» Articles » PMID: 31259174

Biofilm Adaptation to Different Temperatures Seen Through Shotgun Proteomics

Overview
Journal Front Nutr
Date 2019 Jul 2
PMID 31259174
Citations 22
Authors
Affiliations
Soon will be listed here.
Abstract

is a foodborne pathogen that can cause invasive severe human illness (listeriosis) in susceptible patients. Most human listeriosis cases appear to be caused by consumption of refrigerated ready-to-eat foods. Although initial contamination levels in foods are usually low, the ability of these bacteria to survive and multiply at low temperatures allows it to reach levels high enough to cause disease. This study explores the set of proteins that might have an association with adaptation to different temperatures. Cultures were grown in biofilm, the most widespread mode of growth in natural and industrial realms. Protein extractions were performed from three different growth temperatures (10, 25, and 37°C) and two growth phases (early stage and mature biofilm). subproteomes were targeted using three extraction methods: trypsin-enzymatic shaving, biotin-labeling and cell fractionation. The different subproteomes obtained were separated and analyzed by shotgun proteomics using high-performance liquid chromatography combined with tandem mass spectrometry (LC-OrbiTrap LTQVelos, ThermoFisher Scientific). A total of 141 (biotinylation), 98 (shaving) and 910 (fractionation) proteins were identified. Throughout the 920 unique proteins identified, many are connected to basic cell functions, but some are linked with thermoregulation. We observed some noteworthy protein abundance shifts associated with the major adaptation to cold mechanisms present in , namely: the role of ribosomes and the stressosome with a higher abundance of the general stress protein Ctc (Rl25) and the general stress transcription factor sigma B (σ), changes in cell fluidity and motility seen by higher levels of foldase protein PrsA2 and flagellin (FlaA), the uptake of osmolytes with a higher abundance of glycine betaine (GbuB) and carnitine transporters (OpucA), and the relevance of the overexpression of chaperone proteins such as cold shock proteins (CspLA and Dps). As for 37°C, we observed a significantly higher percentage of proteins associated with transcriptional or translational activity present in higher abundance upon comparison with the colder settings. These contrasts of protein expression throughout several conditions will enrich databases and help to model the regulatory circuitry that drives adaptation of to environments.

Citing Articles

Recent advances in examining the factors influencing the efficacy of biocides against Listeria monocytogenes biofilms in the food industry: A systematic review.

Arthur M, Afari E, Alexa E, Zhu M, Gaffney M, Celayeta J Compr Rev Food Sci Food Saf. 2024; 24(1):e70083.

PMID: 39736097 PMC: 11684510. DOI: 10.1111/1541-4337.70083.


Differential analysis of transcriptome of psychrophilic bacteria under different culture temperatures.

Xu C, Yang L, Zhu R, Zhang J, Li Y, Chao C Technol Health Care. 2024; 32(4):2251-2264.

PMID: 38517814 PMC: 11322704. DOI: 10.3233/THC-231022.


Contrasting genes conferring short- and long-term biofilm adaptation in .

Monteith W, Pascoe B, Mourkas E, Clark J, Hakim M, Hitchings M Microb Genom. 2023; 9(10).

PMID: 37850975 PMC: 10634452. DOI: 10.1099/mgen.0.001114.


Antimicrobial Activity of Sertraline on .

Wang Y, Li L, Cai P, Olsen R, Peng S, Meng H Int J Mol Sci. 2023; 24(5).

PMID: 36902108 PMC: 10002541. DOI: 10.3390/ijms24054678.


Anti-Biofilm Activity of Cell Free Supernatants of Selected Lactic Acid Bacteria against Isolated from Avocado and Cucumber Fruits, and from an Avocado Processing Plant.

Masebe R, Thantsha M Foods. 2022; 11(18).

PMID: 36141000 PMC: 9498153. DOI: 10.3390/foods11182872.


References
1.
Pontinen A, Markkula A, Lindstrom M, Korkeala H . Two-Component-System Histidine Kinases Involved in Growth of Listeria monocytogenes EGD-e at Low Temperatures. Appl Environ Microbiol. 2015; 81(12):3994-4004. PMC: 4524140. DOI: 10.1128/AEM.00626-15. View

2.
Junttila J, Niemela S, Hirn J . Minimum growth temperatures of Listeria monocytogenes and non-haemolytic Listeria. J Appl Bacteriol. 1988; 65(4):321-7. DOI: 10.1111/j.1365-2672.1988.tb01898.x. View

3.
Angelidis A, Smith G . Role of the glycine betaine and carnitine transporters in adaptation of Listeria monocytogenes to chill stress in defined medium. Appl Environ Microbiol. 2003; 69(12):7492-8. PMC: 310023. DOI: 10.1128/AEM.69.12.7492-7498.2003. View

4.
Chan Y, Raengpradub S, Boor K, Wiedmann M . Microarray-based characterization of the Listeria monocytogenes cold regulon in log- and stationary-phase cells. Appl Environ Microbiol. 2007; 73(20):6484-98. PMC: 2075049. DOI: 10.1128/AEM.00897-07. View

5.
Autret N, Raynaud C, Dubail I, Berche P, Charbit A . Identification of the agr locus of Listeria monocytogenes: role in bacterial virulence. Infect Immun. 2003; 71(8):4463-71. PMC: 166014. DOI: 10.1128/IAI.71.8.4463-4471.2003. View