Metallo-beta-lactamase-producing spp. is a major challenge for therapeutic treatment of nosocomial infections. This study is aimed at determining the prevalence of MBL-producing spp. among 87 clinical isolates of spp. from the Korle-Bu Teaching Hospital, Accra, between August 2014 and July 2015. spp. was identified by standard bacteriological method, and resistance to different antibiotics was assessed with the Kirby-Bauer disc diffusion method. Meropenem-resistant isolates were screened for enzyme activity using the modified Hodge test (MHT) and combined disc test (CDT). Additionally, multiplex PCR was used to determine MBL genes presence (VIM IMP, and NDM). All isolates showed high resistance to cefotaxime (90.8%), ceftazidime (75.9%), cotrimoxazole (70.1%), ciprofloxacin (64.4%), gentamicin (72.4%), levofloxacin (67.8%), and meropenem (59.8%). A total of 54 (62.1%) of isolates were multidrug-resistant. Out of 52 (59.8%) meropenem-resistant , 3 (5.8%) were carbapenemase producers by MHT, whilst, 23 (44.2%) were CDT positive. There was no significant difference between the resistance pattern of amikacin, ceftazidime, cotrimoxazole, ciprofloxacin, and meropenem amongst CDT-positive and CDT-negative isolates ( > 0.05). A total of 7/87 (8.1%) CDT-positive isolates harboured NDM; of these, 4 (57.1%) were from wound swabs, urine ( = 2) (28.6%), and ear swab ( = 1) (14.3%). The study revealed that less than 9% of spp. contained NDM encoding genes. Strict antibiotics usage plan and infection control measures are required to prevent the spread of these resistance genes.
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http://dx.doi.org/10.1155/2020/3852419 | DOI Listing |
Infect Dis Ther
November 2024
Pfizer, 75014, Paris, France.
The spread of carbapenemase-producing gram-negative pathogens, especially those producing metallo-β-lactamases (MBLs), has become a major health concern. MBLs are molecularly the most diverse carbapenemases, produced by a wide spectrum of gram-negative organisms, including the Enterobacterales, Pseudomonas spp., Acinetobacter baumannii, and Stenotrophomonas maltophilia, and can hydrolyze most β-lactams using metal ion cofactors in their active sites.
View Article and Find Full Text PDFMicrobiol Spectr
June 2024
Medical Affairs, Shionogi B.V., London, United Kingdom.
Unlabelled: Carbapenem-resistant Enterobacterales represent a major health threat and have few approved therapeutic options. Enterobacterales isolates were collected from hospitalized inpatients from 49 sites in six European countries (1 January-31 December 2020) and underwent susceptibility testing to cefiderocol and β-lactam/β-lactamase inhibitor combinations. Meropenem-resistant (MIC >8 mg/L) and cefiderocol-susceptible isolates were analyzed by PCR, and cefiderocol-resistant isolates by whole-genome sequencing, to identify resistance mechanisms.
View Article and Find Full Text PDFInt J Antimicrob Agents
July 2024
Infectious Diseases and Intensive Care Units, Pontchaillou University Hospital, Rennes, France. Electronic address:
Microbiol Immunol
January 2024
Centro de Bacteriologia, Instituto Adolfo Lutz, São Paulo, Brazil.
J Anesth Analg Crit Care
July 2022
Department of Surgical, Oncological and Oral Science (Di.Chir.On.S.), University of Palermo, Palermo, Italy.
Carbapenem-resistant Gram-negative bacteria are frequent causes of sepsis and septic shock in intensive care unit (ICU) and thus considered a public health threat. Until now, the best available therapies consist of combinations of preexisting or new antibiotics with β-lactamase inhibitors (either new or preexisting). Several mechanisms of resistance, especially those mediated by metallo-β-lactamases (MBL), are responsible for the inefficacy of these treatments, leaving an unmet medical need.
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