Department of Entomology, Centro de Pesquisas Aggeu Magalhães-FIOCRUZ, Recife-PE, Brazil.
Appl Environ Microbiol. 2012 Sep;78(17):6321-6. doi: 10.1128/AEM.01199-12. Epub 2012 Jul 6.
Bin toxin from Bacillus sphaericus acts on Culex quinquefasciatus larvae by binding to Cqm1 midgut-bound receptors, and disruption of the cqm1 gene is the major cause of resistance. The goal of this work was to screen for a laboratory-selected resistance cqm1(REC) allele in field populations in the city of Recife, Brazil, and to describe other resistance-associated polymorphisms in the cqm1 gene. The cqm1(REC) allele was detected in the four nontreated populations surveyed at frequencies from 0.001 to 0.017, and sequence analysis from these samples revealed a novel resistant allele (cqm1(REC-D16)) displaying a 16-nucletotide (nt) deletion which is distinct from the 19-nt deletion associated with cqm1(REC). Yet a third resistant allele (cqm1(REC-D25)), displaying a 25-nt deletion, was identified in samples from a treated area exposed to B. sphaericus. A comparison of the three deletion events revealed that all are located within the same 208-nt region amplified during the screening procedure. They also introduce equivalent frameshifts in the sequence and generate the same premature stop codon, leading to putative transcripts encoding truncated proteins which are unable to locate to the midgut epithelium. The populations analyzed in this study contained a variety of alleles with mutations disrupting the function of the corresponding Bin toxin receptor. Their locations reveal a hot spot that can be exploited to assess the resistance risk through DNA screening.
球形芽孢杆菌的 Bin 毒素通过与 Cqm1 中肠结合受体结合作用于致倦库蚊幼虫,而 cqm1 基因的破坏是产生抗药性的主要原因。本研究的目的是筛选巴西累西腓市田间种群中经实验室选择的抗性 cqm1(REC)等位基因,并描述 cqm1 基因中其他与抗药性相关的多态性。在所调查的四个未经处理的种群中,检测到 cqm1(REC)等位基因的频率从 0.001 到 0.017,对这些样本的序列分析显示了一个新的抗性等位基因(cqm1(REC-D16)),其存在 16 个核苷酸(nt)的缺失,与与 cqm1(REC)相关的 19-nt 缺失不同。在暴露于球形芽孢杆菌的处理区的样本中还发现了第三个抗性等位基因(cqm1(REC-D25)),其存在 25-nt 的缺失。对这三个缺失事件的比较表明,它们都位于筛选过程中扩增的相同的 208-nt 区域内。它们还在序列中引入了等效的移码,并产生了相同的过早终止密码子,导致编码无法定位到中肠上皮的截短蛋白的假定转录本。本研究分析的种群含有各种突变破坏相应 Bin 毒素受体功能的等位基因。它们的位置揭示了一个热点,可以通过 DNA 筛选来评估抗性风险。