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Soybean [Glycine max (L.) Merr.] rust is caused by the fungal pathogen Phakopsora pachyrhizi. Six rust resistance loci (Rpp1, 2, 3, 4, 5, and 6) have been reported. Crosses were made between 75 resistant plant introductions (PIs) and a susceptible elite line or cultivar. Bulked segregant analysis (BSA) was used to determine if the PI resistance genes mapped to a previously identified locus or to an unreported locus. Fifty-two PIs had resistance genes that mapped to the Rpp3 region on chromosome 6 of the soybean genome. A set of P. pachyrhizi isolates was used to further characterize the resistance of these PIs. Forty-two of the PIs exhibited the same reaction profiles as either PI 462312 (Rpp3) or ‘Hyuuga’ (Rpp3 and Rpp5) to the panel of isolates. The fine mapping of Rpp1, Rpp3, and Rpp4 and the availability of the SoySNP50K Infinium Chip data on the USDA Soybean Germplasm Collection made it possible to use BSA and isolate data on these PIs to determine in retrospect how effective haplotype analysis would be in narrowing down the PIs to those likely to have a unique source of resistance. Thirty-seven of the 52 PIs (71%) mapping to the Rpp3 region had a haplotype identical to that of PI 462312. A combination of these analyses could prove useful in more rapidly narrowing down resistant PIs to those likely to carry a unique resistance gene.

Soybean rust (SBR), caused by Syd. and P. Syd., is a threat to soybean [ (L.) Merr.], production in regions of the world where winters are not cold enough to completely eliminate the many hosts of the fungus, so resistant soybean cultivars would be useful in managing this disease. Resistant germplasm accessions have been identified, and resistance () genes have been mapped to six independent loci, but the high degree of virulence variability among populations and isolates means that the level of resistance to different populations and isolates can vary considerably. Greenhouse assays were conducted from 2008 until 2013 in which seedlings of soybean plant introductions were challenged with bulk isolates collected in the state of Georgia. Accessions were included in the tests either because they carried known genes or because they had appeared resistant to SBR in previous field assays. The resistance was assessed on the basis of infection type, visible urediniospore development, and sometimes lesion density. With a few exceptions, most of the accessions that appeared resistant as adult plants in the field also had resistance reactions as seedlings, and these reactions were generally similar or identical in the different years that the greenhouse assays were conducted. This study demonstrates that greenhouse seedling reactions should usually be reliable indicators of adult plant resistance to related isolates or populations, and confirms the resistance of more than 100 soybean germplasm accessions to fungal isolates and field populations from Georgia.

Between 2009 and 2012, 118 soybean [Glycine max (L.) Merr.] accessions from the USDA Soybean Germplasm Collection were screened for resistance to soybean rust (Phakopsora pachyrhizi) at up to five locations in the southeastern United States. In 2009, plant introductions (PIs) from maturity groups III through IX were evaluated for relative disease severity and intensity of sporulation from uredinia compared with 12 susceptible cultivars from the same range of maturity groups. Resistance evaluations were based primarily on disease severity and intensity of sporulation from rust pustules. To assess resistance at several nurseries, a rust index score was calculated from the severity and sporulation ratings. Many of the PIs were moderately to highly resistant at the 2009 locations between Alabama and South Carolina, but the P. pachyrhizi population in Bossier City, LA, was virulent on most of those accessions. The 2011 rating data from Quincy, FL, indicated an increase in the virulence of the pathogen there since 2009, and this trend was observed again in 2012. In contrast, many of the same PIs developed substantially less soybean rust in Attapulgus, GA, in 2012. Despite the comparatively greater disease that many accessions had in Louisiana in 2009 and in Quincy in 2011 and 2012, at least 78 PIs were resistant in Georgia in 2012, and 20 of those were at least moderately resistant in both Florida and Georgia that year. No accessions were immune to rust at all of the nurseries, but PI 200492 (Rpp1), PI 547875 (a backcross line with Rpp1), and PI 567102B (Rpp6) were the most resistant of the accessions with named resistance genes and were among the most resistant accessions overall. Among the most resistant accessions with unknown resistance genes, PI 416826A, PI 417125, PI 567034, and PI 567104B consistently had effective levels of resistance in different locations and years. Information about the most resistant PIs and their reactions to soybean rust infection across years and locations will be useful for the development of rust-resistant soybean cultivars in the United States. D.R. Walker and R.L. Nelson, USDA-ARS, Soybean/Maize Germ plasm, Pathology and Genetics Research Unit and Dep. of Crop Sci