首页> 外文期刊>Parasitology >BnSP-7 toxin, a basic phospholipase A2 from Bothrops pauloensis snake venom, interferes with proliferation, ultrastructure and infectivity of Leishmania (Leishmania) amazonensis
【24h】

BnSP-7 toxin, a basic phospholipase A2 from Bothrops pauloensis snake venom, interferes with proliferation, ultrastructure and infectivity of Leishmania (Leishmania) amazonensis

机译:BnSP-7毒素,一种来自鲍氏两栖蛇蛇毒的碱性磷脂酶A2,会干扰亚马逊利什曼原虫(Leishmania)的增殖,超微结构和感染性

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

This paper reports the effects of BnSP-7 toxin, a catalytically inactive phospholipase A2 from Bothrops pauloensis snake venom, on Leishmania (Leishmania) amazonensis. BnSP-7 presented activity against promastigote parasite forms both in the MTT assay, with IC50 of 58·7 μg mL -1 of toxin, and a growth curve, inhibiting parasite proliferation 60-70% at concentrations of 50-200 μg mL-1 of toxin 96? h after treatment. Also, the toxin presented effects on amastigotes, reducing parasite viability by 50% at 28·1 μg mL-1 and delaying the amastigote-promastigote differentiation process. Ultrastructural studies showed that BnSP-7 caused severe morphological changes in promastigotes such as mitochondrial swelling, nuclear alteration, vacuolization, acidocalcisomes, multiflagellar aspects and a blebbing effect in the plasma membrane. Finally, BnSP-7 interfered with the infective capacity of promastigotes in murine peritoneal macrophages, causing statistically significant infectivity-index reductions (P05) of 20-35%. These data suggest that the BnSP-7 toxin is an important tool for the discovery of new parasite targets that can be exploited to develop new drugs for treating leishmaniasis.
机译:本文报道了来自Bothrops pauloensis蛇毒的一种催化失活的磷脂酶A2 BnSP-7毒素对亚马逊利什曼原虫(Leishmania)的影响。 BnSP-7在MTT分析中均表现出针对前鞭毛体寄生虫形式的活性,IC50为58·7μgmL -1毒素,并且在浓度为50-200μgmL-1时具有生长曲线,抑制了60-70%的寄生虫增殖。毒素96?治疗后h。此外,该毒素还对变形虫产生了影响,在28·1μgmL-1浓度下将寄生虫的生存力降低了50%,并延迟了假孢子虫-前鞭毛虫的分化过程。超微结构研究表明,BnSP-7引起了前鞭毛体的严重形态变化,例如线粒体肿胀,核改变,空泡化,酸性钙化酶体,多鞭毛形态和质膜起泡效应。最后,BnSP-7干扰了前鞭毛体在鼠腹膜巨噬细胞中的感染能力,导致统计学上显着的感染指数降低(20%至35%)(P <05)。这些数据表明,BnSP-7毒素是发现新的寄生虫靶标的重要工具,可以利用该靶标开发用于治疗利什曼病的新药。

著录项

相似文献

  • 外文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号