PcLys-i3, an invertebrate lysozyme, is involved in the antibacterial immunity of the red swamp crayfish, Procambarus clarkii

Dev Comp Immunol. 2018 Oct:87:109-115. doi: 10.1016/j.dci.2018.05.020. Epub 2018 May 31.

Abstract

Antimicrobial peptides (AMPs) play important roles in innate immunity against pathogens and lysozymes are a particularly type of AMP. Lysozymes are hydrolytic enzymes that are characterized by their ability to cleave the beta-(1,4)-glycosidic bond between N-acetylmuramic acid and N-acetylglucosamine in peptidoglycan, which is the major bacterial cell wall polymer. In this work, a lysozyme was identified from Procambarus clarkii and designated PcLys-i3. Quantitative RT-PCR was used to analyze the tissue distribution and expression profiles of PcLys-i3. PcLys-i3 was present in all tested tissues and had high expression levels in gills, stomach and intestine. The expression levels of PcLys-i3 were up-regulated in gills and intestine after challenge with Vibrio parahaemolyticus, Staphylococcus aureus and Aeromonas hydrophila. PcLys-i3 and PcFer proteins can enhance the bacterial elimination in crayfish, whereas the bacterial elimination was weakened when the expression level of PcLys-i3 or PcFer RNAs was suppressed by RNAi. Recombinant PcLys-i3 and PcFer significantly reduced the mortality of crayfish with bacterial infections. Further study found that PcLys-i3 could interact with PcFer in vitro. Finally, the PcLys-i3 and PcFer proteins could bind to bacteria and inhibit bacterial replication. These results suggest that both PcLys-i3 and PcFer play important roles in the antibacterial immunity of red swamp crayfish.

Keywords: Innate immunity; Lysozymes; Procambarus clarkii; Vibrio parahaemolyticus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aeromonas hydrophila / immunology
  • Aeromonas hydrophila / physiology
  • Animals
  • Anti-Bacterial Agents / immunology*
  • Anti-Bacterial Agents / metabolism
  • Arthropod Proteins / genetics
  • Arthropod Proteins / immunology*
  • Arthropod Proteins / metabolism
  • Astacoidea / genetics
  • Astacoidea / immunology*
  • Astacoidea / microbiology
  • Gene Expression Profiling / methods
  • Gills / immunology
  • Gills / metabolism
  • Gills / microbiology
  • Host-Pathogen Interactions
  • Intestinal Mucosa / metabolism
  • Intestines / immunology
  • Intestines / microbiology
  • Muramidase / genetics
  • Muramidase / immunology*
  • Muramidase / metabolism
  • RNA Interference
  • Staphylococcus aureus / immunology
  • Staphylococcus aureus / physiology
  • Up-Regulation
  • Vibrio / immunology
  • Vibrio / physiology

Substances

  • Anti-Bacterial Agents
  • Arthropod Proteins
  • Muramidase