Single-cell transcriptomics reveals expression profiles of Trypanosoma brucei sexual stages.


Journal

PLoS pathogens
ISSN: 1553-7374
Titre abrégé: PLoS Pathog
Pays: United States
ID NLM: 101238921

Informations de publication

Date de publication:
03 2022
Historique:
received: 01 11 2021
accepted: 06 02 2022
revised: 22 03 2022
pubmed: 8 3 2022
medline: 23 4 2022
entrez: 7 3 2022
Statut: epublish

Résumé

Early diverging lineages such as trypanosomes can provide clues to the evolution of sexual reproduction in eukaryotes. In Trypanosoma brucei, the pathogen that causes Human African Trypanosomiasis, sexual reproduction occurs in the salivary glands of the insect host, but analysis of the molecular signatures that define these sexual forms is complicated because they mingle with more numerous, mitotically-dividing developmental stages. We used single-cell RNA-sequencing (scRNAseq) to profile 388 individual trypanosomes from midgut, proventriculus, and salivary glands of infected tsetse flies allowing us to identify tissue-specific cell types. Further investigation of salivary gland parasite transcriptomes revealed fine-scale changes in gene expression over a developmental progression from putative sexual forms through metacyclics expressing variant surface glycoprotein genes. The cluster of cells potentially containing sexual forms was characterized by high level transcription of the gamete fusion protein HAP2, together with an array of surface proteins and several genes of unknown function. We linked these expression patterns to distinct morphological forms using immunofluorescence assays and reporter gene expression to demonstrate that the kinetoplastid-conserved gene Tb927.10.12080 is exclusively expressed at high levels by meiotic intermediates and gametes. Further experiments are required to establish whether this protein, currently of unknown function, plays a role in gamete formation and/or fusion.

Identifiants

pubmed: 35255094
doi: 10.1371/journal.ppat.1010346
pii: PPATHOGENS-D-21-02201
pmc: PMC8939820
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1010346

Subventions

Organisme : Biotechnology and Biological Sciences Research Council
ID : BB/R016437/1
Pays : United Kingdom
Organisme : Biotechnology and Biological Sciences Research Council
ID : BB/R010188/1
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 206194/Z/17/Z
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 220185/Z/20/Z
Pays : United Kingdom

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Virginia M Howick (VM)

Institute of Biodiversity, Animal Health, and Comparative Medicine, University of Glasgow, Glasgow, United Kingdom.
Wellcome Centre for Integrative Parasitology, University of Glasgow, Glasgow, United Kingdom.
Parasites and Microbes Programme, Wellcome Sanger Institute, Hinxton, United Kingdom.

Lori Peacock (L)

School of Biological Sciences, University of Bristol, Bristol, United Kingdom.
Bristol Veterinary School, University of Bristol, Langford, United Kingdom.

Chris Kay (C)

School of Biological Sciences, University of Bristol, Bristol, United Kingdom.

Clare Collett (C)

School of Biological Sciences, University of Bristol, Bristol, United Kingdom.

Wendy Gibson (W)

School of Biological Sciences, University of Bristol, Bristol, United Kingdom.

Mara K N Lawniczak (MKN)

Parasites and Microbes Programme, Wellcome Sanger Institute, Hinxton, United Kingdom.

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Classifications MeSH