Abstract
We have examined the genetics of systemic resistance in Phaseolus vulgaris to azuki bean mosaic virus (AzMV) and cowpea aphid-borne mosaic virus (CABMV) and the relationship of this resistance to a phenotypically similar resistance to watermelon mosaic virus (WMV) and soybean mosaic virus (SMV). In P. vulgaris cv ‘Great Northern 1140’ (GN1140), resistance to SMV and WMV has been attributed to the genes Smv and Wmv, respectively, which have been shown to segregate as a unit. Systemic resistance to AzMV is conferred by two incompletely dominant alleles, Azm1 and Azm2, at unlinked loci. At least three resistance alleles must be present at these two loci for systemic resistance to be expressed in the plant. Systemic resistance to CABMV in GN 1140 is conditioned by a dominant allele that has been designated Cam2. Under some environmental conditions, a recessive allele at an unlinked locus, cam3, also controls a resistant response to CABMV. Resistance to AzMV and CABMV does not assort independently from Wmv/Smv, but also does not consistently cosegregate, suggesting that perhaps in each case one of the factors involved in resistance is associated with Smv/Wmv.
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References
Ali M (1950) Genetics of resistance to the common bean mosaic virus in the bean (Phaseolus vulgaris L.). Phytopathology 40:69–79
Bennetzen JL, Hulbert SH (1992) Organization, instability and evolution of plant disease resistance genes. Plant Mol Biol 20: 575–580
Benscher D, Pappu SS, Niblett CL, Rybicki EP, Bird J (1993) Biological and molecular characterization of potyviruses from Passiflora. Phyotopathology 83:1422
Bijaisoradat M, Kuhn CW (1985) Nature of resistance in soybean to cowpea chlorotic mottle virus. Phytopathology 75:351–355
Blauth JR (1994) Genetic analysis of resistance to pepper mottle potyvirus and tobacco etch potyvirus in pepper, genus Capsicum. PhD thesis, Cornell University, Ithaca, N.Y.
Bos L (1992) Potyviruses, chaos or order? Arch Virol [Suppl 5]: 31–46
Clark M, Adams A (1977) Characteristics of the microplate method of enzyme-linked immunosorbent assay for the detection of plant viruses. J Gen Virol 34:475–483
Day KL (1984) Resistance to bean common mosaic virus in Phaseolus Vulgaris L. PhD thesis, University of Birmingham, Birmingham, UK
Dijkstra J, Khan J (1992) A proposal for a bean common mosaic subgroup of potyviruses. Arch Virol [Suppl] 5: 389–395
Drijfhout E (1978) Genetic interaction between Phaseolus vulgaris and bean common mosaic virus with implications for strain identification and breeding for resistance. Agric Res Rep 872. Pudoc, Wageningen
Ellingboe A (1981) Changing concepts in host-pathogen genetics. Annu Rev Phytopathol 19:125–143
Fisher ML, Kyle MM (1994) Inheritance of resistance to potyviruses in Phaseolus vulgaris L. III. Cosegregation of phenotypically similar dominant responses to nine potyviruses. Theor Appl Gen 89:818–823
Fraser R (1986) Genes for resistance to plant viruses. CRC Crit Rev Plant Sci 3:257–294
Fraser R (1992) The genetics of plant-virus interactions: implications for plant breeding. Euphytica 63:175–185
Hollings M, Brunt A (1981) Potyviruses. Handbook of plant virus infections: comparative diagnosis. Elsevier/North Holland, Amsterdam, pp 731–807
Jones D, Thomas C, Hammond-Kosack K, Balint-Kurti P, Jones DG (1994) Isolation of the tomato Cf-9 gene for resistance to Cladosporium fulvum by transposon tagging. Science 266:789–793
Khan J, Lohuis D, Goldbach R, Dijkstra J (1993) Sequence data to setttle the taxonomic position of bean common mosaic virus and blackeye cowpea mosaic virus isolates. J Gen Virol 74:2243–2249
Kyle M (1988) The I gene and broad spectrum plant virus resistance in Phaseolus vulgaris L. PhD thesis, Cornell University, Ithaca, N.Y.
Kyle MM, Dickson MH (1988) Linkage of hypersensitivity to five potyviruses with the B locus for seed coat in Phaseolus vulgaris L. J Hered 79:308–311
Kyle MM, Provvidenti R (1987) Inheritance of resistance to potato y viruses in Phaseolus vulgaris L. I. Two independent genes for resistance to watermelon mosaic virus-2. Theor Appl Genet 74:595–600
Kyle MM, Provvidenti R (1993a) Inheritance of resistance to potyviruses in Phaseolus vulgaris L. II. Inheritance, linkage relations, and utility of a gene for lethal systemic necrosis to soybean mosaic virus. Theor Appl Genet 86:189–196
Kyle MM, Provvidenti R (1993b) Genetics of broad spectrum virus resistance in bean and pea. In: Kyle MM (ed) Resistance to viral diseases of vegetables: genetics and breeding. Timber Press, Portland, Ore., pp 153–166
Leisner SM, Turgeon R, Howell SH (1993) Effects of host plant development and genetic determinants on the long-distance movement of cauliflower mosaic virus in Arabidopsis. Plant Cell 5:191–202
Martin GB, Brommonschenkel SH, Chunwongse J, Frary A, Ganal MW, Spivey R, Wu T, Earle ED, Tanksley SD (1993) Map-based cloning of protein kinase gene conferring disease resistance in tomato. Science 262:1432–1436
McKern N, Shukla D, Barnett O, Vetten H, Dijkstra J, Whittaker L, Ward C (1992) Coat protein properties suggest that azuki bean mosaic virus, blackeye cowpea mosaic virus, peanut stripe virus, and three isolates from soybean are all strains of the same potyvirus. Intervirology 33:121–134
Mink G, Silbernagel M (1992) Serological and biological relationships among viruses in the bean common mosaic virus subgroup. Arch Virol [Suppl 5]: 397–406
Pink DAC, Lot H, Johnson R (1992) Novel pathotypes of lettuce mosaic virus — breakdown of a durable resistance? Euphytica 63:169–174
Provvidenti R (1974) Inheritance of resistance to watermelon mosaic virus-2 in Phaseolus vulgaris. Phytopathology 64:1448–1450
Provvidenti R (1983) Two useful selections of the bean cultivar Black Turtle Soup for viral identification. Bean Improv Coop Ann Rep 26:73–75
Provvident R (1993a) Genetics of resistance to viral diseases of bean. In: Kyle MM (ed) Resistance to viral diseases of vegetables: genetics and breeding. Timber Press, Portland, Ore., pp 112–152
Provvidenti R (1993b) Resistance to three strains of passionfruit woodiness virus in Phaseolus vulgaris. Bean Improv Coop Ann Rep 36:137–138
Provvidenti R, Gonsalves D, Ranalli R (1982) Inheritance of resistance to soybean mosaic virus in Phaseolus vulgaris. J Hered 73:302–303
Provvidenti R, Gonsalves D, Taiwo K (1983) Inheritance of resistance to blackeye cowpea mosaic and cowpea aphid-borne mosaic viruses in Phaseolus vulgaris. J Hered 74:60–61
Pryor T (1987) The origin and structure of fungal disease resistance genes in plants. Trends Genet 3(6): 157–161
Rybicki EP, Shukla DD (1992) Coat protein phylogeny and systematics of potyviruses. Arch Virol [Suppl 5] 5: 139–170
Shukla D, Ward C (1988) Amino acid sequence homology of coat proteins as a basis for identification and classification of the potyvirus group. J Gen Virol 69:2703–2710
Taiwo M, Gonsalves D, Provvidenti R, Thurston H (1982) Partial characterization and grouping of isolates of blackeye cowpea mosaic and cowpea aphid borne mosaic viruses. Phytopathology 72:590–569
Tsuchizaki T, Omura T (1987) Relationships among bean common mosaic virus, blackeye cowpea mosaic virus, azuki mosaic virus, and soybean mosaic virus. Ann Phytopathol Soc Jpn 53:478–488
Ward C, McKern N, Frenkel M, Shukla D (1992) Sequence data as the major criterion for potyvirus classification. Arch Virol [Suppl 5] 5:283–297
Whitham S, Dinesh-Kumar S, Choi D, Hehl R, Corr C, Baker B (1994) The product of the tobacco mosaic virus resistance gene N: similarity to Toll and the interleukin-1 receptor. Cell 78:1101–1115
Wintermantel WM, Anderson EJ, Schoelz JE (1993) Identification of domains within gene VI of cauliflower mosaic virus that influence systemic infection of Nicotiana bigelovii in a light-dependent manner. Virology 196:789–798
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Fisher, M.L., Kyle, M.M. Inheritance of resistance to potyviruses in Phaseolus vulgaris L. IV. Inheritance, linkage relations, and environmental effects on systemic resistance to four potyviruses. Theoret. Appl. Genetics 92, 204–212 (1996). https://doi.org/10.1007/BF00223377
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DOI: https://doi.org/10.1007/BF00223377