Hi-Jack
Hi-Jack infers pathway-level metabolite-hijacking interactions between hosts and obligate intracellular pathogens to identify host metabolic reactions and metabolites exploited by pathogens.
Key Features:
- Metabolite Hijacking Concept: Encodes the concept that pathogens hijack host metabolic pathways to redirect resources toward pathogen proliferation, particularly protein production.
- Comprehensive Metabolic Network Analysis: Searches host and pathogen metabolic network data to identify candidate reactions where hijacking may occur.
- Novel Scoring Function: Applies a scoring function to rank candidate hijacked reactions and to prioritize frequently implicated metabolites.
- Pathway Interaction Identification: Maps interconnections between host and pathogen metabolic pathways to reveal specific biochemical interactions.
Scientific Applications:
- Analysis of obligate intracellular pathogens (Mycobacterium tuberculosis, Mtb): Applied to Mtb to identify host metabolic targets and to reveal potential metabolic strategies used during infection.
- Identification of hijacked host pathways: Identifies human pathways likely targeted for hijacking, including carbohydrate metabolism, lipid metabolism, and amino acid metabolism.
- Mapping cross-species pathway linkages: Reveals specific interconnections such as human fatty acid biosynthesis linked to Mtb biosynthesis of unsaturated fatty acids and the human pentose phosphate pathway linked to Mtb lipopolysaccharide biosynthesis.
Methodology:
Integrates host and pathogen metabolic network data and applies a scoring function to rank candidate hijacked reactions, identify implicated pathways, and highlight frequently hijacked metabolites.
Topics
Details
- Tool Type:
- command-line tool
- Operating Systems:
- Linux, Windows, Mac
- Added:
- 8/3/2017
- Last Updated:
- 11/25/2024
Operations
Publications
Kleftogiannis D, Wong L, Archer JA, Kalnis P. Hi-Jack: a novel computational framework for pathway-based inference of host–pathogen interactions. Bioinformatics. 2015;31(14):2332-2339. doi:10.1093/bioinformatics/btv138. PMID:25758402.
PMID: 25758402