Point mutations in the sodium channel gene conferring tau‐fluvalinate resistance in Varroa destructor

BACKGROUND: Sodium channels (SCs) in mites and insects are target sites for pesticides, including pyrethroids. Point mutations in the SC gene have been reported to change the structural conformation of the protein and its sensitivity to pesticides. To find mutations in the SC gene of the mite Varroa...

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Published in:Pest management science Vol. 70; no. 6; pp. 889 - 894
Main Authors: Hubert, Jan, Nesvorna, Marta, Kamler, Martin, Kopecky, Jan, Tyl, Jan, Titera, Dalibor, Stara, Jitka
Format: Journal Article
Language:English
Published: Chichester, UK John Wiley & Sons, Ltd 01-06-2014
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Summary:BACKGROUND: Sodium channels (SCs) in mites and insects are target sites for pesticides, including pyrethroids. Point mutations in the SC gene have been reported to change the structural conformation of the protein and its sensitivity to pesticides. To find mutations in the SC gene of the mite Varroa destructor (VmNa), the authors analysed the VmNa gene sequences available in GenBank and prepared specific primers for the amplification of two fragments containing the regions coding for (i) the domain II S4–S6 region (bp 2805–3337) and (ii) the domain III S4‐3′ terminus region (bp 4737–6500), as determined according to the VmNa cDNA sequence AY259834. RESULTS: Sensitive and resistant mite populations did not differ in the amino acid sequences of the III S4‐3′ terminus VmNa region. However, differences were found in the IIS4–IIS6 fragment. In the resistant population, the mutation C(3004) → G resulted in the substitution L(1002) → V (codon ctg → gtg) at the position equivalent to that of the housefly L925 in the domain II S5 helix. Additionally, the mutation F(1052) → L (codon ttc → ctc) at the position equivalent to that of the housefly F975 in the domain II P‐loop connecting segments S5 and S6 was detected in both the resistant and sensitive populations. CONCLUSION: All individuals that survived the tau‐fluvalinate treatment in the bioassay harboured the L(1002) → V mutation combined with the F(1052), while dead individuals from both the sensitive and resistant populations harboured mostly the L(1002) residue and either of the two residues at position 1052. © 2013 Society of Chemical Industry
Bibliography:http://dx.doi.org/10.1002/ps.3679
ArticleID:PS3679
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ISSN:1526-498X
1526-4998
DOI:10.1002/ps.3679