Scientia Agricultura Sinica ›› 2026, Vol. 59 ›› Issue (11): 2374-2386.doi: 10.3864/j.issn.0578-1752.2026.11.006

• PLANT PROTECTION • Previous Articles     Next Articles

Function of c-di-GMP Synthase Rsp1208 of Ralstonia solanacearum Strain GMI 1000

FAN XiaoHan1(), ZHANG WeiJun2, YUAN JinFeng2, ZHAO DongLin1, ZHANG ChengSheng1, ZHANG ZhiFan2(), XU KangWen1()   

  1. 1 Tobacco Research Institute, Chinese Academy of Agricultural Sciences, Qingdao 266101, Shandong
    2 Fenggang Branch of Zunyi Company, Guizhou Provincial Tobacco Company, Zunyi 564200, Guizhou
  • Received:2026-02-10 Accepted:2026-04-03 Online:2026-06-01 Published:2026-06-03
  • Contact: ZHANG ZhiFan, XU KangWen

Abstract:

【Background】Bacterial wilt is a devastating soil-borne vascular disease caused by Ralstonia solanacearum. As a conserved second messenger in bacteria, c-di-GMP orchestrates multiple pathogenic phenotypes of plant bacterial pathogens. However, the functional characteristics of core c-di-GMP metabolic genes in R. solanacearum remain to be fully elucidated.【Objective】This study aimed to investigate the functions and regulatory mechanisms of c-di-GMP metabolism-associated genes in R. solanacearum GMI 1000, clarify the impacts of key genes on bacterial physiological phenotypes and pathogenicity, refine the c-di-GMP signaling regulatory network, and to provide a theoretical foundations for screening novel control targets and developing green management strategies against bacterial wilt.【Method】Using R. solanacearum GMI 1000 as the material, RT-qPCR was performed to compare the transcriptional profiles of 24 putative c-di-GMP metabolic genes under routine culture and simulated infection conditions. For the most significantly downregulated gene Rsp1208, gene deletion, complementation, enzyme active-site mutagenesis and overexpression strains were constructed via homologous recombination and electroporation. Key physiological phenotypes including growth kinetics, motility, biofilm formation and exopolysaccharide (EPS) yield were systematically quantified. Transcriptional levels of motility- and EPS synthesis-related genes were analyzed by RT-qPCR. Intracellular c-di-GMP content and in vitro diguanylate cyclase activity were detected using LC-MS/MS and thiazole orange fluorescence assay, respectively. Pathogenicity assays on tomato seedlings were conducted using the root-wounding inoculation method.【Result】Under simulated infection conditions, all 24 c-di-GMP metabolic genes were transcriptionally downregulated to varying degrees, among which Rsp1208 showed the most extreme downregulation. The protein encoded by Rsp1208 harbors both GGDEF and EAL domains. Deletion of Rsp1208 significantly increased bacterial motility by 26.57% and EPS production by 85.92%, reduced biofilm formation by 75%, decreased intracellular c-di-GMP levels markedly, and extremely enhanced pathogenicity on tomato. The complemented strain restored wild-type phenotypes, whereas the overexpression strain exhibited attenuated motility, mildly elevated biofilm formation and significantly weakened pathogenicity. Transcriptional levels of motility-related genes (flhC, fliA, fliM, fliC) and EPS synthesis genes (xpsR, epsB) were drastically upregulated in the Rsp1208 deletion mutant. Mutation of the GGDEF active site abolished the c-di-GMP synthetic activity of Rsp1208, while EAL site mutation exerted no significant effect.【Conclusion】Rsp1208 functions as a c-di-GMP diguanylate cyclase through its GGDEF domain, regulating intracellular c-di-GMP homeostasis in R. solanacearum, mediating phenotypic remodeling of motility, biofilm formation and EPS production, and ultimately governing the pathogenicity of the pathogen. These findings deepen the mechanistic understanding of R. solanacearum pathogenesis and provide critical theoretical support for the development of green control technologies against bacterial wilt.

Key words: Ralstonia solanacearum, c-di-GMP, pathogenicity, motility, biofilm

Table 1

Primers used for Rsp1208 gene deletion, complementation, and overexpression vector construction"

引物名称
Primer name
引物序列
Primer sequence
靶标基因
Target gene
退火温度
Annealing temperature (℃)
产物大小
Product size (bp)
用途
Purpose
Rsp1208-F1 gagctcggtacccggggatccAACACGTCGTCGTTGGTGATC 上游
Upstream
56 550 基因克隆
Gene clone
Rsp1208-R1 tatcgtcgatccagCAGCAGCTGGACGAATCGTT
Rsp1208-F2 ctgctgCTGGATCGACGATACGCAGG 下游
Downstream
56 740 基因克隆
Gene clone
Rsp1208-R2 acgacggccagtgccaagcttGAAACCGCCTCCAGCATGG
Rsp1208OE-F agggaacaaaagctgggtaccGTTGCCTGACCGCGAACG 过表达片段
Overexpression fragment
58 1350 基因克隆
Gene clone
Rsp1208OE-R caggaattcgatatcaagcttTTACGGCATCAGATCGCGC
M13F TGTAAAACGACGGCCAGT 55 过表达验证
Overexpression verification
M13R AACAGCTATGACCATGA
Rsp1208-pET30-F taagaaggagatatacatatgTTGCCTGACCGCGAACGATTCGTC 蛋白表达片段
Protein expression fragment
55 1371 基因克隆
Gene clone
Rsp1208-pET30-R ctcgagtgcggccgcaagcttCGGCATCAGATCGCGCGCGCGTTCG

Table 2

Primers used for RT-qPCR"

基因Gene 引物序列Primer sequence
gyrB F: CAAGGGCAAGATCCTGAACG R: GATGATGATGCGGTGGTAGC
flhC F: AAGAGGTGCTGTCGATCACT R: TCACGGTGTGCAACATCTTC
fliA F: CATCGCCAACCAGATGATGG R: GCGGCATAGAACTCGAACTG
fliM F: CATGCCGTACACCATGATCG R: TGTTGAGGATGTCGGACACA
fliC F: ACTACAACGGCAACAAGCTG R: TGGCCATATTGGAAGGTCGT
xpsR CCCGCCAGTTCATTCTTCAG GGACTGATGATCCAGGTGGT
epsB GTGAGCTTGCTCAACGACAT GTCAGCTTCTTGGGCTTCAC

Fig. 1

Screening of genes related to c-di-GMP metabolism in R. solanacearum"

Fig. 2

Domain analysis of Rsp1208 protein and PCR identification of deletion, complementation, point mutation, and overexpression strains"

Fig. 3

Effects of Rsp1208 deletion and overexpression on growth, motility, biofilm, and exopolysaccharide phenotypes of R. solanacearum GMI 1000"

Fig. 4

Transcription levels of related genes in the Rsp1208 deletion mutants"

Fig. 5

Regulation of intracellular c-di-GMP contents in R. solanacearum by Rsp1208 and validation of its in vitro c-di-GMP synthase activity"

Fig. 6

Effects of Rsp1208 deletion and overexpression on the pathogenicity in tomato"

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