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Updated: Jun 28, 2026

Purification and Visualization of Lipopolysaccharide from Gram-negative Bacteria by Hot Aqueous-phenol Extraction
Published on: May 28, 2012
Polysaccharide biosynthesis locus required for virulence of Bacteroides fragilis
M J Coyne1, A O Tzianabos, B C Mallory
1Channing Laboratory, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA.
Abstract:
Bacteroides fragilis, though only a minor component of the human intestinal commensal flora, is the anaerobe most frequently isolated from intra-abdominal abscesses. B. fragilis 9343 expresses at least three capsular polysaccharides-polysaccharide A (PS A), PS B, and PS C. Purified PS A and PS B have been tested in animal models and are both able to induce the formation of intra-abdominal abscesses. Mutants unable to synthesize PS B or PS C still facilitate abscess formation at levels comparable to those of wild-type 9343. To determine the contribution of PS A to abscess formation in the context of the intact organism, the PS A biosynthesis region was cloned, sequenced, and deleted from 9343 to produce a PS A-negative mutant. Animal experiments demonstrate that the abscess-inducing capability of 9343 is severely attenuated when the organism cannot synthesize PS A, despite continued synthesis of the other capsular polysaccharides. The PS A of 9343 contains an unusual free amino sugar that is essential for abscess formation by this polymer. PCR analysis of the PS A biosynthesis loci of 50 B. fragilis isolates indicates that regions flanking each side of this locus are conserved in all strains. The downstream conserved region includes two terminal PS A biosynthesis genes that homology-based analyses predict are involved in the synthesis and transfer of the free amino sugar of PS A. Conservation of these genes suggests that this sugar is present in the PS A of all serotypes and may explain the abscessogenic nature of B. fragilis.
Insights
Polysaccharide A (PS A) from Bacteroides fragilis is crucial for causing intra-abdominal abscesses. Its absence in a mutant severely reduces abscess formation, highlighting PS A's role in virulence.
Area of Science:
- Microbiology
- Immunology
- Pathogenesis
Background:
- Bacteroides fragilis is a common cause of intra-abdominal abscesses.
- B. fragilis produces multiple capsular polysaccharides, including PS A, PS B, and PS C.
- Previous studies showed PS A and PS B can induce abscesses in animal models.
Purpose of the Study:
- To investigate the specific role of Polysaccharide A (PS A) in the abscess-inducing capability of Bacteroides fragilis 9343.
- To determine if PS A is essential for abscess formation by the intact organism.
Main Methods:
- Cloning, sequencing, and deletion of the PS A biosynthesis region in B. fragilis 9343 to create a PS A-negative mutant.
- Animal models to assess the abscess-inducing capability of the wild-type and mutant strains.
- PCR analysis of PS A biosynthesis loci in 50 B. fragilis isolates.
Main Results:
- The PS A-negative mutant showed significantly reduced abscess-inducing capability compared to wild-type 9343.
- Abscess formation was impaired even with the continued synthesis of other polysaccharides (PS B, PS C).
- An unusual free amino sugar in PS A was identified as essential for abscess formation.
Conclusions:
- Polysaccharide A is a key virulence factor for Bacteroides fragilis in intra-abdominal abscess formation.
- The presence of a specific free amino sugar in PS A is critical for its abscessogenic properties.
- Conserved genes involved in free amino sugar synthesis suggest this mechanism is common across B. fragilis serotypes.
Related Concept Videos
Biosynthesis of Polysaccharides
Formation of Lipopolysaccharides
Gene Regulation in Microbial Communities: Quorum Sensing
Bacterial Phylum Bacteroidota
Determinants of Bacterial Pathogenicity and Virulence
Regulation of Bacterial Virulence

