A Double Line of Defense: Heat Shock Proteins and Polyamines Act as Contributing Factors to Drug Resistance of some Plasmodium Parasites

Xolani Henry Makhoba
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引用次数: 2

Abstract

Malaria remains a threat to human life worldwide with children under the age of 5 being the most vulnerable. Plasmodium falciparum, known as the causative agent of the deadliest malaria, survives both in the mosquito vector and human host. The sudden temperature change seems to not affect the parasite’s cellular system. Heat shock proteins and polyamines are the major house-keepers of the parasite’s cellular system to remain viable, despite the temperature changes that the parasite gets exposed to. While heat shock proteins protect newly synthesized proteins until they are properly folded polyamines are needed for cell differentiation, proliferation, and cell growth. In plants for example, polyamines have been reported to act as molecular chaperones when cells are exposed to unfavorable conditions that could be detrimental to cells. In this review, the role of heat shock proteins and polyamines in plasmodium parasite drug resistance and their role in parasite survival are discussed. The current drugs against malaria as well as the alternative future approach towards malarial drug development are reviewed.
双重防线:热休克蛋白和多胺是一些疟原虫耐药的促进因素
疟疾仍然对全世界的人类生命构成威胁,其中5岁以下儿童最为脆弱。恶性疟原虫被认为是最致命的疟疾的病原体,在蚊子载体和人类宿主中都能存活。突然的温度变化似乎不会影响寄生虫的细胞系统。热休克蛋白和多胺是寄生虫细胞系统保持活力的主要管家,尽管寄生虫暴露在温度变化中。当热休克蛋白保护新合成的蛋白质直到它们被正确折叠时,多胺是细胞分化、增殖和细胞生长所需要的。例如,据报道,在植物中,当细胞暴露于可能对细胞有害的不利条件时,多胺充当分子伴侣。本文就热休克蛋白和多胺在疟原虫耐药过程中的作用及其在疟原虫存活中的作用作一综述。综述了目前抗疟疾药物的研究进展,以及未来抗疟疾药物的发展方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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