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Automated Measurement of Cryptococcal Species Polysaccharide Capsule and Cell Body
Published on: January 11, 2018
Identification of polysaccharide capsules among extensively drug-resistant genitourinary Haemophilus parainfluenzae
Aida González-Díaz1,2, Fe Tubau1,2, Miguel Pinto3
1Microbiology Department, Hospital Universitari de Bellvitge, Universitat de Barcelona-IDIBELL, Barcelona, Spain.
Abstract:
The human commensal Haemophilus parainfluenzae is emerging as an opportunistic multidrug-resistant pathogen. The objectives of this work were to characterise a new capsular operon of extensively drug-resistant (XDR) H. parainfluenzae clinical isolates and study their resistance mechanisms using whole-genome sequencing. All strains were resistant to: ß-lactams, via amino acid changes in PBP3 (S385T, I442F, V511A, N526K and V562I); quinolones, by alterations in GyrA (S84F and D88Y) and ParC (S84F and S138T); chloramphenicol, through the presence of catS; macrolides, via the presence of mel and mef(E)-carrying MEGA element; and tetracycline, through the presence of tet(M) and/or tet(B). Phylogenetic analysis revealed high genomic diversity when compared to the H. parainfluenzae genomes available on the NCBI, the isolates from this study being closely related to the Swiss XDR AE-2096513. A full capsular operon showing homology to that of H. influenzae was identified, in accordance with the observation of a capsular structure by TEM. This study describes for the first time a capsular operon in H. parainfluenzae, a major determinant of pathogenicity that may contribute to increased virulence in XDR clinical isolates. Moreover, phylogenetic analysis suggests the possible spread of an XDR-encapsulated strain in Europe.
Insights
Extensively drug-resistant Haemophilus parainfluenzae strains possess a novel capsular operon. This discovery aids in understanding the pathogenicity and spread of these opportunistic multidrug-resistant bacteria.
Area of Science:
- Microbiology
- Genomics
- Pathogen Discovery
Background:
- Haemophilus parainfluenzae, a human commensal, is increasingly recognized as an opportunistic multidrug-resistant pathogen.
- The emergence of extensively drug-resistant (XDR) strains necessitates understanding their genetic basis and virulence factors.
Purpose of the Study:
- To characterize a novel capsular operon in XDR H. parainfluenzae clinical isolates.
- To elucidate the genetic mechanisms underlying multidrug resistance in these isolates using whole-genome sequencing.
Main Methods:
- Whole-genome sequencing of clinical H. parainfluenzae isolates.
- Phylogenetic analysis of genomic data.
- Transmission electron microscopy (TEM) for capsular structure visualization.
Main Results:
- Identification of a complete capsular operon in H. parainfluenzae, homologous to that of H. influenzae.
- Detailed characterization of resistance mechanisms against beta-lactams, quinolones, chloramphenicol, macrolides, and tetracycline.
- Phylogenetic analysis revealed high genomic diversity and close relation to a known Swiss XDR strain, suggesting potential European spread.
Conclusions:
- This study reports the first description of a capsular operon in H. parainfluenzae, a potential virulence determinant.
- The identified capsular operon may contribute to the increased pathogenicity of XDR clinical isolates.
- Phylogenetic findings suggest the possible dissemination of XDR-encapsulated H. parainfluenzae strains across Europe.
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