# Architecture and regulatory functions of c-di-GMP signaling in classical Bordetella species

**Authors:** Denisa Vondrova, Sabrina Laura Mugni, Jan Blumenstein, Clara Kasiztky, Federico Sisti, Julieta Fernández, Jana Kamanova

PMC · DOI: 10.1093/femsre/fuaf065 · FEMS Microbiology Reviews · 2025-12-26

## TL;DR

This paper reviews how the c-di-GMP signaling pathway regulates important functions like virulence and biofilm formation in Bordetella bacteria.

## Contribution

The paper provides a comprehensive overview of the c-di-GMP signaling architecture and its regulatory roles in classical Bordetella species.

## Key findings

- c-di-GMP signaling interacts with the BvgAS system to regulate virulence gene expression.
- The LapD-LapG proteolytic switch controls the BrtA adhesin in Bordetella.
- c-di-GMP suppresses the type III secretion system in these bacteria.

## Abstract

Cyclic di-GMP (c-di-GMP) is a highly conserved bacterial second messenger that regulates important processes such as motility, biofilm formation and virulence. In this review, we investigate the architecture and regulatory functions of c-di-GMP signaling in classical Bordetella species, including B. bronchiseptica, B. parapertussis and B. pertussis. We examine how the c-di-GMP signaling pathway interacts with the BvgAS two-component system and other signaling pathways to coordinate virulence gene expression and surface-associated behaviors in these respiratory pathogens. In particular, we highlight the functions of characterized diguanylate cyclases (DGCs), phosphodiesterases (PDEs) and dual-domain proteins, focusing on regulatory modules such as the BdcA-DdpA scaffold complex, the oxygen-sensing DGC BpeGReg and the LapD-LapG proteolytic switch that controls BrtA adhesin. We also propose a model for the function of BvgR, a PDE-like protein lacking catalytic residues, and discuss how c-di-GMP suppresses the type III secretion system. Importantly, we highlight the diversity of the c-di-GMP network in classical Bordetella species, likely reflecting their evolutionary specialization. To conclude, we outline important open questions and suggest future research directions, including the identification of sensory ligands and c-di-GMP effectors. Overall, our review illustrates the importance of c-di-GMP as a critical, but still incompletely understood, regulatory hub in Bordetella pathogenesis.

This review summarizes current literature on c-di-GMP signaling in classical Bordetella species and examines the molecular architecture of the network and its regulatory roles in Bordetella physiology and pathogenesis.

## Linked entities

- **Genes:** bdcA (oxidoreductase) [NCBI Gene 913828], ddpA (D,D-dipeptide ABC transporter periplasmic binding protein) [NCBI Gene 917292], lapD (cyclic di-GMP receptor LapD) [NCBI Gene 32803494], lapG (cysteine protease LapG) [NCBI Gene 32803493], brtA (bile-regulated transcriptional regulator BrtA) [NCBI Gene 32489313], bvgR (virulence regulation phosphodiesterase BvgR) [NCBI Gene 56479104]
- **Proteins:** bvgR (virulence regulation phosphodiesterase BvgR)
- **Chemicals:** cyclic di-GMP (c-di-GMP) (PubChem CID 137221491)

## Full-text entities

- **Chemicals:** oxygen (MESH:D010100), Cyclic di-GMP (MESH:C062025)
- **Species:** Bordetella bronchiseptica (species) [taxon 518], Bordetella pertussis (species) [taxon 520], Bordetella parapertussis (species) [taxon 519]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12805831/full.md

## References

158 references — full list in the complete paper: https://tomesphere.com/paper/PMC12805831/full.md

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Source: https://tomesphere.com/paper/PMC12805831