Gastric Infection by <i>Cronobacter sakazakii</i> : An <i>In Vitro</i> Insight

Cronobacter sakazakii , an opportunistic foodborne pathogen associated with powdered infant formula, causes severe neonatal infections, yet its interaction with gastric epithelial cells remains poorly characterized. Here, we conducted a preliminary in vitro study to evaluate early host–pathogen responses of C. sakazakii in AGS gastric epithelial cells. AGS cells were exposed to C. sakazakii ATCC 29544 at a multiplicity of infection of 100 for 2 h, and cytotoxicity and transcriptional responses were assessed by viability assay, gentamicin protection assay, and reverse transcription-quantitative polymerase chain reaction. Infection significantly reduced AGS cell viability and increased expression of bacterial virulence-associated genes ( ompA and hfq ) and host inflammatory genes ( IL-8 and NF-ƙB ) compared with mock-infected controls ( p &lt; 0.001). Gentamicin-protected recovery was consistent with bacterial entry into AGS cells, although confirmatory imaging-based analyses were not performed. These findings indicate that C. sakazakii (ATCC 29544) can elicit early cytotoxic and pro-inflammatory responses in AGS gastric epithelial cells under in vitro conditions, supporting the need for confirmatory studies in more physiologically relevant gastric study models.

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Publication Details

Journal
Foodborne Pathogens and Disease
Published
2026-06-16
DOI
https://doi.org/10.1177/15353141261461975
Primary Topic
Enterobacteriaceae and Cronobacter Research
Type
article
Field-Weighted Citation Impact
0.00
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article

Gastric Infection by Cronobacter sakazakii : An In Vitro Insight

Babak Pakbin, Susanne U. Mertens-Talcott
Foodborne Pathogens and Disease
Enterobacteriaceae and Cronobacter Research
article

Gastric Infection by Cronobacter sakazakii : An In Vitro Insight

Babak Pakbin, Susanne U. Mertens-Talcott
article en

Abstract

Cronobacter sakazakii , an opportunistic foodborne pathogen associated with powdered infant formula, causes severe neonatal infections, yet its interaction with gastric epithelial cells remains poorly characterized. Here, we conducted a preliminary in vitro study to evaluate early host–pathogen responses of C. sakazakii in AGS gastric epithelial cells. AGS cells were exposed to C. sakazakii ATCC 29544 at a multiplicity of infection of 100 for 2 h, and cytotoxicity and transcriptional responses were assessed by viability assay, gentamicin protection assay, and reverse transcription-quantitative polymerase chain reaction. Infection significantly reduced AGS cell viability and increased expression of bacterial virulence-associated genes ( ompA and hfq ) and host inflammatory genes ( IL-8 and NF-ƙB ) compared with mock-infected controls ( p &lt; 0.001). Gentamicin-protected recovery was consistent with bacterial entry into AGS cells, although confirmatory imaging-based analyses were not performed. These findings indicate that C. sakazakii (ATCC 29544) can elicit early cytotoxic and pro-inflammatory responses in AGS gastric epithelial cells under in vitro conditions, supporting the need for confirmatory studies in more physiologically relevant gastric study models.

Foodborne Pathogens and Disease
Texas A&M University (US)
Openalex Percentile: Top 7%
Enterobacteriaceae and Cronobacter Research
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