Evidence map›Paper›PMID 41428707›Full record

ArticlePLoS neglected tropical diseases2025

Insecticide resistance levels, spatial distribution, and kdr mutations in the dengue vector Aedes albopictus of Hong Kong.

Shaolin Han, Elliott F Miot, Yunshi Liao, Munsif Ali Khan, Mathilde Rivot, Lilia Tsz-Wing Tang, Jehan Zeb, Ka Mei Szeto, Long Ching, Tsz Him Li and 4 more

Abstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Shaolin HanCentre for Immunology & Infection, Hong Kong SAR, China.
Elliott F MiotCentre for Immunology & Infection, Hong Kong SAR, China.
Yunshi LiaoCentre for Immunology & Infection, Hong Kong SAR, China.
Munsif Ali KhanCentre for Immunology & Infection, Hong Kong SAR, China.
Mathilde RivotCentre for Immunology & Infection, Hong Kong SAR, China.
Lilia Tsz-Wing TangCentre for Immunology & Infection, Hong Kong SAR, China.
Jehan ZebCentre for Immunology & Infection, Hong Kong SAR, China.
Ka Mei SzetoCentre for Immunology & Infection, Hong Kong SAR, China.
Long ChingCentre for Immunology & Infection, Hong Kong SAR, China.
Tsz Him LiCentre for Immunology & Infection, Hong Kong SAR, China.
Xintong HuangState Key Laboratory of Emerging Infectious Diseases, School of Public Health, The University of Hong Kong, Hong Kong SAR, China.
Brinna E L BarlowCentre for Immunology & Infection, Hong Kong SAR, China.
Sebastien MarcombeCentre for Immunology & Infection, Hong Kong SAR, China.
Tommy Tsan-Yuk LamCentre for Immunology & Infection, Hong Kong SAR, China.ORCID 0000-0002-9769-1527

Funding

Hong Kong Jockey Club Global Health Institute (to TTL), and the Fondation pour la Recherche MédicaleInnoHK initiative of the Innovation Technology Commission of the Hong Kong Special Administrative Region Government
6 · The paper itself

Abstract

Aedes albopictus (Skuse), a primary dengue vector in Hong Kong, poses significant challenges to public health due to escalating insecticide resistance in Asia. To address this concern, we evaluated resistance profiles of five field-derived Ae. albopictus populations across Hong Kong using WHO insecticide susceptibility bioassays. Metabolic detoxification using synergists test with piperonyl butoxide (PBO) and target-site mutations referred to as knockdown resistance (kdr) in the voltage-gated sodium channel (VGSC) gene were characterized to elucidate resistance mechanisms. The results show that Ae albopictus populations in Hong Kong exhibited high resistance to commonly used pyrethroids (permethrin, deltamethrin) and the organochlorine dichlorodiphenyltrichloroethane (DDT), as well as emerging resistance to the organophosphate malathion. Resistance to three larvicides, temephos, spinosad, and pyriproxyfen, is likely to be developing, whereas Bacillus thuringiensis israelensis (Bti) still retains efficacy. Sequencing revealed the F1534S/L mutation in VGSC Domain III (29.0% mutation frequency), strongly correlated with pyrethroid survivorship. A minor dual mutation (S406T + L424H) in Domain I was recorded but showing limited phenotypic association. Synergist assays demonstrated partial or full restoration of pyrethroid susceptibility with PBO, implicating cytochrome P450-mediated metabolic resistance as a co-factor. These findings confirm that Ae. albopictus in Hong Kong has evolved multifaceted resistance mechanisms, driven by both target-site mutations and metabolic detoxification. This study provides critical evidence to optimize local vector control strategies and contributes resistance profiles to the Asia-Pacific region, aiding regional efforts to mitigate dengue transmission risks.

Indexed as

AedesInsecticide ResistanceInsecticidesMosquito VectorsVoltage-Gated Sodium ChannelsAnimalsDengueHong KongInsect ProteinsMutationPyrethrinsInsecticidesInsect ProteinsPyrethrinsVoltage-Gated Sodium Channels

Identifiers

PMID41428707
PMCPMC12721537

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.