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Updated: Dec 3, 2025

Methodology for the Study of Horizontal Gene Transfer in Staphylococcus aureus
Published on: March 10, 2017
Staphylococcal Protein A (spa) Locus Is a Hot Spot for Recombination and Horizontal Gene Transfer in Staphylococcus
Alem Zukancic1, Mubin A Khan2, Sumayya J Gurmen1
1Department of Pathobiology, College of Veterinary Medicine, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.
Abstract:
Staphylococcus pseudintermedius is a major canine pathogen but also occasionally colonizes and infects humans. Multidrug-resistant methicillin-resistant S. pseudintermedius (MDR MRSP) strains have emerged globally, making treatment and control of this pathogen challenging. Sequence type 71 (ST71), ST68, and ST45 are the most widespread and successful MDR MRSP clones. The potential genetic factors underlying the clonal success of these and other predominant clones remain unknown. Characterization of the pangenome, lineage-associated accessory genes, and genes acquired through horizontal gene transfer from other bacteria is important for identifying such factors. Here, we analyzed genome sequence data from 622 S. pseudintermedius isolates to investigate the evolution of pathogenicity across lineages. We show that the predominant clones carry one or more lineage-associated virulence genes. The gene encoding staphylococcal protein A (SpA), a key virulence factor involved in immune evasion and a potential vaccine antigen, is deleted in 62% of isolates. Most importantly, we have discovered that the spa locus is a hot spot for recombination and horizontal gene transfer in S. pseudintermedius, where genes related to restriction modification, prophage immunity, mercury resistance, and nucleotide and carbohydrate metabolism have been acquired in different lineages. Our study also establishes that ST45 is composed of two distinct sublineages that differ in their accessory gene content and virulence potential. Collectively, this study reports several previously undetected lineage-associated genetic factors that may have a role in the clonal success of the major MDR MRSP clones. These data provide a framework for future experimental studies on S. pseudintermedius pathogenesis and for developing novel therapeutics against this pathogen.IMPORTANCEStaphylococcus pseudintermedius is a major canine pathogen but can also occasionally infect humans. Identification of genetic factors contributing to the virulence and clonal success of multidrug-resistant S. pseudintermedius clones is critical for the development of therapeutics against this pathogen. Here, we characterized the genome sequences of a global collection of 622 S. pseudintermedius isolates. We show that all major clones, besides carrying core virulence genes, which are present in all strains, carry one or more lineage-specific genes. Many of these genes have been acquired from other bacterial species through a horizontal gene transfer mechanism. Importantly, we have discovered that the staphylococcal protein A gene (spa), a widely used marker for molecular typing of S. pseudintermedius strains and a potential vaccine candidate antigen, is deleted in 62% of strains. Furthermore, the spa locus in S. pseudintermedius acts as a reservoir to accumulate lineage-associated genes with adaptive functions.
Insights
Multidrug-resistant Staphylococcus pseudintermedius clones possess lineage-specific genes contributing to their success. The staphylococcal protein A (spa) gene is frequently deleted, and its locus acts as a hub for acquiring new adaptive genes.
Area of Science:
- Veterinary Microbiology
- Genomics
- Bacterial Pathogenesis
Background:
- Staphylococcus pseudintermedius is a significant canine pathogen with emerging multidrug-resistant (MDR) strains.
- Globally prevalent MDR MRSP clones (ST71, ST68, ST45) pose treatment challenges.
- Understanding genetic factors driving clonal success is crucial for controlling MDR MRSP.
Purpose of the Study:
- To investigate the genomic basis of pathogenicity and clonal success in Staphylococcus pseudintermedius lineages.
- To identify lineage-associated accessory genes and horizontally acquired genes.
- To characterize genetic variations, including deletions and recombination hotspots, in predominant MRSP clones.
Main Methods:
- Genome sequencing and analysis of 622 Staphylococcus pseudintermedius isolates.
- Pangenome analysis to identify lineage-specific accessory genes.
- Investigation of horizontal gene transfer events and recombination hotspots, particularly the spa locus.
Main Results:
- Predominant MRSP clones carry lineage-associated virulence genes.
- The staphylococcal protein A (spa) gene is deleted in 62% of isolates.
- The spa locus is a recombination hotspot, acquiring genes for restriction modification, prophage immunity, mercury resistance, and metabolism.
- ST45 comprises two distinct sublineages with differing accessory gene content and virulence potential.
Conclusions:
- Lineage-specific genetic factors contribute to the success of major MDR MRSP clones.
- The spa locus is a dynamic region involved in acquiring adaptive genes via horizontal gene transfer.
- These findings provide insights into S. pseudintermedius pathogenesis and potential therapeutic targets.
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