» Articles » PMID: 22092717

Listeria Monocytogenes Adapts to Long-term Stationary Phase Survival Without Compromising Bacterial Virulence

Overview
Specialty Microbiology
Date 2011 Nov 19
PMID 22092717
Citations 15
Authors
Affiliations
Soon will be listed here.
Abstract

Bacteria withstand starvation during long-term stationary phase through the acquisition of mutations that increase bacterial fitness. The evolution of the growth advantage in stationary phase (GASP) phenotype results in the ability of bacteria from an aged culture to outcompete bacteria from a younger culture when the two are mixed together. The GASP phenotype was first described for Escherichia coli, but has not been examined for an environmental bacterial pathogen, which must balance long-term survival strategies that promote fitness in the outside environment with those that promote fitness within the host. Listeria monocytogenes is an environmental bacterium that lives as a saprophyte in soil, but is capable of replicating within the cytosol of mammalian cells. Herein, we demonstrate the ability of L. monocytogenes to express GASP via the acquisition of mutations during long-term stationary growth. Listeria monocytogenes GASP occurred through mechanisms that were both dependent and independent of the stress-responsive alternative sigma factor SigB. Constitutive activation of the central virulence transcriptional regulator PrfA interfered with the development of GASP; however, L. monocytogenes GASP cultures retained full virulence in mice. These results indicate that L. monocytogenes can accrue mutations that optimize fitness during long-term stationary growth without negatively impacting virulence.

Citing Articles

cell-to-cell spread bypasses nutrient limitation for replicating intracellular bacteria.

Radhakrishnan P, Theriot J bioRxiv. 2025; .

PMID: 39975404 PMC: 11838505. DOI: 10.1101/2025.01.31.635960.


Pseudomonas putida Dynamics of Adaptation under Prolonged Resource Exhaustion.

Gross J, Katz S, Hershberg R Genome Biol Evol. 2024; 16(6).

PMID: 38849986 PMC: 11179108. DOI: 10.1093/gbe/evae117.


Two Permeases Associated with the Multifunctional CtaP Cysteine Transport System in Listeria monocytogenes Play Distinct Roles in Pathogenesis.

Vaval Taylor D, Xayarath B, Freitag N Microbiol Spectr. 2023; 11(3):e0331722.

PMID: 37199604 PMC: 10269559. DOI: 10.1128/spectrum.03317-22.


Investigating Transcriptomic Induction of Resistance and/or Virulence in Cells Surviving Sublethal Antimicrobial Exposure.

Kokkoni E, Andritsos N, Sakarikou C, Michailidou S, Argiriou A, Giaouris E Foods. 2021; 10(10).

PMID: 34681431 PMC: 8535302. DOI: 10.3390/foods10102382.


Molecular Evolutionary Dynamics of Energy Limited Microorganisms.

Shoemaker W, Polezhaeva E, Givens K, Lennon J Mol Biol Evol. 2021; 38(10):4532-4545.

PMID: 34255090 PMC: 8476154. DOI: 10.1093/molbev/msab195.


References
1.
Zambrano M, Siegele D, Almiron M, Tormo A, Kolter R . Microbial competition: Escherichia coli mutants that take over stationary phase cultures. Science. 1993; 259(5102):1757-60. DOI: 10.1126/science.7681219. View

2.
Garner M, Njaa B, Wiedmann M, Boor K . Sigma B contributes to Listeria monocytogenes gastrointestinal infection but not to systemic spread in the guinea pig infection model. Infect Immun. 2006; 74(2):876-86. PMC: 1360341. DOI: 10.1128/IAI.74.2.876-886.2006. View

3.
STEINHAUS E, BIRKELAND J . Studies on the Life and Death of Bacteria: I. The Senescent Phase in Aging Cultures and the Probable Mechanisms Involved. J Bacteriol. 1939; 38(3):249-61. PMC: 374517. DOI: 10.1128/jb.38.3.249-261.1939. View

4.
Finkel S, Kolter R . Evolution of microbial diversity during prolonged starvation. Proc Natl Acad Sci U S A. 1999; 96(7):4023-7. PMC: 22413. DOI: 10.1073/pnas.96.7.4023. View

5.
Kazmierczak M, Mithoe S, Boor K, Wiedmann M . Listeria monocytogenes sigma B regulates stress response and virulence functions. J Bacteriol. 2003; 185(19):5722-34. PMC: 193959. DOI: 10.1128/JB.185.19.5722-5734.2003. View