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...
Main Authors: | , , , , |
---|---|
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 |
id |
doaj-71b231c34d734581ac7deef288c718cf |
---|---|
record_format |
Article |
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 |
work_keys_str_mv |
AT alexanderiward trypanosomacruziamastigotesthatpersistinthecolonduringchronicstagemurineinfectionshaveareducedreplicationrate AT franciscoolmo trypanosomacruziamastigotesthatpersistinthecolonduringchronicstagemurineinfectionshaveareducedreplicationrate AT richardlatherton trypanosomacruziamastigotesthatpersistinthecolonduringchronicstagemurineinfectionshaveareducedreplicationrate AT martinctaylor trypanosomacruziamastigotesthatpersistinthecolonduringchronicstagemurineinfectionshaveareducedreplicationrate AT johnmkelly trypanosomacruziamastigotesthatpersistinthecolonduringchronicstagemurineinfectionshaveareducedreplicationrate |
_version_ |
1724319634277007360 |