YycH and YycI Regulate Expression of <i>Staphylococcus aureus</i> Autolysins by Activation of WalRK Phosphorylation
2020
Mike Gajdiss | Ian R. Monk | Ute Bertsche | Janina Kienemund | Tanja Funk | Alina Dietrich | Michael Hort | Esther Sib | Timothy P. Stinear | Gabriele Bierbaum
<i>Staphylococcus aureus</i> is a facultative pathogen that can encode numerous antibiotic resistance and immune evasion genes and can cause severe infections. Reduced susceptibility to last resort antibiotics such as vancomycin and daptomycin is often associated with mutations in <i>walRK</i>, an essential two-component regulatory system (TCS). This study focuses on the WalK accessory membrane proteins YycH and YycI and their influence on WalRK phosphorylation. Depletion of YycH and YycI by antisense RNA caused an impaired autolysis, indicating a positive regulatory function on WalK as has been previously described. Phosphorylation assays with full-length recombinant proteins in phospholipid liposomes showed that YycH and YycI stimulate WalK activity and that both regulatory proteins are needed for full activation of the WalK kinase. This was validated in vivo through examining the phosphorylation status of WalR using Phos-tag SDS-PAGE with a <i>yycHI</i> deletion mutant exhibiting reduced levels of phosphorylated WalR. In the <i>yycHI</i> knockdown strain, muropeptide composition of the cell wall was not affected, however, the wall teichoic acid content was increased. In conclusion, a direct modulation of WalRK phosphorylation activity by the accessory proteins YycH and YycI is reported both in vitro and in vivo. Taken together, our results show that YycH and YycI are important in the direct regulation of WalRK-dependent cell wall metabolism.
显示更多 [+] 显示较少 [-]