The diguanylate cyclase GcpA inhibits the production of pectate lyases via the H‐NS protein and RsmB regulatory RNA in Dickeya dadantii

• Published in: Molecular plant pathology Vol. 19; no. 8; pp. 1873 - 1886
• Main Authors: Yuan, Xiaochen, Tian, Fang, He, Chenyang, Severin, Geoffrey B., Waters, Christopher M., Zeng, Quan, Liu, Fengquan, Yang, Ching‐Hong
• Format: Journal Article
• Language: English
• Published: England John Wiley & Sons, Inc 01.08.2018; John Wiley and Sons Inc
• Subjects: Cell walls; Clonal deletion; c‐di‐GMP; Dickeya dadantii; Gene expression; genes; Guanosine; guanosine monophosphate; Kinases; motility; mutants; Original; pectate lyase; PelD gene; Polymerase chain reaction; Proteins; quantitative polymerase chain reaction; reverse transcriptase polymerase chain reaction; Reverse transcription; Ribonucleic acid; RNA; Secretion; soft‐rot pathogen; type III secretion system; virulence; pectate lyase; motility; soft-rot pathogen; c-di-GMP; virulence; type III secretion system
• ISSN: 1464-6722; 1364-3703
• DOI: 10.1111/mpp.12665

Summary Dickeya dadantii 3937 secretes pectate lyases (Pels) to degrade plant cell walls. Previously, we have demonstrated that EGcpB and EcpC function as bis‐(3′,5′)‐cyclic dimeric guanosine monophosphate (c‐di‐GMP)‐specific phosphodiesterases (PDEs) to positively regulate Pel production. However, the diguanylate cyclase (DGC) responsible for the synthesis of c‐di‐GMP and the dichotomous regulation of Pel has remained a mystery. Here, we identified GcpA as the dominant DGC to negatively regulate Pel production by the specific repression of pelD gene expression. Quantitative reverse transcription‐polymerase chain reaction (qRT‐PCR) assays revealed that the expression levels of histone‐like, nucleoid‐structuring protein encoding gene hns and post‐transcriptional regulator encoding genes rsmA and rsmB were significantly affected by GcpA. Deletion of hns or rsmB in the gcpAD418A site‐directed mutant restored its Pel production and pelD expression, demonstrating that H‐NS and RsmB contribute to the GcpA‐dependent regulation of Pel in D. dadantii. In addition, RsmB expression was subject to positive regulation by H‐NS. Thus, we propose a novel pathway consisting of GcpA–H‐NS–RsmB–RsmA–pelD that controls Pel production in D. dadantii. Furthermore, we showed that H‐NS and RsmB are responsible for the GcpA‐dependent regulation of motility and type III secretion system (T3SS) gene expression, respectively. Of the two PDEs involved in the regulation of Pels, only EGcpB regulates pelD expression through the same pathway as GcpA.