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Journal of Clinical Microbiology, July 1998, p. 1871-1876, Vol. 36, No. 7
Department of Parasitology,
Received 25 November 1997/Returned for modification 13 February
1998/Accepted 23 March 1998
Recently, extensions of the range of Echinococcus
multilocularis in Europe and North America and drastic increases
in fox populations in Europe put an increasing proportion of the human population at risk of alveolar echinococcosis. To obtain data on the
local infection pressure, studies of the prevalence of the parasite in
the animals that transmit the parasite, foxes, dogs, and cats, are
urgently required. Such investigations, however, have been hampered by
the need for necropsy of the host animal to specifically diagnose
infection with the parasite. In this study, a nested PCR and an
improved method for DNA extraction were developed to allow the
sensitive and specific diagnosis of E. multilocularis
infections directly from diluted fecal samples from foxes. The target
sequence for amplification is part of the E. multilocularis
mitochondrial 12S rRNA gene. The specificity of the method was
100% when it was tested against 18 isolates (metacestodes and adult
worms) of 11 cestode species, including E. granulosus. The
sensitivity of the method was evaluated by adding egg suspensions and
individual eggs to samples of diluted feces from uninfected foxes. The
presence of one egg was sufficient to give a specific signal. To
confirm the PCR results, an internal probe which hybridized only with
E. multilocularis amplification products but
not with the DNA of other cestodes was constructed. In order to
investigate the applicability of this method for epidemiological studies, 250 wild foxes from a area in southern Germany where echinococcosis is highly endemic were examined by both necropsy and PCR
of rectal contents. The sensitivity correlated with the parasites'
number and stage of maturity. It ranged from 100% (>1,000 gravid
worms) to 70% (<10 nongravid worms). On the basis of positive PCR
results for 165 foxes, the sensitivity of the traditional and widely
used necropsy method was found to be not higher than 76%. We therefore
present this PCR system as an alternative method for the routine
diagnosis of E. multilocularis in carnivores.
0095-1137/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Detection of Echinococcus multilocularis
in the Definitive Host: Coprodiagnosis by PCR as an Alternative
to Necropsy
*
Corresponding author. Mailing address: Department of
Parasitology, University of Hohenheim, Emil-Wolff-Str. 34, 70599 Stuttgart, Germany. Phone: 0049-711-4593076. Fax: 0049-711-4592276. E-mail: dinkelan{at}uni-hohenheim.de.
Journal of Clinical Microbiology, July 1998, p. 1871-1876, Vol. 36, No. 7
0095-1137/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
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