P. Descheemaeker et al., Molecular characterisation of group A streptococci from invasive and non-invasive disease episodes in Belgium during 1993-1994, J MED MICRO, 49(5), 2000, pp. 467-471
Five hundred clinical group A streptococcal (GAS) isolates were collected i
n Belgium during the period 1 Nov, 1993 to 31 Oct. 1994, Clinical and labor
atory data were recorded and isolates were characterised, The presence of t
he genes encoding streptococcal pyrogenic exotoxin types A (speA), B (speB)
, C (speC), F (speF) and streptococcal superantigen (ssa) were determined b
y PCR to target specific sequences. These isolates were also emm-typed and
analysed by pulsed-field gel electrophoresis (PFGE) of genomic macrorestric
tion fragments with the enzyme SmaI. In total, 136 unrelated GAS PFGE types
were identified and genetic diversity was clearly demonstrated. Two GAS PF
GE types predominated; a first PFGE type comprised 66 (13.2%) emm1 isolates
characterised by speA(+), speB(+), speC(-), speF(+) and ssa(-); the second
PFGE type comprised 44 (8.8%) emm12 isolates characterised by speA(-), spe
B(+), speC(+) (or speC-), speF(+) and ssa(-). Indistinguishable PFGE types
were observed among both invasive and non-invasive isolates. Ten different
PFGE types were found among 11 streptococcal toric shock syndrome (STSS) is
olates, and five of these lacked speA, Twenty-five (34.7%) of 72 invasive i
solates gave negative results for speA, speC and ssa. This retrospective st
udy confirmed the observation that the dissemination of one specific clone
cannot be associated with invasive GAS disease and posed a question regardi
ng the role of SPE A as a major virulence factor. Other streptococcal virul
ence factors in conjunction with host factors may determine the outcome of
invasive GAS infection.