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Bloodstream Infections Due to Carbapenemase-Producing Escherichia coli: A Comprehensive Review
Maria Scrascia1, Adriana Antonina Tempesta2, Viviana Cafiso2
1Department of Biosciences, Biotechnology and Environment, University of Bari Aldo Moro, Via Orabona 4, 70125 Bari, Italy.
Carbapenemase-producing Escherichia coli (CP-Ec) is a growing threat due to antimicrobial resistance. Effective management requires enhanced surveillance and infection control to combat CP-Ec bloodstream infections.
Area of Science:
- Microbiology
- Infectious Diseases
- Genomics
Background:
- Carbapenemase-producing Escherichia coli (CP-Ec) is a significant driver of global antimicrobial resistance.
- CP-Ec exhibits genomic plasticity and plasmid-mediated spread, increasingly causing bloodstream infections.
- The prevalence of NDM, OXA-48-like, and KPC carbapenemases in CP-Ec is expanding.
Purpose of the Study:
- To provide a comprehensive review of the global epidemiology of CP-Ec.
- To summarize molecular features, treatment options, and transmission dynamics of CP-Ec.
- To highlight key high-risk clones and their role in international CP-Ec spread.
Main Methods:
- Systematic literature review of global CP-Ec epidemiology.
- Analysis of molecular characteristics, including carbapenemase types and plasmid backbones.
- Examination of clonal structures and transmission dynamics of key CP-Ec clones.
Main Results:
- CP-Ec bloodstream infections are associated with severe outcomes and limited treatment options, especially for NDM producers.
- High-risk clones such as ST410, ST167, and ST131 are major contributors to international CP-Ec dissemination.
- Treatment failures with last-resort antibiotics are increasingly reported for CP-Ec infections.
Conclusions:
- CP-Ec bloodstream infections pose a growing clinical challenge requiring improved management strategies.
- Enhanced global surveillance and genomic epidemiology integration are crucial for controlling CP-Ec.
- Optimized antimicrobial stewardship and targeted infection control are essential to mitigate CP-Ec's impact.
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