Skip to content
DraconiticResearch
Search Sources API
206,690 studies31 sourcesUpdated 27 min ago
Peer-reviewedCC BY 4.0Microbiology Spectrum

A PhoP-regulated type II secretion system drives bacterial competition in Serratia marcescens

  1. 1Instituto de Biología Molecular y Celular de Rosario, Consejo Nacional de Investigaciones Científicas y Técnicas, Universidad Nacional de Rosario, Rosario, Argentina

Abstract

Serratia marcescens is an enteric bacterium that can act as an opportunistic pathogen, with increasing incidence in clinical settings. This is largely due to its ability to express a broad repertoire of virulence factors and acquire antibiotic resistance mechanisms. Consequently, S. marcescens has been designated by the World Health Organization (WHO) as a research priority for the development of alternative antimicrobial strategies. In this study, we identify a previously unrecognized role of the type II secretion system (T2SS) in mediating bacterial competition in the clinical strain S. marcescens RM66262. Phylogenomic analysis reveals that the T2SS is conserved among clinical isolates but absent from most environmental strains, suggesting it confers a selective advantage in host-associated or highly competitive environments. Functional assays demonstrate that the T2SS contributes to both inter- and intraspecies antagonism and acts in concert with the contact-dependent type VI secretion system (T6SS), with both systems contributing additively to bacterial killing through distinct mechanisms. We further show that T2SS expression is positively regulated by the PhoP/PhoQ two-component system through direct binding to its promoter region and is induced in response to competitive cues such as attack by Acinetobacter nosocomialis. Altogether, our findings expand the functional scope of the T2SS beyond classical extracellular virulence, establishing it as a PhoP-regulated system involved in bacterial competition and a promising target for novel anti-virulence strategies.

IMPORTANCE: This work uncovers a previously uncharacterized role for the type II secretion system (T2SS) in Serratia marcescens, demonstrating its involvement in both inter- and intraspecies bacterial competition. The finding that the T2SS is conserved among clinical isolates but largely absent in environmental strains suggests that this system confers a selective advantage in host-associated or high-competition settings. Furthermore, we show that T2SS expression is regulated by the PhoP/PhoQ system and induced by interbacterial contact, underscoring its role in adaptive antagonistic responses. By expanding the known functional scope of the T2SS, this study provides new insights into the ecological strategies of opportunistic pathogens and highlights a promising target for anti-virulence therapeutic development.

Related

  1. Caenorhabditis elegans and Serratia marcescens host-parasite coevolution model strains derived through mutagenesis and experimental evolution
    Samuel Preston Slowinski, Levi T. Morran
    EcoEvoRxivPreprintCC BY-NC-ND 4.0Full textGenetics & genomicsEcoEvoRxiv
  2. Phage therapy for multidrug-resistant Serratia marcescens infection: mechanisms, preclinical evidence, and translational challenges
    Shengting Zhang, Huili Tao, Sha Zhao +1
    Frontiers in MicrobiologyPeer-reviewedCC BY 4.0Full textEcologyCrossrefEurope PMCPMC
  3. Predictive comparison and evaluation of ANN and ANFIS as effective tools in modeling prodigiosin production by Serratia marcescens ND93
    Köksal Erentürk, Neslihan Dikbaş, Sevda Uçar +1
    BMC BiotechnologyPeer-reviewedCC BY-NC-ND 4.0Full textSystems & synthetic biologyPMC
  4. M.FcoHsdM-dependent DNA methylation coordinates secretion-associated gene expression, interbacterial competition, and virulence in Flavobacterium columnare
    R. Zhu, Y. Zhang, Y. Zhu +2
    bioRxivPreprintAll rights reservedFull textMicrobiologybioRxiv
  5. A GacS-mediated regulatory framework coordinates bacterial competition and rhizosphere microbiome remodeling in Pseudomonas fluorescens
    Yuan Luo, Jing Wang, Yi-Nan Ma +3
    MicrobiomePeer-reviewedCC BY-NC-ND 4.0Plant biologyCrossref
BibTeX
@article{sartori2026phopregulated,
  title = {{A PhoP-regulated type II secretion system drives bacterial competition in Serratia marcescens}},
  author = {María Sol Sartori and Brayan S. Arango Gil and Eleonora García Véscovi and Javier F. Mariscotti},
  journal = {Microbiology Spectrum},
  year = {2026},
  month = oct,
  doi = {10.1128/spectrum.02169-26},
  url = {https://doi.org/10.1128/spectrum.02169-26},
  note = {CC BY 4.0},
}
RIS
TY  - JOUR
TI  - A PhoP-regulated type II secretion system drives bacterial competition in Serratia marcescens
AU  - María Sol Sartori
AU  - Brayan S. Arango Gil
AU  - Eleonora García Véscovi
AU  - Javier F. Mariscotti
PY  - 2026
DA  - 2026/10/15
JO  - Microbiology Spectrum
DO  - 10.1128/spectrum.02169-26
UR  - https://doi.org/10.1128/spectrum.02169-26
AB  - Serratia marcescens is an enteric bacterium that can act as an opportunistic pathogen, with increasing incidence in clinical settings. This is largely due to its ability to express a broad repertoire of virulence factors and acquire antibiotic resistance mechanisms. Consequently, S. marcescens has been designated by the World Health Organization (WHO) as a research priority for the development of alternative antimicrobial strategies. In this study, we identify a previously unrecognized role of the type II secretion system (T2SS) in mediating bacterial competition in the clinical strain S. marcescens RM66262. Phylogenomic analysis reveals that the T2SS is conserved among clinical isolates but absent from most environmental strains, suggesting it confers a selective advantage in host-associated or highly competitive environments. Functional assays demonstrate that the T2SS contributes to both inter- and intraspecies antagonism and acts in concert with the contact-dependent type VI secretion system (T6SS), with both systems contributing additively to bacterial killing through distinct mechanisms. We further show that T2SS expression is positively regulated by the PhoP/PhoQ two-component system through direct binding to its promoter region and is induced in response to competitive cues such as attack by Acinetobacter nosocomialis. Altogether, our findings expand the functional scope of the T2SS beyond classical extracellular virulence, establishing it as a PhoP-regulated system involved in bacterial competition and a promising target for novel anti-virulence strategies.  IMPORTANCE: This work uncovers a previously uncharacterized role for the type II secretion system (T2SS) in Serratia marcescens, demonstrating its involvement in both inter- and intraspecies bacterial competition. The finding that the T2SS is conserved among clinical isolates but largely absent in environmental strains suggests that this system confers a selective advantage in host-associated or high-competition settings. Furthermore, we show that T2SS expression is regulated by the PhoP/PhoQ system and induced by interbacterial contact, underscoring its role in adaptive antagonistic responses. By expanding the known functional scope of the T2SS, this study provides new insights into the ecological strategies of opportunistic pathogens and highlights a promising target for anti-virulence therapeutic development.
SN  - 2165-0497
ER  -