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Parasit Vectors. 2019 Apr 11;12(1):167. doi: 10.1186/s13071-019-3416-9.

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

Author information

1
Department of Medical Entomology, Shandong Academy of Medical Sciences, Shandong Institute of Parasitic Diseases, Jining, 272033, Shandong, People's Republic of China. liuhmm163@163.com.
2
Department of Pathogen Biology, Guangdong Provincial Key Laboratory of Tropical Disease Research, School of Public Health, Southern Medical University, Guangzhou, People's Republic of China.
3
Department of Medical Entomology, Shandong Academy of Medical Sciences, Shandong Institute of Parasitic Diseases, Jining, 272033, Shandong, People's Republic of China.
4
Program in Public Health, University of California, Irvine, CA, USA.
5
Department 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.
6
Department of Medical Entomology, Shandong Academy of Medical Sciences, Shandong Institute of Parasitic Diseases, Jining, 272033, Shandong, People's Republic of China. gmq2005@163.com.

Abstract

BACKGROUND:

Culex 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).

METHODS:

Culex 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.

RESULTS:

Larval 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.

CONCLUSIONS:

The 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.

KEYWORDS:

Culex pipiens pallens; Insecticide resistance; L1014F; L1014S; kdr

PMID:
30975185
DOI:
10.1186/s13071-019-3416-9
[Indexed for MEDLINE]
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