Asian soybean rust (ASR), caused by Phakopsora pachyrhizi and recently discovered for the first time in continental United States, has been of concern to the U.S. agricultural industry for more than 30 years. Since little soybean rust resistance is known, and resistance is often difficult to detect or quantitate, we initiated a project to develop a better, more quantitative, method. The methodology determined the average numbers and diameters of uredinia in lesions that developed on leaves of inoculated plants 14 days after inoculation. It was used to compare virulence of P. pachyrhizi isolates from Asia and Australia and P. meibomiae from Puerto Rico and Brazil, collected as many as 30 years earlier, with isolates of P. pachyrhizi recently collected from Africa or South America. Susceptible reactions to P. pachyrhizi resulted in tan-colored lesions containing 1 to 14 uredinia varying greatly in size within individual lesions. In contrast, on these same genotypes at the same time of year, resistance to other P. pachyrhizi isolates was typified by 0 to 6 small uredinia in reddish-brown to dark-brown lesions. Using appropriate rust resistant and rust susceptible genotypes as standards, examination of uredinia 14 days after inoculation allowed quantitative comparisons of sporulation capacities, one measure of susceptibility or resistance to soybean rust. The study verified the presence and ability to detect all known major genes for resistance to soybean rust in the original sources of resistance. It demonstrated that soybean lines derived from the original PI sources, and presumed to possess the resistance genes, in actuality may lack the gene or express an intermediate reaction to the rust pathogen. We suggest that a determination of numbers and sizes of uredinia will detect both major gene and partial resistance to soybean rust.
Soybean rust occurs in all major soybean-growing regions of the world including the North American mainland. Soybean rust, caused by Phakopsora pachyrhizi, is the most destructive foliar disease of soybean, and yield losses of over 50% are common when environmental conditions are conducive for disease development. Heavily infected plants defoliate and mature more rapidly than plants not infected with rust. P. pachyrhizi has a broad host range and can infect many other legumes including some native to Australia. A number of physiological races of the fungus have been reported on these native legumes from Australia and on soybean. In addition, four single genes for rust resistance were previously identified in four different soybean plant introductions. These sources of resistance also have been reported to be susceptible in some field locations and when challenged with certain isolates of P. pachyrhizi. Partial resistance, expressed as reduced pustule number and increased length of latent period, has also been reported but has not been widely used in breeding programs. Yield stability has been used in the past and compares percentage of yields in fungicide and nonfungicide plots. Cultivars or lines with a higher percentage of yield have greater yield stability in the presence of rust. Although soybean rust only recently was found in the continental United States, a proactive project to evaluate the USDA soybean germ plasm collection for rust resistance was initiated in 2002 at the Fort Detrick plant biocontainment facility and at six international locations. Part of this project is to discover soybean lines with greater yield stability, and additional single and partial resistance. To help minimize the impact of soybean rust, the first line of defense will be fungicides, with host resistance and yield stability augmenting the long-term management of soybean rust.
Soybean rust, caused by the fungus Phakopsora pachyrhizi, was detected in the continental United States in 2004. Several new sources of resistance to P. pachyrhizi have been identified in soybean (Glycine max); however, there is limited information about their resistance when challenged with additional U.S. and international isolates. Resistance of 20 soybean (G. max) entries was compared after inoculation with 10 P. pachyrhizi isolates, representing different geographic and temporal origins. Soybean entries included 2 universal susceptible cultivars, 4 sources of soybean rust resistance genes (Rpp1–4), and 4 and 10 resistant entries selected from field trials in Paraguay and Vietnam, respectively. Of the known Rpp1–4 sources of resistance, plant introduction (PI) 459025B (Rpp4) produced reddish-brown (RB) lesions in response to all of the P. pachyrhizi isolates, while PI 230970 (Rpp2) produced RB lesions to all isolates except one from Taiwan, in response to which it produced a susceptible tan (TAN) lesion. PI 200492 (Rpp1) and PI 462312 (Rpp3) produced TAN lesions in response to most P. pachyrhizi isolates. The resistant entries selected from Paraguay and Vietnam varied considerably in their responses to the 10 P. pachyrhizi isolates, with M 103 the most susceptible and GC 84058-18-4 the most resistant. The reaction patterns on these resistant entries to the P. pachyrhizi isolates were different compared with the four soybean accessions with the Rpp genes, indicating that they contain novel sources of rust resistance. Among the P. pachyrhizi isolates, TW 72-1 from Taiwan and IN 73-1 from India produced the most susceptible and resistant reactions, respectively, on the soybean entries.
Phakopsora pachyrhizi, the causal fungus of soybean rust, was discovered in the continental U.S. in November 2004. The presence of this disease in the U.S. may have an impact on soybean (Glycine max) production, as the current commercial varieties are considered to be susceptible, and the use of one or more applications of fungicides will add additional costs to production. One objective of the USDA-ARS research on soybean rust is to identify soybean germplasm with resistance to the disease. There are over 16,000 soybean accessions in the USDA Germplasm Collection located at the University of Illinois. These accessions were evaluated in a two-tiered inoculation program using a mixture of four P. pachyrhizi isolates in Biosafety Level 3 containment greenhouses the FDWSRU. In the first round of evaluations, 16,595 accessions were rated for rust severity. Of these, 3,215 accessions, based on low visual rust severity or the presence of a red-brown reaction, were selected for a second round of evaluation. After the second round of replicated evaluations of the 3,215 accessions, 805 were selected for further evaluation, again based on low mean visual severity or the presence of a red-brown reaction. Some of these selected accessions have the potential to provide soybean rust resistance genes that may be useful for incorporation into commercial soybean cultivars. Accepted for publication 9 November 2005. Published 4 January 2006.
Soybean [Glycine max (L.) Merr.] resistance to soybean rust (SBR) caused by Phakopsora pachyrhizi could reduce reliance on fungicides to manage this disease. The objective of this study was to identify soybean germplasm with resistance to field populations of P. pachyrhizi in the United States. Field evaluations of 576 accessions from the USDA Soybean Germplasm Collection for resistance to SBR were conducted at seven locations in the southern United States between 2006 and 2008. Accessions from maturity groups (MG) 000 to X and North American susceptible check cultivars from each MG except X were rated for disease severity in all year–location environments, and for disease incidence, fungal sporulation, lesion type, and/or uredinia density in certain environments. While none of the accessions was immune in all environments, 64 were resistant in two or more locations each year that they were tested. Some accessions appeared to be more resistant in certain environments than in others. Of the original four Rpp genes described in the literature, Rpp1 provided the highest level of resistance, and among the accessions with uncharacterized Rpp genes, PI 567104B had the highest overall resistance across environments. The plant introductions confirmed to be resistant in these evaluations should be useful sources of genes for resistance to North American populations of P. pachyrhizi
Two soybean accessions, PI 587886 and PI 587880A, previously identified as having resistance to Phakospora pachyrhizi Syd. (soybean rust, SBR) were used to create two populations (POP-1 and POP-2) segregating for SBR resistance. F(2)-derived F(3) (F(2:3)) families from each population were grown in a naturally SBR-infected field in Paraguay to determine inheritance and map resistance genes. Over 6,000 plants from 178 families in POP-1 and over 5,000 plants from 160 families in POP-2 were evaluated at R5 for lesion type: immune reaction (IR), reddish-brown (RB), or tan (TAN) colored lesions. Based on the lesion type present, each F(2:3) family was rated as resistant, segregating or susceptible and this classification was used to infer the F(2)-phenotype and genotype. For both populations, the F(2) segregation ratios fit a 1:2:1 (resistant:segregating:susceptible) ratio expected for a single gene (P > 0.05). The RB lesions occurred almost exclusively in the heterozygous class, indicating incomplete dominance under the conditions of this study. Molecular markers flanking the locations of the known resistance genes were used to map the resistance gene in both populations to the Rpp1 locus. However, evaluation of PI 587886 and PI 587880A against eight P. pachyrhizi isolates indicated that the resistance allele in these two accessions was different from Rpp1. This test also demonstrated that these accessions were resistant to at least one P. pachyrhizi isolate collected in the southern US. This is the first report of using an adult plant field-screen with natural rust pressure to map SBR resistance.
Soybean rust, caused by Phakopsora pachyrhizi, is a devastating foliar disease of soybean that may cause significant yield losses if not managed by well-timed fungicide applications. To determine the effect of fungicide timing on soybean rust severity and soybean yield, field trials were completed in Paraguay (four locations), the United States (two locations), and Zimbabwe (one location) from 2005 to 2006. Treatments at each location included applications of tebuconazole, pyraclostrobin, or a combination of azoxystrobin + propiconazole, and in some locations pyraclostrobin + tebuconazole at the following soybean growth stages (GS): (i) GS R1 (beginning flowering), (ii) GS R3 (beginning pod), (iii) GS R5 (beginning seed), (iv) GS R1 + R3, (v) GS R3 + R5, and (vi) GS R1 + R3 + R5. Soybean yields from plots treated with fungicides were 16 to 114% greater than yields from no fungicide control plots in four locations in Paraguay, 12 to 55% greater in two locations in the United States, and 31% greater in Zimbabwe. In all locations, rust severity measured over time as area under the disease progress curve (AUDPC) was negatively correlated (r = –0.3, P < 0.0001) to yield. The effectiveness of any given treatment (timing of application and product applied) was often dependent on when rust was first detected and the intensity of its development. For example, when soybean rust was first observed before GS R3 (two locations in Paraguay), the plants in plots treated with a fungicide at GS R1 had the lowest AUPDC values and highest yields. When soybean rust was first observed after GS R3, plants treated with a fungicide at GS R3 and/or GS R5 had the lowest AUDPC values and highest yields with a few exceptions.
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