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武汉市公园和农村白纹伊蚊种群电压门控钠离子通道基因突变分析
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作者 吴丽群 雷励 +1 位作者 包继永 陈晓敏 《中华卫生杀虫药械》 CAS 2024年第6期546-550,共5页
目的了解武汉市公园和农村生境中白纹伊蚊种群电压门控钠离子通道(VGSC)基因突变情况。方法2022年6—10月在武汉市2个公园和2个村湾分别采集白纹伊蚊幼虫和蛹,于实验室饲养至成蚊,抽提单只成蚊的基因组DNA,PCR扩增VGSC基因部分片段,测... 目的了解武汉市公园和农村生境中白纹伊蚊种群电压门控钠离子通道(VGSC)基因突变情况。方法2022年6—10月在武汉市2个公园和2个村湾分别采集白纹伊蚊幼虫和蛹,于实验室饲养至成蚊,抽提单只成蚊的基因组DNA,PCR扩增VGSC基因部分片段,测序后分析VGSC基因突变情况,并采用χ^(2)检验对种群间白纹伊蚊VGSC基因3个位点突变型等位基因的分布进行比较分析。结果共检测公园生境白纹伊蚊104只和农村生境白纹伊蚊43只。公园白纹伊蚊种群VGSC基因的1016、1532与1534位点均存在突变,且1016与1534位点及1532与1534位点均存在联合突变;而农村白纹伊蚊种群VGSC基因的1016与1534位点存在突变,1532位点未发现突变,且未发现联合突变现象。公园白纹伊蚊种群1534位点TCC/S和TGC/C突变型等位基因频率高于农村种群,差异具有统计学意义(P﹤0.001),但公园种群和农村种群间1016位点GGA/G突变型等位基因与1532位点ACC/T突变型等位基因的突变频率差异均无统计学意义(P=0.160,P=0.263)。结论公园和农村白纹伊蚊种群VGSC基因突变情况有差异,建议开展白纹伊蚊VGSC基因突变监测,以进一步了解武汉市白纹伊蚊拟除虫菊酯类杀虫剂抗药性迅速发展的作用机制。 展开更多
关键词 白纹伊蚊 抗药性 电压门控钠离子通道基因
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Mutations and intron polymorphisms in voltage-gated sodium channel genes of different geographic populations of Culex pipiens pallens/Culex pipiens quinquefasciatus in China 被引量:1
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作者 Wenyu Li Delong Ma +6 位作者 Qunzheng Mu Xinxin Zhou Dongdong Hua Chunchun Zhao Qiyong Liu Jun Wang Fengxia Meng 《Infectious Diseases of Poverty》 SCIE CAS CSCD 2024年第2期6-16,共11页
Background Culex pipiens pallens and Culex pipiens quinquefasciatus are the dominant species of Culex mosquitoes in China and important disease vectors.Long-term use of insecticides can cause mutations in the voltage-... Background Culex pipiens pallens and Culex pipiens quinquefasciatus are the dominant species of Culex mosquitoes in China and important disease vectors.Long-term use of insecticides can cause mutations in the voltage-gated sodium channel(vgsc)gene of mosquitoes,but little is known about the current status and evolutionary origins of vgsc gene in different geographic populations.Therefore,this study aimed to determine the current status of vgsc genes in Cx.p.pallens and Cx.p.quinquefasciatus in China and to investigate the evolutionary inheritance of neighboring downstream introns of the vgsc gene to determine the impact of insecticides on long-term evolution.Methods Sampling was conducted from July to September 2021 in representative habitats of 22 provincial-level administrative divisions in China.Genomic DNA was extracted from 1308 mosquitoes,the IIS6 fragment of the vgsc gene on the nerve cell membrane was amplified using polymerase chain reaction,and the sequence was used to evaluate allele frequency and knockdown resistance(kdr)frequency.MEGA 11 was used to construct neighborjoining(NJ)tree.PopART was used to build a TCS network.Results There were 6 alleles and 6 genotypes at the L1014 locus,which included the wild-type alleles TTA/L and CTA/L and the mutant alleles TTT/F,TTC/F,TCT/S and TCA/S.The geographic populations with a kdr frequency less than 20.00%were mainly concentrated in the regions north of 38°N,and the geographic populations with a kdr frequency greater than 80.00%were concentrated in the regions south of 30°N.kdr frequency increased with decreasing latitude.And within the same latitude,the frequency of kdr in large cities is relatively high.Mutations were correlated with the number of introns.The mutant allele TCA/S has only one intron,the mutant allele TTT/F has three introns,and the wild-type allele TTA/L has 17 introns.Conclusions Cx.p.pallens and Cx.p.quinquefasciatus have developed resistance to insecticides in most regions of China.The neighboring downstream introns of the vgsc gene gradually decreased to one intron with the mutation of the vgsc gene.Mutations may originate from multiple mutation events rather than from a single origin,and populations lacking mutations may be genetically isolated. 展开更多
关键词 Culex pipiens pallens Culex pipiens quinquefasciatus vgsc gene MUTATION Frequency INTRON HAPLOTYPE China
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日本囊对虾电压门控钠通道基因克隆与组织表达
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作者 刘锦燊 叶海辉 +1 位作者 王桂忠 李少菁 《厦门大学学报(自然科学版)》 CAS CSCD 北大核心 2012年第2期268-273,共6页
利用基因克隆等分子生物学技术,获得日本囊对虾(Marsupenaeus japonicus)的电压门控钠通道(voltage-gatesodium channel,VGSC)蛋白的部分cDNA序列,获得的片段核苷酸长度为2 877bp,可编码954个氨基酸残基,总分子质量约为108.2ku.与同源... 利用基因克隆等分子生物学技术,获得日本囊对虾(Marsupenaeus japonicus)的电压门控钠通道(voltage-gatesodium channel,VGSC)蛋白的部分cDNA序列,获得的片段核苷酸长度为2 877bp,可编码954个氨基酸残基,总分子质量约为108.2ku.与同源蛋白比较结果显示,日本囊对虾的VGSC序列与其他一些物种具有较高相似性,特别是跨膜蛋白结构域具有极高的保守性.基于VGSC氨基酸序列比对绘制的系统树基本能够反映出各物种间的进化关系.以RT-PCR法检测日本囊对虾VGSC的组织表达,结果显示VGSC表达与各组织的功能有极其密切的关系.VGSC mRNA在脑神经节中表达量最高,其次为肝胰腺,说明了钠通道在神经信号传导以及调节内分泌中都起到了重要的作用. 展开更多
关键词 日本囊对虾 电压门控钠通道 基因克隆 组织表达
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A novel strategy for screening mutations in the voltage-gated sodium channel gene of Aedes albopictus based on multiplex PCR-mass spectrometry minisequencing technology 被引量:1
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作者 Qunzheng Mu Xin Zhao +8 位作者 Fengfeng Li Wenyu Li Xinxin Zhou Xinchang Lun Yiguan Wang Dongdong Hua Qiyong Liu Di Xiao Fengxia Meng 《Infectious Diseases of Poverty》 SCIE CAS CSCD 2023年第4期43-53,共11页
Background The current prevention and control strategy forAedes albopictus heavily relies on comprehensive management, such as environmental management and chemical control. However, the wide application of pyrethroid... Background The current prevention and control strategy forAedes albopictus heavily relies on comprehensive management, such as environmental management and chemical control. However, the wide application of pyrethroids has facilitated the development of insecticide resistance, primarily via mutations in the voltage-gated sodium channel (VGSC) gene. This study aims to develop a novel strategy for detecting mutations in the VGSC gene inAe. albopictus using multiplex PCR-mass spectrometry (MPCR-MS) minisequencing technology.Methods We established a new strategy for detecting mutations in the VGSC gene inAe. albopictus using MPCR-MS minisequencing technology. MPCR amplification and mass probe extension (MPE) were first used, followed by single nucleotide polymorphism (SNP) typing mass spectrometry, which allows the simultaneous detection of multiple mutation sites of the VGSC gene in 96 samples ofAe. albopictus. A total of 70 wild-collectedAe. albopictus were used to evaluate the performance of the method by comparing it with other methods.Results Three target sites (1016, 1532, 1534) in the VGSC gene can be detected simultaneously by double PCR amplification combined with matrix-assisted laser desorption ionization-time-of-flight mass spectrometry, achieving a detection limit of 20 fg/μl. We applied this method to 70 wild-collectedAe. albopictus, and the obtained genotypes were consistent with the routine sequencing results, suggesting the accuracy of our method.Conclusions MPCR-MS minisequencing technology provides a sensitive and high-throughput approach toAe. albopictus VGSC gene mutation screening. Compared with conventional sequencing, this method is economical and time-saving. It is of great value for insecticide resistance surveillance in areas with a high risk of vector-borne disease. 展开更多
关键词 Aedes albopictus vgsc gene MUTATION Single nucleotide polymorphisms Multiplex polymerase chain reaction-mass spectrometry mini-sequencing
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