Phosphoglucomutase A mediated regulation of carbon flux is essential for antibiotic and disease persistence inMycobacterium tuberculosis

Abstract

The long-term survival of Mtb mandates judicious utilization of the available resources inside the host. Uninterrupted access to host-derived nutrients holds the key to the success of Mtb. Phosphoglucomutase enzyme besides synthesizing glycogen, which serves as a nutrient reservoir, also helps modulate the carbon flux in different pathogens. Studies on the role of glycogen metabolism in disease progression, reactivation, and drug susceptibility in tuberculosis are severely lacking. To investigate this, we generated an Mtb strain (ΔpgmA) devoid of the gene that encodes for the enzyme phosphoglucomutase A (pgmA). The absence ofpgmAimpedes the ability of the pathogen to survive under nutrient-limiting and reactivation conditions. In the current study, we demonstrate that the absence of cell membrane-associated glycolipids in ΔpgmAcompromised the cell wall integrity and increased the susceptibility of ΔpgmAto various stresses. Interestingly, in comparison to the wild type, low cAMP levels in ΔpgmAimparted an enhanced growth phenotype on cholesterol. Differential gene expression and carbon flux analysis suggest that stored carbon in the form of glycogen is essential for the survival of Mtb under nutrient-limiting conditions. Finally, we demonstrate that thepgmAgene of Mtb is essential for the growth of Mtb inside the host. Overall, this study unveils the significance ofpgmA-mediated regulation of membrane glycolipids and its implication on antibiotic and disease persistence in tuberculosis. Additionally, information derived from this study will help design anti-TB strategies that are novel, short, and more efficient.