Ovomucin and its hydrolysates differentially influenced colitis severity in Citrobacter rodentium-infected mice

Abstract

Egg white protein ovomucin and its hydrolysates were previously reported to exert anti-inflammatory and anti-adhesive activities. However, their potential to regulate pathogen colonization and disease severity has not been fully characterized. To investigate the effects of ovomucin (OVM) and its hydrolysates including ovomucin-protex 26L (OP) and pepsin/pancreatin (OPP) on host resistance to pathogen infection, a well-documented colitis model in mice for attaching and effacing E. coli pathogens, Citrobacter rodentium, was used in the current study. C57Bl/6J female mice were fed on a basal diet supplemented with OVM or the hydrolysates for 3 weeks prior to C. rodentium challenge with the dietary treatments continued for seven days. Body weight was not affected throughout the experimental period. OP supplementation resulted in lower (P < 0.05) pathogen loads at 7 dpi. Attenuated colitis severity was shown in mice that received OVM and OP as indicated by reduced colonic pathological scores and pro-inflammatory response compared with the infected control group. In contrast, OPP consumption resulted in enhanced C. rodentium colonization and disease severity. Notably, reduced microbial diversity indices of the gut microbiota was observed in the OPP-supplemented mice compared with OVM- and OP-supplemented groups. This study showed the potential of OVM and OP to alleviate the severity of colitis induced by infection, while also suggested the opposite outcome of OPP in mitigating enteric infection.

Supplementary files

Article information

Article type
Paper
Submitted
18 Apr 2024
Accepted
03 Jul 2024
First published
18 Jul 2024

Food Funct., 2024, Accepted Manuscript

Ovomucin and its hydrolysates differentially influenced colitis severity in Citrobacter rodentium-infected mice

X. Bao, T. Ju, S. Tollenaar, C. Sergi, B. P. Willing and J. P. Wu, Food Funct., 2024, Accepted Manuscript , DOI: 10.1039/D4FO01813C

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