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Host cellular unfolded protein response signaling regulates Campylobacter jejuni invasion

Campylobacter jejuni is a major cause of bacterial foodborne illness in humans worldwide. Bacterial entry into a host eukaryotic cell involves the initial steps of adherence and invasion, which generally activate several cell-signaling pathways that induce the activation of innate defense systems, w...

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Autores principales: Tentaku, Aya, Shimohata, Takaaki, Hatayama, Sho, Kido, Junko, Nguyen, Anh Quoc, Kanda, Yuna, Fukushima, Shiho, Uebanso, Takashi, Iwata, Taketoshi, Mawatari, Kazuaki, Harada, Nagakatsu, Takahashi, Akira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6188877/
https://www.ncbi.nlm.nih.gov/pubmed/30321237
http://dx.doi.org/10.1371/journal.pone.0205865
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author Tentaku, Aya
Shimohata, Takaaki
Hatayama, Sho
Kido, Junko
Nguyen, Anh Quoc
Kanda, Yuna
Fukushima, Shiho
Uebanso, Takashi
Iwata, Taketoshi
Mawatari, Kazuaki
Harada, Nagakatsu
Takahashi, Akira
author_facet Tentaku, Aya
Shimohata, Takaaki
Hatayama, Sho
Kido, Junko
Nguyen, Anh Quoc
Kanda, Yuna
Fukushima, Shiho
Uebanso, Takashi
Iwata, Taketoshi
Mawatari, Kazuaki
Harada, Nagakatsu
Takahashi, Akira
author_sort Tentaku, Aya
collection PubMed
description Campylobacter jejuni is a major cause of bacterial foodborne illness in humans worldwide. Bacterial entry into a host eukaryotic cell involves the initial steps of adherence and invasion, which generally activate several cell-signaling pathways that induce the activation of innate defense systems, which leads to the release of proinflammatory cytokines and induction of apoptosis. Recent studies have reported that the unfolded protein response (UPR), a system to clear unfolded proteins from the endoplasmic reticulum (ER), also participates in the activation of cellular defense mechanisms in response to bacterial infection. However, no study has yet investigated the role of UPR in C. jejuni infection. Hence, the aim of this study was to deduce the role of UPR signaling via induction of ER stress in the process of C. jejuni infection. The results suggest that C. jejuni infection suppresses global protein translation. Also, 12 h of C. jejuni infection induced activation of the eIF2α pathway and expression of the transcription factor CHOP. Interestingly, bacterial invasion was facilitated by knockdown of UPR-associated signaling factors and treatment with the ER stress inducers, thapsigargin and tunicamycin, decreased the invasive ability of C. jejuni. An investigation into the mechanism of UPR-mediated inhibition of C. jejuni invasion showed that UPR signaling did not affect bacterial adhesion to or survival in the host cells. Further, Salmonella Enteritidis or FITC-dextran intake were not regulated by UPR signaling. These results indicated that the effect of UPR on intracellular intake was specifically found in C. jejuni infection. These findings are the first to describe the role of UPR in C. jejuni infection and revealed the participation of a new signaling pathway in C. jejuni invasion. UPR signaling is involved in defense against the early step of C. jejuni invasion and thus presents a potential therapeutic target for the treatment of C. jejuni infection.
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spelling pubmed-61888772018-10-25 Host cellular unfolded protein response signaling regulates Campylobacter jejuni invasion Tentaku, Aya Shimohata, Takaaki Hatayama, Sho Kido, Junko Nguyen, Anh Quoc Kanda, Yuna Fukushima, Shiho Uebanso, Takashi Iwata, Taketoshi Mawatari, Kazuaki Harada, Nagakatsu Takahashi, Akira PLoS One Research Article Campylobacter jejuni is a major cause of bacterial foodborne illness in humans worldwide. Bacterial entry into a host eukaryotic cell involves the initial steps of adherence and invasion, which generally activate several cell-signaling pathways that induce the activation of innate defense systems, which leads to the release of proinflammatory cytokines and induction of apoptosis. Recent studies have reported that the unfolded protein response (UPR), a system to clear unfolded proteins from the endoplasmic reticulum (ER), also participates in the activation of cellular defense mechanisms in response to bacterial infection. However, no study has yet investigated the role of UPR in C. jejuni infection. Hence, the aim of this study was to deduce the role of UPR signaling via induction of ER stress in the process of C. jejuni infection. The results suggest that C. jejuni infection suppresses global protein translation. Also, 12 h of C. jejuni infection induced activation of the eIF2α pathway and expression of the transcription factor CHOP. Interestingly, bacterial invasion was facilitated by knockdown of UPR-associated signaling factors and treatment with the ER stress inducers, thapsigargin and tunicamycin, decreased the invasive ability of C. jejuni. An investigation into the mechanism of UPR-mediated inhibition of C. jejuni invasion showed that UPR signaling did not affect bacterial adhesion to or survival in the host cells. Further, Salmonella Enteritidis or FITC-dextran intake were not regulated by UPR signaling. These results indicated that the effect of UPR on intracellular intake was specifically found in C. jejuni infection. These findings are the first to describe the role of UPR in C. jejuni infection and revealed the participation of a new signaling pathway in C. jejuni invasion. UPR signaling is involved in defense against the early step of C. jejuni invasion and thus presents a potential therapeutic target for the treatment of C. jejuni infection. Public Library of Science 2018-10-15 /pmc/articles/PMC6188877/ /pubmed/30321237 http://dx.doi.org/10.1371/journal.pone.0205865 Text en © 2018 Tentaku et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://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
Tentaku, Aya
Shimohata, Takaaki
Hatayama, Sho
Kido, Junko
Nguyen, Anh Quoc
Kanda, Yuna
Fukushima, Shiho
Uebanso, Takashi
Iwata, Taketoshi
Mawatari, Kazuaki
Harada, Nagakatsu
Takahashi, Akira
Host cellular unfolded protein response signaling regulates Campylobacter jejuni invasion
title Host cellular unfolded protein response signaling regulates Campylobacter jejuni invasion
title_full Host cellular unfolded protein response signaling regulates Campylobacter jejuni invasion
title_fullStr Host cellular unfolded protein response signaling regulates Campylobacter jejuni invasion
title_full_unstemmed Host cellular unfolded protein response signaling regulates Campylobacter jejuni invasion
title_short Host cellular unfolded protein response signaling regulates Campylobacter jejuni invasion
title_sort host cellular unfolded protein response signaling regulates campylobacter jejuni invasion
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6188877/
https://www.ncbi.nlm.nih.gov/pubmed/30321237
http://dx.doi.org/10.1371/journal.pone.0205865
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