Abstract

Heat shock proteins (HSPs) are a set of highly conserved proteins that can serve as intestinal gate keepers in gut homeostasis. Here, effects of a probiotic, Lactobacillus rhamnosus GG (LGG), and two novel porcine isolates, Lactobacillus johnsonii strain P47-HY and Lactobacillus reuteri strain P43-HUV, on cytoprotective HSP expression and gut barrier function, were investigated in a porcine IPEC-J2 intestinal epithelial cell line model. The IPEC-J2 cells polarized on a permeable filter exhibited villus-like cell phenotype with development of apical microvilli. Western blot analysis detected HSP expression in IPEC-J2 and revealed that L. johnsonii and L. reuteri strains were able to significantly induce HSP27, despite high basal expression in IPEC-J2, whereas LGG did not. For HSP72, only the supernatant of L. reuteri induced the expression, which was comparable to the heat shock treatment, which indicated that HSP72 expression was more stimulus specific. The protective effect of lactobacilli was further studied in IPEC-J2 under an enterotoxigenic Escherichia coli (ETEC) challenge. ETEC caused intestinal barrier destruction, as reflected by loss of cell–cell contact, reduced IPEC-J2 cell viability and transepithelial electrical resistance, and disruption of tight junction protein zonula occludens-1. In contrast, the L. reuteri treatment substantially counteracted these detrimental effects and preserved the barrier function. L. johnsonii and LGG also achieved barrier protection, partly by directly inhibiting ETEC attachment. Together, the results indicate that specific strains of Lactobacillus can enhance gut barrier function through cytoprotective HSP induction and fortify the cell protection against ETEC challenge through tight junction protein modulation and direct interaction with pathogens.

Highlights

  • Control of intestinal disorders in newborns is crucial as they are highly susceptible to pathogens, such as enterotoxigenic Escherichia coli (ETEC)

  • The results indicate that specific strains of Lactobacillus can enhance gut barrier function through cytoprotective Heat shock proteins (HSPs) induction and fortify the cell protection against ETEC challenge through tight junction protein modulation and direct interaction with pathogens

  • Twelve hours of incubation with bacteria showed that the survival of IPEC-J2 cells was partly affected, an effect most likely caused by bacterial growth

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Summary

Introduction

Control of intestinal disorders in newborns is crucial as they are highly susceptible to pathogens, such as enterotoxigenic Escherichia coli (ETEC). The pathogenesis of ETEC starts with bacterial attachment to the host small intestinal epithelium cells (IECs), followed by production of heat-labile and heat-stable enterotoxins. These toxins facilitate more intimate pathogen colonization, disrupt the tight junction (TJ) structure of the mucosal barrier, and result in a ‘leaky’ gut. Physiological Reports published by Wiley Periodicals, Inc. on behalf of the American Physiological Society and The Physiological Society.

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