The aims of the study were to determine the prevalence of Listeria monocyto
genes in the feces of healthy Austrians and to characterize the isolates by
various typing methods.
Stool specimens from 505 healthy volunteers from the Tyrol were tested for
the presence of L. monocytogenes using cold enrichment for 6 months and fiv
e different detection methods: conventional plating onto Palcam and Rapid'L
.MONO agar, immunomagnetic separation (IMS) followed by conventional platin
g, enzyme-linked fluorescent immunoassay (ELFA), ELISA, and PCR.
L. monocytogenes was isolated by conventional plating from one specimen (0.
2%), and a further three were positive on immunomagnetic separation (0.8%).
Only one specimen tested positive with ELFA and EIA, although it tested ne
gative by conventional culture, IMS, and PCR. Eighteen of 505 samples were
positive by PCR (3.6%), and this included three of the four culture-confirm
ed specimens. Serotyping, phage-typing, arsenic cadmium, anti microbial-res
istance typing and pulsed-field gel electrophoresis showed that multiple L.
monocytogenes isolates from three of the four carriers were indistinguisha
ble.
Our data indicate that the Austrian fecal carriage rate is at least 0.8%. I
n view of a listeriosis incidence of 0.16/100,000 per year, the chances of
fecal carriage developing Into listeriosis appear to be very low.