# Mapping Escherichia coli in Women with Simple Urinary Tract Infections: Phenotypic ESBL/AmpC Screening and Whole-Genome Insights from Oman

**Authors:** Aisha Al-Mufarji, Meher Rizvi, Nawal Al-Kindi, Nada Al-Tamtami, Zaaima Al-Jabri

PMC · DOI: 10.3390/antibiotics15020124 · Antibiotics · 2026-01-27

## TL;DR

This study maps drug-resistant Escherichia coli in women with urinary tract infections in Oman, identifying effective antibiotic alternatives and genomic patterns.

## Contribution

The study provides new insights into the prevalence of ESBL-producing E. coli in Omani women and evaluates novel oral antibiotics as carbapenem-sparing options.

## Key findings

- ESBL-producing E. coli accounted for 38–51% of isolates, with ST-131 being the most common sequence type.
- Nitrofurantoin, mecillinam, fosfomycin, and nitroxoline showed 100% activity against ESBL and non-ESBL isolates.
- Genomic analysis revealed blaCTX-M-15 as the dominant ESBL genotype among E. coli isolates.

## Abstract

Background/Objectives: Simple urinary tract infections (sUTIs) are common in women and increasingly affected by multidrug-resistant (MDR) Escherichia coli. Extended-spectrum β-lactamase (ESBL) and AmpC producers restrict oral treatment options and promote carbapenem use. This study aimed to (i) describe the etiology and antimicrobial susceptibility of sUTIs in women of reproductive age in Oman, (ii) determine the prevalence of ESBL/AmpC-producing E. coli, (iii) evaluate nitroxoline, fosfomycin, mecillinam, and temocillin against ESBL and non-ESBL E. coli, and (iv) characterize circulating clones and resistance/virulence determinants using whole-genome sequencing (WGS). Methods: In this multicentric study (September 2022–August 2023), 795 uropathogens from 762 women (15–50 years) with sUTI were collected from four Omani hospitals. Identification and susceptibility testing of E. coli (n = 489) and Klebsiella pneumoniae (n = 140) using BD Phoenix and MALDI-TOF MS was performed (CLSI 2022). Thirty ESBL-producing and 82 non-ESBL E. coli underwent phenotypic ESBL/AmpC testing and evaluation of mecillinam, temocillin, nitroxoline, and fosfomycin. WGS was performed on 26 isolates (23 ESBL, 3 wild type) and analyzed for MLST, and SNP phylogeny using ResFinder, CARD, PlasmidFinder, VirulenceFinder. Statistical significance was set at p < 0.05. Results: E. coli (62%) and K. pneumoniae (18%) were the predominant pathogens. E. coli showed high susceptibility to nitrofurantoin (~97%), carbapenems, aminoglycosides, and piperacillin–tazobactam, but reduced susceptibility to cephalosporins, fluoroquinolones, cotrimoxazole, and ampicillin. ESBL prevalence ranged from 38–51%; AmpC producers were rare (4.6%). Mecillinam, nitroxoline, and fosfomycin exhibited 100% activity against both ESBL and non-ESBL isolates; temocillin showed 89.3% activity in ESBL strains. WGS identified 15 sequence types dominated by ST-131, ST-1193, ST-73, and ST-174, with blaCTX-M-15 as the major ESBL genotype. Conclusions: sUTIs in Oman show a high burden of ESBL-producing E. coli. Nitrofurantoin, mecillinam, fosfomycin, temocillin, and nitroxoline would be effective carbapenem-sparing oral options. Continuous phenotypic and genomic surveillance are crucial to guide antimicrobial therapy and stewardship.

## Linked entities

- **Chemicals:** nitrofurantoin (PubChem CID 6604200), carbapenems (PubChem CID 134085), piperacillin–tazobactam (PubChem CID 461573), cephalosporins (PubChem CID 25058126), cotrimoxazole (PubChem CID 358641), ampicillin (PubChem CID 6249), mecillinam (PubChem CID 36273), temocillin (PubChem CID 171758), nitroxoline (PubChem CID 19910), fosfomycin (PubChem CID 441029)
- **Species:** Escherichia coli (taxon 562), Klebsiella pneumoniae (taxon 573)

## Full-text entities

- **Genes:** mph(A) [NCBI Gene 8319296], Sul2 [NCBI Gene 7324562], ompT [NCBI Gene 3853531], blaTEM-1 [NCBI Gene 9537966], Mrx [NCBI Gene 13909208], sat [NCBI Gene 1238709], traT [NCBI Gene 13907082], Sul1 [NCBI Gene 7872757], iha [NCBI Gene 3654559], OXA-1 [NCBI Gene 8319151], blaDHA-1 [NCBI Gene 13905369], dfrA1 [NCBI Gene 10549022], hlyA [NCBI Gene 7701379], beta-lactamase [NCBI Gene 9284727], H-NS [NCBI Gene 13905950], sitA [NCBI Gene 5962082], CTX-M-14 [NCBI Gene 20492411], dihydropteroate synthase [NCBI Gene 20491868], tet(A [NCBI Gene 15152827], blaOXA-1 [NCBI Gene 17035637], yehA [NCBI Gene 4924785], blaTEM [NCBI Gene 13905334], TEM-1 [NCBI Gene 2716540], ESBL [NCBI Gene 13906541], AmpC [NCBI Gene 7872529], Iron [NCBI Gene 3853509], pap [NCBI Gene 7256836], CTX-M-15 [NCBI Gene 2716485], iss [NCBI Gene 20492777], blaCTX-M-15 [NCBI Gene 9538104], blaCTX-M-14 [NCBI Gene 9720867], dihydrofolate reductase [NCBI Gene 17047053], iutA [NCBI Gene 7324510]
- **Diseases:** AMR (MESH:C565965), nausea (MESH:D009325), neonatal sepsis (MESH:D000071074), dysuria (MESH:D053159), acute pyelonephritis (MESH:D011704), fever (MESH:D005334), cystitis (MESH:D003556), multidrug-resistant infections (MESH:D018088), Antibiotic Resistance (MESH:D004761), flank pain (MESH:D021501), urinary obstruction (MESH:D001748), gastrointestinal symptoms (MESH:D012817), injury to (MESH:D014947), chronic kidney disease (MESH:D051436), bacteriuria (MESH:D001437), diabetes mellitus (MESH:D003920), pulmonary hypersensitivity (MESH:D004342), peripheral neuropathy (MESH:D010523), hemolytic anemia (MESH:D000743), renal disease (MESH:D007674), abdominal discomfort (MESH:D000007), neonatal meningitis (MESH:D007232), bacterial infections (MESH:D001424), bloodstream infections (MESH:D018805), structural, functional, or metabolic abnormalities of the urinary tract (MESH:D014570), ST-1193 (MESH:D010855), glucose-6-phosphate dehydrogenase (G6PD) deficiency (MESH:D005955), Urinary Tract Infections (MESH:D014552), E. coli infection (MESH:D004927), extraintestinal infections (MESH:D007239), preterm birth (MESH:D047928)
- **Chemicals:** meropenem (MESH:D000077731), Cefepime (MESH:D000077723), pivmecillinam (MESH:D000561), CAZ (MESH:D002442), Carbapenem (MESH:D015780), H2O (MESH:D014867), ertapenem (MESH:D000077727), 8-hydroxyquinoline (MESH:D015125), NI (MESH:C005308), Gentamicin (MESH:D005839), tazobactam (MESH:D000078142), CEC (MESH:D002433), FEP (MESH:D011138), MEC (MESH:D000560), yersiniabactin (MESH:C104398), aminoglycoside (MESH:D000617), TMO (MESH:C031367), TE (MESH:D013691), Cefoxitin (MESH:D002440), ciprofloxacin (MESH:D002939), sulfonamide (MESH:D013449), AMC (MESH:D019980), Cefpodoxime (MESH:C053268), cotrimoxazole (MESH:D015662), cefazolin (MESH:D002437), clavulanate (MESH:D019818), CFM (MESH:D020682), ampicillin (MESH:D000667), Imipenem (MESH:D015378), folate (MESH:D005492), polysialic acid (MESH:C021319), beta-Lactam (MESH:D047090), Nitrofurantoin (MESH:D009582), Tetracycline (MESH:D013752), FOS (MESH:D005578), ceftazidime-avibactam (MESH:C000595613), cefuroxime (MESH:D002444), CLED agar (-), quinolone (MESH:D015363), Amikacin (MESH:D000583), fluoroquinolone (MESH:D024841), macrolide (MESH:D018942), Piperacillin-tazobactam (MESH:D000077725), CRO (MESH:D002443), trimethoprim (MESH:D014295), cephalosporin (MESH:D002511)
- **Species:** Enterobacterales (order) [taxon 91347], Escherichia coli (E. coli, species) [taxon 562], Lactobacillus (genus) [taxon 1578], Streptomyces sp. t73 (species) [taxon 1828166], Klebsiella pneumoniae (species) [taxon 573], Homo sapiens (human, species) [taxon 9606], Proteus mirabilis (species) [taxon 584], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395]
- **Cell lines:** -131 — Homo sapiens (Human), Transformed cell line (CVCL_7275), EC 1286 — Homo sapiens (Human), Melanoma, Cancer cell line (CVCL_8037)

## Full text

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## References

92 references — full list in the complete paper: https://tomesphere.com/paper/PMC12937327/full.md

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Source: https://tomesphere.com/paper/PMC12937327