Skip to main content
Applied and Environmental Microbiology logoLink to Applied and Environmental Microbiology
. 1995 Aug;61(8):3069–3075. doi: 10.1128/aem.61.8.3069-3075.1995

Quantitative fluorescence in situ hybridization of Bifidobacterium spp. with genus-specific 16S rRNA-targeted probes and its application in fecal samples.

P S Langendijk 1, F Schut 1, G J Jansen 1, G C Raangs 1, G R Kamphuis 1, M H Wilkinson 1, G W Welling 1
PMCID: PMC167584  PMID: 7487040

Abstract

Three 16S rRNA hybridization probes were developed and tested for genus-specific detection of Bifidobacterium species in the human fecal flora. Variable regions V2, V4, and V8 of the 16S rRNA contained sequences unique to this genus and proved applicable as target sites for oligodeoxynucleotide probes. Determination of the genus specificity of the oligonucleotides was performed by whole-cell hybridization with fluorescein isothiocyanate-labelled probes. To this end, cells were fixed on glass slides, hybridized with the probes, and monitored by videomicroscopy. In combination with image analysis, this allowed quantification of the fluorescence per cell and objective evaluation of hybridization experiments. One of the probes developed was used to determine the population of Bifidobacterium spp. in human fecal samples. A comparison was made with results obtained by cultural methods for enumeration. Since both methods gave similar population estimates, it was concluded that all bifidobacteria in feces were culturable. However, since the total culturable counts were only a fraction of the total microscopic counts, the contribution of bifidobacteria to the total intestinal microflora was overestimated by almost 10-fold when cultural methods were used as the sole method for enumeration.

Full Text

The Full Text of this article is available as a PDF (435.6 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Amann R. I., Krumholz L., Stahl D. A. Fluorescent-oligonucleotide probing of whole cells for determinative, phylogenetic, and environmental studies in microbiology. J Bacteriol. 1990 Feb;172(2):762–770. doi: 10.1128/jb.172.2.762-770.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Amann R. I., Stromley J., Devereux R., Key R., Stahl D. A. Molecular and microscopic identification of sulfate-reducing bacteria in multispecies biofilms. Appl Environ Microbiol. 1992 Feb;58(2):614–623. doi: 10.1128/aem.58.2.614-623.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Amann R., Springer N., Ludwig W., Görtz H. D., Schleifer K. H. Identification in situ and phylogeny of uncultured bacterial endosymbionts. Nature. 1991 May 9;351(6322):161–164. doi: 10.1038/351161a0. [DOI] [PubMed] [Google Scholar]
  4. Benson D., Lipman D. J., Ostell J. GenBank. Nucleic Acids Res. 1993 Jul 1;21(13):2963–2965. doi: 10.1093/nar/21.13.2963. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Giovannoni S. J., DeLong E. F., Olsen G. J., Pace N. R. Phylogenetic group-specific oligodeoxynucleotide probes for identification of single microbial cells. J Bacteriol. 1988 Feb;170(2):720–726. doi: 10.1128/jb.170.2.720-726.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Jansen G. J., Wilkinson M. H., Deddens B., van der Waaij D. Characterization of human faecal flora by means of an improved fluoro-morphometrical method. Epidemiol Infect. 1993 Oct;111(2):265–272. doi: 10.1017/s0950268800056971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Kuritza A. P., Salyers A. A. Use of a species-specific DNA hybridization probe for enumerating Bacteroides vulgatus in human feces. Appl Environ Microbiol. 1985 Oct;50(4):958–964. doi: 10.1128/aem.50.4.958-964.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Larsen N., Olsen G. J., Maidak B. L., McCaughey M. J., Overbeek R., Macke T. J., Marsh T. L., Woese C. R. The ribosomal database project. Nucleic Acids Res. 1993 Jul 1;21(13):3021–3023. doi: 10.1093/nar/21.13.3021. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Meijer-Severs G. J., van Santen E. Variations in the anaerobic faecal flora of ten healthy human volunteers with special reference to the Bacteroides fragilis-group and Clostridium difficile. Zentralbl Bakteriol Mikrobiol Hyg A. 1986 Feb;261(1):43–52. doi: 10.1016/s0176-6724(86)80061-x. [DOI] [PubMed] [Google Scholar]
  10. Meijer B. C., Kootstra G. J., Geertsma D. G., Wilkinson M. H. Effects of ceftriaxone on faecal flora: analysis by micromorphometry. Epidemiol Infect. 1991 Jun;106(3):513–521. doi: 10.1017/s0950268800067571. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Moore W. E., Holdeman L. V. Human fecal flora: the normal flora of 20 Japanese-Hawaiians. Appl Microbiol. 1974 May;27(5):961–979. doi: 10.1128/am.27.5.961-979.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Neefs J. M., Van de Peer Y., De Rijk P., Chapelle S., De Wachter R. Compilation of small ribosomal subunit RNA structures. Nucleic Acids Res. 1993 Jul 1;21(13):3025–3049. doi: 10.1093/nar/21.13.3025. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Raskin L., Stromley J. M., Rittmann B. E., Stahl D. A. Group-specific 16S rRNA hybridization probes to describe natural communities of methanogens. Appl Environ Microbiol. 1994 Apr;60(4):1232–1240. doi: 10.1128/aem.60.4.1232-1240.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Rice C. M., Fuchs R., Higgins D. G., Stoehr P. J., Cameron G. N. The EMBL data library. Nucleic Acids Res. 1993 Jul 1;21(13):2967–2971. doi: 10.1093/nar/21.13.2967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Sladek T. L., Jacobberger J. W. Flow cytometric titration of retroviral expression vectors: comparison of methods for analysis of immunofluorescence histograms derived from cells expressing low antigen levels. Cytometry. 1993;14(1):23–31. doi: 10.1002/cyto.990140106. [DOI] [PubMed] [Google Scholar]
  16. Wagner M., Erhart R., Manz W., Amann R., Lemmer H., Wedi D., Schleifer K. H. Development of an rRNA-targeted oligonucleotide probe specific for the genus Acinetobacter and its application for in situ monitoring in activated sludge. Appl Environ Microbiol. 1994 Mar;60(3):792–800. doi: 10.1128/aem.60.3.792-800.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Ward D. M., Weller R., Bateson M. M. 16S rRNA sequences reveal numerous uncultured microorganisms in a natural community. Nature. 1990 May 3;345(6270):63–65. doi: 10.1038/345063a0. [DOI] [PubMed] [Google Scholar]
  18. Wilkinson M. H., Jansen G. J., van der Waaij D. Computer processing of microscopic images of bacteria: morphometry and fluorimetry. Trends Microbiol. 1994 Dec;2(12):485–489. doi: 10.1016/0966-842x(94)90653-x. [DOI] [PubMed] [Google Scholar]
  19. Wilkinson M. H. Shading correction and calibration in bacterial fluorescence measurement by image processing system. Comput Methods Programs Biomed. 1994 Aug;44(2):61–67. doi: 10.1016/0169-2607(94)90086-8. [DOI] [PubMed] [Google Scholar]
  20. Yamamoto T., Morotomi M., Tanaka R. Species-specific oligonucleotide probes for five Bifidobacterium species detected in human intestinal microflora. Appl Environ Microbiol. 1992 Dec;58(12):4076–4079. doi: 10.1128/aem.58.12.4076-4079.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. van der Waaij D., Berghuis-de Vries J. M., Lekkerkerk Lekkerkerk-v Colonization resistance of the digestive tract in conventional and antibiotic-treated mice. J Hyg (Lond) 1971 Sep;69(3):405–411. doi: 10.1017/s0022172400021653. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. van der Waaij D. The ecology of the human intestine and its consequences for overgrowth by pathogens such as Clostridium difficile. Annu Rev Microbiol. 1989;43:69–87. doi: 10.1146/annurev.mi.43.100189.000441. [DOI] [PubMed] [Google Scholar]

Articles from Applied and Environmental Microbiology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES