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Shift in vacuolar to cytosolic regime of infecting Salmonella from a dual proteome perspective

By applying dual proteome profiling to Salmonella enterica serovar Typhimurium (S. Typhimurium) encounters with its epithelial host (here, S. Typhimurium infected human HeLa cells), a detailed interdependent and holistic proteomic perspective on host-pathogen interactions over the time course of inf...

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Autores principales: Fels, Ursula, Willems, Patrick, De Meyer, Margaux, Gevaert, Kris, Van Damme, Petra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10426988/
https://www.ncbi.nlm.nih.gov/pubmed/37535689
http://dx.doi.org/10.1371/journal.ppat.1011183
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author Fels, Ursula
Willems, Patrick
De Meyer, Margaux
Gevaert, Kris
Van Damme, Petra
author_facet Fels, Ursula
Willems, Patrick
De Meyer, Margaux
Gevaert, Kris
Van Damme, Petra
author_sort Fels, Ursula
collection PubMed
description By applying dual proteome profiling to Salmonella enterica serovar Typhimurium (S. Typhimurium) encounters with its epithelial host (here, S. Typhimurium infected human HeLa cells), a detailed interdependent and holistic proteomic perspective on host-pathogen interactions over the time course of infection was obtained. Data-independent acquisition (DIA)-based proteomics was found to outperform data-dependent acquisition (DDA) workflows, especially in identifying the downregulated bacterial proteome response during infection progression by permitting quantification of low abundant bacterial proteins at early times of infection when bacterial infection load is low. S. Typhimurium invasion and replication specific proteomic signatures in epithelial cells revealed interdependent host/pathogen specific responses besides pointing to putative novel infection markers and signalling responses, including regulated host proteins associated with Salmonella-modified membranes.
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spelling pubmed-104269882023-08-16 Shift in vacuolar to cytosolic regime of infecting Salmonella from a dual proteome perspective Fels, Ursula Willems, Patrick De Meyer, Margaux Gevaert, Kris Van Damme, Petra PLoS Pathog Research Article By applying dual proteome profiling to Salmonella enterica serovar Typhimurium (S. Typhimurium) encounters with its epithelial host (here, S. Typhimurium infected human HeLa cells), a detailed interdependent and holistic proteomic perspective on host-pathogen interactions over the time course of infection was obtained. Data-independent acquisition (DIA)-based proteomics was found to outperform data-dependent acquisition (DDA) workflows, especially in identifying the downregulated bacterial proteome response during infection progression by permitting quantification of low abundant bacterial proteins at early times of infection when bacterial infection load is low. S. Typhimurium invasion and replication specific proteomic signatures in epithelial cells revealed interdependent host/pathogen specific responses besides pointing to putative novel infection markers and signalling responses, including regulated host proteins associated with Salmonella-modified membranes. Public Library of Science 2023-08-03 /pmc/articles/PMC10426988/ /pubmed/37535689 http://dx.doi.org/10.1371/journal.ppat.1011183 Text en © 2023 Fels et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Fels, Ursula
Willems, Patrick
De Meyer, Margaux
Gevaert, Kris
Van Damme, Petra
Shift in vacuolar to cytosolic regime of infecting Salmonella from a dual proteome perspective
title Shift in vacuolar to cytosolic regime of infecting Salmonella from a dual proteome perspective
title_full Shift in vacuolar to cytosolic regime of infecting Salmonella from a dual proteome perspective
title_fullStr Shift in vacuolar to cytosolic regime of infecting Salmonella from a dual proteome perspective
title_full_unstemmed Shift in vacuolar to cytosolic regime of infecting Salmonella from a dual proteome perspective
title_short Shift in vacuolar to cytosolic regime of infecting Salmonella from a dual proteome perspective
title_sort shift in vacuolar to cytosolic regime of infecting salmonella from a dual proteome perspective
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10426988/
https://www.ncbi.nlm.nih.gov/pubmed/37535689
http://dx.doi.org/10.1371/journal.ppat.1011183
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