Abstract

Bifidobacterium pseudocatenulatum LI09 could protect rats from D-galactosamine- (D-GalN-) induced liver injury. However, individual difference in the protective effects of LI09 on the liver injury remains poorly understood. The present study is aimed at determining the multiple intestinal bacteria associated with the better protective effect of LI09 against D-GalN-induced rat liver injury. Two rat cohorts, i.e., the nonsevere and severe cohorts, were divided based on their liver injury severity. Higher level of ALB and lower levels of ALT, AST, TBA, TB, IL-5, and MIP-3α were determined in the nonsevere cohort than the severe cohort. The alpha diversity indices (i.e., observed species, Shannon, and Pielou indices) did not yield significant differences between the intestinal microbiota of the nonsevere and severe cohorts. The intestinal microbiota composition was different between the two cohorts. Ten phylotypes assigned to Bacteroides, Clostridia_UCG-014, Clostridium Lachnospiraceae, Lachnospiraceae_NK4A136, and Parabacteroides were closely associated with the nonsevere cohort, among which, ASV8_Lachnospiraceae_NK4A136 was the most associated one. At the structure level, two groups of phylotypes with most correlations were determined in the intestinal microbiota networks of the two cohorts. Among them, ASV135_Lachnospiraceae_NK4A136 was the most powerful gatekeeper in the microbiota network of the nonsevere cohort. In conclusion, some intestinal bacteria, e.g., Lachnospiraceae_NK4A136, Parabacteroides, and Clostridium, were associated with the better protective effect of LI09 against D-GalN-induced rat liver injury. They were likely to enhance the effectiveness of LI09, and their clinical application deserves further investigation.

Highlights

  • Liver injury could result in critical illness and even mortality in human beings [1, 2]

  • B. pseudocatenulatum LI09 has been determined with protective effects against D-GalN-induced liver injury in rats [16]

  • Individual difference was determined in the protective effects of LI09 on D-GalN-induced rat liver injury based on the Ishak score results

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Summary

Introduction

Liver injury could result in critical illness and even mortality in human beings [1, 2]. The progression of liver injury is associated with the alterations of the gut microbiota [3, 4]. A variety of materials and products are capable of preventing liver diseases via modulating the gut microbiota in the individuals or animal models [5,6,7,8], while some alternative factors, e.g., hormone, were associated with the prevention of liver diseases [9]. Lactobacillus buchneri TCP016 could alleviate the liver injury induced by LPS and D-galactosamine (D-GalN) via reshaping the intestinal microbiota [11]. Pediococcus pentosaceus PP04 was capable of modulating the gut inflammation and intestinal microbiota to relieve the mice liver injury induced by high-fat diet [12]. Bifidobacterium longum LC67 and Lactobacillus plantarum LC27 could restore the disturbance of gut microbiota in mice to attenuate the liver damage induced by 2,4,6-trinitrobenzesulfonic acid [13]

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