scholarly journals Pathogenic Variability of Puccinia coronata f. sp. avenae and P. graminis f. sp. avenae on Oat in South Africa

Plant Disease ◽  
2001 ◽  
Vol 85 (10) ◽  
pp. 1085-1090 ◽  
Author(s):  
B. D. van Niekerk ◽  
Z. A. Pretorius ◽  
W. H. P. Boshoff

Although crown rust (caused by Puccinia coronata f. sp. avenae) and stem rust (caused by Puccinia graminis f. sp. avenae) are generally considered to be the most widespread and damaging diseases of oat (Avena spp.) in South Africa, pathogenic variability has never been studied. During 1997 and 1998, one dominant crown rust pathotype (SBLL) was identified with virulence to resistance genes Pc40, Pc45, Pc46, Pc51, and Pc54. Four other pathotypes (SGLL, PBBB+Pc35, SDQL, and JBBM+Pc35), occurring at low frequencies and further rendering resistance genes Pc35, Pc39, Pc48, Pc50, Pc52, and Pc64 ineffective, were also detected. Resistance gene Pc40 was postulated in Wisconsin X1588-2; Pc51 in Euro, Maluti, Overberg, OX88I 075-106, Perdeberg, and Swartberg; and Pc39 was confirmed in the cultivar Fidler. During the same period, four stem rust pathotypes were identified with virulence to resistance genes Pg1, Pg2, Pg4, Pg8, Pg9, Pg12,Pg15, and Pga. Resistance gene Pga was postulated in Alpha, OX87 080-1, OX88I 075-106, Sederberg, and W94/4; Pg2 and/or Pg4 in Euro, Perdeberg, Potberg, and Swartberg; and Pg9 in Pallinup and Victorian. Collections of wild oat species Avena fatua, A. byzantina, A. sterilis, and A. barbata were susceptible to all crown rust patho-types, while the four stem rust pathotypes were virulent on all species except A. barbata.

2018 ◽  
Vol 2018 ◽  
pp. 1-7
Author(s):  
Arif Abrahim ◽  
Temam Hussein ◽  
Ayele Badebo

Wheat is one of the important major crops of Hararghe Highlands. It is third in land coverage and total production after sorghum and maize. However, the wheat stem rust disease is threatening production of wheat in this region. So, this research was conducted with the following objective: to determine the population of Puccinia graminis f. sp. tritici in Hararghe Highlands. A total of 200 fields were surveyed and stem rust samples were collected and transported to Kulumsa Agricultural Research Center for race analysis. Inoculation of differentials carrying resistance genes Sr24 and Sr-Tmp indicated typical low infection types on all isolates. Isolates EH5, EH8, and EH3 from East Hararghe and WH2, WH1, and WH3 from West Hararghe showed high virulence of infection in all differential lines. Ten (10) races were identified by using Puccinia graminis tritici code system: TTGSK, PTJQK, TTSSK, TTKSK, TRSSK, and TTJQK from East Hararghe and TTTSK and TTSQK from West Hararghe zones. Race TTSSK was most frequent (25%) followed by TTKSK (25%) in East Hararghe. Race TTSSK showed 50% frequency of occurrence in West Hararghe zones. The low frequency of occurrences indicated high variability of the races in the survey areas. Therefore, monitoring of populations of pathogens is important for the national and regional research centers. Detection of pathogen virulence evolution and of currently effective resistance genes is necessary and must be applied within a system of resistance gene management.


Plant Disease ◽  
2021 ◽  
Author(s):  
Suraj Sapkota ◽  
Paul Raymer ◽  
Alfredo Martinez-Espinoza ◽  
Bochra Amina Bahri

Stem rust, caused by Puccinia graminis, and crown rust, caused by P. coronata, are common rust diseases on cool-season grasses (Karakkat et al. 2018), for which long-distance spore dispersal was recorded in northern US (Harder and Haber 1992). During the summers of 2019 and 2020, severe infection of stem rust and crown rust was observed on > 60% of tall fescue (Festuca arundinacea) germplasm plants in a breeding nursery located at the University of Georgia, Griffin GA. Rust-infected leaves first presented uredinia pustules, then black telia towards the end of the season. The uredinia pustules of stem rust and crown rust were brick-red and, yellow and arranged along the host veins, respectively. The urediniospores were one-celled, round to ovoid and measured from 20.75±2.44 μm (crown rust) to 27±3.60 μm long (stem rust). The teliospores were two-celled and measured from 45.75±10.14 μm (stem rust) to 51.60±4.0 μm long (crown rust) (Leonard et al. 2005; Cummins 1971). Urediniospores of both rusts were collected from infected plants in the field in April of 2020 using a Piston vacuum pump (Welch by Gardner Denver Ltd.) and stored at -80 °C in 1.5 ml Eppendorf tubes. Genomic DNA was extracted by grinding the urediniospores in liquid nitrogen using mortar and pestle, followed by the cetyltrimethylammonium bromide method (Doyle and Doyle 1987). The internal transcribed spacer (ITS) region of the ribosomal DNA was amplified using the ITS5-ITS4 primers (White et al. 1990). BLASTn and phylogenetic analyses revealed that the sequence of stem rust (GenBank acc. no. MW430963) and crown rust (GenBank acc. no. MW431324) pathogens had >99% similarity with P. graminis (GenBank acc. no. HQ317538) and P. coronata var. avenae f. sp. avenae (clade V; Liu and Hambleton 2013) (GenBank acc. no. EU014044), respectively. Pathogenicity tests were conducted on the tall fescue cultivar ‘Bandit’. For each rust, 12 pots (10 cm × 10 cm) were planted, each containing 13 seeds in a Sungro professional growing mix soil (Sun Gro Horticulture Distribution Inc.). The plant materials were kept in the greenhouse at 20°C/ 25°C (night/day),15-hrs of light, and watered twice a week for 4-weeks. Urediniospores were recovered from -80°C and allowed to acclimate at room temperature for 1 h. For each rust, 20 ml of suspension containing 1×105 urediniospores ml−1 and 5 μl of Tween-twenty (Agdia Inc. Elkhart, IN) were used to inoculate 6 pots; while 6 control pots were sprayed with sterile water. After inoculation, plants were allowed to dry for 1 h and then transferred to a dark chamber at 20°C and 90% of humidity for 12-15 h. At 10-days post inoculation, all inoculated plants developed rust symptoms identical to those observed in the field, whereas control plants had no symptoms. Stem and crown rust pathogens were re-isolated from the artificially inoculated tall fescue plants. Based on form, size, color and numbers of cells forming the spores, a 1947 Festuca elatior specimen from Georgia mentioning Puccinia coronata (Hanlin 1966), held at the Julian H. Miller Mycological Herbarium (Catalog No. GAM00013162), was discarded as an earlier record of P. coronata var. avenae and could have been misdiagnosed. Due to the fragile integrity of the original infected plant sample as well as the incipient infection, DNA identification was unsuccessful. To our knowledge, this is the first morphological, genetic and taxonomic report of P. graminis and P. coronata var. avenae f. sp. avenae on tall fescue in Georgia, USA


1970 ◽  
Vol 48 (12) ◽  
pp. 2117-2121
Author(s):  
George Fleischmann

All isolates of oat crown rust, Puccinia coronata f. sp. avenae, identified in Canada in 1969 were inoculated onto 12 different lines containing resistance from wild oats, Avena sterilis, collected in Europe and the Middle East. Lines that contain resistance genes Pc-38 and Pc-39, and wild oat collections CI 8081 and F158, provide effective resistance to nearly every culture of crown rust. Regional differences in the level of virulence of crown rust cultures isolated from eastern and western Canada were observed on lines that contain A. sterilis resistance, with cultures of crown rust isolated from the east being generally less virulent than those from western Canada.


1980 ◽  
Vol 22 (4) ◽  
pp. 641-649 ◽  
Author(s):  
J. W. Martens ◽  
R. I. H. McKenzie ◽  
D. E. Harder

Tests of over 1400 Avena accessions, comprising eight species, from Iran, Iraq and Turkey have shown that resistance to oat stem rust caused by Puccinia graminis Pers. f. sp. avenae Eriks and E. Henn. occurs infrequently in the Avena populations of the region and was found only in A. barbata Pott ex Link and A. sterilis L. Resistance to oat crown rust caused by P. coronata Cda f. sp. avenae Eriks, was common in A. barbata from Turkey and in A. sterilis from all three countries. The inheritance of resistance conferred by two genes from the region, Pg-15 and Pc-54 is described. Gene Pg-15, the first stem rust resistance gene found in this region, is partially dominant and independent of the Pg-2, Pg-9, Pg-12 and Pg-13 loci. It conferred resistance to races that are important in North America. Gene Pc-54 was also the first crown rust resistance gene to be identified from this region. It was usually recessive, and allelic or closely linked with gene Pc-35.


Plant Disease ◽  
2010 ◽  
Vol 94 (6) ◽  
pp. 784-784 ◽  
Author(s):  
Z. A. Pretorius ◽  
C. M. Bender ◽  
B. Visser ◽  
T. Terefe

Isolates of Puccinia graminis f. sp. tritici belonging to the Ug99 race group are virulent to a broad spectrum of resistance genes, rendering most of the world's wheat germplasm susceptible to stem rust (3). Following the initial detection of Ug99 (TTKSK, North American [NA] race notation) in Uganda, virulence to the widely used Sr31 resistance gene has been reported from Kenya, Ethiopia, Sudan, and Iran (2,3). In November 2009, a wheat genotype suspected to carry Sr31 showed a susceptible response to stem rust in a disease nursery (29°08′05.02′′S, 30°38′29.18′′E), inoculated with race TTKSP, near Greytown in KwaZulu-Natal, South Africa. Inoculation of urediniospores of the field collection (isolate UVPgt60) onto seedlings of line Federation4*/Kavkaz confirmed virulence for Sr31. In three independent, replicated, and comparative seedling tests, eight single-pustule isolates of UVPgt60 all typed to race PTKST following the NA race nomenclature. These isolates produced compatible infection types (ITs) (3+ to 4) on the Sr31 testers Gamtoos, Sr31/6*LMPG, Federation4*/Kavkaz, Kavkaz, and Clement, whereas isolate UVPgt59 (TTKSP) was avirulent (ITs ;1 to 1) on these genotypes. In addition to Sr31 virulence, the new race differed from TTKSP by producing a lower IT (2 to 2++) on Cns_T.mono_ deriv., the accepted entry for Sr21 in the NA differential set. The UVPgt60 isolates were clearly avirulent on Einkorn (Sr21) (IT ;1=), a response that also differed from those produced by BPGSC, TTKSF, and TTKSP (IT 2). With the exception of Sr21, UVPgt60 isolates had a virulence pattern similar to race TTKST (1), notably the virulence combination for Sr24 and Sr31. Isolate UVPgt60.6 was randomly selected for testing on additional Sr genes and South African wheat cultivars and breeding lines. Similar to the race identification experiments seedling tests were duplicated and compared with reactions produced by TTKSP and other races. Greenhouse temperatures for all seedling tests ranged between 18 and 25°C. On the basis of primary leaf responses, PTKST is avirulent (ITs 0; to 2++) for Sr13, 14, 21, 22, 25, 26, 27, 29, 32, 33, 35, 36, 37, 39, 42, 43, 44, Em, Tmp, and Satu and virulent (ITs 3 to 4) for Sr5, 6, 7b, 8a, 8b, 9a, 9b, 9d, 9e, 9g, 10, 11, 16, 17, 24, 30, 31, 34, 38, 41, and McN. From 103 South African wheat cultivars and lines tested as seedlings, 59 and 47 were susceptible (IT ≥ 3) to races PTKST and TTKSP, respectively. Simple-sequence repeat analysis (4) with selected primer pairs showed that PTKST clusters with isolates belonging to the Ug99 lineage. Subsequent to the collection made at Greytown, stem rust sampled in December 2009 from naturally infected breeders' lines at Cedara (29°32′19.59′′S, 30°16′03.50′′E), KwaZulu-Natal, revealed five isolates with a virulence profile similar to PTKST. On the basis of current evidence it appears that PTKST may be an introduction to South Africa rather than a single-step mutation from local stem rust races. References: (1) Y. Jin et al. Plant Dis. 92:923, 2008. (2) K. Nazari et al. Plant Dis. 93:317, 2009. (3) R. P. Singh et al. Adv. Agron. 98:271, 2008. (4) B. Visser et al. Mol. Plant Pathol. 10:213, 2009.


Plant Disease ◽  
2016 ◽  
Vol 100 (6) ◽  
pp. 1184-1191 ◽  
Author(s):  
Sylwia Sowa ◽  
Edyta Paczos-Grzęda ◽  
Aneta Koroluk ◽  
Sylwia Okoń ◽  
Agnieszka Ostrowska ◽  
...  

Wild oat tetraploids of the section Pachycarpa have already been proven to be a rich source of useful genes but have largely been unexploited for Puccinia coronata resistance. In this study, accessions of Avena magna, A. murphyi, and A. insularis gathered from European and North American gene banks were evaluated at the seedling stage for crown rust reaction using the host–pathogen test and six highly diverse and virulent P. coronata isolates. Of the 92 Avena accessions analyzed, 58.7% were resistant to at least one crown rust race. In all, 37% of the tested accessions reacted nonuniformly, which indicated their heterogeneity. The highest level of resistance was observed in three of the accessions, one of which was verified by flow cytometry as being hexaploid and two of which were verified as being tetraploids. The infection profiles of 19 accessions corresponded to resistance determined by the genes Pc14, Pc39, Pc40, Pc48, Pc50, Pc54, Pc55, Pc61, Pc67, Pc68, Pc97, Pc101, or Pc104. The patterns of infection of the remaining resistant A. magna and A. murphyi accessions allowed us to postulate the presence of potentially novel crown rust resistance genes.


2007 ◽  
Vol 58 (6) ◽  
pp. 639 ◽  
Author(s):  
B. D. McCallum ◽  
T. Fetch ◽  
J. Chong

The major cereal crops grown in Canada are wheat (11 Mha), barley (4 Mha), and oat (1.5 Mha). Over 90% of the total cereal production area is in the western provinces of Manitoba, Saskatchewan,and Alberta. Historically, the disease of major concern in wheat was stem rust, caused by Puccinia graminis f. sp. tritici. The first significant stem rust resistant cultivar in Canada was Thatcher, grown extensively from 1939 until the early 1970s. The stem rust resistance in Thatcher was relatively effective, with the exception of susceptibility to race 15B epidemic in the 1950s. Thatcher, however, was very susceptible to leaf rust, caused by Puccinia triticina. Over time, improved resistance to both stem and leaf rust was achieved with the release of cultivars with additional genes for resistance, primarily Sr2, Sr6, Sr7a, Sr9b, Lr13, Lr14a, Lr16, and Lr34. Over the years genetic resistance has adequately controlled stem rust but leaf rust continues to cause significant losses, partially due to changes in the P. triticina population which reduced the effectiveness of resistance genes such as Lr13 and Lr16. Stripe rust on wheat, caused by Puccinia striiformis f. sp. tritici, was historically a problem under irrigation in southern Alberta, but since 2000 it has been found annually in the central Canadian prairies and southern Ontario. The genetic basis of resistance to stripe rust in most Canadian wheat cultivars has not been determined, although Yr18 provides partial resistance in many cultivars. In contrast to wheat, rust diseases have generally not caused concern for barley producers. Stem rust, caused by P. graminis f. sp. tritici, is the primary concern for barley growers, and has been controlled through use of gene Rpg1 since 1947. In 1988 race QCCJ with virulence on Rpg1 was detected in the prairie region but to date has not caused significant economic losses in barley. The resistance gene rpg4 is effective against QCCJ, but no commercial varieties have yet been produced with rpg4. In oat, both stem rust, caused by Puccinia graminis f. sp. avenae, and crown rust, caused by Puccinia coronata f. sp. avenae, have caused significant yield losses. Both rusts have been controlled mainly through host resistance and early planting. Stem rust resistance genes Pg2 and Pg13 have been the most effective and occur in many current oat cultivars. However, in 1998, 2 races, NA67 and NA76, with virulence on both Pg2 and Pg13 were detected in the prairie region. Currently, race NA67 is predominant in the prairie region and thus all Canadian cultivars are susceptible to stem rust. Since the 1980s, improved resistance to crown rust has been achieved through use of resistance derived from Avena sterilis. Pc39 was the first of the genes derived from this wild relative to be deployed in a new cultivar, followed by the release of cultivars possessing both Pc38 and Pc39. These 2 genes remained effective until the early 1990s. From 1994 onward, a series of cultivars with the highly effective Pc68 gene introgressed from A. sterilis were released. Virulence to Pc68 appeared in 2001, and in 2005 cultivars with this gene were severely rusted. The cultivar Leggett with Pc68 plus the highly effective Pc94 gene from the diploid A. strigosa was released in 2004. Rhamnus cathartica, the alternate host of P. coronata, is widespread in Canada and removal of these woody shrubs in the vicinity of oat fields is important to reduce the severity of crown rust. The increased use of fungicides on all cereals in the past 10 years has been fairly effective in rust control but represents an added input cost for producers.


Plant Disease ◽  
2018 ◽  
Vol 102 (5) ◽  
pp. 955-963
Author(s):  
Brijesh B. Karakkat ◽  
Vonte L. Jackson ◽  
Paul L. Koch

Crown rust (caused by Puccinia coronata) and stem rust (caused by P. graminis) are two common and destructive diseases of turfgrass in the United States. Crown rust has been associated with perennial ryegrass and stem rust with Kentucky bluegrass when identified based solely on fungal morphology. However, recent studies using molecular identification methods have indicated the host–pathogen relationship of rusts on turf to be more complex. Our primary objective was to quickly and accurately identify P. coronata and P. graminis in symptomatic turfgrass leaves over 3 years on turfgrass samples from across the Midwestern United States. Between 2013 and 2015, 413 samples of symptomatic cool-season turfgrass from Wisconsin and surrounding states were screened using real-time polymerase chain reaction. Of these samples, 396 were Kentucky bluegrass and 17% of them contained P. coronata, 69% contained P. graminis, and 13% contained both P. coronata and P. graminis. In addition, both year and location effects were observed on the distribution of Puccinia spp. collected annually from two locations in southern Wisconsin. This research supports previous conclusions that have identified variability among P. graminis and P. coronata host relationships on turfgrass, and further demonstrates that rust fungal populations on Kentucky bluegrass may not be consistent between locations in the same year or over multiple years at the same location. The increasing evidence of variation in the turfgrass rust populations will likely affect future rust management and turfgrass breeding efforts.


Plant Disease ◽  
2013 ◽  
Vol 97 (3) ◽  
pp. 387-392 ◽  
Author(s):  
Mohsen Mohammadi ◽  
Davoud Torkamaneh ◽  
Mehran Patpour

Following emergence of Ug99, the new virulent race of Puccinia graminis f. sp. tritici in Africa, a global effort for identification and utilization of new sources of Ug99-resistant germplasm has been undertaken. In this study, we conducted replicated experiments to evaluate the resistance of Iranian wheat germplasm to the TTKSK lineage of the Ug99 race of P. graminis f. sp. tritici. We also evaluated for presence of stem rust resistance genes (i.e., Sr2, Sr24, Sr26, Sr38, Sr39, Sr31, and Sr1RSAmigo) in wheat cultivars and breeding lines widely cultivated in Iran. Our phenotyping data revealed high levels of susceptibility to Ug99 in Iranian bread wheat germplasm. Our genotyping data revealed that Iranian cultivars do not carry Sr24, Sr26, or Sr1RSAmigo. Only a few salt-tolerant cultivars and breeding lines tested positively for Sr2, Sr31, Sr38, or Sr39 markers. In conclusion, the genetic basis for resistance to Ug99 in Iranian wheat cultivars was found to be vulnerable. Acquiring knowledge about existing resistance genes and haplotypes in wheat cultivars and breeding lines will help breeders, cereal pathologists, and policy makers to select and pyramid effective stem rust resistance genes.


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.


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