Subcellular localization and function study of a secreted phospholipase C from Nocardia seriolae

FEMS Microbiol Lett. 2017 Sep 15;364(17). doi: 10.1093/femsle/fnx143.

Abstract

Fish nocardiosis is a chronic systemic granulomatous disease, and Nocardia seriolae is the main pathogen that causes it. The pathogenesis and virulence factors of N. seriolae are not fully understood. A phospholipase C (PLC), which is likely to be a secreted protein targeting host cell mitochondria, was found by a bioinformatics analysis of the whole genome sequence of N. seriolae. In order to determine the subcellular localization and study the preliminary function of PLC from N. seriolae (NsPLC), in this study gene cloning, secreted protein identification, subcellular localization in host cells and apoptosis detection of NsPLC were carried out. Mass spectrometry analysis of extracellular products from N. seriolae showed that NsPLC was a secreted protein. Subcellular localization of NsPLC-GFP fusion protein in fathead minnow (FHM) cells revealed that the green fluorescence exhibited a punctate distribution near the nucleus and did not co-localize with mitochondria. In addition, an apoptosis assay suggested that apoptosis was induced in FHM cells by the overexpression of NsPLC. This study may lay the foundations for further studies on the function of NsPLC and promote the understanding of the virulence factors and pathogenic mechanism of N. seriolae.

Keywords: Nocardia seriolae; cell apoptosis; overexpression; phospholipase C; secreted protein; subcellular localization.

MeSH terms

  • Animals
  • Apoptosis
  • Cell Line
  • Cloning, Molecular
  • Cyprinidae / microbiology*
  • Cytoplasm / enzymology*
  • Epithelial Cells / cytology
  • Epithelial Cells / microbiology
  • Epithelial Cells / ultrastructure
  • Escherichia coli / genetics
  • Gene Expression
  • Green Fluorescent Proteins / genetics
  • Host-Pathogen Interactions
  • Microscopy, Fluorescence
  • Mitochondria / enzymology
  • Mitochondria / ultrastructure
  • Nocardia / cytology
  • Nocardia / enzymology*
  • Nocardia / genetics
  • Phylogeny
  • Recombinant Fusion Proteins / metabolism
  • Transfection
  • Type C Phospholipases / chemistry*
  • Type C Phospholipases / genetics
  • Type C Phospholipases / metabolism*
  • Virulence Factors / chemistry
  • Virulence Factors / metabolism*

Substances

  • Recombinant Fusion Proteins
  • Virulence Factors
  • Green Fluorescent Proteins
  • Type C Phospholipases