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Identification and geographical distribution of pyrethroid resistance mutations in the poultry red mite Dermanyssus gallinae
Author(s) -
Katsavou Evangelia,
Vlogiannitis Spyros,
KarpTatham Eleanor,
Blake Damer P,
Ilias Aris,
Strube Christina,
Kioulos Ilias,
Dermauw Wannes,
Van Leeuwen Thomas,
Vontas John
Publication year - 2020
Publication title -
pest management science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.296
H-Index - 125
eISSN - 1526-4998
pISSN - 1526-498X
DOI - 10.1002/ps.5582
Subject(s) - pyrethroid , acaricide , biology , knockdown resistance , mite , cypermethrin , genetics , deltamethrin , pesticide resistance , cyfluthrin , veterinary medicine , toxicology , pesticide , ecology , medicine
Background The poultry red mite (PRM) Dermanyssus gallinae is the most common ectoparasite on poultry and causes high economic losses in poultry farming worldwide. Pyrethroid acaricides have been widely used for its control and, consequently, pyrethroid resistance has arisen. In this study we aim to investigate the occurrence of resistance and study the geographical distribution of pyrethroid resistance mutations across PRM populations in Europe. Results Full dose–response contact bioassays revealed very high levels of resistance against several pyrethroids (α‐cypermethrin, fluvalinate, and cyfluthrin) in two PRM populations from Greece, compared to a susceptible reference strain. Resistance was associated with mutations in the gene encoding the target site of pyrethroids, the voltage‐gated sodium channel (VGSC). Mutations, M918L and L925V in domain IIS4‐S5 and F1534L in domain IIIS6, were found at positions known to play a role in pyrethroid resistance in other arthropod species. Subsequent screening by sequencing VGSC gene fragments IIS4‐S5 and IIIS6 revealed the presence and distribution of these mutations in many European populations. In some populations, we identified additional or different mutations including M918V/T, L925M, T929I, I936F, and F1538L. The latter mutation is a possible alternative for F1538I that has been previously associated with pyrethroid resistance in other Acari species. Conclusion We report very high levels of pyrethroid resistance in PRM populations from Greece, as well as the identification and geographical distribution of 10 pyrethroid resistance mutations in PRM populations across Europe. Our results draw attention to the need for an evidence‐based implementation of PRM control, taking acaricide resistance management into consideration. © 2019 Society of Chemical Industry