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Updated: Oct 18, 2025

High-Throughput Transcriptome Analysis for Investigating Host-Pathogen Interactions
Published on: March 5, 2022
A systematic bioinformatics approach for large-scale identification and characterization of host-pathogen shared
Stephen Among James1,2, Hui San Ong1, Ranjeev Hari1
1Centre for Bioinformatics, School of Data Sciences, Perdana University, Damansara Heights, Kuala Lumpur, 50490, Malaysia.
Researchers identified shared genetic sequences between hosts and pathogens, revealing insights into host-pathogen interactions. This discovery has implications for developing new vaccines and drugs against infectious diseases.
Area of Science:
- Bioinformatics
- Genomics
- Molecular Biology
Background:
- Biology is generating vast amounts of data through high-throughput omics technologies.
- Biological databases offer public access to extensive data for knowledge discovery.
- Increasing sequence data for pathogens, like viruses, is crucial due to their impact on human health.
Purpose of the Study:
- To develop and apply a systematic bioinformatics approach for identifying and characterizing shared sequences between hosts and pathogens.
- To analyze the "share-ome" between Flaviviridae viruses and humans.
Main Methods:
- A large-scale, systematic bioinformatics approach was employed.
- Identification and characterization of shared nonamer sequences between host (human) and pathogen (Flaviviridae).
Main Results:
- A total of 2430 nonamers showed 100% identity between Flaviviridae and humans.
- These shared sequences mapped to 16,946 Flaviviridae and 7506 human protein sequences across 125 Flaviviridae species.
- Hepatitis C virus (Hepacivirus C) accounted for the majority (68%) of shared sequences, followed by West Nile, dengue, and Zika viruses.
Conclusions:
- Mapping host-pathogen share-omes has significant implications for vaccine and drug design, diagnostics, and disease surveillance.
- The presented workflow is adaptable for various pathogens, including viral, bacterial, and parasitic agents.
- Characterization of shared sequences offers structural-functional insights into host-pathogen interactions.
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