A Putative Plasmodium RNA-Binding Protein Plays a Critical Role in Female Gamete Fertility and Parasite Transmission to the Mosquito Vector

sexual stage gametocytes are critical for parasite transmission from the human host to the mosquito vector. Mature gametocytes generate fertile male (micro-) or female (macro-) gametes upon activation inside the mosquito midgut. While a number of parasite genes have been described that are critical...

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Veröffentlicht in:Frontiers in cell and developmental biology 2022-04, Vol.10, p.825247
Hauptverfasser: Kumar, Sudhir, Abatiyow, Biley A, Haile, Meseret T, Oualim, Kenza M Z, Leeb, Amanda S, Vaughan, Ashley M, Kappe, Stefan H I
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Sprache:eng
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Zusammenfassung:sexual stage gametocytes are critical for parasite transmission from the human host to the mosquito vector. Mature gametocytes generate fertile male (micro-) or female (macro-) gametes upon activation inside the mosquito midgut. While a number of parasite genes have been described that are critical for gametogenesis and fertility, no parasite gene has been shown to have a unique function in macrogametes. The genome of encodes numerous RNA-binding proteins. We identified a novel protein containing a putative RNA-binding domain, which we named Macrogamete-Contributed Factor Essential for Transmission (MaCFET). This protein is expressed in the asexual and sexual stages. Parasites that carry a deletion of ( ), developed normally as asexual stages, indicating that its function is not essential for the asexual proliferation of the parasite . Furthermore, male and female gametocytes developed normally and underwent activation to form microgametes and macrogametes. However, by utilizing genetic crosses, we demonstrate that parasites suffer a complete female-specific defect in successful fertilization. Therefore, MaCFET is a critical female-contributed factor for parasite transmission to the mosquito. Based on its putative RNA-binding properties, MaCFET might be in involved in the regulation of mRNAs that encode female-specific functions for fertilization or female-contributed factors needed post fertilization.
ISSN:2296-634X
2296-634X
DOI:10.3389/fcell.2022.825247