Investigation of Campylobacter concisus gastric epithelial pathogenicity using AGS cells
is an oral bacterium. Recent studies suggest that may be involved in human gastric diseases. The mechanisms, however, by which causes human gastric diseases have not been investigated. Here we examined the gastric epithelial pathogenicity of using a cell culture model. Six strains and the human gast...
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Published in | Frontiers in microbiology Vol. 14; p. 1289549 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Media S.A
11.01.2024
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Subjects | |
Online Access | Get full text |
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Summary: | is an oral bacterium. Recent studies suggest that
may be involved in human gastric diseases. The mechanisms, however, by which
causes human gastric diseases have not been investigated. Here we examined the gastric epithelial pathogenicity of
using a cell culture model. Six
strains and the human gastric epithelial cell line AGS cells were used. IL-8 produced by AGS cells after incubation with
was measured using enzyme-linked immunosorbent assay (ELISA), and AGS cell apoptosis was determined by caspase 3/7 activities. The effects of
on actin arrangement in AGS cells was determined using fluorescence staining. The effects of
on global gene expression in AGS cells was determined by transcriptomic analysis and quantitative real-time PCR (qRT-PCR). The role of the upregulated
gene in gastric cancer survival was assessed using the Kaplan-Meier method.
induced production of IL-8 by AGS cells with strain variation. Significantly increased caspase 3/7 activities were observed in AGS cells incubated with
strains when compared to AGS cells without bacteria.
induced actin re-arrangement in AGS cells.
upregulated 30 genes in AGS cells and the upregulation of
gene was confirmed by qRT-PCR. The Kaplan-Meier analysis showed that upregulation of
gene is associated with worse survival in gastric cancer patients. Our findings suggest that
may play a role in gastric inflammation and the progression of gastric cancer. Further investigation in clinical studies is warranted. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Edited by: Stuart A. Thompson, Augusta University, United States Reviewed by: Sankarasubramanian Jagadesan, University of Nebraska Medical Center, United States Mohsina Huq, Qassim University, Saudi Arabia |
ISSN: | 1664-302X 1664-302X |
DOI: | 10.3389/fmicb.2023.1289549 |