SUMMARYSixty-nine Staphylococcus aureas strains, 39 of which produced staphylococcal enterotoxin B (SEB + ) and 14 of which were associated with toxic shock (TS +), were studied using the following markers: serotyping, phage typing, antibiotyping, ribotyping, zymotyping and pulsed-field electrophoresis typing. Analysis of the results showed that the enterotoxin B producing strains were derived from at least three clones: the first two consisted of methicillin-susceptible strains, while the third included the methicillin-resistant (MRSA) strains. TS + strains of nongenital origin appeared to be distributed between the three clones, with no specific characters.
INTRODUCTIONThe toxic shock syndrome toxin-i (TSST-1) of Staphylococcus aureus is responsible for staphylococcal toxic shock (TS). Most of the strains of genital origin and 50 % of others belong to the same clone [1]. Among the other S. aureus toxins, staphylococcal enterotoxin B (SEB) has been associated with disease recognized post-mortem [2,3]. Responsible mainly for food poisoning, it has also been associated with toxic shock [4][5][6]. The properties of SEB-producing strains (SEB+) are well documented; Asheshov and co-workers [7] demonstrated that the strains in the 94/96 phage complex were very often SEB+; Melconian and colleagues [8] observed that these strains were lysed mainly by phages of groups II and V; and Dornbusch and Hallander [9] have demonstrated a relationship between oxacillin resistance and toxin production. Recently, Lee and colleagues [10] have shown that TS-associated strains produced either TSST-1, enterotoxin B or, exceptionally, both; they have also shown that SEB+ strains belonged to the same zymotype, suggesting a clonal origin. The aim of the present study was to confirm or refute the existence of an enterotoxin-B producing cell clone by studying the phenotypic and genotypic characters of SEB + strains (whether or not associated with TS) as well as non-producing strains, using six different