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Detection of an Allele Conferring Resistance to Bacillus sphaericus Binary Toxin in Culex quinquefasciatus Populations by Molecular Screening

机译:分子筛查法检测对库克斯库克斯族人群球菌芽孢杆菌二元毒素具有抗性的等位基因

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摘要

The activity of the Bacillus sphaericus binary (Bin) toxin on Culex quinquefasciatus larvae depends on its specific binding to the Cqm1 receptor, a midgut membrane-bound α-glucosidase. A 19-nucleotide deletion in the cqm1 gene (cqm1REC) mediates high-level resistance to Bin toxin. Here, resistance in nontreated and B. sphaericus-treated field populations of C. quinquefasciatus was assessed through bioassays as well as a specific PCR assay designed to detect the cqm1REC allele in individual larvae. Resistance ratios at 90% lethal concentration, gathered through bioassays, were close to 1 and indicate that the selected populations had similar levels of susceptibility to B. sphaericus, comparable to that of a laboratory colony. A diagnostic PCR assay detected the cqm1REC allele in all populations investigated, and its frequency in two nontreated areas was 0.006 and 0.003, while the frequency in the B. sphaericus-treated population was significantly higher. Values of 0.053 and 0.055 were detected for two distinct sets of samples, and homozygote resistant larvae were found. Evaluation of Cqm1 expression in individual larvae through α-glucosidase assays corroborated the allelic frequency revealed by PCR. The data from this study indicate that the cqm1REC allele was present at a detectable frequency in nontreated populations, while the higher frequency in samples from the treated area is, perhaps, correlated with the exposure to B. sphaericus. This is the first report of the molecular detection of a biolarvicide resistance allele in mosquito populations, and it confirms that the PCR-based approach is suitable to track such alleles in target populations.
机译:球形芽孢杆菌二元(Bin)毒素对库克斯库克斯幼虫的活性取决于其与Cqm1受体(中肠膜结合α-葡萄糖苷酶)的特异性结合。 cqm1基因(cqm1REC)中的19个核苷酸缺失介导了对Bin毒素的高水平抗性。在这里,通过生物测定以及旨在检测单个幼虫中cqm1REC等位基因的特异性PCR测定法评估了未处理和经球形芽孢杆菌处理过的西洋参线虫田间种群的抗性。通过生物测定收集的在90%致死浓度下的耐药率接近1,表明所选种群对球形芽孢杆菌的敏感性水平与实验室菌落相当。诊断性PCR检测法在所有调查人群中检测到cqm1REC等位基因,在两个未治疗区域的频率分别为0.006和0.003,而在球形芽孢杆菌治疗人群中的频率明显更高。对于两组不同的样品,检测到的值为0.053和0.055,并且发现了纯合子抗性的幼虫。通过α-葡萄糖苷酶检测评估个体幼虫中Cqm1的表达,证实了PCR显示的等位基因频率。这项研究的数据表明,cqm1REC等位基因在未经处理的人群中以可检测的频率存在,而来自经过处理的区域的样品中较高的频率可能与暴露于球形芽孢杆菌有关。这是对蚊虫种群中的抗生物杀虫剂等位基因进行分子检测的第一份报告,它证实了基于PCR的方法适合追踪目标人群中的此类等位基因。

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