Significance of Na+ in the fish pathogen, Vibrio anguillarum, under energy depleted condition

FEMS Microbiology Letters

Volumn 234, Issue 1, 2004, Pages 163-167

  Fujiwara Nagata, Erina ^a   Eguchi, Mitsuru ^a  

^a KINKI UNIVERSITY   (Japan)

Author keywords

Energy; Fish pathogen; Marine; Na+; Starvation survival; Vibrio anguillarum

Indexed keywords

SEA WATER; SODIUM ION;

ARTICLE; BACTERIAL GROWTH; BACTERIAL MEMBRANE; BACTERIAL STRAIN; BACTERIAL SURVIVAL; BACTERIOPLANKTON; CONTROLLED STUDY; ENERGY METABOLISM; FISH; LISTONELLA ANGUILLARUM; NONHUMAN; PRIORITY JOURNAL; RESPIRATORY CHAIN; SODIUM DEPLETION;

ANIMALS; BIOMASS; CARBONYL CYANIDE M-CHLOROPHENYL HYDRAZONE; CELL MEMBRANE; COLONY COUNT, MICROBIAL; CULTURE MEDIA; ELECTRON TRANSPORT; ENERGY METABOLISM; FISH DISEASES; FISHES; ION TRANSPORT; MEMBRANE POTENTIALS; NA(+)-K(+)-EXCHANGING ATPASE; SODIUM CHLORIDE; VIBRIO; WATER MICROBIOLOGY;

LISTONELLA ANGUILLARUM; VIBRIO; VIBRIO ANGUSTUM;

EID: 1942470022     PISSN: 03781097     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.femsle.2004.03.026     Document Type: Article

References (29)

1. Taylar B.T. Marine habitats, bacteria. Lederberg J., Alexander M., Hopwood D.A., Iglewski B.H., Laskin A.I. Encyclopedia of Microbiology. vol. 3 (M-R):1989;29-44 Academic Press, New York.
2. Dimroth P. Sodium ion transport decarboxylases and other aspects of sodium ion cycling in bacteria. Microbiol. Rev. 51:1987;320-340.
3. + in pH homeostasis and growth of the marine bacterium Vibrio alginolyticus. J. Gen. Microbiol. 138:1992;1271-1276.
4. McCarter L.L. Polar flagellar motility of the Vibrionaceae. Microbiol. Mol. Biol. Rev. 65:2001;445-462.
5. Häse C.C., Fedorova N.D., Galperin M.Y., Dibrov P.A. Sodium ion cycle in bacterial pathogens: evidence from cross-genome comparisons. Microbiol. Mol. Biol. Rev. 65:2001;353-370.
6. Kogure K. Bioenergetics of marine bacteria. Curr. Opin. Biotechnol. 9:1998;278-282.
7. +-translocating NADH-quinone reductase of marine and halophilic bacteria. J. Bioenerg. Biomembr. 25:1993;385-391.
8. +-translocating NADH-quinone reductase in marine bacteria using a PCR technique. Can. J. Microbiol. 46:2000;325-332.
9. +-translocating NADH-quinone reductase from the marine Vibrio alginolyticus. Biochim. Biophys. Acta. 1505:2001;37-44.
10. Östling J., Holmquist L., Flärdh K., Svenblad B., Jouper-jaan Å., Kjelleberg S. Starvation and recovery of Vibrio. Kjelleberg S. Starvation in bacteria. 1993;103-127 Plenum Press, New York.
11. Nyström T. Translational fidelity, protein oxidation, and senescence: lessons from bacteria. Ageing Res. Rev. 1:2002;693-703.
12. Nyström T. Conditional senescence in bacteria: death of the immortals. Mol. Microbiol. 48:2003;17-23.
13. Muroga K., Iida M., Matsumoto H. Detection of Vibrio anguillarum from waters. Bull. Japan. Soc. Sci. Fish. 52:1986;641-647.
14. Larsen J.L. Vibrio anguillarum: influence of temperature, pH, NaCl concentration and incubation time on growth. J. Appl. Bacteriol. 57:1984;237-246.
15. +-dependent respiratory chain in Vibrio anguillarum, a fish pathogen, in comparison with other marine Vibrios. FEMS Microbiol. Ecol. 44:2003;225-230.
16. Humphrey B., Kjelleberg S., Marshall K.C. Responses of marine bacteria under starvation conditions at a solid-water interface. Appl. Environ. Microbiol. 45:1983;43-47.
17. Miyamoto N., Eguchi M. Direct detection of a fish pathogen, Vibrio anguillarum serotype J-O-1, in freshwater by fluorescent antibody technique. Fish. Sci. 63:1997;253-257.
18. Miyamoto N., Eguchi M. Response to low osmotic stress in a fish pathogen, Vibrio anguillarum. FEMS Microbiol. Ecol. 22:1997;225-231.
19. Nyström T., Marden P., Kjelleberg S. Relative changes in incorporation rates of leucine and methionine during starvation of two bacteria isolated from marine waters. FEMS Microbiol. Ecol. 38:1986;285-292.
20. Huq A., Colwell R. Vibrios in the marine and estuarine environments. J. Mar. Biotechnol. 3:1995;60-63.
21. Kita-Tsukamoto K., Oyaizu H., Nanba K., Simidu U. Phylogenetic relationships of marine bacteria, mainly members of the family Vibrionaceae, determined on the basis of 16S rRNA sequences. Int. J. Syst. Bacteriol. 43:1993;8-19.
22. MacLeod R.A., Matula T.I. Nutrition and metabolism of marine bacteria. XI. Some characteristics of the lytic phenomenon. Can. J. Microbiol. 8:1962;883-896.
23. + in preventing lysis of a slightly halophilic Vibrio alginolyticus. Can. J. Microbiol. 19:1973;563-571.
24. Unemoto T., Hayashi M., Terao K. Lysis of halophilic Vibrio alginolyticus and Vibrio costicolus induced by chaotropic anions. Biochim. Biophys. Acta. 500:1977;425-431.
25. Ericsson M., Hanstorp D., Hagberg P., Enger J., Nyström T. Sorting out bacterial viability with optical tweezers. J. Bacteriol. 182:2000;5551-5555.
26. Nyström T., Gustavsson N. Maintenance energy requirement: what is required for stasis survival of Escherichia coli? Biochim. Biophys. Acta. 1365:1998;225-231.
27. Wada M., Kogure K. Membrane bioenergetics in reference to marine bacterial culturability. Colwell R.R., Grimes D.J. Nonculturable microorganisms in the environment. 2000;47-55 ASM press, Washington, DC.
28. +-dependent activation in the respiratory chain of marine Vibrio alginolyticus. J. Biochem. 85:1979;1461-1467.
29. Hörmansdorfer S., Wentges H., Neugebaur-Büchler K., Bauer J. Isolation of Vibrio alginolyticus from seawater aquaria. Int. J. Hyg. Environ. Health. 203:2000;169-175.