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Association of blaVIM-2, blaPDC-35, blaOXA-10, blaOXA-488 and blaVEB-9 β-Lactamase Genes with Resistance to Ceftazidime-Avibactam and Ceftolozane-Tazobactam in Multidrug-Resistant Pseudomonas aeruginosa

Sid Ahmed, Mazen, 1970- (author)
Örebro universitet,Institutionen för naturvetenskap och teknik,Department of Laboratory Medicine and Pathology, Microbiology Division, Hamad Medical Corporation, Doha, Qatar,The Life Science Centre-Biology
Khan, Faisal Ahmad, 1986- (author)
Örebro universitet,Institutionen för naturvetenskap och teknik,The Life Science Centre-Biology
Hadi, Hamad Abdel (author)
Communicable Diseases Center, Hamad Medical Corporation, Doha, Qatar; Division of Infectious Diseases, Department of Medicine, Hamad Medical Corporation, Doha, Qatar
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Skariah, Sini (author)
Department of Microbiology and Immunology, Weill Cornell Medicine-Qatar, Doha, Qatar
Sultan, Ali A. (author)
Department of Microbiology and Immunology, Weill Cornell Medicine-Qatar, Doha, Qatar
Salam, Abdul (author)
Department of Epidemiology and Biostatistics, King Fahad Specialist Hospital, Dammam, Saudi Arabia
Al Khal, Abdul Latif (author)
Communicable Diseases Center, Hamad Medical Corporation, Doha, Qatar; Division of Infectious Diseases, Department of Medicine, Hamad Medical Corporation, Doha, Qatar
Söderquist, Bo, 1955- (author)
Örebro universitet,Institutionen för medicinska vetenskaper
Ibrahim, Emad Bashir (author)
Department of Laboratory Medicine and Pathology, Microbiology Division, Hamad Medical Corporation, Doha, Qatar; Department of Microbiology and Immunology, Weill Cornell Medicine-Qatar, Doha, Qatar
Omrani, Ali S (author)
Jass, Jana, 1963- (author)
Örebro universitet,Institutionen för naturvetenskap och teknik,The Life Science Centre-Biology
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 (creator_code:org_t)
2022-01-19
2022
English.
In: Antibiotics. - : MDPI. - 2079-6382. ; 11:2
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Ceftazidime-avibactam and ceftolozane-tazobactam are approved for the treatment of complicated Gram-negative bacterial infections including multidrug-resistant (MDR) Pseudomonas aeruginosa. Resistance to both agents has been reported, but the underlying mechanisms have not been fully explored. This study aimed to correlate β-lactamases with phenotypic resistance to ceftazidime-avibactam and/or ceftolozane-tazobactam in MDR-P. aeruginosa from Qatar. A total of 525 MDR-P. aeruginosa isolates were collected from clinical specimens between 2014 and 2017. Identification and antimicrobial susceptibility were performed by the BD PhoenixTM system and gradient MIC test strips. Of the 75 sequenced MDR isolates, 35 (47%) were considered as having difficult-to-treat resistance, and 42 were resistant to ceftazidime-avibactam (37, 49.3%), and/or ceftolozane-tazobactam (40, 53.3%). They belonged to 12 sequence types, with ST235 being predominant (38%). Most isolates (97.6%) carried one or more β-lactamase genes, with blaOXA-488 (19%) and blaVEB-9 (45.2%) being predominant. A strong association was detected between class B β-lactamase genes and both ceftazidime-avibactam and ceftolozane-tazobactam resistance, while class A genes were associated with ceftolozane-tazobactam resistance. Co-resistance to ceftazidime-avibactam and ceftolozane-tazobactam correlated with the presence of blaVEB-9, blaPDC-35, blaVIM-2, blaOXA-10 and blaOXA-488. MDR-P. aeruginosa isolates resistant to both combination drugs were associated with class B β-lactamases (blaVIM-2) and class D β-lactamases (blaOXA-10), while ceftolozane-tazobactam resistance was associated with class A (blaVEB-9), class C (blaVPDC-35), and class D β-lactamases (blaOXA-488).

Subject headings

NATURVETENSKAP  -- Biologi -- Mikrobiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Microbiology (hsv//eng)

Keyword

P. aeruginosa
PDC-35
VEB-9
antimicrobial resistance
ceftazidime–avibactam
ceftolozane–tazobactam
β-lactamases

Publication and Content Type

ref (subject category)
art (subject category)

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