# Epidemiology and genomics of azithromycin-resistant extensively drug-resistant Salmonella enterica serovar Typhimurium in Taiwan

**Authors:** Yu-Ping Hong, Ying-Shu Liao, Bo-Han Chen, You-Wun Wang, Ru-Hsiou Teng, Shiu-Yun Liang, Hsiao Lun Wei, Jui-Hsien Chang, Chien-Shun Chiou

PMC · DOI: 10.1128/aac.01334-25 · Antimicrobial Agents and Chemotherapy · 2026-02-19

## TL;DR

A new highly drug-resistant strain of Salmonella is spreading in Taiwan, and genomic analysis shows how it evolved from less resistant strains.

## Contribution

Identification of the genetic evolution and spread of azithromycin-resistant extensively drug-resistant Salmonella in Taiwan.

## Key findings

- AziR-XDR S. Typhimurium strains emerged from MDR ancestors via IS26-mediated resistance gene acquisitions.
- All AziR-XDR isolates carry additional resistance genes on plasmids, increasing resistance to multiple antibiotics.
- The HC50_13 subclone has increased notably in Taiwan since 2021.

## Abstract

The recent emergence of azithromycin-resistant extensively drug-resistant (AziR-XDR) Salmonella enterica serovar Typhimurium (S. Typhimurium) in Taiwan poses a significant public health concern. To investigate the genetic basis and the evolutionary dynamics, we analyzed 60 isolates collected between 2007 and 2024, comprising multidrug-resistant (MDR, n = 45) and AziR-XDR (n = 15) isolates from human and animal sources. Whole-genome sequencing analysis revealed that 36 of 45 MDR isolates and all AziR-XDR isolates belonged to the HC50_13 subclone (differing by ≤ 50 core genes) and clustered within the HC20_152604 cluster (differing by ≤ 20 core genes) and the SNP cluster PDS000042202. All HC50_13 MDR isolates and AziR-XDR isolates carried core resistance genes including aac(3)-IId, aph(3’’)-Ib, aph(6)-Id, blaTEM-1, floR, sul2, tet(A) on type 2 IncC plasmids, and AziR-XDR isolates carried additional antimicrobial resistance genes (ARGs) on the plasmids, including blaDHA-1, dfrA17, mph(A), qnrB, and sul1, conferring additional resistance to azithromycin, trimethoprim, third-generation cephalosporins, and fluoroquinolones. AziR-XDR S. Typhimurium strains belonging to the HC50_13 subclone were initially identified in 2016 and have notably increased in Taiwan since 2021. The subclone was likely evolved from MDR ancestor strains by multiple IS26-mediated acquisitions of additional resistance cassettes. Our findings demonstrate how MDR S. Typhimurium can evolve locally into highly resistant strains. This underscores the need for genomic surveillance and coordinated antimicrobial stewardship in Taiwan and globally to prevent further dissemination of the highly resistant HC20_152604 clade.

## Linked entities

- **Genes:** aac(3)-IId (aminoglycoside N-acetyltransferase AAC(3)-IId) [NCBI Gene 50216977], aph(3'')-Ib (aminoglycoside O-phosphotransferase APH(3'')-Ib) [NCBI Gene 23448054], floR (chloramphenicol/florfenicol efflux MFS transporter FloR) [NCBI Gene 57334229], sul-2 (Sulfatase N-terminal domain-containing protein) [NCBI Gene 179194], tet(A) (tetracycline efflux MFS transporter Tet(A)) [NCBI Gene 33941499], dfrA17 (trimethoprim-resistant dihydrofolate reductase DfrA17) [NCBI Gene 83039323], sul-1 (Putative extracellular sulfatase Sulf-1 homolog) [NCBI Gene 180619]
- **Chemicals:** azithromycin (PubChem CID 447043), trimethoprim (PubChem CID 5578)

## Full-text entities

- **Genes:** tet(A) [NCBI Gene 13909704], blaTEM-1 [NCBI Gene 24955828], sul2 [NCBI Gene 24955642], mph(A) [NCBI Gene 7693044], sul1 [NCBI Gene 13909701], floR [NCBI Gene 24955634]
- **Chemicals:** azithromycin (MESH:D017963), fluoroquinolones (MESH:D024841), trimethoprim (MESH:D014295), cephalosporins (MESH:D002511)
- **Species:** Salmonella enterica subsp. enterica serovar Typhimurium (no rank) [taxon 90371], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

32 references — full list in the complete paper: https://tomesphere.com/paper/PMC13041382/full.md

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Source: https://tomesphere.com/paper/PMC13041382