Evidence map›Paper›PMID 41793682›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2026

Whole-Genome Analysis of Multidrug-Resistant Escherichia coli from Bloodstream Infections in Iraqi Cancer Patients.

Watheq Mohammed Al-Jewari, Bassam Abdul Rasool Hassan, Abu Bakar Abdul Majeed, Muhamad Faiz Othman, Ahmed Zuhair Abdulhameed Alsammarraie, Mohammed Kamil Al Qayyim, Musaab Kadhim Alabboodi

Abstract readMulticenter Study
In one paragraph

Article in Asian Pacific journal of cancer prevention : APJCP, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Watheq Mohammed Al-JewariDepartment of Pharmacology and Life Sciences, Faculty of Pharmacy, Universiti Teknologi MARA, 42300 Bandar Puncak Alam, Selangor, Malaysia.
Bassam Abdul Rasool HassanDepartment of Pharmacy, Al Rafidain University College, 10001, Baghdad, Iraq.
Abu Bakar Abdul MajeedDepartment of Pharmacology and Life Sciences, Faculty of Pharmacy, Universiti Teknologi MARA, 42300 Bandar Puncak Alam, Selangor, Malaysia.
Muhamad Faiz OthmanDepartment of Pharmacy Practice and Clinical Pharmacy, Faculty of Pharmacy, Universiti Teknologi MARA, 42300 Bandar Puncak Alam, Selangor, Malaysia.
Ahmed Zuhair Abdulhameed AlsammarraieMedical Oncology Department, Oncology Teaching Hospital Baghdad, Baghdad, Iraq.
Mohammed Kamil Al QayyimDepartment of Haematology, Medical City Complex, Haematology and Transplant Centre, Baghdad, Iraq.
Musaab Kadhim AlabboodiMedical Oncology Department, Alamal National Hospital for Cancer Treatment, Baghdad, Iraq.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn Iraq, oncology patients with bloodstream infections face escalating treatment challenges due to rising antimicrobial resistance in Escherichia coli, compounded by limited diagnostic capacity and restricted therapeutic options. However, data from oncology settings in Iraq are limited. This study aimed to characterize and compare the antimicrobial resistance gene profiles of multidrug-resistant and antibiotic-sensitive E. coli isolates from cancer patients, to inform infection control and stewardship strategies.

methodsA prospective, multicenter investigation was conducted in three oncology hospitals in Baghdad. Fifty-five Escherichia coli bloodstream isolates, 36 multidrug-resistant (MDR) (65.5%) and 19 antibiotic-sensitive (34.5%), underwent phenotypic susceptibility testing using VITEK® 2 and disk diffusion. Whole-genome sequencing (Illumina MiSeq) was performed, and antimicrobial resistance genes (ARGs) were identified using AMRFinderPlus and classified by functional category.

resultsMDR isolates showed a broad resistome dominated by efflux systems. Across all isolates, a total of 36 unique antimicrobial resistance genes were identified, underscoring substantial resistome diversity., efflux pump genes were detected in 100%, β-lactamase genes in 88.9%, macrolide resistance genes in 66.7%, tetracycline resistance genes in 55.6%, and aminoglycoside resistance genes in 41.7%. Representative determinants included AcrAB-TolC/EmrAB-TolC/MdtABC-TolC (efflux) and BlaEC family/CMY-42/TEM types (β-lactams). Among sensitive isolates, only 11 antibiotic-associated genes, mainly efflux or regulators (e.g., acrF, emrD, emrR, emrY, tolC; regulators marR, evgA; target parC; others baeS, cpxA, cysB), overlapped with MDR, suggesting a shared core that is insufficient alone for phenotypic resistance without additional high-level mechanisms.

conclusionsMultidrug-resistant E. coli from oncology patients harbor dense, efflux-driven resistomes supplemented by diverse β-lactamases and other resistance determinants, while sensitive isolates retain a limited core set of genes. Genomic surveillance in cancer centers is critical for anticipating resistance emergence and informing targeted antimicrobial strategies.

Indexed as

BacteremiaDrug Resistance, Multiple, BacterialEscherichia coliEscherichia coli InfectionsGenome, BacterialNeoplasmsAnti-Bacterial AgentsFemaleFollow-Up StudiesHumansIraqMaleMicrobial Sensitivity TestsMiddle AgedPrognosisProspective StudiesAnti-Bacterial Agentsantimicrobial resistancecancer patientsEscherichia coliwhole-genome sequencing

Identifiers

PMID41793682
PMCPMC13570634

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