A direct PCR detection method for Clostridium tyrobutyricum spores in up to 100 milliliters of raw milk

Author:

Herman L M1,De Block J H1,Waes G M1

Affiliation:

1. Government Dairy Research Station, Agricultural Research Centre Ghent, Melle, Belgium.

Abstract

A direct detection method for Clostridium tyrobutyricum spores in up to 100 ml of raw milk is presented. The bacterial spores are concentrated by centrifugation after chemical extraction of the milk components. The vegetative cells are selectively lysed, and their DNA is digested and washed away. Afterwards, the DNA is liberated from the spores by microwave treatment. For the identification of the C. tyrobutyricum DNA, a two-step PCR method with two nested pairs of primers is used. The primers were derived from the 16S-23S rRNA spacer region of C. tyrobutyricum, and the specificity of each of them for C. tyrobutyricum is demonstrated. The detection limit can be estimated to be between 3 and 30 spores in 100 ml of raw milk.

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

Reference19 articles.

1. Dénombrement des spores de Clostridium tyrobutyricum par filtration sur membrane et culture sur milieu gélosé;Abgrall B.;Le Lait,1985

2. Large sample simultaneous confidence intervals for the multinomial probabilities based on transformations of the cell frequencies;Bailey B. J. R.;Thecnometrics,1980

3. The 16S/23S ribosomal spacer region as a target for DNA probes to identify eubacteria;Barry T.;PCR Methods Appl.,1991

4. Immuno détection des spores de Clostridium tyrobutyricum agent du gonflement butyrique des fromages. Sci;Bergère J. L.;Aliments,1987

5. Spore properties of clostridia occurring in cheese;Bergère J. L.;J. Appl. Bacteriol.,1970

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