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Published on: February 19, 2019
A genome-led study on the pathogenesis of Fusobacterium necrophorum infections
Gary Thapa1, Ambikesh Jayal2, Elvis Sikazwe3
1Public Health Wales Microbiology Aberystwyth, Bronglais General Hospital, Aberystwyth, UK.
Abstract:
Fusobacterium necrophorum causes a range of mild to life threatening infections and there is uncertainty in terms of diagnosis and treatment due to the lack of knowledge on their pathogenic mechanisms. This study characterised genomes of F. necrophorum to compare their virulence factors and investigate potential infection markers. 27 isolates of F. necrophorum from patients with pharyngotonsillitis were subjected to whole genome sequencing and compared with 42 genomes published in the NCBI database. Phylogenomics, pangemome, pan-GWAS and virulome were analysed to study strain variations with reference to virulence factors. Core genome based phylogenomic tree exhibited three clades of which Clade A belonged to F. necrophorum subsp necrophorum, clades B and C were F. necrophorum subsp funduliforme. Pan-GWAS and Pan-Virulome suggest some marker genes associated with clinical sources of isolation that needs further validation. Our study highlights some interesting features of the pathogenesis of F. necrophorum infections. Although the animal isolate genomes had some marker genes, the genomes of human isolates did not exhibit clear correlation to their clinical sources of isolation. This prompts to think of other mechanisms such as co-infections or host factors that can be involved in the pathogenesis.
Insights
Genomic analysis of Fusobacterium necrophorum reveals strain variations and potential virulence markers. Further research is needed to understand pathogenesis, as human isolates lacked clear correlations to clinical sources.
Area of Science:
- Microbiology
- Genomics
- Infectious Diseases
Background:
- Fusobacterium necrophorum causes diverse infections with poorly understood pathogenic mechanisms, complicating diagnosis and treatment.
- Limited knowledge on virulence factors hinders effective management of F. necrophorum infections.
Purpose of the Study:
- To characterize F. necrophorum genomes for comparative analysis of virulence factors.
- To identify potential genetic markers associated with F. necrophorum infections and clinical sources.
Main Methods:
- Whole genome sequencing of 27 F. necrophorum isolates from pharyngotonsillitis patients.
- Comparative analysis with 42 public NCBI genomes using phylogenomics, pangenomics, pan-GWAS, and virulome analysis.
Main Results:
- Phylogenomic analysis identified three distinct clades: F. necrophorum subsp. necrophorum (Clade A) and F. necrophorum subsp. funduliforme (Clades B and C).
- Pan-GWAS and Pan-Virulome analyses suggested potential marker genes linked to isolation sources, requiring further validation.
- Human isolates did not show a clear correlation between genome markers and clinical sources, unlike some animal isolates.
Conclusions:
- Genomic characterization provides insights into F. necrophorum pathogenesis and strain diversity.
- The lack of clear genomic markers in human isolates suggests the involvement of co-infections or host factors in disease development.
- Further investigation into non-genomic factors is crucial for a comprehensive understanding of F. necrophorum pathogenicity.
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