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Published online 8 September 2006
Published in Crop Sci 46:2338-2339 (2006)
© 2006 Crop Science Society of America
677 S. Segoe Rd., Madison, WI 53711 USA
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REGISTRATIONS OF GERMPLASMS

Registration of Common Bacterial Blight Resistant White Kidney Bean Germplasm Line USWK-CBB-17

P.N. Miklasa,*, J.R. Smithb and S.P. Singhc

a USDA-ARS, Vegetable & Forage Crop Res. Unit, 24106 N. Bunn Rd., Prosser, WA 99350
b USDA-ARS, Crop Genetics & Production Res. Unit, P.O. Box 345, Stoneville, MS 38776-0345
c Univ. of Idaho, Kimberly Research & Extension Center, Kimberly, ID 83341

* Corresponding author (pmiklas{at}pars.ars.usda.gov)

White kidney bean (Phaseolus vulgaris L.) germplasm line USWK-CBB-17 (Reg. no. GP-261, PI 642447) was developed by USDA-ARS in cooperation with the Idaho Agricultural Experiment Station and released in 2006. This line was bred with a high level of resistance to common bacterial blight (Xap) caused by Xanthomonas axonopodis pv. phaseoli Starr & Garces 1950 emend. (Vauterin et al., 1995) = X. campestris pv. phaseoli (Smith) Dye. Common bacterial blight is a major seed-borne disease endemic to the U.S. bean production regions east of the continental divide and problematic in Colorado, Michigan, Minnesota, Nebraska, New York, North Dakota, and Wisconsin. USDK-CBB-17 possesses two major QTL that confer a high level of resistance to Xap. Marker-assisted selection using the SAP6 sequenced characterized amplified region (SCAR) marker tightly linked with a QTL derived from great northern landrace cultivar Montana No. 5 (Miklas et al., 2000, 2003) and SU91 SCAR marker with a QTL from breeding line XAN 159 (Pedraza et al., 1997) facilitated the development of USWK-CBB-17.

USWK-CBB-17 (previously tested as PS99–499–3-2-B-2) is an F5–derived line derived from the cross 98MSU-837//I9566–21–4-2/USLK-2. 98MSU-837 is an advanced white kidney breeding line from Michigan State University with high yield potential. USLK-2 is a light red kidney breeding line released by USDA-ARS (Miklas et al., 2002) that possesses I and bc-3 genes for resistance to Bean common mosaic virus (BCMV) and Bean common mosaic necrosis virus (BCMNV). I9566–21–4-2 is an F3–derived line from the cross ‘Montcalm’/XAN 159 selected for the presence of SAP6 and SU91 markers and resistance to common bacterial blight in greenhouse leaf inoculation assays. XAN 159, with the pedigree ‘UI-114’/PI319441//PI319443/3/‘Masterpiece,’ is an advanced breeding line from CIAT with resistance to common bacterial blight derived via interspecific hybridization with tepary bean (Phaseolus acutifolius A. Gray var. latifolius Freeman) (Thomas and Waines, 1984). XAN 159 is the source of a major resistance QTL linked with the SU91 SCAR marker (Pedraza et al., 1997). Montcalm with the pedigree GN No.1/‘Dark Red Kidney’ is a dark red kidney cultivar from Michigan State University with moderate resistance to common bacterial blight conferred by a major QTL linked with the SAP6 SCAR marker (Miklas et al., 2000) that was derived from Montana No. 5 via ‘Great Northern No. 1’ (Miklas et al., 2003).

Marker-assisted selection was used to identify an F1 plant (PS99–499B) from the last cross with the presence of SAP6 and SU91 markers and advanced to F2. The F2 was planted in the field at the Washington State University, Irrigated Agriculture Research and Extension Center, Roza Unit, at Prosser, WA, and screened for plant and seed type. An F3 progeny from an F2 single-plant selection (PS99–499B-3) was tested for reaction to common bacterial blight in leaf inoculation tests conducted at the USDA-ARS Tropical Agriculture Research Station at Mayaguez, Puerto Rico. An individual F3 plant (PS99–499B-3–2) with high level resistance and confirmed to possess SAP6 and SU91 markers was advanced to F4. The F4 progeny-row was grown in the field at Prosser and harvested in bulk (PS99–499B-3–2-B). The F3:5 bulk was screened for leaf reaction to common bacterial blight in the University of Idaho greenhouse at Kimberly, ID. An individual F5 plant (PS99–499B-3–2-B-2) with high level resistance and possessing SAP6 and SU91 markers was selected to produce USWK-CBB-17 that was subsequently increased for three generations and evaluated in multiple greenhouse tests for reaction to common bacterial blight and examined in the field for yield and maturity.

USWK-CBB-17, in a greenhouse leaf inoculation test conducted at Kimberly, ID, in December 2004, had a mean disease score of 4.8 based on a 1-to-9 scale, where 1 is no visible common bacterial blight and 9 is completely susceptible. In comparison, the dark red kidney bean Montcalm had a mean disease score of 8.7. In a repeated test in December 2005, USWK-CBB-17 scored 3.9 compared to 8.0 for Montcalm and 7.7 for ‘Beluga’ large white alubia (Kelly et al., 1999). USWK-CBB-17 possesses both the SAP6 and SU91 markers linked with major QTL for resistance derived from Montana No. 5 (via Montcalm) and tepary bean (via XAN 159), respectively. USWK-CBB-17 exhibits a much higher level of resistance to common bacterial blight than commercially available white kidney bean cultivars.

USWK-CBB-17 exhibits a Type I determinate bush growth habit typical of white kidney bean. Yield was 98% of Beluga at the Washington State University Research Farm at Othello, Washington, in 2005. Average weight of 100 seeds was 41 g, which is slightly less than the 44 g for Beluga. USWK-CBB-17 matured in 91 d, the same as Beluga. Seed appearance was rated commercially acceptable for the white kidney market class. USWK-CBB-17 also exhibits a hypersensitive resistance response to the NL-3 strain of BCMNV in Prosser greenhouse tests, which infers presence of the I gene for resistance to BCMV. This germplasm line is also resistant to Beet curly top virus (BCTV).

USWK-CBB-17 will be most useful for incorporating resistance to common bacterial blight into the white kidney market class but also into other large-seeded market classes and green bean of Andean origin as well. Seed will be maintained by USDA-ARS at Prosser, WA, and provided in small quantities on written request. We ask that appropriate recognition of source be given when this germplasm contributes to the development of a new cultivar or germplasm line.

NOTES

Registration by CSSA.

Received for publication April 14, 2006.

REFERENCES





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