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Plasmodium falciparum gametocytes: still many secrets of a hidden life.

机译:恶性疟原虫配子体细胞:仍然是隐藏生活的许多秘密。

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Sexual differentiation and parasite transmission are intimately linked in the life cycle of malaria parasites. The specialized cells providing this crucial link are the Plasmodium gametocytes. These are formed in the vertebrate host and are programmed to mature into gametes emerging from the erythrocytes in the midgut of a blood-feeding mosquito. The ensuing fusion into a zygote establishes parasite infection in the insect vector. Although key mechanisms of gametogenesis and fertilization are becoming progressively clear, the fundamental biology of gametocyte formation still presents open questions, some of which are specific to the human malaria parasite Plasmodium falciparum. Developmental commitment to sexual differentiation, regulation of stage-specific gene expression, the profound molecular and cellular changes accompanying gametocyte specialization, the requirement for tissue-specific sequestration in P. falciparum gametocytogenesis are proposed here as areas for future investigation. The epidemiological relevance of parasite transmission from humans to mosquito in the spread of malaria and of Plasmodium drug resistance genes indicates that understanding molecular mechanisms of gametocyte formation is highly relevant to design strategies able to interfere with the transmission of this disease.
机译:性别差异和寄生虫传播与疟疾寄生虫的生命周期密切相关。提供这个关键环节的专门细胞是疟原虫配子细胞。它们在脊椎动物宿主中形成,并被编程为成熟,从采血蚊子中肠的红细胞中形成配子。随后融合到合子中,在昆虫载体中建立了寄生虫感染。尽管配子发生和受精的关键机制变得越来越清晰,但配子细胞形成的基本生物学仍然存在悬而未决的问题,其中一些是人类疟疾寄生虫恶性疟原虫特有的。在此提出了对性别分化的发展承诺,阶段特异性基因表达的调节,配子细胞专门化伴随的深刻的分子和细胞变化,恶性疟原虫配子发生的组织特异性螯合的要求,作为今后研究的领域。疟疾和疟原虫耐药基因传播中从人到蚊的寄生虫传播的流行病学相关性表明,了解配子形成的分子机制与能够干扰该疾病传播的设计策略高度相关。

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