Skip to main content

Diversity and frequency of kdr mutations within Anopheles sinensis populations from Guangxi, China

Abstract

Background

Anopheles sinensis is a major vector of malaria in China and its control is under great threat as the development of insecticide resistance. Voltage-gated sodium channel (VGSC) is the target of several classes of insecticides. Genetic mutations of VGSC have been documented to confer knockdown resistance (kdr) to dichlorodiphenyltrichloroethane (DDT) and pyrethroids in mosquitoes. To control this vector efficiently, it is important to know the resistance-associated genetic mutations, their distribution frequencies and genealogical relations.

Methods

Three hundreds and thirteen (313) adults of An. sinensis collected from nine locations across Guangxi Zhuang Autonomous Region were used. The partial sequence of the An. sinensis voltage gated sodium channel gene (AS-VGSC) containing codon 1014 was sequenced. PHASE2.1 was used to construct the haplotypes of each individual, and the accuracy of haplotypes was further confirmed by clone sequencing. The genealogical relations of kdr mutations in AS-VGSC was analysed using TCS 2.1 and Network 5.0.

Results

Sixteen AS-VGSC haplotypes including seven haplotypes carrying non-synonymous mutations at codon 1014, and fifty-five AS-VGSC genotypes were identified from 313 mosquitoes collected from nine geographical locations across Guangxi. The number of haplotypes in each of the nine populations ranged from 5 to 13. The frequency of haplotypes carrying kdr mutations ranged from 2.7 to 80.0 % within the nine populations, of which 1014C was unexpectedly high in the northeast of Guangxi. Genealogical analysis suggested multiple origins of kdr mutations in An. sinensis.

Conclusion

Diverse haplotypes of AS-VGSC are distributed in Guangxi. The presence of haplotypes carrying mutations at codon 1014 indicates a risk of pyrethroid and DDT resistance. The kdr mutations show differential distribution geographically, with high frequencies occurred in the northeast of Guangxi. Genealogical analysis suggests multiple origins of kdr mutations in An. sinensis populations in Guangxi. These findings have important practical implications for the sustainability of An. sinensis control programmes.

Background

Anopheles sinensis is a major vector of malaria in China and countries of Southeast Asia. Chemical control of vector has played an important role in malaria control and elimination [1]. In China, DDT has been widely used for indoor residual spray (IRS) since 1950s, and pyrethroids for insecticide-treated bed nets (ITNs) since 1980s [2]. Unfortunately, long-term and large-scale use of pyrethroids has led to increasing insecticide resistance in Chinese An. sinensis [3, 4], which poses a major threat to malaria control.

The voltage-gated sodium channel protein is the major target for pyrethroids and DDT [5]. Although there have been debates [68], many studies have demonstrated that mutations at codon 1014 of VGSC cause resistance to both pyrethroids and DDT in many arthropod species [5, 6]. 1014F/S/H mutations can reduce sodium channel sensitivity to pyrethroids in Xenopus oocytes [915], and provide protection to pyrethroids and DDT [9]. In An. sinensis, significant positive correlations between kdr allele frequency and bioassay-based resistance phenotype have been documented [1619]. Recent years, kdr mutation has been used as a molecular mark for monitoring pyrethroid resistance in An. sinensis in China [19].

Guangxi Zhuang Autonomous Region was once a malaria-endemic region. Before 1949, there were more than 5 million malaria patients per year [20]. Thanks to the “National Malaria Control Programme”, the “Basically Eliminating Malaria” strategy and the “Action Plan of Malaria Elimination (2010–2020)” implemented since 1955, 2000, and 2010 respectively in China [21, 22], the malaria burden has been substantially reduced, with one indigenous and 2068 imported cases being reported from 2010 to 2015 in Guangxi [22]. Although Guangxi has already achieved remarkable accomplishments in eliminating malaria, the risk of malaria re-emergence remains partly due to increasing cross-border population migration and the unique natural environment (e.g. rice fields) suitable for mosquito breeding in Guangxi [2225].

As the historical use in vector control and continuing use in agriculture of different insecticides, not only the geographical distribution and density of malaria vectors are likely to change, insecticide resistance is expected to be selected as well. Recent investigations have shown that An. sinensis has replaced Anopheles minimus to be the main malaria vector in Guangxi [24]. However, the status of insecticide resistance in An. sinensis is less understood in this region up to date. As an effort in this direction, the distribution and frequency of VGSC mutations that possibly lead to resistance to DDT and pyrethroids were investigated in nine field populations of An. sinensis collected extensively across Guangxi in this study.

Methods

Samples

Anopheles sinensis adults used in the study were caught by light trap (wave length 365 nm) from July to September in 2014, around farmers’ houses at different geographical locations across Guangxi. The sampling sites were part of the malaria vector monitoring sites that were set up partly because there were imported malaria cases observed since 2010 in these regions. A brief description of the sampling sites was provided in Additional file 1. The farmers living at the sampling sites usually use mosquito-coil (largely containing pyrethroids) to prevent mosquitoes, and apply insecticides (e.g. pyrethroids) for crop protection.

The collected individual mosquitoes were first morphologically identified using the determination key provided by [26]. Anopheles sinensis adults were put into 100-μl Eppendorf tubes containing 100 % ethanol solution, and kept at 4 °C until use. The accuracy of morphological classification was guaranteed by molecular detection of ten randomly selected adults from each population using the rDNA-ITS2 method [27].

PCR amplification of partial AS-VGSC sequence

The genomic DNA of individual adult mosquitoes was prepared as described elsewhere [28, 29]. A fragment containing codon 1014 of AS-VGSC gene was amplified using primers kdr-F (5′-TGCCACTCCGTGTGTTTAGA-3′) and kdr-R (5′-GAGCGATGATGATCCGAAAT-3′) [16]. The PCR mixture (30 μl) consisted of 6 μl DNA template, 0.4 μl Takara Taq Polymerase, 3 μl 10xTaq Buffer, 3 μl 2.5 μM dNTPs, 0.6 μl kdr-F, 0.6 μl kdr-R and 16.4 μl ddH2O. The reaction programme was 95 °C for 5 min, followed by 36 cycles each with 95 °C for 30 s, 55 °C for 30 s, 72 °C for 30 s, and by a final extension of 10 min at 72 °C. PCR products were gel-purified and sequenced using the forward primer kdr-F (BGI, China).

Haplotype identification and genealogical analysis

Genotype data were carefully inspected by using Chromas (Technelysium Pty Ltd, Australia). AS-VGSC haplotypes were constructed by software PHASE2.1 (http://www.bioinf.man.ac.uk/resources/phase/) from the genotype data. The presence (and accuracy) of haplotypes constructed in heterozygotes was confirmed by sequencing of three to five clones derived from 12 representative heterozygotes. Genealogical relations among haplotypes were analysed using Network 5.0 [30] and TCS2.1 [31].

Results

Identification of polymorphic sites in the AS-VGSC gene

The gene of An. sinensis voltage sensitive sodium channel (KE525266.1)contains 31 exons and 30 introns. A ~325 bp-in-length sequence was sequenced through direct sequencing of each purified PCR product. The partial sequence (267 bp), excluding the primer sequence and covering partial exon 19 (169 bp), intron 19 (64 bp)and partial exon 20 (34 bp), was used for further analysis (Fig. 1). Two synonymous mutations (C/G at PS1, T/C at PS9) were observed. Five polymorphic sites were found in the intron 19 (PS4–8). Non-synonymous mutations were identified in the second (T/G/C) and third nucleotide (G/T) of codon 1014 (PS2 and 3).

Fig. 1
figure 1

The polymorphic sites (PS) identified in the fragment of AS-VGSC gene

Haplotype diversity of AS-VGSC gene

From the sequence data of 313 individuals, sixteen AS-VGSC haplotypes were identified (Table 1). The number of haplotypes in each of the nine populations ranged from 5 (Guigang) to 13 (Yulin). Three haplotypes (1014L2, 1014L3 and 1014L8) were detected in all the nine populations, while 1014L7 was uniquely distributed in Nanning. 1014L1 was the predominant haplotype for Nanning and Yulin, 1014L2 for Baise and Hechi, and 1014L8 was most abundant in Wuzhou (Table 2).

Table 1 Haplotypes identified or/and used in this study
Table 2 Haplotypes of the AS-VGSC gene and their frequencies (%) in nine An. sinensis populations from Guangxi, China

Point mutations at position 1014 of the domain II of the VGSC protein have been documented to confer kdr [5, 6]. In this study, three types of kdr mutations were detected: TTT (1014F), TCG (1014S), and TGT (1014C). Accordingly, seven haplotypes carrying kdr mutations, namely 1014F1, 1014F2, 1014S1, 1014S2, 1014S3, 1014S4 and 1014C1 respectively were identified (Table 1), in the frequencies ranging from 2.7 to 80.0 % in the nine populations (Fig. 2). In the four populations in the northeast (Guigang, Guilin, Hezhou and Liuzhou), the frequencies of kdr mutations were more than 50.0 %, predominated by 1014C1. In contrast, only 1014S in a low frequency (<5 %) was observed in the two western populations (Baise and Nanning). Three types of kdr mutations coexisted in the other three populations (Hechi, Wuzhou, Yilin) in a frequency from 11.6 to 33.3 %.

Fig. 2
figure 2

Distribution of haplotypes in Anopheles sinensis in Guangxi. BS, HC, HZ, GG, GL, LZ, NN, WZ and YL are the abbreviations for Baise, Hechi, Hezhou, Guigang, Guilin, Liuzhou, Nanning, Wuzhou and Yulin respectively

Fifty-five AS-VGSC genotypes were detected (Additional file 2). Among the nine populations, the predominant genotype was largely population-specific. According to the encoding amino acid at position 1014, all the 55 genotypes could be grouped into wild-type (1014L/1014L), mutant-type (1014F/1014F, 1014C/1014C and 1014F/1014C), heterozygous-type (1014L/1014S, 1014L/1014C and 1014L/1014F) (Table 3). Wild-type was found in all the nine populations, in frequencies ranging from 5.3 to 94.6 %. No mutant-type individual was observed in Baise, Hechi, Nanning and Yulin. The mutant homozygote 1014F/1014F was only observed in Hezhou in a low frequency of 3.7 %, while 1014C/1014C homozygote was detected in Guigang (60.0 %), Hezhou (42.1 %), Liuzhou (22.3 %), Guilin (15.8 %) and Wuzhou (8.3 %).

Table 3 Frequency of VGSC genotypes in nine An. sinensis populations from Guangxi China, grouped according to the amino acid at position 1014 of VGSC

Genealogical analysis of kdr mutations

To estimate the evolutionary relationship of kdr mutations, sixteen haplotypes identified in this study and ten haplotypes retrieved from GenBank database (Table 1) were used to construct a network using TCS 2.1 and Network 5.0. The two software generated identical results for our dataset, thus only the network produced by Network 5.0 was displayed (Fig. 3).

Fig. 3
figure 3

Network showing the genealogy of AS-VGSC haplotypes. Empty circle means the wildtype haplotype (without 1014 mutation), solid circles mean mutant haplotypes with 1014 mutation (black 1014F, grey 1014S, dark green 1014C). The size of each circle is proportional to the corresponding frequency of a certain haplotype identified in Guangxi province. Straight line indicates the possible mutational step. The note above the line referred to the mutation position and base. Haplotypes marked with Asterisk mean that these haplotypes are retrieved from GenBank. H represents the type of intron haplotypes (see Table 1 for details)

The network analysis revealed complex reticulate pattern and multiple independent mutation events leading to kdr haplotypes. For example, haplotype 1014F1 was possibly derived from 1014L1, while 1014F2 from 1014L3; 1014S1, S2, S3 and S4 were perhaps the results of an independent mutational step from four different wild haplotypes 1014L5, 1014L2, 1014L3 and 1014L4 respectively.

The genealogical analysis also revealed that a single mutation (T165C) might result in the resistant phenotype from the susceptible one. For example, 1014S2 shared identical intron sequence with 1014L2, L5 and S1, and a single mutation (T165C) might change the susceptible 1014L2 to the resistant 1014S2.

Discussion

Sequence analysis reveals that the sodium channel gene of An. sinensis has diverse genetic mutations. From 313 mosquitoes collected from Guangxi, 16 haplotypes were identified (Tables 1, 2). The number and frequency of AS-VGSC haplotypes are different among the nine populations from Guangxi. Overall, the 1014L1, 1014L2 and 1014C1 rank the top three haplotypes. Some haplotypes, for example 1014L2, 1014L3 and 1014L8, are widespread, and some haplotypes such as 1014L7 are restricted to a particular location (Table 2). Less number of haplotypes detected in Hezhou and Guigang may be related to the relative small sample size and/or strong selective pressure leading to 1014C1 in a high frequency. The high polymorphism of AS-VGSC may be partly explained by their large population size, wide distribution range of An. sinensis [14], diverse natural landscapes and different local insecticide selective pressure.

Three non-synonymous mutations (TTT for 1014F, TGT for 1014C and TCG for 1014S) were identified in this work. However, the TTC-encoding 1014F, previously found in Korea [32] and in Anhui and Sichuan of China [19], was not detected in Guangxi. The presence of L1014W substitution was reported based on the direct sequencing data of only one An. sinensis heterozygote from Guiping of Guangxi [17]. This result is questionable and needs reconfirmation, because 1014F/W is not the only possibility encoded by the individual genotype T(T/G)(T/G). In this and another study [33], sequencing of cloned fragment with the T(T/G)(T/G) template resolved into two alleles, TTG and TGT, encoding 1014L/C rather than 1014F/W.

Differential kdr distribution patterns were observed in the nine examined An. sinensis populations from Guangxi. Overall, haplotypes carrying 1014C mutation are widespread and present in high frequencies in the northeast, while 1014S is rare and distributed in the west (Table 1; Fig. 2). Notably, four of the nine populations with kdr allele frequencies higher than 50 % were located in the northeast of Guangxi, while only 1014S in a frequency less than 5 % was detected in the two western populations. Geographically, the frequency of kdr mutations decreased towards south and west from northeast. This pattern is in keeping with previous observations that a high kdr mutation frequency was detected in the central China which is located northeast to Guangxi [19, 34, 40], and kdr alleles were less prevalent in Yunnan and Hainan which are in the west and south to Guangxi respectively [16, 18, 19, 34, 40].

Considering the fact that haplotype 1014C1 and 1014F1, detected in samples of this study, are also distributed in central China (Table 1), it is possible that migration of An. sinensis population from central China through Hunan and Guizhou, may contribute to the occurrence of 1014C1 and 1014F1 in the northeast of Guangxi. The obvious distinction in the geographic distribution of each allele between populations in the west and in the northeast is likely a combined consequence of independent mutational events in different geographic locations and the geographical barriers limiting gene flow imposed by the mountainous landscapes of Guangxi. Theoretically, selective pressure may play a role in shaping the frequency of insecticide resistance-associated mutation in a population. However, it was not possible to assess the contribution of local selection of insecticides to the existing kdr distribution pattern because application history of insecticides was not known for samples used in this study.

Previous studies have documented that the predominant kdr allele is L1014 F [4, 12, 13, 16, 19, 3335, 40], the high frequency of 1014C1 in the five An. sinensis populations in northeast of Guangxi (Fig. 3) is unexpected. 1014C was present in An. sinensis samples collected in Anhui, Guizhou, Henan, Hubei, Hunan, Jiangsu and Shandong of China [16, 19, 34, 40] and in Korea [33], and was also found in VGSC of other mosquito species, such as Culex pipiens pipiens from China [36] and Anopheles albimanus from Mexico and Nicaragu [37]. These observations indicate that 1014C is a conserved mutation in mosquitoes and widely distributed. Why 1014C1 is prevalent in the five populations remains to be investigated. One possibility is that 1014C1 may provide a better protection, or/and a lower fitness cost, than other kdr alleles such as the classical 1014F.

The geographic distribution pattern and the genealogical analysis of kdr haplotypes strongly suggests that kdr mutations are not singly originated. For example, there are at least two independent mutation events giving rise to 1014F or 1014S haplotypes from a wild haplotype through a single mutational step (Table 1; Fig. 3). Multiple origins of resistance alleles via point mutations at the voltage-gated sodium channel gene have also been characterized in other insect species [38, 39]. Interestingly, 1014C1 and 1014F1 is co-distributed in Guangxi and share the same intron (Tables 1, 2). The network analysis indicates that only one mutational step is able to change 1014F1 to 1014C1 (Fig. 3). Based on these observations, it is hypothesized that 1014C1 may represent a kdr allele evolved via a sequential progression from 1014F1 and perhaps has gradually replaced 1014F1.

Conclusions

Sixteen AS-VGSC haplotypes were identified in An. sinensis from Guangxi, suggesting diverse genetic mutations in the AS-VGSC gene. Three types of kdr mutations (1014F, 1014S and 1014C) were detected in Guangxi. Genealogical analysis suggests multiple origins of kdr mutations in An. sinensis. Although a direct link between kdr mutations and level of insecticide resistance has not been established due to the unavailability of susceptibility data for the samples used in this study, the high frequency of kdr mutation (>50 %) in Guigang, Guilin, Hezhou and Liuzhou indicates a risk of resistance to pyrethroids and DDT in An. sinensis in these areas. The heterogeneities in the geographic distribution and multiple origins of kdr alleles highlight the need of a location-customized strategy for monitoring and management of insecticide resistance.

Abbreviations

VGSC :

voltage-gated sodium channel

kdr :

knockdown resistance

DDT:

dichlorodiphenyltrichloroethane

ITNs:

insecticide-treated bed nets

IRS:

indoor residual spray

References

  1. Enayati A, Hemingway J. Malaria management: past, present, and future. Annu Rev Entomol. 2010;55:569–91.

    Article  CAS  PubMed  Google Scholar 

  2. Lu B. Integrated mosquito management Second edition. 2nd ed. Beijing: Science Press; 1999.

    Google Scholar 

  3. Wang DQ, Xia ZG, Zhou SS, Zhou XN, Wang RB, Zhang QF. A potential threat to malaria elimination: extensive deltamethrin and DDT resistance to Anopheles sinensis from the malaria-endemic areas in China. Malar J. 2013;12:164.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  4. Zhang HW, Liu Y, Hu T, Zhou RM, Chen JS, Qian D, et al. Knockdown resistance of Anopheles sinensis in Henan province China. Malar J. 2015;14:137.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  5. Dong K, Du Y, Rinkevich F, Nomura Y, Xu P, Wang L, et al. Molecular biology of insect sodium channels and pyrethroid resistance. Insect Biochem Mol Biol. 2014;50:1–17.

    Article  PubMed  PubMed Central  Google Scholar 

  6. Silva APB, Santos JMM, Martins AJ. Mutations in the voltage-gated sodium channel gene of anophelines and their association with resistance to pyrethroids—a review. Parasit Vectors. 2014;7:450.

    Article  PubMed  PubMed Central  Google Scholar 

  7. Brooke BD. kdr: can a single mutation produce an entire insecticide resistance phenotype? Trans R Soc Trop Med Hyg. 2008;102:524–5.

    Article  PubMed  Google Scholar 

  8. Donnelly MJ, Corbel V, Weetman D, Wilding CS, Williamson MS, Black WCT. Does kdr genotype predict insecticide-resistance phenotype in mosquitoes? Trends Parasitol. 2009;25:213–9.

    Article  CAS  PubMed  Google Scholar 

  9. Burton MJ, Melloe IR, Duce IR, Davies TGE, Field LM, Williamson MS. Differential resistance of insect sodium channels with kdr mutations to deltamethrin, permethrin and DDT. Insect Biochem Mol Biol. 2011;41:723–32.

    Article  CAS  PubMed  Google Scholar 

  10. Du YZ, Nomura Y, Satar G, Hu ZN, Nauen R, He SY, et al. Molecular evidence for dual pyrethroid-receptor sites on a mosquito sodium channel. Proc Natl Acad Sci USA. 2013;110:11785–90.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  11. Smith TJ, Lee SH, Ingles PJ, Knipple DC, Soderlund DM. The L1014F point mutation in the house fly Vssc1 sodium channel confers knockdown resistance to pyrethroids. Insect Biochem Mol Biol. 1997;27:807–12.

    Article  CAS  PubMed  Google Scholar 

  12. Tan JG, Liu ZQ, Nomura Y, Goldin AL, Dong K. Alternative splicing of and an insect sodium channel gene generates pharmacologically distinct sodium channels. J Neurosci. 2002;22:5300–9.

    CAS  PubMed  PubMed Central  Google Scholar 

  13. Tan JG, Liu ZQ, Wang RW, Huang ZY, Chen AC, Gurevitz M, et al. Identification of amino acid residues in the insect sodium channel critical for pyrethroid binding. Mol Pharmacol. 2005;67:513–22.

    Article  CAS  PubMed  Google Scholar 

  14. Usherwood PNR, Vais H, Khambay BPS, Davies TGE, Williamson MS. Sensitivity of the Drosophila para sodium channel to DDT is not lowered by the super-kdr mutation M918T on the IIS4-S5 linker that profoundly reduces sensitivity to permethrin and deltamethrin. FEBS Lett. 2005;579:6317–25.

    Article  CAS  PubMed  Google Scholar 

  15. Vais H, Williamson MS, Goodson SJ, Devonshire AL, Warmke JW, Usherwood PN, et al. Activation of Drosophila sodium channels promotes modification by deltamethrin-Reductions in affinity caused by knock-down resistance mutations. J Gen Physiol. 2000;11:305–18.

    Article  Google Scholar 

  16. Zhong D, Chang X, Zhou G, He Z, Fu F, Yan Z, et al. Relationship between knockdown resistance, metabolic detoxification and organismal resistance to pyrethroids in Anopheles sinensis. PLoS ONE. 2013;8:e55475.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  17. Tan WL, Li CX, Wang ZM, Liu MD, Dong YD, Feng XY, et al. First Detection of multiple knockdown resistance (kdr) like mutations in voltage-gated sodium channel using three new genotyping methods in Anopheles sinensis from Guangxi Province, China. J Med Entomol. 2012;49:1012–20.

    Article  CAS  PubMed  Google Scholar 

  18. Qin Q, Li YJ, Zhong DB, Zhou N, Chang XL, Li C, et al. Insecticide resistance of Anopheles sinensis in Hainan Island, a malaria-endemic area of China. Parasit Vectors. 2014;7:92.

    Article  PubMed  PubMed Central  Google Scholar 

  19. Wang Y, Yu WQ, Shi H, Yang ZZ, Xu JN, Ma YJ, et al. Historical survey of the kdr mutations in the populations of Anopheles sinensis in China in 1996–2014. Malar J. 2015;14:120.

    Article  PubMed  PubMed Central  Google Scholar 

  20. Li J, Wei S, Yang Y, Li J. Analysis of the prevalence of imported malaria in Guangxi from 2012 to 2013. J Pathog Biology. 2015;10:180–3.

    Google Scholar 

  21. Li JH, Li J, Qin YX, Guo CK, Huang YM, Lin Z. Appraisal of the effect and measures on control malaria for 60 years in Guangxi. J Trop Med. 2014;14:361–4.

    Google Scholar 

  22. Li J, Yang Y, Zhang W, Wei S, Lin K. Mid-term assessment report of malaria elimination action plan in Guangxi. China Tropical Medicine. 2016;16:305–10.

    Google Scholar 

  23. Lu G, Zhou S, Horstick O, Wang X, Liu Y, Müller O. Malaria outbreaks in China (1990–2013): a systematic review. Malar J. 2014;13:269.

    Article  PubMed  PubMed Central  Google Scholar 

  24. Lin K, Huang Y, Li J, Mao W, Li J, Xun Y, et al. Malaria vector Anopheles investigation analysis after malaria was basically eliminated in Guangxi. J Med Pest Control. 2014;30:963–6.

    Google Scholar 

  25. Guo C, Li J, Qin Y. Investigation on geographical distribution, ecological feature and malaria transmission of Anopheles in Guangxi. Chin J Vector Biol Control. 2007;18:112–5.

    Google Scholar 

  26. Lu B, Wu H. Classification and identification of important medical insects of China. 1st ed. China: Henan Science and Technology Publishing House; 2003.

    Google Scholar 

  27. Joshi D, Park MH, Saeung A, Choochote W, Min GS. Multiplex assay to identify Korean vectors of malaria. Mol Ecol Resour. 2010;10:748–50.

    Article  CAS  PubMed  Google Scholar 

  28. Feng X, Yang C, Yang Y, Li J, Lin K, Li M, Qiu X. Distribution and frequency of G119S mutation in ace1 gene within Anopheles sinensis populations from Guangxi, China. Malar J. 2015;14:470.

    Article  PubMed  PubMed Central  Google Scholar 

  29. Rinkevich FD, Zhang L, Hamm RL, Brady SG, Lazzaro BP, Scott JG. Frequencies of the pyrethroid resistance alleles of Vssc1 and CYP6D1 in house flies from the eastern United States. Insect Mol Biol. 2006;15:157–67.

    Article  CAS  PubMed  Google Scholar 

  30. Bandelt H, Forster P, Rohl A. Median-joining networks for inferring intraspecific phylogenies. Mol Biol Evol. 1999;16:37–48.

    Article  CAS  PubMed  Google Scholar 

  31. Clement M, Posada D, Crandall K. TCS: a computer program to estimate gene genealogies. Mol Ecol. 2000;9:1657–9.

    Article  CAS  PubMed  Google Scholar 

  32. Kang S, Jung J, Lee S, Hwang H, Kim W. The polymorphism and the geographical distribution of the knockdown resistance (kdr) of Anopheles sinensis in the Republic of Korea. Malar J. 2012;11:151–8.

    Article  PubMed  PubMed Central  Google Scholar 

  33. Kim H, Baek JH, Lee WJ, Lee SH. Frequency detection of pyrethroid resistance allele in Anopheles sinensis populations by realtime PCR amplification of specific allele (rtPASA). Pestic Biochem Phys. 2007;87:54–61.

    Article  CAS  Google Scholar 

  34. Chang XL, Zhong DB, Fang Q, Hartsel J, Zhou GF, Shi LN, et al. Multiple resistances and complex mechanisms of Anopheles sinensis mosquito: a major obstacle to mosquito-borne diseases control and elimination in China. PLoS Neglect Trop Dis. 2014;8:e2889.

    Article  Google Scholar 

  35. Bai L, Zhu GD, Zhou HY, Tang JX, Li JL, Xu S, et al. Development and application of an AllGlo probe-based qPCR assay for detecting knockdown resistance (kdr) mutations in Anopheles sinensis. Malar J. 2014;13:379.

    Article  PubMed  PubMed Central  Google Scholar 

  36. Wang ZM, Li CX, Xing D, Yu YH, Liu N, Xue RD, et al. Detection and widespread distribution of sodium channel alleles characteristic of insecticide resistance in Culex pipiens complex mosquitoes in China. Med Vet Entomol. 2012;26:228–32.

    Article  PubMed  Google Scholar 

  37. Lol JC, Castellanos ME, Liebman KA, Lenhart A, Pennington PM, Padilla NR. Molecular evidence for historical presence of knock-down resistance in Anopheles albimanus, a key malaria vector in Latin America. Parasit Vectors. 2013;6:268.

    Article  PubMed Central  Google Scholar 

  38. Rinkevich FD, Hedtke SM, Leichter CA, Harris SA, Su C, Brady SG, et al. Multiple origins of kdr-type resistance in the house fly. Musca domestica. PLoS One. 2012;7:e52761.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  39. Pinto J, Lynd A, Vicente JL, Santolamazza F, Randle NP, Gentile G, et al. Multiple origins of knockdown resistance mutations in the afrotropical mosquito vector Anopheles gambiae. PLoS ONE. 2007;2:e1243.

    Article  PubMed  PubMed Central  Google Scholar 

  40. Chang X, Zhong D, Lo E, Fang Q, Bonizzoni M, Wang X, et al. Landscape genetic structure and evolutionary genetics of insecticide resistance gene mutations in Anopheles sinensis. Parasit Vectors. 2016;9:228.

    Article  PubMed  PubMed Central  Google Scholar 

Download references

Authors’ contributions

XHQ, CY and XYF conceived the study. CY performed the experiment and XYF identified the species. CY, ZSH and XHQ analyzed the data. XHQ, CY, ZSH and XYF wrote the paper. XYF and ML contributed to sample collection. All authors read and approved the final manuscript.

Acknowledgements

The authors thank the reviewers for their constructive comments and suggestions.

Competing interests

The authors declare that they have no competing interests.

Availability of data and matarials

All the datasets are presented in the main paper.

Funding

This work was supported by Grants No. 2012CB114103 and 2012ZX10004219. The funders had no role in the study design, data collection, analysis, decision to publish or preparation of the manuscript.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Xinghui Qiu.

Additional information

Chan Yang and Xiangyang Feng contributed equally to this work.

Additional files

Additional file 1. Brief description of Anopheles sinensis collection sites in Guangxi.

12936_2016_1467_MOESM2_ESM.doc

Additional file 2. Genotypes of the AS-VGSC gene and their frequency in nine An. sinensis populations from Guangxi, China.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Yang, C., Feng, X., Huang, Z. et al. Diversity and frequency of kdr mutations within Anopheles sinensis populations from Guangxi, China. Malar J 15, 411 (2016). https://doi.org/10.1186/s12936-016-1467-3

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12936-016-1467-3

Keywords