Bacterial Protein Toxin Research Cluster, Institute of Molecular Biosciences, Mahidol University, Nakorn-Pathom, 73170, Thailand.
Department of Protozoology, Faculty of Tropical Medicine, Mahidol University, Ratchadewee, Bangkok, 10400, Thailand.
Parasit Vectors. 2018 Sep 20;11(1):515. doi: 10.1186/s13071-018-3110-3.
Mosquitoes transmit many vector-borne infectious diseases including malaria, dengue, chikungunya, yellow fever, filariasis, and Japanese encephalitis. The insecticidal δ-endotoxins Cry4, Cry11, and Cyt produced from Bacillus thuringiensis have been used for bio-control of mosquito larvae. Cry δ-endotoxins are synthesised as inactive protoxins in the form of crystalline inclusions in which they are processed to active toxins in larval midgut lumen. Previously, we demonstrated that the activated Cry4Ba toxin has to alter the permeability of the peritrophic membrane (PM), allowing toxin passage across PM to reach specific receptors on microvilli of larval midgut epithelial cells, where the toxin undergoes conformational changes, followed by membrane insertion and pore formation, resulting in larval death. A peritrophic membrane (PM)-binding calcofluor has been proposed to inhibit chitin formation and enhance baculovirus infection of lepidopteran Trichoplusia ni.
In this study, Aedes aegypti larvae were fed with the calcofluor and Cry4Ba toxin to investigate the effect of this agent on the toxicity of the Cry4Ba toxin.
Calcofluor displayed an enhancing effect when co-fed with the Cry4Ba wild-type toxin. The agent could restore the killing activity of the partially active Cry4Ba mutant E417A/Y455A toward Ae. aegypti larvae. PM destruction was observed after larval challenge with calcofluor together with the toxin. Interestingly, calcofluor increased Cry4Ba toxin susceptibility toward semi-susceptible Culex quinquefasciatus larvae. However, calcofluor alone or in combination with the toxin showed no mortality effect on non-susceptible fresh-water fleas, Moina macrocopa.
Our results suggest that PM may contribute to the resistance of the mosquito larvae to Cry4Ba toxin. The PM-permeability alternating calcofluor might be a promising candidate for enhancing insect susceptibility, which will consequently improve Cry4Ba efficacy in field settings in the future.
蚊子传播多种媒介传播的传染病,包括疟疾、登革热、基孔肯雅热、黄热病、丝虫病和日本脑炎。苏云金芽孢杆菌产生的杀虫δ-内毒素 Cry4、Cry11 和 Cyt 已被用于控制蚊虫幼虫。Cry δ-内毒素以晶体包含物的形式合成无活性原毒素,在幼虫中肠腔的溶酶体中被加工成活性毒素。此前,我们证明激活的 Cry4Ba 毒素必须改变围食膜 (PM) 的通透性,允许毒素穿过 PM 到达幼虫中肠上皮细胞微绒毛上的特定受体,在那里毒素发生构象变化,随后膜插入和孔形成,导致幼虫死亡。已提出一种围食膜 (PM)-结合的钙荧光素来抑制几丁质形成并增强杆状病毒对鳞翅目昆虫三化螟的感染。
在这项研究中,用钙荧光素和 Cry4Ba 毒素喂养埃及伊蚊幼虫,以研究该试剂对 Cry4Ba 毒素毒性的影响。
钙荧光素与 Cry4Ba 野生型毒素共喂养时显示出增强作用。该试剂可以恢复 Cry4Ba 部分活性 E417A/Y455A 突变体对埃及伊蚊幼虫的致死活性。在用毒素处理幼虫后观察到 PM 破坏。有趣的是,钙荧光素增加了 Cry4Ba 毒素对半敏感的致倦库蚊幼虫的敏感性。然而,钙荧光素单独或与毒素联合对非敏感的淡水蚤,大型蚤,没有致死作用。
我们的结果表明 PM 可能有助于蚊子幼虫对 Cry4Ba 毒素的抗性。PM 通透性交替的钙荧光素可能是一种有前途的候选物,可提高昆虫的敏感性,从而提高 Cry4Ba 在未来田间环境中的功效。