Hostname: page-component-78c5997874-j824f Total loading time: 0 Render date: 2024-11-15T07:25:25.530Z Has data issue: false hasContentIssue false

Genetic analysis of Okra Yellow Vein Mosaic Virus disease resistance in wild relative of okra Abelmoschus angulosus Wall. ex Wight & Arn

Published online by Cambridge University Press:  14 March 2019

SamanthiKumari Wasala*
Affiliation:
Plant Genetic Resources Centre, Gannoruwa, Peradeniya, Sri Lanka
Sumudu I. Senevirathne
Affiliation:
Plant Genetic Resources Centre, Gannoruwa, Peradeniya, Sri Lanka
Jayantha Bandara Senanayake
Affiliation:
Field Crops Research and Development Institute, Mahailluppalla, Sri Lanka
Anuradini Navoditha
Affiliation:
Field Crops Research and Development Institute, Mahailluppalla, Sri Lanka
*
*Corresponding author. E-mail: [email protected]

Abstract

Wild relative of okra, Abelmoschus angulosus Wall. ex Wight & Arn. was identified as a resistant germplasm for Okra Yellow Vein Mosaic Virus (OYVMV) which is the devastating disease for okra cultivation in Sri Lanka. The mode of resistance of OYVMV in A. angulosus was studied with the aim of tagging responsible genes for the disease resistance. Wide hybridization was performed between A. angulosus and highly virus susceptible A. esculentus variety, MI-7. Very poor seed setting was observed in F1 and F2 generations due to post zygotic abortion. Disease screening was carried out using F1 and F2:3 populations along with parents in the field under induced disease pressure. Disease severity index and area under disease progress curve were calculated to measure disease severity. Number of genes segregating for OYVMV disease resistance was calculated for the F2:3 generation. Modified Wright's formula was used to estimate the effective gene number and mode of inheritance by a quantitative method. A χ2 test was performed for qualitative analysis. Plants of A. angulosus were totally free of virus incidence while 100% disease incidence was observed in the variety MI-7. F2:3 population showed between and within progeny segregation for disease incidence. Results indicated that the disease susceptibility was dominant over resistance. χ2 analysis revealed that the segregation of disease severity was significantly fit to the gene model of 9:6:1 (χ2 = 0.1757 at P ≤ 0.05) suggesting the disease resistance in A. angulosus is governing by two recessive genes in an additive manner. Result was confirmed by the quantitative analysis.

Type
Research Article
Copyright
Copyright © NIAB 2019 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Ali, M, Hossain, MZ and Sarker, NC (2000) Inheritance of Yellow Vein Mosaic Virus (YVMV) tolerance in a cultivar of okra (Abelmoschus esculentus (L.) Moench). Euphytica 111: 205209.Google Scholar
Ali, S, Khan, MA, Habib, A, Rasheed, S and Iftikhar, Y (2005) Correlation of environmental conditions with okra yellow vein mosaic virus and Bemisia tabaci population density. International Journal of Agriculture & Biology 7: 142144.Google Scholar
Arora, D, Jindal, SK and Singh, K (2008) Genetics of resistance to yellow vein mosaic virus in inter-varietal crosses of okra (Abelmoschus esculentus L. Moench). SABRAO Journal of Breeding and Genetics 40: 93103.Google Scholar
Basnet, BR, Singh, RP, Herrera-Faessel, SA, Ibrahim, AMH, Huerta-Espino, V and Rudd, JC (2013) Genetic analysis of adult plant resistance to yellow rust and leaf rust in common spring wheat Quaiu 3. Plant Disease 97: 728736.Google Scholar
Bjarko, ME and Line, RF (1988) Heritability and number of genes controlling leaf rust resistance in four cultivars of wheat. Phytopathology 78: 457461.Google Scholar
Charrier, A (1984) Genetic Resources of the Genus Abelmoschus Med. (okra). Rome, Italy: International Board for Plant Genetic Resources Secretariat, 61 pp.Google Scholar
Cockerham, CC (1983) Covariance of relatives from self-fertilization. Crop Science 23: 11771180.Google Scholar
DOA (Department of Agriculture) (1990) Okra. Crop Recommendation Technoguide. Sri Lanka: Ministry of Agriculture Development and Research, pp. 7679.Google Scholar
García-Cano, E, Resende, RO, Boiteux, LS, Giordano, LB, Fernández-Muñoz, R and Moriones, E (2008) Phenotypic expression, stability, and inheritance of a recessive resistance to monopartite begomoviruses associated with tomato yellow leaf curl disease in tomato. Phytopathology 98: 618627.Google Scholar
Jambhale, ND and Nerkar, YS (1981) Inheritance of resistance to okra yellow vein mosaic disease in interspecific crosses of Abelmoschus. Theory of Applied Genetics 60: 313316.Google Scholar
Jose, J and Usha, R (2003) Bhendi yellow vein mosaic disease in India is caused by association of a satellite with a begomovirus. Virology 7: 305310.Google Scholar
Luke, HH, Barnett, RD and Pfahler, PL (1975) Inheritance of horizontal resistance to crown rust in oats. Phytopathology 65: 631632.Google Scholar
MacDiarmid, R (2005) RNA silencing in productive virus infections. Annual Review of Phytopathology 43: 523544.Google Scholar
McKinney, HH (1923) Influence of soil temperature and moisture on infection of wheat seedlings by Helminthosporium sativum. Journal of Agriculture Research 26: 195217.Google Scholar
Patel, P, Malik, SK, Negi, KS, John, J, Yadav, S, Chaudhari, G and Bhat, KV (2013) Pollen germination characteristics, pollen–pistil interaction and reproductive behaviour in interspecific crosses among Abelmoschus esculentus Moench and its wild relatives. Grana 52: 114.Google Scholar
Samarajeewa, PK (2003) Wild Abelmoschus species in the improvement of okra. In: Conservation and use of crop wild relatives. In: Proceedings of the joint department of agriculture, Sri Lanka and National Institute of Agribiological sciences, Japan, workshop held on 3rd February 2003, pp. 97108.Google Scholar
Samarajeewa, PK and Rathnayake, RMUSK (2004) Disease resistance and genetic variation of wild relatives of okra (Abelmoschus esculentus L.). Annals of the Sri Lanka Department of Agriculture 6: 167176.Google Scholar
Sankara, RK and Acharyya, P (2012) Incidence of yellow vein mosaic virus disease of okra (Abelmoschus esculentus (L.) Moench) under summer and rainy environments. International Journal of Current Research 4: 1821.Google Scholar
Sastry, KSM and Singh, SJ (1974) Effect of yellow vein mosaic virus infection on growth and yield of okra crop. Indian Phytopathology 27: 294297.Google Scholar
Senavirathne, HMSI, Wasala, SK, Senanayake, DMJB, Weerasekara, D, Wickramasinghe, HAM and Deepal, PKGA (2016) Characterization and detection of Yellow Vain disease of okra (Abelmoachus esculentus L. Meonch) in Sri Lanka. Tropical Agriculture Research 27: 360369.Google Scholar
Senjam, P, Senapati, BK, Chattopadhyay, and Datta, S (2018) Genetic control of yellow vein mosaic virus disease tolerance in Abelmoschus esculentus (L.) Moench. Journal of Genetics 97: 2533.Google Scholar
Seth, T, Chattopadhyay, A, Dutta, S, Hazra, P and Singh, B (2017) Genetic control of yellow vein mosaic virus disease in okra and its relationship with biochemical parameters. Euphytica 213: 30.Google Scholar
Sharma, BR and Dhillon, TS (1983) Genetics of resistance to yellow vein mosaic virus in interspecific crosses of okra (Abelmoschus spp.). Genetica Agraria 37: 267275.Google Scholar
Sharma, BR and Sharma, DP (1984) Breeding for resistance to yellow vein mosaic virus in okra. Indian Journal of Agricultural Sciences 54: 917920.Google Scholar
Singh, HB, Joshi, BS, Khanna, PP and Gupta, PS (1962) Breeding for field resistance to yellow vein mosaic in bhindi. Indian Journal of Genetics and Plant Breeding 22: 137138.Google Scholar
Singh, B, Mathura, R, Kalloo, G, Satpathy, S and Pandey, KK (2007) Wild taxa of okra (Abelmoschus Species): reservoir of genes for resistance to biotic stresses. Acta Horticulture 752: 323328.Google Scholar
Steel, RDG and Torrie, JH (1980) Principles and Procedures of Statistics A Biometrical Approach, 2nd edn. New Yolk: McGraw-Hill.Google Scholar
Thakur, MR (1976) Inheritance of yellow vein mosaic in a cross of okra species Abelmoschus esculentus x A. manihot subsp. manihot. SABRAO Journal of Breeding and Genetics 8: 6973.Google Scholar
Vashisht, VK, Sharma, BR and Dhillon, GS (2001) Genetics of resistance to yellow vein mosaic virus in okra. Crop Improvement 28: 218225.Google Scholar
Wilcoxon, RD, Skovmand, B and Atif, AF (1975) Evaluation of wheat cultivars for ability to retard development of stem rust. Annals of Applied Biology 80: 275281.Google Scholar
Wright, S (1968) Evolution and Genetics of Populations. Vol 1. Genetic and Biometric Foundations. Chicago, IL: University of Chicago Press, pp. 469.Google Scholar