Abstract
Exopolysaccharides (EPS) are critical components of the biofilm matrix, and ppGpp has been demonstrated to positively influence biofilm formation. Here, we elucidate the underlying mechanism by which ppGpp regulates EPS production by facilitating HpaR1 to modulate the expression of the gum cluster in the phytopathogen Xanthomonas campestris pv. campestris (Xcc). ppGpp affected the yield of EPS without influencing its primary or advanced structure, as confirmed by Fourier transform infrared spectroscopy and scanning electron microscopy. Expression of the gum cluster, which governs EPS biosynthesis in Xcc, was down-regulated in the ppGpp-deficient mutant (ΔrelAΔspoT) compared to the wild type (WT). Comparison of EPS production between knock-out mutants of the gum cluster and ppGpp-deficient mutant revealed that the gum cluster was a key determinant of EPS production, with ppGpp acting upstream of the gum cluster. Transcriptomic and qPCR analyses indicated that ppGpp modulated global transcription in Xcc, positively regulating expression of hpaR1, which encodes the transcription factor for the gum cluster. This regulatory role was further substantiated by electrophoretic mobility shift assays, which showed that ppGpp enhanced the DNA-binding activity of HpaR1. Furthermore, genetic complementation with hpaR1 restored EPS production, confirming its functional role in this regulatory pathway. In summary, these findings provide novel insights into the molecular mechanisms linking ppGpp signaling to EPS production in X. campestris pv. campestris.
Data availability
The RNA-seq raw data of this study has been deposited in the Sequence Read Archive (SRA) database under accession number PRJNA1011498 (https://www.ncbi.nlm.nih.gov/bioproject/ PRJNA1011498).
References
Kaur, N. & Dey, P. Bacterial exopolysaccharides as emerging bioactive macromolecules: from fundamentals to applications. Res. Microbiol. 174, 104024 (2023).
Bagnol, R., Grijpma, D., Eglin, D. & Moriarty, T. F. The production and application of bacterial exopolysaccharides as biomaterials for bone regeneration. Carbohyd. Polym. 291, 119550 (2022).
Pammel, L. H. Bacteriosis of rutabaga (Bacillus campestris n. sp.). Iowa State Coll. Agric. Exp. Stn. Bull. 27, 130–134 (1894).
Williams, P. H. Black rot: a continuing threat to the world crucifers. Plant Dis. 64, 736–742 (1980).
Alvarez, A. M. In Mechanisms of Resistance to Plant Diseases (eds Slusarenko, A. J., Fraser, R. S. S. & van Loon, L. C.) 21–52 (Springer Netherlands, 2000).
Qiu, J. & He, Y. Advances in applications and research of xanthan gum. Acta Laser Biol. Sin. 28, 385–393 (2019).
Yun, M. H. et al. Xanthan induces plant susceptibility by suppressing callose deposition. Plant Physiol. 141, 178–187 (2006).
Kakkar, A., Nizampatnam, N. R., Kondreddy, A., Pradhan, B. B. & Chatterjee, S. Xanthomonas campestris cell–cell signaling molecule DSF (diffusible signal factor) elicits innate immunity in plants and is suppressed by the exopolysaccharide xanthan. J. Exp. Bot. 66, 6697–6714 (2015).
Ielpi, L., Couso, R. O. & Dankert, M. A. Sequential assembly and polymerization of the polyprenol-linked pentasaccharide repeating unit of the xanthan polysaccharide in Xanthomonas campestris. J. Bacteriol. 175, 2490–2500 (1993).
Katzen, F., Becker, A., Zorreguieta, A., Pühler, A. & Ielpi, L. Promoter analysis of the Xanthomonas campestris pv. campestris gum operon directing biosynthesis of the xanthan polysaccharide. J. Bacteriol. 178, 4313–4318 (1996).
Galván, E. M. et al. Xanthan chain length is modulated by increasing the availability of the polysaccharide copolymerase protein GumC and the outer membrane polysaccharide export protein GumB. Glycobiology 23, 259–272 (2013).
Katzen, F. et al. Xanthomonas campestris pv. campestris gum mutants: Effects on xanthan biosynthesis and plant virulence. J. Bacteriol. 180, 1607–1617 (1998).
Tang, J. et al. Genetic and molecular analysis of a cluster of rpf genes involved in positive regulation of synthesis of extracellular enzymes and polysaccharide in Xanthomonas campestris pathovar campestris. Mol. Gen. Genet. 226, 409–417 (1991).
Slater, H., Alvarez-Morales, A., Barber, C. E., Daniels, M. J. & Dow, J. M. A two-component system involving an HD-GYP domain protein links cell–cell signalling to pathogenicity gene expression in Xanthomonas campestris. Mol. Microbiol. 38, 986–1003 (2000).
Barber, C. E. et al. A novel regulatory system required for pathogenicity of Xanthomonas campestris is mediated by a small diffusible signal molecule. Mol. Microbiol. 24, 555–566 (1997).
Chin, K.-H. et al. The cAMP receptor-like protein CLP is a novel c-di-GMP receptor linking cell–cell signaling to virulence gene expression in Xanthomonas campestris. J. Mol. Biol. 396, 646–662 (2010).
Tao, F., He, Y.-W., Wu, D.-H., Swarup, S. & Zhang, L.-H. The cyclic nucleotide monophosphate domain of Xanthomonas campestris global regulator Clp defines a new class of cyclic di-GMP effectors. J. Bacteriol. 192, 1020–1029 (2010).
de Crecy-Lagard, V. et al. A Xanthomonas campestris pv. campestris protein similar to catabolite activation factor is involved in regulation of phytopathogenicity. J. Bacteriol. 172, 5877–5883 (1990).
Su, H.-Z. et al. Characterization of the GntR family regulator HpaR1 of the crucifer black rot pathogen Xanthomonas campestris pathovar campestris. Sci. Rep. 6, 19862 (2016).
Atkinson, G. C., Tenson, T. & Hauryliuk, V. The RelA/SpoT homolog (RSH) superfamily: distribution and functional evolution of ppGpp synthetases and hydrolases across the tree of life. PLoS ONE 6, e23479 (2011).
Hauryliuk, V., Atkinson, G. C., Murakami, K. S., Tenson, T. & Gerdes, K. Recent functional insights into the role of (p)ppGpp in bacterial physiology. Nat. Rev. Microbiol. 13, 298–309 (2015).
Irving, S. E., Choudhury, N. R. & Corrigan, R. M. The stringent response and physiological roles of (pp)pGpp in bacteria. Nat. Rev. Microbiol. 19, 256–271 (2021).
Ronneau, S. & Hallez, R. Make and break the alarmone: regulation of (p)ppGpp synthetase/hydrolase enzymes in bacteria. FEMS Microbiol. Rev. 43, 389–400 (2019).
Xiao, H. et al. Residual guanosine 3’,5’-bispyrophosphate synthetic activity of relA null mutants can be eliminated by spoT null mutations. J. Biol. Chem. 266, 5980–5990 (1991).
Srivatsan, A. & Wang, J. D. Control of bacterial transcription, translation and replication by (p)ppGpp. Curr. Opin. Microbiol. 11, 100–105 (2008).
Liu, K., Bittner, A. N. & Wang, J. D. Diversity in (p)ppGpp metabolism and effectors. Curr. Opin. Microbiol. 24, 72–79 (2015).
Bai, K. et al. RNA-Seq analysis discovers the critical role of Rel in ppGpp synthesis, pathogenicity, and the VBNC state of Clavibacter michiganensis. Phytopathology 112, 1844–1858 (2022).
Bai, K. et al. The role of RelA and SpoT on ppGpp production, stress response, growth regulation and pathogenicity in Xanthomonas campestris pv. campestris. Microbiol. Spectr. 9, e02057–02021 (2021).
Wang, J., Gardiol, N., Burr, T., Salmond, G. P. & Welch, M. RelA-dependent (p)ppGpp production controls exoenzyme synthesis in Erwinia carotovora subsp. atroseptica. J. Bacteriol. 189, 7643–7652 (2007).
Yang, H. W., Yu, M., Lee, J. H., Chatnaparat, T. & Zhao, Y. The stringent response regulator (p) ppGpp mediates virulence gene expression and survival in Erwinia amylovora. BMC Genomics 21, 261 (2020).
Zhang, Y., Teper, D., Xu, J. & Wang, N. Stringent response regulators (p)ppGpp and DksA positively regulate virulence and host adaptation of Xanthomonas citri. Mol. Plant Pathol. 20, 1550–1565 (2019).
Xu, X. et al. Bacterial alarmone (p)ppGpp mediates the pathogenicity of Clavibacter michiganensis via a dual mechanism that affects both enzyme production and the Tat secretion system. mSystems 10, e0013525 (2025).
Lemos, J. A. C., Brown, T. A. & Burne, R. A. Effects of RelA on key virulence properties of planktonic and biofilm populations of Streptococcus mutans. Infect. Immu. 72, 1431–1440 (2004).
Ge, X. et al. Bifunctional enzyme SpoT is involved in biofilm formation of Helicobacter pylori with multidrug resistance by upregulating efflux pump Hp1174 (gluP). Antimicrob. Agents Ch. 62, e00957–18 (2018).
Gupta, K. R., Kasetty, S. & Chatterji, D. Novel functions of (p)ppGpp and Cyclic di-GMP in mycobacterial physiology revealed by phenotype microarray analysis of wild-type and isogenic strains of Mycobacterium smegmatis. Appl. Environ. Microb. 81, 2571–2578 (2015).
Nguyen, D. et al. Active starvation responses mediate antibiotic tolerance in biofilms and nutrient-limited bacteria. Science 334, 982–986 (2011).
Taylor, C. M. et al. Listeria monocytogenes relA and hpt mutants are impaired in surface-attached growth and virulence. J. Bacteriol. 184, 621–628 (2002).
Li, W., Liu, M., Siddique, M. S., Graham, N. & Yu, W. Contribution of bacterial extracellular polymeric substances (EPS) in surface water purification. Environ. Pollut. 280, 116998 (2021).
Guibaud, G., Comte, S., Bordas, F., Dupuy, S. & Baudu, M. Comparison of the complexation potential of extracellular polymeric substances (EPS), extracted from activated sludges and produced by pure bacteria strains, for cadmium, lead and nickel. Chemosphere 59, 629–638 (2005).
Liao, B. Q., Allen, D. G., Droppo, I. G., Leppard, G. G. & Liss, S. N. Surface properties of sludge and their role in bioflocculation and settleability. Water Res 35, 339–350 (2001).
Zhang, P. et al. Extracellular protein analysis of activated sludge and their functions in wastewater treatment plant by shotgun proteomics. Sci. Rep. 5, 12041 (2015).
Pandian, V., Babinastarlin, S., Shankar, T., Sivakumar, T. & Kasirajan, A. Quantification and characterization of exopolysaccharides from Bacillus subtilis (MTCC 121). Adv. Biol. Res. 5, 71–76 (2011).
Vinothkanna, A. et al. Structural characterization, functional and biological activities of an exopolysaccharide produced by probiotic Bacillus licheniformis AG-06 from Indian polyherbal fermented traditional medicine. Int. J. Biol. Macromol. 174, 144–152 (2021).
An, S.-Q. et al. Systematic mutagenesis of all predicted gntR genes in Xanthomonas campestris pv. campestris reveals a GntR family transcriptional regulator controlling hypersensitive response and virulence. Mol. Plant Microbe . 24, 1027–1039 (2011).
Valentini, M. & Filloux, A. Biofilms and Cyclic di-GMP (c-di-GMP) Signaling: lessons from Pseudomonas aeruginosa and other bacteria. J. Biol. Chem. 291, 12547–12555 (2016).
Ryan, R. P. et al. Cyclic di-GMP signalling in the virulence and environmental adaptation of Xanthomonas campestris. Mol. Microbiol. 63, 429–442 (2006).
Hallez, R., Delaby, M., Sanselicio, S. & Viollier, P. H. Hit the right spots: cell cycle control by phosphorylated guanosines in alphaproteobacteria. Nat. Rev. Microbiol. 15, 137–148 (2017).
Shyp, V. et al. Reciprocal growth control by competitive binding of nucleotide second messengers to a metabolic switch in Caulobacter crescentus. Nat. Microbiol. 6, 59–72 (2021).
Fung, D. K., Trinquier, A. E. & Wang, J. D. Crosstalk between (p)ppGpp and other nucleotide second messengers. Curr. Opin. Microbiol. 76, 102398 (2023).
Turner, P., Barber, C. & Daniels, M. Behaviour of the transposons Tn5 and Tn7 in Xanthomonas campestris pv. campestris. Mol. Gen. Genet. 195, 101–107 (1984).
Zhang, Y., Zhang, Y., Zhang, B., Wu, X. & Zhang, L. Q. Effect of carbon sources on production of 2,4-diacetylphloroglucinol in Pseudomonas fluorescens 2P24. Acta Microbiol. Sin. 58, 1202–1212 (2018).
Kessler, B., de Lorenzo, V. & Timmis, K. N. A general system to integrate lacZ fusions into the chromosomes of gram-negative eubacteria: regulation of the Pm promoter of the Tol plasmid studied with all controlling elements in monocopy. Mol. Gen. Genet. 233, 293–301 (1992).
Berg, T., Tesoriero, L. & Hailstones, D. L. PCR-based detection of Xanthomonas campestris pathovars in Brassica seed. Plant Pathol. 54, 416–427 (2005).
Staskawicz, B., Dahlbeck, D., Keen, N. & Napoli, C. Molecular characterization of cloned avirulence genes from race 0 and race 1 of Pseudomonas syringae pv. glycinea. J. Bacteriol. 169, 5789–5794 (1987).
Osbourn, A. E., Clarke, B. R., Stevens, B. J. H. & Daniels, M. J. Use of oligonucleotide probes to identify members of two-component regulatory systems in Xanthomonas campestris pathor campestris. Mol. Gen. Genet. 222, 145–151 (1990).
Bai, K. et al. Transcriptional profiling of Xanthomonas campestris pv. campestris in viable but nonculturable state. BMC Genomics 24, 105 (2023).
Radonic, A. et al. Guideline to reference gene selection for quantitative real-time PCR. Biochem. Bioph. Res. Co. 313, 856–862 (2004).
Pfaffl, M. W. A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res. 29, 2002–2007 (2001).
Bai, K. et al. Evaluation of optimal reference genes for the normalization by qPCR in viable but nonculturable state in Xanthomonas campestris pv. campestris. J. Phytopathol. 170, 399–407 (2022).
Li, B. & Dewey, C. N. RSEM: accurate transcript quantification from RNA-Seq data with or without a reference genome. BMC Bioinforma. 12, 323 (2010).
Robinson, M. D., McCarthy, D. J. & Smyth, G. K. edgeR: a Bioconductor package for differential expression analysis of digital gene expression data. Bioinformatics 26, 139–140 (2010).
Han, C. et al. Majorbio Cloud 2024: update single-cell and multiomics workflows. iMeta 3, e217 (2024).
Acknowledgements
This work was supported by the Natural Science Foundation of Henan Province (number 252300423649) and the Beijing Municipal Natural Science Foundation (number 6222025).
Author information
Authors and Affiliations
Contributions
K.B. conceived and designed the research, performed the experiments, analyzed and interpreted the data, and wrote the manuscript. X.X. performed the experiments, analyzed and interpreted the data, and wrote the manuscript. C.Y. and H.Y. helped carry out the experiments. M.L. analyzed the data. N.J. and J.L. designed the research. J.Z. and Z.W. revised the manuscript. L.L. conceived and designed the research and revised the manuscript. All authors read and approved the final manuscript.
Corresponding author
Ethics declarations
Competing interests
The authors declare no competing interests.
Additional information
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary information
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Bai, K., Xu, X., Yu, C. et al. The ppGpp-HpaR1-gum regulatory pathway modulates exopolysaccharides production in Xanthomonas campestris pv. campestris. npj Biofilms Microbiomes (2026). https://doi.org/10.1038/s41522-026-00926-8
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/s41522-026-00926-8