A comparative analysis of alternative splicing patterns in Atlantic salmon (Salmo Salar) in response to Moritella viscosa and sea lice (Lepeophtheirus salmonis) infection.

Atlantic salmon Moritella viscosa alternative splicing immune response post-transcriptional regulation sea lice

Journal

Fish & shellfish immunology
ISSN: 1095-9947
Titre abrégé: Fish Shellfish Immunol
Pays: England
ID NLM: 9505220

Informations de publication

Date de publication:
03 May 2024
Historique:
received: 06 01 2024
revised: 19 04 2024
accepted: 02 05 2024
medline: 6 5 2024
pubmed: 6 5 2024
entrez: 5 5 2024
Statut: aheadofprint

Résumé

Moritella viscosa (M. viscosa) and sea lice (Lepeophtheirus salmonis) are severe pathogens that primarily infect the skin of Atlantic salmon (Salmo salar), which cause significant economic losses in the farming industry. However, the pathogenesis and molecular mechanisms underlying the host's immune defence at the post-transcriptional level remain unclear. Alternative splicing (AS) is an evolutionarily conserved post-transcriptional mechanism that can greatly increase the richness of the transcriptome and proteome. In this study, transcriptomic data derived from skin tissues of Atlantic salmon after M. viscosa and sea lice infections were used to examine the AS profiles and their differential expression patterns. In total, we identified 33,044 AS events (involving 13,718 genes) in the control (CON) group, 35,147 AS events (involving 14,340 genes) in the M. viscosa infection (MV) group, and 30,364 AS events (involving 13,142 genes) in the sea lice infection (LC) group. Among the five types of AS identified in our study (i.e. skipped exon (SE), alternative 5´ splice site (A5SS), alternative 3´ splice site (A3SS), mutually exclusive exon (MXE), and retained intron (RI)), SE was the most prevalent type in all three groups (i.e. CON, MV, and LC groups). Decreased percent-spliced-in (PSI) levels were observed in SE events under both MV- and LC-infected conditions, suggesting that MV or LC infection elevated exon-skipping isoforms and promoted the selection of shorter transcripts in numerous DAS genes. In addition, most of the differential AS genes were associated with pathways related to mRNA regulation, epithelial or muscle development, and immune response. These findings provide novel insights into the role of AS in host-pathogen interactions in fish species and represent the first comparative analysis of AS in response to bacterial and parasitic infections in fish.

Identifiants

pubmed: 38705547
pii: S1050-4648(24)00251-1
doi: 10.1016/j.fsi.2024.109606
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

109606

Informations de copyright

Copyright © 2024. Published by Elsevier Ltd.

Auteurs

Shengnan Gao (S)

Department of Infectious Diseases and Public Health, Jockey Club College of Veterinary Medicine and Life Sciences, City University of Hong Kong, Kowloon Tong, Hong Kong; State Key Lab of Marine Pollution, City University of Hong Kong, Kowloon Tong, Hong Kong.

Suxu Tan (S)

Institute of Aquatic Biotechnology, College of Life Sciences, Qingdao University, Qingdao, 266071, China.

Sara L Purcell (SL)

Department of Pathology and Microbiology, Atlantic Veterinary College, University of Prince Edward Island, Charlottetown, PE, C1A 4P3, Canada.

Shona K Whyte (SK)

Department of Pathology and Microbiology, Atlantic Veterinary College, University of Prince Edward Island, Charlottetown, PE, C1A 4P3, Canada.

Kathleen Parrish (K)

Department of Pathology and Microbiology, Atlantic Veterinary College, University of Prince Edward Island, Charlottetown, PE, C1A 4P3, Canada.

Liang Zhong (L)

Department of Infectious Diseases and Public Health, Jockey Club College of Veterinary Medicine and Life Sciences, City University of Hong Kong, Kowloon Tong, Hong Kong.

Shucheng Zheng (S)

State Key Lab of Marine Pollution, City University of Hong Kong, Kowloon Tong, Hong Kong.

Yuxuan Zhang (Y)

Department of Infectious Diseases and Public Health, Jockey Club College of Veterinary Medicine and Life Sciences, City University of Hong Kong, Kowloon Tong, Hong Kong.

Ruoxi Zhu (R)

Department of Infectious Diseases and Public Health, Jockey Club College of Veterinary Medicine and Life Sciences, City University of Hong Kong, Kowloon Tong, Hong Kong.

Ladan Jahangiri (L)

Department of Infectious Diseases and Public Health, Jockey Club College of Veterinary Medicine and Life Sciences, City University of Hong Kong, Kowloon Tong, Hong Kong.

Runsheng Li (R)

Department of Infectious Diseases and Public Health, Jockey Club College of Veterinary Medicine and Life Sciences, City University of Hong Kong, Kowloon Tong, Hong Kong.

Mark D Fast (MD)

Department of Pathology and Microbiology, Atlantic Veterinary College, University of Prince Edward Island, Charlottetown, PE, C1A 4P3, Canada.

Wenlong Cai (W)

Department of Infectious Diseases and Public Health, Jockey Club College of Veterinary Medicine and Life Sciences, City University of Hong Kong, Kowloon Tong, Hong Kong; State Key Lab of Marine Pollution, City University of Hong Kong, Kowloon Tong, Hong Kong. Electronic address: wenlocai@cityu.edu.hk.

Classifications MeSH