Changes in Atlantic salmon (Salmo salar) epidermal mucus protein composition profiles following infection with sea lice (Lepeophtheirus salmonis)

Russell H. Easy, Neil W. Ross

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121 Citas (Scopus)

Resumen

The mucus protein profile of Atlantic salmon (Salmo salar) and changes due to infection with sea lice (Lepeophtheirus salmonis) were examined. Two-dimensional gel electrophoresis was performed on salmon skin mucus and comparisons between control and infected fish mucus were made. LC MS/MS identified intracellular proteins, calmodulin, actin, and hemopexin and plasma proteins, such as apolipoproteins, lectin, plasminogen and transferrin. Plasma proteins in the mucus may result from either direct expression by epidermal cells, leakage of plasma or via a secondary circulation system. Therefore, RT-PCR was used to measure mRNA of transferrin and lectin in Atlantic salmon skin. Transferrin expression was observed suggesting direct expression by the epidermis. Lectin expression was not detected suggesting another mechanism of entry into mucus, either leakage from plasma or secondary circulation. The lack of observable albumin on 2D gels, suggests that mucus lectin may arise from the secondary circulation route. Interestingly, β-actin was a significant component of Atlantic salmon mucus. Cleaved actin and transferrin fragments were observed and positively correlated with sea lice infection suggestive of proteolytic activity. Increased levels of cleaved transferrin during sea lice infection may activate the nitrous oxide response of salmon macrophages, as part of the fish's immune response to sea lice infection.

Idioma originalEnglish
Páginas (desde-hasta)159-167
Número de páginas9
PublicaciónComparative Biochemistry and Physiology - Part D: Genomics and Proteomics
Volumen4
N.º3
DOI
EstadoPublished - sep. 2009
Publicado de forma externa

Nota bibliográfica

Funding Information:
The authors thank Paul Merlin of Merlin Sea Farms for salmon smolts, and Cook aquaculture for sea lice; Ron Melanson for help with fish husbandry and Mark Fast, Denise Muise, Sangeetha Subramanian and Steve Leadbetter for sampling. The authors thank Kenneth Chisholm and Devanand Pinto of the proteomics facility at NRC-IMB for assistance with the mass spectrometry analysis. This research was funded by the National Research Council — Institute for Marine Biosciences.

ASJC Scopus Subject Areas

  • Biochemistry
  • Physiology
  • Molecular Biology
  • Genetics

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