Phenotypic characterization of soybean genotypes for rust (Phakopsora pachyrhizi sydow) resistance
Abstract
The present investigation was carried out to phenotypically characterize 30 soybean genotypes for resistance to rust caused by Phakopsora pachyrhizi Sydow. The genotypes were evaluated under field conditions at Agricultural Research Station, Kasbe-Digraj, Sangli, during Kharif 2018 in a randomized block design with three replications. Rust severity was assessed using the 0-9 disease-rating scale and percent disease intensity (PDI) was calculated following standard phytopathometric procedures. None of the genotypes showed an absolutely resistant reaction. KDS-753 recorded a highly resistant reaction, whereas CAUMS-1, KS-103, KDS-726, KDS-1009 and PS-1637 were moderately resistant. Six genotypes were susceptible and the remaining genotypes were highly susceptible. The identified highly resistant and moderately resistant genotypes may serve as useful donors for soybean rust resistance breeding, molecular characterization and gene-pyramiding programmes.
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Introduction
Soybean (Glycine max (L.) Merr.) is an important oilseed and protein crop and is often described as a "miracle crop" or "golden bean" because its seed generally contains about 38-42% protein and 18-20% oil (Anonymous, 2022; Tiwari, 2022) [1,34] . Soybean protein has a favorable amino-acid profile and contributes substantially to human food, livestock feed and vegetable-oil requirements (Anonymous, 2022; Tiwari, 2022) [1,34] . Asian soybean rust, caused mainly by Phakopsora pachyrhizi Sydow, is one of the most destructive foliar diseases of soybean in tropical and subtropical soybean-growing regions (Bromfield, 1984; Goellner et al., 2010; Reis, 2022) [4,11,29] . The pathogen is an obligate biotroph, produces abundant urediniospores and can infect leaves rapidly under humid conditions, resulting in premature defoliation, reduced pod filling and heavy yield losses under favourable epidemics (Miles et al., 2003; Dalla Lana et al., 2015; Godoy et al., 2016) [24,7,12] . Rust symptoms commonly begin as small chlorotic to greyish lesions that later turn tan to reddish-brown, usually on the lower leaf surface, where uredinia develop and release spores (Miles et al., 2005; Hartman et al., 2015) [23,13] . Disease development is favoured by moderate temperature, high humidity and prolonged leaf wetness, and the pathogen can spread over long distances through wind-borne urediniospores (Bonde et al., 2006; Schmale and Ross, 2015; Belinelli et al., 2025) [3,32,2] . In India, soybean rust has been reported as an economically important disease in several soybean-growing areas, including Maharashtra, Karnataka and Madhya Pradesh (Rao et al., 1995; Mahajan et al., 2019) [28,20] . The epidemic occurrence of rust during favourable seasons has emphasized the need for systematic screening of germplasm and incorporation of resistance into adapted varieties (Khot et al., 2010; Kurundkar et al., 2011; Mahajan et al., 2019) [15,16,20] . Host resistance is considered a sustainable component of rust management; however, resistance governed by single major genes can be overcome by virulent pathogen populations (Pham et al., 2009; Twizeyimana and Hartman, 2012) [27,35] . Therefore, resistant donor identification, differential reaction studies, new Rpp-source discovery and integration with molecular characterization are required for durable resistance breeding (Whitham et al., 2016; Childs et al., 2018; Dormatey et al., 2020) [38,6,9] . Because soybean rust epidemics are influenced by airborne inoculum movement, host susceptibility and favourable weather, field screening remains important for identifying resistant donors that can be confirmed later through molecular and multilocation studies (Hartman et al., 2015; Martinelli et al., 2015; Mueller et al., 2016; Belinelli et al., 2025) [13,21,25,2] . Broadening the resistance base through wild and related legume sources, gene pyramiding and host-pathogen studies is important for improving the durability of soybean rust resistance (Kawashima et al., 2016; Dormatey et al., 2020) [14, 9] . Transfer of a pigeonpea-derived resistance gene into soybean demonstrated that related legumes can provide valuable resistance resources against Asian soybean rust (Kawashima et al., 2016) [14] . Accurate phenotypic screening remains essential because molecular tools, image-based phenotyping and advanced disease-detection methods require reliable field-based disease classification for validation ( [22,21,5,31] . Hence, the present study was undertaken to characterize soybean genotypes for rust reaction and to identify resistant or moderately resistant genotypes useful for further crop improvement (Mayee and Datar, 1986; Martinelli et al., 2015) [22,21] .
Material and Methods
Experimental material
The experimental material consisted of 30 soybean genotypes collected from different sources. The list of genotypes and their pedigree is presented in Table 1.
Experimental method
The field experiment was conducted at Agricultural Research Station, Kasbe-Digraj, Sangli, during Kharif 2018.
The experiment was laid out in a randomized block design with three replications and all recommended agronomic practices were followed to raise a healthy crop according to university recommendations.
Screening for rust resistance
Rust severity was recorded on five randomly selected plants from each plot using the 0-9 scale proposed for plant-disease assessment (Mayee and Datar, 1986) [22] . The rating scale used for rust assessment is given in Table 2. More than 50% area covered, lesions/pustules very common on all parts, defoliation common; death of plants common; damage more than 50%. Percent Disease Intensity (PDI) was calculated using the standard formula suggested by Wheeler (1969) [37] 𝑃𝐷𝐼 = Sum of individual disease ratings (Number of plants examined × Maximum disease grade) × 100
The categorization of soybean genotypes on the basis of PDI is presented in Table 3. [33,19,17] . [30, 20, 7] . The comparative performance of the top-yielding genotypes and the relationship between rust severity and seed yield are illustrated in Fig. 1 and Fig. 2.
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