Campylobacter jejuni Modulates Reactive Oxygen Species Production and NADPH Oxidase 1 Expression in Human Intestinal Epithelial Cells

Campylobacter jejuni is the major bacterial cause of foodborne gastroenteritis worldwide. Mechanistically, how this pathogen interacts with intrinsic defence machinery of human intestinal epithelial cells (IECs) remains elusive. To address this, we investigated how C. jejuni counteracts the intracel...

Full description

Bibliographic Details
Main Authors: Geunhye Hong, Cadi Davies, Zahra Omole, Janie Liaw, Anna D. Grabowska, Barbara Canonico, Nicolae Corcionivoschi, Brendan W. Wren, Nick Dorrell, Abdi Elmi, Ozan Gundogdu
Format: Article
Language:English
Published: Hindawi-Wiley 2023-01-01
Series:Cellular Microbiology
Online Access:http://dx.doi.org/10.1155/2023/3286330
_version_ 1811165468626518016
author Geunhye Hong
Cadi Davies
Zahra Omole
Janie Liaw
Anna D. Grabowska
Barbara Canonico
Nicolae Corcionivoschi
Brendan W. Wren
Nick Dorrell
Abdi Elmi
Ozan Gundogdu
author_facet Geunhye Hong
Cadi Davies
Zahra Omole
Janie Liaw
Anna D. Grabowska
Barbara Canonico
Nicolae Corcionivoschi
Brendan W. Wren
Nick Dorrell
Abdi Elmi
Ozan Gundogdu
author_sort Geunhye Hong
collection DOAJ
description Campylobacter jejuni is the major bacterial cause of foodborne gastroenteritis worldwide. Mechanistically, how this pathogen interacts with intrinsic defence machinery of human intestinal epithelial cells (IECs) remains elusive. To address this, we investigated how C. jejuni counteracts the intracellular and extracellular reactive oxygen species (ROS) in IECs. Our work shows that C. jejuni differentially regulates intracellular and extracellular ROS production in human T84 and Caco-2 cells. C. jejuni downregulates the transcription and translation of nicotinamide adenine dinucleotide phosphate (NAPDH) oxidase (NOX1), a key ROS-generating enzyme in IECs and antioxidant defence genes CAT and SOD1. Furthermore, inhibition of NOX1 by diphenylene iodonium (DPI) and siRNA reduced C. jejuni ability to interact, invade, and intracellularly survive within T84 and Caco-2 cells. Collectively, these findings provide mechanistic insight into how C. jejuni modulates the IEC defence machinery.
first_indexed 2024-04-10T15:37:37Z
format Article
id doaj.art-44ad18a07c584fa8ba09f381bec1ebca
institution Directory Open Access Journal
issn 1462-5822
language English
last_indexed 2024-04-10T15:37:37Z
publishDate 2023-01-01
publisher Hindawi-Wiley
record_format Article
series Cellular Microbiology
spelling doaj.art-44ad18a07c584fa8ba09f381bec1ebca2023-02-13T01:08:47ZengHindawi-WileyCellular Microbiology1462-58222023-01-01202310.1155/2023/3286330Campylobacter jejuni Modulates Reactive Oxygen Species Production and NADPH Oxidase 1 Expression in Human Intestinal Epithelial CellsGeunhye Hong0Cadi Davies1Zahra Omole2Janie Liaw3Anna D. Grabowska4Barbara Canonico5Nicolae Corcionivoschi6Brendan W. Wren7Nick Dorrell8Abdi Elmi9Ozan Gundogdu10Faculty of Infectious and Tropical DiseasesFaculty of Infectious and Tropical DiseasesFaculty of Infectious and Tropical DiseasesFaculty of Infectious and Tropical DiseasesDepartment of BiophysicsDepartment of Biomolecular SciencesBacteriology BranchFaculty of Infectious and Tropical DiseasesFaculty of Infectious and Tropical DiseasesFaculty of Infectious and Tropical DiseasesFaculty of Infectious and Tropical DiseasesCampylobacter jejuni is the major bacterial cause of foodborne gastroenteritis worldwide. Mechanistically, how this pathogen interacts with intrinsic defence machinery of human intestinal epithelial cells (IECs) remains elusive. To address this, we investigated how C. jejuni counteracts the intracellular and extracellular reactive oxygen species (ROS) in IECs. Our work shows that C. jejuni differentially regulates intracellular and extracellular ROS production in human T84 and Caco-2 cells. C. jejuni downregulates the transcription and translation of nicotinamide adenine dinucleotide phosphate (NAPDH) oxidase (NOX1), a key ROS-generating enzyme in IECs and antioxidant defence genes CAT and SOD1. Furthermore, inhibition of NOX1 by diphenylene iodonium (DPI) and siRNA reduced C. jejuni ability to interact, invade, and intracellularly survive within T84 and Caco-2 cells. Collectively, these findings provide mechanistic insight into how C. jejuni modulates the IEC defence machinery.http://dx.doi.org/10.1155/2023/3286330
spellingShingle Geunhye Hong
Cadi Davies
Zahra Omole
Janie Liaw
Anna D. Grabowska
Barbara Canonico
Nicolae Corcionivoschi
Brendan W. Wren
Nick Dorrell
Abdi Elmi
Ozan Gundogdu
Campylobacter jejuni Modulates Reactive Oxygen Species Production and NADPH Oxidase 1 Expression in Human Intestinal Epithelial Cells
Cellular Microbiology
title Campylobacter jejuni Modulates Reactive Oxygen Species Production and NADPH Oxidase 1 Expression in Human Intestinal Epithelial Cells
title_full Campylobacter jejuni Modulates Reactive Oxygen Species Production and NADPH Oxidase 1 Expression in Human Intestinal Epithelial Cells
title_fullStr Campylobacter jejuni Modulates Reactive Oxygen Species Production and NADPH Oxidase 1 Expression in Human Intestinal Epithelial Cells
title_full_unstemmed Campylobacter jejuni Modulates Reactive Oxygen Species Production and NADPH Oxidase 1 Expression in Human Intestinal Epithelial Cells
title_short Campylobacter jejuni Modulates Reactive Oxygen Species Production and NADPH Oxidase 1 Expression in Human Intestinal Epithelial Cells
title_sort campylobacter jejuni modulates reactive oxygen species production and nadph oxidase 1 expression in human intestinal epithelial cells
url http://dx.doi.org/10.1155/2023/3286330
work_keys_str_mv AT geunhyehong campylobacterjejunimodulatesreactiveoxygenspeciesproductionandnadphoxidase1expressioninhumanintestinalepithelialcells
AT cadidavies campylobacterjejunimodulatesreactiveoxygenspeciesproductionandnadphoxidase1expressioninhumanintestinalepithelialcells
AT zahraomole campylobacterjejunimodulatesreactiveoxygenspeciesproductionandnadphoxidase1expressioninhumanintestinalepithelialcells
AT janieliaw campylobacterjejunimodulatesreactiveoxygenspeciesproductionandnadphoxidase1expressioninhumanintestinalepithelialcells
AT annadgrabowska campylobacterjejunimodulatesreactiveoxygenspeciesproductionandnadphoxidase1expressioninhumanintestinalepithelialcells
AT barbaracanonico campylobacterjejunimodulatesreactiveoxygenspeciesproductionandnadphoxidase1expressioninhumanintestinalepithelialcells
AT nicolaecorcionivoschi campylobacterjejunimodulatesreactiveoxygenspeciesproductionandnadphoxidase1expressioninhumanintestinalepithelialcells
AT brendanwwren campylobacterjejunimodulatesreactiveoxygenspeciesproductionandnadphoxidase1expressioninhumanintestinalepithelialcells
AT nickdorrell campylobacterjejunimodulatesreactiveoxygenspeciesproductionandnadphoxidase1expressioninhumanintestinalepithelialcells
AT abdielmi campylobacterjejunimodulatesreactiveoxygenspeciesproductionandnadphoxidase1expressioninhumanintestinalepithelialcells
AT ozangundogdu campylobacterjejunimodulatesreactiveoxygenspeciesproductionandnadphoxidase1expressioninhumanintestinalepithelialcells