# Clinical Presentation, Detection, and Immunopathogenesis of Mycoplasma hyosynoviae Field Isolates in Experimentally Inoculated Pigs

**Authors:** Nubia R. Macedo, Bailey L. Arruda, Luis G. Giménez-Lirola, Ganwu Li, Locke Karriker, Jordi Mora, María J. Clavijo

PMC · DOI: 10.3390/pathogens15010066 · 2026-01-08

## TL;DR

This study examines how two strains of Mycoplasma hyosynoviae affect pigs, showing differences in disease severity and immune response.

## Contribution

The study reveals strain-specific differences in pathogenesis and immune response in pigs infected with Mycoplasma hyosynoviae.

## Key findings

- Lameness was observed in inoculated pigs, with mild to moderate clinical signs.
- The high-virulence strain caused lesions and was detected in synovial fluid, unlike the low-virulence strain.
- Serum IgG levels increased, but only IL-1β, IL-6, and TNF-α cytokines were elevated at 7 days post-inoculation.

## Abstract

Mycoplasma hyosynoviae is a significant pathogen in swine populations, contributing to polyarthritis and lameness in growing pigs. This study characterizes the clinical presentation, pathogen detection, immune response, and lesion development following experimental inoculation with two distinct M. hyosynoviae strains. Pigs were inoculated with either a low- or high-virulence strain and monitored for 18 days. Lameness was observed throughout the study, with affected pigs exhibiting mild to moderate clinical signs. M. hyosynoviae was often detected in the tonsils, while detection in oral fluids was transient. Serum IgG levels increased significantly in the inoculated groups. IL-1β, IL-6, and TNF-α cytokines were elevated only at 7 DPI, whereas IL-8, IL-10, and IFN-γ levels were unchanged in both inoculated groups. Notably, only pigs inoculated with the high-virulence strain developed lesions, and M. hyosynoviae was detected only in the synovial fluid by PCR from this group. These findings highlight strain-dependent differences in the pathogenesis of M. hyosynoviae. The pathological differences between these strains suggest variations in adherence factors, immune evasion capabilities, or metabolic adaptability. Further research is warranted to elucidate the genetic determinants of virulence and the protective role of humoral and cellular immune responses in M. hyosynoviae infection.

## Linked entities

- **Proteins:** IL1B (interleukin 1 beta), IL6 (interleukin 6), TNF (tumor necrosis factor), CXCL8 (C-X-C motif chemokine ligand 8), IL10 (interleukin 10), IFNG (interferon gamma)
- **Diseases:** polyarthritis (MONDO:0024280)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** IL10 (Interleukin 10 level) [NCBI Gene 103158318], TNF (tumor necrosis factor) [NCBI Gene 397086] {aka TNFSF2, TNFa}, IFNG (interferon gamma) [NCBI Gene 396991], IL1B (interleukin 1 beta) [NCBI Gene 397122] {aka IL1B1}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 396880] {aka AMCF-I, IL8}, IL6 (interleukin 6) [NCBI Gene 399500] {aka IL-6}, IGG (Immunoglobulin G level) [NCBI Gene 102658792]
- **Diseases:** Lameness (MESH:D007794), polyarthritis (MESH:D001168), M. hyosynoviae infection (MESH:C566367)
- **Species:** Metamycoplasma hyosynoviae (species) [taxon 29559], Sus scrofa (pig, species) [taxon 9823]

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12845361/full.md

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Source: https://tomesphere.com/paper/PMC12845361