 16 May 2023

Kalia NP, Singh S, Hards K, Cheung CY, Sviriaeva E, Banaei-Esfahani A, Aebersold R, Berney M, Cook GM, Pethe K (2023) M. tuberculosis relies on trace oxygen to maintain energy homeostasis and survive in hypoxic environments. https://doi.org/10.1016/j.celrep.2023.112444

» Cell Rep 42:112444. PMID: 37115669 Open Access

Kalia Nitin Pal, Singh Samsher, Hards Kiel, Cheung Chen-Yi, Sviriaeva Ekaterina, Banaei-Esfahani Amir, Aebersold Ruedi, Berney Michael, Cook Gregory M, Pethe Kevin (2023) Cell Rep

Abstract: The bioenergetic mechanisms by which Mycobacterium tuberculosis survives hypoxia are poorly understood. Current models assume that the bacterium shifts to an alternate electron acceptor or fermentation to maintain membrane potential and ATP synthesis. Counterintuitively, we find here that oxygen itself is the principal terminal electron acceptor during hypoxic dormancy. M. tuberculosis can metabolize oxygen efficiently at least two orders of magnitude below the concentration predicted to occur in hypoxic lung granulomas. Despite a difference in apparent affinity for oxygen, both the cytochrome bcc:aa3 and cytochrome bd oxidase respiratory branches are required for hypoxic respiration. Simultaneous inhibition of both oxidases blocks oxygen consumption, reduces ATP levels, and kills M. tuberculosis under hypoxia. The capacity of mycobacteria to scavenge trace levels of oxygen, coupled with the absence of complex regulatory mechanisms to achieve hierarchal control of the terminal oxidases, may be a key determinant of long-term M. tuberculosis survival in hypoxic lung granulomas. • Keywords: Microbiology, Bioenergetics, Cytochrome bcc-aa3, Cytochrome bd, Dormancy, Granuloma, Hypoxia, Persisters, Terminal oxidase, Tuberculosis • Bioblast editor: Plangger M

Labels: MiParea: Respiration Pathology: Infectious Stress:Hypoxia Organism: Eubacteria

Preparation: Intact organism, Intact cells

Coupling state: ET

HRR: Oxygraph-2k

2023-05

@@ Line 2: / Line 2: @@
 |title=Kalia NP, Singh S, Hards K, Cheung CY, Sviriaeva E, Banaei-Esfahani A, Aebersold R, Berney M, Cook GM, Pethe K (2023) ''M. tuberculosis'' relies on trace oxygen to maintain energy homeostasis and survive in hypoxic environments. https://doi.org/10.1016/j.celrep.2023.112444
 |info=Cell Rep 42:112444. [https://pubmed.ncbi.nlm.nih.gov/37115669 PMID: 37115669 Open Access]
-|authors=Kalia NP, Singh S, Hards K, Cheung CY, Sviriaeva E, Banaei-Esfahani A, Aebersold R, Berney M, Cook GM, Pethe K
+|authors=Kalia Nitin Pal, Singh Samsher, Hards Kiel, Cheung Chen-Yi, Sviriaeva Ekaterina, Banaei-Esfahani Amir, Aebersold Ruedi, Berney Michael, Cook Gregory M, Pethe Kevin
 |year=2023
 |journal=Cell Rep
-|abstract=The bioenergetic mechanisms by which Mycobacterium tuberculosis survives hypoxia are poorly understood. Current models assume that the bacterium shifts to an alternate electron acceptor or fermentation to maintain membrane potential and ATP synthesis. Counterintuitively, we find here that oxygen itself is the principal terminal electron acceptor during hypoxic dormancy. M. tuberculosis can metabolize oxygen efficiently at least two orders of magnitude below the concentration predicted to occur in hypoxic lung granulomas. Despite a difference in apparent affinity for oxygen, both the cytochrome bcc:aa3 and cytochrome bd oxidase respiratory branches are required for hypoxic respiration. Simultaneous inhibition of both oxidases blocks oxygen consumption, reduces ATP levels, and kills M. tuberculosis under hypoxia. The capacity of mycobacteria to scavenge trace levels of oxygen, coupled with the absence of complex regulatory mechanisms to achieve hierarchal control of the terminal oxidases, may be a key determinant of long-term M. tuberculosis survival in hypoxic lung granulomas.
+|abstract=The bioenergetic mechanisms by which ''Mycobacterium tuberculosis'' survives hypoxia are poorly understood. Current models assume that the bacterium shifts to an alternate electron acceptor or fermentation to maintain membrane potential and ATP synthesis. Counterintuitively, we find here that oxygen itself is the principal terminal electron acceptor during hypoxic dormancy. ''M. tuberculosis'' can metabolize oxygen efficiently at least two orders of magnitude below the concentration predicted to occur in hypoxic lung granulomas. Despite a difference in apparent affinity for oxygen, both the cytochrome bcc:aa3 and cytochrome bd oxidase respiratory branches are required for hypoxic respiration. Simultaneous inhibition of both oxidases blocks oxygen consumption, reduces ATP levels, and kills ''M. tuberculosis'' under hypoxia. The capacity of mycobacteria to scavenge trace levels of oxygen, coupled with the absence of complex regulatory mechanisms to achieve hierarchal control of the terminal oxidases, may be a key determinant of long-term ''M. tuberculosis'' survival in hypoxic lung granulomas.
 |keywords=Microbiology, Bioenergetics, Cytochrome bcc-aa3, Cytochrome bd, Dormancy, Granuloma, Hypoxia, Persisters, Terminal oxidase, Tuberculosis
 |editor=[[Plangger M]]
@@ Line 11: / Line 11: @@
 {{Labeling
 |area=Respiration
+|diseases=Infectious
+|injuries=Hypoxia
+|organism=Eubacteria
+|preparations=Intact organism, Intact cells
+|couplingstates=ET
 |instruments=Oxygraph-2k
 |additional=2023-05
 }}