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Development of a sensitive and reliable reverse transcription droplet digital PCR assay for the detection of citrus yellow vein clearing virus.
Liu, Yingjie; Wang, Yingli; Wang, Qin; Zhang, Yanhui; Shen, Wanxia; Li, Ruhui; Cao, Mengji; Chen, Lei; Li, Xue; Zhou, Changyong; Zhou, Yan.
Afiliación
  • Liu Y; National Citrus Engineering Research Center, Citrus Research Institute, Southwest University, Chongqing, 400712, China.
  • Wang Y; Academy of Agricultural Sciences, Southwest University, Chongqing, 400712, China.
  • Wang Q; National Citrus Engineering Research Center, Citrus Research Institute, Southwest University, Chongqing, 400712, China.
  • Zhang Y; Academy of Agricultural Sciences, Southwest University, Chongqing, 400712, China.
  • Shen W; National Citrus Engineering Research Center, Citrus Research Institute, Southwest University, Chongqing, 400712, China.
  • Li R; Academy of Agricultural Sciences, Southwest University, Chongqing, 400712, China.
  • Cao M; National Citrus Engineering Research Center, Citrus Research Institute, Southwest University, Chongqing, 400712, China.
  • Chen L; Academy of Agricultural Sciences, Southwest University, Chongqing, 400712, China.
  • Li X; National Citrus Engineering Research Center, Citrus Research Institute, Southwest University, Chongqing, 400712, China.
  • Zhou C; USDA-ARS, National Germplasm Resources Laboratory, Beltsville, MD, 20705, USA.
  • Zhou Y; National Citrus Engineering Research Center, Citrus Research Institute, Southwest University, Chongqing, 400712, China.
Arch Virol ; 164(3): 691-697, 2019 Mar.
Article en En | MEDLINE | ID: mdl-30535807
ABSTRACT
In 2009, a new viral disease of citrus caused by citrus yellow vein clearing virus (CYVCV) was first discovered in China. CYVCV is considered to be the most serious pathogen affecting lemon production. In this study, a sensitive and reliable reverse transcription droplet digital polymerase chain reaction (RT-ddPCR) assay was developed to detect and quantify CYVCV without references. The specificity of the assay was demonstrated by its failure to amplify other relevant citrus viruses. The quantitative linearity, sensitivity and accuracy of RT-ddPCR for detecting CYVCV were compared to those of real-time RT-PCR. The results showed that both methods had a high degree of linearity (R2 = 0.9776) and quantitative correlation. Furthermore, RT-ddPCR was found to be 100 times more sensitive than real-time RT-PCR, and it can therefore be used to detect CYVCV in individual arthropods. In summary, the results demonstrated that the RT-ddPCR assay is a promising approach for quantitative detection of CYVCV with high precision and accuracy.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades de las Plantas / Citrus / Reacción en Cadena de la Polimerasa de Transcriptasa Inversa / Flexiviridae Tipo de estudio: Diagnostic_studies / Evaluation_studies País/Región como asunto: Asia Idioma: En Año: 2019 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades de las Plantas / Citrus / Reacción en Cadena de la Polimerasa de Transcriptasa Inversa / Flexiviridae Tipo de estudio: Diagnostic_studies / Evaluation_studies País/Región como asunto: Asia Idioma: En Año: 2019 Tipo del documento: Article