Cosegregation of Avr4 and Avr6 in Phytophthora sojae

1996 ◽  
Vol 74 (5) ◽  
pp. 800-802 ◽  
Author(s):  
Mark Gijzen ◽  
Helga Förster ◽  
Michael D. Coffey ◽  
Brett Tyler

The F2 progeny resulting from a cross of Phytophthora sojae race 2 (avirulent on Rps4 and Rps6) and race 7 (virulent on Rps4 and Rps6) were tested for their ability to cause disease on soybean plants carrying the Rps4 or the Rps6 resistance genes. Of 55 F2 progeny analyzed, 41 individuals were avirulent on both of these genes and 14 were virulent on Rps4 and Rps6, indicating that avirulence on Rps4 and Rps6 is dominant and linked. These results support the suggestion that the soybean–Phytophthora relationship is a gene for gene interaction and that the presumptive Avr4 and Avr6 genes are either tightly linked or identical. Keywords: avirulence, genetic mapping, Glycine max, incomplete dominance, Phytophthora megasperma f.sp. glycinea.

Author(s):  
Rawnaq Chowdhury ◽  
Connie Tande ◽  
Emmanuel Z Byamukama

Phytophthora root and stem rot, caused by Phytophthora sojae, is an important disease of soybean (Glycine max L.) in South Dakota. Because P. sojae populations are highly diverse and resistance genes deployed in commercial soybean varieties often fail to manage the disease, this study was initiated to determine P. sojae pathotype distribution in South Dakota. A total of 216 P. sojae isolates were baited from soil collected from 422 soybean fields in South Dakota in 2013-2015 and 2017. The pathotype of each isolate was determined by inoculating 10 seedlings of 13 standard soybean P. sojae differential lines using the hypocotyl inoculation technique. Of the 216 pathotyped isolates, 48 unique pathotypes were identified. The virulence complexity of isolates ranged from virulence on one Rps gene (Rps7) to virulence on 13 Rps genes and mean complexity was 5.2. Harosoy (Rps7), Harlon (Rps1a), Williams 79 (Rps 1c), William 82 (Rps1k), Harosoy 13XX (Rps1b), were susceptible to 98, 80, 78, 73, 72% of the isolates, respectively. These results highlight the highly diverse P. sojae pathotypes in South Dakota and the likely Rps genes to fail in commercial soybean varieties


1995 ◽  
Vol 73 (S1) ◽  
pp. 506-510 ◽  
Author(s):  
Jürgen Ebel ◽  
Markus Feger ◽  
Ulrich Kissel ◽  
Axel Mithöfer ◽  
Tom Waldmüller ◽  
...  

Inducible plant defenses against potential pathogens are thought to be activated by signal compounds released during early stages of the infection process. In the incompatible interaction between soybean (Glycine max L.) and the oomycete Phytophthora megasperma f.sp. glycinea (= Phytophthora sojae) a rapid, localized phytoalexin response is activated at the level of transcription. The phytoalexin response is also stimulated in various soybean tissues, including cultured cells, following treatment with an elicitor derived from the cell walls of the fungus. The best characterized elicitors of P. megasperma for soybean are the branched (1→3)- and (1→6)-linked β-glucans, structural polysaccharides of the hyphal walls. The glucans are naturally released during the early stages of germination of the fungal cysts in a host-independent manner. Cyclic β-glucans of Bradyrhizobium japonicum USDA 110, a symbiont of soybean, arc not active in inducing phytoalexin production in soybean. When tested in combination, B. japonicum β-glucans inhibited stimulation of phytoalexin accumulation by the fungal glucans. Surface-localized glucan-binding proteins exist in soybean cells that display high affinity and specificity for the fungal β-glucans, including an elicitor-active hepta-β-glucoside fragment derived from the polysaccharide, suggesting that elicitor action involves a transmembrane signalling process. The main component of the soybean β-glucan binding sites appears to be a 70-kDa protein. Hepta-β-glucoside binding sites exist in several other legumes, such as bean (Phaseolus vulgaris L.), pea (Pisum sativum L.), and lupine (Lupinus albus L.). The signalling process initiated by the β-glucan elicitor, which leads to the activation of the phytoalexin defense response in soybean, involves changes in the permeability of the plasma membrane to Ca2+ and H+. Chloride channel antagonists are more efficient than calcium channel antagonists in inhibiting both the phytoalexin response and the inducible ion fluxes. The results present evidence that the observed permeability changes of the plasma membrane are primary events in the transduction of the elicitor signal(s) by the challenged soybean cells. Key words: soybean (Glycine max), Phytophthora megasperma f.sp. glycinea, β-glucan elicitor, elicitor-binding proteins, phytoalexins, Ca2+.


2004 ◽  
Vol 17 (4) ◽  
pp. 394-403 ◽  
Author(s):  
Weixing Shan ◽  
Minh Cao ◽  
Dan Leung ◽  
Brett M. Tyler

We have used map-based approaches to clone a locus containing two genes, Avr1b-1 and Avr1b-2, required for avirulence of the oomycete pathogen Phytophthora sojae (Kaufmann & Gerdemann) on soybean plants carrying resistance gene Rps1b. Avr1b-1 was localized to a single 60-kb bacterial artificial chromosome (BAC) clone by fine-structure genetic mapping. Avr1b-1 was localized within the 60-kb region by identification of an mRNA that is expressed in a race-specific and infection-specific manner and that encodes a small secreted protein. When the Avr1b-1 protein was synthesized in the yeast Pichia pastoris and the secreted protein infiltrated into soybean leaves, it triggered a hypersensitive response specifically in host plants carrying the Rps1b resistance gene. This response eventually spread to the entire inoculated plant. In some isolates of P. sojae virulent on Rps1b-containing cultivars, such as P7081 (race 25) and P7076 (race 19), the Avr1b-1 gene had numerous substitution mutations indicative of strong divergent selection. In other isolates, such as P6497 (race 2) and P9073 (race 25), there were no substitutions in Avr1b-1, but Avr1b-1 mRNA did not accumulate. Genetic complementation experiments with P6497 revealed the presence of a second gene, Avr1b-2, required for the accumulation of Avr1b-1 mRNA. Avr1b-2 was genetically mapped to the same BAC contig as Avr1b-1, using a cross between P7064 (race 7) and P6497. The Avr1k gene, required for avirulence on soybean cultivars containing Rps1k, was mapped to the same interval as Avr1b-1.


Plant Disease ◽  
1998 ◽  
Vol 82 (5) ◽  
pp. 555-559 ◽  
Author(s):  
D. E. Kyle ◽  
C. D. Nickell ◽  
R. L. Nelson ◽  
W. L. Pedersen

Phytophthora rot, caused by Phytophthora sojae, is a damaging disease of soybean (Glycine max (L.) Merr.) throughout the soybean-producing regions of the world. The discovery of new sources of resistance in soybean is vital in maintaining control of Phytophthora rot, because races of the pathogen have been discovered that can attack cultivars with commonly used resistance genes. The objectives of this study were to investigate the distribution and diversity of Phytophthora-resistant soybean in southern China and identify sources that confer resistance to multiple races for implementation into breeding programs. Soybean accessions obtained from southern China were evaluated for their response to races 1, 3, 4, 5, 7, 10, 12, 17, 20, and 25 of P. sojae using the hypocotyl inoculation technique in the greenhouse at Urbana, Illinois in 1996 and 1997. Accessions were identified that confer resistant responses to multiple races of the pathogen. These accessions may provide sources of resistance for control of Phytophthora rot of soybean in the future. The majority of the accessions with resistance to eight or more of the ten races tested were from the provinces of Hubei, Jiangsu, and Sichuan in southern China. Based on the evaluated accessions, these provinces appear to be valuable sources of Phytophthora-resistant soybean.


Plant Disease ◽  
2020 ◽  
Vol 104 (7) ◽  
pp. 1888-1893
Author(s):  
Jin Yang ◽  
Sujiao Zheng ◽  
Xiaomen Wang ◽  
Wenwu Ye ◽  
Xiaobo Zheng ◽  
...  

Phytophthora root and stem rot caused by Phytophthora sojae is a destructive disease that afflicts soybean plants throughout the world. The use of resistant soybean cultivars is the primary means of managing this disease, as well as the most effective and economical approach. There are abundant soybean germplasm resources in China that could be deployed for breeding programs; however, the resistance genes (Rps genes) in most cultivars are unknown, leading to uncertainty concerning which are resistant cultivars for use. The resistance genes Rps1a, Rps1c, and Rps1k prevent root and stem rot caused by most P. sojae isolates within a Chinese field population. This study identified three Rps genes in Chinese domestic soybean cultivars using three related avirulence genes by particle bombardment. The complex genetic diversity of soybean cultivars and P. sojae strains has made it difficult to define single Rps genes without molecular involvement. Gene cobombardment is a method for identifying Rps genes quickly and specifically. We showed that cultivars Dongnong 60 and Henong 72 contained Rps1a, while Hedou 19, Henong 76, 75-3, Wandou 21020, Zheng 196, Wandou 28, Heinong 71, and Wandou 29 all contained Rps1c. The cultivars Jidou 12, Henong 72, Heinong 71, and Wandou 29 contained Rps1k. The cultivar Henong 72 contained both Rps1a and Rps1k, while Wandou 29 and Heinong 71 contained both Rps1c and Rps1k. We then evaluated the phenotype of 11 domestic soybean cultivars reacting to P. sojae using the isolates P6497 and Ps1. The 11 domestic cultivars were all resistant to P6497 and Ps1. This research provides source materials and parent plant strains containing Rps1a, Rps1c, and Rps1k for soybean breeding programs.


2003 ◽  
Vol 93 (5) ◽  
pp. 633-639 ◽  
Author(s):  
Terrance Z. Ye ◽  
Rong-Cai Yang ◽  
Francis C. Yeh

We have developed a new complementary model of gene interaction between diploid host and haploid pathogen by allowing for arbitrary levels of dominance in the host. This model enables us to assess the effects of overdominance, incomplete dominance, and underdominance on the equilibrium frequencies of resistance and virulence genes and on the stability of equilibria. Our model reduces to a gene-for-gene model when complete dominance of resistance is assumed. Computer simulations show that our model has two new features. First, when there is overdominance or underdominance of resistance, the internal equilibrium points exist even when there is no cost of unnecessary virulence or when there is a cost of necessary virulence at the balance between cost of unnecessary virulence and effectiveness of resistance. Second, the occurrence of stable resistance and virulence polymorphism is strongly dependent on the level of dominance. These two features suggest the need for caution when using the gene-for-gene model, especially in the presence of overdominance or underdominance. Our model is particularly suitable for studying the coevolutionary dynamics between hybrid populations and their pathogens in natural pathosystems.


2021 ◽  
Vol 219 ◽  
pp. 112312
Author(s):  
Yinlong Xiao ◽  
Ying Du ◽  
Yue Xiao ◽  
Xiaohong Zhang ◽  
Jun Wu ◽  
...  

1981 ◽  
Vol 38 (1) ◽  
pp. 99-112
Author(s):  
Paulo R.C. Castro ◽  
Roberto S. Moraes

This research deals with the effects of growth regulators on flowering and pod formation in soybean plant (Glycine max cv. Davis). Under greenhouse conditions, soybean plants were sprayed with 2,3,5-triiodobenzoic acid (TIBA) 20 ppm, Agrostemmin (1g/10 ml/3 l) gibberellic acid (GA) 100 ppm, and (2-chloroethyl) trimethylammonium chloride (CCC) 2,000 ppm. Application of TIBA increased number of flowers. 'Davis' soybean treated with CCC and TIBA presented a tendency to produce a lower number of pods.


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