Catabolite Repression and Virulence Gene Expression in Listeria monocytogenes

• Published in: Current microbiology 2004-08, Vol.49 (2), p.95-98
• Main Authors: Gilbreth, S.E, Benson, A.K, Hutkins, R.W
• Format: Article
• Language: English
• Subjects: animal pathogenic bacteria; Arbutin - metabolism; Bacteria; bacterial proteins; Bacterial Proteins - genetics; bacterial toxins; Bacterial Toxins - genetics; Benzyl Alcohols - metabolism; Carbohydrate Metabolism; Carbohydrates; Cellobiose - metabolism; culture media; Fermentation; gene expression regulation; Gene Expression Regulation, Bacterial; glucose; Glucose - metabolism; Glucosides; Heat-Shock Proteins - genetics; Hemolysin Proteins; Listeria monocytogenes; Listeria monocytogenes - genetics; Listeria monocytogenes - growth & development; Listeria monocytogenes - metabolism; listeriolysin; listeriosis; Maltose - metabolism; Mannose - metabolism; microbial physiology; Microbiology; pathogenesis; Peptide Termination Factors; Sugar; Sugar Alcohols - metabolism; sugars; Trans-Activators - genetics; transcription (genetics); Transcription, Genetic; Trehalose - metabolism; Virulence Factors - genetics; Virulence Factors - metabolism
• ISSN: 0343-8651; 1432-0991
• DOI: 10.1007/s00284-004-4204-z

Previous studies have suggested that carbohydrates may affect expression of virulence genes in Listeria monocytogenes. Which carbohydrates influence virulence gene expression and how carbohydrates mediate expression, however, is not clear. The goal of this work was to examine how carbohydrates affect virulence gene expression in L. monocytogenes 10403S. Growth studies were conducted in medium containing glucose and various sugars. Metabolism of arbutin, arabitol, cellobiose, mannose, maltose, trehalose, and salicin were repressed in the presence of glucose. Only when glucose was consumed were these sugars fermented, indicating that catabolite repression by glucose had occurred. To determine whether virulence gene expression was also influenced by catabolite repression, we performed primer extension experiments, using primers for hly and prfA, which encode for a hemolysin and the regulator protein PrfA, respectively. In the presence of cellobiose and arbutin, transcription of hemolysin was reduced. However, none of the sugars affected transcription of prfA. The results demonstrate that catabolite repression occurs in L. monocytogenes and suggests that, at least in strain 10403S, cellobiose and arbutin repress expression of hemolysin.