生物
恶性疟原虫
疟疾
转录组
计算生物学
传输(电信)
向性
基因
病毒学
进化生物学
遗传学
基因表达
免疫学
计算机科学
病毒
电信
作者
Eliana Real,Virginia M. Howick,Farah A. Dahalan,Kathrin Witmer,Juliana Cudini,Clare Andradi-Brown,Joshua Blight,Mira S. Davidson,Sunil Kumar Dogga,Adam J. Reid,Jake Baum,Mara Lawniczak
标识
DOI:10.1038/s41467-021-23434-z
摘要
Abstract Malaria parasites have a complex life cycle featuring diverse developmental strategies, each uniquely adapted to navigate specific host environments. Here we use single-cell transcriptomics to illuminate gene usage across the transmission cycle of the most virulent agent of human malaria - Plasmodium falciparum . We reveal developmental trajectories associated with the colonization of the mosquito midgut and salivary glands and elucidate the transcriptional signatures of each transmissible stage. Additionally, we identify both conserved and non-conserved gene usage between human and rodent parasites, which point to both essential mechanisms in malaria transmission and species-specific adaptations potentially linked to host tropism. Together, the data presented here, which are made freely available via an interactive website, provide a fine-grained atlas that enables intensive investigation of the P. falciparum transcriptional journey. As well as providing insights into gene function across the transmission cycle, the atlas opens the door for identification of drug and vaccine targets to stop malaria transmission and thereby prevent disease.
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