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. 1997 Jul;63(7):2863–2869. doi: 10.1128/aem.63.7.2863-2869.1997

A novel means to develop strain-specific DNA probes for detecting bacteria in the environment.

V G Matheson 1, J Munakata-Marr 1, G D Hopkins 1, P L McCarty 1, J M Tiedje 1, L J Forney 1
PMCID: PMC168583  PMID: 9212434

Abstract

A simple means to develop strain-specific DNA probes for use in monitoring the movement and survival of bacteria in natural and laboratory ecosystems was developed. The method employed amplification of genomic DNA via repetitive sequence-based PCR (rep-PCR) using primers specific for repetitive extragenic palindromic (REP) elements, followed by cloning of the amplified fragments. The cloned fragments were screened to identify those which were strain specific, and these were used as probes for total genomic DNA isolated from microbial communities and subjected to rep-PCR. To evaluate the utility of the approach, we developed probes specific for Burkholderia cepacia G4 and used them to determine the persistence of the strain in aquifer sediment microcosms following bioaugmentation. Two of four probes tested were found to specifically hybridize to DNA fragments of the expected sizes in the rep-PCR fingerprint of B. cepacia G4 but not to 64 genetically distinct bacteria previously isolated from the aquifer. One of these probes, a 650-bp fragment, produced a hybridization signal when as few as 10 CFU of B. cepacia G4 were present in a mixture with 10(6) CFU nontarget strains, indicating that the sensitivity of these probes was comparable to those of other PCR-based detection methods. The probes were used to discriminate groundwater and microcosm samples that contained B. cepacia G4 from those which did not. False-positive results were obtained with a few samples, but these were readily identified by using hybridization to the second probe as a confirmation step. The general applicability of the method was demonstrated by constructing probes specific to three other environmental isolates.

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Selected References

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  1. Amann R. I., Ludwig W., Schleifer K. H. Phylogenetic identification and in situ detection of individual microbial cells without cultivation. Microbiol Rev. 1995 Mar;59(1):143–169. doi: 10.1128/mr.59.1.143-169.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Atlas R. M., Williams J. F., Huntington M. K. Legionella contamination of dental-unit waters. Appl Environ Microbiol. 1995 Apr;61(4):1208–1213. doi: 10.1128/aem.61.4.1208-1213.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bjourson A. J., Stone C. E., Cooper J. E. Combined subtraction hybridization and polymerase chain reaction amplification procedure for isolation of strain-specific Rhizobium DNA sequences. Appl Environ Microbiol. 1992 Jul;58(7):2296–2301. doi: 10.1128/aem.58.7.2296-2301.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Boye M., Ahl T., Molin S. Application of a strain-specific rRNA oligonucleotide probe targeting Pseudomonas fluorescens Ag1 in a mesocosm study of bacterial release into the environment. Appl Environ Microbiol. 1995 Apr;61(4):1384–1390. doi: 10.1128/aem.61.4.1384-1390.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Cook D., Sequeira L. The use of subtractive hybridization to obtain a DNA probe specific for Pseudomonas solanacearum race 3. Mol Gen Genet. 1991 Jul;227(3):401–410. doi: 10.1007/BF00273930. [DOI] [PubMed] [Google Scholar]
  6. Deneer H. G., Boychuk I. Species-specific detection of Listeria monocytogenes by DNA amplification. Appl Environ Microbiol. 1991 Feb;57(2):606–609. doi: 10.1128/aem.57.2.606-609.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Dimri G. P., Rudd K. E., Morgan M. K., Bayat H., Ames G. F. Physical mapping of repetitive extragenic palindromic sequences in Escherichia coli and phylogenetic distribution among Escherichia coli strains and other enteric bacteria. J Bacteriol. 1992 Jul;174(14):4583–4593. doi: 10.1128/jb.174.14.4583-4593.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Fries M. R., Forney L. J., Tiedje J. M. Phenol- and toluene-degrading microbial populations from an aquifer in which successful trichloroethene cometabolism occurred. Appl Environ Microbiol. 1997 Apr;63(4):1523–1530. doi: 10.1128/aem.63.4.1523-1530.1997. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Hulton C. S., Higgins C. F., Sharp P. M. ERIC sequences: a novel family of repetitive elements in the genomes of Escherichia coli, Salmonella typhimurium and other enterobacteria. Mol Microbiol. 1991 Apr;5(4):825–834. doi: 10.1111/j.1365-2958.1991.tb00755.x. [DOI] [PubMed] [Google Scholar]
  10. Jansson J. K. Tracking genetically engineered microorganisms in nature. Curr Opin Biotechnol. 1995 Jun;6(3):275–283. doi: 10.1016/0958-1669(95)80048-4. [DOI] [PubMed] [Google Scholar]
  11. Judd A. K., Schneider M., Sadowsky M. J., de Bruijn F. J. Use of repetitive sequences and the polymerase chain reaction technique to classify genetically related Bradyrhizobium japonicum serocluster 123 strains. Appl Environ Microbiol. 1993 Jun;59(6):1702–1708. doi: 10.1128/aem.59.6.1702-1708.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Koeuth T., Versalovic J., Lupski J. R. Differential subsequence conservation of interspersed repetitive Streptococcus pneumoniae BOX elements in diverse bacteria. Genome Res. 1995 Nov;5(4):408–418. doi: 10.1101/gr.5.4.408. [DOI] [PubMed] [Google Scholar]
  13. Kogan S. C., Doherty M., Gitschier J. An improved method for prenatal diagnosis of genetic diseases by analysis of amplified DNA sequences. Application to hemophilia A. N Engl J Med. 1987 Oct 15;317(16):985–990. doi: 10.1056/NEJM198710153171603. [DOI] [PubMed] [Google Scholar]
  14. Lee C. Y., Pan S. F., Chen C. H. Sequence of a cloned pR72H fragment and its use for detection of Vibrio parahaemolyticus in shellfish with the PCR. Appl Environ Microbiol. 1995 Apr;61(4):1311–1317. doi: 10.1128/aem.61.4.1311-1317.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Leser T. D., Boye M., Hendriksen N. B. Survival and activity of Pseudomonas sp. strain B13(FR1) in a marine microcosm determined by quantitative PCR and an rRNA-targeting probe and its effect on the indigenous bacterioplankton. Appl Environ Microbiol. 1995 Apr;61(4):1201–1207. doi: 10.1128/aem.61.4.1201-1207.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Louws F. J., Fulbright D. W., Stephens C. T., de Bruijn F. J. Specific genomic fingerprints of phytopathogenic Xanthomonas and Pseudomonas pathovars and strains generated with repetitive sequences and PCR. Appl Environ Microbiol. 1994 Jul;60(7):2286–2295. doi: 10.1128/aem.60.7.2286-2295.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Lupski J. R., Weinstock G. M. Short, interspersed repetitive DNA sequences in prokaryotic genomes. J Bacteriol. 1992 Jul;174(14):4525–4529. doi: 10.1128/jb.174.14.4525-4529.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Mahbubani M. H., Bej A. K., Miller R., Haff L., DiCesare J., Atlas R. M. Detection of Legionella with polymerase chain reaction and gene probe methods. Mol Cell Probes. 1990 Jun;4(3):175–187. doi: 10.1016/0890-8508(90)90051-z. [DOI] [PubMed] [Google Scholar]
  19. Manulis S., Valinsky L., Lichter A., Gabriel D. W. Sensitive and specific detection of Xanthomonas campestris pv. pelargonii with DNA primers and probes identified by random amplified polymorphic DNA analysis. Appl Environ Microbiol. 1994 Nov;60(11):4094–4099. doi: 10.1128/aem.60.11.4094-4099.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Nascimento E. R., Yamamoto R., Khan M. I. Mycoplasma gallisepticum F-vaccine strain-specific polymerase chain reaction. Avian Dis. 1993 Jan-Mar;37(1):203–211. [PubMed] [Google Scholar]
  21. Nelson M. J., Montgomery S. O., O'neill E. J., Pritchard P. H. Aerobic metabolism of trichloroethylene by a bacterial isolate. Appl Environ Microbiol. 1986 Aug;52(2):383–384. doi: 10.1128/aem.52.2.383-384.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Recorbet G., Picard C., Normand P., Simonet P. Kinetics of the persistence of chromosomal DNA from genetically engineered Escherichia coli introduced into soil. Appl Environ Microbiol. 1993 Dec;59(12):4289–4294. doi: 10.1128/aem.59.12.4289-4294.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Seal S. E., Jackson L. A., Daniels M. J. Isolation of a Pseudomonas solanacearum-specific DNA probe by subtraction hybridization and construction of species-specific oligonucleotide primers for sensitive detection by the polymerase chain reaction. Appl Environ Microbiol. 1992 Nov;58(11):3751–3758. doi: 10.1128/aem.58.11.3751-3758.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Sharples G. J., Lloyd R. G. A novel repeated DNA sequence located in the intergenic regions of bacterial chromosomes. Nucleic Acids Res. 1990 Nov 25;18(22):6503–6508. doi: 10.1093/nar/18.22.6503. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Southern E. M. Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol. 1975 Nov 5;98(3):503–517. doi: 10.1016/s0022-2836(75)80083-0. [DOI] [PubMed] [Google Scholar]
  26. Tas E., Kaijalainen S., Saano A., Lindström K. Isolation of a Rhizobium galegae strain-specific DNA probe. Microb Releases. 1994 Jul;2(4):231–237. [PubMed] [Google Scholar]
  27. Thiem S. M., Krumme M. L., Smith R. L., Tiedje J. M. Use of molecular techniques to evaluate the survival of a microorganism injected into an aquifer. Appl Environ Microbiol. 1994 Apr;60(4):1059–1067. doi: 10.1128/aem.60.4.1059-1067.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Uyttendaele M., Schukkink R., van Gemen B., Debevere J. Detection of Campylobacter jejuni added to foods by using a combined selective enrichment and nucleic acid sequence-based amplification (NASBA). Appl Environ Microbiol. 1995 Apr;61(4):1341–1347. doi: 10.1128/aem.61.4.1341-1347.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Versalovic J., Kapur V., Mason E. O., Jr, Shah U., Koeuth T., Lupski J. R., Musser J. M. Penicillin-resistant Streptococcus pneumoniae strains recovered in Houston: identification and molecular characterization of multiple clones. J Infect Dis. 1993 Apr;167(4):850–856. doi: 10.1093/infdis/167.4.850. [DOI] [PubMed] [Google Scholar]
  30. Versalovic J., Koeuth T., Lupski J. R. Distribution of repetitive DNA sequences in eubacteria and application to fingerprinting of bacterial genomes. Nucleic Acids Res. 1991 Dec 25;19(24):6823–6831. doi: 10.1093/nar/19.24.6823. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Voytek M. A., Ward B. B. Detection of ammonium-oxidizing bacteria of the beta-subclass of the class Proteobacteria in aquatic samples with the PCR. Appl Environ Microbiol. 1995 Apr;61(4):1444–1450. doi: 10.1128/aem.61.4.1444-1450.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Woods C. R., Jr, Versalovic J., Koeuth T., Lupski J. R. Analysis of relationships among isolates of Citrobacter diversus by using DNA fingerprints generated by repetitive sequence-based primers in the polymerase chain reaction. J Clin Microbiol. 1992 Nov;30(11):2921–2929. doi: 10.1128/jcm.30.11.2921-2929.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Yamamoto S., Harayama S. PCR amplification and direct sequencing of gyrB genes with universal primers and their application to the detection and taxonomic analysis of Pseudomonas putida strains. Appl Environ Microbiol. 1995 Mar;61(3):1104–1109. doi: 10.1128/aem.61.3.1104-1109.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. de Bruijn F. J. Use of repetitive (repetitive extragenic palindromic and enterobacterial repetitive intergeneric consensus) sequences and the polymerase chain reaction to fingerprint the genomes of Rhizobium meliloti isolates and other soil bacteria. Appl Environ Microbiol. 1992 Jul;58(7):2180–2187. doi: 10.1128/aem.58.7.2180-2187.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]

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