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2009 | 58 | 4 |

Tytuł artykułu

Viable but non-culturable state [VBNC] of Escherichia coli related to EnvZ under the effect of pH, starvation and osmotic stress in sea water

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
When exposed extreme environmental conditions such as sea water, bacteria have been shown different survival strategy for continue their life. One of this strategy known as viable but nonculturable (VBNC) state which is very important for nondifferiation bacteria. VBNC cells cause serious human health problems. Little is known, however, about the genetic mechanisms underlying the VBNC state. Under different environmental conditions, porins are important in the survival strategy of bacteria. EnvZ/OmpR work together as regulators of ompF and ompC gene expression. It is known that the EnvZ system has a role in VBNC state. In this study we tried to find out the viability of EnvZ, OmpC and OmpF mutant E. coli under stress effect of osmolarity, pH and starvation. Bacteria were suspended in filtered-autoclaved sea water microcosms and numbers determined over 25 day incubation periods by plate count (PC), direct viable count (DVC) and count of cells capable of respiration (RCC). As regard to results, alkaline pH affected E. coli more than acidic pH, which led to decline in number. On the contrary glycine betaine addition to sea water protected E. coli porin mutants and also reduced the death rate of bacteria. Under the effect of pH, osmotic stress and starvation stress, wild type E. coli and porin mutants entered a dormant state or became VBNC with the exception of MSZ31 (envZ mutant) E.coli cells which did not enter the VBNC state under the three tested stress conditions. This study is the first report to demonstrate that E. coli could not enter the VBNC state in the lack of EnvZ product under the stress of osmolarity, pH and starvation and the relationship between EnvZ and VBNC state are not affected by pH, osmolarity and starvation.

Wydawca

-

Rocznik

Tom

58

Numer

4

Opis fizyczny

p.307-317,fig.,ref.

Twórcy

autor
  • Dumlupinar University, Kutahya, Turkey
autor
autor
autor

Bibliografia

  • Aiba H., F. Nakasai, S. Mizushima and T. Mizuno. 1989. Evidence for the physiological importance of the phosphotransfer between the two regulatory components, EnvZ and OmpR in Escherichia coli. J. Biol. Chem. 264: 14090-14094.
  • Barcina I., P. Lebaron and J. Vives-Rego. 1997. Survival of allochthonous bacteria in aquatic systems: a biological approach. FEMS Microbiol. Ecol. 23: 1-9.
  • Colwell R.R. and D.J. Gray. 2000. Nonculturable Microorganisms in the Environment. American Society for Microbiology, Washington, DC, USA.
  • Darcan C., R. Özkanca and K.P. Flint. 2003. Survival of nonspecific porin-deficient mutants of Escherichia coli in Black Sea water. Letts. App. Microbiol. 37: 380-385.
  • Darcan C., R. Özkanca and Ö. Ídil. 2009. The role of RpoS, H-NS and AcP on the pH-dependent OmpC and OmpF porin expressions of Escherichia coli at different pH. African Journal of Biotechnology 8: 1845-1854.
  • Darcan C., 2005. An investigation on the effect of pH, starvation and osmotic stress on outer membrane porin protein synthesis level of Escherichia coli in the black sea water. Ph. D. Thesis, Deparment of Biology, Ondokuz Mayis University, 180 p.
  • Dawe L.L. and W.E. Penrose. 1978. "Bactericidal" property of seawater: death ordebilition? Appl. Environ. Microbiol. 35: 829-833.
  • Davies C.M. and L.M. Evison. 1991. Sunlight and survival of enteric bacteria in natural waters. J. Appl. Bacteriol. 70: 265-279
  • D'Souza-Ault M., L.T. Smith and G.M. Smith. 1993 Roles of N-acetylglutaminylglutamine amide and glycine betaine in adaptation of Pseudomonas aeruginosa to osmotic stress. Appl. Environ. Microbiol. 59: 473-478.
  • Ferrario M., B.R. Ernsting, D.W. Borstm, D.E. Wiese, R.M. Blumenthal and R.G. Matthews. 1995. The leucine-responsive regulatory protein of Escherichia coli negatively regulates transcription of ompC and micF and positively regulates translation of ompF. J. Bacteriol. 177: 103-113.
  • Forst S. and M. Inouye. 1988. Environmentally regulated gene expression for membrane proteins in Escherichia coli. Anna. Rev. Cell Biol. 4: 21-42.
  • Forst S., D. Comeau, S. Norioka and M. Inouye. 1987. Localization and membrane topology of EnvZ, a protein involved in osmoregulation of OmpF and OmpC in Escherichia coli. J. Biol. Chem. 262: 16433-16438.
  • Forst S., J. Delgado and M. Inouye. 1989. Phosphorylation of OmpR by the osmosensor EnvZ modulates the expression of the ompF and ompC genes of Escherichia coli. Proc. Natl. Acad. Sci. 86: 6052-6056.
  • Gurijala K.R. and M. Alexander. 1990. Explanation for the decline of bacteria introduced into lake waters. Micro. Ecol. 20: 231-244.
  • Hall M.N. and T.J. Silhavy. 1981. The ompB locus and the regulation of the major outer membrane porin proteins of Escherichia coli K-12. J. Mol. Biol. 146: 23-43.
  • Igo M.M. and T.J. Silhavy. 1988. EnvZ, a transmembrane environmental sensor of Escherichia coli K12, is phophorylated in vitro. J. Bacteriol. 170: 5971-5973.
  • Kaeriyama M., K.Machida, A. Kitakaze, H. Wang, Q. Lao, T. Fukamachi, H. Saito and H. Kobayashi. 2006. OmpC and OmpF are required for growth under hyperosmotic stress above pH 8 in Escherichia coli. Letts. Appl. Microbiol. 42: 196-201.
  • Kjelleberg S. and M. Hermannsson. 1987. Short-term responses to energy fluctuation by marine heterotrophic bacteria. In "Microbes in the sea" Ed Mitchell, R., and Sleigh, A. pp. 203-219. Chichester: John Wiley.
  • Koebnik R., K.P. Locher and P. Van Gelder. 2000. Structure and function of bacterial outer membrane proteins: barrels in a nutshell. Mol. Microbiol. 37: 239-253.
  • Kömerik N. and M. Wilson. 2002. Factors influencing the susceptibility of gram-negative bacteria to toluidine blue O-mediated lethal photosensitization. J. Appl. Microbiol. 92: 618-623.
  • Kogure K., U. Simidu and N. Taga. 1979. A tentative direct microscopic method for counting living marine bacteria. Can. J. Microbiol. 25: 415-420.
  • Kussovski V.K., A.E. Hristov and T.S. Radoucheva. 2001. Proflavine-mediated inactivation of Salmonella dublin exposed to visible sunlight in natural fresh water. Microbios 105: 119-125.
  • Liu X. and T. Ferenci. 1998. Regulation of porin-mediated outer membrane permeability by nutrient limitation in Escherichia coli. J. Bacteriol. 180: 3917-3922
  • Liu X. and T. Ferenci. 2001. An analysis of multifactorial influences on the transcriptional control of ompF and ompC porin expression under nutrient limitation. Microbiology 147: 2981-2989.
  • McCambridge J. and T.A. McMeekin. 1983. Effect of solar radiation and predacious micro-organisms on survival of faecal and other bacteria. Appl. Environ. Microbiol. 41: 1083-1087.
  • Muela A., C. Seco, E. Camafeita, I. Arana, M. Orruno, J.A. Lopez and I. Barcina. 2008. Changes in Escherichia coli outer membrane subproteome under environmental conditions inducing the viable but nonculturable state. FEMS Microbiol. Ecol. 64 (1), 28-36.
  • Munro P.M., J.M. Gauthier, A. Breittemayer and J. Bongiovanni. 1989. Influence of osmoregulation process on starvation survival of Escherichia coli in sea water. Appl. Environ. Microbiol. 55: 2017-2024.
  • Nikaido H. and M. Vaara. 1985. Molecular basis of bacterial outer membrane permeability. Microbiol. Rev. 49: 1-32.
  • Özkanca R. 1993. Survival and physiological status of Escherichia coli in lake water under different nutrient conditions. Ph. D. Thesis. Department of Biological Sciences, University of Warwick, England.
  • Özkanca R. and K.P. Flint. 2002. The effect of starvation stress on the porin protein expression of Escherichia coli in lake water. Lett. Appl. Microbiol. 35: 533-537.
  • Özkanca R., N. Şahin, K. Itik, E. Kariptaş and K.P. Flint. 2002. The effect of toluidine blue on the survival, dormancy and outer membrane porin proteins (OmpC and OmpF) of Salmonella typhimurium LT2 in seawater. J. Appl. Microbiol. 92: 1097-1104.
  • Rodriguez G.G., D. Phipps, K. Ishiguro and H.F. Ridgway. 1992. Use of a fluorescent redox probe for direct visualization of actively respiring bacteria. Appl. Environ. Microbiol. 58: 1801-1808.
  • Roth W.G., M.P. Leckie and D.N. Dietzler. 1988. Restoration of colony-forming activity in osmotically stressed Escherichia coli by betaine. Appl. Environ. Microbiol. 54: 3142-3146.
  • Rozen Y. and S. Belkin. 2001. Survival of enteric bacteria in sea-water. FEMS Microbiol. Rev. 25: 513-529.
  • Russo F.D. and T.J. Silhavy. 1991. EnvZ controls the concentration of phosphorylated OmpR to mediate osmoregulation of the porin genes. J. Mol. Biol. 222: 567-580.
  • Sainz T., J. Perez, J. Villaseca, U. Hernandez, C. Eslava, G. Mendoza and C. Wache. 2005. Survival to different acid challenges and outer membrane profiles of pathogenic Escherichia coli strains isolated from pozol, a Mexican typical maize fermented food. Int. J. Food Microbiol. 105: 357-367.
  • Sato M, K. Machida, E. Arikado, H. Saito, T. Kakegawa and H. Kobayashi. 2000. Expression of outer membrane proteins in Escherichia coli growing at acid pH. Appl. Environ. Microbiol. 66: 943-947.
  • Sinton L.W., C.H. Hall, P.A. Lynch and R.J. Davies-Colley. 2002. Sunlight inactivation of faecal indicator bacteria and bacteriophages from waste stabilization pond effluent in fresh and saline waters. Appl. Environ. Microbiol. 68: 1122-1131.
  • Sylvester D.M., R. Taylor and T.R. Lattann. 2001. Viable but nonculturable bacteria: a public health threat? Infect. Dis. Rev. 3: 70-82.
  • Tsui P., V. Helu and M. Freundlich. 1988. Altered osmoregulation of ompF in integration host factor mutants of Escherichia coli. J. Bacteriol. 170: 4950-4953.
  • Wang Y., L. Wang, Y. Sun, Y. Chen, L. Zhu, L. Guo, B. Luo and H. Wang. 2007. Disrupted ompC causes osmosis sensitivity of Escherichia coli in alkaline medium. J. Genetics and Genomics 34: 1131-1138.

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Bibliografia

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