首页> 外文期刊>Acta Virologica: International Journal >Simultaneous detection of papaya ringspot virus, papaya leaf distortion mosaic virus, and papaya mosaic virus by multiplex real-time reverse transcription PCR
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Simultaneous detection of papaya ringspot virus, papaya leaf distortion mosaic virus, and papaya mosaic virus by multiplex real-time reverse transcription PCR

机译:多重实时逆转录PCR同时检测木瓜环斑病毒,木瓜叶片畸变花叶病毒和木瓜花叶病毒

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Both the single infection of papaya ringspot virus (PRSV), papaya leaf distortion mosaic virus (PLDMV) or papaya mosaic virus (PapMV) and double infection of PRSV and PLDMV or PapMV which cause indistinguishable symptoms, threaten the papaya industry in Hainan Island, China. In this study, a multiplex real-time reverse transcription PCR (RT-PCR) was developed to detect simultaneously the three viruses based on their distinctive melting temperatures (Tms): 81.0 +/- 0.8 degrees C for PRSV, 84.7 +/- 0.6 degrees C for PLDMV, and 88.7 +/- 0.4 degrees C for PapMV. The multiplex real-time RT-PCR method was specific and sensitive in detecting the three viruses, with a detection limit of 1.0 x 10(1), 1.0 x 10(2), and 1.0 x 10(2) copies for PRSV, PLDMV, and PapMV, respectively. Indeed, the reaction was 100 times more sensitive than the multiplex RT-PCR for PRSV, and 10 times more sensitive than multiplex RT-PCR for PLDMV. Field application of the multiplex real-time RT-PCR demonstrated that some non-symptomatic samples were positive for PLDMV by multiplex real-time RT-PCR but negative by multiplex RT-PCR, whereas some samples were positive for both PRSV and PLDMV by multiplex real-time RT-PCR assay but only positive for PLDMV by multiplex RT-PCR. Therefore, this multiplex real-time RT-PCR assay provides a more rapid, sensitive and reliable method for simultaneous detection of PRSV, PLDMV, PapMV and their mixed infections in papaya.
机译:番木瓜环斑病毒(PRSV),番木瓜叶片畸变花叶病毒(PLDMV)或番木瓜花叶病毒(PapMV)的单次感染以及PRSV和PLDMV或PapMV的双重感染均导致难以区分的症状,威胁着中国海南岛的番木瓜产业。在这项研究中,开发了一种实时多重逆转录PCR(RT-PCR),以基于三种病毒的独特解链温度(Tms)同时检测这三种病毒:PRSV为81.0 +/- 0.8摄氏度,PRSV为84.7 +/- 0.6对于PLDMV,温度为0摄氏度,对于PapMV为88.7 +/- 0.4摄氏度。多重实时RT-PCR方法对三种病毒的检测具有特异性和敏感性,对于PRSV,PLDMV的检出限为1.0 x 10(1),1.0 x 10(2)和1.0 x 10(2)拷贝,和PapMV。实际上,对于PRSV,该反应的敏感性比多重RT-PCR高100倍,对于PLDMV,该反应的敏感性比多重RT-PCR高10倍。多重实时RT-PCR的现场应用表明,一些非症状样本通过多重实时RT-PCR对PLDMV呈阳性,但通过多重RT-PCR呈阴性,而一些样品对PRSV和PLDMV呈阳性实时RT-PCR检测,但多重RT-PCR仅对PLDMV呈阳性。因此,这种多重实时RT-PCR分析提供了一种更快速,灵敏和可靠的方法,用于同时检测木瓜中的PRSV,PLDMV,PapMV及其混合感染。

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