IrFC - An Ixodes ricinus injury-responsive molecule related to Limulus Factor C
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
24924263
DOI
10.1016/j.dci.2014.05.016
PII: S0145-305X(14)00152-9
Knihovny.cz E-resources
- Keywords
- Complement, Innate immunity, Limulus Clotting Factor C, Phagocytosis, RNA interference, Tick Ixodes ricinus,
- MeSH
- Borrelia immunology MeSH
- Candida albicans immunology MeSH
- Escherichia coli immunology MeSH
- Gene Expression MeSH
- Phagocytosis MeSH
- Ixodes enzymology genetics immunology microbiology MeSH
- Complement System Proteins physiology MeSH
- RNA, Messenger biosynthesis genetics MeSH
- Micrococcus luteus immunology MeSH
- Molecular Sequence Data MeSH
- Enzyme Precursors biosynthesis genetics MeSH
- Immunity, Innate MeSH
- Arthropod Proteins biosynthesis genetics MeSH
- Serine Endopeptidases biosynthesis genetics MeSH
- Up-Regulation immunology MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Complement System Proteins MeSH
- Limulus clotting factor C MeSH Browser
- RNA, Messenger MeSH
- Enzyme Precursors MeSH
- Arthropod Proteins MeSH
- Serine Endopeptidases MeSH
Limulus Clotting Factor C is a multi-domain serine protease that triggers horseshoe crab hemolymph clotting in the presence of trace amounts of bacterial lipopolysaccharides. Here we describe and functionally characterize an homologous molecule, designated as IrFC, from the hard tick Ixodes ricinus. Tick Factor C consists of an N-terminal cysteine-rich domain, four complement control protein (sushi) modules, an LCCL domain, a truncated C-lectin domain and a C-terminal trypsin-type domain. Developmental expression profiling by quantitative real-time PCR revealed that the irfc mRNA is expressed in all stages including eggs. In tissues dissected from adult I. ricinus females, the irfc mRNA is present mainly in tick hemocytes and accordingly, indirect immunofluorescence microscopy localized IrFC intracellularly, in tick hemocytes. Irfc mRNA levels were markedly increased upon injection of sterile saline, or different microbes, demonstrating that the irfc gene transcription occurs in response to injury. This indicates a possible role of IrFC in hemolymph clotting and/or wound healing, although these defense mechanisms have not been yet definitely demonstrated in ticks. RNAi silencing of irfc expression resulted in a significant reduction in phagocytic activity of tick hemocytes against the Gram-negative bacteria Chryseobacterium indologenes and Escherichia coli, but not against the yeast, Candida albicans. This result suggests that IrFC plays a role in the tick primordial complement system and as such possibly mediates transmission of tick-borne pathogens.
References provided by Crossref.org
Tick Immune System: What Is Known, the Interconnections, the Gaps, and the Challenges
Acquisition of exogenous haem is essential for tick reproduction
Deep Sequencing Analysis of the Ixodes ricinus Haemocytome
GENBANK
KJ150729