Turn on more accessible mode
Skip to main content
Turn off more accessible mode
PCD
Sign In
|
PCD
This Site: PCD
All Sites
People
Advanced Search
PCD
HOME
INTRODUCTION
WHO
WHAT
WHERE
PUBLICATIONS
RELATED SITES
CONTACT
PCD
>
PCD Publications
>
Assays to detect β-tubulin codon 200 polymorphism in Trichuris trichiura and Ascaris lumbricoides
PCD Publications
: Assays to detect β-tubulin codon 200 polymorphism in Trichuris trichiura and Ascaris lumbricoides
Title
Assays to detect β-tubulin codon 200 polymorphism in Trichuris trichiura and Ascaris lumbricoides
Author
Diawara, A., Drake, L.J., Suswillo, R.R., Kihara, J., Bundy, D.A.P., Scott, M.E., Halpenny, C., Stothard, J.R., Prichard, R.K.
Year
2009
Publisher
PLoS Neg. Trop. Dis
Issue & Pages
3(3):e397
Summary
Background: The soil-transmitted helminths (STH) Ascaris lumbricoides and Trichuris trichiura are gastrointestinal parasites causing many disabilities to humans, particularly children. The benzimidazole (BZ) drugs, albendazole (ALB) and
mebendazole (MBZ), are commonly used for mass treatment for STH. Unfortunately, there is concern that increased use of
anthelmintics could select for resistant populations of these human parasites. In veterinary parasites, and lately in filarial
nematodes, a single amino acid substitution from phenylalanine to tyrosine, known to be associated with benzimidazole resistance, has been found in parasite b-tubulin at position 200. We have developed pyrosequencer assays for codon 200 (TTC or TAC) in A. lumbricoides and T. trichiura to screen for this single nucleotide polymorphism (SNP).
Method and Findings: Pyrosequencing assays were developed and evaluated for detecting the TTC or TAC SNP at codon 200 in b-tubulin in A. lumbricoides and T. trichiura. Genomic DNA from individual worms, eggs isolated from individual adult worms or from fecal samples with known treatment history and origin, were sequenced at b-tubulin by pyrosequencing,
and genotypes were confirmed by conventional sequencing. The assays were applied to adult worms from a benzimidazolenaıve population in Kenya. Following this, these assays were applied to individual worms and pooled eggs from people in East Africa (Uganda and Zanzibar) and Central America (Panama) where mass anthelmintic drug programs had been implemented. All A. lumbricoides samples were TTC. However, we found 0.4% homozygous TAC/TAC in T. trichiura worms from non-treated people in Kenya, and 63% of T. trichiura egg pools from treated people in Panama contained only TAC.
Conclusion: Although the codon 200 TAC SNP was not found in any of the A. lumbricoides samples analyzed, a rapid genotyping assay has been developed that can be used to examine larger populations of this parasite and to monitor for
possible benzimidazole resistance development. The TAC SNP at codon 200, associated with benzimidazole resistance in
other nematodes, does occur in T. trichiura, and a rapid assay has been developed to allow populations of this parasite to be
monitored for the frequency of this SNP. Sample sizes were small, anthelmintic efficacy was not assessed, and treated and
non-treated samples were from different locations, so these frequencies cannot be extrapolated to other populations of T.
trichiura or to a conclusion about resistance to treatment. The occurrence of the TAC SNP at codon 200 of b-tubulin in T.
trichiura may explain why benzimidazole anthelmintics are not always highly effective against this species of STH. These
assays will be useful in assessing appropriate treatment in areas of high T. trichiura prevalence and in monitoring for
possible resistance development in these STH.
Topic
Worms
Full Text
Full Text
Attachments
Created at 16/04/2009 14:31 by NEW-SERVER3\AWoolnough
Last modified at 16/04/2009 14:31 by NEW-SERVER3\AWoolnough
Use this page to add attachments to an item.
Name