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1.
BMC Infect Dis ; 24(1): 378, 2024 Apr 06.
Artículo en Inglés | MEDLINE | ID: mdl-38582858

RESUMEN

INTRODUCTION: Carbapenem-resistant gram-negative bacilli are a worldwide concern because of high morbidity and mortality rates. Additionally, the increasing prevalence of these bacteria is dangerous. To investigate the extent of antimicrobial resistance and prioritize the utility of novel drugs, we evaluated the molecular characteristics and antimicrobial susceptibility profiles of carbapenem-resistant Enterobacterales, Pseudomonas aeruginosa and Acinetobacter baumannii in Ecuador in 2022. METHODS: Ninety-five clinical isolates of carbapenem non-susceptible gram-negative bacilli were collected from six hospitals in Ecuador. Carbapenem resistance was confirmed with meropenem disk diffusion assays following Clinical Laboratory Standard Institute guidelines. Carbapenemase production was tested using a modified carbapenemase inactivation method. Antimicrobial susceptibility was tested with a disk diffusion assay, the Vitek 2 System, and gradient diffusion strips. Broth microdilution assays were used to assess colistin susceptibility. All the isolates were screened for the blaKPC, blaNDM, blaOXA-48, blaVIM and blaIMP genes. In addition, A. baumannii isolates were screened for the blaOXA-23, blaOXA-58 and blaOXA-24/40 genes. RESULTS: Carbapenemase production was observed in 96.84% of the isolates. The blaKPC, blaNDM and blaOXA-48 genes were detected in Enterobacterales, with blaKPC being predominant. The blaVIM gene was detected in P. aeruginosa, and blaOXA-24/40 predominated in A. baumannii. Most of the isolates showed co-resistance to aminoglycosides, fluoroquinolones, and trimethoprim/sulfamethoxazole. Both ceftazidime/avibactam and meropenem/vaborbactam were active against carbapenem-resistant gram-negative bacilli that produce serin-carbapenemases. CONCLUSION: The epidemiology of carbapenem resistance in Ecuador is dominated by carbapenemase-producing K. pneumoniae harbouring blaKPC. Extensively drug resistant (XDR) P. aeruginosa and A. baumannii were identified, and their identification revealed the urgent need to implement strategies to reduce the dissemination of these strains.


Asunto(s)
Carbapenémicos , beta-Lactamasas , Humanos , Carbapenémicos/farmacología , Meropenem , Epidemiología Molecular , Ecuador/epidemiología , Pruebas de Sensibilidad Microbiana , beta-Lactamasas/genética , Proteínas Bacterianas/genética , Antibacterianos/farmacología , Bacterias Gramnegativas/genética , Klebsiella pneumoniae/genética , Pseudomonas aeruginosa/genética
2.
Med Mycol ; 59(7): 664-671, 2021 Jul 06.
Artículo en Inglés | MEDLINE | ID: mdl-33305313

RESUMEN

An increasing number of outbreaks due to resistant non-albicans Candida species have been reported worldwide. Between 2014 and 2016, Candida isolates causing invasive candidiasis were recovered in a Mexican hospital. Isolates were identified to species level and antifungal susceptibility was determined. In the time period studied, 74 invasive candidiasis cases were identified, with 38% (28/74) caused by Candida parapsilosis, out of which 54% (15/28) were fluconazole resistant. The ERG11 gene was sequenced for 12 recoverable fluconazole-resistant C. parapsilosis isolates and SNPs identified. The 12 isolates had one common silent point mutation in ERG11 (T591C) and seven isolates had an additional (A395T) mutation, which corresponded to Y132F. Four of the isolates carrying this mutation were closely related within the same cluster by microsatellite typing. This is the first report of an invasive candidiasis outbreak in Mexico due to azole-resistant C. parapsilosis associated with the Y132F substitution.


Asunto(s)
Antifúngicos/farmacología , Azoles/farmacología , Candida parapsilosis/efectos de los fármacos , Candida parapsilosis/genética , Candidiasis Invasiva/epidemiología , Brotes de Enfermedades/estadística & datos numéricos , Proteínas Fúngicas/genética , Mutación/efectos de los fármacos , Adulto , Sustitución de Aminoácidos , Farmacorresistencia Fúngica , Femenino , Hospitales Generales/estadística & datos numéricos , Humanos , Masculino , México , Pruebas de Sensibilidad Microbiana , Persona de Mediana Edad , Mutación/genética , Estudios Retrospectivos
3.
Mycopathologia ; 182(11-12): 1005-1014, 2017 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-28685375

RESUMEN

Metabolic control improves outcomes associated with mucormycosis. The aim of this study was to compare the in vitro proliferation of Rhizopus oryzae in blood of individuals with and without diabetes at different glycaemic levels. Ninety-five individuals were included. Blood samples from each participant were incubated with sporangiospores of R. oryzae. The germination, filamentation and growth of R. oryzae were compared at different time points. Four groups were defined, one without (group A, n = 30) and three with diabetes: group B (HbA1c ≤7%, N = 24), group C (HbA1c 7.1-9%, N = 20) and group D (HbA1c > 9%, N = 21). The percentage of germinated sporangiospores was higher in the group A after 6 h (group A 56% ± 3, group B 35% ± 4, group C 48% ± 4, group D 46% ± 1.4, p = 0.01), 12 h (group A 54% ± 1.4, group B 19% ± 4, group C 16% ± 1, group D 9.5% ± 5, p < 0.001) and 24 h (group A 29% ± 1, group B 12% ± 4, group C 13.5% ± 3.5, group D 12% ± 1, p < 0.01). The filamentation was higher in groups with diabetes. Group B showed higher filamentation grade than group A at 6 h (0.4 ± 0.04 vs 1 ± 0.09, p < 0.001) and 24 h (1.6 ± 0.05 vs 2.1 ± 0.1, p = 0.05). In conclusion, R. oryzae proliferation was higher among diabetic individuals, including good glycaemic control, than among non-diabetic individuals.


Asunto(s)
Sangre/microbiología , Diabetes Mellitus/sangre , Susceptibilidad a Enfermedades/sangre , Rhizopus/crecimiento & desarrollo , Esporas Fúngicas/crecimiento & desarrollo , Adulto , Anciano , Anciano de 80 o más Años , Análisis Químico de la Sangre , Proliferación Celular , Femenino , Germinación , Hemoglobina Glucada/análisis , Índice Glucémico , Carga Glucémica , Humanos , Hierro/sangre , Masculino , Persona de Mediana Edad , Mucormicosis/metabolismo , Mucormicosis/microbiología
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