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Molecular Characteristics of Colistin Resistance in Acinetobacter baumannii and the Activity of Antimicrobial Combination Therapy in a Tertiary Care Medical Center in Lebanon.
Abou Fayad, Antoine; Haraoui, Louis-Patrick; Sleiman, Ahmad; Hussein, Hadi; Grenier, Frédéric; Derbaj, Ghada; Itani, Dana; Iweir, Sereen; Sherri, Nour; Bazzi, Wael; Rasheed, Sari; Tanelian, Arax; Miari, Mariam; El Hafi, Bassam; Kanj, Souha S; Kanafani, Zeina A; Daoud, Ziad; Araj, George F; Matar, Ghassan M.
Affiliation
  • Abou Fayad A; Department of Experimental Pathology, Immunology and Microbiology, Faculty of Medicine, American University of Beirut, Beirut 1107 2020, Lebanon.
  • Haraoui LP; Center for Infectious Diseases Research, American University of Beirut, Beirut 1107 2020, Lebanon.
  • Sleiman A; World Health Organization (WHO) Collaborating Center for Reference and Research on Bacterial Pathogens, Beirut 1107 2020, Lebanon.
  • Hussein H; Department of Microbiology and Infectious Diseases, Faculty of Medicine and Health Sciences, Université de Sherbrooke, Sherbrooke, QC J1K 2R1, Canada.
  • Grenier F; Centre de recherche Charles-Le Moyne, Hôpital Charles-Le Moyne, Greenfield Park, QC J4V 2G9, Canada.
  • Derbaj G; Department of Experimental Pathology, Immunology and Microbiology, Faculty of Medicine, American University of Beirut, Beirut 1107 2020, Lebanon.
  • Itani D; Center for Infectious Diseases Research, American University of Beirut, Beirut 1107 2020, Lebanon.
  • Iweir S; World Health Organization (WHO) Collaborating Center for Reference and Research on Bacterial Pathogens, Beirut 1107 2020, Lebanon.
  • Sherri N; Department of Experimental Pathology, Immunology and Microbiology, Faculty of Medicine, American University of Beirut, Beirut 1107 2020, Lebanon.
  • Bazzi W; Center for Infectious Diseases Research, American University of Beirut, Beirut 1107 2020, Lebanon.
  • Rasheed S; World Health Organization (WHO) Collaborating Center for Reference and Research on Bacterial Pathogens, Beirut 1107 2020, Lebanon.
  • Tanelian A; Department of Biology, Faculty of Science, Université de Sherbrooke, Sherbrooke, QC J1K 2R1, Canada.
  • Miari M; Department of Experimental Pathology, Immunology and Microbiology, Faculty of Medicine, American University of Beirut, Beirut 1107 2020, Lebanon.
  • El Hafi B; Center for Infectious Diseases Research, American University of Beirut, Beirut 1107 2020, Lebanon.
  • Kanj SS; World Health Organization (WHO) Collaborating Center for Reference and Research on Bacterial Pathogens, Beirut 1107 2020, Lebanon.
  • Kanafani ZA; Department of Experimental Pathology, Immunology and Microbiology, Faculty of Medicine, American University of Beirut, Beirut 1107 2020, Lebanon.
  • Daoud Z; Center for Infectious Diseases Research, American University of Beirut, Beirut 1107 2020, Lebanon.
  • Araj GF; World Health Organization (WHO) Collaborating Center for Reference and Research on Bacterial Pathogens, Beirut 1107 2020, Lebanon.
  • Matar GM; Department of Experimental Pathology, Immunology and Microbiology, Faculty of Medicine, American University of Beirut, Beirut 1107 2020, Lebanon.
Microorganisms ; 12(2)2024 Feb 08.
Article in En | MEDLINE | ID: mdl-38399753
ABSTRACT
(1)

Background:

Infections with pan-drug-resistant (PDR) bacteria, such as A. baumannii, are becoming increasingly common, especially in healthcare facilities. In this study, we selected 15 colistin-resistant clinical A. baumannii isolates from a hospital in Beirut, Lebanon, to test combination therapies and determine their sequence types (STs) and the mechanism of colistin resistance using whole-genome sequencing (WGS). (2)

Methods:

Antimicrobial susceptibility testing via broth microdilution against 12 antimicrobials from different classes and growth rate assays were performed. A checkerboard assay was conducted on PDR isolates using six different antimicrobials, each in combination with colistin. Genomic DNA was extracted from all isolates and subjected to WGS. (3)

Results:

All isolates were resistant to all tested antimicrobials with the one exception that was susceptible to gentamicin. Combining colistin with either meropenem, ceftolozane-tazobactam, or teicoplanin showed synergistic activity. Sequencing data revealed that 67% of the isolates belonged to Pasteur ST2 and 33% to ST187. Furthermore, these isolates harbored a number of resistance genes, including blaOXA-23. Mutations in the pmrC gene were behind colistin resistance. (4)

Conclusions:

With the rise in antimicrobial resistance and the absence of novel antimicrobial production, alternative treatments must be found. The combination therapy results from this study suggest treatment options for PDR ST2 A. baumannii-infected patients.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Microorganisms Year: 2024 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Microorganisms Year: 2024 Document type: Article Affiliation country: