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. 1995 Feb;61(2):448–455. doi: 10.1128/aem.61.2.448-455.1995

Tracking the Response of Burkholderia cepacia G4 5223-PR1 in Aquifer Microcosms

J Winkler, K N Timmis, R A Snyder
PMCID: PMC1388346  PMID: 16534928

Abstract

The introduction of bacteria into the environment for bioremediation purposes (bioaugmentation) requires analysis and monitoring of microbial population dynamics to define persistence and activity from both efficacy and risk assessment perspectives. Burkholderia cepacia G4 5223-PR1 is a Tn5 insertion mutant which constitutively expresses a toluene ortho-monooxygenase that degrades trichloroethylene (TCE). This ability of G4 5223-PR1 to degrade TCE without aromatic induction may be useful for bioremediation of TCE-containing aquifers and groundwater. Thus, a simulated aquifer sediment system and groundwater microcosms were used to monitor the survival of G4 5223-PR1. The fate of G4 5223-PR1 in sediment was monitored by indirect immunofluorescence microscopy, a colony blot assay, and growth on selective medium. G4 5223-PR1 was detected immunologically by using a highly specific monoclonal antibody which reacted against the O-specific polysaccharide chain of the lipopolysaccharides of this organism. G4 5223-PR1 survived well in sterilized groundwater, although in nonsterile groundwater microcosms rapid decreases in the G4 5223-PR1 cell population were observed. Ten days after inoculation no G4 5223-PR1 cells could be detected by selective plating or immunofluorescence. G4 5223-PR1 survival was greater in a nonsterile aquifer sediment microcosm, although after 22 days of elution the number of G4 5223-PR1 cells was low. Our results demonstrate the utility of monoclonal antibody tracking methods and the importance of biotic interactions in determining the persistence of introduced microorganisms.

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Selected References

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  1. Abelson P. H. Inefficient remediation of ground-water pollution. Science. 1990 Nov 9;250(4982):733–733. doi: 10.1126/science.2237418. [DOI] [PubMed] [Google Scholar]
  2. Brettar I., Höfle M. G. Influence of ecosystematic factors on survival of Escherichia coli after large-scale release into lake water mesocosms. Appl Environ Microbiol. 1992 Jul;58(7):2201–2210. doi: 10.1128/aem.58.7.2201-2210.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bérubé A., Trudel M., Payment P. Rapid detection and identification of Legionella pneumophila by a membrane immunoassay. Appl Environ Microbiol. 1989 Jun;55(6):1640–1641. doi: 10.1128/aem.55.6.1640-1641.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Christensen B., Torsvik T., Lien T. Immunomagnetically captured thermophilic sulfate-reducing bacteria from north sea oil field waters. Appl Environ Microbiol. 1992 Apr;58(4):1244–1248. doi: 10.1128/aem.58.4.1244-1248.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Darveau R. P., Hancock R. E. Procedure for isolation of bacterial lipopolysaccharides from both smooth and rough Pseudomonas aeruginosa and Salmonella typhimurium strains. J Bacteriol. 1983 Aug;155(2):831–838. doi: 10.1128/jb.155.2.831-838.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Gonzalez J. M., Sherr E. B., Sherr B. F. Size-selective grazing on bacteria by natural assemblages of estuarine flagellates and ciliates. Appl Environ Microbiol. 1990 Mar;56(3):583–589. doi: 10.1128/aem.56.3.583-589.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Hancock R. E., Wieczorek A. A., Mutharia L. M., Poole K. Monoclonal antibodies against Pseudomonas aeruginosa outer membrane antigens: isolation and characterization. Infect Immun. 1982 Jul;37(1):166–171. doi: 10.1128/iai.37.1.166-171.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Hofstra H., Dankert J. Antigenic cross-reactivity of major outer membrane proteins in enterobacteriaceae species. J Gen Microbiol. 1979 Apr;111(2):293–302. doi: 10.1099/00221287-111-2-293. [DOI] [PubMed] [Google Scholar]
  9. Hofstra H., Dankert J. Major outer membrane proteins: common antigens in enterobacteriaceae species. J Gen Microbiol. 1980 Jul;119(1):123–131. doi: 10.1099/00221287-119-1-123. [DOI] [PubMed] [Google Scholar]
  10. Huang H. C., Schuurink R., Denny T. P., Atkinson M. M., Baker C. J., Yucel I., Hutcheson S. W., Collmer A. Molecular cloning of a Pseudomonas syringae pv. syringae gene cluster that enables Pseudomonas fluorescens to elicit the hypersensitive response in tobacco plants. J Bacteriol. 1988 Oct;170(10):4748–4756. doi: 10.1128/jb.170.10.4748-4756.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Huq A., Colwell R. R., Rahman R., Ali A., Chowdhury M. A., Parveen S., Sack D. A., Russek-Cohen E. Detection of Vibrio cholerae O1 in the aquatic environment by fluorescent-monoclonal antibody and culture methods. Appl Environ Microbiol. 1990 Aug;56(8):2370–2373. doi: 10.1128/aem.56.8.2370-2373.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Jain R. K., Sayler G. S. Problems and potential for in situ treatment of environmental pollutants by engineered microorganisms. Microbiol Sci. 1987 Feb;4(2):59–63. [PubMed] [Google Scholar]
  13. Krumme M. L., Timmis K. N., Dwyer D. F. Degradation of trichloroethylene by Pseudomonas cepacia G4 and the constitutive mutant strain G4 5223 PR1 in aquifer microcosms. Appl Environ Microbiol. 1993 Aug;59(8):2746–2749. doi: 10.1128/aem.59.8.2746-2749.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Kyhse-Andersen J. Electroblotting of multiple gels: a simple apparatus without buffer tank for rapid transfer of proteins from polyacrylamide to nitrocellulose. J Biochem Biophys Methods. 1984 Dec;10(3-4):203–209. doi: 10.1016/0165-022x(84)90040-x. [DOI] [PubMed] [Google Scholar]
  15. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  16. Luk J. M., Lindberg A. A. Rapid and sensitive detection of Salmonella (O:6,7) by immunomagnetic monoclonal antibody-based assays. J Immunol Methods. 1991 Mar 1;137(1):1–8. doi: 10.1016/0022-1759(91)90387-u. [DOI] [PubMed] [Google Scholar]
  17. McPhail G. D., Finn T., Isaacson P. G. A useful low temperature method for post-embedding electron immunocytochemistry in routine histopathology. J Pathol. 1987 Mar;151(3):231–238. doi: 10.1002/path.1711510311. [DOI] [PubMed] [Google Scholar]
  18. Nybroe O., Johansen A., Laake M. Enzyme-linked immunosorbent assays for detection of Pseudomonas fluorescens in sediment samples. Lett Appl Microbiol. 1990 Dec;11(6):293–296. doi: 10.1111/j.1472-765x.1990.tb00185.x. [DOI] [PubMed] [Google Scholar]
  19. Ramos-González M. I., Ruiz-Cabello F., Brettar I., Garrido F., Ramos J. L. Tracking genetically engineered bacteria: monoclonal antibodies against surface determinants of the soil bacterium Pseudomonas putida 2440. J Bacteriol. 1992 May;174(9):2978–2985. doi: 10.1128/jb.174.9.2978-2985.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Ramos J. L., Wasserfallen A., Rose K., Timmis K. N. Redesigning metabolic routes: manipulation of TOL plasmid pathway for catabolism of alkylbenzoates. Science. 1987 Jan 30;235(4788):593–596. doi: 10.1126/science.3468623. [DOI] [PubMed] [Google Scholar]
  21. Roszak D. B., Colwell R. R. Survival strategies of bacteria in the natural environment. Microbiol Rev. 1987 Sep;51(3):365–379. doi: 10.1128/mr.51.3.365-379.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Shields M. S., Reagin M. J. Selection of a Pseudomonas cepacia strain constitutive for the degradation of trichloroethylene. Appl Environ Microbiol. 1992 Dec;58(12):3977–3983. doi: 10.1128/aem.58.12.3977-3983.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Stanier R. Y., Palleroni N. J., Doudoroff M. The aerobic pseudomonads: a taxonomic study. J Gen Microbiol. 1966 May;43(2):159–271. doi: 10.1099/00221287-43-2-159. [DOI] [PubMed] [Google Scholar]
  24. Steinmetz I., Rheinheimer C., Bitter-Suermann D. Rapid identification of legionellae by a colony blot assay based on a genus-specific monoclonal antibody. J Clin Microbiol. 1992 Apr;30(4):1016–1018. doi: 10.1128/jcm.30.4.1016-1018.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Tsai C. M., Frasch C. E. A sensitive silver stain for detecting lipopolysaccharides in polyacrylamide gels. Anal Biochem. 1982 Jan 1;119(1):115–119. doi: 10.1016/0003-2697(82)90673-x. [DOI] [PubMed] [Google Scholar]
  26. VENABLE J. H., COGGESHALL R. A SIMPLIFIED LEAD CITRATE STAIN FOR USE IN ELECTRON MICROSCOPY. J Cell Biol. 1965 May;25:407–408. doi: 10.1083/jcb.25.2.407. [DOI] [PMC free article] [PubMed] [Google Scholar]

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