Molecular validation of Tomato Yellow Leaf curl Virus (TYLCV) (Ty-1/3, Ty-2 and Ty-3), Fusarium wilt (I-2) and Root- Knot Nematode (Mi-1) resistance in the breeding lines of tomato (Solanum lycopersicum L.)
2024
Arumugam Nithyanandam1, T. Saraswathi2*, L. Pugalendhi1, C. Indu Rani1, N. Manivannan3, S. Harish 4 and N. Manikanda Boopathi5
Gene based molecular screening for disease resistance has become a prominent and widely adopted approach in contemporary tomato breeding programs, both in the public and private sectors. The effectiveness of disease-resistant molecular screening relies on the selection of suitable markers that span the entire genomic region for accurate identification of resistant alleles. In this study, various co-dominant and dominant Sequence Characterized Amplified Region (SCAR) markers were employed to screen for resistance genes associated with Tomato yellow leaf curl virus (TyLCV) Ty-1, Ty-2, Ty-3, Fusarium wilt (race-2) I-2, and Root-knot Nematode ((Meloidogyne incognita) Mi-1. The selected markers exhibited high robustness in distinguishing between resistant and susceptible lines. Co-dominant SCAR markers M2 (Ty-1 gene) and TG0302 (Ty-2 gene) efficiently identify homozygous or heterozygous alleles in Tomato yellow leaf curl virus (TyLCV) screening. The P6-25 marker for Ty-3 gene discerns Ty-3, Ty-3a, and Ty-3b alleles, enhancing allele specificity. In Fusarium wilt I-2 gene screening, I-2/5 ensures accurate identification, while in Root-knot Nematode Mi-1 gene screening, co-dominant marker Mi-23 reliably identify and distinguishes homozygous or heterozygous resistant lines without false positives for I-2 and Mi-1 genes. This streamlined marker assisted approach optimizes disease resistance screening in tomato breeding, providing valuable insights for disease resistant cultivar development.
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