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1.
Lett Appl Microbiol ; 72(6): 774-782, 2021 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-33544912

RESUMEN

The study was performed to compare real-time PCR after nucleic acid extraction directly from stool samples as well as from samples stored and transported on Whatman papers or flocked swabs at ambient temperature in the tropics. In addition, the possible suitability for a clear determination of likely aetiological relevance of PCR-based pathogen detections based on cycle threshold (Ct) values was assessed. From 632 Tanzanian children <5 years of age with and without gastrointestinal symptoms, 466 samples were subjected to nucleic acid extraction and real-time PCR for gastrointestinal viral, bacterial and protozoan pathogens. Equal or even higher frequencies of pathogen detections from Whatman papers or flocked swabs were achieved compared with nucleic acid extraction directly from stool samples. Comparison of the Ct values showed no significant difference according to the nucleic acid extraction strategy. Also, the Ct values did not allow a decision whether a detected pathogen was associated with gastrointestinal symptoms.


Asunto(s)
Heces/microbiología , Heces/parasitología , Enfermedades Gastrointestinales/diagnóstico , Manejo de Especímenes , Animales , Bacterias/clasificación , Bacterias/genética , Niño , Enfermedades Gastrointestinales/microbiología , Enfermedades Gastrointestinales/parasitología , Tracto Gastrointestinal/microbiología , Tracto Gastrointestinal/parasitología , Humanos , Masculino , Parásitos/clasificación , Parásitos/genética , Reacción en Cadena en Tiempo Real de la Polimerasa , Tanzanía , Virus/clasificación , Virus/genética
2.
Lett Appl Microbiol ; 68(6): 509-513, 2019 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-30761564

RESUMEN

In-house loop-mediated isothermal amplification (LAMP) procedures for the detection of paratyphoid fever-associated bacteria on serovar level were evaluated. Therefore, LAMP primers for Salmonella genus, for two LAMP schemes for S. Paratyphi A, for S. Paratyphi B and for S. Paratyphi C were tested with DNA from culture isolates from strain collections and spiked blood cultures against published PCR protocols targeting the same micro-organisms. Sensitivity and specificity for DNA from culture isolates verified by LAMP ranged from 80·0 to 100·0% and 96·1 to 100·0% vs 65 to 100% and 98·7 to 100% for the PCR approaches. For the spiked blood culture materials, sensitivity and specificity for LAMP ranged from 87·5 to 100·0% and 96·7 to 100·0% vs from 60 to 100% and 98·2 to 100% for PCR. In conclusion, LAMP for paratyphoid fever shows comparable performance characteristics as PCR. Due to its easy application, the procedure is well suited for surveillance purposes in resource-limited settings. SIGNIFICANCE AND IMPACT OF THE STUDY: The use of easy-to-apply, point-of-care-testing-like loop-mediated isothermal amplification (LAMP) for the diagnosis of paratyphoid fever is evaluated. This approach can contribute to low-threshold availability of surveillance options for resource limited settings. Easy-to-teach and easy-to-apply LAMP schemes with similar performance characteristics as PCR are provided. The described test evaluation is of particular use for surveillance and public health experts.


Asunto(s)
ADN Bacteriano/genética , Técnicas de Amplificación de Ácido Nucleico/métodos , Fiebre Paratifoidea/diagnóstico , Salmonella/genética , Salmonella/aislamiento & purificación , Cultivo de Sangre , Cartilla de ADN/genética , Humanos , Fiebre Paratifoidea/microbiología , Reacción en Cadena de la Polimerasa , Prueba de Estudio Conceptual , Sensibilidad y Especificidad
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