Clostridium perfringens type C (C. perfringens type C) is one of the main microbial pathogens responsible for piglet
diarrhea worldwide, causing substantial economic losses for pig-rearing industries. The
mitogen-activated protein kinase (MAPK) signaling pathway is a key regulator of
inflammatory bowel disease, especially necrotic
enteritis. However, whether and how the MAPK signaling pathway is involved in regulating the process of piglet
diarrhea when challenged by C. perfringens type C are still unknown. Here, we screened 38 differentially expressed genes (DEGs) in piglets' ileum tissues experimentally infected with C. perfringens type C that were enriched in the Sus scrofa MAPK signaling pathway, based on our previous transcriptome data. Of these DEGs, 12 genes (
TRAF2, MAPK8, and GADD45G, among others) were upregulated whereas 26 genes (MAPK1, TP53, and CHUK, among others) were downregulated in the infected group. Our results showed that MAPK1, TP53, MAPK8, MYC, and CHUK were in the core nodes of the PPI network. Additionally, we obtained 35 lncRNAs from the sequencing data, which could be trans-targeted to MAPK signaling pathway genes and were differentially expressed in the ileum tissues infected with C. perfringens. We used qRT-PCR to verify the expression levels of genes and lncRNAs related to the MAPK signaling pathway; their expression patterns were consistent with
RNA sequencing data. Our results provide strong support for deeply exploring the role of the MAPK signaling pathway in
diarrhea caused by C. perfringens type C.