Testing for 'total' Enterobacteriaceae, coliforms and Escherichia coli as m
arker organisms in foods and detection of specific pathogens of the family
Enterobacteriaceae, including pathogenic E. coli, Salmonella, Shigella and
Yersinia spp. is widely applied in many food control laboratories. This rev
iew describes some recent developments in culture media for these organisms
. Methods for enumeration of E. coli include the standard MPN technique, a
membrane-filter method and the use of media containing chromogenic and fluo
rogenic indicators for beta-D-glucuronidase (GUD) activity. Shiga toxin-pro
ducing E. coli O157 strains usually do not ferment sorbitol and an GUD-nega
tive. These characteristics are used in selective media for these organisms
, such as cefixime tellurite sorbitol MacConkey agar. For the detection of
salmonellae, motility enrichment in Modified Semisolid Rappaport-Vassiliadi
s (MSRV) medium shows equal or better results than the use of standard Rapp
aport-Vassiliadis broth. Addition of nitrofurantoin to diagnostic semisolid
salmonella agar and to xylose lysine desoxycholate agar favours the isolat
ion of S. enteritidis. Recently developed salmonella media use different se
lective and diagnostic properties, such as acid formation from propylene gl
ycol, glucuronate fermentation, fermentation of glycerol and addition of Te
rgitol 4 as selective agent. The isolation of Shigella spp. from foods is r
ather difficult and further evaluation of suggested isolation systems and t
he development of more effective methods for the isolation of this pathogen
are needed. Yersinia enterocolitica includes both pathogenic and nonpathog
enic biotypes and serogroups. As no single procedure will recover all patho
genic strains of Y. enterocolitica, the use of two isolation procedures in
parallel is recommended. (C) 1998 Elsevier Science B.V. All rights reserved
.