Dépôt numérique
RECHERCHER

Transcriptional profiling of macrophages reveals distinct parasite stage-driven signatures during early infection by Leishmania donovani

Téléchargements

Téléchargements par mois depuis la dernière année

Plus de statistiques...

Chaparro, Visnu; Graber, Tyson; Alain, Tommy et Jaramillo, Maritza ORCID logoORCID: https://orcid.org/0000-0002-1910-5684 (2022). Transcriptional profiling of macrophages reveals distinct parasite stage-driven signatures during early infection by Leishmania donovani Scientific Reports , vol. 12 , nº 6369. pp. 1-13. DOI: 10.1038/s41598-022-10317-6.

[thumbnail of Transcriptional profiling of macrophages reveals distinct parasite stage-driven signatures during early infection by Leishmania donovani.pdf]
Prévisualisation
PDF - Version publiée
Disponible sous licence Creative Commons Attribution.

Télécharger (1MB) | Prévisualisation

Résumé

Macrophages undergo swift changes in mRNA abundance upon pathogen invasion. Herein we describe early remodelling of the macrophage transcriptome during infection by amastigotes or promastigotes of Leishmania donovani. Approximately 10-16% of host mRNAs were differentially modulated in L. donovani-infected macrophages when compared to uninfected controls. This response was partially stage-specific as a third of changes in mRNA abundance were either exclusively driven by one of the parasite forms or significantly different between them. Gene ontology analyses identified categories associated with immune functions (e.g. antigen presentation and leukocyte activation) among significantly downregulated mRNAs during amastigote infection while cytoprotective-related categories (e.g. DNA repair and apoptosis inhibition) were enriched in upregulated transcripts. Interestingly a combination of upregulated (e.g. cellular response to IFNβ) and repressed (e.g. leukocyte activation, chemotaxis) immune-related transcripts were overrepresented in the promastigote-infected dataset. In addition, Ingenuity Pathway Analysis (IPA) associated specific mRNA subsets with a number of upstream transcriptional regulators predicted to be modulated in macrophages infected with L. donovani amastigotes (e.g. STAT1 inhibition) or promastigotes (e.g. NRF2, IRF3, and IRF7 activation). Overall, our results indicate that early parasite stage-driven transcriptional remodelling in macrophages contributes to orchestrate both protective and deleterious host cell responses during L. donovani infection.

Type de document: Article
Mots-clés libres: Parasitology, Transcriptomics, Gene regulation in immune cells, Immune evasion, Infection
Centre: Centre INRS-Institut Armand Frappier
Date de dépôt: 10 juill. 2022 14:13
Dernière modification: 10 juill. 2022 14:13
URI: https://espace.inrs.ca/id/eprint/12749

Gestion Actions (Identification requise)

Modifier la notice Modifier la notice