STREPTOCOCCAL PYROGENIC EXOTOXIN-A, STREPTOLYSIN-O, EXOENZYMES, SEROTYPE AND BIOTYPE PROFILES OF STREPTOCOCCUS-PYOGENES ISOLATES FROM PATIENTS WITH TOXIC-SHOCK-SYNDROME AND OTHER SEVERE INFECTIONS
H. Mulleralouf et al., STREPTOCOCCAL PYROGENIC EXOTOXIN-A, STREPTOLYSIN-O, EXOENZYMES, SEROTYPE AND BIOTYPE PROFILES OF STREPTOCOCCUS-PYOGENES ISOLATES FROM PATIENTS WITH TOXIC-SHOCK-SYNDROME AND OTHER SEVERE INFECTIONS, Zentralblatt fur Bakteriologie, 286(3), 1997, pp. 421-433
The determination of protein M and T serotypes, biotypes and pyrogenic
(erythrogenic) exotoxin A (SPE A), streptolysin O (SLO), streptokinas
e (SK), hyaluronidase (HA) and cysteine proteinase release by 212 S. p
yogenes isolates from patients with severe invasive group A streptococ
cal (GAS) infections, among them 74 cases of streptococcal toxic shock
syndrome (STSS) has been investigated. M1 or M3 serotypes were expres
sed by 25% of the isolates (53/212), whereas 59% (125/212) belonged to
15 other different serotypes and 16% (34/212) were untypeable. Of the
74 isolates from STSS patients, 42% (31/74) expressed M1 and to a les
ser extent M3 serotypes versus 19% of the non STSS isolates (26/138).
Among the ten different biotypes known, biotypes 1 and 3 were prevalen
t, particularly the former in the case of STSS isolates. SPE A was det
ectably produced by about 25% (54/212) of the strains. However, as hig
h as 40.5% of the STSS isolates (30/74) versus 17.4% of non STSS isola
tes (24/138) released SPE A. Moreover, 67% of the SPE A producing stra
ins were of serotype M1 or M3. SK and HA were released by 71% and 10%
of the isolates respectively. All strains released SLO (4 to 256 HU/ml
) and 85% cysteine proteinase. No relationship between toxin or enzyme
titer and the type of disease or clinical origin of the strains was f
ound. Culture supernatants of all isolates showed moderate to high lym
phocyte transforming activity with index values ranging from 14.5 to 5
0.3 including those strains which did not release detectable amounts o
f SPE A suggesting that SPE C and other mitogenic factor(s) are releas
ed by the isolates investigated.