Quantitative PCR method for sensitive detection of ruminant fecal pollution in freshwater and evaluation of this method in alpine karstic regions

Appl Environ Microbiol. 2006 Aug;72(8):5610-4. doi: 10.1128/AEM.00364-06.

Abstract

A quantitative TaqMan minor-groove binder real-time PCR assay was developed for the sensitive detection of a ruminant-specific genetic marker in fecal members of the phylum Bacteroidetes. The qualitative and quantitative detection limits determined were 6 and 20 marker copies per PCR, respectively. Tested ruminant feces contained an average of 4.1 x 10(9) marker equivalents per g, allowing the detection of 1.7 ng of feces per filter in fecal suspensions. The marker was detected in water samples from a karstic catchment area at levels matching a gradient from negligible to considerable ruminant fecal influence (from not detectable to 10(5) marker equivalents per liter).

Publication types

  • Evaluation Study

MeSH terms

  • Animals
  • Bacteroidetes / classification
  • Bacteroidetes / genetics
  • Bacteroidetes / isolation & purification*
  • Feces / microbiology*
  • Fresh Water / microbiology*
  • Genetic Markers*
  • Molecular Sequence Data
  • Polymerase Chain Reaction / methods*
  • Ruminants / microbiology*
  • Sensitivity and Specificity
  • Sequence Analysis, DNA
  • Water Pollution
  • Water Supply

Substances

  • Genetic Markers

Associated data

  • GENBANK/DQ364808
  • GENBANK/DQ364809
  • GENBANK/DQ364810
  • GENBANK/DQ364811
  • GENBANK/DQ364812
  • GENBANK/DQ364813
  • GENBANK/DQ364814
  • GENBANK/DQ364815
  • GENBANK/DQ364816
  • GENBANK/DQ364817
  • GENBANK/DQ364818
  • GENBANK/DQ364819
  • GENBANK/DQ364820
  • GENBANK/DQ364821
  • GENBANK/DQ364822