2003
DOI: 10.1016/j.jviromet.2003.08.009
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Detection of norovirus (GI, GII), Sapovirus and astrovirus in fecal samples using reverse transcription single-round multiplex PCR

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Cited by 232 publications
(185 citation statements)
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“…Detection and genotyping of rotavirus was performed following the procedures of Rodríguez-Díaz et al (2009). Detection of sapovirus, norovirus and astrovirus was carried out using the primers described by Yan et al (2003) with a multiplex Reverse transcriptase (RT)-PCR using the standard conditions described in a commercial kit (Superscript III one step RT-PCR; Invitrogen, Genome Biotechnologies). The presence of hepatitis A was established in a monoplex RT-PCR as described elsewhere (Sánchez et al 2002).…”
Section: Methodsmentioning
confidence: 99%
“…Detection and genotyping of rotavirus was performed following the procedures of Rodríguez-Díaz et al (2009). Detection of sapovirus, norovirus and astrovirus was carried out using the primers described by Yan et al (2003) with a multiplex Reverse transcriptase (RT)-PCR using the standard conditions described in a commercial kit (Superscript III one step RT-PCR; Invitrogen, Genome Biotechnologies). The presence of hepatitis A was established in a monoplex RT-PCR as described elsewhere (Sánchez et al 2002).…”
Section: Methodsmentioning
confidence: 99%
“…Therefore, a rapid and sensitive assay is preferred to screen for the presence of these viruses in diarrheal fecal specimens. In a previous study, we developed a reverse transcription single-round multiplex polymerase chain reaction (RT-smPCR) assay for the simultaneous detection of norovirus (genogroup I, genogroup II), sapovirus and astrovirus in fecal specimens (Yan et al, 2003). Recently, we developed another RT multiplex PCR for one-step amplification of all subgenera A to F adenoviruses, and group A and C rotaviruses.…”
mentioning
confidence: 99%
“…A stool suspension of approximately 10% was prepared in Dulbecco's Phosphate Buffered Saline (DPBS) using the selected human norovirus positive sample (HuNoV GII/4 positive sample) and precleared by centrifugation at 13,000 rpm for 15 min at 4℃ (7,8). Genomic RNA was extracted from stool supernatant using the QIAamp Viral RNA mini kit (Qiagen), according to the manufacturer's protocol.…”
Section: Rna Extraction From Stool Samples and Gene Amplification By mentioning
confidence: 99%