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Transcriptome profiling and differential expression analysis of the immune-related genes during the acute phase of infection with Photobacterium damselae subsp. damselae in silver pomfret (Pampus argenteus).

Authors :
Nawaz, Mateen
Li, Xionglin
Yue, Xinyuan
Gouife, Moussa
Huang, Kejing
Chen, Suyang
Ma, Rongrong
Jiang, Jianhu
Zhou, Suming
Jin, Shan
Wang, Yajun
Xie, Jiasong
Source :
Fish & Shellfish Immunology. Dec2022, Vol. 131, p342-348. 7p.
Publication Year :
2022

Abstract

Silver pomfret has been widely cultured in China due to its high economic value. Photobacterium damselae subsp. damselae (PDD) is a Gram-negative bacterium that has been shown to infect many fish species. To increase knowledge of the molecular mechanisms of the host defense against PDD , we conducted transcriptome analysis of head kidney in silver pomfret at 24 h and 72 h post-infection (hpi) via Illumina sequencing. The de novo assembly resulted in the identification of 79,063 unigenes, with 59,386 (75.11%) successfully annotated in public databases (NR, NT, KO, Swiss-Prot, Pfam, GO, and KOG databases). Comparison of gene expression profiles between PBS-injected fish (sham control) and PDD- challenged fish revealed 329 and 570 differentially expressed genes (DEGs) were screened at 24 hpi and 72 hpi, respectively. The DEGs were enriched in multiple immune-related pathways such as Hepatitis C, Gastric acid secretion, CAMs and Leukocyte transendothelial migration pathways, Primary immunodeficieny, ECM-receptor interaction, PI3K-Akt signaling pathway. The data obtained in the present study offers valuable information for acute immune response of silver pomfret challenged with PDD , which will facilitate further investigations on strategies against Photobacterium spp. infection in teleosts. • Silver pomfret head kidney transcriptome was sequenced following acute infection with PDD. • 329 and 570 DEGs were differentially expressed between control and PDD -infected fish, respectively. • The DEG KEGG analysis revealed that 134 and 208 pathways were significantly assigned at 24 and 72 hpi, respectively. • Quantitative PCR analysis of the selected DEGs confirmed that the generated RNA-seq data are a reliable resource. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10504648
Volume :
131
Database :
Academic Search Index
Journal :
Fish & Shellfish Immunology
Publication Type :
Academic Journal
Accession number :
160734900
Full Text :
https://doi.org/10.1016/j.fsi.2022.10.020