Abstract
Pseudomonas aeruginosa is a serious pathogen involved in nosocomial infections. Its pathogenicity is owed to rich production of virulence factors (VIFs) regulated by several complex hierarchical signal systems depending on environmental conditions, medium composition, and the presence of certain active compounds in it. Choline (Ch), which exists in patient tissues, and ethanol (Et), whose consumption aggravates infections, were reported to augment this microbe virulence. The goal of the present study was to show the effect of Et addition to P. aeruginosa cultures in two media (minimal culture medium [MM] and Eagon-Grelet medium [EGM]) in the absence or presence of Ch on its VIF levels. In MM, Et sharply repressed the basal and Ch-induced levels of the P. aeruginosa lectins PA-IL (galactose-specific) and PA-IIL (fucose/mannose-binding) and proteolytic activities, while increasing C6-HSL (autoinducer), hemolytic phospholipase C (PLC-H), and phosphatase levels. In EGM, it profoundly increased lectin, protease, pyocyanin, rhamnolipid (RhaL), autoinducer, and slightly phosphatase levels, but reduced Ch-induced protease, PLC-H, and acid phosphatase activities, except the short-chain HSL levels, which were increased by Et in combination with Ch. The presented results enlighten part of the complex molecular basis of Et-induced aggravation of P. aeruginosa infections due to increasing the bacterium virulence, which runs in parallel to suppression of the patient’s immunity.
Similar content being viewed by others
Literature Cited
Brown MRW, Scott Foster JHS (1970) A simple diagnostic milk medium for Pseudomonas aeruginosa. J Clin Pathol 23:172–177
Byng GS, Eustice DC, Jensen RA (1979) Biosynthesis of phenazine pigments in mutant and wild-type cultures of Pseudomonas aeruginosa. J Bacteriol 138:846–852
Chen AH, Innis SM, Davidson AG, James SJ (2005) Phosphatidylcholine and lysophosphatidylcholine excretion is increased in children with cystic fibrosis and is associated with plasma homocysteine, S-adenosylhomocysteine, and S-adenosylmethionine. Am J Clin Nutr 81:686–691
Ciocci G, Mitchell EP, Cautier C, Wimmerova M, Sudakevitz D, Perez S, Gilboa-Garber N, Imberty A (2003) Structural basis of calcium and galactose recognition by the lectin PA-IL of Pseudomonas aeruginosa. FEBS Lett 555:297–301
de Roux A, Cavalcanti M, Marcos MA, Garcia E, Ewig S, Mensa J, Torres A (2006) Impact of alcohol abuse in the etiology and severity of community-acquired pneumonia. Chest 129:1219–1225
DeVault JD, Kimbara K, Chakrabarty AM (1990) Pulmonary dehydration and infection in cystic fibrosis: evidence that ethanol activates alginate gene expression and induction of mucoidy in Pseudomonas aeruginosa. Mol Microbiol 4:737–745
Eagon RG (1956) Studies on polysaccharide formation by Pseudomonas fluorescens. Can J Microbiol 2:673–677
Faunce DE, Garner JL, Llanas JN, Patel PJ, Gregory MS, Duffner LA, Gamelli RL, Kovacs EJ (2003) Effect of acute ethanol exposure on the dermal inflammatory response after burn injury. Alcohol Clin Exp Res 27:1199–1206
Fiske CH, Subbarow J (1925) The colorimetric determination of phosphorus. J Biol Chem 66:375–400
Gilboa-Garber N (1972) Purification and properties of hemagglutinin from Pseudomonas aeruginosa and its reaction with human blood cells. Biochim Biophys Acta 273:165–173
Gilboa-Garber N (1982) Pseudomonas aeruginosa lectins. Methods Enzymol 83:378–385
Gilboa-Garber N (1997) Multiple aspects of Pseudomonas aeruginosa lectins. Nova Acta Leopold 75:153–177
Gilboa-Garber N, Garber N (1989) Microbial lectin cofunction with lytic activities as a model for a general basic lectin role. FEMS Microbiol Rev 63:211–221
Gilboa-Garber N, Zakut V, Mizrahi L (1973) Production of cholinesterase by Pseudomonas aeruginosa, its regulation by glucose and cyclic AMP and inhibition by antiserum. Biochim Biophys Acta 297:120–124
Glick J, Garber N, Shohet D (1987) Surface haemagglutinating activity of Pseudomonas aeruginosa. Microbios 50:69–80
Greenberg SS, Zhao X, Hua L, Wang JF, Nelson S, Ouyang J (1999) Ethanol inhibits lung clearance of Pseudomonas aeruginosa by a neutrophil and nitric oxide-dependent mechanism, in vivo. Alcohol Clin Exp Res 23:735–744
Imberty A, Wimmerova M, Mitchell EP, Gilboa-Garber N (2004) Structures of the lectins from Pseudomonas aeruginosa : insights into the molecular basis for host glycan recognition. Microb Infect 6:221–228
Jerrells TR (1991) Immunodeficiency associated with ethanol abuse. Adv Exp Med Biol 288:229–236
Johnson MK, Boese-Marrazzo D (1980) Production and properties of heat-stable extracellular hemolysin from Pseudomonas aeruginosa. Infect Immun 29:1028–1033
Lisa TA, Garrido MN, Domenech CE (1983) Induction of acid phosphatase and cholinesterase activities in Ps. aeruginosa and their in-vitro control by choline, acetylcholine and betaine. Mol Cell Biochem 50:149–155
Lowry OH, Rosebrough NJ, Farr AL, Randall RJ (1951) Protein measurement with the folin phenol reagent. J Biol Chem 193:265–272
Lucchesi GI, Lisa TA, Domenech CE (1989) Choline and betaine as inducer agents of Pseudomonas aeruginosa phospholipase C activity in high phosphate medium. FEMS Microbiol Lett 48:335–338
Matsufuji M, Nakata K, Yoshimoto A (1997) High production of rhamnolipids by Pseudomonas aeruginosa growing on ethanol. Biotechnol Lett 19:1213–1215
McClean KH, Winson MK, Fish L, Taylor A, Chhabra SR, Camara M, Daykin M, Lamb JH, Swift S, Bycroft BW, Stewart GSAB, Williams P (1997) Quorum sensing and Chromobacterium violaceum: exploitation of violacein production and inhibition for the detection of N-acylhomoserine lactones. Microbiology 143:3703–3711
Mitchell E, Houles C, Sudakevitz D, Wimmerova M, Gautier C, Perez S, Wu AM, Gilboa-Garber N, Imberty A (2002) Structural basis for oligosaccharide-mediated adhesion of Pseudomonas aeruginosa in the lung of cystic fibrosis patients. Nature Struct Biol 9:918–921
Nicas TI, Iglewski BH (1985) The contribution of exoproducts to virulence of Pseudomonas aeruginosa. Can J Microbiol 31:387–392
Pearson JP, Passador L, Iglewski BH, Greenberg EP (1995) A second N-acylhomoserine lactone signal produced by Pseudomonas aeruginosa. Proc Natl Acad Sci USA 92:1490–1494
Sage AE, Vasil ML (1997) Osmoprotectant-dependent expression of plcH, encoding the hemolytic phospholipase C, is subject to novel catabolite repression control in Pseudomonas aeruginosa PAO1. J Bacteriol 179:4874–4881
Schlictman D, Kubo M, Shankar S, Chakrabarty AM (1995) Regulation of nucleoside diphosphate kinase and secretable virulence factors in Pseudomonas aeruginosa: roles of algR2 and algH. J Bacteriol 177:2469–2474
Schuster M, Greenberg EP (2006) A network of networks: quorum-sensing gene regulation in Pseudomonas aeruginosa. Int J Med Microbiol 296:73–81
Sokol PA, Ohman DE, Iglewski BH (1979) A more sensitive plate assay for detection of protease production by Pseudomanas aeruginosa. J Clin Microbiol 9:538–540
Wagner VE, Frelinger JG, Barth RK, Iglewski BH (2006) Quorum sensing: dynamic response of Pseudomonas aeruginosa to external signals. Trends Microbiol 14:55–58
Winzer K, Falconer C, Garber NC, Diggle SP, Camara M, Williams P (2000) The Pseudomonas aeruginosa lectins PA-IL and PA-IIL are controlled by quorum sensing and by RpoS. J Bacteriol 182:6401–6411
Zhang P, Bagby GJ, Happel KI, Summer WR, Nelson S (2002) Pulmonary host defenses and alcohol. Front Biosci 7:1314–1330
Acknowledgments
The research, which is part of N. Katri’s Ph.D. thesis, was supported by Bar-Ilan University research funds. The authors thank Ms. Sharon Victor and Ms. Ela Gindy for their great help in the preparation of the manuscript and graphic presentation.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Katri, N., Gilboa-Garber, N. Ethanol Effects on Pseudomonas aeruginosa Lectin, Protease, Hemolysin, Pyocyanin, Autoinducer, and Phosphatase Levels Depending on Medium Composition and Choline Presence. Curr Microbiol 54, 296–301 (2007). https://doi.org/10.1007/s00284-006-0441-7
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00284-006-0441-7