Infection and immunity, September 2017, Vol.85(9)
During infection, senses and responds to stress; such responses may be modulated by MisRS (NGO0177 and NGO0176), a two-component system that is a homolog of CpxRA. In , CpxRA senses and responds to envelope stress; CpxA is a sensor kinase/phosphatase for CpxR, a response regulator. When a mutant is grown in medium containing glucose, CpxR is phosphorylated by acetyl phosphate but cannot be dephosphorylated, resulting in constitutive activation. Kandler and coworkers (J. L. Kandler, C. L. Holley, J. L. Reimche, V. Dhulipala, J. T. Balthazar, A. Muszyński, R. W. Carlson, and W. M. Shafer, Antimicrob Agents Chemother 60:4690-4700, 2016, https://doi.org/10.1128/AAC.00823-16) showed that MisR (CpxR) is required for the maintenance of membrane integrity and resistance to antimicrobial peptides, suggesting a role in gonococcal survival Here, we evaluated the contributions of MisR and MisS (CpxA) to gonococcal infection in a murine model of cervicovaginal colonization and identified MisR-regulated genes using RNA sequencing (RNA-Seq). The deletion of or severely reduced the capacity of to colonize mice or maintain infection over a 7-day period and reduced microbial fitness after exposure to heat shock. Compared to the wild type (WT), the inactivation of identified 157 differentially regulated genes, most of which encoded putative envelope proteins. The inactivation of identified 17 differentially regulated genes compared to the WT and 139 differentially regulated genes compared to the mutant, 111 of which overlapped those differentially expressed in the comparison of the WT versus the mutant. These data indicate that an intact MisRS system is required for gonococcal infection of mice. Provided the MisR is constitutively phosphorylated in the mutant, the data suggest that controlled but not constitutive activation is required for gonococcal infection in mice.
Cpxra ; Misrs ; Neisseria Gonorrhoeae ; RNA-Seq ; Envelope Stress ; Genes ; Infection ; Mice ; Bacterial Proteins -- Metabolism ; Gonorrhea -- Microbiology ; Neisseria Gonorrhoeae -- Pathogenicity ; Protein Kinases -- Metabolism ; Reproductive Tract Infections -- Microbiology ; Virulence Factors -- Metabolism
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