Salmonella Infections among Pediatric Population in Qatar: Phenotypic Resistance and Associated Genotypic Determinants
التاريخ
2021-04-23المؤلف
Al Hadidi, SAbdelrahman, H
Al Thani, A
Ibrahim, E
Yassine, HM
Doiphode, S
Eltai, NO
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البيانات الوصفية
عرض كامل للتسجيلةالملخص
Salmonella is a significant public health burden worldwide and being the
most common bacterial diarrheal illness among infants and young children. In
the last few years, Qatar reports a high incidence of salmonellosis outbreaks
coupled with a significant increase of Multidrug-Resistant (MDR) among
pediatric populations every year. This study aims to elucidate the molecular
mechanisms underlying resistance to ceftriaxone, cefepime, amoxicillinclavulanate
tetracycline, trimethoprim-sulfamethoxazole, chloramphenicol, and
azithromycin among Salmonella isolated from the pediatric population. A total
of 246 Salmonella isolates were collected from children under 18 years old
admitted to the Pediatric Emergency Center (PEC), Hamad Medical Corporation
(HMC) from Jan. 2018 to Dec 2019 with gastroenteritis. Isolates were tested
for antibiotic susceptibility against nineteen relevant antibiotics using E-test.
Resistance was confirmed using PCR-specific primers for 38 genes. Resistance
was detected against 14 antibiotics, and 38.2% of isolates were resistant to
at least one antibiotic. Overall, we reported 23.9%, resistance to tetracycline
21.1%, ampicillin 18.7%, AMC, and 13% sulfamethoxazole-trimethoprim.
Further, 16.2% of the isolates were Multidrug-Resistant (MDR), with 4.1%
being Extended-Spectrum β Lactamase (ESBL) producers. 90% of ESBL
producers harbored one of bla CTX-M-Group. Class 1 AMC resistant samples
showed the highest resistance to different antibiotics. Our results indicate a high
antimicrobial resistance pattern of Salmonella and the presence of Class (1)
cassette that involves the transmission and expression of the resistance among
AMC resistance isolates, which might lead to increased multi-drug resistance.
This study provides evidence guidance to activate and implement the pillars
of an antimicrobi
DOI/handle
http://hdl.handle.net/10576/18401المجموعات
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