Antimicrobial Susceptibility and Characterization of Extended-Spectrum β-Lactamase-Producing Escherichia coli Isolated from Stools of Primary Healthcare Patients in Ethiopia.
Deneke WoldeTadesse EgualeHaile AlemayehuGirmay MedhinAklilu Feleke HaileMateja PirsKatja Strasek SmrdelJana AvberšekDarja KušarTjaša Cerar KišekTea JankoAndrej SteyerMateja Erdani KreftPublished in: Antibiotics (Basel, Switzerland) (2024)
Antimicrobial resistance of Escherichia coli is a growing problem in both developed and developing countries. This study aimed to investigate the phenotypic antimicrobial resistance of E. coli isolates ( n = 260) isolated from the stool specimen of patients attending public health facilities in Addis Ababa and Hossana. This study also aimed to characterize phenotypically confirmed extended-spectrum beta-lactamase (ESBL)-producing E. coli isolates ( n = 22) using whole-genome sequencing. Resistance to 18 different antimicrobials was assessed using the disc diffusion method according to the European Committee on Antimicrobial Susceptibility Testing (EUCAST) guidelines. The highest resistance rate among the E. coli isolates was found for ampicillin (52.7%), followed by trimethoprim-sulfamethoxazole (29.6%). Of all isolates, 50 (19.2%) were multidrug-resistant and 22 (8.5%) were ESBL producers. ESBL genes were detected in 94.7% of the sequenced E. coli isolates, and multiple β-lactamase genes were detected in 57.9% of the isolates. The predominant ESBL gene identified was bla CTX-M-15 (78.9%). The bla TEM-1B gene was detected in combination with other ESBL genes in 57.9% of the isolates, while only one of the sequenced isolates contained the bla TEM-1B gene alone. The bla CTX-M-3 gene was detected in three isolates. The genes bla CTX-M-15 and bla TEM-1B as well as bla CTX-M-15 and bla TEM-169 were confirmed to coexist in 52.6% and 10.5% of the sequenced E. coli isolates, respectively. In addition, bla OXA-1 was identified together with bla CTX-M-15 and bla TEM-1B in one isolate, and in one isolate, bla TEM-169 together with bla CTX-M-15 and bla TEM-1B was found. The results obtained show that measures need to be taken to reduce the spread of drug resistance and ensure the long-term use of available antimicrobials.
Keyphrases
- klebsiella pneumoniae
- escherichia coli
- multidrug resistant
- antimicrobial resistance
- genetic diversity
- genome wide
- genome wide identification
- public health
- healthcare
- drug resistant
- gram negative
- acinetobacter baumannii
- end stage renal disease
- biofilm formation
- copy number
- ejection fraction
- newly diagnosed
- prognostic factors
- chronic kidney disease
- genome wide analysis
- tertiary care