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Phenotypic and genotypic characteristics of Arcanobacterium haemolyticum isolated from clinical samples in a Danish
Osama Sammra1, Alice Friis-Møller, Anna Balbutskaya
1Institut für Pharmakologie und Toxikologie, Justus-Liebig-Universität Gießen, Schubertstr 81, 35392, Gießen, Germany.
Abstract:
Six Arcanobacterium haemolyticum strains isolated from six patients of two hospitals in Denmark were identified phenotypically, also including matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS) analysis, and by genotypic methods. The latter were performed by sequencing 16S rDNA and glyceraldehyde 3-phosphate dehydrogenase encoding gene gap and by amplification of an A. haemolyticum specific region of 16S-23S rDNA intergenic spacer region and 23S rDNA. The six A. haemolyticum strains were further investigated for the presence of seven potential virulence genes encoding arcanolysin, phospholipase D, hemolysin A, CAMP factor family protein, collagen binding protein, neuraminidase A and neuraminidase H which appeared to be present in two (seven virulence genes), two (six virulence genes) and two strains (four virulence genes), respectively. The phenotypic and genotypic properties described in the present study might help to reliably identify and further characterize A. haemolyticum isolated from human patients, a species which seems to be of increasing importance.
Insights
This study identifies six Arcanobacterium haemolyticum strains using phenotypic and genotypic methods, including MALDI-TOF MS. Virulence gene analysis reveals varying profiles, aiding in the characterization of this increasingly important bacterial species.
Area of Science:
- Medical Microbiology
- Bacterial Pathogenesis
Background:
- Arcanobacterium haemolyticum is a bacterial species of increasing clinical importance.
- Accurate identification and characterization are crucial for understanding its pathogenicity.
Purpose of the Study:
- To phenotypically and genotypically characterize Arcanobacterium haemolyticum strains isolated from human patients.
- To investigate the presence and distribution of key virulence genes in these strains.
Main Methods:
- Phenotypic identification including matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS).
- Genotypic identification via 16S rDNA and gap gene sequencing, and 16S-23S rDNA intergenic spacer region amplification.
- Detection of seven potential virulence genes (arcanolysin, phospholipase D, hemolysin A, CAMP factor family protein, collagen binding protein, neuraminidase A, neuraminidase H).
Main Results:
- Six Arcanobacterium haemolyticum strains were successfully identified from Danish hospitals.
- Genotypic analysis confirmed phenotypic identification.
- Virulence gene analysis showed varying presence, with strains harboring between four and seven genes.
Conclusions:
- The combined phenotypic and genotypic approaches provide reliable methods for identifying and characterizing Arcanobacterium haemolyticum.
- Understanding the virulence gene profiles is essential for assessing the pathogenic potential of clinical isolates.
- This study contributes to the growing knowledge of Arcanobacterium haemolyticum as a significant human pathogen.
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