# Genomic Characterization of Potential Opportunistic Zoonotic Streptococcus parasuis Isolated in China

**Authors:** Gang Liu, Yu Liu, Zhikang Jiang, Kang Liu, Xianwen Wang, Juyuan Hao, He Kong, Yajie Yu, Zicheng Ding, Min Li, Xianjie Han

PMC · DOI: 10.3390/pathogens14040395 · Pathogens · 2025-04-18

## TL;DR

This study analyzes the genomes of two Streptococcus parasuis strains from pigs in China to understand their potential zoonotic threat and drug resistance.

## Contribution

The study identifies key virulence and antibiotic resistance genes in S. parasuis and links mobile genetic elements to drug resistance.

## Key findings

- srtC, ctpV, and sugC are key virulence genes in S. parasuis, though their pathogenic potential is lower than in S. suis serotype 2.
- S. parasuis shows resistance to aminoglycosides, macrolides, tetracyclines, and oxazolidinones but is susceptible to some oxazolidinone-class antibiotics.
- Mobile genetic elements are associated with antibiotic resistance in the studied S. parasuis strains.

## Abstract

(1) Background: S. parasuis is a potential opportunistic zoonotic pathogen that can infect pigs, cattle, and humans, composed of former members of S. suis serotypes 20, 22, and 26. In recent years, unclassified serotypes and a serotype 11 S. parasuis have been discovered. (2) Methods: We characterized two S. parasuis strains (FZ1 and FZ2) isolated from brain samples of paralyzed pigs and examined evolutionary divergence among 22 available S. parasuis and 8 serotype 2 S. suis genomes through whole-genome sequencing and comparative genomic analysis. We compared virulence genes (VGs) and antibiotic resistance genes (ARGs) and analyzed mobile genetic elements (MGEs) in FZ1 and FZ2. (3) Results: Comparative genomics revealed that srtC, ctpV, and sugC may represent key virulence determinants in S. parasuis, although their pathogenic potential appears attenuated compared to serotype 2 S. suis. In addition, S. parasuis exhibited primary resistance to aminoglycosides, macrolides, tetracyclines, and oxazolidinones, while demonstrating heightened susceptibility to oxazolidinone-class antibiotics. Moreover, we found an important association between MGEs and antibiotic resistance in S. parasuis FZ1 and FZ2. (4) Conclusions: This study provides new insights into the genomic and evolutionary characteristics of S. parasuis and provides a new basis for the study of bacterial pathogenesis and drug resistance in the future.

## Linked entities

- **Genes:** srtC (Ebp pilus assembly class C sortase) [NCBI Gene 60893491], ctpV (copper-exporting ATPase) [NCBI Gene 885254], sugC (sugar ABC transporter ATP-binding protein SugC) [NCBI Gene 887104]
- **Chemicals:** oxazolidinones (PubChem CID 73949)
- **Species:** Streptococcus parasuis (taxon 1501662), Streptococcus suis (taxon 1307)

## Full-text entities

- **Chemicals:** tetracyclines (MESH:D013754), macrolides (MESH:D018942), aminoglycosides (MESH:D000617), oxazolidinone (MESH:D023303)
- **Species:** Streptococcus suis (species) [taxon 1307], Sus scrofa (pig, species) [taxon 9823], Streptococcus parasuis (species) [taxon 1501662], Homo sapiens (human, species) [taxon 9606], Bos taurus (bovine, species) [taxon 9913]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12030105/full.md

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12030105/full.md

## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12030105/full.md

---
Source: https://tomesphere.com/paper/PMC12030105