Abstract

In order to survive external stresses, bacteria need to adapt quickly to changes in their environment. One adaptive mechanism is to coordinate and alter their gene expression by using two-component systems (TCS). TCS are composed of a sensor kinase that activates a transcriptional response regulator by phosphorylation. TCS are involved in motility, virulence, nutrient acquisition, and envelope stress in many bacteria. The pathogenic bacteria Salmonella enterica serovar Typhi (S. Typhi) possess 30 TCSs, is specific to humans, and causes typhoid fever. Here, we have individually deleted each of the 30 response regulators. We have determined their role during interaction with host cells (epithelial cells and macrophages). Deletion of most of the systems (24 out of 30) resulted in a significant change during infection. We have identified 32 new phenotypes associated with TCS of S. Typhi. Some previously known phenotypes associated with TCSs in Salmonella were also confirmed. We have also uncovered phenotypic divergence between Salmonella serovars, as distinct phenotypes between S. Typhi and S. Typhimurium were identified for cpxR. This finding highlights the importance of specifically studying S. Typhi to understand its pathogenesis mechanisms and to develop strategies to potentially reduce typhoid infections.

Highlights

  • Bacteria possess a variety of systems that enable them to respond to diverse signals received from the external environment

  • These signals are mainly detected by two-component systems (TCS) composed of a histidine sensor kinase (SK) and a response regulator (RR)

  • These TCS were all detected in the genome of the closely related serovar Typhimurium

Read more

Summary

Introduction

Bacteria possess a variety of systems that enable them to respond to diverse signals received from the external environment. These signals are mainly detected by two-component systems (TCS) composed of a histidine sensor kinase (SK) and a response regulator (RR). The SK partner of the TCS is located in the inner membrane and generally comprises two domains, a receiver and a transmitter domain that contains a kinase activity with a conserved histidine residue. The RR proteins are located in the cytoplasm and comprise two domains, a receiver domain in the N-terminal section of the protein containing a conserved aspartate residue and a response domain in the C-terminal of the protein. The SK activates the RR through transfer of its phosphorylated group to the conserved RR aspartate residue

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call