首页> 外文期刊>BMC Pharmacology >In vitro susceptibility to pentavalent antimony in Leishmania infantum strains is not modified during in vitro or in vivo passages but is modified after host treatment with meglumine antimoniate
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In vitro susceptibility to pentavalent antimony in Leishmania infantum strains is not modified during in vitro or in vivo passages but is modified after host treatment with meglumine antimoniate

机译:婴儿利什曼原虫菌株对五价锑的体外敏感性在体外或体内传代过程中并未改变,但在接受葡甲胺葡甲胺的宿主治疗后有所改变

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Background Leishmaniasis is a common parasitic disease in Southern Europe, caused by Leishmania infantum. The failures of current treatment with pentavalent antimonials are partially attributable to the emergence of antimony-resistant Leishmania strains. This study analyses the in vitro susceptibility to pentavalent antimony of intracellular amastigotes from a range of L. infantum strains, derived from the same infected animal, during in vitro and in vivo passages and after host treatment with meglumine antimoniate. Results SbV-IC50 values for strains from two distinct isolates from the same host and one stock after two years of culture in NNN medium and posterior passage to hamster were similar (5.0 ± 0.2; 4.9 ± 0.2 and 4.4 ± 0.1 mgSbV/L, respectively). In contrast, a significant difference (P V-IC50 values in the stocks obtained before and after treatment of hosts with meglumine antimoniate (4.7 ± 0.4 mgSbV/L vs. 7.7 ± 1.5 mgSbV/L). Drug-resistance after drug pressure in experimentally infected dogs increased over repeated drug administration (6.4 ± 0.5 mgSbV/L after first treatment vs. 8.6 ± 1.4 mgSbV/L after the second) (P Conclusions These results confirm previous observations on strains from Leishmania/HIV co-infected patients and indicate the effect of the increasing use of antimony derivatives for treatment of canine leishmaniasis in endemic areas on the emergence of Leishmania antimony-resistant strains.
机译:背景技术利什曼病是由婴儿利什曼原虫引起的在南欧常见的寄生虫病。当前用五价锑治疗的失败部分归因于抗锑利什曼原虫菌株的出现。这项研究分析了在体外和体内传代以及用葡甲胺锑酸盐进行宿主治疗后,来自同一感染动物的一系列L. infantum菌株的胞内变形虫对五价锑的体外敏感性。结果在NNN培养基中培养两年并且仓鼠向后传递后,来自同一宿主和一只种群的两个不同分离株的菌株的Sb V -IC50值相似(5.0±0.2; 4.9±0.2和分别为4.4±0.1 mgSb V / L)。相反,在用葡甲胺锑酸盐处理宿主之前和之后获得的原种中,PV(s -IC50值具有显着差异(4.7±0.4 mgSb V / L与7.7±1.5 mgSb < sup> V / L)。反复给药后,实验感染犬的药压后耐药性增加(首次治疗后为6.4±0.5 mgSb V / L,而8.6±1.4 mgSb第二秒后 V / L)(P结论)这些结果证实了以前对利什曼原虫/ HIV合并感染患者株的观察结果,并表明增加使用锑衍生物治疗地方性犬利什曼病的效果地区出现了利什曼原虫抗锑菌株。

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