Laboratory of Microbiology, Parasitology and Hygiene (LMPH), University of Antwerp, Universiteitsplein 1, B-2610, Wilrijk, Belgium.
Department of Parasitology, Charles University, Vinicna 7, CZ-12844, Prague 2, Czech Republic.
Int J Parasitol Drugs Drug Resist. 2019 Dec;11:1-7. doi: 10.1016/j.ijpddr.2019.09.003. Epub 2019 Sep 10.
To gain insight into the propagation of miltefosine (MIL) resistance in visceral leishmaniasis, this laboratory study explored development of resistant parasites with a defective miltefosine transporter (MT) in sand flies.
Infectivity, colonization of stomodeal valve and metacyclogenesis of a MIL-resistant (MIL-R) Leishmania infantum LEM3323 line with a defective MT were assessed in the natural sand fly vectors Phlebotomus perniciosus and Lutzomyia longipalpis. Given our recent description of partial drug dependency of the MT-deficient line, the impact of MIL pre-exposure on sand fly infectivity was explored as well.
A significant reduction in sand fly infection, stomodeal valve colonization and differentiation into metacyclics (determined by a lower flagellum/cell body length ratio) was observed in both vectors for MIL-R as compared to the isogenic parent MIL-susceptible line. Re-introduction of the wildtype MT gene into MIL-R tended to partially rescue the capacity to infect sand flies. Pre-exposure to MIL did not alter infectivity of the MIL-R line.
The MIL resistant L. infantum LEM3323 line is significantly hampered in its development and transmissibility potential in two sand fly vector species. Additional studies are warranted to evaluate whether this applies to other visceral Leishmania parasites with acquired MIL-resistance.
深入了解米替福新(MIL)耐药性在内脏利什曼病中的传播,本实验室研究探索了在沙蝇中具有缺陷米替福新转运蛋白(MT)的耐药寄生虫的发展。
在自然传播媒介白蛉属和长角血蝉中评估了具有缺陷 MT 的 MIL 耐药(MIL-R)利什曼原虫 LEM3323 系的感染力、气门阀定植和前鞭毛体形成。鉴于我们最近描述了 MT 缺陷系的部分药物依赖性,还探索了 MIL 预暴露对沙蝇感染力的影响。
与同基因亲代 MIL 敏感系相比,在两种载体中,MIL-R 的感染白蛉的能力、气门阀定植和分化为前鞭毛体(通过降低鞭毛/细胞体长度比来确定)均显著降低。野生型 MT 基因的重新引入倾向于部分恢复感染白蛉的能力。MIL 预暴露并未改变 MIL-R 系的感染力。
在两种沙蝇媒介物种中,MIL 耐药的利什曼原虫 LEM3323 系在其发育和传播潜力方面受到严重阻碍。需要进一步研究以评估其他获得性 MIL 耐药的内脏利什曼原虫寄生虫是否适用。