Evidence map›Paper›PMID 30975185›Full record

ArticleParasites & vectors2019

Trends in insecticide resistance in Culex pipiens pallens over 20 years in Shandong, China.

Hongmei Liu, Lihua Xie, Peng Cheng, Jiabao Xu, Xiaodan Huang, Haifang Wang, Xiao Song, Lijuan Liu, Huaiwei Wang, Jingxuan Kou and 3 more

Open access · goldAbstract read
In one paragraph

Article in Parasites & vectors, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
7.3field-weighted citation impact, top 3% 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

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

15 citing papers in PubMed, 50 citations in OpenAlex.

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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

13 authors at 3 institutions in 2 countries.

Hongmei LiuDepartment of Medical Entomology, Shandong Academy of Medical Sciences, Shandong Institute of Parasitic Diseases, Jining, 272033, Shandong, People's Republic of China. liuhmm163@163.com.
Lihua XieDepartment of Pathogen Biology, Guangdong Provincial Key Laboratory of Tropical Disease Research, School of Public Health, Southern Medical University, Guangzhou, People's Republic of China.
Peng ChengDepartment of Medical Entomology, Shandong Academy of Medical Sciences, Shandong Institute of Parasitic Diseases, Jining, 272033, Shandong, People's Republic of China.
Jiabao XuDepartment of Pathogen Biology, Guangdong Provincial Key Laboratory of Tropical Disease Research, School of Public Health, Southern Medical University, Guangzhou, People's Republic of China.
Xiaodan HuangDepartment of Medical Entomology, Shandong Academy of Medical Sciences, Shandong Institute of Parasitic Diseases, Jining, 272033, Shandong, People's Republic of China.
Haifang WangDepartment of Medical Entomology, Shandong Academy of Medical Sciences, Shandong Institute of Parasitic Diseases, Jining, 272033, Shandong, People's Republic of China.
Xiao SongDepartment of Medical Entomology, Shandong Academy of Medical Sciences, Shandong Institute of Parasitic Diseases, Jining, 272033, Shandong, People's Republic of China.
Lijuan LiuDepartment of Medical Entomology, Shandong Academy of Medical Sciences, Shandong Institute of Parasitic Diseases, Jining, 272033, Shandong, People's Republic of China.
Huaiwei WangDepartment of Medical Entomology, Shandong Academy of Medical Sciences, Shandong Institute of Parasitic Diseases, Jining, 272033, Shandong, People's Republic of China.
Jingxuan KouDepartment of Medical Entomology, Shandong Academy of Medical Sciences, Shandong Institute of Parasitic Diseases, Jining, 272033, Shandong, People's Republic of China.
Guiyun YanProgram in Public Health, University of California, Irvine, CA, USA.
Xiao-Guang ChenDepartment of Pathogen Biology, Guangdong Provincial Key Laboratory of Tropical Disease Research, School of Public Health, Southern Medical University, Guangzhou, People's Republic of China. xgchen2001@hotmail.com.
Maoqing GongDepartment of Medical Entomology, Shandong Academy of Medical Sciences, Shandong Institute of Parasitic Diseases, Jining, 272033, Shandong, People's Republic of China. gmq2005@163.com.
Shandong First Medical University · CNSouthern Medical University · CNUniversity of California, Irvine · US

Funding

University of California Health Participation in the National COVID Cohort Collaborative (N3C)UL1TR001414 · NCATS · UNIVERSITY OF CALIFORNIA-IRVINE · PI COOPER, DAN M, VILAIN, ERIC J. · 2015 to 2023
$35.1M
China Postdoctoral Science Foundation funded project 2017M622733medical and health science and technology development project of Shandong Province 2016WS0393National Natural Science Foundation of China 81471985National Natural Science Foundation of China 81528013National Natural Science Foundation of China 81672059National Natural Science Foundation of China 81702034Natural Science Foundation of Guangdong Province, China 2014A030312016NCATS NIH HHS UL1 TR001414
6 · The paper itself

Abstract

backgroundCulex pipiens pallens is the most abundant Culex mosquito species in northern China and is an important vector of bancroftian filariasis and, potentially, West Nile virus. Insecticides, particularly pyrethroids, are widely used for adult mosquito control. Insecticide resistance has become common in several mosquito species, and vector control is the main method currently available to prevent disease transmission. The voltage-gated sodium channel (Vgsc) gene is the target site of pyrethroids, and mutations in this gene cause knockdown resistance (kdr).

methodsCulex pipiens pallens larvae were collected from May to November over two decades, from 1992 to 2018, in four cities in Shandong Province, China. The World Health Organization (WHO) standard resistance bioassay was applied to test the resistance levels of Cx. p. pallens larvae to five different insecticides and to test deltamethrin resistance in adults, using the F1 generation. Mutations at Vgsc codon 1014 were also screened in 471 adult samples collected in 2014 to determine the association between kdr mutations and phenotypic resistance.

resultsLarval resistance against deltamethrin showed an increasing trend from the 1990s until 2018, which was statistically significant in all populations; resistance to cypermethrin increased significantly in mosquitoes from the Zaozhuang population. However, larval resistance to other insecticides remained relatively stable. Larval resistance against deltamethrin was consistent with adult bioassays in 2014, in which all tested populations were highly resistant, with mortality rates ranging from 39.4 to 55.23%. The L1014S and L1014F mutations were both observed in five Cx. p. pallens populations, with L1014F significantly associated with deltamethrin resistance.

conclusionsThe long-term dataset from Shandong demonstrates major increases in pyrethroid resistance over a 20-year period. The L1014F kdr mutation may be considered a viable molecular marker for monitoring pyrethroid resistance in Cx. p. pallens.

Indexed as

Insecticide ResistanceAnimalsChinaCulexFemaleInsecticidesMutationNitrilesPyrethrinsVoltage-Gated Sodium ChannelsdecamethrinInsecticidesNitrilesPyrethrinsVoltage-Gated Sodium ChannelsCulex pipiens pallensInsecticide resistancekdrL1014FL1014S

Identifiers

PMID30975185
PMCPMC6460514
OpenAlexW2946508034

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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.