Oat endosperm proteins associated with resistance to stem rust of oats

Genome ◽  
1992 ◽  
Vol 35 (1) ◽  
pp. 120-125 ◽  
Author(s):  
N. K. Howes ◽  
J. Chong ◽  
P. D. Brown

The presence of oat (Avena sativa L.) endosperm proteins, extracted with dimethylformamide mercaptoethanol – sodium dodecylsulfate and separated by dodecylsulfate polyacrylamide gel electrophoresis, was compared among cv. Rodney (carrying Pg4) and Rodney 0 derived backcross lines carrying single known genes Pg1, Pg2, Pg3, Pg8, Pg9, Pg13, Pg15, and Pg16, for stem rust resistance, and among other lines or cultivars with or without these genes. Most single-gene lines had polypeptide patterns similar to that of Rodney 0, a near-isogenic line with no known stem rust resistance. However, lines Rodney Pg3 and Rodney Pg9 were missing a 25.3-kDa avenin present in Rodney 0 and present in lines or cultivars that did not carry Pg9. The Rodney Pg13 line and several lines or cultivars that carried Pg13 were missing a 56.6-kDa polypeptide present in Rodney 0 and in several lines and cultivars that did not carry this gene. These results suggest that the Pg3/Pg9 and Pg13 loci were associated with the loci controlling the synthesis of the 25.3- and 56.6-kDa polypeptides, respectively. Results from genetic studies showed that gene Pg13 was linked in repulsion (linkage value 4.2 ± 1.9 cM) to the 56.6-kDa polypeptide locus.Key words: electrophoresis, oats, proteins, rust resistance.


1969 ◽  
Vol 11 (2) ◽  
pp. 266-274 ◽  
Author(s):  
K. N. Kao ◽  
D. R. Knott

The inheritance of pathogenicity in wheat stem rust was studied in selfed cultures of races 29 and 111, F1 and F2 cultures of a cross between the two races and cultures from a backcross to race 29. The various cultures were tested on Marquis and Prelude and on a series of lines of these varieties carrying single genes for stem rust resistance. Virulence on Sr 5, Sr 6, Sr 8, Sr 9a, Sr 14 and a gene in Marquis was recessive and in each case there was a single gene for virulence corresponding to each gene for resistance. Virulence on Sr 1 was possibly controlled by two dominant complementary genes. There appeared to be two alleles for virulence on Prelude, one dominant and one recessive.



Genome ◽  
1990 ◽  
Vol 33 (1) ◽  
pp. 115-118 ◽  
Author(s):  
S. J. Singh ◽  
R. A. McIntosh

Leaf rust resistance in five triticale cultivars was controlled by a single gene designated LrSatu. This gene was closely linked in coupling with the stem rust resistance gene SrSatu believed to be located on chromosome 3R. Approximately 50% of lines in the 17th International Triticale Screening Nursery possessed SrSatu and LrSatu. Lines carrying SrSatu and LrSatu occurred more frequently among complete than in substituted triticale lines.Key words: × Triticosecale Wittmack, P. graminis f.sp. tritici, P. recondita f.sp. tritici, leaf rust, stem rust, rust resistnace, genetic linkage.



Plant Disease ◽  
2006 ◽  
Vol 90 (1) ◽  
pp. 113-113 ◽  
Author(s):  
R. Wanyera ◽  
M. G. Kinyua ◽  
Y. Jin ◽  
R. P. Singh

Stem rust resistance in wheat cultivars with Sr31 has been effective and durable worldwide for more than 30 years. Isolates of Puccinia graminis f. sp. tritici with virulence to Sr31 were detected in Uganda in 1999 (1). During 2003 and 2004, a majority of current Kenyan cultivars and a large portion of CIMMYT wheat germplasm with gene Sr31 planted in Kenya were susceptible to stem rust. Six isolates collected during 2004 at different locations in Kenya were tested for virulence on the 16 North American stem rust race differentials with the following Sr genes: Sr5, 6, 7b, 8a, 9a, 9b, 9d, 9e, 9g, 10, 11, 17, 21, 30, 36, and Tmp. An extended set of designated Sr genes (Sr13, 19, 22, 24, 25, 26, 29, 31, 32, 33, 35, 37, 39, 40, 44, and Wld-1) was also tested at the seedling stage. An isolate from Uganda collected in 1999 with virulence on Sr31 was used for comparison. Urediniospores suspended in a lightweight mineral oil were inoculated onto 7-day-old seedlings. Inoculated plants were placed in a dew chamber for 14 h at 18°C in the dark and then for an additional period of 3 to 4 h placed under fluorescent light. Plants were incubated in a greenhouse at 18 ± 2°C with a photoperiod of 16 h. Infection types (IT), described by Stakman et al. (3), were assessed after 14 days postinoculation. All isolates from Kenya exhibited a low infection type (IT 0) on line W2691SrTt-1 (donor of Sr36), a low infection type (IT 2) on cv. Triumph 64 (donor of SrTmp), and high infection types (IT 3 or 4) on all other lines in the differential set (2); thus these isolates were keyed to race TTKS. The virulence pattern of the isolate collected in 1999 from Uganda was identical to that from Kenya on the differential set and on the extended set of designated Sr genes. In this study, these isolates produced a high infection type (IT 3) on Einkorn and CnSSr21Tm (a derivative of Triticum monococcum in Chinese Spring background), two sources of Sr21 used in our study, whereas the isolate with Sr31-virulence from Uganda in 1999 was reported to be avirulent on Sr21 (1). These isolates produced high infection types on single gene lines with Sr31 and winter wheat cvs. Custer, Foster, GA-Dozier, Patton, and Pioneer 26R61, which were known to carry the 1BL.1RS translocation with Sr31. These isolates were also virulent on SrWld-1, a gene used in spring wheat for its resistance to North American stem rust isolates. In addition to Sr36 and SrTmp, other stem rust resistance genes that were effective against TTKS at the seedling stage include Sr13, 22, 24, 25, 26, 27, 29, 32, 33, 35, 37, 39, 40, and 44. Cultivars, breeding germplasm, and single gene lines are currently being evaluated for adult plant reaction in Kenya. Results from this study indicated that stem rust isolates with virulence on Sr31 are now wide spread in the Eastern Africa highlands and pose a threat to wheat production in the region, as well as in other wheat production areas where Sr31 resistance is important. A rapid deployment of effective resistance genes to this race in breeding programs throughout Eastern Africa and Asia is needed to reduce this threat. References: (1) Z. A. Pretorius et al. Plant Dis. 84:203, 2000. (2) A. P. Roelfs and J. W. Martens. Phytopathology 78:526, 1988. (3) E. C. Stakman et al. U.S. Department of Agriculture. ARS E-617, 1962.



1970 ◽  
Vol 48 (8) ◽  
pp. 1439-1443 ◽  
Author(s):  
P. Bartoš ◽  
G. J. Green ◽  
P. L. Dyck

Thirty-four European wheat cultivars were classified into eight groups according to their reactions to seven North American races of Puccinia graminis f. sp. tritici. Cultivars of seven groups were crossed with a variety or single gene line having similar rust reactions. These crosses indicated that the resistance of Hybrid 80-3, Stabil, and Vrakuňská (group 1) was conferred by stem rust resistance gene Sr5; Admonter Früh (group 2) carries Sr5 and an unidentified gene; Flevina (group 4) carries Sr11; Erythrospermum 974 (group 5) carries Sr5 and Sr8; Étoile de Choisy (group 6) carries an unidentified gene for moderate resistance to all the races used; and Mironovskaja 808 (group 7) and Belocerkovskaja 198 (group 8) each carry an unidentified gene. The five cultivars in group 3 were not studied genetically but they react like Marquis and may carry Sr7b.



1999 ◽  
Vol 89 (12) ◽  
pp. 1214-1217 ◽  
Author(s):  
Donald E. Harder

Infection types produced by Puccinia graminis f. sp. avenae on plants of Avena sativa with the stem rust resistance gene Pg10 are characterized by moderate-sized uredinia surrounded by an area of chlorosis and a larger variable zone of dark brown necrosis. This study was undertaken to assess the effectiveness of gene Pg10 as a source of resistance to stem rust and to determine the interactions of this gene with other common Pg genes. A derived Pg10 line was tested with 58 distinct pathotypes of P. graminis f. sp. avenae and was crossed to substituted single-gene lines carrying the resistance gene Pg1, Pg2, Pg3, Pg4, Pg8, Pg9, Pg13, Pg15, Pg16, or Pga. The Pg10 line showed moderate resistance to all 58 patho-types, and there was no indication of specificity in virulence by any isolate. Gene Pg10 was inherited independently of the other Pg genes and had a complementary effect on the expression of resistance by these genes. An effective level of resistance conferred by Pg10 was demonstrated in a field nursery artificially inoculated with P. graminis f. sp. avenae. It was concluded that Pg10 is a potentially useful source of stem rust resistance in oat breeding, with its main attributes being an apparent broad base of resistance, ease of combining with other Pg genes, and complementary effects on the expression of other Pg genes



Plant Disease ◽  
2021 ◽  
Author(s):  
Kumarse Nazari ◽  
Ezgi Kurtulus ◽  
Handan Kavaz ◽  
Omer M. Ozturk ◽  
Yesim Egerci ◽  
...  

Severe wheat stem rust caused by Puccinia graminis Pers.:Pers. f. sp. tritici Erikss. (Pgt) can result in complete crop failure. In recent years, the increasing frequency and the early onset of stem rust in Central West Asia and North Africa (CWANA) has become a big concern. The Sr24 resistance gene, one of the most effective stem rust resistance genes effective against most P. graminis f. sp. tritici races worldwide, has been widely deployed. Until the recent establishment of virulence to Sr24 within the Ug99 lineage of the pathogen in Africa (Hei et al. 2020; Jin et al. 2008; Patpour et al. 2015), Iraq (Nazari et al., 2021), occasional detections of races virulent to Sr24 were reported in South Africa (Le Roux and Rijkenberg 1987), India (Bhardwaj et al. 1990), Germany (Olivera Firpo et al. 2017), Georgia (Olivera, et al. 2019), and Western Siberia (Skolotneva et al., 2020). During the rust surveys conducted in Sinops, Samsun, and Kastomonu in the Black Sea region in northern Turkey in 2018, 19 isolates were collected. Single pustule (SP) isolates were developed and used in race analysis in the Biosafety Rust Laboratory, Regional Cereal Rust Research Center (RCRRC), Izmir, Turkey. Sample recovery, experimental procedures for pre-inoculation, inoculation, incubation, and race typing were conducted as previously described (Nazari et al. 2021). Among the tested SP isolates, two isolates showed a high infection type (IT) of 33+ on the Sr24 tester line (Little Club/Agent) and a low infection type of 11+ for the source of Sr31 (Benno/6*LMPG-6). Eight SP isolates were further developed from the high IT 33+ pustules collected from the Sr24 tester line. After spore multiplications, they were used in inoculation of the 20 North American stem rust single-gene lines used to differentiate races of P. graminis f. sp. tritici, plus Trident (Sr38+), Siouxland (Sr24+Sr31), and Sisson (Sr31+Sr36). Five SP-derived isolates with IT 33+ on the Sr24 single-gene line collected from Samsun (Alacam – Etyemez; Location: N 41.61889 E 35.55722) and Sinop (Merkez-Sanlıoglu; Location: N 41.85556 E 35.04889) were identified as race TKKTP and the remaining three SP isolates as race TKTTP. In 2020, we detected two isolates of TKKTP among the stem rust samples from Tunisia submitted to RCRRC. These two isolates were collected from bread wheat cultivars Heydna and Tahmet at a trial site near Bou Salem in Western Tunisia (Location: N 36.5351 E 8.95486). Based on the negative results of the Stage 1 test using a suite of four real-time polymerase chain reaction assays diagnostic for the Ug99 race group developed by Szabo (2012), these two races should not belong to the Ug99 race group when compared to the reference Ug99 race TTKTT from Kenya. These races were virulent to Sr5, Sr21, Sr9e, Sr7b, Sr6, Sr8a, Sr9g, Sr9b, Sr30, Sr17, Sr9a, Sr9d, Sr10, SrTmp, Sr24, Sr38, and SrMcN. In addition to these genes, race TKTTP was virulent to Sr36. Both races were avirulent to Sr11 and Sr31. To our knowledge, this is the first report of P. graminis f. sp. tritici races with the Sr24 virulence in Turkey and Tunisia. The results reflect an increasing trend of virulence to Sr24 in the pathogen populations, and raise a great concern given the deployment of the Sr24 resistance gene in widely grown wheat cultivars worldwide.



Crop Science ◽  
1969 ◽  
Vol 9 (6) ◽  
pp. 838-839 ◽  
Author(s):  
L. H. Edwards ◽  
N. D. Williams ◽  
F. J. Gough ◽  
K. L. Lebsock


Crop Science ◽  
1982 ◽  
Vol 22 (2) ◽  
pp. 393-399 ◽  
Author(s):  
D. R. Knott


Crop Science ◽  
1978 ◽  
Vol 18 (3) ◽  
pp. 365-369 ◽  
Author(s):  
D. R. Knott ◽  
R. A. McIntosh


Crop Science ◽  
1995 ◽  
Vol 35 (5) ◽  
pp. 1445-1450 ◽  
Author(s):  
David P. Horvath ◽  
Lynn S. Dahleen ◽  
Jo‐Ann Stebbing ◽  
Greg Penner


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