Tissue and Time Optimization for Real-Time Detection of Apple Mosaic Virus and Apple Necrotic Mosaic Virus Associated with Mosaic Disease of Apple ( Malus domestica )

• Published in: Viruses 2023-03, Vol.15 (3), p.795
• Main Authors: Nabi, Sajad Un, Mir, Javid Iqbal, Yasmin, Salwee, Din, Ambreena, Raja, Wasim H, Madhu, G S, Parveen, Shugufta, Mansoor, Sheikh, Chung, Yong Suk, Sharma, Om Chand, Sheikh, Muneer Ahmad, Al-Misned, Fahad A, El-Serehy, Hamed A
• Format: Article
• Language: English
• Subjects: Apple; Asymptomatic; Autumn; Bromoviridae; Cultivars; detection; Diagnosis; Disease; Diseases and pests; Fruits; Gene banks; Gene expression; Genetic aspects; High temperature; Identification and classification; Ilarvirus; Leaves; Malus; Malus domestica; mosaic; Mosaic disease; Mosaic Viruses; Optimization; Plant Diseases; Plant Viruses; Planting; Plants; Polymerase chain reaction; Reverse transcription; RNA viruses; Seasons; Seeds; spatial; Summer; temporal; Trees; Variance analysis; virus; Virus diseases of plants; Viruses
• ISSN: 1999-4915; 1999-4915
• DOI: 10.3390/v15030795

Besides apple mosaic virus (ApMV), apple necrotic mosaic virus (ApNMV) has also been found to be associated with apple mosaic disease. Both viruses are unevenly distributed throughout the plant and their titer decreases variably with high temperatures, hence requiring proper tissue and time for early and real-time detection within plants. The present study was carried out to understand the distribution and titer of ApMV and ApNMV in apple trees from different plant parts (spatial) during different seasons (temporal) for the optimization of tissue and time for their timely detection. The Reverse Transcription-Polymerase Chain Reaction (RT-PCR) and Reverse Transcription-quantitative Polymerase Chain Reaction (RT-qPCR) was carried out to detect and quantify both viruses in the various plant parts of apple trees during different seasons. Depending on the availability of tissue, both ApMV and ApNMV were detected in all the plant parts during the spring season using RT-PCR. During the summer, both viruses were detected only in seeds and fruits, whereas they were detected in leaves and pedicel during the autumn season. The RT-qPCR results showed that during the spring, the ApMV and ApNMV expression was higher in leaves, whereas in the summer and autumn, the titer was mostly detected in seeds and leaves, respectively. The leaves in the spring and autumn seasons and the seeds in the summer season can be used as detection tissues through RT-PCR for early and rapid detection of ApMV and ApNMV. This study was validated on 7 cultivars of apples infected with both viruses. This will help to accurately sample and index the planting material well ahead of time, which will aid in the production of virus-free, quality planting material.