Using scRNA-seq to Identify Transcriptional Variation in the Malaria Parasite Ookinete Stage

The crossing of the mosquito midgut epithelium by the malaria parasite motile ookinete form represents the most extreme population bottleneck in the parasite life cycle and is a prime target for transmission blocking strategies. However, we have little understanding of the clonal variation that exis...

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Main Authors: Kathrin Witmer, Farah Aida Dahalan, Tom Metcalf, Arthur M. Talman, Virginia M. Howick, Mara K. N. Lawniczak
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-03-01
Series:Frontiers in Cellular and Infection Microbiology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fcimb.2021.604129/full
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spelling doaj-88890f7ac9334ac889ae2f04375cb72c2021-03-01T14:24:33ZengFrontiers Media S.A.Frontiers in Cellular and Infection Microbiology2235-29882021-03-011110.3389/fcimb.2021.604129604129Using scRNA-seq to Identify Transcriptional Variation in the Malaria Parasite Ookinete StageKathrin Witmer0Farah Aida Dahalan1Tom Metcalf2Arthur M. Talman3Arthur M. Talman4Virginia M. Howick5Virginia M. Howick6Virginia M. Howick7Mara K. N. Lawniczak8Parasites and Microbes Programme, Wellcome Sanger Institute, Hinxton, United KingdomDepartment of Life Sciences, Imperial College London, London, United KingdomParasites and Microbes Programme, Wellcome Sanger Institute, Hinxton, United KingdomParasites and Microbes Programme, Wellcome Sanger Institute, Hinxton, United KingdomMIVEGEC, IRD, CNRS, University of Montpellier, Montpellier, FranceParasites and Microbes Programme, Wellcome Sanger Institute, Hinxton, United KingdomInstitute of Biodiversity, Animal Health and Comparative Medicine, College of Medical Veterinary and Life Sciences, University of Glasgow, Glasgow, United KingdomWellcome Centre for Integrative Parasitology, College of Medical Veterinary and Life Sciences, University of Glasgow, Glasgow, United KingdomParasites and Microbes Programme, Wellcome Sanger Institute, Hinxton, United KingdomThe crossing of the mosquito midgut epithelium by the malaria parasite motile ookinete form represents the most extreme population bottleneck in the parasite life cycle and is a prime target for transmission blocking strategies. However, we have little understanding of the clonal variation that exists in a population of ookinetes in the vector, partially because the parasites are difficult to access and are found in low numbers. Within a vector, variation may result as a response to specific environmental cues or may exist independent of those cues as a potential bet-hedging strategy. Here we use single-cell RNA-seq to profile transcriptional variation in Plasmodium berghei ookinetes across different vector species, and between and within individual midguts. We then compare our results to low-input transcriptomes from individual Anopheles coluzzii midguts infected with the human malaria parasite Plasmodium falciparum. Although the vast majority of transcriptional changes in ookinetes are driven by development, we have identified candidate genes that may be responding to environmental cues or are clonally variant within a population. Our results illustrate the value of single-cell and low-input technologies in understanding clonal variation of parasite populations.https://www.frontiersin.org/articles/10.3389/fcimb.2021.604129/fullookinetePlasmodiumscRNA-seqtranscriptomicsmalariaAnopheles
collection DOAJ
language English
format Article
sources DOAJ
author Kathrin Witmer
Farah Aida Dahalan
Tom Metcalf
Arthur M. Talman
Arthur M. Talman
Virginia M. Howick
Virginia M. Howick
Virginia M. Howick
Mara K. N. Lawniczak
spellingShingle Kathrin Witmer
Farah Aida Dahalan
Tom Metcalf
Arthur M. Talman
Arthur M. Talman
Virginia M. Howick
Virginia M. Howick
Virginia M. Howick
Mara K. N. Lawniczak
Using scRNA-seq to Identify Transcriptional Variation in the Malaria Parasite Ookinete Stage
Frontiers in Cellular and Infection Microbiology
ookinete
Plasmodium
scRNA-seq
transcriptomics
malaria
Anopheles
author_facet Kathrin Witmer
Farah Aida Dahalan
Tom Metcalf
Arthur M. Talman
Arthur M. Talman
Virginia M. Howick
Virginia M. Howick
Virginia M. Howick
Mara K. N. Lawniczak
author_sort Kathrin Witmer
title Using scRNA-seq to Identify Transcriptional Variation in the Malaria Parasite Ookinete Stage
title_short Using scRNA-seq to Identify Transcriptional Variation in the Malaria Parasite Ookinete Stage
title_full Using scRNA-seq to Identify Transcriptional Variation in the Malaria Parasite Ookinete Stage
title_fullStr Using scRNA-seq to Identify Transcriptional Variation in the Malaria Parasite Ookinete Stage
title_full_unstemmed Using scRNA-seq to Identify Transcriptional Variation in the Malaria Parasite Ookinete Stage
title_sort using scrna-seq to identify transcriptional variation in the malaria parasite ookinete stage
publisher Frontiers Media S.A.
series Frontiers in Cellular and Infection Microbiology
issn 2235-2988
publishDate 2021-03-01
description The crossing of the mosquito midgut epithelium by the malaria parasite motile ookinete form represents the most extreme population bottleneck in the parasite life cycle and is a prime target for transmission blocking strategies. However, we have little understanding of the clonal variation that exists in a population of ookinetes in the vector, partially because the parasites are difficult to access and are found in low numbers. Within a vector, variation may result as a response to specific environmental cues or may exist independent of those cues as a potential bet-hedging strategy. Here we use single-cell RNA-seq to profile transcriptional variation in Plasmodium berghei ookinetes across different vector species, and between and within individual midguts. We then compare our results to low-input transcriptomes from individual Anopheles coluzzii midguts infected with the human malaria parasite Plasmodium falciparum. Although the vast majority of transcriptional changes in ookinetes are driven by development, we have identified candidate genes that may be responding to environmental cues or are clonally variant within a population. Our results illustrate the value of single-cell and low-input technologies in understanding clonal variation of parasite populations.
topic ookinete
Plasmodium
scRNA-seq
transcriptomics
malaria
Anopheles
url https://www.frontiersin.org/articles/10.3389/fcimb.2021.604129/full
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