ESβL and MβL Production in Gram-Negative Bacteria Isolated From HIV Seropositive Individuals
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نوع سند: مقاله ژورنالی
زبان: English
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شناسه ملی سند علمی:
JR_JCMI-9-4_002
تاریخ نمایه سازی: 14 آذر 1402
Abstract:
Background: Extended-spectrum β-lactamase (ESβL) or metallo-β-lactamase (MβL) production by gramnegative
bacteria in immunocompromised patients poses a serious therapeutic challenge for infection
control and is associated with infections with a higher morbidity/mortality, especially in developing
countries. This study aimed to phenotypically evaluate the production of ESβL as well as MβL in ۷۵ gramnegative
bacterial isolates from clinical samples of the human immunodeficiency virus (HIV) positive
individuals.
Methods: Bacterial identification was by chromogenic media, analytical profile index ۲۰ E, and ۲۰ NE kits,
and ESβL production was tested by double-disc synergy test (DDST) and combination disc method, while
MβL production was screened with imipenem ethylene diamine tetra-acetic acid (EDTA) combined disc
and EDTA-disc potentiation with ceftazidime.
Results: Altogether, ۵۷ isolates (۷۶.۰%) produced ESβL either with DDST (۶), combination disc method (۴۹),
or both (۲). DDST detected the ESβL enzyme in ۱۰.۷% of the tested isolates which were all Pseudomonas
aeruginosa. None of the bacterial isolates revealed MβL production with the imipenem/imipenem-EDTA
method, whereas ۲۶.۷% of tested isolates produced MβL with EDTA-disc potentiation using ceftazidime
out of which ۶۵.۰% were P. aeruginosa. Moreover, ESβL/MβL co-production was evident in ۲۲.۷% of the
tested bacterial isolates with P. aeruginosa constituting ۶۴.۷%.
Conclusion: ESβL and MβL co-production among the studied isolates indicates a heightened resistance to
β-lactam antibiotics, suggesting grave health consequences, especially in immunocompromised individuals
with already limiting therapeutic options in the region. The study revealed higher ESβL production
compared to MβL production in isolates, with the predominating producing specie being P. aeruginosa,
and higher ESβL and MβL detection by the combination disc method and EDTA-disc potentiation using
ceftazidime, respectively.
Keywords:
Authors
Folasade M.Adeyemi
Department of Microbiology, Faculty of Basic and Applied Sciences, Osun State University, Osogbo, Nigeria
Omotayo O.Oyedara
Department of Microbiology, Faculty of Basic and Applied Sciences, Osun State University, Osogbo, Nigeria- Departamento de Microbiología e Inmunología, Facultad de Ciencias Biologicas, Universidad Autonoma de Nuevo Leon, San Nicolas de los Garza, Nuevo Le
Abideen A.Wahab
Department of Microbiology, Faculty of Basic and Applied Sciences, Osun State University, Osogbo, Nigeria
Sunday B.Akinde
Department of Microbiology, Faculty of Basic and Applied Sciences, Osun State University, Osogbo, Nigeria