Changes in Photosynthesis of Wheat Plants Infected with Wheat Stem Rust (Puccinia graminis f.sp. tritici)

1985 ◽  
Vol 112 (2) ◽  
pp. 165-172 ◽  
Author(s):  
R. Berghaus ◽  
H. J. Reisener
Plant Disease ◽  
2005 ◽  
Vol 89 (2) ◽  
pp. 159-163 ◽  
Author(s):  
P. D. Peterson ◽  
K. J. Leonard ◽  
J. D. Miller ◽  
R. J. Laudon ◽  
T. B. Sutton

A federal and state program operated from 1918 until the 1980s to eradicate common barberry (Berberis vulgaris), the alternate host of Puccinia graminis, from the major areas of cereal production in the United States. Over 500 million bushes were destroyed nationally during the program, approximately 1 million in Minnesota. Some sites in Minnesota where barberry bushes were destroyed remained in the “active” class when eradication was phased out in the 1980s. Active sites were defined as those on which there was still a possibility of emergence of barberry seedlings or sprouts arising from the parent bush. In the present study, from 1998 to 2002, 72 of the approximately 1,200 active sites in Minnesota were surveyed. Areas within 90 m of mapped locations of previously destroyed bushes were searched carefully at each site. Reemerged barberry plants were found on 32 sites. The reproductive status and GPS coordinates were recorded for each reemerged bush. More than 90% of the barberry bushes were found in counties with less than 400 ha of wheat per county, mostly in southeastern Minnesota, but one bush was found in a major wheat-producing county in northwestern Minnesota. Reemergence of barberry may serve as a source of new wheat stem rust races in future epidemics.


Plant Disease ◽  
2020 ◽  
Vol 104 (7) ◽  
pp. 1939-1943
Author(s):  
Xian Xin Wu ◽  
Qiu Jun Lin ◽  
Xin Yu Ni ◽  
Qian Sun ◽  
Rong Zhen Chen ◽  
...  

Wheat stem rust, caused by Puccinia graminis f. sp. tritici, is one of the most serious fungal diseases in wheat production, seriously threatening the global supply of wheat and endangering food security. The present study was conducted to evaluate wheat monogenic lines with known Sr genes to the most prevalent P. graminis f. sp. tritici races in China. In addition, wheat lines introduced from the International Maize and Wheat improvement Center (CIMMYT) with resistance to the Ug99 race group were also evaluated with the prevalent Chinese P. graminis f. sp. tritici races. The monogenic lines containing Sr9e, Sr21, Sr26, Sr31, Sr33, Sr35, Sr37, Sr38, Sr47, and SrTt3 were effective against races 21C3CTTTM, 34C0MRGSM, and 34C3MTGQM at both seedling and adult-plant stages. In contrast, monogenic lines containing Sr6, Sr7b, Sr8a, Sr9a, Sr9b, Sr9d, Sr9f, Sr9g, Sr13, Sr16, Sr18, Sr19, Sr20, Sr24, Sr28, Sr29, and Sr34 were highly susceptible to these races at both seedling and adult-plant stages. Lines with Sr5, Sr10, Sr13, Sr14, Sr15, Sr17, Sr21, Sr22, Sr23, Sr25, Sr27, Sr29, Sr30, Sr32, Sr36, and Sr39 were resistant to one or more of the tested races. Among the 123 CIMMYT lines, 38 (30.9%) showed varying levels of susceptibility to Chinese P. graminis f. sp. tritici races. The results should be useful for breeding wheat cultivars with resistance to stem rust.


Plant Disease ◽  
2012 ◽  
Vol 96 (4) ◽  
pp. 590-590 ◽  
Author(s):  
Z. A. Pretorius ◽  
L. J. Szabo ◽  
W. H. P. Boshoff ◽  
L. Herselman ◽  
B. Visser

Seven races have been described in the Ug99 race group of Puccinia graminis f. sp. tritici (2). Ug99-related races previously recorded in South Africa are TTKSF, TTKSP, and PTKST (4). In December 2010, severe stem rust infection of the winter wheat cv. Matlabas was observed for the first time in South Africa. Race analysis using the 20 North American (NA) stem rust differential lines and letter code system classified the race as TTKSF. In comparative infection studies in a greenhouse, cv. Matlabas seedlings were susceptible (infection type [IT] 4) to isolate UVPgt61/1 (TTKSF+) collected from Afrikaskop in the eastern Free State, whereas the cultivar was resistant (IT 1 to 2) to stem rust isolates 2013 (TTKSF), UVPgt55 (TTKSF), UVPgt59 (TTKSP), and UVPgt60 (PTKST). Isolate 2013 represents the original collection of race TTKSF in South Africa (1). In addition to the NA differentials, no variation in the IT range of seedlings of lines with Sr7a, 8b, 12, 13, 14, 16, 18, 19, 22, 25, 26, 27, 28, 29, 32, 33, 34, 35, 39, 41, 42, 43, 44, Em, R, Tt2, and Satu was observed between UVPgt61/1 and UVPgt55. With the exception of cv. Matlabas, ITs of 106 South African cultivars likewise did not differentiate UVPgt61/1 and UVPgt55. Seedling IT studies were conducted at least twice. Microsatellite analysis (4) showed that all single pustule isolates established from the original Matlabas isolate formed part of the Ug99 group. When characterized with selected single nucleotide polymorphisms (SNPs), all single pustule isolates shared an identical genotype that differed from UVPgt55 (TTKSF), a foreign introduction into South Africa (1,3). SNP genotype analysis suggests that UVPgt61/1 is genetically dissimilar to UVPgt55, as is Zim1009, another TTKSF+ isolate that was collected from Birchenough in Zimbabwe. Studies are underway to determine the identity of the defeated Sr gene in Matlabas and the cultivar has been added to the South African stem rust differential set. TTKSF+ is the eighth race detected in the Ug99 group. Since no other cultivars or advanced lines were found to carry the Matlabas gene, it is unlikely that race TTKSF+ will threaten wheat production in South Africa. However, the occurrence of a new Ug99-related race emphasizes the variability within this internationally important group. References: (1) W. H. P. Boshoff et al. Plant Dis. 86:922, 2002. (2) R. F. Park et al. Euphytica 179:109, 2011. (3) B. Visser et al. Mol. Plant Pathol. 10:213, 2009. (4) B. Visser et al. Euphytica 179:119, 2011.


Plant Disease ◽  
2020 ◽  
Vol 104 (1) ◽  
pp. 293-293
Author(s):  
Tsegaab Tesfaye ◽  
Alemayehu Chala ◽  
Elfinesh Shikur ◽  
David Hodson ◽  
Les J. Szabo

1969 ◽  
Vol 47 (11) ◽  
pp. 1816-1817 ◽  
Author(s):  
P. G. Williams

Hyphae of the wheat stem rust fungus form short, lateral projections under conditions of artificial culture that are unfavorable for saprophytic growth. It is suggested that the structures are homologous with the haustoria of intercellular rust mycelium.


1971 ◽  
Vol 13 (1) ◽  
pp. 119-127 ◽  
Author(s):  
A. K. Sanghi ◽  
N. H. Luig

Nine genes conditioning resistance to cultures of P. graminis tritici (possessing unusual genes for avirulence), P. graminis secalis, and sexual or somatic hybrids between these formae speciales were found in the wheat cultivars Mentana and Yalta. In Mentana, Sr8 operated against all six cultures utilized; but in Yalta, Sr11 conditioned resistance to only two hybrid cultures. In addition, four other genes in Mentana and three genes in Yalta operated against the cultures.The present study indicates that hybridization between wheat stem rust and rye stem rust can be important in producing new combinations of virulence genes which can attack known genes for resistance in wheat. The implications of such hybridization in relation to the transference to wheat of resistance in rye to P. graminis tritici are discussed.


1976 ◽  
Vol 54 (19) ◽  
pp. 2204-2214 ◽  
Author(s):  
Mishael Oichoe Osoro ◽  
G. J. Green

Experiments were designed to show whether or not virulence genes reduce fitness and bring about stabilizing selection. The competitive abilities of seven related races of Puccinia graminis f. sp. tritici were studied on seedlings of three to five susceptible wheat varieties by growing mixtures of the races in greenhouses, growth cabinets, and field plots. In experiments in which simple races with few virulence genes were mixed with complex races with one, two, or three extra virulence genes, the complex races predominated after 4 to 10 generations in five of the six mixtures, and the simple race predominated in one mixture. A complex race predominated over simple races in the field experiment. It was concluded that virulence genes did not impair the fitness of the wheat stem rust races studied.In one race mixture studied in growth cabinets the complex race predominated at 25 °C, and the simple race, at 15 °C. Temperature did not differentially influence the competitive abilities of the races in three other mixtures.Incubation periods for all races were shorter at higher temperatures, but races C18(15B-1L) and C33(15B-1L) developed faster than races C9(15B-1L), C37(15), C38(15B-1L), C42(15), and C49(15) at all temperatures. In addition, races C18(15B-1L) and C33(15B-1L) produced more urediospores per pustule than races C9(15B-1L), C37(15), and C49(15). The differences in incubation period and spore production are considered to be the most important factors studied and they could cause the differences in aggressiveness of the seven races.


2006 ◽  
Vol 96 (1) ◽  
pp. 96-104 ◽  
Author(s):  
F. J. Keiper ◽  
M. S. Haque ◽  
M. J. Hayden ◽  
R. F. Park

Sequence-tagged microsatellite profiling was used to develop 110 microsatellites for Puccinia graminis f. sp. tritici (causal agent of wheat stem rust). Low microsatellite polymorphism was exhibited among 10 pathogenically diverse P. graminis f. sp. tritici isolates collected from Australian cereal growing regions over a period of at least 70 years, with two polymorphic loci detected, each revealing two alleles. Limited cross-species amplification was observed for the wheat rust pathogens, P. triticina (leaf rust) and P. striiformis f. sp. tritici (stripe rust). However, very high transferability was revealed with P. graminis f. sp. avenae (causal agent of oat stem rust) isolates. A genetic diversity study of 47 P. graminis f. sp. avenae isolates collected from an Australia-wide survey in 1999, and a historical group of 16 isolates collected from Australian cereal growing regions from 1971 to 1996, revealed six polymorphic microsatellite loci with a total of 15 alleles. Genetic analysis revealed the presence of several clonal lineages and subpopulations in the pathogen population, and wide dispersal of identical races and genotypes throughout Australian cereal-growing regions. These findings demonstrated the dynamic population structure of this pathogen in Australia and concur with the patterns of diversity observed in pathogenicity studies.


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