In vivo and in vitro assessment of host-parasite interaction between the parasitic copepod Brachiella thynni (Copepoda; Lernaeopodidae) and the farmed Atlantic bluefin tuna (Thunnus thynnus)

Fish Shellfish Immunol. 2020 Nov:106:814-822. doi: 10.1016/j.fsi.2020.08.001. Epub 2020 Aug 23.

Abstract

The Atlantic bluefin tuna (ABFT; Thunnus thynnus) today represents one of the economically most important species for Croatian fisheries industry. Although the most diverse and abundant parasitofauna is usually found in the largest specimens of wild ABFT, the opposite was observed in captivity where parasite populations significantly decline by the end of the farming cycle. Copepod Brachiella thynni, is a skin parasite frequently parasitizing tuna, whose population also decreases in number throughout the rearing process. In order to better understand the immunity mechanisms underlying ABFT reaction to B. thynni infection, we studied expression profiles of immunity related genes; interleukin 1β (il1β), tumour necrosis factors (tnfα1, tnfα2), complement component 4 (c4) and caspase 3 (casp3), in peripheral blood leukocytes (PBLs) during in vitro stimulation by B. thynni protein extracts (i.e. antigens) and in infected tissues at B. thynni parasitation site. Finally, a histopathological analysis of semi-thin and ultra-thin sections of tissues surrounding B. thynii attachment site was performed to evaluate the severity of parasite-induced lesions and identify involved cell lineages. In vitro stimulation of ABFT PBLs with B. thynii antigens caused a dose-depended upregulation of selected genes, among which tnfα1 showed the highest induction by both concentrations of B. thynni protein extract. However, targeted genes were not significantly upregulated in the infected tissue. Also, no significant alterations in ultrastructure of epithelial layers surrounding B. thynii attachment site were noticed, except local tissue erosion, necrosis of squamous epithelium and proliferation of rodlet and goblet cells. Our results suggest that B. thynii has evolved strategies to successfully bypass both innate immune response and the connective-tissue proliferation processes. Therefore, the observed disappearance of this copepod by the end of the rearing process is more likely related to its limited lifespan on the host and its inability to complete the life cycle in the rearing cages, rather than host's reaction.

Keywords: Atlantic bluefin tuna; Copepoda; Cytokines; Fish parasites; Parasite protein extracts.

MeSH terms

  • Animals
  • Aquaculture
  • Caspase 3 / genetics
  • Complement C3 / genetics
  • Complement C4 / genetics
  • Copepoda / physiology*
  • Female
  • Host-Parasite Interactions / genetics
  • Host-Parasite Interactions / immunology*
  • Interleukin-1beta / genetics
  • Leukocytes / immunology
  • Tumor Necrosis Factors / genetics
  • Tuna / genetics
  • Tuna / immunology*
  • Tuna / parasitology*

Substances

  • Complement C3
  • Complement C4
  • Interleukin-1beta
  • Tumor Necrosis Factors
  • Caspase 3