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1.
BMC Microbiol ; 24(1): 347, 2024 Sep 14.
Artículo en Inglés | MEDLINE | ID: mdl-39277715

RESUMEN

BACKGROUND: Linezolid-resistant Enterococcus faecium (LRE) is a global priority pathogen. Thirteen LRE were reported from clinical specimens between November 2021 and April 2023 at two laboratories in Karachi, Pakistan. We aimed to investigate the strain types and genes associated with linezolid resistance among these isolates. Whole genome sequencing (WGS) was performed and analyzed by multilocus sequence typing (MLST). The presence of linezolid resistance genes was identified using ResFinder v4.1.11 and the LRE-finder tool. RESULTS: Twelve isolates belonged to clonal complex 17 (CC17); ST80 (n = 10), ST612 (n = 1) and ST1380 (n = 1). Six isolates showed the presence of optrA gene and G2576T mutations in the 23S rRNA gene, while six showed poxtA and cfr(D) genes. One isolate showed the combination of optrA, cfr(D) and poxtA genes. CONCLUSION: Our findings show the circulation of CC17 sequence types with a known outbreak potential and we identified molecular mechanisms of resistance that were not previously reported from Pakistan.


Asunto(s)
Antibacterianos , Farmacorresistencia Bacteriana , Enterococcus faecium , Infecciones por Bacterias Grampositivas , Linezolid , Pruebas de Sensibilidad Microbiana , Tipificación de Secuencias Multilocus , Secuenciación Completa del Genoma , Enterococcus faecium/genética , Enterococcus faecium/efectos de los fármacos , Enterococcus faecium/aislamiento & purificación , Enterococcus faecium/clasificación , Pakistán , Linezolid/farmacología , Humanos , Antibacterianos/farmacología , Farmacorresistencia Bacteriana/genética , Infecciones por Bacterias Grampositivas/microbiología , Infecciones por Bacterias Grampositivas/epidemiología , ARN Ribosómico 23S/genética , Femenino , Masculino , Genoma Bacteriano/genética , Genómica , Adulto , Proteínas Bacterianas/genética , Persona de Mediana Edad , Mutación
2.
Front Public Health ; 10: 773704, 2022.
Artículo en Inglés | MEDLINE | ID: mdl-35372207

RESUMEN

Introduction: Quality-assured antimicrobial susceptibility testing (AST) depends upon the knowledge and skills of laboratory staff. In many low- and middle-income countries (LMICs), including Pakistan, such types of knowledge and skills are limited. Therefore, the objective of this study was to use openaccess online courses to improve the knowledge of laboratory staff involved in the detection and reporting of antimicrobial resistance (AMR). Methodology: Seven online modules comprising 22 courses aimed at strengthening the laboratory detection of Antimicrobial resistance (AMR) were developed. The courses were uploaded onto the website www.parn.org.pk. Participants had an option of selecting courses of their interest. Online registration and completion of a pre-course assessment (pre-test) were essential for enrolment. However, participation in post-course assessment (post-test) was optional. The number of registered participants and the proportion of participants who completed each course were computed. A paired t-test was used to assess the increase between mean pre- and post-test scores. The association between the participants working in public vs. private laboratories and course completion rates were determined using the chi-square test. Results: A total of 227 participants from Pakistan (March 2018 to June 2020) were registered. The largest number of registered participants and the highest completion rate were noted for AST and biosafety courses, while quality-related courses attracted a lower interest. A comparison of pre- and post-test performance using the paired mean score for the individual courses showed a statistically significant (the value of p < 0.05) improvement in 13/20 assessed courses. A higher course completion rate was observed in participants from public vs. private sector laboratories (56.8 vs. 30.8%, the value of p = 0.005). Conclusions: Our study suggests a promising potential for open online courses (OOCs) toward addressing knowledge gaps in laboratory practice in resource limited settings.


Asunto(s)
Farmacorresistencia Bacteriana , Educación a Distancia , Competencia Profesional , Antibacterianos , Humanos , Internet , Laboratorios , Pakistán
3.
J Coll Physicians Surg Pak ; 25(11): 781-4, 2015 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-26577960

RESUMEN

OBJECTIVE: To evaluate the sealing ability of two different types of Glass Ionomer Cements (GICs) used for sandwich restorations and assess the effect of acid etching of GIC on microleakage at GIC-resin composite interface. STUDY DESIGN: Experimental study. PLACE AND DURATION OF STUDY: Department of Operative, DIEKIOHS (DUHS) and NED University, Karachi, from February to June 2011. METHODOLOGY: Eighty cavities were prepared on the proximal surfaces of 40 permanent human premolars (2 cavities per tooth), assigned to 4 groups (n=20) and restored as follows: Group CIE - Conventional GIC (CI) was applied onto the axial and cervical cavity walls, allowed setting for 5 minutes and acid etched (E) along the cavity margins with 37% phosphoric acid for 15 seconds, washed for 30 seconds and dried; the adhesive system was applied and light cured for 10 seconds, completing the restoration with composite resin light cured for 40 seconds; Group CIN - same as Group CIE, except for acid etching of the CI surface; Group RME - same as CIE, but using a resin modified GIC (RMGIC); Group RMN - same as Group RME, except for acid etching of the RMGIC surface. Specimens were soaked in 1% methylene blue dye solution at 37ºC for 24 hours, rinsed under running water for 15 minutes, bisected mesiodistally and dye penetration was measured following the ISO/TS 11405-2003 standard. Kruskal Wallis and post Hoc tests significant differences in the microleakage among all the four groups. RESULTS: There was a significant difference between the two groups of GICs (RMGIC and CI, p=0.001). There was no significant difference in between the two sub-groups that is between CIN and CIE (p=0.656), and between Groups RME and RMN (p=0.995). CONCLUSION: Phosphoric acid etching of GIC, prior to the placement of composite resin, does not improve the sealing ability of sandwich restorations. RMGIC was more effective in preventing dye penetration at the GIC-resin composite dentine interfaces than CI.


Asunto(s)
Resinas Compuestas/química , Cementos Dentales/química , Filtración Dental/clasificación , Materiales Dentales/química , Cementos de Ionómero Vítreo/química , Cementos de Resina/química , Grabado Ácido Dental/métodos , Preparación de la Cavidad Dental/métodos , Restauración Dental Permanente , Dentina , Recubrimientos Dentinarios/química , Humanos , Resinas Sintéticas/química
4.
J Pak Med Assoc ; 62(10): 995-8, 2012 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-23866432

RESUMEN

OBJECTIVE: To compare phenotypic and genotypic methods of yeast identification. METHODS: The in-vitro cross-sectional study was conducted from January 2006 to May 2009. Invasive yeasts isolated at the clinical microbiology laboratory at the Aga Khan University (AKU), Karachi, Pakistan, were identified. Speciation by phenotypic and molecular methods was compared. All yeasts isolated during the study period from blood and other invasive sites were identified using standard methods. Isolates were shipped to Mycotic Diseases Branch, Centres for Disease Control and Prevention, Atlanta, Georgia, USA, for identification by Luminex flow cytometric multianalyte profiling (xMAP) system. Ribosomal ITS2 DNA sequencing was performed on isolates not identified by Luminex. RESULT: Of the 214 invasive yeasts evaluated, Candida species were 209 (97.7%) while the frequency of non-Candida species was 5 (2.3%). Overall agreement between phenotypic and molecular identification was 81.3%, 90.3% amongst the more common Candida species, and only 38.8% amongst the uncommon yeasts. CONCLUSION: Phenotypic methods of identification proved adequate for common Candida species, but were deficient in recognising rare Candida and non-Candida yeasts, highlighting the importance of molecular methods for identification.


Asunto(s)
Técnicas de Tipificación Micológica/métodos , Micosis/microbiología , Levaduras/clasificación , Levaduras/genética , Candida/clasificación , Candida/genética , Candida/aislamiento & purificación , Estudios Transversales , Citometría de Flujo , Genotipo , Humanos , Técnicas In Vitro , Micosis/epidemiología , Pakistán/epidemiología , Fenotipo , Reacción en Cadena de la Polimerasa , Levaduras/aislamiento & purificación
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