Slow growing behavior in African trypanosomes during adipose tissue colonization
BRINGAUD, Frederic
Centre de résonance magnétique des systèmes biologiques [CRMSB]
Microbiologie Fondamentale et Pathogénicité [MFP]
< Réduire
Centre de résonance magnétique des systèmes biologiques [CRMSB]
Microbiologie Fondamentale et Pathogénicité [MFP]
Langue
EN
Article de revue
Ce document a été publié dans
Nature Communications. 2022, vol. 13, n° 1, p. 7548
Résumé en anglais
Abstract When Trypanosoma brucei parasites, the causative agent of sleeping sickness, colonize the adipose tissue, they rewire gene expression. Whether this adaptation affects population behavior and disease treatment ...Lire la suite >
Abstract When Trypanosoma brucei parasites, the causative agent of sleeping sickness, colonize the adipose tissue, they rewire gene expression. Whether this adaptation affects population behavior and disease treatment remained unknown. By using a mathematical model, we estimate that the population of adipose tissue forms (ATFs) proliferates slower than blood parasites. Analysis of the ATFs proteome, measurement of protein synthesis and proliferation rates confirm that the ATFs divide on average every 12 h, instead of 6 h in the blood. Importantly, the population of ATFs is heterogeneous with parasites doubling times ranging between 5 h and 35 h. Slow-proliferating parasites remain capable of reverting to the fast proliferation profile in blood conditions. Intravital imaging shows that ATFs are refractory to drug treatment. We propose that in adipose tissue, a subpopulation of T. brucei parasites acquire a slow growing behavior, which contributes to disease chronicity and treatment failure.< Réduire
Project ANR
Alliance française contre les maladies parasitaires - ANR-11-LABX-0024
Interactions métaboliques entre les adipocytes et les trypanosomes, un nouveau paradigme pour les trypanosomoses - ANR-19-CE15-0004
Interactions métaboliques entre les adipocytes et les trypanosomes, un nouveau paradigme pour les trypanosomoses - ANR-19-CE15-0004