Synthetic enterotoxin B DNA probes for detection of enterotoxigenic Staphylococcus aureus strains

Author:

Notermans S1,Heuvelman K J1,Wernars K1

Affiliation:

1. Laboratory of Water and Food Microbiology, National Institute of Public Health and Environmental Hygiene, Bilthoven, The Netherlands.

Abstract

DNA-DNA colony hybridization experiments with three different synthetic probes were carried out with 210 strains of Staphylococcus aureus. The synthetic probes encoded the amino acids 15 to 29 (probe 1), 179 to 192 (probe 2), and 207 to 219 (probe 3) of staphylococcal enterotoxin B (SEB). The amino acid sequences of these parts of SEB are identical to those of SEC1. All 21 SEB-producing strains tested reacted with each of the three probes. Of the 69 SEC-producing strains, 21 reacted with probe 1, none reacted with probe 2, and all 69 reacted with probe 3. With other strains no hybridization signals were obtained. The results presented here show that with a single synthetic DNA probe (probe 3) both SEB- and SEC-producing strains are detectable.

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

Reference18 articles.

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2. BergdoU M. S. 1979. Staphylococcal intoxications p. 443. In H. Rieman and F. L. Bryan (ed.) Food-borne infections and intoxications 2nd ed. Academic Press Inc. New York.

3. Nucleotide sequence of the staphylococcal enterotoxin Cl gene and relatedness to other pyrogenic toxins;Bohach G. A.;Mol. Gen. Genet.,1987

4. Purification and partial characterization of enterotoxin C produced by Staphylococcus aureus strain 137;Borja C. R.;Biochemistry,1967

5. The microslide gel double diffusion test for the detection and assay of staphylococcal enterotoxins;Casman E. P.;Health Lab. Sci.,1969

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