Potential of emodepside for vector-borne disease control.

IF 2.4 3区 医学 Q3 INFECTIOUS DISEASES Malaria Journal Pub Date : 2025-01-11 DOI:10.1186/s12936-025-05250-8
Pattarapon Khemrattrakool, Thitipong Hongsuwong, Theerawit Phanphoowong, Patchara Sriwichai, Kittiyod Poovorawan, Joel Tarning, Kevin C Kobylinski
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Abstract

Background: Emodepside is an anthelmintic used in veterinary medicine that is currently under investigation in human clinical trials for the treatment of soil-transmitted helminths and possibly Onchocerca volvulus. Emodepside targets the calcium-activated voltage-gated potassium slowpoke 1 (SLO-1) channels of presynaptic nerves of pharynx and body wall muscle cells of nematodes leading to paralysis, reduced locomotion and egg laying, starvation, and death. Emodepside also has activity against Drosophila melanogaster SLO-1 channels. Orthologous SLO-1 genes are present in Anopheles gambiae and Aedes aegypti, suggesting that emodepside may have activity against mosquitoes.

Methods: Both Anopheles dirus and Ae. aegypti were blood-fed emodepside across a range of concentrations (1-10,000 nM) and mosquito survival was monitored for 10 days. Co-feeding experiments were also performed with An. dirus blood fed ivermectin at the concentrations that kills 25% (LC25) and 50% (LC50) of mosquitoes with and without emodepside at clinical peak concentration in humans (Cmax) and five times the Cmax, and mosquito survival was monitored for 10 days.

Results: Emodepside had weak mosquito-lethal effects in An. dirus but none observed in Ae. aegypti at the concentrations evaluated. The An. dirus emodepside LC50 was 4,623 [4,159-5,066] ng/ml which is > 100-fold greater than the peak concentrations seen in human. The ivermectin and emodepside co-feed experiment with An. dirus did not indicate any altered effect of ivermectin on mosquito survival when emodepside co-fed at human Cmax or five times that of the human Cmax.

Conclusions: Emodepside was not lethal to An. dirus at human-relevant concentrations and had no effect on Ae. aegypti survival. Thus, mass distribution of emodepside does not appear to be a potential tool for vector-borne disease control. Emodepside induced mortality in An. dirus does suggest that the SLO-1 channel could be a potential target for novel vector control and may warrant further investigation.

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emodepide在媒介传播疾病控制中的潜力。
背景:Emodepside是一种用于兽药的驱虫药,目前正在研究用于治疗土壤传播蠕虫和可能的盘尾丝虫的人体临床试验。Emodepside作用于线虫咽部和体壁肌细胞突触前神经的钙激活电压门控钾慢泡1 (lo -1)通道,导致瘫痪、运动和产卵减少、饥饿和死亡。Emodepside也对果蝇的sl1通道有活性。冈比亚按蚊和埃及伊蚊中均存在同源的sl -1基因,提示emodepide可能具有抗蚊活性。方法:选取大按蚊和伊蚊;对埃及伊蚊按浓度范围(1-10,000 nM)进行血喂,监测蚊子存活10天。与An共饲试验。按含和不含emodepside的伊维菌素在人体内临床峰值浓度(Cmax)和5倍于Cmax的浓度分别饲喂25% (LC25)和50% (LC50)的伊维菌素,监测蚊虫存活10 d。结果:emodep甙对安县有较弱的杀蚊作用。但在伊蚊中没有发现。埃及伊蚊的浓度评估。一个。大鼠血药苷LC50为4,623 [4,159 ~ 5,066]ng/ml,是人血药苷峰值浓度的近100倍。伊维菌素与emodepide共饲试验。当emodepside与人类Cmax或人类Cmax的5倍共同喂食时,没有显示伊维菌素对蚊子存活的影响有任何改变。结论:Emodepside对An无致死性。对伊蚊无影响。蚊生存。因此,大规模分布的emodepide似乎不是媒介传播疾病控制的潜在工具。emodepide致An的死亡率。dirus确实表明,SLO-1通道可能是新型病媒控制的潜在目标,可能值得进一步研究。
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来源期刊
Malaria Journal
Malaria Journal 医学-寄生虫学
CiteScore
5.10
自引率
23.30%
发文量
334
审稿时长
2-4 weeks
期刊介绍: Malaria Journal is aimed at the scientific community interested in malaria in its broadest sense. It is the only journal that publishes exclusively articles on malaria and, as such, it aims to bring together knowledge from the different specialities involved in this very broad discipline, from the bench to the bedside and to the field.
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