家庭用蚊駆除スプレーが殺虫剤耐性を促進する可能性を解明(Backyard Mosquito Sprays May Be Fueling Insecticide Resistance)

2026-07-17 ノースカロライナ州立大学(NC State)

米国ノースカロライナ州立大学(NC State University)の研究チームは、住宅の庭で行われる蚊の殺虫剤散布が、ヒトスジシマカ(Aedes albopictus)の殺虫剤抵抗性を急速に進化させている可能性を2件の研究で明らかにした。研究では、2016~2024年にノースカロライナ州ウェイク郡で採集した2,273匹を対象に、ピレスロイド系殺虫剤に対するノックダウン抵抗性(kdr)変異を解析した。その結果、2016~2017年には抵抗性は確認されなかったが、2018年に初めて検出され、2023年には調査住宅区画の84%で抵抗性変異が確認され、全個体の39%が変異を保有していた。また、抵抗性は資産価値の高い住宅地ほど高い傾向があり、民間業者や家庭での殺虫剤散布が局所的な選択圧となって抵抗性拡大を促している可能性が示された。研究チームは、薬剤散布だけに依存せず、水たまりの除去など幼虫の発生源対策を組み合わせた総合的害虫管理(IPM)を推進することが、将来的な防除効果の維持に重要であると提言している。

<関連情報>

世界的に侵入しているヒトスジシマカ(Aedes albopictus)におけるノックダウン耐性の社会経済的予測因子 Socioeconomic predictors of knockdown resistance in the globally invasive tiger mosquito Aedes albopictus

Cole D. Butler;Jessica Y. Ding;Jennifer Baltzegar;Zachary S. Brown;Martha O. Burford Reiskind;Michael H. Reiskind
Royal Society Open Science  Published:08 Jul 2026
DOI:https://doi.org/10.1098/rsos.251678

家庭用蚊駆除スプレーが殺虫剤耐性を促進する可能性を解明(Backyard Mosquito Sprays May Be Fueling Insecticide Resistance)

Abstract

The tiger mosquito Aedes albopictus (Skuse) is a nuisance biter and vector for many dangerous pathogens. Population control of this species primarily relies on the spraying of chemical insecticides. However, the emergence of insecticide resistance, otherwise known as knockdown resistance (kdr), jeopardizes control and is a serious threat to public health. Effectively managing resistance requires us first to understand the conditions that predict its evolution. Here, we investigate the association between total property value (TPV) and the frequency of kdr in Ae. albopictus populations in Raleigh, North Carolina, USA. We hypothesized that kdr frequency correlates with TPV, because we speculate that wealthier neighbourhoods apply chemical insecticides more frequently. We tested this hypothesis by sampling mosquito populations from 31 different residential blocks across the city and along a TPV gradient. Overall, we found a high frequency of kdr (39%) over a spatially heterogeneous distribution that was significantly correlated with TPV. We find evidence supporting a connection between socioeconomic factors and the rise of insecticide resistance, something not previously documented for this species. This suggests that economic interventions may be a promising approach to resistance management in this and other contexts.

 

郊外に生息するヒトスジシマカにおけるノックダウン耐性の出現と空間分布 Emergence and spatial distribution of knockdown resistance in a suburban population of Aedes albopictus

Jennifer F. Baltzegar,Cole D. Butler,Jessica Y. Ding,Chay M. Beeson,E. M. X. Reed,Michael H. Reiskind & Martha O. Burford Reiskind
Parasites & Vectors  Published:27 June 2026
DOI:https://doi.org/10.1186/s13071-026-07519-6  Unedited version

Abstract

Background
Aedes albopictus is a major vector of arboviral diseases and is often targeted by pyrethroid-based mosquito control in residential areas. While knockdown resistance (kdr) mutations are well-documented in Ae. aegypti, their emergence in Ae. albopictus has been less studied, particularly in suburban environments, where insecticide application is often uncoordinated. Understanding the temporal and spatial dynamics of resistance evolution in this context is critical for preserving the effectiveness of public health interventions.

Methods
We conducted longitudinal sampling of Ae. albopictus populations in Wake County, North Carolina, from 2016 to 2024. Using a novel allele-specific PCR melt curve assay, we genotyped 2,669 mosquitoes at the F1534S locus in the voltage-gated sodium channel gene. Resistance allele frequencies were calculated annually and mapped across the county for three key years, representing the pre-emergence (2016), initial detection (2018), and widespread phases of resistance development (2023). Selection and dominance were estimated using the Wright–Fisher approximate Bayesian computation algorithm for locus F1534S.

Results
The F1534S resistance allele was first detected in 2018 at a central neighborhood in Wake County. By 2023, the allele had become distributed throughout the sampling region, with the highest observed frequencies near the site of first detection. Resistance allele frequency peaked at 0.36 in 2023, accompanied by an increase in heterozygous and homozygous resistance genotypes. Temporally sampled sites showed consistent trends in rising frequencies of the resistance allele, with all temporally sampled locations harboring resistance genotypes by 2022. The resistance allele was estimated to have a high selection coefficient and to be partially recessive in this population.

Conclusions
Our findings reveal rapid emergence and spatial distribution of the F1534S kdr allele in a suburban population of Ae. albopictus. The observed distribution of resistance alleles is consistent with strong genetic selection. These results highlight the need for proactive resistance monitoring and integrated management strategies that address private-sector contributions to insecticide selection pressure.

1207植物保護
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