Genome-Wide DNA Methylation and RNA Analysis Reveal Potential Mechanism of Resistance toStreptococcus agalactiaein GIFT Strain of Nile Tilapia (Oreochromis niloticus)
Author(s) -
Qiaomu Hu,
Qiuwei Ao,
Yun Tan,
Gan Xi,
Yongju Luo,
Jiajie Zhu
Publication year - 2020
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1901496
Subject(s) - nile tilapia , oreochromis , streptococcus agalactiae , biology , strain (injury) , dna methylation , mechanism (biology) , genetics , genome , gene , dna , fish <actinopterygii> , fishery , microbiology and biotechnology , streptococcus , bacteria , gene expression , anatomy , physics , quantum mechanics
Streptococcus agalactiae is an important pathogenic bacterium causing great economic loss in Nile tilapia ( Oreochromis niloticus) culture. Resistant and susceptible groups sharing the same genome showed significantly different resistance to S. agalactiae in the genetically improved farmed tilapia strain of Nile tilapia. The resistance mechanism is unclear. We determined genome-wide DNA methylation profiles in spleen of resistant and susceptible O. niloticus at 5 h postinfection with S. agalactiae using whole-genome bisulfite sequencing. The methylation status was higher in the spleen samples from resistant fish than in the susceptible group. A total of 10,177 differentially methylated regions were identified in the two groups, including 3725 differentially methylated genes (DMGs) (3129 hyper-DMGs and 596 hypo-DMGs). The RNA sequencing showed 2374 differentially expressed genes (DEGs), including 1483 upregulated and 891 downregulated. Integrated analysis showed 337 overlapping DEGs and DMGs and 82 overlapping DEGs and differentially methylated region promoters. By integrating promoter DNA methylation with gene expression, we revealed four immune-related genes (Arnt2, Nhr38, Pcdh10, and Ccdc158) as key factors in epigenetic mechanisms contributing to pathogen resistance. Our study provided systematic methylome maps to explore the epigenetic mechanism and reveal the methylation loci of pathogen resistance and identified methylation-regulated genes that are potentially involved in defense against pathogens.
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