Mixed infection of two mandariviruses identified by high-throughput sequencing in Kinnow mandarin and development of their specific detection using duplex RT-PCR

• Published in: 3 Biotech 2024-06, Vol.14 (6), p.170, Article 170
• Main Authors: Kumar, Rakesh, Gupta, Nitika, Sharma, Susheel Kumar, Kishan, Gopi, Srivastava, Nishant, Khan, Zainul A., Kumar, Ashwini, Baranwal, Virendra Kumar
• Format: Article
• Language: English
• Subjects: Agriculture; Bioinformatics; Biomaterials; Biotechnology; Cancer Research; Chemistry; Chemistry and Materials Science; Clearing; Electron microscopy; Fragments; Gene sequencing; Genomes; Leaves; Mandarins; Mixed infection; Next-generation sequencing; Original Article; Plant viruses; Polymerase chain reaction; rRNA; Stem Cells; Target detection; Viruses
• ISSN: 2190-572X; 2190-5738
• DOI: 10.1007/s13205-024-04011-9

In the current study, high-throughput sequencing (HTS) was used to identify viruses associated with the Kinnow mandarin ( Citrus reticulata ) plants exhibiting yellow vein clearing, mottling, and chlorosis symptoms at experimental farm of ICAR-Indian Agricultural Research Institute, New Delhi, India. During November 2022, leaf samples of symptomatic and asymptomatic Kinnow mandarin trees were collected, subjected to HTS and one of the representative symptomatic samples was subjected to leaf-dip electron microscopy (EM). In the EM results, flexuous virus particles typical of mandarivirus were observed. Ribosomal RNA was depleted from total RNA of pooled samples and RNA sequencing was done using NovaSeq 6000. Host unaligned reads were de novo assembled into contigs, which were annotated through BLASTn using database of plant viruses/viroids reference genomes (NCBI). Results of assembled contigs revealed near-complete genomes of two mandariviruses, i.e. , citrus yellow vein clearing virus (CYVCV) and citrus yellow mottle-associated virus (CiYMaV). The values of fragments per kilo base transcript length per million fragments mapped estimation indicated the dominance of CYVCV in HTS data and it was also confirmed through krona plot distribution of viruses in the pooled samples. A rapid and reliable duplex RT-PCR assay was also developed and standardized for the simultaneous detection of both CYVCV and CiYMaV in a pooled Kinnow mandarin sample. The developed duplex RT-PCR was then validated for the presence of these viruses in individual Kinnow mandarin samples. The specificity and sensitivity results confirmed that primers were highly specific to their targets and able to detect viruses up to 10 –2 dilutions of RNA in standard and duplex RT-PCR. Therefore, the developed rapid duplex RT-PCR can be used for virus indexing and production of virus-free Kinnow mandarin plants for certification programs.