# Molecular Epidemiological Surveillance of Carbapenem-Resistant Gram-Negative Bacteria in Southern Lebanon

**Authors:** Anwar Al Souheil, Hadi Hussein, Ziad Jabbour, Sara Barada, Jose-Rita Gerges, Ghada Derbaj, Abdallah Kurdi, Hassan Jamil Kazma, Nour Nahouli, Ali Hasan Najem, Abdallah Medlej, Wael Zorkot, Rana El Hajj, Mahmoud I. Khalil, Ghassan M. Matar, Antoine Abou Fayad

PMC · DOI: 10.3390/antibiotics14111124 · 2025-11-07

## TL;DR

This study uses genome sequencing to track drug-resistant bacteria in hospitals in southern Lebanon, revealing widespread resistance and the need for better surveillance.

## Contribution

The first molecular characterization of carbapenem-resistant Gram-negative bacteria in South Lebanon using next-generation sequencing.

## Key findings

- Pseudomonas spp. and Escherichia coli were the most common CR-GNB isolates.
- Most isolates carried plasmid-associated resistance genes, indicating potential for spread.
- Phylogenetic analysis showed shared genetic profiles across hospitals, suggesting transmission.

## Abstract

Introduction: Carbapenem-resistant Gram-negative bacteria (CR-GNB) are rapidly spreading pathogens that increase morbidity and mortality in hospital settings and significantly restrict available treatment options worldwide. The lack of molecular epidemiological data and the limited use of next-generation sequencing (NGS) in South Lebanon have hindered comprehensive surveillance efforts. This study represents the first molecular characterization of CR-GNB in this region. Methods: A total of 477 clinical Gram-negative bacterial isolates were collected from intensive care unit (ICU) patients admitted to various hospitals in South Lebanon in 2023. Of these, 131 CR-GNB were subjected to whole-genome sequencing using the Illumina MiSeq platform. K-mer-based species identification, multilocus sequence typing (MLST), antimicrobial resistance (AMR) gene profiling, and plasmid analysis were performed using multiple bioinformatic tools. Phylogenetic analysis was conducted using SaffronTree. Results: K-mer-based identification revealed that the predominant species among CR-GNB isolates were Pseudomonas spp. and Escherichia coli (26.7% each), followed by Klebsiella pneumoniae (19.8%), Acinetobacter baumannii (17.6%), Proteus mirabilis (4.6%), Enterobacter cloacae (2.3%), Achromobacter spp. (1.5%), and Citrobacter freundii (0.8%). Based on antimicrobial susceptibility testing, isolates were classified as follows: 0.8% as pan drug-resistant (PDR), 40.5% as extensively drug-resistant (XDR), and 52.7% as multidrug-resistant (MDR) and 6.1% as antimicrobial-resistant (AMR). All isolates harbored AMR genes, with the following distribution: 2% blaVIM, 5% blaNDM-1, 27% blaNDM-5, 65% blaOXA-type, and 1% blaDIM-1. Plasmid-associated AMR genes were detected in 58% of isolates; among these, 96% carried Inc-family plasmids, 57% Col plasmids, and 11% replication-associated elements (rep). Phylogenetic analysis demonstrated that certain isolates exhibited both hospital-specific and shared genetic profiles, indicating widespread dissemination across multiple healthcare facilities, as well as evidence of local emergence and ongoing transmission. Conclusions: The high prevalence of CR-GNB harboring resistance genes and plasmids underscores the urgent need for NGS-based genomic surveillance in South Lebanon. Implementing such strategies is essential for tracking resistance genes, identifying clonal outbreaks, and guiding effective infection control interventions to mitigate the spread of CR-GNB.

## Linked entities

- **Species:** Pseudomonas sp. #P (taxon 299395), Escherichia coli (taxon 562), Klebsiella pneumoniae (taxon 573), Acinetobacter baumannii (taxon 470), Proteus mirabilis (taxon 584), Enterobacter cloacae (taxon 550), Citrobacter freundii (taxon 546)

## Full-text entities

- **Diseases:** infection (MESH:D007239)
- **Chemicals:** Carbapenem (MESH:D015780)
- **Species:** Citrobacter freundii (species) [taxon 546], Enterobacter cloacae (species) [taxon 550], Klebsiella pneumoniae (species) [taxon 573], Proteus mirabilis (species) [taxon 584], Acinetobacter baumannii (species) [taxon 470], Homo sapiens (human, species) [taxon 9606], Escherichia coli (E. coli, species) [taxon 562]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12649687/full.md

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Source: https://tomesphere.com/paper/PMC12649687