Abstract
A method was developed for the detection of Giardia cysts by using the polymerase chain reaction (PCR) and the giardin gene as the target. DNA amplification by PCR, using giardin DNA as the target, resulted in detection of both live and dead cysts. When giardin mRNA was used as the target, the ability to amplify cDNA by PCR depended on the mode of killing. Cysts killed by freezing were not detected by PCR when giardin mRNA was the target. Cysts killed by heating or exposure to monochloramine, however, gave positive detection signals for both DNA and giardin mRNA targets. The amount of giardin mRNA and total RNA was significantly increased in live cysts following the induction of excystation. Cysts killed by freezing, heating, or exposure to monochloramine did not show a change in RNA content. The detection of the giardin gene by PCR permits a sensitive and specific diagnosis for Giardia spp. Discrimination between live and dead cysts can be made by measuring the amounts of RNA or PCR-amplified product from the giardin mRNA target before and after the induction of excystation.
MeSH Terms
Animals
Base Sequence
Blotting, Southern
Cytoskeletal Proteins/genetics
DNA, Protozoan/analysis
Electrophoresis, Polyacrylamide Gel
Female
Giardia/isolation & purification,metabolism,pathogenicity
Male
Mice
Molecular Sequence Data
Polymerase Chain Reaction
Protozoan Proteins/genetics
Sensitivity and Specificity
Chemicals
Cytoskeletal Proteins
DNA, Protozoan
Protozoan Proteins
giardin protein, Giardia lamblia
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Mahbubani M H
Department of Biology, University of Louisville, Kentucky 40292.
Bej A K
Perlin M
Schaefer F W
Jakubowski W
Atlas R M
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