Two-Component Signal Transduction Systems of Pathogenic Bacteria As Targets for Antimicrobial Therapy: An Overview

Sandeep Tiwari(Universidade Federal de Minas Gerais), Syed Babar Jamal(Universidade Federal de Minas Gerais), Syed Shah Hassan(Universidade Federal de Minas Gerais), Paulo Vinícius Sanches Daltro de Carvalho(Universidade Federal de Minas Gerais), S. Almeida(Universidade Federal de Minas Gerais), Debmalya Barh(Universidade Federal de Minas Gerais), Preetam Ghosh(Virginia Commonwealth University), Artur Silva(Universidade Federal do Pará), Thiago Luiz de Paula Castro(Universidade Federal da Bahia), Vasco Azevedo(Universidade Federal de Minas Gerais)
Frontiers in Microbiology
October 10, 2017
Cited by 216Open Access
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Abstract

The bacterial communities in a wide range of environmental niches sense and respond to numerous external stimuli for their survival. Primarily, a source they require to follow up this communication is the two-component signal transduction system (TCS), which typically comprises a sensor Histidine kinase for receiving external input signals and a response regulator that conveys a proper change in the bacterial cell physiology. For numerous reasons, TCSs have ascended as convincing targets for antibacterial drug design. Several studies have shown that TCSs are essential for the coordinated expression of virulence factors and, in some cases, for bacterial viability and growth. It has also been reported that the expression of antibiotic resistance determinants may be regulated by some TCSs. In addition, as a mode of signal transduction, phosphorylation of histidine in bacteria differs from normal serine/threonine and tyrosine phosphorylation in higher eukaryotes. Several studies have shown the molecular mechanisms by which TCSs regulate virulence and antibiotic resistance in pathogenic bacteria. In this review, we list some of the characteristics of the bacterial TCSs and their involvement in virulence and antibiotic resistance. Furthermore, this review lists and discusses inhibitors that have been reported to target TCSs in pathogenic bacteria.


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