# Genomic Epidemiology of Carbapenem-Resistant Acinetobacter baumannii Isolated from Patients Admitted to Intensive Care Units in Network Hospitals in Southern Thailand

**Authors:** Arnon Chukamnerd, Komwit Surachat, Rattanaruji Pomwised, Prasit Palittapongarnpim, Kamonnut Singkhamanan, Sarunyou Chusri

PMC · DOI: 10.3390/antibiotics15020133 · Antibiotics · 2026-01-28

## TL;DR

This study used genomic data to track the spread of antibiotic-resistant Acinetobacter baumannii in southern Thai hospitals, finding a dominant strain linked to high resistance and virulence.

## Contribution

The study provides new insights into the genomic epidemiology of CRAB in southern Thailand, identifying a high-risk ST2 lineage with widespread hospital circulation.

## Key findings

- Sequence type ST2 was the most prevalent and associated with high resistance and virulence.
- blaOXA-23 was the dominant resistance gene in diverse plasmid combinations.
- Clade B (ST2) was linked to bloodstream and soft tissue infections.

## Abstract

Background/Objectives: Carbapenem-resistant Acinetobacter baumannii (CRAB) is classified as an urgent-threat pathogen because of its resistance to nearly all available antibiotics, resulting in high morbidity and mortality rates. However, data on the molecular epidemiology of CRAB isolates in southern Thailand are limited. This study aimed to investigate the genomic epidemiology of CRAB isolates within a hospital network in lower southern Thailand. Methods: Whole-genome sequencing data of CRAB clinical isolates (n = 224) were obtained from a previous study. Additional isolates (n = 70) were included, for which genomic DNA was extracted and sequenced. In total, 294 isolates were collected from patients across seven hospitals in southern Thailand between 2019 and 2020. Their genomes were analyzed using several bioinformatic tools. Results: A high proportion of isolates were obtained from sputum samples of patients with CRAB infection or colonization. Sequence type (ST) 2 was the most frequent ST and was classified in the quadrant with high resistance and virulence. The Sankey diagram showed that ST2 was the dominant and most versatile CRAB lineage circulating across major hospitals, commonly associated with pneumonia, and that diverse resistance genes and plasmid combinations were dominated by blaOXA-23. The core single-nucleotide polymorphism (SNP)-based phylogenetic tree revealed clades A1 (ST215), A2 (multiple STs), and B (ST2). Bloodstream, skin, and soft tissue infections were predominantly observed in clade B. Conclusions: Our analysis revealed widespread circulation of a high-risk ST2 CRAB lineage with enhanced resistance and virulence across hospital networks in the studied region, highlighting the importance of genomics-informed surveillance for controlling CRAB dissemination.

## Linked entities

- **Diseases:** pneumonia (MONDO:0005249)
- **Species:** Acinetobacter baumannii (taxon 470)

## Full-text entities

- **Genes:** SIL1 (SIL1 nucleotide exchange factor) [NCBI Gene 64374] {aka BAP, MSS, ULG5}, LIN9 (lin-9 DREAM MuvB core complex component) [NCBI Gene 286826] {aka BARA, BARPsv, Lin-9, TGS, TGS2}, PEBP1 (phosphatidylethanolamine binding protein 1) [NCBI Gene 5037] {aka HCNP, HCNPpp, HEL-210, HEL-S-34, HEL-S-96, PBP}, VDAC1 (voltage dependent anion channel 1) [NCBI Gene 7416] {aka PORIN, VDAC-1}, ADSS2 (adenylosuccinate synthase 2) [NCBI Gene 159] {aka ADEH, ADSS, ADSS 2}, ST2 (suppression of tumorigenicity 2) [NCBI Gene 6761], SELENBP1 (selenium binding protein 1) [NCBI Gene 8991] {aka EHMTO, HEL-S-134P, LPSB, MTO, SBP56, SP56}, SDCBP (syndecan binding protein) [NCBI Gene 6386] {aka MDA-9, MDA9, SDCBP1, ST1, SYCL, TACIP18}
- **Diseases:** systemic diseases (MESH:D034721), Pneumonia (MESH:D011014), pleural effusion (MESH:D010996), CRAB (MESH:D000151), chronic kidney disease (MESH:D051436), pulmonary disease (MESH:D008171), diabetes mellitus (MESH:D003920), skin/ (MESH:D012871), SSTI (MESH:D018461), injury to (MESH:D014947), infectious disease (MESH:D003141), BSI (MESH:D018805), Colonization (MESH:D003108), STs (MESH:D010855), coronary artery disease (MESH:D003324), UTI (MESH:D014552), cerebrovascular disease (MESH:D002561), peritonitis (MESH:D010538), infection (MESH:D007239), hypertension (MESH:D006973), ascites (MESH:D001201)
- **Chemicals:** lipid A (MESH:D008050), gentamicin (MESH:D005839), tetracyclines (MESH:D013754), meropenem (MESH:D000077731), levofloxacin (MESH:D064704), iron (MESH:D007501), Carbapenem (MESH:D015780), CAZ (MESH:D002442), ertapenem (MESH:D000077727), tigecycline (MESH:D000078304), lincosamide (MESH:D055231), ciprofloxacin (MESH:D002939), sulfonamide (MESH:D013449), aminoglycoside (MESH:D000617), chloramphenicol (MESH:D002701), beta-lactams (MESH:D047090), agarose (MESH:D012685), TMP/SMX (MESH:D015662), Lipopolysaccharide (MESH:D008070), imipenem (MESH:D015378), rifampicin (MESH:D012293), fluoroquinolones (MESH:D024841), amikacin (MESH:D000583), macrolides (MESH:D018942), piperacillin/tazobactam (MESH:D000077725), tetracycline (MESH:D013752), AMK (-)
- **Species:** Enterobacter (genus) [taxon 547], Klebsiella pneumoniae (species) [taxon 573], Pseudomonas aeruginosa (species) [taxon 287], Enterococcus faecium (species) [taxon 1352], Acinetobacter baumannii (species) [taxon 470], Homo sapiens (human, species) [taxon 9606], Staphylococcus aureus (species) [taxon 1280]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12937475/full.md

## References

50 references — full list in the complete paper: https://tomesphere.com/paper/PMC12937475/full.md

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Source: https://tomesphere.com/paper/PMC12937475