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1.
Rev. Soc. Bras. Med. Trop ; 47(3): 302-306, May-Jun/2014. tab, graf
Artículo en Inglés | LILACS | ID: lil-716392

RESUMEN

Introduction This study confirmed the absence of natural infection with Xenotropic murine leukemia virus-related virus (XMRV) or XMRV-related disease in human populations of the Brazilian Amazon basin. We demonstrated that 803 individuals of both sexes, who were residents of Belem in the Brazilian State of Pará, were not infected with XMRV. Methods Individuals were divided into 4 subgroups: healthy individuals, individuals infected with human immunodeficiency virus, type 1 (HIV-1), individuals infected with human T-lymphotrophic virus, types 1 or 2 (HTLV-1/2), and individuals with prostate cancer. XMRV infection was investigated by nested PCR to detect the viral gag gene and by quantitative PCR to detect pol. Results There was no amplification of either gag or pol segments from XRMV in any of the samples examined. Conclusions This study supports the conclusions of the studies that eventually led to the retraction of the original study reporting the association between XMRV and human diseases. .


Asunto(s)
Adulto , Femenino , Humanos , Masculino , Persona de Mediana Edad , Infecciones por VIH/virología , Infecciones por HTLV-I/virología , Infecciones por HTLV-II/virología , Neoplasias de la Próstata/virología , Infecciones por Retroviridae/complicaciones , Virus Relacionado con el Virus Xenotrópico de la Leucemia Murina/genética , Brasil , ADN Viral/genética , Reacción en Cadena de la Polimerasa
2.
Korean Journal of Blood Transfusion ; : 155-160, 2013.
Artículo en Coreano | WPRIM | ID: wpr-117793

RESUMEN

BACKGROUND: Xenotropic murine leukemia virus-related virus (XMRV) has been detected in peripheral blood mononuclear cells (PBMNs), therefore, it has been regarded as being infectious and transmittable by transfusion. Thus, we attempted to detect XMRV in blood samples in order to confirm the absence of XMRV from blood donors. METHODS: We achieved 165 blood donors and four chronic fatigue syndrome (CFS) patients. We performed real-time polymerase chain reaction using the LightCycler 480 (Roche, Penzberg, Germany) for the gag and env genes of the XMRV genome. DNA was extracted from peripheral blood samples. We used Uracil-N-Glycosylase in order to prevent contamination and DNA extracted from mouse embryonic fibroblasts (MEF) for amplification control. RESULTS: No XMRV was detected in any of the blood donors in both the gag and env genes. In four CFS patients, amplification was not detected in the gag gene. In two of four CFS patients, amplifications were detected and the melting temperature was in agreement with that of MEF control in the env gene. CONCLUSION: Although XMRV was not present in blood samples from blood donors, this is the first report on XMRV in Korean blood donors. We confirmed the absence of XMRV in Korean blood donors, the same as studies reported in other countries.


Asunto(s)
Animales , Humanos , Ratones , Donantes de Sangre , ADN , Síndrome de Fatiga Crónica , Fibroblastos , Congelación , Genes env , Genes gag , Genoma , Reacción en Cadena en Tiempo Real de la Polimerasa , Virus Relacionado con el Virus Xenotrópico de la Leucemia Murina
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