LPS-Induced Liver Injury of Magang Geese through Toll-like Receptor and MAPK Signaling Pathway

Bingxin Li; Longsheng Hong; Yindan Luo; Bingqi Zhang; Ziyu Yu; Wanyan Li; Nan Cao; Yunmao Huang; Danning Xu; Yugu Li; Yunbo Tian

doi:10.3390/ani13010127

LPS-Induced Liver Injury of Magang Geese through Toll-like Receptor and MAPK Signaling Pathway

Animals (Basel). 2022 Dec 28;13(1):127. doi: 10.3390/ani13010127.

Authors

Bingxin Li^{1

2}, Longsheng Hong^{2

3}, Yindan Luo¹, Bingqi Zhang^{1

2}, Ziyu Yu^{1

2}, Wanyan Li^{1

2}, Nan Cao^{1

2}, Yunmao Huang^{1

2}, Danning Xu^{1

2}, Yugu Li^{2

3}, Yunbo Tian^{1

2}

Affiliations

¹ College of Animal Science & Technology, Zhongkai University of Agriculture and Engineering, Guangzhou 510225, China.
² Guangdong Province Key Laboratory of Waterfowl Healthy Breeding, Guangzhou 510225, China.
³ College of Veterinary Medicine, South China Agricultural University, Guangzhou 510642, China.

Abstract

Lipopolysaccharide (LPS) is one of the main virulence factors of Gram-negative bacteria. In the process of waterfowl breeding, an inflammatory reaction due to LPS infection is easily produced, which leads to a decline in waterfowl performance. The liver plays a vital role in the immune response and the removal of toxic components. Therefore, it is necessary to study the mechanism of liver injury induced by LPS in goose. In this study, a total of 100 1-day-old goslings were randomly divided into a control group and LPS group after 3 days of pre-feeding. On days 21, 23, and 25 of the formal experiment, the control group was intraperitoneally injected with 0.5 mL normal saline, and the LPS group was intraperitoneally injected with LPS 2 mg/(kg body weight) once a day. On day 25 of the experiment, liver samples were collected 3 h after the injection of saline and LPS. The results of histopathology and biochemical indexes showed that the livers of the LPS group had liver morphological structure destruction and inflammatory cell infiltration, and the levels of ALT and AST were increased. Next, RNA sequencing analysis was used to determine the abundances and characteristics of the transcripts, as well as the associated somatic mutations and alternative splicing. We screened 727 differentially expressed genes (DEGs) with p < 0.05 and |log2(Fold Change)| ≥ 1, as the thresholds; GO and KEGG enrichment analysis showed that LPS-induced liver injury may be involved in the Toll-like receptor signaling pathway, MAPK signaling pathway, NOD-like receptor signaling pathway, FoxO, and PPAR signaling pathway. Finally, we intersected the genes enriched in the key pathway of LPS-induced liver injury with the top 50 key genes in protein−protein interaction networks to obtain 28 more critical genes. Among them, 17 genes were enriched in Toll-like signaling pathway and MAPK signaling pathway. Therefore, these results suggest that LPS-induced liver injury in geese may be the result of the joint action of Toll-like receptor, MAPK, NOD-like receptor, FoxO, and PPAR signaling pathway. Among them, the TLR7-mediated MAPK signaling pathway plays a major role.

Keywords: LPS; MAPK; Toll-like receptor; goose; liver injury.

Abstract

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