Newly excysted juveniles (NEJs) of Fasciola gigantica induce mice liver fibrosis and M2 macrophage-like phenotype in vivo

Microb Pathog. 2020 Feb:139:103909. doi: 10.1016/j.micpath.2019.103909. Epub 2019 Dec 3.

Abstract

Liver flukes of animals are parasitic flatworms of major socioeconomic importance in many countries. Particularly, Fasciola gigantica is a leading cause of production losses to the livestock (mainly sheep and cattle) and meat industries due to clinical disease, reduced weight gain and milk production, and deaths. Immune responses induced by helminth have been extensively studied, but there is limited information on this aspect by F. gigantica, especially on macrophages induced with this parasite. Studies have shown that host immune responses induced by parasitic infection is greatly correlated with the macrophage polarization axis. In the present study, we used the murine model of F. gigantica to explore the interaction of host and F. gigantica. We found F. gigantica NEJs promoted pathology and fibrosis of mice liver, and the enlargement of mice spleen. We also showed that macrophages were recruited to mice peritoneal cavity at 5 days post infection. By evaluating the expression of genetic markers of M2 macrophages such as Arg-1, Ym1 and RELMɑ, and genetic marker of M1 macrophages iNOS, we showed that M2 macrophages were induced by F. gigantica. M2 macrophages are central to the immune response during helminth infection, and our findings in this study provided insight into the immune interaction between F. gigantica and host.

Keywords: Fasciola gigantica; Fibrosis; M2 macrophages; Newly excysted juveniles (NEJs).

MeSH terms

  • Animals
  • Fasciola / genetics
  • Fasciola / growth & development
  • Fasciola / physiology*
  • Fasciola hepatica / growth & development
  • Fasciola hepatica / physiology*
  • Fascioliasis / immunology
  • Fascioliasis / parasitology*
  • Fascioliasis / pathology
  • Female
  • Humans
  • Liver Cirrhosis / immunology
  • Liver Cirrhosis / parasitology*
  • Liver Cirrhosis / pathology
  • Macrophages / immunology
  • Macrophages / parasitology*
  • Male
  • Mice
  • Phenotype