BMC Microbiology· 2026Q1
Pathogenicity and genome-informed virulence features of Glaesserella parasuis serovar 13 in piglets
- 0citations
- Q1SCImago
- 2026year
Short summary
Glaesserella parasuis serovar 13 strain W2 caused dose-dependent mortality and severe pulmonary injury in piglets, with whole-genome sequencing revealing numerous putative virulence factors related to immune modulation, nutrient acquisition, and adhesion.
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Key points
- Glaesserella parasuis serovar 13 strain W2 induced dose-dependent mortality and severe pulmonary injury in a piglet challenge model.
- The strain disseminated to multiple tissues and body fluids following intraperitoneal challenge.
- Whole-genome sequencing revealed a 2.36 Mb chromosome and identified multiple putative virulence-associated homologs.
- These homologs are primarily related to immune modulation, nutrient acquisition, adhesion, stress adaptation, and surface structure remodeling.
- Antimicrobial resistance screening detected resistance-associated homologs but no definitive acquired resistance genes.
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Abstract
Glaesserella parasuis is an important swine pathogen that causes Glässer’s disease, a systemic disease associated with polyserositis, arthritis, meningitis, and pneumonia. Serovar 13 is generally considered highly pathogenic and has been linked to severe clinical disease in pigs; however, integrated evidence on its experimental pathogenicity and complete genomic characteristics remains limited. In this study, we systematically characterized G. parasuis serovar 13 strain W2, a clinical isolate recovered from the lung of a piglet with severe systemic disease, by combining a piglet challenge model, whole-genome sequencing, and comparative genomic analysis. W2 caused dose-dependent mortality after intraperitoneal challenge, disseminated to multiple tissues and body fluids, and induced dose-associated pulmonary injury, indicating marked pathogenic effects in this intraperitoneal challenge model. Sequencing results revealed that W2 contained a complete circular chromosome of 2.36 Mb without detectable plasmid replicons, and taxonomic analyses confirmed its placement within G. parasuis. Genome annotation identified multiple putative virulence-associated homologs mainly related to immune modulation, nutrient acquisition, adhesion, stress adaptation, and surface structure remodeling. Predicted prophage-like regions, genomic islands, and CRISPR array-like loci further suggested genomic plasticity in this strain. Antimicrobial resistance screening identified resistance-associated homologs but no definitive acquired resistance genes. Overall, W2 is a serovar 13 clinical isolate that exhibited marked pathogenic effects in a piglet intraperitoneal challenge model. Genome analysis identified multiple putative virulence-associated features, although their contributions to the observed phenotype remain to be established.
The authors' abstract, as published at the source. BMC Microbiology, 2026 · DOI ↗
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