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ARID 调控恶性疟原虫雄性配子体发生和雌性育性,对寄生虫向蚊子传播至关重要。

ARID Regulates P. falciparum Malaria Parasite Male Gametogenesis and Female Fertility and Is Critical for Parasite Transmission to the Mosquito Vector.

机构信息

Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, Washington, USA.

Molecular Botany Lab, Swami Devanand Post Graduate College, Math-Lar, Deoria, Uttar Pradesh, India.

出版信息

mBio. 2022 Jun 28;13(3):e0057822. doi: 10.1128/mbio.00578-22. Epub 2022 May 31.

DOI:10.1128/mbio.00578-22
PMID:35638735
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9239086/
Abstract

Sexual reproduction of Plasmodium falciparum parasites is critical to the spread of malaria in the human population. The factors that regulate gene expression underlying formation of fertilization-competent gametes, however, remain unknown. Here, we report that P. falciparum expresses a protein with an AT-rich interaction domain (ARID) which, in other organisms, is part of chromatin remodeling complexes. P. falciparum ARID (ARID) localized to the parasite nucleus and is critical for the formation of male gametes and fertility of female gametes. ARID gene deletion () gametocytes showed downregulation of gene expression important for gametogenesis, antigenic variation, and cell signaling and for parasite development in the mosquito. Our study identifies ARID as a critical nuclear protein involved in regulating the gene expression landscape of mature gametocytes. This establishes fertility and also prepares the parasite for postfertilization events that are essential for infection of the mosquito vector. Successful completion of the life cycle requires formation of mature gametocytes and their uptake by the female mosquito vector in an infected blood meal. Inside the mosquito midgut the parasite undergoes gametogenesis and sexual reproduction. In the present study, we demonstrate that ARID is essential for male gametogenesis and female fertility and, thereby, transmission to the mosquito vector. ARID possibly regulates the chromatin landscape of stage V gametocytes and targeting ARID function may provide new avenues into designing interventions to prevent malaria transmission.

摘要

疟原虫寄生虫的有性繁殖对于疟疾在人类中的传播至关重要。然而,调节形成受精能力配子的基因表达的因素仍然未知。在这里,我们报告疟原虫表达一种具有富含 AT 的相互作用结构域(ARID)的蛋白质,在其他生物体中,它是染色质重塑复合物的一部分。疟原虫 ARID(ARID)定位于寄生虫核内,对于雄性配子体的形成和雌性配子体的育性至关重要。ARID 基因缺失()配子体表现出与配子发生、抗原变异和细胞信号传导以及寄生虫在蚊子中的发育有关的重要基因表达下调。我们的研究将 ARID 鉴定为一种参与调节成熟配子体基因表达图谱的关键核蛋白。这确立了育性,并为受精后事件做好准备,这些事件对于感染蚊子媒介至关重要。成功完成生命周期需要形成成熟的配子体并被感染的血液餐中的雌性蚊子载体吸收。在蚊子的中肠中,寄生虫经历配子发生和有性繁殖。在本研究中,我们证明 ARID 对于雄性配子体发生和雌性育性至关重要,从而传播给蚊子媒介。ARID 可能调节阶段 V 配子体的染色质景观,靶向 ARID 功能可能为设计预防疟疾传播的干预措施提供新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b514/9239086/61093cbc3ba5/mbio.00578-22-f006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b514/9239086/f3eafd81e366/mbio.00578-22-f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b514/9239086/c403312505f2/mbio.00578-22-f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b514/9239086/817495420966/mbio.00578-22-f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b514/9239086/c37a4880f9ac/mbio.00578-22-f004.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b514/9239086/61093cbc3ba5/mbio.00578-22-f006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b514/9239086/f3eafd81e366/mbio.00578-22-f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b514/9239086/c403312505f2/mbio.00578-22-f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b514/9239086/817495420966/mbio.00578-22-f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b514/9239086/c37a4880f9ac/mbio.00578-22-f004.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b514/9239086/61093cbc3ba5/mbio.00578-22-f006.jpg

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