# Genomic epidemiological analysis reveals new insights into the resurgence of Mycoplasma pneumoniae in China

**Authors:** Xue Wang, Dandan Zheng, Cheng Gong, Ming Luo, Aihua Li, Xuecong Duan, Chengcheng Wang, Geng Hu, Xuejiao Guan, Fan Yang, Fang Huang, Lihong Chen

PMC · DOI: 10.3389/fcimb.2025.1611519 · Frontiers in Cellular and Infection Microbiology · 2025-11-07

## TL;DR

This study analyzed the resurgence of Mycoplasma pneumoniae in Beijing, China, using genomic data to understand its spread and genetic changes.

## Contribution

The study reveals that the 2023 M. pneumoniae outbreak in Beijing was due to existing strains, not new variants, with distinct genomic features.

## Key findings

- The 2023 outbreak was caused by pre-existing M. pneumoniae strains, not new variants.
- ST3 and ST14 were the dominant sequence types, with increasing macrolide resistance in ST14.
- Genomic analysis showed high similarity among Beijing strains and distinct regional clustering.

## Abstract

After coronavirus disease 2019 pandemic restrictions, Mycoplasma pneumoniae (M. pneumoniae) re-surged widely across the world. This study aimed to determine the genomic epidemiological characteristics of resurging M. pneumoniae, which has dominated the respiratory infection outbreak in Beijing, China, since mid-September 2023.

M. pneumoniae samples were collected from patients with acute respiratory-tract infections in Beijing in 2018–2023. A total of 160 M. pneumoniae genomes were sequenced via probe-capture-based approach. The genetic features of M. pneumoniae were characterized by multilocus sequence typing and comparative genomic analysis.

In total, 160 patients with M. pneumoniae infections were enrolled. ST3 (n = 93) and ST14 (n = 65) were the predominant sequence types. The macrolide-resistant mutation rate of ST3 was maintained at 100%, whereas that of ST14 increased rapidly. Comparative genomic analysis revealed 99% to > 99% similarity among the Beijing strains from 2023 when aligned to the reference M129 genome. The major variation occurs in the P1 gene. MAUVE indicated a lack of rearrangement, yet it included four subtype-specific insertions and non-conserved hsdS genes. The phylogenetic tree showed that strains from Asia and other world regions clustered into distinct clades, with significant evolutionary differences. Further genomic analyses identified some Asia-dominant genetic variations in genes associated with genome stability, pathogenesis, and drug resistance.

The 2023 outbreak of M. pneumoniae was not attributable to a novel variant but stemmed from the resurgence of the pre-existing strains. Our genomic epidemiological findings demonstrated that the endemic strains in different regions exhibit distinct genomic characteristics, associated with genomic stability.

## Linked entities

- **Genes:** CRYGFP (crystallin gamma F, pseudogene) [NCBI Gene 1423], hsdS (type I restriction/modification system specificity determinant HsdS) [NCBI Gene 887695]

## Full-text entities

- **Diseases:** M. pneumoniae infections (MESH:C566367), respiratory infection (MESH:D012141), coronavirus disease 2019 (MESH:D000086382)
- **Chemicals:** macrolide (MESH:D018942)
- **Species:** Mycoplasmoides pneumoniae (Filterable agent of primary atypical pneumonia, species) [taxon 2104], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

52 references — full list in the complete paper: https://tomesphere.com/paper/PMC12634620/full.md

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Source: https://tomesphere.com/paper/PMC12634620