- Citado por SciELO
- Citado por Google
- Similares em SciELO
- Similares em Google
versão On-line ISSN 1984-7033
Crop Breed. Appl. Biotechnol. vol.12 no.1 Viçosa mar. 2012
Advances on molecular studies of the interaction soybean - Asian rust
Avanços dos estudos moleculares da interação da soja - ferrugem asiática
Aguida Maria Alves Pereira MoralesI, *; Aluízio BorémI; Michelle A GrahamII; Ricardo Vilela AbdelnoorIII
IUniversidade Federal de Viçosa (UFV), Departamento de Fitotecnia, 36.570-000, Viçosa, MG, Brazil. *E-mail: email@example.com
IICorn Insects and Crop Genetics Research (USDA), 50011, Ames, IA, USA
IIIEmbrapa Soja, 86001-970, Londrina, PR, Brazil
Effective management practices are essential for controlling rust outbreaks. The main control method used is the application of fungicides, which increases substantially the cost of production and is harmful to the environment. Prevention is still the best way to avoid more significant losses in soybean yields. Alternatives, such as planting resistant varieties to the fungus, are also important. The use of resistant or tolerant varieties is the most promising method for controlling Asian soybean rust. Recently, five dominant genes resistant to soybean rust were described: Rpp1, Rpp2, Rpp3, Rpp4 and Rpp5. However, little is known about the molecular interaction among soybean plant and soybean rust and on the molecular pathway triggered by pathogen recognition. Understanding the molecular mechanisms involved in defense responses is of primary importance for planning strategies to control stress and, consequently, to increase plant adaptation to limiting conditions.
Key words: Phakopsora pachyrhizi, resistance, plant-pathogen, molecular biology.
Práticas efetivas são necessárias para o controle da ferrugem. O principal método de controle utilizado é a aplicação de fungicidas, o que aumentará substancialmente o custo de produção e são prejudiciais ao meio ambiente. A prevenção ainda é a melhor maneira de evitar mais perdas significativas na produção de soja. Alternativas, como o plantio de variedades resistentes ao fungo, também são importantes. O uso de variedades resistentes ou tolerantes é o método mais promissor para o controle da ferrugem asiática da soja. Recentemente, cinco genes de resistência a ferrugem da soja foram descritos Rpp1, Rpp2, Rpp3, Rpp4 e Rpp5. No entanto, pouco se sabe sobre a interação molecular entre a planta e ferrugem da soja e as rotas desencadeadas na planta pelo reconhecimento do patógeno. Compreender os mecanismos moleculares envolvidos nas respostas de defesa é de primordial importância no planejamento de estratégias para controle do estresse e, consequentemente, para aumentar a adaptação das plantas a condições limitantes.
Palavras chave: Phakopsora pachyrhizi, resistência, planta-patógeno, biologia molecular.
ASIAN SOYBEAN RUST
Asian Soybean Rust (ASR) is caused by Phakopsora pachyrhizi Syd. and Syd; uredial anamorph; Malupa sojae (syn. Uredo sojae); Domain Eukaryota; Kingdom Fungi; Phylum Basidiomycota; Order Uredinales; Class Urediniomycetes; Family Phakopsoraceae; Genus Phakopsora (Index Fungorum 2010). Rust is considered a polycyclic disease. The fungus is able to complete several generations in a single cycle of the host. Temperatures and humidity that favor the growth and development of soybean plants also favor the development of rust (Zambolin 2006). According to Freire et al. (2008) the South and North American continents were free of P. pachyrhizi until 2001. Then P. pachyrhizi was reported in Paraguay (Morel and Yorinori 2002), and became established in Bolivia, Argentina (Rossi 2003) and Brazil (Yorinori et al. 2005) in 2002/2003. In 2004, ASR was reported for the first time in the USA (Schneider et al. 2005). These authors estimated that the disease caused yield losses from 10 to 80 %.
According to Ono et al. (1992) P. pachyrhizi and Phakopsora meibomiae have wide host ranges and are able to sporulate on 31 species in 17 genera of leguminous plants. Rust samples taken from wild host plants are able to infect a broad range of plant species in greenhouse environments (Jarvie 2009). Recently, new host species from 25 genera were identified in evaluations made in greenhouses, including 12 genera that had not been reported previously (Slaminko et al. 2008). The presence of a susceptible host, viable pathogen spores and suitable environmental conditions are prerequisites for the development of a soybean rust epidemic. The optimum temperature for urediniospore germination ranges between 12 and 27 °C. Urediniospore germination is greater in darkness and requires a period of leaf moisture. Germination takes about 6 hours in optimum temperature and moisture conditions (Kochman 1977).
First symptoms of ASR could be described as small water-soaked lesions that develop into grey, tan to dark brown or reddish brown (RB) lesions (uredinia) particularly on abaxial leaf surfaces (Sinclair 1989). The color of the lesion depends on lesion age and interaction with the host genotype. RB lesions with little sporulation indicate a resistant reaction, whereas tan lesions with much sporulation indicate a susceptible reaction. The number of pustules per lesion increases with age of the lesion and groups of spores (urediniospores) are expelled from each pustule (uredinia) through a central pore (Sinclair 1989).
The disease destroys leaf tissue resulting in lower photosynthetic activity, premature defoliation and reduced life cycle. In addition, the premature leaf abscission prevents grain maturation (Sinclair 1989), and the rust infection during pod formation or seed fill can cause embryo abortion and pod abscission (Yorinori et al. 2005). The cumulative effect of rust on the production leads to a decrease in the number of pods and seed and a reduction in seed weight (Sinclair 1989).
P. pachyrhizi forms asexual uredospores on short stalks within a uredium 5-8 days after inoculation on colonized leaves. Uredospores are released from uredia through an ostiole and dispersed by wind. Under appropriate conditions, uredospores germinate a single germ tube and the penetration occurs directly through epidermis, but can also occur through stomatal openings (Zambolin 2006). Penetration by P. pachyrhizi starts with the formation of a funnel-shaped structure, termed appressorial cone, within the appressorium. This cone is contiguous with the cell wall of the penetration hypha, which is also called transepidermal vesicle. During penetration, the epidermal cells collapse become disorganized and show signs of cell death (Panstruga 2003, Mendgen et al. 2006). After penetration, the hypha grows through the epidermal cell and reaches the intercellular space. The primary hypha may branch to form a secondary one and finally, haustorium mother cells differentiate in close contact with mesophyll cells. The haustorium provides a wide contact surface inside the host cell for acquisition of sugars and amino acids through a symport proton gradient (Mendgen et al. 2006).
A recent study depicted a two-year field trial in Brazil where soybean rust was responsible for 37-67 % of soybean seed yield losses (Kumudini et al. 2008). This study coincided with yield losses observed in Asia up to 80 % (Miles et al. 2003). Effective management practices are essential for controlling rust outbreaks. The main control method used is the application of fungicides, which substantially increases the cost of production and is harmful to the environment (Zambolim 2006). The chemical group most often used for rust control is a mixture of strobilurin and triazole.
Prevention is still the best way to avoid more significant losses in soybean production. The method is to offset the timing of soybean production and pods maturation in condition that does not favor P. pachyrhizi. In addition, lowering inoculum levels by implementation of a soybean-free period is important. Alternatives such as using resistant varieties to the fungus are also important. However, resistance does not mean that the disease does not occur, but allows greater stability and efficiency of chemical control (Anuário Brasileiro de Soja 2009). Recently, soybean cultivars resistant to the fungus were released in Brazil. These varieties boast characteristics that curb fungal growth and ensure higher production stability, reducing the losses induced by the disease, and the environmental impacts caused by repeated fungicide applications.
MOLECULAR INTERACTION BETWEEN SOYBEAN AND ASR
Immunity to P. pachyrhizi occurs when no visual lesions are produced by the soybean plant. A resistant response leads to the formation of RB lesions indicating a hypersensitive reaction. A susceptible response occurs when tan lesions develop, indicating fungal growth and development. The genetics of resistance of the only five dominant genes to specific soybean rust isolates has been described: Rpp1, Rpp2, Rpp3, Rpp4 and Rpp5 (Bromfield and Hartwig 1980, Mclean and Byth 1980, Hartwig and Bromfield 1983, Hartwig 1986, Garcia et al. 2008).
In order to identify new sources of resistance in soybean, Miles et al. (2006) evaluated the entire germplasm collection (16,000 accessions) of the United States Department of Agriculture (USDA) against a mixture of five P. pachyrhizi isolates. After two rounds of evaluation, only 850 accessions were identified with partial tolerance or resistance reactions to P. pachyrhizi, which correlates to less than 5 % of USDA germplasm collection.
Resistance alleles different from those already described in the literature were also identified in several other genotypes (Laperuta et al. 2008, Pierozzi et al. 2008). When the disease was first detected in Brazil, all the described resistance genes were effective against the fungus. However, in 2003, a new race of P. pachyrhizi broke the resistance conferred by genes Rpp1 and Rpp3 while Rpp2, Rpp4 and Rpp5 remained resistant.
Although Rpp2- and Rpp4-mediated resistances have been stable in Brazil (Hartman et al. 2005), only dominantly inherited R gene-mediated resistance against P. pachyrhizi has been overcome in nature several times because of the great capacity of the fungus to develop new race. Generally, this scenario of breakdown of R gene-mediated resistance is known as the 'boom and bust' syndrome. In addition to pyramiding known Rpp resistance genes into modern cultivars to create a more durable and broad-spectrum disease resistance, the selection of novel sources of resistance to P. pachyrhizi is desirable (Goellner et al. 2010).
Along with single gene resistance, partial resistance to soybean rust has been described (Hartman et al. 2005). This kind of resistance may be controlled by minor genes and may be expressed as reduced uredinial number and size, a longer latent period and other components related to fungal reproduction. Recently, the average number of uredinia per lesion and the average uredinial diameter were reported to be components of partial resistance in soybean rust and were a reflection of fungal growth in the host tissue (Bonde et al. 2006). All described Rpp genes have already been mapped on soybean chromosomes (Chr), Rpp1 was mapped on chromosome 18, Rpp2 on Chr 16, Rpp3 on Chr 6, Rpp4 on Chr 18 and Rpp5 on Chr 3 (Hyten et al. 2007, Garcia et al. 2008, Silva et al. 2008, Hyten et al. 2009). Additionally, some alleles was mapped on the same chromosome, for exemple, Rpp1b was also mapped on Chr 18, while Rpp Hyuuga was also mapped on Chr 6 (Monteros et al. 2007, Chakraborty et al. 2009)
Despite the physical location of the Rpp genes and the recent release of the soybean genome (Schmutz et al. 2010), none of them was cloned yet. However, significant progress has been made towards cloning Rpp4, which remained the most stable gene when challenged against isolates of fungus from different parts of the world (Yamaoka et al. 2002, Bonde et al. 2006). Sequencing of the mapped region in the susceptible genotype Williams 82 identified a cluster of three resistance genes, CC-NBS-LRR (coiled-coil, nucleotide-binding site, leucine-rich repeats), within a 2cM region on chromosome 18, which shows sequence similarly to the lettuce RGC2 family of resistance genes (Meyer et al. 2009). In addition, Virus-induced gene silencing (VIGS) demonstrated that silencing of the Rpp4 candidate genes diminished resistance in PI459025B (that carries Rpp4 resistance allele), confirming that one of the genes in the cluster is responsible for resistance.
There is a clear evidence of evolutionary forces acting on the Rpp4 locus. Differences in gene number between Wm82 and PI459025B are likely due to duplication or unequal recombination. In addition, given the similarity of all Rpp4 candidate genes between genotypes, it is possible that small amino acids differences may play a key role in resistance (Meyer et al. 2009).
Little is known about the molecular interaction among soybean and P. pachyrhizi and the defense pathways triggered by pathogen recognition. Understanding the molecular mechanisms involved in defense responses is of primary importance to plan strategies for controlling stress and consequently to increase plant adaptation in limiting conditions. The development of sequencing techniques and gene expression analysis on a large scale, combined with new bioinformatics tools for data analysis have facilitated the structuring of extremely valuable databases to create strategies for genetic engineering.
Given the rarity of Asian rust resistance in soybean, few genomic tools are available for examining the resistance of P. pachyrhizi in immune (R) genomes. Therefore, rust resistance research has focused on genotype independent platforms like microarray analyses to identify genes involved in resistance and susceptibility. Van de Mortel et al. (2007) used the soybean affymetrix gene chip to study changes in gene expression in resistant and susceptible genotypes when inoculated with ASR. A biphasic gene response to P. pachyrhizi infection was seen in both genotypes. Differences in gene expression between inoculated and mock plants peaked at 12 hours post inoculation (hpi) and returned to almost basal levels by 24 hpi, in both resistant and susceptible genotype. At 72 hpi a second larger wave of defense gene expression could be observed, which was earlier in the resistant than in the susceptible interaction. The early transcriptional response observed in susceptible and resistant plants might represent a general response of soybean to the nonspeciûc recognition of any pathogen, presumably by interaction with microbe-associated or microbe-induced molecular patterns (MAMPs and MIMPs) (Mackey and Mcfall 2006). By contrast, the second likely response relates to R-gene detection of P. pachyrhizi (Posada-Buitrago and Frederick 2005, Tremblay et al. 2009).
In a similar approach, Panthee et al. (2007) identified genes, which might be involved in a defense response against P. pachyrhizi by susceptible soybean cv.5601 plants 72h after infection (hai) using microarray. Most of the induced genes had defense and stress related functions such as genes encoding an SA-related protein, heat shock protein (HSP), leaf senescence-associated receptor like kinase, and chalcone synthase. Recently, Pandey et al. (2011) combined the work of Van de Mortel et al. (2007) with VIGS, to screen 140 candidate genes that might play a role in Rpp2-mediated resistance toward P. pachyrhizi. This study identified 11 genes that compromised Rpp2-mediated resistance when silenced, including GmEDS1, GmNPR1, GmPAD4, GmPAL1, five predicted transcription factors, an O-methyl transferase, and a cytochrome P450 monooxygenase. Additionally, a large scale transcript profiling approach conducted with soybean plants (accession PI200492) has revealed an up-regulation in gene expression for lipoxygenases and peroxidases in an incompatible interaction, suggesting an important function for these genes in Rpp1-mediated resistance (Choi et al. 2008).
Using laser capture microdissection, Tremblay et al. (2010) isolated susceptible soybean palisade and mesophyll cells showing signs of infection, extracted the RNA and performed transcriptome profiling. A total of 2,982 genes were differentially expressed, from which 685 were up-regulated and 2,297 were down regulated. Complementary to transcriptional analyses in the host, gene transcript profiling has also been performed with the fungus (Posada-Buitrago and Frederick 2005, Tremblay et al. 2009). A recent study of gene expression within P. pachyrhizi germinating spores allowed the identification of 488 unique expressed sequence tags (ESTs). One hundred eighty nine of these ESTs showed significant similarly (E-value < 10-5) to sequences deposited in the NCBI non-redundant protein database. These genes were assigned putative roles in primary metabolism, gene and protein expression, cell structure and growth, cell division, cell signaling and cell communication (Posada-Buitrago and Frederick 2005). Recently, a cDNA library was constructed based on the separation of uredinia from host tissue by using laser-captured microdissection (Tremblay et al. 2009). About 80 % of identified genes in this study shared no homology to previously described Phakopsora genes. This result demonstrates stage-speciûc gene expression in the development of uredinia.
While the techniques have proven effective at looking at genes downstream of Rpp genes, more research is needed to identify potential candidate genes that could be used to engineer sustainable resistance into soybean against P. pachyrhizi.
The use of resistant varieties is the optimal control strategy due to the value of a technology already being aggregated to the seed. The rust resistance genes have been incorporated in breeding programs in Brazil and the United States. Resistant varieties with genes of greater resistance were released; however, the resistance stability is uncertain, once the large number of races of this fungus already described proves the great variability of the pathogen. As a result, the use of fungicides is still necessary to ensure the survival of resistant varieties. Recently, research on Asian soybean rust has mainly focused on host range studies, epidemiology and the evaluation of yield loss and control measures. These studies have predominantly centered on the diseased plant. However, as soybean cultivars with resistance to all known races of P. pachyrhizi are not available yet, more basic research on this pathogen is also necessary. Elements in the infection process of the fungus and possibilities of interference to adapt new plant protection strategies need to be identified.
Anuário Brasileiro de Soja (2009) Editora Gazeta, Santa Cruz do Sul, 127p. [ Links ]
Bonde MR, Nester SE, Austin CN, Stone CL, Frederick RD, Hartman GL and Miles MR (2006) Evaluation of virulence of Phakopsora pachyrhizi and P. meibomiae isolates. Plant Disease 90: 708-716. [ Links ]
Bromfield KR and Hartwig EE (1980) Resistance to soybean rust and mode of inheritance. Crop Science 20: 254-255. [ Links ]
Chakraborty N, Curley J, Frederick RD, HytenDL, Nelson RL, Hartman GL and Diers B (2009) Mapping and confirmation of a new allele at Rpp1 from soybean PI 594538A conferring RB lesion-type resistance to soybean rust. Crop Science 49: 783-790. [ Links ]
Choi J, Alkharouf N, Schneider K, Matthews B and Frederick R (2008) Expression patterns in soybean resistant to Phakopsora pachyrhizi reveal the importance of peroxidases and lipoxygenases. Functional & Integrative Genomics 8: 314-359. [ Links ]
Freire MCM, Oliveira LO, Almeida AMR, Schuster I, Moreira MA, Liebenberg MM and Mienie CMS (2008) Evolutionary history of Phakopsora pachyrhizi (the Asian soybean rust) in Brazil based on nucleotide sequences of the internal transcribed spacer region of the nuclear ribosomal DNA. Genetics and Molecular Biology 31: 920-931. [ Links ]
Garcia A, Calvo É, Souza Kiihl R, Harada A, Hiromoto D and Vieira L (2008) Molecular mapping of soybean rust (Phakopsora pachyrhizi) resistance genes: discovery of a novel locus and alleles. Theoretical and Applied Genetics 117: 545-553. [ Links ]
Goellner K, Loehrer Langenback C, Conrath U, Akoch EC and Schaffrat HU (2010) Phakopsora pachyrhizi, the causal agent of Asian soybean rust. Molecular Plant Pathology 2: 169-177. [ Links ]
Hartman GL, Miles MR and Frederick RD (2005) Breeding for resistance to soybean rust. Plant Disease 89: 664-666. [ Links ]
Hartwig EE (1986) Identification of a fourth major gene conferring resistance to soybean rust. Crop Science 26: 1135-1136. [ Links ]
Hartwig EE and Bromfield KR (1983) Relationships among 3 genes conferring specific resistance to rust in soybeans. Crop Science 23: 237-239. [ Links ]
Hyten DL, Hartman GL, Nelson RL, Frederick RD, Concibido VC, Narvel JM and Cregan PB (2007) Map location of the Rpp1 locus that confers resistance to soybean rust in soybean. Crop Science 47: 837-838. [ Links ]
Hyten DL, Smith JR, Frederick RD, Tuchekr ML, Song Q andCregan PB (2009) Bulked segregant analysis using the Golden Gate assay to locate the Rpp3 locus that confers resistance to soybean rust in soybean. Crop Science 49: 265-271. [ Links ]
Jarvie JA (2009) A review of soybean rust from a South African perspective. South African Journal of Science 105: 103-108. [ Links ]
Kochman JK (1977) Soybean rust in Australia. In Ford RE and Sinclair JB (eds) Rust of soybean-The problem and research needs. International Agricultural Publications, Manila, p. 44-48. [ Links ]
Kumudini S, Godoy CV, Board JE, Omielan J and Tollenaar M (2008) Mechanisms involved in soybean rust-induced yield reduction. Crop Science 48: 2334-2342. [ Links ]
Laperuta LDC, Arias CAA, Ribeiro AS, Rachid BF, Pierozzi PHB, Toledo JFF, Pípolo AE and Carneiro GED (2008) New Genes conferring resistance to asian soybean rust: allelic testing for the Rpp2 and Rpp4 Loci. Pesquisa Agropecuária Brasileira 43: 1741-1747. [ Links ]
Mackey D and McFall AJ (2006) MAMPs and MIMPs: proposed classiûcations for inducers of innate immunity. Molecular Microbiology 61: 1365-1371. [ Links ]
McLean RJ and Byth D (1980) Inheritance of resistance to rust (Phakopsora pachyrhizi) in soybean. Australian Journal of Agricultural Research 31: 951-956. [ Links ]
Mendgen K, Krieg PA, Rebagliati MR, Maniatis T, Zinn K and Green MR (2006) Volatiles modulate the development of plant pathogenic rust fungi. Planta 224: 1353-1361. [ Links ]
Meyer JDF, Silva DCG, Yang C, Pedley KF, Zhang C, Van de Mortel M, Hill JH, Shoemaker RC, Abdelnoor RV, Whitham SA and Graham MA (2009) Identification and analyses of candidate genes for Rpp4-mediated resistance to Asian soybean rust in Soybean. Plant Physiology 150: 295-307. [ Links ]
Miles MR, Frederick RD and Hartman GL (2006) Evaluation of soybean germplasm for resistance to Phakopsora pachyrhizi. Online. Plant Health Progress doi: 10.1094/PHP- 2006-0104-01-RS. [ Links ]
Monteros MJ, Missaoui AM, Phillips DV, Walker DR and Boerma HR (2007) Mapping and confirmation of the 'Hyuuga' red-brown lesion resistance gene for Asian soybean rust. Crop Science 47: 829-834. [ Links ]
Morel WM and Yorinori JT (2002) Situacion de la roja de la soja en el Paraguay. Boletin de Diulgacion N° 44. Ministerio de Agricultura y Granaderia, Centro Regional de Investigacion Agricola, Capitan Miranda, Paraguay. [ Links ]
Ono Y, Buritica P and Hennen JF (1992) Delimitation of Phakopsora, Physopella and Cerotelium and their species on Leguminosae. Mycological Research 96: 825-850. [ Links ]
Pandey AK, Yang C, Zhang C, Graham MA, Horstman HD, Lee Y, Zabotina OA, Hill JH, Pedley KF and Whitham SA (2011) Functional analysis of the asian soybean rust resistance pathway mediated by Rpp2. Molecular Plant-Microbe Interactions 24: 194-206. [ Links ]
Panthee DR, Yuan JS, Wright DL, Marois JJ, Mailhot D and Stewart JRCN (2007) Gene expression analysis in soybean in response to the causal agent of Asian soybean rust (Phakopsora pachyrhizi Sydow) in an early growth stage. Functional and Integrative Genomics 7: 291-301. [ Links ]
Panstruga R (2003) Establishing compatibility between plants and obligate biotrophic pathogens. Current Opinion in Plant Biology 6: 320-326. [ Links ]
Pierozzi PHB, Ribeiro AS, Moreira JUV, Laperuta LC, Rachid BF, Lima WF, Arias CAA, Olivera MF and Toledo JFF (2008) New soybean (Glycine max, Fabales, Fabaceae) sources of qualitative genetic resistance to Asian soybean rust caused by Phakopsora pachyrhizi (Uredinales, Phakopsoraceae). Genetics and Molecular Biology 31: 505-511. [ Links ]
Posada-Buitrago ML and Frederick RD (2005) Expressed sequence tag analysis of the soybean rust pathogen Phakopsora pachyrhizi. Fungal Genetics and Biology 42: 949-962. [ Links ]
Rossi RL (2003) First report of Phakopsora pachyrhizi, the causal organism of soybean rust in the province of Misiones, Argentina. Plant Disease 87: 102. [ Links ]
Schmutz J, Cannon SB, Schlueter J, Ma J, Mitros T, Nelson W, Hyten DL, Song Q, Thelen JJ and Cheng J (2010) Genome sequence of the palaeopolyploid soybean. Nature 463: 178-183 [ Links ]
Schneider RW, Hollier CA, Whitam HK, Palm ME, McKemy JM, Hernández JR, Levy L, and DeVries-Paterson R (2005) First report of soybean rust caused by Phakopsora pachyrhizi in the continental United States. Plant Disease 89: 774-774 [ Links ]
Silva DCG, Yamanaka N, Brogin RL, Arias CAA, Nepomuceno AL, Di Mauro AO, Pereira SS, Nogueira LM, Passianoto ALL and Abdelnoor RV (2008b) Molecular mapping of two loci that confer resistance to Asian rust in soybean. Theoretical and Applied Genetics 117: 57-63. [ Links ]
Sinclair JB (1989) Threats to soybean production in the tropics: red leaf blotch and leaf rust. Plant Disease 73: 604-606. [ Links ]
Slaminko TL, Miles MR, Frederick RD, Bonde MR and Hartman GL (2008) New legume hosts of Phakopsora pachyrhizi Based on Greenhouse Evaluations. Plant Disease 92: 767-771. [ Links ]
Tremblay A, Hosseini P, Alkharouf N, Li S and Matthews BF (2010) Transcriptome analysis of a compatible response by Glycine max to Phakopsora pachyrhizi infection. Plant Science 179: 183-193. [ Links ]
Tremblay A, Li S, Scheffler BE and Matthews BF (2009) Laser capture microdissection and expressed sequence tag analysis of uredinia formed by Phakopsora pachyrhizi, the causal agent of Asian soybean rust. Physiological and Molecular Plant Pathology 73: 163-174. [ Links ]
Van de Mortel M, Recknor JC, Graham MA, Nettleton D, Dittman JD, Nelson RT, Godoy CV, Abdelnoor RV, Almeida AMR, Baum TJ and Whitham SA (2007) Distinct biphasic mRNA changes in response to Asian soybean rust infection. Molecular Plant-Microbe Interactions 20: 887-899. [ Links ]
Yamaoka Y, Fujiwara Y, Kakishima M, Katsuya K, Yamada K and Hagiwara H (2002) Pathogenic races of Phakopsora pachyrhizi on soybean and wild host plants collected in Japan. Journal of General Plant Pathology 68: 52-56. [ Links ]
Yorinori JT, Paiva WM, Frederick RD, Costamilan LM, Bertagnoli PF, Hartman GL, Godoy CV and Nunes JJ (2005) Epidemics of soybean rust (Phakopsora pachyrhizi) in Brazil and Paraguay from 2001 to 2003. Plant Disease 89: 675-677. [ Links ]
Zambolin L (2006) Manejo integrado da ferrugem asiática da soja. In Zambolin L. (ed.) Ferrugem asiática da soja. Suprema, Viçosa, 139p. [ Links ]
Received 11 November 2011
Accepted 6 February 2012