Effect of osmotic stress and culture density on invasiveness of Listeria monocytogenes strains

International Journal of Food Microbiology

Volumn 144, Issue 3, 2011, Pages 440-445

  Walecka, Ewa ^a   Molenda, Jerzy ^a   Karpíšková, Renata ^b   Bania, Jacek ^a  

^a WROC AW UNIVERSITY OF ENVIRONMENTAL AND LIFE SCIENCES   (Poland)

^b NATIONAL INSTITUTE OF PUBLIC HEALTH   (Czech Republic)

Author keywords

Growth phase; Invasiveness; Listeria monocytogenes; Osmotic stress; Plaque forming

Indexed keywords

SODIUM CHLORIDE;

ARTICLE; BACTERIAL GROWTH; BACTERIUM CULTURE; CONCENTRATION (PARAMETERS); CONTROLLED STUDY; HUMAN; HUMAN CELL; LISTERIA MONOCYTOGENES; MICROBIAL POPULATION DYNAMICS; NONHUMAN; OSMOTIC STRESS; SPECIES INVASION;

BACTERIAL PROTEINS; GENE EXPRESSION REGULATION, BACTERIAL; HT29 CELLS; HUMANS; LISTERIA MONOCYTOGENES; SODIUM CHLORIDE; STRESS, PHYSIOLOGICAL; TIME FACTORS;

LISTERIA MONOCYTOGENES;

EID: 78649987213     PISSN: 01681605     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ijfoodmicro.2010.10.032     Document Type: Article

References (22)

1. Bo Andersen J., Roldgaard B.B., Christensen B.B., Licht T.R. Oxygen restriction increases the infective potential of Listeria monocytogenes in vitro in Caco-2 cells and in vivo in guinea pigs. BMC Microbiol. 2007, 7:55.
2. Bierne H., Sabet C., Personnic N., Cossart P. Internalins: a complex family of leucine-rich repeat-containing proteins in Listeria monocytogenes. Microbes Infect. 2007, 9:1156-1166.
3. Boor K.J. Bacterial stress responses: what doesn't kill them can make them stronger. PLoS Biol. 2006, 4:e23.
4. Chowduhry R., Sahu G.K., Das J. Stress response in pathogenic bacteria. J. Biosci. 1996, 21:149-160.
5. Conte M.P., Petrone G., Di Biase A.M., Ammendolia M.G., Superti F., Seganti L. Acid tolerance in Listeria monocytogenes influences invasiveness of enterocyte-like cells and macrophage-like cells. Microb. Pathog. 2000, 29:137-144.
6. Doumith M., Buchrieser C., Glaser P., Jacquet C., Martin P. Differentiation of the major Listeria monocytogenes serovars by multiplex PCR. J. Clin. Microbiol. 2004, 42:3819-3822.
7. Garner M.R., James K.E., Callahan M.C., Wiedmann M., Boor K.J. Exposure to salt and organic acids increases the ability of Listeria monocytogenes to invade Caco-2 cells but decreases its ability to survive gastric stress. Appl. Environ. Microbiol. 2006, 72:5384-5395.
8. Kazmierczak M.J., Wiedmann M., Boor K.J. Contributions of Listeria monocytogenes sigmaB and PrfA to expression of virulence and stress response genes during extra- and intracellular growth. Microbiology 2006, 152:1827-1838.
9. Kim H., Marquis H., Boor K.J. SigmaB contributes to Listeria monocytogenes invasion by controlling expression of inlA and inlB. Microbiology 2005, 151:3215-3222.
10. Kolter R.D., Siegele A., Tormo A. The stationary phase of the bacterial life cycle. Annu. Rev. Microbiol. 1993, 47:855-874.
11. Mead P.S., Slutsker L., Dietz V., McCaig L.F., Bresee J.S., Shapiro C., Griffin P.M., Tauxe R.V. Food-related illness and death in the United States. Emerg. Infect. Dis. 1999, 5:607-625.
12. Pfaffl M.W. A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res. 2001, 29:2002-2007.
13. Olesen I., Vogensen F.K., Jespersen L. Gene transcription and virulence potential of Listeria monocytogenes strains after exposure to acidic and NaCl stress. Foodborne Pathog. Dis. 2009, 6:669-680.
14. Rees C.E., Dodd C.E., Gibson P.T., Booth I.R., Stewart G.S. The significance of bacteria in stationary phase to food microbiology. Int. J. Food Microbiol. 1995, 28:263-275.
15. Roche S.M., Gracieux P., Milohanic E., Albert I., Virlogeux-Payant I., Témoin S., Grépinet O., Kerouanton A., Jacquet C., Cossart P., Velge P. Investigation of specific substitutions in virulence genes characterizing phenotypic groups of low-virulence field strains of Listeria monocytogenes. Appl. Environ. Microbiol. 2005, 71:6039-6048.
16. Roche S.M., Velge P., Bottreau E., Durier C., Marquet-van der Mee N., Pardon P. Assessment of the virulence of Listeria monocytogenes: agreement between a plaque-forming assay with HT-29 cells and infection of immunocompetent mice. Int. J. Food Microbiol. 2001, 68:33-44.
17. Sue D., Fink D., Wiedmann M., Boor K.J. Sigma B-dependent gene induction and expression in Listeria monocytogenes during osmotic and acid stress conditions simulating the intestinal environment. Microbiology 2004, 150:3843-3855.
18. Vázquez-Boland J.A., Kuhn M., Berche P., Chakraborty T., Domínguez-Bernal G., Goebel W., González-Zorn B., Wehland J., Kreft J. Listeria pathogenesis and molecular virulence determinants. Clin. Microbiol. Rev. 2001, 14:584-640.
19. Velge P., Bottreau E., Van-Langendonck N., Kaeffer B. Cell proliferation enhances entry of Listeria monocytogenes into intestinal epithelial cells by two proliferation-dependent entry pathways. J. Med. Microbiol. 1997, 46:681-692.
20. Werbrouck H., Grijspeerdt K., Botteldoorn N., Van Pamel E., Rijpens N., Van Damme J., Uyttendaele M., Herman L., Van Coillie E. Differential inlA and inlB expression and interaction with human intestinal and liver cells by Listeria monocytogenes strains of different origins. Appl. Environ. Microbiol. 2006, 72:3862-3871.
21. Werbrouck H., Vermeulen A., Van Coillie E., Messens W., Herman L., Devlieghere F., Uyttendaele M. Influence of acid stress on survival, expression of virulence genes and invasion capacity into Caco-2 cells of Listeria monocytogenes strains of different origins. Int. J. Food Microbiol. 2009, 31:140-146.
22. Zhou X., Jiao X., Wiedmann M. Listeria monocytogenes in the Chinese food system: strain characterization through partial actA sequencing and tissue-culture pathogenicity assays. J. Med. Microbiol. 2005, 54:217-224.