Evidence map›Paper›PMID 35505385›Full record

ArticleParasites & vectors2022

Spatial heterogeneity of knockdown resistance mutations in the dengue vector Aedes albopictus in Guangzhou, China.

Xueli Zheng, Zihao Zheng, Shanshan Wu, Yong Wei, Lei Luo, Daibin Zhong, Guofa Zhou

Open access · goldAbstract read
In one paragraph

Article in Parasites & vectors, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.2field-weighted citation impact, top 13% of its field
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

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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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. F1534SFrontiers in cellular and infection microbiology · 2026
    Article
  4. Mechanisms and genetic mutations of pyrethroid resistance inFrontiers in cellular and infection microbiology · 2025
    Article
  5. Article
  6. Article
  7. Article
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

7 authors at 3 institutions in 2 countries.

Xueli Zheng *Department of Pathogen Biology, School of Public Health, Southern Medical University, Guangzhou, Guangdong, China. zhengxueli2001@126.com.
Zihao Zheng *Department of Pathogen Biology, School of Public Health, Southern Medical University, Guangzhou, Guangdong, China.
Shanshan WuDepartment of Pathogen Biology, School of Public Health, Southern Medical University, Guangzhou, Guangdong, China.
Yong WeiDepartment of Pathogen Biology, School of Public Health, Southern Medical University, Guangzhou, Guangdong, China.
Lei LuoGuangzhou Center for Disease Control and Prevention, Guangzhou, China.
Daibin ZhongProgram in Public Health, School of Medicine, University of California, Irvine, CA, USA.
Guofa ZhouProgram in Public Health, School of Medicine, University of California, Irvine, CA, USA.
Southern Medical University · CNUniversity of California, Irvine · USGuangzhou Center for Disease Control and Prevention · CN

Funding

Guangzhou Science, Technology and Innovation Commission No. 201804020084the National Natural Science Foundation of China No. 31630011
6 · The paper itself

Abstract

backgroundThe city of Guangzhou has been the epicenter of dengue fever in China since the 1990s, with Aedes albopictus being the primary vector. The main method used to control vectors and prevent dengue fever has been the application of chemical insecticides; however, this control strategy has resulted in the development of resistance to these insecticides in mosquitoes. Here we report our investigation of the patterns of knockdown resistance (kdr) mutations in 15 field populations of Ae. albopictus collected from 11 districts in Guangzhou.

resultsFour mutant alleles (V1016G, F1534S, F1534C, F1534L) were detected in domain II and III of the voltage-gated sodium channel (VGSC) gene. Various allele frequencies of kdr mutations were observed (3.1-25.9% for V1016G, 22.6-85.5% for F1534S, 0-29.0% for F1534L, 0.6-54.2% for F1534C). Seven kdr haplotypes (VF, VS, VL, VC, GF, GC, GS) were identified; the highest frequency of haplotypes was found for the single mutant haplotype VS (50.8%), followed by the wild-type VF haplotype (21.7%) and the single mutant haplotype VC (11.9%). Of the three double mutant haplotypes, GF was the most frequent (8.8%), followed by GC (1.2%) and GS (0.8%). Aedes albopictus showed spatial heterogeneity in deltamethrin resistance in populations collected in Guangzhou. We also observed significant differences in haplotype frequency. The frequency of the VC haplotype was significantly higher in high-risk dengue areas than in low-risk ones.

conclusionsThe kdr allele V1016G was discovered for the first time in Guangzhou. Genetic isolation in mosquito populations and long-term insecticide selection seem to be responsible for the persistent, patchy distribution of kdr mutant alleles. The small-scale spatial heterogeneity in the distribution and frequency of kdr mutations may have important implications for vector control operations and insecticide resistance management strategies.

Indexed as

AedesDengueInsecticidesAnimalsChinaMosquito VectorsMutationInsecticidesAedes albopictusGuangzhouHaplotype frequencyInsecticide resistanceVoltage-gated sodium channel gene

Identifiers

PMID35505385
PMCPMC9066732
OpenAlexW4225299862

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LicenceCC BY
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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.