# Molecular Epidemiology of Escherichia coli Clinical Isolates From a Tertiary Care Hospital in Uttarakhand, India: Insights Into Antimicrobial Resistance (AMR) Burden, Virulence Profiles, and High-Risk Lineages

**Authors:** Ranjana Rohilla, Mohit Bhatia, Varun Shamanna, Geetha Nagaraj, Pratima Gupta, Balram Ji Omar, Harshitha Gk, K L Ravikumar

PMC · DOI: 10.7759/cureus.102613 · Cureus · 2026-01-30

## TL;DR

This study analyzes E. coli isolates from a hospital in India to understand their resistance to antibiotics and virulence traits, revealing high levels of drug resistance and concerning bacterial clones.

## Contribution

The study provides genomic insights into E. coli clinical isolates in India, highlighting high-risk lineages with combined virulence and multidrug resistance.

## Key findings

- 90% of isolates showed multidrug resistance, with universal resistance to fluoroquinolones and third-generation cephalosporins.
- 76% of isolates carried carbapenemase genes, and the most common sequence type was ST167.
- Virulence factors like fim, pap, and iutA were prevalent, with no diarrheagenic E. coli pathotypes identified.

## Abstract

Introduction

Escherichia coli (E. coli) is a major cause of extraintestinal infections and a leading contributor to antimicrobial resistance (AMR), particularly in low- and middle-income countries. The increasing convergence of multidrug resistance and virulence within high-risk clones poses serious challenges to treatment and infection control. Genomic data on circulating clinical E. coli lineages from India remain limited. This study aimed to characterize the population structure, AMR determinants, virulence profiles, and plasmid content of clinical E. coli isolates using whole-genome sequencing (WGS).

Methods

An exploratory study was conducted on 50 clinical E. coli isolates collected between January 2018 and October 2020 from diverse clinical specimens at a tertiary care teaching hospital in Uttarakhand, India. Antimicrobial susceptibility testing was performed using the VITEK 2 Compact system and interpreted according to the Clinical and Laboratory Standards Institute (CLSI) guidelines. WGS was carried out on the Illumina MiSeq platform. In silico analyses included phylogrouping, multilocus sequence typing (MLST), serotyping, AMR gene detection, virulence factor profiling, and plasmid replicon typing.

Results

Multidrug resistance was observed in the majority (45/50 (90%)) of the isolates. Universal phenotypic resistance was noted to fluoroquinolones (50/50 (100%)) and third-generation cephalosporins (50/50 (100%)), while carbapenem resistance was detected in 35/50 (70%). Tigecycline and colistin retained in vitro activity in 47/50 (94%) and 50/50 (100%) isolates, respectively. Genomic analysis identified extended-spectrum beta-lactamases (ESBL) genes in all isolates and carbapenemase genes (blaNDM-1, blaNDM-5, blaOXA-181) in 38/50 (76%), with high genotype-phenotype concordance. The predominant sequence type was ST167 (15/50 (30%)), followed by ST410, ST648, ST405, and ST131. Virulence profiling demonstrated predominance of ExPEC-associated adhesins (fim, pap, afa) and iron acquisition systems (iutA, fyuA, iroN). No classical diarrheagenic E. coli pathotypes were identified. IncF-type plasmids were the most prevalent.

Conclusion

This study highlights the alarming convergence of virulence and multidrug resistance among dominant E. coli clones in a tertiary care setting in India. The findings underscore the value of WGS-based surveillance in guiding antimicrobial stewardship and strengthening infection control strategies.

## Linked entities

- **Genes:** ZMYM2 (zinc finger MYM-type containing 2) [NCBI Gene 7750], REG3A (regenerating family member 3 alpha) [NCBI Gene 5068], AFA (ankyloblepharon filiforme adnatum) [NCBI Gene 170], iutA (ferric siderophore receptor) [NCBI Gene 1026206], fyuA (receptor precursor-mostly Fe transport) [NCBI Gene 11639363], iroN (TonB-dependent siderophore receptor protein) [NCBI Gene 1254300]
- **Chemicals:** carbapenems (PubChem CID 134085), tigecycline (PubChem CID 54686904), colistin (PubChem CID 5311054)
- **Species:** Escherichia coli (taxon 562)

## Full-text entities

- **Genes:** pap [NCBI Gene 7256836], blaNDM-1 [NCBI Gene 13906127], rmtB [NCBI Gene 13906405], Iron [NCBI Gene 3853509], iutA [NCBI Gene 7324510], blaCTX-M-15 [NCBI Gene 9538104], blaTEM [NCBI Gene 13905334], aadA1 [NCBI Gene 13906545], mph [NCBI Gene 13905635], blaOXA-1 [NCBI Gene 17035637], cat [NCBI Gene 2847485], ESBL [NCBI Gene 13906541], cmlA [NCBI Gene 9846099], qnrS1 [NCBI Gene 20467117], tetB [NCBI Gene 18157666], sat [NCBI Gene 1238709]
- **Diseases:** nosocomial infections (MESH:D003428), diarrheal disease (MESH:D004403), Infections (MESH:D007239), pleural or peritoneal infections (MESH:D010538), UTIs (MESH:D014552), wound infections (MESH:D014946), ExPEC (MESH:D004927), neonatal meningitis (MESH:D007232), Gram-negative infections (MESH:D016905), infectious diseases (MESH:D003141), BSIs (MESH:D018805), respiratory infections (MESH:D012141), MDR (MESH:D018088), AMR (MESH:D060467), meningitis (MESH:D008580)
- **Chemicals:** -lactamases (-), nitrofurantoin (MESH:D009582), penicillins (MESH:D010406), tetracycline (MESH:D013752), cephalosporins (MESH:D002511), heme (MESH:D006418), macrolides (MESH:D018942), ceftriaxone (MESH:D002443), piperacillin-tazobactam (MESH:D000077725), quinolone (MESH:D015363), Fluoroquinolone (MESH:D024841), amikacin (MESH:D000583), imipenem (MESH:D015378), ampicillin (MESH:D000667), beta-lactam (MESH:D047090), chloramphenicol (MESH:D002701), folate (MESH:D005492), aminoglycoside (MESH:D000617), enterobactin (MESH:D004758), yersiniabactin (MESH:C104398), ciprofloxacin (MESH:D002939), Tigecycline (MESH:D000078304), nalidixic acid (MESH:D009268), Carbapenem (MESH:D015780), tetracyclines (MESH:D013754), meropenem (MESH:D000077731), levofloxacin (MESH:D064704), gentamicin (MESH:D005839)
- **Species:** Homo sapiens (human, species) [taxon 9606], Ehrlichia sp. IE-C (species) [taxon 371764], Escherichia coli (E. coli, species) [taxon 562], Escherichia coli O25b:H4-ST131 (no rank) [taxon 941322]
- **Mutations:** E84V, S80I, E460D, D87N, S83L, S458T, S458A, E123D, I529L, A108V, Y358N
- **Cell lines:** ATCC 25922 — Homo sapiens (Human), Lung adenocarcinoma, Cancer cell line (CVCL_0023)

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## References

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Source: https://tomesphere.com/paper/PMC12964320