scholarly journals piRNA-3312: A Putative Role for Pyrethroid Resistance in Culex pipiens pallens (Diptera: Culicidae)

2017 ◽  
Vol 54 (4) ◽  
pp. 1013-1018 ◽  
Author(s):  
Juxin Guo ◽  
Wenyun Ye ◽  
Xianmiao Liu ◽  
Xueli Sun ◽  
Qin Guo ◽  
...  
2016 ◽  
Vol 115 (12) ◽  
pp. 4511-4517 ◽  
Author(s):  
Mengmeng Tian ◽  
Bingqian Liu ◽  
Hongxia Hu ◽  
Xixi Li ◽  
Qin Guo ◽  
...  

2019 ◽  
Author(s):  
Qiqi Shi ◽  
Peng Cheng ◽  
Chongxing Zhang ◽  
Lijuan Liu ◽  
Xiao Song ◽  
...  

Abstract Background Long-lasting overdependence on insecticides has led to the rapid spread of pyrethroid resistance in mosquito vectors, which is of great concern to the general public. There are many studies on metabolic resistance and target resistance, but fewer studies have been conducted on cuticle resistance and behaviour resistance. The cuticle of mosquitoes has been hypothesized to play a role in insecticide resistance by reducing penetration or sequestering insecticides. Methods We used RNA sequencing (RNA-seq) to analyse the transcriptome of cypermethrin-resistant and cypermethrin-susceptible strains of Culex pipiens pallens . Sequenced 6 samples using an Illumina HiSeq platform, and generated approximately 6.66 Gb bases from each sample on average. Mapping the sequenced reads to a reference genome and reconstructing the transcripts, through gene expression analysis, we detected differentially expressed genes (DEGs) among the samples. Followed Gene Ontology (GO) classification and functional enrichment. Finally, we screened the genes of cuticle proteins associated with drug resistance throughout the genome, selected the significant DEGs with a log2 fold change>3.0 and Padj<0.05, and applied real-time fluorescence quantitative PCR to verify the DEGs. Results We obtained 13,517 novel transcripts, of which 8,653 were previously unknown splicing events for known genes, 665 were novel coding transcripts without any known features, and 4,199 were long noncoding RNA. A total of 1035, 944, and 657 genes were upregulated in comparisons between samples, and 2680, 1215, and 975 genes were downregulated in comparisons between samples. Finally, among all samples, 167 genes upregulated, and 145 genes downregulated. The GO classification and functional enrichment of DEGs as follows: molecular function, 224 genes; cellular component, 149 genes; and biological process, 272 genes. The expression of XM_001863852 and XM_001845881 in resistant strains of Culex pipiens pallens was lower than that in the laboratory sensitive strain, with fold changes in expression of 0.177 and 0.548, respectively; the expression of the XM_001845883.1 in the resistant strain was higher than that in the susceptible strain, and a 2.281-fold change in expression. Conclusions The results provide a reference for resistance mechanisms through the mosquito cuticle, furthermore, could provide a new perspective for disease vector control.


2017 ◽  
Vol 116 (9) ◽  
pp. 2489-2497 ◽  
Author(s):  
Wenyun Ye ◽  
Xianmiao Liu ◽  
Juxin Guo ◽  
Xueli Sun ◽  
Yan Sun ◽  
...  

2021 ◽  
Author(s):  
Yang Xu ◽  
Yang Zhou ◽  
Xixi Li ◽  
Lei Ma ◽  
Dan Zhou ◽  
...  

Abstract The cuticle protein (CP) encoded by CPR63 plays a role in deltamethrin resistance in Culex pipiens pallens. Herein, we investigated the distribution of CPR63 transcripts in this organism, and revealed high expression levels in legs and wings. Furthermore, expression of CPR63 in the legs of deltamethrin-resistant (DR) strains were 1.79-fold higher than in deltamethrin-susceptible (DS) strains. Cuticle analysis of small interfering RNA (siRNA) groups by scanning electron microscopy (SEM) revealed a significantly thinner procuticle of the tarsi in the siCPR63 group than the siNC (negative control (group). Transmission electron microscopy (TEM) revealed that the procuticle, exocuticle and endocuticle thickness of the tarsi were significantly thinner in the siCPR63 group than the siNC group. Our results illuminate the resistance mechanism of CPRs and demonstrate that CPR63 contributes to the resistance phenotype by thickening the cuticle and substantially reducing uptake of insecticides.


2020 ◽  
Vol 13 (1) ◽  
Author(s):  
Yang Xu ◽  
Xiaoshan Yang ◽  
Xiaohong Sun ◽  
Xixi Li ◽  
Zhihan Liu ◽  
...  

Abstract Background Culex pipiens pallens poses a serious threat to human health because of its widespread distribution, high carrier capacity for several arboviruses, frequent human-biting, and growth in urban environments. Pyrethroid insecticides have been mainly used to control adult Cx. pipiens pallens during outbreaks of mosquito-borne diseases. Unfortunately, mosquitoes have developed resistance, rendering the insecticides ineffective. Cuticular resistance is the primary mechanism of pyrethroid resistance. Previously, we revealed that cuticular protein of low complexity CPLCG5 is a major cuticular protein associated with deltamethrin resistance in Cx. pipiens pallens, which is enriched in the cuticle of mosquitoes’ legs and participates in pyrethroid resistance by forming a rigid matrix. However, the regulatory mechanisms of its transcription remain unknown. Results First, qRT-PCR analysis revealed that the expression of FTZ-F1 (encoding Fushi tarazu-Factor 1) was ~ 1.8-fold higher in the deltamethrin-resistant (DR) than deltamethrin-susceptible (DS) strains at 24 h post-eclosion (PE) and ~ 2.2-fold higher in the DR strain than in the DS strain at 48 h PE. CPLCG5 and FTZ-F1 were co-expressed in the legs, indicating that they might play an essential role in the legs. Dual luciferase reporter assays and EMSA (electrophoretic mobility shift experiments) revealed that FTZ-F1 regulates the transcription of CPLCG5 by binding to the FTZ-F1 response element (− 870/− 864). Lastly, knockdown of FTZ-F1 not only affected CPLCG5 expression but also altered the cuticle thickness and structure of the legs, increasing the susceptibility of the mosquitoes to deltamethrin in vivo. Conclusions The results revealed that FTZ-F1 regulates the expression of CPLCG5 by binding to the CPLCG5 promoter region, altering cuticle thickness and structure, and increasing the susceptibility of mosquitoes to deltamethrin in vivo. This study revealed part of the mechanism of cuticular resistance, providing a deeper understanding of insecticide resistance.


2014 ◽  
Vol 114 (2) ◽  
pp. 699-706 ◽  
Author(s):  
Zhentao Lei ◽  
Yuan Lv ◽  
Weijie Wang ◽  
Qin Guo ◽  
Feifei Zou ◽  
...  

2020 ◽  
Author(s):  
Qiqi Shi ◽  
Peng Cheng ◽  
Chongxing Zhang ◽  
Lijuan Liu ◽  
Xiao Song ◽  
...  

Abstract Background A long-lasting overdependence on insecticides has led to the rapid spread of pyrethroid resistance in mosquito vectors, which poses a great risk to the general public. Although there are many studies on metabolic resistance and target resistance, few have investigated cuticle resistance and behaviour resistance. The cuticle of mosquitoes has been hypothesized to play a role in insecticide resistance by reducing penetration or sequestering insecticides.Methods We used RNA sequencing (RNA-seq) to analyse the transcriptome of cypermethrin-resistant and cypermethrin-susceptible strains of Culex pipiens pallens. We sequenced 6 samples using an Illumina HiSeq platform and generated approximately 6.66 Gb bases from each sample on average. Mapping the sequenced reads to a reference genome and reconstructing the transcripts via gene expression analysis, we detected differentially expressed genes (DEGs) among the samples. Followed Gene Ontology (GO) classification and functional enrichment. Finally, we screened the genes of cuticle proteins associated with drug resistance throughout the genome, selected the significant DEGs with a log2 fold change > 3.0 and Padj < 0.05, and applied real-time fluorescence quantitative polymerase chain reaction (PCR) to verify the DEGs. Results We obtained 13,517 novel transcripts, of which 8,653 were previously unknown splicing events for known genes, 665 were novel coding transcripts without any known features, and 4,199 were long non-coding RNA (lncRNA). A total of 1035, 944, and 657 genes were upregulated in comparisons between the samples, and 2680, 1215, and 975 genes were downregulated in comparisons between the samples. Finally, among all samples, 167 genes were upregulated and 145 genes were downregulated. The GO classification and functional enrichment of DEGs were as follows: molecular function, 224 genes; cellular component, 149 genes; and biological process, 272 genes. The expression of XM_001863852 and XM_001845881 in resistant strains of Culex pipiens pallens was lower than that in the laboratory sensitive strain, with 0.177 and 0.548-fold change in expression, respectively; the expression of the XM_001845883.1 in the resistant strain was higher than that in the susceptible strain, with a 2.281-fold change in expression.Conclusions Our results provide a reference for resistance mechanisms via the mosquito cuticle as well as a new perspective for disease vector control.


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