基于基因敲除抗性(kdr)突变的中国长江流域白纹伊蚊(双翅目:库蚊科)检测与种群遗传分析。

IF 2.6 4区 医学 Q3 INFECTIOUS DISEASES
Zu Ma, Qing Liu, Ming Wang, Yu-tong Du, Jing-wen Xie, Zi-ge Yi, Jing-hong Cai, Tong-yan Zhao, Heng-duan Zhang
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引用次数: 0

摘要

背景:白纹伊蚊是基孔肯雅、登革热、黄热病和寨卡病毒的重要病媒。杀虫剂通常是快速降低病媒种群密度的最有效工具,尤其是在虫媒病毒疾病爆发期间。然而,杀虫剂(尤其是拟除虫菊酯类杀虫剂)的大量使用导致世界各地出现了抗药性蚊虫种群。电压门控钠通道(VGSC)基因突变是白纹伊蚊对杀虫剂产生抗药性的主要原因之一,也被称为 "抗性敲除"(kdr)突变。了解与杀虫剂抗药性相关的基因突变是开发快速抗药性诊断技术的先决条件。方法:我们报告了对长江流域 7 个省市 22 个采样点的 541 份白纹伊蚊标本中 kdr 基因突变的 PCR 基因分型结果。扩增了 VGSC 基因结构域 II 和结构域 III 的部分 DNA 序列。随后对这些DNA片段进行了测序,以发现可能介导拟除虫菊酯抗性(kdr)的基因突变。对 22 个白纹伊蚊种群中 kdr 突变的频率和分布进行了评估。结果:1016位点的kdr突变有2个等位基因,3种基因型:V/V(73.38%)、V/G(26.43%)和G/G(0.18%)。1016G 同源突变仅在重庆的 CQSL 株系中发现一例,在上海的 SHJD 株系、江苏的 NJDX 株系和湖北的 HBQN 株系中均未发现 1016G 突变。1532个位点有两个等位基因和三种基因型,分别为I/I(88.35%)、I/T(8.50%)和T/T(3.14%)。共有 1534 个位点有四个等位基因和六个基因型:F/F(49.35%)、F/S(19.96%)、F/C(1.48%)和 F/L(0.18%);S/S(23.66%)和 C/C(5.36%)。仅在重庆和湖北的白纹伊蚊种群中发现了 F1534C 突变的单倍型,仅在重庆的三个地理品系中发现了 C1534C 突变的单倍型。1534S 突变的单倍型仅见于四川和上海的白纹伊蚊种群。F1534L 仅在河北青海发现。上海的白纹伊蚊种群与其他地区(除四川外)的白纹伊蚊种群的遗传分化程度较高,重庆的种群与长江中下游(湖北、江苏、江西和安徽)的种群的遗传分化程度较低。上海和四川的单倍型多样性和核苷酸多样性较低。系统进化分析和序列比较显示,1016位点分为三个分支,其中携带1016突变的A支系和B支系主要发生在江苏,携带1016突变的C支系主要发生在重庆,这表明1016G至少有两个起源。IIIS6系统进化分析和序列比较发现,F1534S、F1534C和I1532T可分为两个分支,表明IIIS6有两个起源;结论:结合kd基因突变的分布,IIIS6有两个起源:结合kdr突变的分布和种群遗传学分析,我们推断除了除虫菊酯抗性突变的本地选择外,来自其他地区的白纹伊蚊的扩散和定殖可能是长江流域部分白纹伊蚊种群出现kdr突变的原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Detection and population genetic analysis of Aedes albopictus (Diptera: Culicidae) based on knockdown resistance (kdr) mutations in the Yangtze River basin of China

Background

Aedes albopictus is an important vector of chikungunya, dengue, yellow fever and Zika viruses. Insecticides are often the most effective tools for rapidly decreasing the density of vector populations, especially during arbovirus disease outbreaks. However, the intense use of insecticides, particularly pyrethroids, has led to the selection of resistant mosquito populations worldwide. Mutations in the voltage-gated sodium channel (VGSC) gene are one of the main drivers of insecticide resistance in Ae. albopictus and are also known as “knockdown resistance” (kdr) mutations. Knowledge about genetic mutations associated with insecticide resistance is a prerequisite for developing techniques for rapid resistance diagnosis. Here, we report studies on the origin and dispersion of kdr haplotypes in samples of Ae. albopictus from the Yangtze River Basin, China;

Methods

Here, we report the results of PCR genotyping of kdr mutations in 541 Ae. albopictus specimens from 22 sampling sites in 7 provinces and municipalities in the Yangtze River Basin. Partial DNA sequences of domain II and domain III of the VGSC gene were amplified. These DNA fragments were subsequently sequenced to discover the possible genetic mutations mediating knockdown resistance (kdr) to pyrethroids. The frequency and distribution of kdr mutations were assessed in 22 Ae. albopictus populations. Phylogenetic relationships among the haplotypes were used to infer whether the kdr mutations had a single or multiple origins;

Results

The kdr mutation at the 1016 locus had 2 alleles with 3 genotypes: V/V (73.38%), V/G (26.43%) and G/G (0.18%). The 1016G homozygous mutation was found in only one case in the CQSL strain in Chongqing, and no 1016G mutations were detected in the SHJD (Shanghai), NJDX (Jiangsu) or HBQN (Hubei) strains. A total of 1532 locus had two alleles and three genotypes, I/I (88.35%), I/T (8.50%) and T/T (3.14%). A total of 1534 locus had four alleles and six genotypes: F/F (49.35%), F/S (19.96%), F/C (1.48%) and F/L (0.18%); S/S (23.66%); and C/C (5.36%). Haplotypes with the F1534C mutation were found only in Ae. albopictus populations in Chongqing and Hubei, and C1534C was found only in three geographic strains in Chongqing. Haplotypes with the 1534S mutation were found only in Ae. albopictus populations in Sichuan and Shanghai. F1534L was found only in HBYC. The Ae. albopictus populations in Shanghai were more genetically differentiated from those in the other regions (except Sichuan), and the genetic differentiation between the populations in Chongqing and those in the middle-lower reaches of the Yangtze River (Huber, Jiangsu, Jiangxi, and Anhui) was lower. Shanghai and Sichuan displayed low haplotype diversity and low nucleotide diversity. Phylogenetic analysis and sequence comparison revealed that the 1016 locus was divided into three branches, with the Clade A and Clade B branches bearing the 1016 mutation occurring mostly in Jiangsu and the Clade C branch bearing the 1016 mutation occurring mostly in Chongqing, suggesting at least two origins for 1016G. IIIS6 phylogenetic analysis and sequence comparison revealed that F1534S, F1534C and I1532T can be divided into two branches, indicating that IIIS6 has two origins;

Conclusions

Combined with the distribution of kdr mutations and the analysis of population genetics, we infer that besides the local selection of pyrethroid resistance mutations, dispersal and colonization of Ae. albopictus from other regions may explain why kdr mutations are present in some Ae. albopictus populations in the Yangtze River Basin.

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来源期刊
Infection Genetics and Evolution
Infection Genetics and Evolution 医学-传染病学
CiteScore
8.40
自引率
0.00%
发文量
215
审稿时长
82 days
期刊介绍: (aka Journal of Molecular Epidemiology and Evolutionary Genetics of Infectious Diseases -- MEEGID) Infectious diseases constitute one of the main challenges to medical science in the coming century. The impressive development of molecular megatechnologies and of bioinformatics have greatly increased our knowledge of the evolution, transmission and pathogenicity of infectious diseases. Research has shown that host susceptibility to many infectious diseases has a genetic basis. Furthermore, much is now known on the molecular epidemiology, evolution and virulence of pathogenic agents, as well as their resistance to drugs, vaccines, and antibiotics. Equally, research on the genetics of disease vectors has greatly improved our understanding of their systematics, has increased our capacity to identify target populations for control or intervention, and has provided detailed information on the mechanisms of insecticide resistance. However, the genetics and evolutionary biology of hosts, pathogens and vectors have tended to develop as three separate fields of research. This artificial compartmentalisation is of concern due to our growing appreciation of the strong co-evolutionary interactions among hosts, pathogens and vectors. Infection, Genetics and Evolution and its companion congress [MEEGID](http://www.meegidconference.com/) (for Molecular Epidemiology and Evolutionary Genetics of Infectious Diseases) are the main forum acting for the cross-fertilization between evolutionary science and biomedical research on infectious diseases. Infection, Genetics and Evolution is the only journal that welcomes articles dealing with the genetics and evolutionary biology of hosts, pathogens and vectors, and coevolution processes among them in relation to infection and disease manifestation. All infectious models enter the scope of the journal, including pathogens of humans, animals and plants, either parasites, fungi, bacteria, viruses or prions. The journal welcomes articles dealing with genetics, population genetics, genomics, postgenomics, gene expression, evolutionary biology, population dynamics, mathematical modeling and bioinformatics. We also provide many author benefits, such as free PDFs, a liberal copyright policy, special discounts on Elsevier publications and much more. Please click here for more information on our author services .
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