# The emergence of chromosomally located blaCTX-M subtypes in Salmonella enterica serotype Kentucky ST198 isolated from diarrhea patients, food, and environmental sources in Henan, China

**Authors:** Haoyu Qi, Menghan Li, Yanfen Li, Ruichao Li, Ying Cui, Lingling Wu, Meng Zhang, Guangwei Zhang, Yongli Li

PMC · DOI: 10.3389/fmicb.2026.1758643 · Frontiers in Microbiology · 2026-02-04

## TL;DR

This study examines drug-resistant Salmonella Kentucky ST198 isolates in China, revealing chromosomal resistance genes and the need for surveillance.

## Contribution

Identifies chromosomally located blaCTX-M subtypes in Salmonella Kentucky ST198 and their resistance patterns.

## Key findings

- Salmonella Kentucky ST198 isolates from China show multi-drug resistance with chromosomally located blaCTX-M genes.
- Phylogenetic analysis grouped isolates into two clades with distinct resistance gene locations.
- Continuous surveillance is needed to control the spread of extensively drug-resistant Salmonella Kentucky ST198.

## Abstract

Recently, with the resistance to medically important antimicrobial agents, Salmonella enterica serovar Kentucky ST198 has attracted continuous attention. In this study, we present the prevalence, antimicrobial resistance (AMR) mechanisms, and comparative genomics study of 68 Salmonella Kentucky ST198 isolates exhibiting distinct AMR patterns, from patients, food, and environmental sources in Henan Province, China.

We evaluated the genomic and antimicrobial resistance characteristics of Salmonella Kentucky ST198 obtained from foodborne disease and food safety surveillance in Henan, China, during 2018–2022, using whole-genome sequencing and antibiotic susceptibility testing.

Among 1,574 Salmonella isolates, 68 S. Kentucky ST198 isolates were identified, all of which exhibited multi-drug resistance (MDR). Each strain carried between 5 and 19 antimicrobial resistance genes. Phylogenetic analysis revealed that isolates identified in China were clustered into two clades (ST198-1 and ST198-2), characterized by a specific point mutation in the gyrA gene and closely related to European isolates. Comparative genomics showed that acquisition of MDR region in clade ST198-2 conferred resistance to azithromycin, fosfomycin, cefotaxime, rifamycin, chloramphenicol, florfenicol, trimethoprim, and ampicillin. Most blaCTX-M genes were chromosomally located except one strain carrying blaCTX-M-27 on plasmid p0111. In clade ST198-2, blaCTX-M-55 or blaCTX-M-64 genes were detected within the MDR region, while in clade ST198-1, blaCTX-M-14b was inserted into the coding gene clusters of the T6SS, located chromosomally. Considering the extensively drug-resistant nature of the isolates, continuous surveillance and effective measures to control the transmission of Salmonella Kentucky ST198 are urgently needed.

## Linked entities

- **Genes:** blaCTX-M (CTX-M family extended-spectrum class A beta-lactamase) [NCBI Gene 85161177], GYRA (DNA GYRASE A) [NCBI Gene 820238]
- **Chemicals:** azithromycin (PubChem CID 447043), fosfomycin (PubChem CID 441029), cefotaxime (PubChem CID 5742673), rifamycin (PubChem CID 6324616), chloramphenicol (PubChem CID 5959), florfenicol (PubChem CID 114811), trimethoprim (PubChem CID 5578), ampicillin (PubChem CID 6249)
- **Diseases:** diarrhea (MONDO:0001673)

## Full-text entities

- **Genes:** VIM (vimentin) [NCBI Gene 7431], PLPPR5 (phospholipid phosphatase related 5) [NCBI Gene 163404] {aka LPPR5, PAP2, PAP2D, PRG5}, ADI1 (acireductone dioxygenase 1) [NCBI Gene 55256] {aka APL1, ARD, ARD', Fe-ARD, HMFT1638, MTCBP1}, strA [NCBI Gene 13923317], MFT2 (Trichoepithelioma, multiple familial, 2) [NCBI Gene 100188881] {aka TEM}, strB [NCBI Gene 24957187], CUL9 (cullin 9) [NCBI Gene 23113] {aka H7AP1, PARC}
- **Diseases:** infection (MESH:D007239), AMR (MESH:D060467), type II (MESH:D006938), MDR (MESH:D018088), cgMLST (MESH:D020512), ESBLs (MESH:C579922), foodborne disease (MESH:D005517), non-typhoidal Salmonella (NTS) infections (MESH:D014435), diarrhea (MESH:D003967)
- **Chemicals:** trimethoprim (MESH:D014295), cephalosporins (MESH:D002511), sulphonamides (MESH:D013449), macrolides (MESH:D018942), quinolone (MESH:D015363), Ciprofloxacin (MESH:D002939), fluoroquinolone (MESH:D024841), Streptomycin (MESH:D013307), CFX (MESH:D002440), -lactamase (-), sulfamethoxazole (MESH:D013420), cefotaxime (MESH:D002439), azithromycin (MESH:D017963), aminoglycoside (MESH:D000617), tetracycline (MESH:D013752), fosfomycin (MESH:D005578), penicillin (MESH:D010406), rifamycin (MESH:C023808), beta-lactam (MESH:D047090), gentamicin (MESH:D005839), lincomycin (MESH:D008034), chloramphenicol (MESH:D002701), florfenicol (MESH:C035534), CFZ (MESH:C057223), ampicillin-sulbactam (MESH:C035444), AMS (MESH:D000576), ampicillin (MESH:D000667), AMP (MESH:D000249), imipenem (MESH:D015378), nalidixic acid (MESH:D009268), mph (MESH:C041626), CAZ (MESH:D002442), carbapenem (MESH:D015780), tetracyclines (MESH:D013754), sulfamethoxazole-trimethoprim (MESH:D015662), cefazolin (MESH:D002437)
- **Species:** Salmonella enterica subsp. enterica serovar Kentucky (no rank) [taxon 192955], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Homo sapiens (human, species) [taxon 9606], Gallus gallus (bantam, species) [taxon 9031], Sapovirus GI.1 (no rank) [taxon 1398550], Escherichia coli ATCC 25922 (strain) [taxon 1322345], Salmonella enterica (species) [taxon 28901]
- **Mutations:** T57S, Asp87Gly, D87N, S83F, Asp87Tyr, S80I
- **Cell lines:** pHA22057 — Homo sapiens (Human), Finite cell line (CVCL_2Y68), p14076B — Homo sapiens (Human), Transformed cell line (CVCL_EH19), IS26 — Rattus norvegicus (Rat), Transformed cell line (CVCL_8806)

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## References

47 references — full list in the complete paper: https://tomesphere.com/paper/PMC12913533/full.md

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Source: https://tomesphere.com/paper/PMC12913533