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疟原虫配子表面 184kDa 蛋白 Pb184 的 C 端区域有助于受精和雄配子与残体的结合。

The C-terminal region of the Plasmodium berghei gamete surface 184-kDa protein Pb184 contributes to fertilization and male gamete binding to the residual body.

机构信息

Laboratory of Veterinary Parasitology, School of Veterinary Medicine, Kitasato University, Aomori, Towada, 034-8628, Japan.

出版信息

Parasit Vectors. 2024 Jul 13;17(1):304. doi: 10.1186/s13071-024-06374-7.

Abstract

BACKGROUND

Malaria, a global health concern, is caused by parasites of the Plasmodium genus, which undergo gametogenesis in the midgut of mosquitoes after ingestion of an infected blood meal. The resulting male and female gametes fuse to form a zygote, which differentiates into a motile ookinete. After traversing the midgut epithelium, the ookinete differentiates into an oocyst on the basal side of the epithelium.

METHODS

Membrane proteins with increased gene expression levels from the gamete to oocyst stages in P. berghei were investigated utilizing PlasmoDB, the functional genomic database for Plasmodium spp. Based on this analysis, we selected the 184-kDa membrane protein, Pb184, for further study. The expression of Pb184 was further confirmed through immunofluorescence staining, following which we examined whether Pb184 is involved in fertilization using antibodies targeting the C-terminal region of Pb184 and biotin-labeled C-terminal region peptides of Pb184.

RESULTS

Pb184 is expressed on the surface of male and female gametes. The antibody inhibited zygote and ookinete formation in vitro. When mosquitoes were fed on parasite-infected blood containing the antibody, oocyst formation decreased on the second day after feeding. Synthesized biotin-labeled peptides matching the C-terminal region of Pb184 bound to the female gamete and the residual body of male gametes, and inhibited differentiation into ookinetes in the in vitro culture system.

CONCLUSIONS

These results may be useful for the further studying the fertilization mechanism of Plasmodium protozoa. There is also the potential for their application as future tools to prevent malaria transmission.

摘要

背景

疟疾是一种全球性的健康问题,由疟原虫属寄生虫引起,这些寄生虫在蚊子摄入受感染的血液后,在中肠中进行配子生殖。由此产生的雄性和雌性配子融合形成合子,合子分化为可运动的动合子。穿过中肠上皮细胞后,动合子在上皮细胞的基底侧分化为卵囊。

方法

利用 PlasmoDB(疟原虫属的功能基因组数据库)研究了配子到卵囊阶段基因表达水平增加的膜蛋白。基于此分析,我们选择了 184kDa 的膜蛋白 Pb184 进行进一步研究。通过免疫荧光染色进一步证实了 Pb184 的表达,然后我们使用针对 Pb184 C 端区域的抗体和生物素标记的 Pb184 C 端区域肽来检查 Pb184 是否参与受精。

结果

Pb184 表达在雄性和雌性配子的表面。该抗体抑制了体外合子和动合子的形成。当蚊子吸食含有抗体的寄生虫感染血液时,在吸食后的第二天卵囊形成减少。与 Pb184 C 端区域匹配的合成生物素标记肽结合到雌性配子和雄性配子的残余体上,并抑制了体外培养系统中动合子的分化。

结论

这些结果可能有助于进一步研究疟原虫的受精机制。它们也有可能作为未来预防疟疾传播的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c2a/11246575/959b4147279d/13071_2024_6374_Fig1_HTML.jpg

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