Targeting highly conserved 3′-untranslated region of pecluviruses for sensitive broad-spectrum detection and quantitation by RT-PCR and assessment of phylogenetic relationships

• Published in: Journal of virological methods 2010-11, Vol.169 (2), p.385-390
• Main Authors: Dieryck, B., Delfosse, P., Reddy, A.S., Bragard, C.
• Format: Article
• Language: English
• Subjects: 3' Untranslated Regions; 3′-Untranslated region; Africa, Western; Arachis - virology; Biological and medical sciences; Broad-spectrum detection; Conserved Sequence; DNA Primers - genetics; Fundamental and applied biological sciences. Psychology; India; Microbiology; Molecular Sequence Data; Peanut clump virus; Phytopathology. Animal pests. Plant and forest protection; Plant Diseases - virology; Plant Viruses - classification; Plant Viruses - genetics; Plant Viruses - isolation & purification; Plant viruses and viroids; Reverse Transcriptase Polymerase Chain Reaction - methods; RNA, Viral - genetics; Sensitivity and Specificity; Sequence Analysis, DNA; Techniques used in virology; Virology; Virology - methods; Virus quantitation
• ISSN: 0166-0934; 1879-0984
• DOI: 10.1016/j.jviromet.2010.08.010

The 3′-end region of many virus isolates has been shown to possess conserved sequences in addition to the presence of numerous genomic and subgenomic RNAs. Utilizing these sequences, a broad-spectrum reverse transcription-polymerase chain reaction protocol has been developed to detect all the known Indian peanut clump virus and Peanut clump virus isolates, that cause peanut clump diseases in West Africa and India. The primers were targeted at the highly conserved 3′-untranslated regions of the PCV RNA-1 and RNA-2. The conservation was confirmed by sequencing these untranslated regions of RNA-1 for six isolates and RNA-2 for one isolate. The conserved structure of the RNA-1 and RNA-2 was observed and the importance of this region for the virus survival was confirmed. The primers were also designed for virus quantitation using a Taqman ®-based real-time RT-PCR. The use of RT-PCR and real-time quantitative RT-PCR improved the sensitivity of PCV detection compared to ELISA. RT-PCR also led to the detection of IPCV and PCV on two new natural hosts: Oldenlandia aspera and Vigna subterranea. Real-time RT-PCR is considered to be an ideal tool for identifying resistant sources to both IPCV and PCV.