TY - JOUR
T1 - Metabolically active neutrophils represent a permissive niche for Mycobacterium tuberculosis
AU - Andrews, J. Tucker
AU - Zhang, Zijing
AU - Prasad, G. V.R.Krishna
AU - Huey, Fischer
AU - Nazarova, Evgeniya V.
AU - Wang, Jocelyn
AU - Ranaraja, Ananya
AU - Weinkopff, Tiffany
AU - Li, Lin Xi
AU - Mu, Shengyu
AU - Birrer, Michael J.
AU - Huang, Stanley Ching Cheng
AU - Zhang, Nan
AU - Argüello, Rafael J.
AU - Philips, Jennifer A.
AU - Mattila, Joshua T.
AU - Huang, Lu
N1 - Publisher Copyright:
© 2024 The Authors
PY - 2024/10
Y1 - 2024/10
N2 - Mycobacterium tuberculosis (Mtb)-infected neutrophils are often found in the airways of patients with active tuberculosis (TB), and excessive recruitment of neutrophils to the lung is linked to increased bacterial burden and aggravated pathology in TB. The basis for the permissiveness of neutrophils for Mtb and the ability to be pathogenic in TB has been elusive. Here, we identified metabolic and functional features of neutrophils that contribute to their permissiveness in Mtb infection. Using single-cell metabolic and transcriptional analyses, we found that neutrophils in the Mtb-infected lung displayed elevated mitochondrial metabolism, which was largely attributed to the induction of activated neutrophils with enhanced metabolic activities. The activated neutrophil subpopulation was also identified in the lung granulomas from Mtb-infected non-human primates. Functionally, activated neutrophils harbored more viable bacteria and displayed enhanced lipid uptake and accumulation. Surprisingly, we found that interferon-γ promoted the activation of lung neutrophils during Mtb infection. Lastly, perturbation of lipid uptake pathways selectively compromised Mtb survival in activated neutrophils. These findings suggest that neutrophil heterogeneity and metabolic diversity are key to their permissiveness for Mtb and that metabolic pathways in neutrophils represent potential host-directed therapeutics in TB.
AB - Mycobacterium tuberculosis (Mtb)-infected neutrophils are often found in the airways of patients with active tuberculosis (TB), and excessive recruitment of neutrophils to the lung is linked to increased bacterial burden and aggravated pathology in TB. The basis for the permissiveness of neutrophils for Mtb and the ability to be pathogenic in TB has been elusive. Here, we identified metabolic and functional features of neutrophils that contribute to their permissiveness in Mtb infection. Using single-cell metabolic and transcriptional analyses, we found that neutrophils in the Mtb-infected lung displayed elevated mitochondrial metabolism, which was largely attributed to the induction of activated neutrophils with enhanced metabolic activities. The activated neutrophil subpopulation was also identified in the lung granulomas from Mtb-infected non-human primates. Functionally, activated neutrophils harbored more viable bacteria and displayed enhanced lipid uptake and accumulation. Surprisingly, we found that interferon-γ promoted the activation of lung neutrophils during Mtb infection. Lastly, perturbation of lipid uptake pathways selectively compromised Mtb survival in activated neutrophils. These findings suggest that neutrophil heterogeneity and metabolic diversity are key to their permissiveness for Mtb and that metabolic pathways in neutrophils represent potential host-directed therapeutics in TB.
UR - http://www.scopus.com/inward/record.url?scp=85197214675&partnerID=8YFLogxK
U2 - 10.1016/j.mucimm.2024.05.007
DO - 10.1016/j.mucimm.2024.05.007
M3 - Article
C2 - 38844208
AN - SCOPUS:85197214675
SN - 1933-0219
VL - 17
SP - 825
EP - 842
JO - Mucosal Immunology
JF - Mucosal Immunology
IS - 5
ER -