# Whole-Genome Sequence Analysis of Colistin-Resistant, mcr-Harboring Escherichia coli Isolated from a Swine Slaughterhouse in Thailand

**Authors:** Ratchadaporn Boripun, Pakpoom Tadee, Ravisa Warin, Naparat Suttidate, Doan Hoang Phu, Hidenori Kabeya, Chaithep Poolkhet, Sumalee Boonmar, Suchawadee Tesakul, Yanika Klainiem, Nuttapong Pavana

PMC · DOI: 10.3390/antibiotics15020135 · Antibiotics · 2026-01-29

## TL;DR

This study found high levels of colistin-resistant E. coli in a Thai swine slaughterhouse, highlighting risks of antibiotic resistance spreading through the food chain.

## Contribution

The study provides genomic insights into colistin-resistant E. coli isolates from livestock in Thailand, revealing high multidrug resistance and virulence gene prevalence.

## Key findings

- 73.21% of E. coli isolates harbored mcr genes, with mcr-1 being the most common.
- 75% of isolates exhibited multidrug resistance with 22 distinct resistance profiles.
- Whole genome sequencing confirmed multiple resistance and virulence genes in selected isolates.

## Abstract

The emergence of colistin-resistant Escherichia coli (E. coli) in livestock poses a major public health concern due to its zoonotic potential and multidrug resistance (MDR). The study aimed to detect mobilized colistin resistance genes (mcr-1 to mcr-9) in E. coli isolates, along with characterizing their antimicrobial susceptibility, resistance genes, virulence genes, and whole genome sequencing. We investigated E. coli contamination in a swine slaughterhouse in Nakhon Si Thammarat Province, Thailand. A total of 200 fecal samples were collected and screened for E. coli using selective media supplemented with colistin. A total of 200 fecal samples were collected from a swine slaughterhouse and screened for E. coli using selective media supplemented with colistin. Presumptive E. coli isolates were confirmed by PCR, followed by molecular detection of mcr-1 to mcr-9 genes. Antimicrobial susceptibility testing was performed using the disk diffusion method. Selected isolates were further analyzed for additional antimicrobial resistance genes and virulence associated genes by PCR. Whole genome sequencing was conducted on representative isolates exhibiting high levels of antimicrobial resistance. Our results showed that out of 200 fecal samples, 124 presumptive E. coli isolates were recovered from a swine slaughterhouse using selective media containing colistin. PCR confirmation identified 112 isolates (90.32%) as E. coli. Molecular detection of mobilized colistin resistance (mcr) genes (82 isolates, 73.21%) demonstrated that mcr-1 (50.89%) was the most prevalent, followed by mcr-9 (25.89%) and mcr-3 (24.11%). Overall, the 82 mcr E. coli isolates showed the highest level of resistance to ampicillin (97.56%), followed by tetracycline (95.12%), piperacillin (73.17%), and chloramphenicol (65.85%). For non-mcr E. coli isolates, the highest resistance percentage was observed for ampicillin (96.67%), followed by piperacillin (80%) and tetracycline (73.33%). Among the isolates, 75% exhibited MDR phenotypes, showing 22 distinct resistance profiles. The most common MDR pattern was AMP-PIP-TE-C-S (12.5%). Additional antimicrobial resistance genes, including aadA, ampC, and blaTEM, were detected in over 60% of a subset of 30 tested isolates. The virulence gene analysis revealed that eae (74.10%), associated with enteropathogenic E. coli (EPEC), was the predominant pathotype. Whole genome sequencing of five selected isolates confirmed the presence of multiple antimicrobial resistance and virulence determinants. In conclusion, this study reveals a high prevalence of MDR E. coli harboring colistin resistance genes (mcr-1 to mcr-9) in a swine slaughterhouse in southern Thailand. The findings highlight the potential risk of zoonotic transmission of antimicrobial resistant E. coli through the food production chain and emphasize the importance of continuous genomic surveillance and prudent antimicrobial use in livestock production systems.

## Linked entities

- **Genes:** MCR1 (cytochrome-b5 reductase) [NCBI Gene 853707], mcr3 (ncRNA) [NCBI Gene 14515894], aadA (aminoglycoside adenyltransferase) [NCBI Gene 1252782], ampC (beta-lactamase) [NCBI Gene 878149], eae (T3SS intimin) [NCBI Gene 915471]
- **Chemicals:** colistin (PubChem CID 5311054), ampicillin (PubChem CID 6249), tetracycline (PubChem CID 54675776), piperacillin (PubChem CID 43672), chloramphenicol (PubChem CID 5959)
- **Species:** Escherichia coli (taxon 562), Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** aadA2 [NCBI Gene 13906555], colicin [NCBI Gene 6383669], aadA [NCBI Gene 7872390], floR [NCBI Gene 13905643], tetC [NCBI Gene 6275977], aadA1 [NCBI Gene 13906545], blaTEM [NCBI Gene 13905334], ermB [NCBI Gene 9846007], yehA [NCBI Gene 4924785], AmpC [NCBI Gene 7872529], dfrA14 [NCBI Gene 20493539], aphA1 [NCBI Gene 4246774], ESBL [NCBI Gene 13906541], dfrA12 [NCBI Gene 13906804], tir [NCBI Gene 8319157], cmlA [NCBI Gene 9846099], OqxB [NCBI Gene 5962056], aac3-IId [NCBI Gene 18157945], qnrS1 [NCBI Gene 20467117], nleA [NCBI Gene 39727474], tetB [NCBI Gene 18157666], OqxA [NCBI Gene 5962055], ompT [NCBI Gene 3853531], mphA [NCBI Gene 8319296], etpD [NCBI Gene 5290910], traJ [NCBI Gene 4364256], traT [NCBI Gene 13907082]
- **Diseases:** nosocomial infections (MESH:D003428), mcr (MESH:D014086), HUS (MESH:D006463), infections (MESH:D007239), colitis (MESH:D003092), EAEC (MESH:D004927), enteric (MESH:D004751), bacterial infections (MESH:D001424), fecal (MESH:D005242), Gram-negative infections (MESH:D016905), mcr-1.1 (MESH:D015658), intestinal diseases (MESH:D007410), injury to (MESH:D014947), MDR (MESH:D018088), AMR (MESH:D060467), diarrhea (MESH:D003967), foodborne infection (MESH:D005517)
- **Chemicals:** -lactamases (-), S (MESH:D013455), penicillin (MESH:D010406), streptogramin (MESH:D025361), tetracycline (MESH:D013752), trimethoprim (MESH:D014295), cephalosporins (MESH:D002511), ceftriaxone (MESH:D002443), macrolides (MESH:D018942), amikacin (MESH:D000583), quinolone (MESH:D015363), AMP (MESH:D000667), pirlimycin (MESH:C034093), agarose (MESH:D012685), beta-lactam (MESH:D047090), chloramphenicol (MESH:D002701), folate (MESH:D005492), Enrofloxacin (MESH:D000077422), TE (MESH:D013691), enterobactin (MESH:D004758), Aminoglycoside (MESH:D000617), piperacillin (MESH:D010878), yersiniabactin (MESH:C104398), lactose (MESH:D007785), cortisol (MESH:D006854), amoxicillin-clavulanic (AMC) acid (MESH:D019980), sulfonamide (MESH:D013449), Agar (MESH:D000362), Streptomycin (MESH:D013307), C (MESH:D002244), iron (MESH:D007501), tetracyclines (MESH:D013754), gentamicin (MESH:D005839)
- **Species:** Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Macrotrachela sp. CR (species) [taxon 1659203], Homo sapiens (human, species) [taxon 9606], Ehrlichia sp. IE-C (species) [taxon 371764], Gallus gallus (bantam, species) [taxon 9031], Salmonella (genus) [taxon 590], Escherichia coli (E. coli, species) [taxon 562], Escherichia coli O157:H7 (no rank) [taxon 83334], Mesorhizobium sp. CR11 (species) [taxon 1837347], Sus scrofa (pig, species) [taxon 9823], Enterobacterales (order) [taxon 91347]
- **Cell lines:** :H7 — Bos taurus (Bovine), Spontaneously immortalized cell line (CVCL_HG38)

## Full text

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## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12937216/full.md

## References

85 references — full list in the complete paper: https://tomesphere.com/paper/PMC12937216/full.md

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Source: https://tomesphere.com/paper/PMC12937216