Gilthead seabream ( Sparus aurata L.) innate defence against the parasite Enteromyxum leei (Myxozoa)

Parasitology. 2006 Jan;132(Pt 1):95-104. doi: 10.1017/S0031182005008759.

Abstract

The humoral innate immune response of gilthead seabream (Sparus aurata L.) against the myxozoan Enteromyxum leei has been studied. At 10, 22, 38, 52 and 108 days of cohabitation fish were sampled to examine gut histology and to determine serum innate immune parameters and the mRNA expression of pro-inflammatory cytokines (IL-1beta and TNFalpha) in head-kidney. The parasite was successfully transmitted to 45% of the recipient fish and prevalence reached a maximum (62.5%) at the last sampling time (108 days). Recipient fish started to die after 74 days of cohabitation. In general, alternative complement activity was higher whereas the peroxidase level was lower in recipient fish than in controls. Moreover, IL-1beta mRNA expression increased while the TNFalpha gene expression decreased in recipient fish. These data demonstrate the involvement of complement activity in the defence mechanisms of the gilthead seabream against the myxosporean E. leei. Within the recipient fish group, few differences were observed in the studied immune parameters between E. leei-parasitized and non-parasitized recipient fish. Parasitological and immunological implications of E. leei infections in Mediterranean fish farms are discussed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Complement System Proteins / metabolism
  • Fish Diseases / immunology*
  • Fish Diseases / parasitology
  • Fish Diseases / transmission
  • Immunity, Innate
  • Interleukin-1 / metabolism
  • Peroxidase / blood
  • Prevalence
  • Protozoan Infections, Animal / immunology*
  • Protozoan Infections, Animal / parasitology
  • Protozoan Infections, Animal / transmission
  • Sea Bream / immunology*
  • Sea Bream / parasitology
  • Time Factors
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Interleukin-1
  • Tumor Necrosis Factor-alpha
  • Complement System Proteins
  • Peroxidase