Cyclic di‐GMP sensing histidine kinase PdtaS controls mycobacterial adaptation to carbon sources. Issue 4 (27th March 2021)

• Record Type: Journal Article
• Authors: Hariharan, Vignesh Narayan; Yadav, Rahul; Thakur, Chandrani; Singh, Albel; Gopinathan, Renu; Singh, Devendra Pratap; Sankhe, Gaurav; Malhotra, Vandana; Chandra, Nagasuma; Bhatt, Apoorva; Saini, Deepak Kumar
• Is Part Of: FASEB journal. Volume 35:Issue 4(2021)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2021-03-27
• Subjects: c‐di‐GMP -- nutrient starvation -- two‐component system; Biology -- Periodicals; Biology, Experimental -- Periodicals; 570
• DOI: 10.1096/fj.202002537RR
• Languages: English
• ISSNs: 0892-6638

Abstract

Abstract: Cell signaling relies on second messengers to transduce signals from the sensory apparatus to downstream signaling pathway components. In bacteria, one of the most important and ubiquitous second messenger is the small molecule cyclic diguanosine monophosphate (c‐di‐GMP). While the biosynthesis, degradation, and regulatory pathways controlled by c‐di‐GMP are well characterized, the mechanisms through which c‐di‐GMP controls these processes are not entirely understood. Herein we present the report of a c‐di‐GMP sensing sensor histidine kinase PdtaS (Rv3220c), which binds to c‐di‐GMP at submicromolar concentrations, subsequently perturbing signaling of the PdtaS‐PdtaR (Rv1626) two‐component system. Aided by biochemical analysis, genetics, molecular docking, FRET microscopy, and structural modelling, we have characterized the binding of c‐di‐GMP in the GAF domain of PdtaS. We show that a pdtaS knockout in Mycobacterium smegmatis is severely compromised in growth on amino acid deficient media and exhibits global transcriptional dysregulation. The perturbation of the c‐di‐GMP‐PdtaS‐PdtaR axis results in a cascade of cellular changes recorded by a multiparametric systems' approach of transcriptomics, unbiased metabolomics, and lipid analyses.