Riveron Jacob M, Ibrahim Sulaiman S, Chanda Emmanuel, Mzilahowa Themba, Cuamba Nelson, Irving Helen, Barnes Kayla G, Ndula Miranda, Wondji Charles S
Vector Biology Department, Liverpool School of Tropical Medicine, Pembroke place, Liverpool, L3 5QA, UK.
BMC Genomics. 2014 Sep 27;15(1):817. doi: 10.1186/1471-2164-15-817.
Pyrethroid resistance in the major malaria vector Anopheles funestus is rapidly expanding across Southern Africa. It remains unknown whether this resistance has a unique origin with the same molecular basis or is multifactorial. Knowledge of the origin, mechanisms and evolution of resistance are crucial to designing successful resistance management strategies.
Here, we established the resistance profile of a Zambian An. funestus population at the northern range of the resistance front. Similar to other Southern African populations, Zambian An. funestus mosquitoes are resistant to pyrethroids and carbamate, but in contrast to populations in Mozambique and Malawi, these insects are also DDT resistant. Genome-wide microarray-based transcriptional profiling and qRT-PCR revealed that the cytochrome P450 gene CYP6M7 is responsible for extending pyrethroid resistance northwards. Indeed, CYP6M7 is more over-expressed in Zambia [fold-change (FC) 37.7; 13.2 for qRT-PCR] than CYP6P9a (FC15.6; 8.9 for qRT-PCR) and CYP6P9b (FC11.9; 6.5 for qRT-PCR), whereas CYP6P9a and CYP6P9b are more highly over-expressed in Malawi and Mozambique. Transgenic expression of CYP6M7 in Drosophila melanogaster coupled with in vitro assays using recombinant enzymes and assessments of kinetic properties demonstrated that CYP6M7 is as efficient as CYP6P9a and CYP6P9b in conferring pyrethroid resistance. Polymorphism patterns demonstrate that these genes are under contrasting selection forces: the exceptionally diverse CYP6M7 likely evolves neutrally, whereas CYP6P9a and CYP6P9b are directionally selected. The higher variability of CYP6P9a and CYP6P9b observed in Zambia supports their lesser role in resistance in this country.
Pyrethroid resistance in Southern Africa probably has multiple origins under different evolutionary forces, which may necessitate the design of different resistance management strategies.
主要疟疾传播媒介——斯氏按蚊对拟除虫菊酯的抗性正在撒哈拉以南非洲迅速蔓延。目前尚不清楚这种抗性是否源于同一分子基础的单一源头,还是多因素导致的。了解抗性的起源、机制和进化对于制定成功的抗性管理策略至关重要。
在此,我们确定了赞比亚斯氏按蚊种群在抗性前沿北部范围的抗性概况。与撒哈拉以南非洲的其他种群类似,赞比亚的斯氏按蚊对拟除虫菊酯和氨基甲酸酯具有抗性,但与莫桑比克和马拉维的种群不同,这些昆虫对滴滴涕也具有抗性。基于全基因组微阵列的转录谱分析和定量逆转录聚合酶链反应(qRT-PCR)显示,细胞色素P450基因CYP6M7是导致拟除虫菊酯抗性向北扩展的原因。实际上,CYP6M7在赞比亚的过表达程度[倍数变化(FC)为37.7;qRT-PCR为13.2]高于CYP6P9a(FC为15.6;qRT-PCR为8.9)和CYP6P9b(FC为11.9;qRT-PCR为6.5),而CYP6P9a和CYP6P9b在马拉维和莫桑比克的过表达程度更高。CYP6M7在黑腹果蝇中的转基因表达,以及使用重组酶的体外试验和动力学特性评估表明,CYP6M7在赋予拟除虫菊酯抗性方面与CYP6P9a和CYP6P9b一样有效。多态性模式表明,这些基因受到不同的选择压力:异常多样的CYP6M7可能呈中性进化,而CYP6P9a和CYP6P9b则受到定向选择。在赞比亚观察到的CYP6P9a和CYP6P9b较高变异性支持了它们在该国抗性中作用较小的观点。
撒哈拉以南非洲的拟除虫菊酯抗性可能在不同的进化力量下有多个起源,这可能需要设计不同的抗性管理策略。