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2023 (English)In: Microbiology Spectrum, E-ISSN 2165-0497, Vol. 11, no 2, article id e03671-22Article in journal (Refereed) Published
Abstract [en]
Malaria inflicts the highest rate of morbidity and mortality among the vector-borne diseases. The dramatic bottleneck of parasite numbers that occurs in the gut of the obligatory mosquito vector provides a promising target for novel control strategies. Using single-cell transcriptomics, we analyzed Plasmodium falciparum development in the mosquito gut, from unfertilized female gametes through the first 20 h after blood feeding, including the zygote and ookinete stages. This study revealed the temporal gene expression of the ApiAP2 family of transcription factors and of parasite stress genes in response to the harsh environment of the mosquito midgut. Further, employing structural protein prediction analyses, we found several upregulated genes predicted to encode intrinsically disordered proteins (IDPs), a category of proteins known for their importance in regulation of transcription, translation, and protein-protein interactions. IDPs are known for their antigenic properties and may serve as suitable targets for antibody- or peptide-based transmission suppression strategies. In total, this study uncovers the P. falciparum transcriptome from early to late parasite development in the mosquito midgut, inside its natural vector, which provides an important resource for future malaria transmission-blocking initiatives.
Keywords
malaria, Plasmodium falciparum, mosquito midgut, scRNA-seq, single cell, stage transition, transmission
National Category
Cell Biology Bioinformatics and Computational Biology Microbiology
Research subject
Molecular Bioscience
Identifiers
urn:nbn:se:su:diva-215086 (URN)10.1128/spectrum.03671-22 (DOI)000939731800001 ()36847501 (PubMedID)2-s2.0-85153879865 (Scopus ID)
Funder
NIH (National Institutes of Health), R01AI031478Science for Life Laboratory, SciLifeLabSwedish Research Council, VR-N/TSwedish Research Council, SFO programSwedish Research Council, 2021-06602
2023-02-282023-02-282025-02-05Bibliographically approved