TOMATO yellow leaf curl disease (TYLCD) is a significant limitation factor in tomato
crops and ranks among the top 10 plant viruses affecting the production of many crops,
particularly tomatoes, leading to considerable economic losses without an efficient control
strategy till now. In this study, PCR technique was used to amplify partial sequences (670 bp) of
tomato yellow leaf curl virus (TYLCV) genome, specifically spanning the trans-activator protein
(C2), replication enhancer protein (C3) genes, as well as partial parts of replication (Rep) and
coat protein (CP) genes. These sequences were obtained from naturally infected tomato plants
collected from different governorates in Egypt. The DNA sequence analyses of the current
Egyptian isolate was annotated and deposited in the GenBank with an accession ID MZ546492,
revealing high nucleotide sequence identities (99.3 %) to TYLCV isolates in the GenBank.
The transmission and host range assays confirmed that the whitefly is the sole transmitter, and
tomatoes, zucchini, cucumber, pepper, jimsonweed, and common bean as a host for TYLCV.
To explore alternative control strategies, an in-silico approach was employed to generate the
possible siRNA-producing sequences that could be used to knock down TYLCV in infected
plants. The current findings support the development of a rapid, reliable, and robust molecular
detection and identification tool of TYLCV in tomato germplasm to ensure the safe and
sustainable production of TYLCV-free tomatoes. Additionally, in silico analysis indicated the
possibility of using siRNA to control TYLCV.
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