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Chronic exposure to arsenic in drinking water can lead to resistance to antimonial drugs in a mouse model of visceral leishmaniasis

机译:在小鼠内脏利什曼病模型中,长期暴露于饮用水中的砷可能导致对锑药物的耐药性

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摘要

The Indian subcontinent is the only region where arsenic contamination of drinking water coexists with widespread resistance to antimonial drugs that are used to treat the parasitic disease visceral leishmaniasis. We have previously proposed that selection for parasite resistance within visceral leishmaniasis patients who have been exposed to trivalent arsenic results in cross-resistance to the related metalloid antimony, present in the pentavalent state as a complex in drugs such as sodium stibogluconate (Pentostam) and meglumine antimonate (Glucantime). To test this hypothesis, Leishmania donovani was serially passaged in mice exposed to arsenic in drinking water at environmentally relevant levels (10 or 100 ppm). Arsenic accumulation in organs and other tissues was proportional to the level of exposure and similar to that previously reported in human liver biopsies. After five monthly passages in mice exposed to arsenic, isolated parasites were found to be completely refractory to 500 ?g?mL?1 Pentostam compared with the control passage group (38.5 ?g?mL?1) cultured in vitro in mouse peritoneal macrophages. Reassessment of resistant parasites following further passage for 4 mo in mice without arsenic exposure showed that resistance was stable. Treatment of infected mice with Pentostam confirmed that resistance observed in vitro also occurred in vivo. We conclude that arsenic contamination may have played a significant role in the development of Leishmania antimonial resistance in Bihar because inadequate treatment with antimonial drugs is not exclusive to India, whereas widespread antimonial resistance is.
机译:印度次大陆是唯一的饮用水砷污染并存的地区,该地区普遍存在对用于治疗内脏利什曼病的寄生虫药的抗药性。我们以前曾建议在暴露于三价砷的内脏利什曼病患者中选择对寄生虫的耐药性会导致对相关准金属锑的交叉耐药,该锑以五价态形式存在于药物中,如stibogluconate(Pentostam)和葡甲胺的复合物。锑酸盐(Glucantime)。为了验证这一假设,在与环境相关水平(10或100 ppm)的饮用水中接触砷的小鼠中连续传代了Leishmania donovani。砷在器官和其他组织中的积累与暴露水平成正比,与人体肝活检中先前报道的相似。与暴露在小鼠腹膜巨噬细胞中的对照组相比(38.5 µg?mL?1),在暴露于砷的小鼠中经过五个月的传代后,发现分离出的寄生虫对500 µg?mL?1的戊喷坦完全不敏感。在没有砷暴露的小鼠中进一步传代4个月后,对抗药性寄生虫的重新评估表明抗药性是稳定的。用戊喷坦处理感染的小鼠证实,体外观察到的耐药性也在体内发生。我们得出的结论是,砷污染可能在比哈尔邦的利什曼原虫耐药性发展中发挥了重要作用,因为对锑药物的不充分治疗并非印度独有,而广泛的锑耐药性则是这种情况。

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