1. Development of a new amplification-refractory mutation system for detection of a single nucleotide polymorphism linked to drug resistance in Ancylostoma caninum
- Author
-
Rabelo Ém and Furtado Lf
- Subjects
Ancylostoma ,Nonsense mutation ,Drug Resistance ,Single-nucleotide polymorphism ,Polymerase Chain Reaction ,Polymorphism, Single Nucleotide ,Sensitivity and Specificity ,Frameshift mutation ,Tubulin ,Genetics ,Animals ,Missense mutation ,Codon ,Molecular Biology ,Gene ,Anthelmintics ,biology ,Reproducibility of Results ,Sequence Analysis, DNA ,General Medicine ,biology.organism_classification ,Molecular biology ,Isotype ,Mutation ,Mutation (genetic algorithm) ,Benzimidazoles ,Ancylostoma caninum - Abstract
Single nucleotide polymorphisms at codons 167, 198, and 200 in the β-tubulin isotype 1 gene have been associated with benz-imidazole resistance. Until now, the only mutation observed in Ancy-lostoma caninum was at codon 200 of this gene. However, the standard-ized methodologies used to detect mutations in this species are faulty. The objective of this study was to standardize a molecular technique based on amplification-refractory mutation system-polymerase chain reaction (ARMS-PCR) for detecting the mutation at codon 200 in the A. caninum β-tubulin isotype 1 gene. Controls were synthesized both for the absence of the mutation, using conventional PCR, and for the presence of the mutation, using the Megaprimer-PCR technique. After standardization of the ARMS-PCR using the controls, the technique was validated through an analysis of 75 A. caninum DNA samples, fol-lowed by sequencing. The results revealed that the developed technique has high sensitivity, specificity, and reproducibility, which allow its ap-plication in the field.
- Published
- 2015