Egypt. J. Phytopathol., Vol. 43, No. 1-2, pp. 179-186 (2015)
Virulent Race Overcome Wheat Stem Rust
Resistance Gene Sr27 in Egypt
M.A. Hasan
Wheat Diseases Res. Dept., Plant Pathol. Res. Inst., ARC, Giza, Egypt
ABSTRACT
riticale is an excellent source of resistance to wheat stem rust, caused
by Puccinia graminis f. sp. tritici. Stem rust historically is one of the
most destructive disease of wheat (Triticum aestivum L.) worldwide.
Deployment of resistant genotypes successfully prevented rust epidemics
over the past several decades. This is primarily due to the ongoing
incorporation of effective stem rust resistance genes into new wheat
breeding material, this may placed the pathogen under great selection
pressure. Although Sr27 has little effect on the commercial wheat
production, it has a major impact on the commercial triticale cultivars. In
Egypt, high levels of stem rust infection were observed on wheat cultivar
(Cooring) which carrying Sr27 grown at Gemmiza Research Station
during May 2015. Samples collected from rusted stems of wheat cultivar
(Cooring) were cut and artificialally inoculated on primary leaves of 8-
day-old seedlings of highly susceptible wheat Cv. Morocco. Four single
pustules were collected and race analysis was don. Results showed that
out of the four identified races, race QQQCM was the most virulent one
on wheat seedling carrying Sr27 with infection type (4), whereas the rest
of races were a virulent to Sr27. This race (QQQCM) first time to appear
in Egypt from previous identified races. Regarding to the performance of
20 stem rust resistant genes at seedling stage, (Sr
9e,7b,8a,9g,30,17,9a,9d,10,31and Sr38 ) were resistant to race QQQCM,
meanwhile the rest Srs were susceptible.
T
Keywords: Stem rust, resistant genes.
INTRODUCTION
Stem rust of wheat caused by the fungus Puccinia graminis Pers. f. sp.
tritici Eriks. & E.Henn. is the most destructive disease on wheat
worldwide. Successful control of the disease over three decades through
the use of genetic resistance has resulted in a sharp decline in research
activity in recent years (El-Daoudi, et al.,1995).
Occurrence of new races in a geographic/ epidemiologic regions can
be attributed to the migration from an outside such as spread of race
TTKS, in East Africa commonly known as Ug99 to anther countries
Singh, et al.,2006. Wheat stem rust resistant gene Sr27(3A.3R
translocation) is one of the most important gene posses resistant to stem
rust especially in triticale, whereas virulence on Sr27 is rare Acosta,
1962. Harder et al., 1972 isolated an east African culture virulent on
Pembina line with Sr27. McIntosh et al., 1983 showed that isolates of P.
graminis f. sp. tritici from triticale cv. Coorong were virulent on wheat
seedlings with Sr27. The results were accepted as evidence that the
resistance gene in Coorong and many other triticale lines developed in
Mexico was Sr27. Virulence on triticale genotypes with Sr27 was found
in South Africa in 1988 Smith and Le Roux, 1992. McIntosh et al.,
1983 showed that Sr27 occurred at high frequency in lines present in
nurseries distributed from CIMMYT and gave warning of genetic
vulnerability.
The value of adult plant resistance in protecting wheat genotypes
against such virulent stem rust races could be achieved by combining
many genes of resistance in a single genotypes that conferred high level
of generalized resistance against the pathogens. In this respect, Brennan
et al., 1988 stated that a breeding program should develop rust resistant
cultivars conditioned with resistance genes (both race- specific and race-
non specific resistance). The inheritance of adult plant resistance has
often been considered as a complex, but there is also an evidence that it is
oligogenic Barcellos et al.,2000. The identification of genes conferring
stem rust adult plant resistance would be a significant step towards a good
control of such disease Manninger et al.,1998; Nazim et al.,2001; and
Mousa et al.,2004.
The objective of this study was to identify and characterize the new
race that overcome the resistant gene Sr27 which governing the resistance
in triticale.
MATERIALS AND METHODS
The collected samples from the infected wheat genotypes Coorong
carrying Sr27 were used to identify physiologic race(s) that overcome the
resistance of Sr27. The collected samples (rusted stems) were kept in
glassine envelopes (8 x 15 cm). Rust samples, were left at room
temperature for 24 hours to remove the humidity in the samples. After
that samples were preserved in dissector in fridge till usage. The infected
specimens were transferred to the very susceptible wheat cv. Morocco.
The method of inoculation was carried out as described by Stakman et
al., 1962. Eight days old seedlings were sprayed with an atomizer in the
inoculation chambers with water then inoculated by shaking and brushing
rusted materials over the plants and sprayed gently again with water in
order to induce “dew” on the plant. Finally, the inoculated plants were
kept in damp chambers for 24 hours to allow the rust spores to germinate
and cause infection. Inoculated plants were transferred and placed on
benches in the greenhouse and kept for 14 day. After developing the rust
symptomes, four single pustules were separately isolated from the sample
and inoculated again on very susceptible wheat cultivar seedlings
Morocco to obtain enough urediospores for inoculate the differential sets.
Infection types (IT) were scored after 14 days using the 0–4 scale of
Stakman et al.,1962. Infection types were categorized as either being
Low( resistant 0, 0; 1 and 2) or High ( susceptible 3 & 4)The differential
host series consisted of wheat rust monogenic lines, arranged in five
subsets Table (1). Races were assigned using the international Pgt-code as
suggested by Roelfs and Martens 1988.
Table (1). Pgt-code races of Puccinia graminis f. sp. Tritici
subset
Infection types produced on host lines with Sr
1
2
3
4
5
5
11
36
9a
24
21
6
9b
9d
31
9e
8a
30
10
38
7b
9g
17
Tmp
MCN
B
C
D
F
G
H
J
K
L
M
N
P
Q
R
S
T
Low
Low
Low
Low
Low
Low
Low
Low
High
High
High
High
High
High
High
High
Low
Low
Low
Low
High
High
High
High
Low
Low
Low
Low
High
High
High
High
Low
Low
High
High
Low
Low
High
High
Low
Low
High
High
Low
Low
High
High
Low
High
Low
High
Low
High
Low
High
Low
High
Low
High
Low
High
Low
High
RESULTS
Race analysis:
Race analysis from the infected wheat triticale Cooring (figure
1and 2) showed that four races were identified based on their reaction on
20 differential sets listed on table 1. Most of the identified races varied in
their virulence on stem rust resistance gene Sr27, this indicated a high
level of variation both in quantity and virulence spectrum. The obtained
data (Table 2and 3), revealed that the identified races posses different
infection types on Sr27 ranged from (0, to 4). Race QQQCM was the
virulent one on Sr27 which gave susceptible reaction with infection type
(4), meanwhile the rest races showed a virulent infection types(0,-1-2).
On the other hand race KKBBB was less aggressive on the differential
sets which overcome the resistance of six stem rust resistant genes ( Sr
21, 9e,7b, 6, 8a and Sr 9g). Races TTMCC and BCPPL were intermediate
in its effect on the resistant genes.
Table 2: Infection type produced on Sr27 with the identified races
No. Race I.T No. Race I.T
1 QQQCM 4 3 BCPPL 2
2 TTMCC 0, 4 KKBBB 1
Table 3: Infection types of twenty differential lines in addition to
Sr 27
inoculated with four single pustules.
Sr
genes
Infection Type/single pustules
1 2 3 4
Set 1
1 Sr5 H H L L
2 Sr21 H H L H
3 Sr9e L H L H
4 Sr7b L H L H
set 2
1 Sr11 H H L L
2 Sr6 H H L H
3 Sr8a L H L H
4 Sr9g L H H H
Set 3
1 Sr36 H H H L
2 Sr9b H L L L
3 Sr30 L L H L
4 Sr17 L H H L
Set 4
1 Sr9a L L H L
2 Sr9d L L L L
3 Sr10 L L H L
4 SrTMP H H H L
Set 5
1 Sr24 H L H L
2 Sr31 L L L L
3 Sr38 L L L L
4 SrMcN H H L L
Sr 27 H L L L
Race QQQCM TTMCC BCPPL KKBBB
Concerning a virulence/virulence formulae of data presented in
Table (4) race QQQCM was the virulent one on Sr27 and nine stem rust
resistant genes, i.e (Sr5,21,11,6,36,9b, TMP,24 and SrMcN). On the other
hand race KKBBB was less aggressive on stem rust resistant genes which
showed virulence on six stem rust resistant genes ( Sr21, 9e,7b, 6 ,8a and
9g), meanwhile it was a virulent on Sr27 . Races TTMCC and BCPPL
were a virulent on Sr27and virulent on different stem rust resistant genes .
Figure 1: Infected wheat triticale Cooring with Sr27 at Gemmiza
Research Station
During May 2015
Figure 2:
Table 4: A virulence / Virulence pattern of identified races
No. Race A virulence /Virulence genes
1 QQQCM Sr9e,7b,8a,9g,30,17,9a,9d,10,31,38/
2 TTMCC Sr9b,30, 9a,9d, 10,24,31,38,27/
3 BCPPL Sr5, 21, 9e, 7b; 11, 6, 8a,
Sr9b,9d,31,38,McN,27/
4 KKBBB Sr5,11,36,9b,30,17,9a,9d,10,TMP,24,
31,38,McN,27/
Effectiveness of stem rust resistant genes was assessed. Sr31 and Sr38
were completely effective to all identified races whereas Sr9g, Sr36 and
SrTMP were the least effective .
Discussion
Wheat stem rust is the most important disease of wheat all over the
world. The pathogen is able to produce new races that can attack
previously resistant varieties and develop rapidly under optimal
environmental conditions which results in a serious yield loss. Hence,
monitoring the disease and its races is of great importance for sustainable
wheat management programs. Race analysis of samples collected from
wheat triticale (cooring) which carrying Sr27, revealed that race QQQCM
was the virulent one on Sr27, meanwhile the rest races were avirulent.
Race QQQCM showed high infection type (4) on some important stem
rust genes i.e, Sr36, Sr24 and SrMcN.In this respect McIntosh et, al.
1983 showed that isolates of P. graminis f. sp. tritici from triticale cv.
Coorong were virulent on wheat seedlings with Sr27. Also he found that
Sr27 occurred at high frequency in lines present in nurseries distributed
from CIMMYT. Olivera et, al. (2013) repotted that, three South African
P. graminis f. sp. tritici isolates UVPgt53, UVPgt56 and UVPgt57 were
virulent on Sr27.He showed that these isolates were virulent on 8 stem
rust resistant genes Sr8a 9a 9b 9d 9g 10 11 McN.
REFERENCES
Acosta A.C.( 1962). The transfer of stem rust resistance from rye to
wheat. Dissertation Abstracts 23, 34-35.
Barcellos, A.L., A. P. Roelfs and M.I.B. de Moraes-Fernands (2000).
Inheritance of adult plant leaf rust resistance in the Brazilian
cultivars Toropi. Plant Dis. 84:90-93.
Brennan, J.P. and Murray, G.M. (1988). Australian wheat diseases —
assessing their economic importance. Agricultural Science
New Series 1, 26-35.
Harder, D.E., Mathenge, G.R. and Mwaura, L.K.( 1972). Physiologic
specialization and epidemiology of wheat stem rust in east
Africa. Phytopathology 62, 166- 171.
El-Daoudi, Y.H.; Mamluk, O.F.; Abu El-Naga, S.A.; Ahmed,M.S.;
Bekele, E.; Nabila, A. El-Sherif and Khalifa,M.O. (1995).
Virulence survey of Puccinia graminis f.sp. tritici and genes
conferring resistance to wheat stem rust in the Nile Valley
countries, Yemen and Syria during 1992/93 and 1993/94.
Egypt. J. Appl. Sci., 11 (3): 90-110.
McIntosh, R.A.(1983). Induced mutations of rust resistance genes in
wheat. In 'Induced Mutations for Disease Resistance in Crop
Plants II'. pp. 115-118. (International Atomic Energy Agency:
Vienna.)
Manninger, K.; Sosz, M.C.; Falusi, J. and Mesterhazy, A. (1998).
Postulation of resistance genes to wheat stem rust in winter
wheat genotypes from Szeged. Acta Phytopathologica
Entomologica., 33:37-42.
Mousa, M.M.; Najeeb, M.A.; Boulot, O.A. and Youssef, W.A.(2004).
Probable genes for stem rust resistance in some Egyptian wheat
varieties. Egypt. J. Appl. Sci., 19:151-163
Nazim, M.S.; Awad, M.A.; Boulot, O.A.; Abu El-Naga, S.A.and
Abdel Hamid, I. (2001). Durable resistance to stem rust in some
Egyptian wheat cultivars. Mun. J. Agric. Res., 26(6):1485-1499.
Olivera, P. D., Pretorius, Z. A., Badebo, A., and Jin, Y. (2013).
Identification of resistance to races of Puccinia graminis f. sp.
tritici with broad virulence in triticale (×Triticosecale). Plant Dis.
97:479-484
Roelfs, A.P. and Martens, J.W. (1988). An international system of
nomenclature for Puccinia graminis f. sp. tritici. Phytopath.,
78(5):526-533.
Smith, J. and Le Roux, J. (1992). First report of wheat stem rust
virulence for Sr27 in South Africa. Vorträge für
Pflanzenzüchtung 24, 109-110.
Singh, R.P., Hodson D.P.; Jin, Y.; Huerta-Espino, J.; Kinyua, M.G.;
Wanyera R.; Njau, P. and Ward, R.W. (2006) Current status,
likely migration and strategies to mitigate the threat to wheat
production from race Ug99 (TTKS)
Stakman, E.C.; D.M. Stewart and W.Q. Loegering (1962).
Identification of physiological races of Puccinia graminis var.
tritici USDA-ARS. Bull, E617. U.S. Govt. Print Office,
Washington DC.
Sr 27
Sr 27Sr 2720158QQQCMSr 274Sr 9e, 7b, 8a, 9g, 30, 17, 9a, 9d, 10, 31
and 38QQQCM

virulence on Sr 27

  • 1.
    Egypt. J. Phytopathol.,Vol. 43, No. 1-2, pp. 179-186 (2015) Virulent Race Overcome Wheat Stem Rust Resistance Gene Sr27 in Egypt M.A. Hasan Wheat Diseases Res. Dept., Plant Pathol. Res. Inst., ARC, Giza, Egypt ABSTRACT riticale is an excellent source of resistance to wheat stem rust, caused by Puccinia graminis f. sp. tritici. Stem rust historically is one of the most destructive disease of wheat (Triticum aestivum L.) worldwide. Deployment of resistant genotypes successfully prevented rust epidemics over the past several decades. This is primarily due to the ongoing incorporation of effective stem rust resistance genes into new wheat breeding material, this may placed the pathogen under great selection pressure. Although Sr27 has little effect on the commercial wheat production, it has a major impact on the commercial triticale cultivars. In Egypt, high levels of stem rust infection were observed on wheat cultivar (Cooring) which carrying Sr27 grown at Gemmiza Research Station during May 2015. Samples collected from rusted stems of wheat cultivar (Cooring) were cut and artificialally inoculated on primary leaves of 8- day-old seedlings of highly susceptible wheat Cv. Morocco. Four single pustules were collected and race analysis was don. Results showed that out of the four identified races, race QQQCM was the most virulent one on wheat seedling carrying Sr27 with infection type (4), whereas the rest of races were a virulent to Sr27. This race (QQQCM) first time to appear in Egypt from previous identified races. Regarding to the performance of 20 stem rust resistant genes at seedling stage, (Sr 9e,7b,8a,9g,30,17,9a,9d,10,31and Sr38 ) were resistant to race QQQCM, meanwhile the rest Srs were susceptible. T Keywords: Stem rust, resistant genes. INTRODUCTION Stem rust of wheat caused by the fungus Puccinia graminis Pers. f. sp. tritici Eriks. & E.Henn. is the most destructive disease on wheat
  • 2.
    worldwide. Successful controlof the disease over three decades through the use of genetic resistance has resulted in a sharp decline in research activity in recent years (El-Daoudi, et al.,1995). Occurrence of new races in a geographic/ epidemiologic regions can be attributed to the migration from an outside such as spread of race TTKS, in East Africa commonly known as Ug99 to anther countries Singh, et al.,2006. Wheat stem rust resistant gene Sr27(3A.3R translocation) is one of the most important gene posses resistant to stem rust especially in triticale, whereas virulence on Sr27 is rare Acosta, 1962. Harder et al., 1972 isolated an east African culture virulent on Pembina line with Sr27. McIntosh et al., 1983 showed that isolates of P. graminis f. sp. tritici from triticale cv. Coorong were virulent on wheat seedlings with Sr27. The results were accepted as evidence that the resistance gene in Coorong and many other triticale lines developed in Mexico was Sr27. Virulence on triticale genotypes with Sr27 was found in South Africa in 1988 Smith and Le Roux, 1992. McIntosh et al., 1983 showed that Sr27 occurred at high frequency in lines present in nurseries distributed from CIMMYT and gave warning of genetic vulnerability. The value of adult plant resistance in protecting wheat genotypes against such virulent stem rust races could be achieved by combining many genes of resistance in a single genotypes that conferred high level of generalized resistance against the pathogens. In this respect, Brennan et al., 1988 stated that a breeding program should develop rust resistant cultivars conditioned with resistance genes (both race- specific and race- non specific resistance). The inheritance of adult plant resistance has often been considered as a complex, but there is also an evidence that it is oligogenic Barcellos et al.,2000. The identification of genes conferring stem rust adult plant resistance would be a significant step towards a good control of such disease Manninger et al.,1998; Nazim et al.,2001; and Mousa et al.,2004.
  • 3.
    The objective ofthis study was to identify and characterize the new race that overcome the resistant gene Sr27 which governing the resistance in triticale. MATERIALS AND METHODS The collected samples from the infected wheat genotypes Coorong carrying Sr27 were used to identify physiologic race(s) that overcome the resistance of Sr27. The collected samples (rusted stems) were kept in glassine envelopes (8 x 15 cm). Rust samples, were left at room temperature for 24 hours to remove the humidity in the samples. After that samples were preserved in dissector in fridge till usage. The infected specimens were transferred to the very susceptible wheat cv. Morocco. The method of inoculation was carried out as described by Stakman et al., 1962. Eight days old seedlings were sprayed with an atomizer in the inoculation chambers with water then inoculated by shaking and brushing rusted materials over the plants and sprayed gently again with water in order to induce “dew” on the plant. Finally, the inoculated plants were kept in damp chambers for 24 hours to allow the rust spores to germinate and cause infection. Inoculated plants were transferred and placed on benches in the greenhouse and kept for 14 day. After developing the rust symptomes, four single pustules were separately isolated from the sample and inoculated again on very susceptible wheat cultivar seedlings Morocco to obtain enough urediospores for inoculate the differential sets. Infection types (IT) were scored after 14 days using the 0–4 scale of Stakman et al.,1962. Infection types were categorized as either being Low( resistant 0, 0; 1 and 2) or High ( susceptible 3 & 4)The differential host series consisted of wheat rust monogenic lines, arranged in five subsets Table (1). Races were assigned using the international Pgt-code as suggested by Roelfs and Martens 1988.
  • 4.
    Table (1). Pgt-coderaces of Puccinia graminis f. sp. Tritici subset Infection types produced on host lines with Sr 1 2 3 4 5 5 11 36 9a 24 21 6 9b 9d 31 9e 8a 30 10 38 7b 9g 17 Tmp MCN B C D F G H J K L M N P Q R S T Low Low Low Low Low Low Low Low High High High High High High High High Low Low Low Low High High High High Low Low Low Low High High High High Low Low High High Low Low High High Low Low High High Low Low High High Low High Low High Low High Low High Low High Low High Low High Low High RESULTS Race analysis: Race analysis from the infected wheat triticale Cooring (figure 1and 2) showed that four races were identified based on their reaction on 20 differential sets listed on table 1. Most of the identified races varied in their virulence on stem rust resistance gene Sr27, this indicated a high
  • 5.
    level of variationboth in quantity and virulence spectrum. The obtained data (Table 2and 3), revealed that the identified races posses different infection types on Sr27 ranged from (0, to 4). Race QQQCM was the virulent one on Sr27 which gave susceptible reaction with infection type (4), meanwhile the rest races showed a virulent infection types(0,-1-2). On the other hand race KKBBB was less aggressive on the differential sets which overcome the resistance of six stem rust resistant genes ( Sr 21, 9e,7b, 6, 8a and Sr 9g). Races TTMCC and BCPPL were intermediate in its effect on the resistant genes. Table 2: Infection type produced on Sr27 with the identified races No. Race I.T No. Race I.T 1 QQQCM 4 3 BCPPL 2 2 TTMCC 0, 4 KKBBB 1 Table 3: Infection types of twenty differential lines in addition to Sr 27 inoculated with four single pustules. Sr genes Infection Type/single pustules 1 2 3 4 Set 1 1 Sr5 H H L L 2 Sr21 H H L H 3 Sr9e L H L H 4 Sr7b L H L H set 2 1 Sr11 H H L L 2 Sr6 H H L H 3 Sr8a L H L H 4 Sr9g L H H H Set 3 1 Sr36 H H H L 2 Sr9b H L L L 3 Sr30 L L H L
  • 6.
    4 Sr17 LH H L Set 4 1 Sr9a L L H L 2 Sr9d L L L L 3 Sr10 L L H L 4 SrTMP H H H L Set 5 1 Sr24 H L H L 2 Sr31 L L L L 3 Sr38 L L L L 4 SrMcN H H L L Sr 27 H L L L Race QQQCM TTMCC BCPPL KKBBB Concerning a virulence/virulence formulae of data presented in Table (4) race QQQCM was the virulent one on Sr27 and nine stem rust resistant genes, i.e (Sr5,21,11,6,36,9b, TMP,24 and SrMcN). On the other hand race KKBBB was less aggressive on stem rust resistant genes which showed virulence on six stem rust resistant genes ( Sr21, 9e,7b, 6 ,8a and 9g), meanwhile it was a virulent on Sr27 . Races TTMCC and BCPPL were a virulent on Sr27and virulent on different stem rust resistant genes . Figure 1: Infected wheat triticale Cooring with Sr27 at Gemmiza Research Station During May 2015
  • 7.
    Figure 2: Table 4:A virulence / Virulence pattern of identified races No. Race A virulence /Virulence genes 1 QQQCM Sr9e,7b,8a,9g,30,17,9a,9d,10,31,38/ 2 TTMCC Sr9b,30, 9a,9d, 10,24,31,38,27/ 3 BCPPL Sr5, 21, 9e, 7b; 11, 6, 8a, Sr9b,9d,31,38,McN,27/ 4 KKBBB Sr5,11,36,9b,30,17,9a,9d,10,TMP,24, 31,38,McN,27/
  • 8.
    Effectiveness of stemrust resistant genes was assessed. Sr31 and Sr38 were completely effective to all identified races whereas Sr9g, Sr36 and SrTMP were the least effective . Discussion Wheat stem rust is the most important disease of wheat all over the world. The pathogen is able to produce new races that can attack previously resistant varieties and develop rapidly under optimal environmental conditions which results in a serious yield loss. Hence, monitoring the disease and its races is of great importance for sustainable wheat management programs. Race analysis of samples collected from wheat triticale (cooring) which carrying Sr27, revealed that race QQQCM was the virulent one on Sr27, meanwhile the rest races were avirulent. Race QQQCM showed high infection type (4) on some important stem rust genes i.e, Sr36, Sr24 and SrMcN.In this respect McIntosh et, al. 1983 showed that isolates of P. graminis f. sp. tritici from triticale cv. Coorong were virulent on wheat seedlings with Sr27. Also he found that Sr27 occurred at high frequency in lines present in nurseries distributed from CIMMYT. Olivera et, al. (2013) repotted that, three South African P. graminis f. sp. tritici isolates UVPgt53, UVPgt56 and UVPgt57 were virulent on Sr27.He showed that these isolates were virulent on 8 stem rust resistant genes Sr8a 9a 9b 9d 9g 10 11 McN. REFERENCES Acosta A.C.( 1962). The transfer of stem rust resistance from rye to wheat. Dissertation Abstracts 23, 34-35. Barcellos, A.L., A. P. Roelfs and M.I.B. de Moraes-Fernands (2000). Inheritance of adult plant leaf rust resistance in the Brazilian cultivars Toropi. Plant Dis. 84:90-93. Brennan, J.P. and Murray, G.M. (1988). Australian wheat diseases — assessing their economic importance. Agricultural Science New Series 1, 26-35. Harder, D.E., Mathenge, G.R. and Mwaura, L.K.( 1972). Physiologic
  • 9.
    specialization and epidemiologyof wheat stem rust in east Africa. Phytopathology 62, 166- 171. El-Daoudi, Y.H.; Mamluk, O.F.; Abu El-Naga, S.A.; Ahmed,M.S.; Bekele, E.; Nabila, A. El-Sherif and Khalifa,M.O. (1995). Virulence survey of Puccinia graminis f.sp. tritici and genes conferring resistance to wheat stem rust in the Nile Valley countries, Yemen and Syria during 1992/93 and 1993/94. Egypt. J. Appl. Sci., 11 (3): 90-110. McIntosh, R.A.(1983). Induced mutations of rust resistance genes in wheat. In 'Induced Mutations for Disease Resistance in Crop Plants II'. pp. 115-118. (International Atomic Energy Agency: Vienna.) Manninger, K.; Sosz, M.C.; Falusi, J. and Mesterhazy, A. (1998). Postulation of resistance genes to wheat stem rust in winter wheat genotypes from Szeged. Acta Phytopathologica Entomologica., 33:37-42. Mousa, M.M.; Najeeb, M.A.; Boulot, O.A. and Youssef, W.A.(2004). Probable genes for stem rust resistance in some Egyptian wheat varieties. Egypt. J. Appl. Sci., 19:151-163 Nazim, M.S.; Awad, M.A.; Boulot, O.A.; Abu El-Naga, S.A.and Abdel Hamid, I. (2001). Durable resistance to stem rust in some Egyptian wheat cultivars. Mun. J. Agric. Res., 26(6):1485-1499. Olivera, P. D., Pretorius, Z. A., Badebo, A., and Jin, Y. (2013). Identification of resistance to races of Puccinia graminis f. sp. tritici with broad virulence in triticale (×Triticosecale). Plant Dis. 97:479-484 Roelfs, A.P. and Martens, J.W. (1988). An international system of nomenclature for Puccinia graminis f. sp. tritici. Phytopath., 78(5):526-533.
  • 10.
    Smith, J. andLe Roux, J. (1992). First report of wheat stem rust virulence for Sr27 in South Africa. Vorträge für Pflanzenzüchtung 24, 109-110. Singh, R.P., Hodson D.P.; Jin, Y.; Huerta-Espino, J.; Kinyua, M.G.; Wanyera R.; Njau, P. and Ward, R.W. (2006) Current status, likely migration and strategies to mitigate the threat to wheat production from race Ug99 (TTKS) Stakman, E.C.; D.M. Stewart and W.Q. Loegering (1962). Identification of physiological races of Puccinia graminis var. tritici USDA-ARS. Bull, E617. U.S. Govt. Print Office, Washington DC. Sr 27 Sr 27Sr 2720158QQQCMSr 274Sr 9e, 7b, 8a, 9g, 30, 17, 9a, 9d, 10, 31 and 38QQQCM