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Clinical and Diagnostic Laboratory Immunology, July 1999, p. 479-482, Vol. 6, No. 4
Institut für Hygiene und Mikrobiologie,
Universität Würzburg, 97080 Würzburg,
Germany1; Parasitology Unit,
Institut Pasteur de Madagascar, 101 Antananarivo,
Madagascar2; and Department of
Parasitology, Regional Hospital of Saint-Pierre, La
Réunion3
Received 11 November 1998/Returned for modification 10 February
1999/Accepted 18 March 1999
A Taenia solium metacestode cDNA expression library in
the lambda ZAPII vector was screened with pooled sera from patients with neurocysticercosis. Sixty primary clones were identified and shown
to belong to two classes. The clones NC-3 and NC-9 did not reveal any
significant homologies to sequences deposited in the databases and were
further characterized. Both recombinant antigens were expressed as
glutathione S-transferase fusion proteins and applied
for serological diagnosis of human cysticercosis. An enzyme-linked
immunosorbent assay was established and evaluated with 27 serum samples
of La Réunion and Madagascar patients with cysticercosis.
Diagnosis in these patients was established with radiological and
serological procedures. For antigen NC-3 a sensitivity of 96.3% and a
specificity of 91.5% for the serodiagnosis were achieved. In contrast,
the sensitivity of antigen NC-9 was only 33.3%.
1071-412X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Serological Diagnosis of Human Cysticercosis by Use of
Recombinant Antigens from Taenia solium Cysticerci
*
Corresponding author. Mailing address: Institut
für Hygiene und Mikrobiologie, Universitat Würzburg,
Josef-Schneider-Strasse 2, 97080 Würzburg, Germany.
Phone: (0931) 201-3931 Fax: (0931) 201-3445. E-mail:
fmuehlschlegel{at}hygiene.uni-wuerzburg.de.
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