Trypanosoma cruzi amastigotes that persist in the colon during chronic stage murine infections have a reduced replication rate

Chronic Trypanosoma cruzi infections are typically lifelong, with small numbers of parasites surviving in restricted tissue sites, which include the gastrointestinal tract. There is considerable debate about the replicative status of these persistent parasites and whether there is a role for dormanc...

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Main Authors: Alexander I. Ward, Francisco Olmo, Richard L. Atherton, Martin C. Taylor, John M. Kelly
Format: Article
Language:English
Published: The Royal Society 2020-12-01
Series:Open Biology
Subjects:
Online Access:https://royalsocietypublishing.org/doi/pdf/10.1098/rsob.200261
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spelling doaj-71b231c34d734581ac7deef288c718cf2021-01-28T15:12:22ZengThe Royal SocietyOpen Biology2046-24412020-12-01101210.1098/rsob.200261200261Trypanosoma cruzi amastigotes that persist in the colon during chronic stage murine infections have a reduced replication rateAlexander I. WardFrancisco OlmoRichard L. AthertonMartin C. TaylorJohn M. KellyChronic Trypanosoma cruzi infections are typically lifelong, with small numbers of parasites surviving in restricted tissue sites, which include the gastrointestinal tract. There is considerable debate about the replicative status of these persistent parasites and whether there is a role for dormancy in long-term infection. Here, we investigated T. cruzi proliferation in the colon of chronically infected mice using 5-ethynyl-2′deoxyuridine incorporation into DNA to provide ‘snapshots’ of parasite replication status. Highly sensitive imaging of the extremely rare infection foci, at single-cell resolution, revealed that parasites are three times more likely to be in S-phase during the acute stage than during the chronic stage. By implication, chronic infections of the colon are associated with a reduced rate of parasite replication. Despite this, very few host cells survived infection for more than 14 days, suggesting that T. cruzi persistence continues to involve regular cycles of replication, host cell lysis and re-infection. We could find no evidence for wide-spread dormancy in parasites that persist in this tissue reservoir.https://royalsocietypublishing.org/doi/pdf/10.1098/rsob.200261trypanosoma cruzichronic infectiondormancyproliferationreplication
collection DOAJ
language English
format Article
sources DOAJ
author Alexander I. Ward
Francisco Olmo
Richard L. Atherton
Martin C. Taylor
John M. Kelly
spellingShingle Alexander I. Ward
Francisco Olmo
Richard L. Atherton
Martin C. Taylor
John M. Kelly
Trypanosoma cruzi amastigotes that persist in the colon during chronic stage murine infections have a reduced replication rate
Open Biology
trypanosoma cruzi
chronic infection
dormancy
proliferation
replication
author_facet Alexander I. Ward
Francisco Olmo
Richard L. Atherton
Martin C. Taylor
John M. Kelly
author_sort Alexander I. Ward
title Trypanosoma cruzi amastigotes that persist in the colon during chronic stage murine infections have a reduced replication rate
title_short Trypanosoma cruzi amastigotes that persist in the colon during chronic stage murine infections have a reduced replication rate
title_full Trypanosoma cruzi amastigotes that persist in the colon during chronic stage murine infections have a reduced replication rate
title_fullStr Trypanosoma cruzi amastigotes that persist in the colon during chronic stage murine infections have a reduced replication rate
title_full_unstemmed Trypanosoma cruzi amastigotes that persist in the colon during chronic stage murine infections have a reduced replication rate
title_sort trypanosoma cruzi amastigotes that persist in the colon during chronic stage murine infections have a reduced replication rate
publisher The Royal Society
series Open Biology
issn 2046-2441
publishDate 2020-12-01
description Chronic Trypanosoma cruzi infections are typically lifelong, with small numbers of parasites surviving in restricted tissue sites, which include the gastrointestinal tract. There is considerable debate about the replicative status of these persistent parasites and whether there is a role for dormancy in long-term infection. Here, we investigated T. cruzi proliferation in the colon of chronically infected mice using 5-ethynyl-2′deoxyuridine incorporation into DNA to provide ‘snapshots’ of parasite replication status. Highly sensitive imaging of the extremely rare infection foci, at single-cell resolution, revealed that parasites are three times more likely to be in S-phase during the acute stage than during the chronic stage. By implication, chronic infections of the colon are associated with a reduced rate of parasite replication. Despite this, very few host cells survived infection for more than 14 days, suggesting that T. cruzi persistence continues to involve regular cycles of replication, host cell lysis and re-infection. We could find no evidence for wide-spread dormancy in parasites that persist in this tissue reservoir.
topic trypanosoma cruzi
chronic infection
dormancy
proliferation
replication
url https://royalsocietypublishing.org/doi/pdf/10.1098/rsob.200261
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