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Carbapenem-resistant Enterobacterales and Causing Infection in Africa and the Middle East: a Surveillance Study from the ATLAS Programme (2018-20)

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Date 2022 Jun 23
PMID 35733913
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Abstract

Objectives: To determine the susceptibility of Enterobacterales (5457) and (1949) isolated from hospitalized patients in Africa (three countries) and the Middle East (five countries) in 2018-20 to a panel of 11 antimicrobials and to identify β-lactamase/carbapenemase genes in isolates with meropenem-non-susceptible and/or ceftazidime/avibactam-resistant phenotypes.

Methods: CLSI broth microdilution testing generated MICs that were interpreted using CLSI (2021) breakpoints. β-Lactamase/carbapenemase genes were identified using multiplex PCR assays.

Results: Enterobacterales isolates were highly susceptible to amikacin (96.7%), ceftazidime/avibactam (96.6%) and tigecycline (96.0%), and slightly less susceptible to meropenem (94.3%). In total, 337 Enterobacterales isolates (6.2% of all Enterobacterales isolates) carried one or more carbapenemase genes: 188 isolates carried a serine carbapenemase (178 OXA, 10 KPC) and 167 isolates carried an MBL (18 isolates carried both an MBL and an OXA). NDM-1 was the most common MBL identified (64.1% of NDM enzymes; 59.9% of all MBLs). OXA-48 (47.8%) and OXA-181 (38.8%) were the most common OXAs detected. isolates were most susceptible to ceftazidime/avibactam (89.1%) and amikacin (88.9%). Only 73.1% of isolates were meropenem susceptible. The majority (68.1%) of isolates tested for carbapenemase/β-lactamase genes were negative. In total, 88 isolates (4.5% of all isolates) carried one or more carbapenemase genes: 81 isolates carried an MBL and 8 carried a GES carbapenemase (1 isolate carried genes for both).

Conclusions: Carbapenemase detection was closely associated with meropenem-non-susceptible phenotypes for Enterobacterales (89.1%) but not for (24.2%). Wide geographic variation in carbapenemase type and frequency of detection was observed.

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References
1.
Moghnieh R, Kanafani Z, Tabaja H, Sharara S, Awad L, Kanj S . Epidemiology of common resistant bacterial pathogens in the countries of the Arab League. Lancet Infect Dis. 2018; 18(12):e379-e394. DOI: 10.1016/S1473-3099(18)30414-6. View

2.
Kazmierczak K, Rabine S, Hackel M, McLaughlin R, Biedenbach D, Bouchillon S . Multiyear, Multinational Survey of the Incidence and Global Distribution of Metallo-β-Lactamase-Producing Enterobacteriaceae and Pseudomonas aeruginosa. Antimicrob Agents Chemother. 2015; 60(2):1067-78. PMC: 4750703. DOI: 10.1128/AAC.02379-15. View

3.
Alghoribi M, Binkhamis K, Alswaji A, Alhijji A, Alsharidi A, Balkhy H . Genomic analysis of the first KPC-producing Klebsiella pneumoniae isolated from a patient in Riyadh: A new public health concern in Saudi Arabia. J Infect Public Health. 2020; 13(4):647-650. DOI: 10.1016/j.jiph.2020.01.003. View

4.
Olalekan A, Onwugamba F, Iwalokun B, Mellmann A, Becker K, Schaumburg F . High proportion of carbapenemase-producing Escherichia coli and Klebsiella pneumoniae among extended-spectrum β-lactamase-producers in Nigerian hospitals. J Glob Antimicrob Resist. 2019; 21:8-12. DOI: 10.1016/j.jgar.2019.09.007. View

5.
Lansbury L, Lim B, Baskaran V, Lim W . Co-infections in people with COVID-19: a systematic review and meta-analysis. J Infect. 2020; 81(2):266-275. PMC: 7255350. DOI: 10.1016/j.jinf.2020.05.046. View