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Novel large-scale chromosomal transfer in Bacteroides fragilis contributes to its pan-genome and rapid environmental
Fasahath Husain1, Kevin Tang2, Yaligara Veeranagouda3
11Brentwood Biomedical Research Institute, Los Angeles, CA, USA.
Abstract:
Bacteroides fragilis, an important component of the human gastrointestinal microbiota, can cause lethal extra-intestinal infection upon escape from the gastrointestinal tract. We demonstrated transfer and recombination of large chromosomal segments from B. fragilis HMW615, a multidrug resistant clinical isolate, to B. fragilis 638R. In one example, the transfer of a segment of ~435 Kb/356 genes replaced ~413 Kb/326 genes of the B. fragilis 638R chromosome. In addition to transfer of antibiotic resistance genes, these transfers (1) replaced complete divergent polysaccharide biosynthesis loci; (2) replaced DNA inversion-controlled intergenic shufflons (that control expression of genes encoding starch utilization system outer membrane proteins) with more complex, divergent shufflons; and (3) introduced additional intergenic shufflons encoding divergent Type 1 restriction/modification systems. Conjugative transposon-like genes within a transferred segment and within a putative integrative conjugative element (ICE5) ~45 kb downstream from the transferred segment both encode proteins that may be involved in the observed transfer. These data indicate that chromosomal transfer is a driver of antigenic diversity and nutrient adaptation in Bacteroides that (1) contributes to the dissemination of the extensive B. fragilis pan-genome, (2) allows rapid adaptation to a changing environment and (3) can confer pathogenic characteristics to host symbionts.
Insights
Large chromosomal segments transferred between Bacteroides fragilis strains, driving antigenic diversity and adaptation. This process disseminates the B. fragilis pan-genome and can confer pathogenic traits.
Area of Science:
- Microbiology
- Genetics
- Bacterial Pathogenesis
Background:
- Bacteroides fragilis is a key human gut microbe.
- This bacterium can cause severe infections outside the gastrointestinal tract.
- Understanding its genetic adaptability is crucial for public health.
Purpose of the Study:
- To investigate the mechanisms and consequences of large chromosomal segment transfer in Bacteroides fragilis.
- To determine how such transfers impact bacterial adaptation, diversity, and pathogenicity.
Main Methods:
- Conjugation experiments were performed between multidrug-resistant B. fragilis HMW615 and B. fragilis 638R.
- Whole-genome sequencing and comparative genomic analysis were used to identify transferred segments.
- Bioinformatic tools were employed to analyze gene content, including polysaccharide biosynthesis loci, shufflons, and restriction/modification systems.
Main Results:
- Demonstrated transfer and recombination of large chromosomal segments (~435 Kb) between B. fragilis strains.
- Transferred segments replaced existing loci, including polysaccharide biosynthesis genes and DNA inversion-controlled shufflons.
- Introduced new shufflons encoding restriction/modification systems and antibiotic resistance genes.
- Identified potential roles for conjugative transposon-like genes and an integrative conjugative element (ICE5) in mediating transfer.
Conclusions:
- Chromosomal transfer significantly drives antigenic diversity and nutrient adaptation in Bacteroides.
- This process facilitates the spread of the extensive B. fragilis pan-genome.
- Rapid adaptation to environmental changes and acquisition of pathogenic characteristics are key outcomes.
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