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Prevalence and distribution of ampc beta-lactamase producing escherichia coli and klebsiella pneumoniae isolates obtained from urine samples at a tertiary care hospital in the caribbean.
Thoms Rodriguez, Camille-Ann; Dawson, Felecia; Cameron, Jenene; Seah, Christine; Reid, Marvin; Melano, Roberto G; Gossell-Williams, Maxine.
Affiliation
  • Thoms Rodriguez CA; Department of Microbiology, The University of the West Indies, Kingston, Jamaica.
  • Dawson F; Department of Microbiology, The University Hospital of the West Indies, Kingston, Jamaica.
  • Cameron J; Department of Basic Medical Sciences, The University of the West Indies, Kingston, Jamaica.
  • Seah C; Department of Microbiology, The University Hospital of the West Indies, Kingston, Jamaica.
  • Reid M; Department of Clinical Lab and Microbiology Sciences, Public Health Ontario Laboratory, Toronto, ON, Canada.
  • Melano RG; Caribbean Institute for Health Research, The University of the West Indies, Kingston, Kingston, Jamaica.
  • Gossell-Williams M; Department of Clinical Lab and Microbiology Sciences, Public Health Ontario Laboratory, Toronto, ON, Canada.
Front Cell Infect Microbiol ; 12: 1015633, 2022.
Article in En | MEDLINE | ID: mdl-36329819
ABSTRACT

Introduction:

The aim of this study was to investigate the prevalence and distribution of AmpC beta-lactamases (BLs) in uropathogens (E. coli and K. pneumoniae) at the University Hospital of the West Indies Jamaica (UHWI).

Method:

De-duplicated consecutive urine samples, collected from January to March 2020 at the UHWI, were analyzed. Screening and phenotypic confirmatory tests were conducted using resistance to cefoxitin and the Disc Approximation Test (DAT) respectively, for isolates of interest. Multiplex PCR was performed on cefoxitin resistant (CR) isolates for the detection of bla CIT, bla MOX, bla FOX, bla ACC, and bla DHA genes. Whole genome sequencing (WGS) was used to further detect AmpC BL genes in PCR negative isolates with indeterminate phenotypic results.

Results:

Sixty-four Gram negative isolates were obtained from 61 patients (55% female), aged 18 months to 88 years old. At least 35% (26) had complicated urinary tract infections. Only 7 out of 64 isolates were E. coli or K. pneumoniae, had antibiograms suggestive of possible AmpC BL production and were CR. DATs confirmed AmpC BL in two of these (1 K. pneumoniae; 1 E. coli), one tested negative (E. coli) and four had inconclusive results (K. pneumoniae). PCR detected bla DHA and bla CIT in two CR isolates. WGS further detected bla CMY-42 in one isolate. The prevalence of screened CR isolates with AmpC BL is 57.14% (4 of 7), representing 6.25% of the sample. AmpC BL producers tested had 100% susceptibility to meropenem and nitrofurantoin.

Conclusion:

AmpC BL prevalence among E. coli and K. pneumoniae, common urinary pathogens, in the studied isolates is low. Although cefoxitin screening is helpful, phenotypic screening using the DAT can yield indeterminate results best clarified by molecular testing.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Escherichia coli / Klebsiella pneumoniae Type of study: Prevalence_studies / Risk_factors_studies Limits: Female / Humans / Male Language: En Journal: Front Cell Infect Microbiol Year: 2022 Document type: Article Affiliation country: Jamaica

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Escherichia coli / Klebsiella pneumoniae Type of study: Prevalence_studies / Risk_factors_studies Limits: Female / Humans / Male Language: En Journal: Front Cell Infect Microbiol Year: 2022 Document type: Article Affiliation country: Jamaica