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Appl Environ Microbiol. 1995 Apr; 61(4): 1444–1450.
PMCID: PMC167402
PMID: 7538277

Detection of ammonium-oxidizing bacteria of the beta-subclass of the class Proteobacteria in aquatic samples with the PCR.

Abstract

The PCR was used as the basis for the development of a sensitive and specific assay for the detection of ammonium-oxidizing bacteria belonging to the beta-subclass of the class Proteobacteria. PCR primers were selected on the basis of nucleic acid sequence data available for seven species of nitrifiers in this subclass. The specificity of the ammonium oxidizer primers was evaluated by testing known strains of nitrifiers, several serotyped environmental nitrifier isolates, and other members of the Proteobacteria, including four very closely related, nonnitrifying species (as determined by rRNA sequence analysis). DNA extracts from 19 bacterio-plankton samples collected from Lake Bonney, Antarctica, and the Southern California Bight were assayed for the presence of ammonium oxidizers. By using a two-stage amplification procedure, ammonium oxidizers were detected in samples collected from both sites. Chemical data collected simultaneously support the occurrence of nitrification and the presence of nitrifiers. This is the first report describing PCR primers specific for ammonium-oxidizing bacteria and the successful amplification of nitrifier genes coding for rRNA from DNA extracts from natural samples. This application of PCR is of particular importance for the detection and study of microbes, such as autotrophic nitrifiers, which are difficult or impossible to isolate from indigenous microbial communities.

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Selected References

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  • Abbaszadegan M, Huber MS, Gerba CP, Pepper IL. Detection of enteroviruses in groundwater with the polymerase chain reaction. Appl Environ Microbiol. 1993 May;59(5):1318–1324. [PMC free article] [PubMed] [Google Scholar]
  • Amann R, Springer N, Ludwig W, Görtz HD, Schleifer KH. Identification in situ and phylogeny of uncultured bacterial endosymbionts. Nature. 1991 May 9;351(6322):161–164. [PubMed] [Google Scholar]
  • Belser LW, Schmidt EL. Serological diversity within a terrestrial ammonia-oxidizing population. Appl Environ Microbiol. 1978 Oct;36(4):589–593. [PMC free article] [PubMed] [Google Scholar]
  • CARLUCCI AF, PRAMER D. Factors influencing the plate method for determining abundance of bacteria in sea water. Proc Soc Exp Biol Med. 1957 Nov;96(2):392–394. [PubMed] [Google Scholar]
  • Distel DL, DeLong EF, Waterbury JB. Phylogenetic characterization and in situ localization of the bacterial symbiont of shipworms (Teredinidae: Bivalvia) by using 16S rRNA sequence analysis and oligodeoxynucleotide probe hybridization. Appl Environ Microbiol. 1991 Aug;57(8):2376–2382. [PMC free article] [PubMed] [Google Scholar]
  • Fliermans CB, Bohlool BB, Schmidt EL. Autecological study of the chemoautotroph Nitrobacter by immunofluorescence. Appl Microbiol. 1974 Jan;27(1):124–129. [PMC free article] [PubMed] [Google Scholar]
  • Giovannoni SJ, Britschgi TB, Moyer CL, Field KG. Genetic diversity in Sargasso Sea bacterioplankton. Nature. 1990 May 3;345(6270):60–63. [PubMed] [Google Scholar]
  • Head IM, Hiorns WD, Embley TM, McCarthy AJ, Saunders JR. The phylogeny of autotrophic ammonia-oxidizing bacteria as determined by analysis of 16S ribosomal RNA gene sequences. J Gen Microbiol. 1993 Jun;139(Pt 6):1147–1153. [PubMed] [Google Scholar]
  • Jinks-Robertson S, Gourse RL, Nomura M. Expression of rRNA and tRNA genes in Escherichia coli: evidence for feedback regulation by products of rRNA operons. Cell. 1983 Jul;33(3):865–876. [PubMed] [Google Scholar]
  • Kogure K, Simidu U, Taga N. A tentative direct microscopic method for counting living marine bacteria. Can J Microbiol. 1979 Mar;25(3):415–420. [PubMed] [Google Scholar]
  • Kopecka H, Dubrou S, Prevot J, Marechal J, López-Pila JM. Detection of naturally occurring enteroviruses in waters by reverse transcription, polymerase chain reaction, and hybridization. Appl Environ Microbiol. 1993 Apr;59(4):1213–1219. [PMC free article] [PubMed] [Google Scholar]
  • Roszak DB, Colwell RR. Survival strategies of bacteria in the natural environment. Microbiol Rev. 1987 Sep;51(3):365–379. [PMC free article] [PubMed] [Google Scholar]
  • Schmidt TM, DeLong EF, Pace NR. Analysis of a marine picoplankton community by 16S rRNA gene cloning and sequencing. J Bacteriol. 1991 Jul;173(14):4371–4378. [PMC free article] [PubMed] [Google Scholar]
  • Seal SE, Jackson LA, Daniels MJ. 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. [PMC free article] [PubMed] [Google Scholar]
  • Soriano S, Walker N. Isolation of ammonia-oxidizing autotrophic bacteria. J Appl Bacteriol. 1968 Dec;31(4):493–497. [PubMed] [Google Scholar]
  • Stahl DA, Lane DJ, Olsen GJ, Pace NR. Characterization of a Yellowstone hot spring microbial community by 5S rRNA sequences. Appl Environ Microbiol. 1985 Jun;49(6):1379–1384. [PMC free article] [PubMed] [Google Scholar]
  • Steffan RJ, Atlas RM. DNA amplification to enhance detection of genetically engineered bacteria in environmental samples. Appl Environ Microbiol. 1988 Sep;54(9):2185–2191. [PMC free article] [PubMed] [Google Scholar]
  • Steffan RJ, Goksøyr J, Bej AK, Atlas RM. Recovery of DNA from soils and sediments. Appl Environ Microbiol. 1988 Dec;54(12):2908–2915. [PMC free article] [PubMed] [Google Scholar]
  • Sykes PJ, Neoh SH, Brisco MJ, Hughes E, Condon J, Morley AA. Quantitation of targets for PCR by use of limiting dilution. Biotechniques. 1992 Sep;13(3):444–449. [PubMed] [Google Scholar]
  • Teske A, Alm E, Regan JM, Toze S, Rittmann BE, Stahl DA. Evolutionary relationships among ammonia- and nitrite-oxidizing bacteria. J Bacteriol. 1994 Nov;176(21):6623–6630. [PMC free article] [PubMed] [Google Scholar]
  • Tsai YL, Olson BH. Detection of low numbers of bacterial cells in soils and sediments by polymerase chain reaction. Appl Environ Microbiol. 1992 Feb;58(2):754–757. [PMC free article] [PubMed] [Google Scholar]
  • Völsch A, Nader WF, Geiss HK, Nebe G, Birr C. Detection and analysis of two serotypes of ammonia-oxidizing bacteria in sewage plants by flow cytometry. Appl Environ Microbiol. 1990 Aug;56(8):2430–2435. [PMC free article] [PubMed] [Google Scholar]
  • Walsh PS, Metzger DA, Higuchi R. Chelex 100 as a medium for simple extraction of DNA for PCR-based typing from forensic material. Biotechniques. 1991 Apr;10(4):506–513. [PubMed] [Google Scholar]
  • Ward BB, Carlucci AF. Marine ammonia- and nitrite-oxidizing bacteria: serological diversity determined by immunofluorescence in culture and in the environment. Appl Environ Microbiol. 1985 Aug;50(2):194–201. [PMC free article] [PubMed] [Google Scholar]
  • Ward BB, Perry MJ. Immunofluorescent Assay for the Marine Ammonium-Oxidizing Bacterium Nitrosococcus oceanus. Appl Environ Microbiol. 1980 Apr;39(4):913–918. [PMC free article] [PubMed] [Google Scholar]
  • Ward DM, Weller R, Bateson MM. 16S rRNA sequences reveal numerous uncultured microorganisms in a natural community. Nature. 1990 May 3;345(6270):63–65. [PubMed] [Google Scholar]
  • Wegmüller B, Lüthy J, Candrian U. Direct polymerase chain reaction detection of Campylobacter jejuni and Campylobacter coli in raw milk and dairy products. Appl Environ Microbiol. 1993 Jul;59(7):2161–2165. [PMC free article] [PubMed] [Google Scholar]

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