16S rDNA sequencing of Ruminococcus albus and Ruminococcus flavefaciens: Design of a signature probe and its application in adult sheep

Denis O. Krause, Brian P. Dalrymple, Wendy J. Smith, Roderick I. Mackie, Christopher S. McSweeney

Research output: Contribution to journalArticle

Abstract

The ruminococci are an important group of fibrolytic bacteria inhabiting the rumen. Seventeen strains of presumptively identified Ruminococcus were evaluated by a combination of nearly complete and partial 16S rDNA sequence that identified all strains as either Ruminococcus albus or Ruminococcus flavefaciens. All sequences fell into cluster IV of the clostridia, while other species of ruminococci (eg. Ruminococcus obeum, Ruminococcus gnavus, Ruminococcus lactaris) fall into cluster XIVa of the clostridia. Ruminococcus cluster IV sequences were used to design a 165 rRNA oligonucleotide probe to assess the relative abundance of target populations in a stable ruminal environment. A stable population (animals fed eight times per day) was established in sheep so that statistically robust comparisons could be made in the absence of variation due to diurnal rumen fluctuations. The steady state populations were sampled six times over a 24 d period and direct microscopic counts (DC), total culturable counts (TCC), and total cellulolytic counts (CEL) were determined. DC and culturable data (TCC and CEL) were compared with relative abundance estimates of Rominococcus IV and Fibrobacter succinogenes. A combination of the Ruminococcus and F. succinogenes probes accounted for 4.0% of the bacterial population and cellulolytic bacteria (measured by most-probable numbers) were 5.2% of the total culturable count. These data suggest that a major portion of the Ruminococcus and Fibrobacter diversity has been cultured and is represented by available sequences. Steady state populations were measured over several days in three sheep and an estimate of variation in DC, TCC, CEL and 16S-based data were obtained. These variance estimates could be used to determine the theoretical sample sizes required to obtain statistically significant differences under different experimental conditions.

Original languageEnglish (US)
Pages (from-to)1797-1807
Number of pages11
JournalMicrobiology
Volume145
Issue number7
DOIs
StatePublished - Jul 1999

Fingerprint

Ruminococcus
Ribosomal DNA
Sheep
Fibrobacter
Clostridium
Rumen
Population
Bacteria
Oligonucleotide Probes
Health Services Needs and Demand
Population Dynamics
Sample Size

Keywords

  • 16S rDNA
  • Phylogeny
  • Rumen
  • Ruminococcus
  • Statistics

ASJC Scopus subject areas

  • Microbiology

Cite this

16S rDNA sequencing of Ruminococcus albus and Ruminococcus flavefaciens : Design of a signature probe and its application in adult sheep. / Krause, Denis O.; Dalrymple, Brian P.; Smith, Wendy J.; Mackie, Roderick I.; McSweeney, Christopher S.

In: Microbiology, Vol. 145, No. 7, 07.1999, p. 1797-1807.

Research output: Contribution to journalArticle

Krause, Denis O. ; Dalrymple, Brian P. ; Smith, Wendy J. ; Mackie, Roderick I. ; McSweeney, Christopher S. / 16S rDNA sequencing of Ruminococcus albus and Ruminococcus flavefaciens : Design of a signature probe and its application in adult sheep. In: Microbiology. 1999 ; Vol. 145, No. 7. pp. 1797-1807.
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