This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Bogosian, G.
Right arrow Articles by O'Neil, J. P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bogosian, G.
Right arrow Articles by O'Neil, J. P.

 Previous Article  |  Next Article 

Journal of Bacteriology, September 2000, p. 5070-5075, Vol. 182, No. 18
0021-9193/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.

Recovery of Hydrogen Peroxide-Sensitive Culturable Cells of Vibrio vulnificus Gives the Appearance of Resuscitation from a Viable but Nonculturable State

Gregg Bogosian,* Noelle D. Aardema, Edward V. Bourneuf, Patricia J. L. Morris, and Julia P. O'Neil

Monsanto Company, Chesterfield, Missouri 63198

Received 15 March 2000/Accepted 19 June 2000

The viabilities of five strains of Vibrio vulnificus were evaluated during the storage of the organisms in sterile seawater at 5°C. The number of CFU was measured by plate count methods on rich media. The total cell numbers were determined by direct microscopic count methods. The titer of CFU declined logarithmically to undetectable levels over a period of 2 to 3 weeks, while the total cell numbers were unchanged. Midway through each study, higher culturable cell counts began to be observed on plates containing catalase or sodium pyruvate; during the latter stages of the study, the plate counts on such media were up to 1,000-fold higher than those on unsupplemented plates. Because autoclaving is known to generate hydrogen peroxide in rich media, and because catalase and sodium pyruvate are known to eliminate hydrogen peroxide, it appears that the conditions of the experiments led to the selection of a hydrogen peroxide-sensitive culturable cell subpopulation. At the time of the final stage of the decline in viability of each culture, hydrogen peroxide-sensitive cells were the only culturable cells present. Warming samples of the cultures to room temperature led to the growth of these residual culturable cells, utilizing nutrients provided by the nonculturable cells. The cells that grew recovered hydrogen peroxide resistance. When mixtures of culturable and nonculturable cells were diluted to the point where only nonculturable cells were present, or when the hydrogen peroxide-sensitive culturable cells had declined to undetectable levels, warming had no effect; no culturable cells were recovered. Warming has been reported to "resuscitate" nonculturable cells. Recognition of the existence of hydrogen peroxide-sensitive culturable cell populations, as well as their ability to grow to high levels in the warmed seawater microcosms, leads instead to the conclusion that while warming permits culturable cells to grow, it has no effect on nonculturable cells.


* Corresponding author. Mailing address: Monsanto BB3M, 700 Chesterfield Parkway, Chesterfield, MO 63198. Phone: (636) 737-6149. Fax: (636) 737-7002. E-mail: gregg.bogosian{at}monsanto.com.


Journal of Bacteriology, September 2000, p. 5070-5075, Vol. 182, No. 18
0021-9193/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Morris, J. J., Kirkegaard, R., Szul, M. J., Johnson, Z. I., Zinser, E. R. (2008). Facilitation of Robust Growth of Prochlorococcus Colonies and Dilute Liquid Cultures by "Helper" Heterotrophic Bacteria. Appl. Environ. Microbiol. 74: 4530-4534 [Abstract] [Full Text]  
  • Alam, M., Sultana, M., Nair, G. B., Siddique, A. K., Hasan, N. A., Sack, R. B., Sack, D. A., Ahmed, K. U., Sadique, A., Watanabe, H., Grim, C. J., Huq, A., Colwell, R. R. (2007). Viable but nonculturable Vibrio cholerae O1 in biofilms in the aquatic environment and their role in cholera transmission. Proc. Natl. Acad. Sci. USA 104: 17801-17806 [Abstract] [Full Text]  
  • Moreau, P. L. (2007). The Lysine Decarboxylase CadA Protects Escherichia coli Starved of Phosphate against Fermentation Acids. J. Bacteriol. 189: 2249-2261 [Abstract] [Full Text]  
  • Drake, S. L., Elhanafi, D., Bang, W., Drake, M. A., Green, D. P., Jaykus, L. A. (2006). Validation of a Green Fluorescent Protein-Labeled Strain of Vibrio vulnificus for Use in the Evaluation of Postharvest Strategies for Handling of Raw Oysters. Appl. Environ. Microbiol. 72: 7205-7211 [Abstract] [Full Text]  
  • Vattakaven, T., Bond, P., Bradley, G., Munn, C. B. (2006). Differential Effects of Temperature and Starvation on Induction of the Viable-but-Nonculturable State in the Coral Pathogens Vibrio shiloi and Vibrio tasmaniensis.. Appl. Environ. Microbiol. 72: 6508-6513 [Abstract] [Full Text]  
  • Wood, D. N., Chaussee, M. A., Chaussee, M. S., Buttaro, B. A. (2005). Persistence of Streptococcus pyogenes in Stationary-Phase Cultures. J. Bacteriol. 187: 3319-3328 [Abstract] [Full Text]  
  • Barer, M. R., Bogosian, G., Steck, T. R. (2004). The Viable but Nonculturable Concept, Bacteria in Urine Samples, and Occam's Razor. J. Clin. Microbiol. 42: 5434-5435 [Full Text]  
  • Stevenson, B. S., Eichorst, S. A., Wertz, J. T., Schmidt, T. M., Breznak, J. A. (2004). New Strategies for Cultivation and Detection of Previously Uncultured Microbes. Appl. Environ. Microbiol. 70: 4748-4755 [Abstract] [Full Text]  
  • Maalej, S., Denis, M., Dukan, S. (2004). Temperature and growth-phase effects on Aeromonas hydrophila survival in natural seawater microcosms: role of protein synthesis and nucleic acid content on viable but temporarily nonculturable response. Microbiology 150: 181-187 [Abstract] [Full Text]  
  • Campbell, M. S., Wright, A. C. (2003). Real-Time PCR Analysis of Vibrio vulnificus from Oysters. Appl. Environ. Microbiol. 69: 7137-7144 [Abstract] [Full Text]  
  • Gupte, A. R., de Rezende, C. L. E., Joseph, S. W. (2003). Induction and Resuscitation of Viable but Nonculturable Salmonella enterica Serovar Typhimurium DT104{dagger}. Appl. Environ. Microbiol. 69: 6669-6675 [Abstract] [Full Text]  
  • Pinhassi, J., Berman, T. (2003). Differential Growth Response of Colony-Forming {alpha}- and {gamma}-Proteobacteria in Dilution Culture and Nutrient Addition Experiments from Lake Kinneret (Israel), the Eastern Mediterranean Sea, and the Gulf of Eilat. Appl. Environ. Microbiol. 69: 199-211 [Abstract] [Full Text]  
  • Smith, R. J., Newton, A. T., Harwood, C. R., Barer, M. R. (2002). Active but nonculturable cells of Salmonella enterica serovar Typhimurium do not infect or colonize mice. Microbiology 148: 2717-2726 [Abstract] [Full Text]  
  • Mascher, F., Moenne-Loccoz, Y., Schnider-Keel, U., Keel, C., Haas, D., Defago, G. (2002). Inactivation of the Regulatory Gene algU or gacA Can Affect the Ability of Biocontrol Pseudomonas fluorescens CHA0 To Persist as Culturable Cells in Nonsterile Soil. Appl. Environ. Microbiol. 68: 2085-2088 [Abstract] [Full Text]  
  • Grey, B., Steck, T. R. (2001). Concentrations of Copper Thought To Be Toxic to Escherichia coli Can Induce the Viable but Nonculturable Condition. Appl. Environ. Microbiol. 67: 5325-5327 [Abstract] [Full Text]  
  • Kolling, G. L., Matthews, K. R. (2001). Examination of Recovery In Vitro and In Vivo of Nonculturable Escherichia coli O157:H7. Appl. Environ. Microbiol. 67: 3928-3933 [Abstract] [Full Text]  
  • Keer, J., Smeulders, M. J., Williams, H. D. (2001). A purF mutant of Mycobacterium smegmatis has impaired survival during oxygen-starved stationary phase. Microbiology 147: 473-481 [Abstract] [Full Text]