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Increased frequency of the T929I and L932F mutations associated with knockdown resistance in permethrin-resistant populations of the human head louse, Pediculus capitis, from California, Florida, and Texas

Author:
Gao, Jian-Rong, Yoon, Kyong Sup, Lee, Si Hyeock, Takano-Lee, Miwako, Edman, John D., Meinking, Terri L., Taplin, David, Clark, J. Marshall
Source:
Pesticide biochemistry and physiology 2003 v.77 no.3 pp. 115-124
ISSN:
0048-3575
Subject:
DNA, Pediculus humanus capitis, amino acid substitution, bioassays, diagnostic techniques, gene frequency, genes, heterozygosity, homozygosity, insecticide resistance, monitoring, mortality, nerve tissue, nucleotide sequences, pediculosis, permethrin, pests, point mutation, resistance management, sequence analysis, sodium channels, California, Ecuador, Florida, Panama, Texas
Abstract:
The resistance levels of different human head louse populations from the USA to 1% permethrin were evaluated using permethrin-impregnated, filter paper disk-contact bioassay. Populations from southern California, south Florida and south central Texas showed 1.5-, 3.1-, and 1.5- to 5.1-fold resistance compared to insecticide-susceptible head louse populations from Panama or Ecuador. Permethrin-resistant or permethrin-susceptible homozygous or heterozygous genotypes were determined from sequences of PCR-amplified genomic DNA fragments of the voltage-sensitive sodium channel α-subunit gene by the presence of a T or C, or both, respectively, at nucleotide positions 36 and 44 in the sequence. The presence of a T at both these positions resulted in the amino acid substitutions, T929I and L932F, respectively. Of the 424 louse samples examined that had the T929I mutation, all also possessed the L932F mutation, indicating that the two mutations were tightly linked. The southern California population was phenotypically determined by bioassay to be comprised of 45% resistant individuals and had a resistant allele frequency of 0.53 by DNA sequence analysis. The south Florida population was phenotypically determined to consist of 87% resistant individuals and had a resistant allele frequency of 0.97. The four Texas populations varied in the level of resistance and in resistant allele frequency. The Mathis population was phenotypically determined to consist of 15% resistant individuals and had a resistant allele frequency of 0.33. However, the populations from San Antonio, Mansfield, and Corpus Christi were likewise phenotyped to have 91%, 94%, and 100%, respectively, resistant individuals and a 0.98, 1.00 and 1.00, respectively, resistant allele frequency. The log survival time versus logit mortality regression lines of susceptible-homozygotes, resistant-homozygotes, and heterozygotes determined that the resistance trait was complete recessive. Thus, the presence of homozygotes of the T929I and L932F mutations in the voltage-sensitive sodium channel correlated well with increased survival time following exposure to permethrin and indicates that a knockdown-type nerve insensitivity mechanism is functioning as the major mechanism causing permethrin resistance in USA head louse populations. Our results substantiate that permethrin resistance in human head louse population in the USA is widespread but variable. Permethrin resistance is highly correlated with the presence of the T929I and L932F point mutations, which are suitable for detection by a variety of DNA-based diagnostic techniques [Pest Manag. Sci. 57 (2001) 968]. Large-scale monitoring of permethrin resistance is possible utilizing these techniques and would provide critical information necessary for the development of an effective resistance management program for pediculosis.
Agid:
2786567