Molecular Characterization of OXA-198 Carbapenemase-Producing Pseudomonas aeruginosa Clinical Isolates

Author:

Bonnin Rémy A.1234ORCID,Bogaerts Pierre56,Girlich Delphine1234,Huang Te-Din56,Dortet Laurent1234,Glupczynski Youri56,Naas Thierry1234ORCID

Affiliation:

1. EA7361, Université Paris Sud, Université Paris-Saclay, LabEx LERMIT, Le Kremlin-Bicêtre, France

2. Bacteriology-Hygiene Unit, AP-HP, Hôpital Bicêtre, Le Kremlin-Bicêtre, France

3. Associated French National Reference Center for Antibiotic Resistance: Carbapenemase-Producing Enterobacteriaceae, Le Kremlin-Bicêtre, France

4. Evolution and Ecology of Resistance to Antibiotics Unit, Institut Pasteur, AP-HP, Université Paris Sud, Paris, France

5. Belgian National Reference Laboratory for Monitoring of Antimicrobial Resistance in Gram-Negative Bacteria, CHU UCL Namur-Site Mont Godinne, Yvoir, Belgium

6. Institut de Recherche Expérimentale et Clinique, Pôle Mont Godinne, Université Catholique de Louvain, Leuven, Belgium

Abstract

ABSTRACT Carbapenemase-producing Pseudomonadaceae have increasingly been reported worldwide, with an ever-increasing heterogeneity of carbapenem resistance mechanisms, depending on the bacterial species and the geographical location. OXA-198 is a plasmid-encoded class D β-lactamase involved in carbapenem resistance in one Pseudomonas aeruginosa isolate from Belgium. In the setting of a multicenter survey of carbapenem resistance in P. aeruginosa strains in Belgian hospitals in 2013, three additional OXA-198-producing P. aeruginosa isolates originating from patients hospitalized in one hospital were detected. To reveal the molecular mechanism underlying the reduced susceptibility to carbapenems, MIC determinations, whole-genome sequencing, and PCR analyses to confirm the genetic organization were performed. The plasmid harboring the bla OXA-198 gene was characterized, along with the genetic relatedness of the four P. aeruginosa isolates. The bla OXA-198 gene was harbored on a class 1 integron carried by an ∼49-kb IncP-type plasmid proposed as IncP-11. The same plasmid was present in all four P. aeruginosa isolates. Multilocus sequence typing revealed that the isolates all belonged to sequence type 446, and single-nucleotide polymorphism analysis revealed only a few differences between the isolates. This report describes the structure of a 49-kb plasmid harboring the bla OXA-198 gene and presents the first description of OXA-198-producing P. aeruginosa isolates associated with a hospital-associated cluster episode.

Funder

Université Paris Sud

JPIAMR

Belgium Ministry of Social Affairs

Agence Nationale de la Recherche

Assistance Publique-Hôpitaux de Paris

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

Reference25 articles.

1. World Health Organization. 2014. Antimicrobial resistance: global report on surveillance 2014. World Health Organization, Geneva, Switzerland. http://www.who.int/drugresistance/documents/surveillancereport/en.

2. Nordmann P, Naas T. 2009. P. aeruginosa and β-lactams, p 157–174. In Courvalin P, LeClercq R, Rice LB (ed), Antibiogram. ASM Press, Washington, DC.

3. Structural and Functional Aspects of Class A Carbapenemases

4. Emerging broad-spectrum resistance in Pseudomonas aeruginosa and Acinetobacter baumannii : Mechanisms and epidemiology

5. Global Spread of Carbapenemase-producingEnterobacteriaceae

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