Research Article | | Peer-Reviewed

Evaluation of Adult Plant Resistance in Bread Wheat (Triticum aestivum L.) Genotypes to Wheat Stem Rust (Puccinia graminis f. sp. tritici) Races in Ethiopia

Received: 8 November 2025     Accepted: 15 December 2025     Published: 29 December 2025
Views:       Downloads:
Abstract

A field experiment was conducted during the 2021 main cropping season using an augmented design to evaluate adult plant resistance in bread wheat genotypes against wheat stem rust (Puccinia graminis f. sp. tritici) in Ethiopia. Final rust severity (FRS), coefficient of infection (CI), and relative area under the disease progress curve (rAUDPC) were used to identify slow rusting genotypes. These parameters proved reliable for assessing resistance. Eleven Pgt races were tested on 20 near-isogenic lines carrying single stem rust resistance genes. Greenhouse results showed seven lines were resistant to all races. Genotypes were grouped based on infection types: Group I (e.g., genotypes 40 and 56) showed low infection types (ITs); Group II (e.g., genotypes 2, 3, 12, 13, 43, 91, 98) showed high ITs; Group III included 68 lines with variable reactions. TTKTF and TKPTF caused the highest ITs, while TTKTT showed the lowest. Thirty slow rusting genotypes were identified based on field FRS (Trace MS to 25 MS) and seedling ITs (2+ to 4). These cultivars offer valuable genetic resources for wheat improvement programs targeting durable resistance to stem rust. These findings demonstrate the importance of combining field-based slow rusting parameters with greenhouse race-specific evaluations to obtain a comprehensive understanding of resistance. The identification of genotypes with stable resistance across multiple environments provides a strong foundation for breeding programs aimed at durable stem rust resistance. Such cultivars are particularly valuable in Ethiopia, where stem rust epidemics pose a recurring threat to wheat production and national food security. This study contributes to the global effort of developing improved wheat varieties by offering genetic resources that can be integrated into international breeding pipelines. By highlighting both race-specific and slow rusting resistance, the research underscores the need for continuous monitoring of pathogen variability and the deployment of diverse resistance genes to ensure long-term effectiveness.

Published in American Journal of Plant Biology (Volume 10, Issue 4)
DOI 10.11648/j.ajpb.20251004.16
Page(s) 121-132
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2025. Published by Science Publishing Group

Keywords

Lines, Near-isogenic, Seedling, Slow Rusting, Races, Resistance

1. Introduction
Wheat rust diseases stem rust (Puccinia graminis f. sp. tritici), leaf rust (Puccinia triticina), and yellow rust (Puccinia striiformis f. sp. tritici) are major constraints to global wheat production. In Ethiopia, stem rust and yellow rust are particularly damaging to productivity. Recent studies estimate annual global losses from these rusts at 15.04 million tons, equivalent to US $2.9 billion . Resistance to wheat rusts is broadly categorized into race-specific and race-non-specific types. Race-specific resistance is qualitative and often short-lived due to the rapid evolution of virulent pathogen races . In contrast, race-non-specific resistance commonly referred to as slow rusting is expressed at adult plant stages and governed by adult plant resistance (APR) genes. Though moderate when acting alone, APR genes contribute significantly to durable resistance when combined with major genes and minor QTLs .
East Africa has been designated a hotspot for stem rust evolution. In 1998, race TTKSK (Ug99) was first identified in Uganda and later detected in Ethiopia in 2003 . Ug99 is virulent to Sr31, a key resistance gene in many cultivars, rendering much of the Ethiopian germplasm susceptible . In 2012, race TKTTF was first detected at trace levels in Ethiopia and reached epidemic levels by November 2013, causing 100% yield loss in cultivars like Digalu (SrTmp) . Unlike Ug99, TKTTF is genetically distinct. Subsequent surveys in 2014–2015 identified nine additional Pgt races in Ethiopia, including TKTTF, TTTTF, TTKSK, TRTTF, PKTTF, TTTSF, SJPQC, JRCSF, and JRCQC . In 2018, race TTKTT emerged, showing virulence to SrTmp, Sr24, and Sr31, and overcoming nearly all resistance genes except Sr36 .
Understanding the genetic basis of resistance to P. graminis f. sp. tritici is essential for effective breeding and deployment of resistant cultivars. Gene postulation is a rapid and widely used method for identifying resistance genes . Analysing the genetic background of resistant genotypes provides a foundation for strategic breeding and disease management. Therefore, this study aimed to evaluate advanced bread wheat lines for seedling resistance genes and identify slow rusting genotypes suitable for wheat improvement programs in Ethiopia.
2. Materials and Methods
2.1. Pathogen Materials
A total of eleven stem rust races were obtained from Ambo Agricultural Research Center. The races were initially identified at Ambo from samples collected from different wheat-growing areas in Ethiopia. The race designation was based on the letter code nomenclature system , modified to further delineate races in the TTKSK lineage . All isolates were derived from a single pustule, increased in isolation, and stored at -80°C. To get sufficient fresh spores of each isolate was multiplied on the susceptible check McNair 701 (CItr 15288). The races were selected based on their prevalence and virulence spectra as indicated (Table 1).
Table 1. Virulence/Avirulence Spectra of Pgt Races Used in Seedling Tests of Bread Wheat Genotypes in the Greenhouse at Ambo Agricultural Research Center in 2021/22.

Race

Virulence

Avirulence

TKTTF

5, 21, 9e, 7b, 6, 8a, 9g, 36, 9b, 30, 17, 9a, 9d, 10, Tmp, 38, McN

11, 24, 31

TTTTF

5, 21, 9e, 7b, 11, 6, 8a, 9g, 36, 9b, 30, 17, 9a, 9d, 10, Tmp, 38, McN

24, 31,

TKPTF

5, 21, 9e, 7b, 6, 8a, 9g, 36, 30, 9g, 9a, 9d, 10, Tmp, 38, McN

11, 9b, 24, 31,

TRTTF

5, 21, 9e, 7b, 11, 6, 9g, 36, 9b, 30, 17, 9a, 9d, 10, Tmp, 38, McN

8a, 24, 31,

TKKTF

5, 21, 9e, 7b, 6, 8a, 9g, 9b, 30, 17, 9a, 9d, 10, Tmp, 38, McN

11, 36, 24, 31,

RRTTF

5, 21, 7b, 11, 6, 9g, 36, 9b, 30, 17, 9a, 9d, 10, Tmp, 38, McN

9e, 8a, 24, 31

TTRTF

5, 21, 9e, 7b, 11, 6, 8a, 9g, 36, 9b, 17, 9a, 9d, 10, Tmp, 38, McN

30, 24, 31,

JRCQC

21, 9e, 11, 6, 9g, 17, 9a, 9d, McN

5, 7b, 8a, 36, 9b, 30, 10, Tmp, 24, 31, 38

TTKSK

5, 21, 9e, 7b, 11, 6, 8a, 9g, 9b, 30, 17, 9a, 9d, 10, 31, 38, McN

36, Tmp, 24

TTKTF

5, 21, 9e, 7b, 11, 6, 8a, 9g, 9b, 30, 17, 9a, 9d, 10, Tmp, 38, McN

36, 24, 31

TTKSK

5, 21, 9e, 7b, 11, 6, 8a, 9g, 9b, 30, 17, 9a, 9d, 10, 31, 38, McN

36, Tmp, 24,

TTKTT

5, 21, 9e, 7b, 11, 6, 8a, 9g, 9b, 30, 17, 9a, 9d, 10, Tmp, 24, 31, 38, McN

36

2.2. Seedling Test Procedures
The experiment was conducted at Ambo Agricultural Research Center (AARC) following the inoculation and disease assessment protocols described by . Five to seven seeds of each bread wheat genotype, including commercial varieties and a susceptible check, were planted in 3 cm diameter plastic pots filled with a soil, compost, and sand mixture in a 2:1:1 ratio. A set of stem rust differential lines was planted alongside the test genotypes. The experiment was arranged in a Completely Randomized Design (CRD) with two replications. The universally susceptible wheat cultivar McNair 701 (CItr 15288) was used as a control to monitor the virulence of each Pgt race. Seven days after sowing, when the first leaf was fully expanded, seedlings were inoculated with selected Pgt races. Spores derived from single pustules were suspended in mineral oil (Soltrol 170) and sprayed onto the seedlings. After allowing the oil to evaporate, a fine mist of water was applied to induce artificial dew and promote spore germination. To prevent cross-contamination, inoculated seedlings were enclosed in plastic bags (145 mm × 235 mm) and sealed at the base with rubber bands . Seedlings were incubated in the dark for 18–24 hours at 18 °C and 95% relative humidity in a dew chamber. They were then exposed to fluorescent light for three hours, followed by gradual drying to acclimate them to the greenhouse environment. After drying, seedlings were transferred to the growth room or greenhouse for disease development. Fourteen days post-inoculation, plants were scored for infection types (ITs) using the 0–4 scale described by . ITs of “0”, “;”, “;1”, “1”, “1+”, “2−”, “2”, and “2+” were classified as low infection types, while “3−”, “3”, “3+”, and “4” were considered high infection types (Figure 1).
Figure 1. Infection Types of P. Graminis f. sp. Tritici and Host Response.
Table 2. Description of Infection Types Used in Classifying the Reactions of Stem Rust on Wheat Seedling Leaves .

Host response

IT

Disease symptoms

Immune

0

No uredinia or other macroscopic sign of infection

Nearly immune

;

No uredinia, but hypersensitive necrotic or chlorotic flecks present

Very resistant

1

Small uredinia surrounded by necrosis

Moderately resistant

2

Small to medium uredinia are often surrounded by chlorosis or necrosis; green islands may be surrounded by chlorotic or necrotic border

Heterogeneous

X

Random distribution of variable-sized uredines on a single leaf

Moderately susceptible

3

Medium-sized uredinia that may be associated with chlorosis

Susceptible

4

Large uredinia without chlorosis

2.3. Host Materials
A total of 100 bread wheat genotypes, selected from breeding populations, were evaluated for adult plant resistance to stem rust. The commercial varieties Hachalu and Madda Walabu were included as resistant and susceptible checks, respectively.
2.4. Data Collection
Stem rust severity was recorded six times at seven-day intervals, beginning at the onset of disease symptoms. Disease scoring was performed using the modified Cobb Scale , which estimates the percentage of leaf area affected by rust pustules.
Table 3. Host Response and Constant Values Used in Disease Severity Assessment .

Field response

Constant value

R

0.2

MR

0.4

M

0.6

MS

0.8

S

1.0

2.5. Average Coefficient of Infection (ACI)
The Average Coefficient of Infection (ACI) was calculated by multiplying the recorded percentage severity of stem rust by a constant value corresponding to the host response, as described by . These constants reflect the degree of susceptibility or resistance and are presented in Table 1. ACI provides a more refined estimate of disease impact by integrating both severity and host reaction.
Area Under the Disease Progress Curve (AUDPC)
The Area Under the Disease Progress Curve (AUDPC) was computed to quantify disease development over time. It was calculated using the formula:
AUDPC = Σ [(yᵢ + yᵢ₊₁) / 2] × (tᵢ₊₁ - tᵢ)
The final Rust Severity (FRS): FRS is the last disease severity scores in modified Cobb’s scale.
Where:
yi and yi+1 are the disease severities at time points ti and ti+1, respectively.
n is the total number of observations.
t represents the time (in days) between disease assessments.
AUDPC provides a cumulative measure of disease intensity over the assessment period and is widely used to compare genotypes for partial resistance.
rAUDPC %: AUDPC value of a genotyeAUDPC of local or the most susceptible genotype×100
2.6. Agronomic Data
Days to 50% heading: the number of days from planting to the time when 50% of plants showed head on plot basis,
Thousand kernel weights (TKW): the weight of thousand kernels sampled at random from the total grains harvested from each experimental plot was measured.
Grain yield (GY): Grain yield in grams per plot was recorded and translated to Kg per ha.
2.7. Data Analysis
All measured quantitative parameters including Coefficient of infection (CI), Final Rust severity (FRS), Area Under Disease Progressive Curve (AUDPC), Disease progress rate (r-value), Relative of Area Under Disease Progressive curve (rAUDPC), yield and yield related parameters were subjected to descriptive analysis.
3. Results and Discussion
3.1. Seedling Response to Eleven Wheat Stem Rust Pathotypes
The infection responses of 100 bread wheat genotypes evaluated against eleven Puccinia graminis f. sp. tritici (Pgt) races are summarized in Figure 2. Across all seedling assays, the susceptible control cultivar McNair 701 consistently exhibited compatible infection types (ITs) ranging from 3 to 4 against all eleven Pgt races, confirming the effectiveness of the inoculation and the virulence of the pathotypes.
The high levels of infection achieved in each experiment enabled reliable scoring of ITs across all genotypes. A wide range of variation was observed in the genotypic responses to the stem rust races (Figure 3), indicating substantial genetic diversity in resistance.
Based on their IT scores, genotypes were classified into three categories: resistant, susceptible, and heterogeneous (Figure 2). The majority of genotypes displayed resistant reactions, with IT scores of 1 or 2. However, a significant number of genotypes were susceptible to race TTKTF, followed by TKPTF, which notably affected several popular wheat varieties.
Among the tested races, TTKTT induced the lowest infection types on some bread wheat genotypes, suggesting the presence of effective resistance genes against this race. Conversely, the highest ITs were recorded for other races, highlighting differential virulence patterns and genotype-specific responses.
Figure 2. Seedling Infection Responses of Bread Wheat Genotypes to Eleven Stem Rust Races.
Figure 3. Seedling Responses of Bread Wheat Genotypes to Multiple Stem Rust Pathotypes.
3.2. Classification of Stem Rust Resistance in Bread Wheat Genotypes
3.2.1. Group I: Genotypes Resistant to All Isolates
Two bread wheat genotypes demonstrated resistance to all eleven Puccinia graminis f. sp. tritici (Pgt) races evaluated at the seedling stage (Table 4). These genotypes consistently exhibited low infection types (ITs), indicating the presence of effective resistance mechanisms.
Table 4. Bread Wheat Genotypes Showing Resistance to All Eleven Pgt Races at Seedling Stage.

SN

TTKTT

TTTTF

TKTTF

TTKSK

JRCQC

TRTTF

TKKTF

TTRTF

TTKTF

TKPTF

RRTTF

Ag_sr

SIN_SR

40

;1

2

2-

;1

2-

;1

2+

;1+

;1+

2+

2+

Trs

5ms

56

;1

;1

2-

;1

;1

;1

;1+

;1+

2-

;1+

;1

Trs

5ms

To accurately postulate the underlying stem rust resistance genes in these lines, further testing with additional Pgt isolates exhibiting diverse virulence profiles is required. Moreover, the use of near-isogenic lines carrying known Sr genes would enhance the precision of gene postulation and help identify the specific resistance genes present in these genotypes.
3.2.2. Group II: Bread Wheat Genotypes Lacking Effective Resistance Genes
Seedling evaluation revealed that all Puccinia graminis f. sp. tritici (Pgt) races produced high infection types on one particular bread wheat breeding line, comparable to the universally susceptible check cultivar McNair 701 (Table 5). This consistent susceptibility across all races indicates the absence of effective seedling resistance in this genotype.
In total, seven genotypes were classified in this group, all exhibiting high infection types to the eleven Pgt races tested. These lines are presumed to lack known stem rust resistance genes and may serve as susceptible checks or baselines in future resistance screening efforts (Table 2).
Table 5. Bread Wheat Genotypes Showing Susceptibility to all Pgt Races at Seedling Stage.

SN

TTKTT

TTTTF

TKTTF

TTKSK

JRCQC

TRTTF

TKKTF

TTRTF

TTKTF

TKPTF

RRTTF

2

3-

3-

3-

3-

3-

3

4

3

3-

3-

3

3

3-

3

3-

3-

3

2+

4

3-

3-

3-

3

12

3-

3-

3

3-

3

3

3+

3+

3-

3

3

13

3-

3-

3-

3-

3-

3

3

3-

3-

3

3

43

3

3-

3

3-

3-

3

3

3

3

3

3

91

3-

3

3

3-

3

3+

3

3

3

3

3+

98

3-

3-

3-

3

3-

3

3

3-

3-

3

3-

3.3. Slow Rusting of Wheat Stem Rust Resistance
The AUPC is one of the indicators of slow-wheat stem rusting at field conditions . At Sinana tested site the tested wheat genotypes were categorized into two distinct groups for wheat stem rust slow-rusting resistance, based on the AUDPC values. Wheat genotypes that exhibited AUDPC values less than 300 ranging from 5 to 290 showed a high level of partial or slow-rusting resistance to wheat stem rust, consisting of 30 bread wheat genotypes. However, in this tested location, high AUDPC values of more than 300 ranged from 301 to 540, indicating low slow-rusting or low partial resistance. This study was similarly discussed with the evaluation of wheat genotypes for slow-rusting resistance to leaf and stem rust diseases which distinguished into low partial resistance and high wheat slow stem rusting on the bases of AUDPC.
Table 6. The Identified High Partial Resistance of Wheat Stem Rust on 30 the Bread Wheat Genotypes During 2022 Main Cropping Season.

Geno

TTKTT

Sin_FRS

Ag_FRS

AUDPC

GY (Kg/ha)

Geno

TTKTT

Sin_FRS

Ag_FRS

AUDPC

GY (Kgha)

2

3-

5s

15s

94

2336.25

70

3

15s

20s

120

2530

3

3-

20s

25s

280

915

72

3-

5s

20s

116

2393.75

13

3-

10s

10s

175

1301.25

77

3-

10s

20s

120

3006.25

15

3-

10s

15s

139

1911.25

79

3-

5ms

20s

116

3408.75

17

2+

20s

20s

123

375

82

3-

5ms

25s

145

1791.25

22

3-

10s

25s

133

1765

84

3-

10s

15s

95

2087.5

35

3

5s

10ms

59

1126.25

86

3-

5s

25s

141

3283.75

37

3-

trs

10ms

58

1177.5

91

3-

5s

15s

91

1957.5

39

3-

trms

10ms

40

2298.75

92

3

5s

20s

124

1231.25

43

3

15s

20s

275

1983.75

93

3-

trmss

20s

108

1762.5

47

3-

15s

20s

100

2528.75

94

3-

trmss

15s

200

1830

51

2+

5s

10ms

61

3042.5

95

3-

5ms

15s

200

1597.5

55

3-

10s

15s

137

2007.5

96

3-

10mss

20s

225

1400

62

3-

15s

20s

108

1776.25

97

3-

trms

15s

180

1275

65

3-

15s

15s

94

1567.5

98

3-

5ms

10ms

65

2268.75

*Gntp= Genotype; TTKTT= Race; Sin_FRS= Sinana Final Rust Severity; Ag_FRS= Agarfa Final Rust Severity; AUDPC = Area under Disease Progress Curve; GY=Grain Yield
3.4. Relationship Between Wheat Stem Rust Traits and Yield Parameters
Pearson’s correlation analysis revealed a highly significant positive correlation (p < 0.001) among key slow-rusting parameters of wheat stem rust, as presented in Table 3. At the Agarfa site during the 2021/22 main cropping season, the correlation coefficient between Coefficient of Infection (CI) and Area Under Disease Progress Curve (AUDPC) was r = 0.80, indicating a strong and consistent association between these two epidemiological traits.
This strong correlation suggests that genotypes with higher CI values also tend to accumulate greater disease pressure over time, as reflected by higher AUDPC values. These findings align with the observations of , who noted that slow-rusting parameters such as CI and AUDPC reliably reflect the rate of disease development and are associated with components of partial resistance, including low receptivity, longer latent periods, and smaller pustule size.
Similar results have been reported by , and , further supporting the utility of these parameters in identifying genotypes with durable, non-race-specific resistance.
Table 7. Pearson’s Correlation Coefficients Between Stem Rust Epidemiological Parameters and Yield-Related Traits at Agarfa (2022 Main Season).

CI-II

CI-III

CI-IV

CI-V

AUDPC

DH

DM

Stand

PH

Yield

TKW

CI-II

1.00

CI-III

0.80

1.00

CI-IV

0.72

0.85

1.00

CI-V

0.08

0.24

0.30

1.00

AUDPC

0.57

0.74

0.79

0.80

1.00

DH

-0.31

-0.34

-0.25

0.13

-0.10

1.00

DM

-0.16

-0.07

-0.12

-0.03

-0.09

0.10

1.00

Stand

-0.22

-0.25

-0.20

0.06

-0.10

0.30

0.11

1.00

PH

0.13

0.24

0.12

0.00

0.11

-0.13

-0.03

-0.01

1.00

Yield

-0.21

-0.20

-0.21

-0.07

-0.18

0.28

0.16

0.48

-0.02

1.00

TKW

-0.02

-0.06

-0.14

-0.28

-0.24

-0.04

0.07

0.09

0.14

0.46

1.00

CI= correlation coefficients; DH=Days Heading; DM= Days Maturity; PH= plant height TKW=Thousand Kernel weighty; AUDPC = Area under Disease Progress Curve
Table 8. Pearson’s Correlations Between Stem Rust Epidemiological Parameters and Yield-Related Traits at Sinana (2022 Main Cropping Season).

CIV

DH (no)

DM (no)

Std (no)

PH (cm)

Yld (kg)

TKW (g)

SL (cm)

SPS (no)

Tlr (no)

SP (no)

CIV

1

DH

-0.01

1

DM

-0.05

0.34

1

Stand

-0.06

0.21

0.01

1

PH

-0.02

-0.07

-0.03

0.31

1

Yield

-0.18

0.24

0.02

0.43

0.37

1

TKW

-0.27

0.09

-0.04

0.11

0.32

0.61

1

SL

0.02

0.15

0.05

-0.01

0.11

0.2

0.24

1

SS

-0.11

0.27

0.15

-0.03

0.02

0.04

-0.02

0.24

1

Tiller

0.07

0.05

-0.07

-0.03

-0.03

-0.07

0

0.04

0.09

1

SSP

0.11

0.25

0.08

0.28

0.14

0.33

0.17

0.21

0.2

-0.03

1

CI= correlation coefficients; DH=Days Heading; DM= Days
4. Conclusion and Recommendations
Seedling resistance was observed in several advanced wheat lines and cultivars. Seven lines showed resistance to all eleven races, while 68 lines had varied reactions. Lines with single-gene race-specific resistance are recommended for crossing programs. Those with high infection types should be used in adult plant resistance studies.
Abbreviations

AARC

Ambo Agricultural Research Center

CRD

Completely Randomized Design

Pgt

Puccinia Graminis Tritici

CI

Coefficient Infection

IT

Infection Iype

AUDPC

Area Under Disease Progress Curve

FRS

Final Rust Severity

LIT

Low Infection Type

HIT

High Infection Type

Acknowledgments
The author gratefully acknowledges the Oromia Agricultural Research Institute for financial support, and Sinana Agricultural Research Center for providing logistical assistance. Special thanks are extended to the Plant Pathology Research team and technical assistants for their valuable contribution to data collection.
Author Contributions
Tamene Mideksa: Conceptualization, Data curation, Formal Analysis, Funding acquisition, Investigation, Methodology, Software, Writing – original draft
Zerihun Eshetu: Data curation, Formal Analysis, Investigation, Software
Conflicts of Interest
The authors declare no conflicts of interest.
Appendix
Table A1. Plant Materials Used in the Study.Plant Materials Used in the Study.Plant Materials Used in the Study.

No

Cross Name

1

MUCUY

2

ATTILA*2/PBW65*2//KACHU/6/BECARD #1/5/KIRITATI/4/2*SERI.1B*2/3/KAUZ*2/BOW//KAUZ

3

BORL14/ABLEU

4

BORL14/ABLEU

5

ABLEU//KACHU/DANPHE

6

SUP152*2/BECARD//KACHU/DANPHE

7

HUW234+LR34/PRINIA//INQALAB 91*2/KUKUNA/3/FRET2*2/SHAMA/4/2*BECARD//ND643/2*WBLL1

8

KACHU//WBLL1*2/BRAMBLING*2/6/BECARD #1/5/KIRITATI/4/2*SERI.1B*2/3/KAUZ*2/BOW//KAUZ

9

KACHU//WBLL1*2/BRAMBLING*2/6/BECARD #1/5/KIRITATI/4/2*SERI.1B*2/3/KAUZ*2/BOW//KAUZ

10

FRNCLN*2/TECUE #1*2/3/ATTILA*2/PBW65*2//MURGA

11

ABLEU*2/BORL14

12

ABLEU*2/BORL14

13

SUP152*2/TECUE #1//2*ABLEU

14

PAURAQ/VILLA JUAREZ F2009*2/4/WBLL1/FRET2//PASTOR*2/3/MURGA

15

BECARD/CHYAK/3/2*PBW343*2/KUKUNA*2//FRTL/PIFED

16

ATTILA/3*BCN//BAV92/3/PASTOR/4/TACUPETO F2001*2/BRAMBLING/5/PAURAQ*2/6/FRNCLN*2/TECUE #1

17

WBLL4/KUKUNA//WBLL1/3/WBLL1*2/BRAMBLING/4/2*PCAFLR/KINGBIRD #1//KIRITATI/2*TRCH

18

BORL14//KACHU/KIRITATI

19

BORL14//KACHU/KIRITATI

20

KACHU/DANPHE//KFA/2*KACHU

21

KACHU/DANPHE//KFA/2*KACHU

22

KACHU/DANPHE//KFA/2*KACHU

23

KACHU//KIRITATI/2*TRCH/3/KFA/2*KACHU

24

ND643/2*WBLL1/4/WHEAR/KUKUNA/3/C80.1/3*BATAVIA//2*WBLL1/5/BORL14

25

SUP152/2*DANPHE #1//BORL14

26

SUP152/2*DANPHE #1//BORL14

27

KRONSTAD F2004/KENYA SUNBIRD//WHEAR/KRONSTAD F2004/3/WBLL1*2/BRAMBLING*2//BAVIS

28

KENYA SUNBIRD/2*KACHU/3/SWSR22T.B./2*BLOUK #1//WBLL1*2/KURUKU

29

PFAU/MILAN/5/CHEN/AEGILOPS SQUARROSA (TAUS)//BCN/3/VEE#7/BOW/4/PASTOR/6/2*BAVIS #1/7/BORL14

30

WHEAR/KUKUNA/3/C80.1/3*BATAVIA//2*WBLL1*2/4/NIINI #1/5/KACHU/DANPHE

31

BECARD//ND643/2*WBLL1/3/KACHU/DANPHE

32

KFA/2*KACHU*2//MUTUS*2/CHONTE

33

KACHU//KIRITATI/WBLL1*2/3/TAITA

34

ATTILA/3*BCN//BAV92/3/PASTOR/4/TACUPETO F2001*2/BRAMBLING/5/PAURAQ*2/6/SUP152/KENYA SUNBIRD

35

KACHU/BECARD//WBLL1*2/BRAMBLING*2/3/VILLA JUAREZ F2009/DANPHE #1

36

ND643/2*TRCH//BECARD/3/BECARD*2/4/MUU/FRNCLN

37

WBLL1*2/BRAMBLING//WBLL1*2/SHAMA/3/WBLL1*2/BRAMBLING*2/6/KAUZ//ALTAR 84/AOS/3/PASTOR/4/873.97/5/MUNAL #1

38

HEILO//MILAN/MUNIA/3/KIRITATI/2*TRCH/4/2*KACHU/KIRITATI

39

VILLA JUAREZ F2009/DANPHE #1//MUTUS*2/CHONTE/4/ATTILA*2/PBW65//FRNCLN/3/FRANCOLIN #1

40

MUTUS*2/HARIL #1/3/SWSR22T.B./2*BLOUK #1//WBLL1*2/KURUKU/4/MUTUS*2/HARIL #1

41

PASTOR/3/VORONA/CNO79//KAUZ/4/MILAN/OTUS//ATTILA/3*BCN/5/MUNAL #1/6/2*KFA/2*KACHU

42

WHEAR/KUKUNA/3/C80.1/3*BATAVIA//2*WBLL1*2/4/KENYA SUNBIRD*2/5/ABLEU

43

WHEAR/KUKUNA/3/C80.1/3*BATAVIA//2*WBLL1*2/4/KENYA SUNBIRD*2/5/ABLEU

44

WHEAR/KUKUNA/3/C80.1/3*BATAVIA//2*WBLL1/4/PAURAQUE #1/5/WHEAR/KUKUNA/3/C80.1/3*BATAVIA//2*WBLL1/6/2*KACHU/DANPHE

45

CHYAK1/VILLA JUAREZ F2009//WBLL1*2/BRAMBLING/7/PRL/2*PASTOR/4/CHOIX/STAR/3/HE1/3*CNO79//2*SERI/5/KIRITATI/2*TRCH/6/ PRL/2*PASTOR/4/CHOIX/STAR/3/HE1/3*CNO79//2*SERI/8/KACHU/DANPHE

46

MUTUS*2//ND643/2*WBLL1/3/2*SWSR22T.B./KACHU//2*KACHU

47

MUTUS*2//ND643/2*WBLL1/3/2*SWSR22T.B./KACHU//2*KACHU

48

SUP152*2/TINKIO #1/4/FRET2*2/SHAMA//KIRITATI/2*TRCH/3/BAJ #1/5/SUP152*2/TINKIO #1

49

WBLL1*2/BRAMBLING//TAM200/TUI/3/VILLA JUAREZ F2009/4/2*BORL14

50

SWSR22T.B./FRANCOLIN #1//2*FRNCLN/5/WHEAR/KUKUNA/3/C80.1/3*BATAVIA//2*WBLL1*2/4/NIINI #1/6/ BORL14

51

KACHU*2/3/ND643//2*PRL/2*PASTOR/4/2*KACHU/DANPHE

52

KACHU*2/3/ND643//2*PRL/2*PASTOR/4/2*KACHU/DANPHE

53

KACHU*2/3/ND643//2*PRL/2*PASTOR/4/2*KACHU/DANPHE

54

PRL/2*PASTOR*2//FH6-1-7/3/COPIO

55

QUAIU/MUNAL//QUAIU #2/3/SUP152/BAJ #1

56

SHORTENED SR26 TRANSLOCATION/4/3*CHIBIA//PRLII/CM65531/3/MISR 2/5/SHORTENED SR26 TRANSLOCATION//2*WBLL1*2/KKTS/3/BECARD

57

WAXWING*2/TUKURU//2*FRNCLN/3/BORL14

58

WHEAR/KUKUNA/3/C80.1/3*BATAVIA//2*WBLL1/4/PAURAQUE #1/5/WHEAR/KUKUNA/3/C80.1/3*BATAVIA//2*WBLL1/6/BORL14

59

PAURAQ/NELOKI/3/WBLL1*2/BRAMBLING*2//BAVIS

60

KACHU/DANPHE*2//MUNAL #1

61

KACHU/DANPHE*2//KFA/2*KACHU

62

KACHU/DANPHE*2//KENYA SUNBIRD/KACHU

63

KACHU/DANPHE*2//KENYA SUNBIRD/KACHU

64

KACHU/DANPHE*2//KENYA SUNBIRD/KACHU

65

BAVIS #1//ND643/2*WBLL1*2/3/BORL14

66

KUTZ/MUCUY

67

WBLL1*2/BRAMBLING//QUAIU/3/KFA/2*KACHU

68

MUTUS/AKURI #1//MUTUS/3/KACHU #1/KIRITATI//KACHU

69

KACHU/DANPHE/3/KACHU//KIRITATI/2*TRCH

70

KACHU/DANPHE/3/KACHU//KIRITATI/2*TRCH

71

KACHU/DANPHE/3/KACHU//KIRITATI/2*TRCH

72

KACHU/DANPHE/3/KACHU//KIRITATI/2*TRCH

73

KACHU/DANPHE/3/KACHU//KIRITATI/2*TRCH

74

KACHU/DANPHE/3/KACHU//KIRITATI/2*TRCH

75

KACHU/DANPHE/3/KACHU//KIRITATI/2*TRCH

76

KACHU/DANPHE/3/KACHU//KIRITATI/2*TRCH

77

KACHU/DANPHE/3/KACHU//KIRITATI/2*TRCH

78

KACHU/DANPHE/3/KACHU//KIRITATI/2*TRCH

79

KACHU/DANPHE/3/KACHU//KIRITATI/2*TRCH

80

KACHU/DANPHE/3/KACHU//KIRITATI/2*TRCH

81

KACHU/DANPHE/3/KACHU//KIRITATI/2*TRCH

82

KACHU/DANPHE/3/KACHU//KIRITATI/2*TRCH

83

KACHU/DANPHE/3/KACHU//KIRITATI/2*TRCH

84

KINGBIRD #1//INQALAB 91*2/TUKURU*2/3/KACHU/KIRITATI

85

BECARD/FRNCLN//KACHU/KIRITATI/3/BOKOTA

86

ROLF07*2/SHORTENED SR26 TRANSLOCATION//SUP152/BAJ #1/3/KACHU #1/KIRITATI//KACHU

87

KENYA SUNBIRD/KACHU/3/2*WBLL1*2/BRAMBLING*2//BAVIS

88

SOKOLL/3/PASTOR//HXL7573/2*BAU/4/WHEAR/SOKOLL/5/2*SUP152/BAJ #1

89

SOKOLL/3/PASTOR//HXL7573/2*BAU/4/MASSIV/PPR47.89C/5/2*BORL14

90

KAUZ//ALTAR 84/AOS/3/MILAN/KAUZ/4/SAUAL/5/SERI.1B//KAUZ/HEVO/3/AMAD*2/4/KIRITATI/6/BORL14/7/KACHU/SAUAL /4/ATTILA*2/PBW65//PIHA/3/ATTILA/2*PASTOR

91

ATTILA*2/PBW65*2//KACHU/6/BECARD #1/5/KIRITATI/4/2*SERI.1B*2/3/KAUZ*2/BOW//KAUZ

92

BORL14/5/ATTILA/3*BCN*2//BAV92/3/KIRITATI/WBLL1/4/DANPHE

93

ATTILA/3*BCN*2//BAV92/3/KIRITATI/WBLL1/4/DANPHE/5/KACHU/DANPHE

94

SUP152/BAJ #1*2/3/KINGBIRD #1//INQALAB 91*2/TUKURU

95

TUKURU//BAV92/RAYON/3/FRNCLN/4/2*FRNCLN*2/TECUE #1

96

ATTILA/3*BCN*2//BAV92/3/KIRITATI/WBLL1/4/DANPHE*2/5/BORL14

97

ATTILA/3*BCN*2//BAV92/3/KIRITATI/WBLL1/4/DANPHE*2/5/BORL14

98

SUP152*2/TECUE #1/5/2*ATTILA/3*BCN*2//BAV92/3/KIRITATI/WBLL1/4/DANPHE

99

KACHU/DANPHE//BORL14

100

KACHU/DANPHE//BORL14

References
[1] Admassu, B., Friedt, W. and Ordon, F., 2012. Stem rust seedling resistance genes in Ethiopian wheat cultivars and breeding lines. African Crop Science Journal, 20(3); 149-162.
[2] Ali, S., Shah, S. J. A., RAHMAN, H. U., Saqib, M. S., Ibrahim, M. and Sajjad, M., 2009. Variability in wheat yield under yellow rust pressure in Pakistan. Turkish Journal of Agriculture and Forestry, 33(6); 537-546.
[3] Ayele B, and Bekele H. (2016). Incidence and Challenges of Rust Diseases in Wheat Production. pp. 41-51. In: Z. Bishaw et al. (eds.) Containing the menace of wheat rusts: Institutional intervention and impacts. Ethiopian Institute of Agricultural Research and International Centre for Agricultural Research in the Dry Areas. Addis Ababa, Ethiopia.
[4] Cao, Q., Hu, Q. H., Khan, S., Wang, Z. J., Lin, A. J., Du, X. and Zhu, Y. G., 2007. Wheat phytotoxicity from arsenic and cadmium separately and together in solution culture and in a calcareous soil. Journal of hazardous materials, 148(1); 377-382.
[5] Flor, H. H., 1956. The complementary genetic systems in flax and flax rust. Adv. Genet. 8: 29-54.
[6] Hei, N. B., Tsegaab T, Getaneh. W, Endale H, B. Hundie, Daniel K, Fikirte, Fufa A, Wubishet A, Teklay A. 2018, Distribution and frequency of wheat stem rust races (Puccinia graminis f. sp. tritici) in Ethiopia. Journal of Agricultural and Crop Research 6(5); 88-96.
[7] Hei, N T. Tsegaab, W. Getaneh, T. Girma, C. Obsa, A. Seyoum, E. Zerihun, K. Nazari, E. Kurtulus, H. Kavaz, I. Ozseven, A. Yoseph., 2020 “First Report of Puccinia graminis f.sp.tritici Race TTKTT in Ethiopia”.
[8] Huerta-Espino, J., Singh, R., Crespo-Herrera, L. A., Villaseñor-Mir, H. E., Rodriguez-Garcia, M. F., Dreisigacker, S., Barcenas-Santana, D. and Lagudah, E., 2020. Adult plant slow rusting genes confer high levels of resistance to rusts in bread wheat cultivars from Mexico. Frontiers in Plant Science, 11; 824.
[9] Huerta-Espino, J., Singh, R. P., German, S., McCallum, B. D., Park, R. F., Chen, W. Q., Bhardwaj, S. C. and Goyeau, H., 2011. Global status of wheat leaf rust caused by Puccinia triticina. Euphytica, 179; 143-160.
[10] Jin, Y., Singh, R. P., Ward, R. W., Wanyera, R., Kinyua, M., Njau, P., et al. (2007). Characterization of seedling infection types and adult plant infection responses of monogenic Sr gene lines to race TTKS of Puccinia graminis f. sp. tritici. Plant Dis. 91, 1096–1099.
[11] Jin Y, Szabo LJ, Pretorius ZA, Singh RP, Ward RW, Fetch TJ. 2008. Detection of virulence to resistance gene Sr24 within race TTKS of Puccinia graminis f. sp. tritici. Plant Dis. 2008; 92: 923±926.
[12] Lagudah, E. S., 2011. Molecular genetics of race non-specific rust resistance in wheat. Euphytica, 179(1); 81-91.
[13] Mabrouk, O. I., El-Orabey, W. M. and Esmail, S. M., 2019. Evaluation of wheat cultivars for slow rusting resistance to leaf and stem rust diseases in Egypt. Egyptian Journal of Phytopathology, 47(2); 1-19.
[14] McNeil, M. D., Kota, R., Paux, E., Dunn, D., McLean, R., Feuillet, C., Li, D., Kong, X., Lagudah, E., Zhang, J. C., Jia, J. Z., Spielmeyer, W., Bellgard, M. and Appels, R. (2008) BAC-derived markers for assaying the stem rust resistance gene, Sr2, in wheat breeding programs. Auarura Ge’erriSfB, 221: 15- 24.
[15] Njau, P. N., Wanyera, R., Macharia, G. K., Macharia, J., Singh, R. and Keller, B., 2009. Resistance in Kenyan bread wheat to recent eastern African isolate of stem rust, Puccinia graminis f. sp. tritici, Ug99. Journal of Plant Breeding and Crop Science, 1(2); 022-027.
[16] Peterson, R. F., Campbell, A. B. and Hannah, A. E., 1948. A diagrammatic scale for estimating rust intensity on leaves and stems of cereals. Canadian journal of research, 26(5); 496-500.
[17] Pretorius, Z. A., Singh, R. P., Wagoire, W. W. and Payne, T. S., 2000. Detection of virulence to wheat stem rust resistance gene Sr31 in Puccinia graminis. f. sp. tritici in Uganda. Plant disease, 84(2); 203-203.
[18] Roelfs, A. P. and Martens, J. W., 1988. An international system of nomenclature for Puccinia graminis f. sp. tritici. Phytopathology, 78(5); 526-533.
[19] Roelfs, A. P., Singh, R. P. and Saari, E. E., 1992. Rust diseases of wheat: concepts and methods of disease management. Cimmyt.
[20] Safavi, S. A., and Afshari, F., 2012. Identification of resistance to Puccinia striiformis f.sp. tritici in some elite wheat genotypes. Journal of Crop Protection 1: 293-302.
[21] Safavi, SA., 2012. Evaluation of slow rusting parameters in thirty seven promising wheat genotypes to yellow rust. Tech. J. Eng. Appl. Sci. 2: 324-329.
[22] Stakman, E. C., Stewart, D. M. and Loegering, W. Q., 1962.. Identification of physiologic races of Puccinia graminis var. tritici. U. S. Dep. Agric. Bur. Entomol. Plant Quarantine Bull. E-617 (Rev.). 53 p.
[23] Stubbs, R. W., 1985. Stripe rust. In Diseases, distribution, epidemiology, and control (pp. 61-101). Academic Press.
[24] Wang ZL, Li LH, He ZH, Duan XY, Zhou YL, et al. (2005) Seedling and adult plant resistance to powdery mildew in Chinese bread wheat cultivars and lines. Plant Disease 89: 457-463.
[25] Wellings, C. R., 2011. Global status of stripe rust: a review of historical and current threats. Euphytica, 179(1); 129-141.
Cite This Article
  • APA Style

    Mideksa, T., Eshetu, Z. (2025). Evaluation of Adult Plant Resistance in Bread Wheat (Triticum aestivum L.) Genotypes to Wheat Stem Rust (Puccinia graminis f. sp. tritici) Races in Ethiopia. American Journal of Plant Biology, 10(4), 121-132. https://doi.org/10.11648/j.ajpb.20251004.16

    Copy | Download

    ACS Style

    Mideksa, T.; Eshetu, Z. Evaluation of Adult Plant Resistance in Bread Wheat (Triticum aestivum L.) Genotypes to Wheat Stem Rust (Puccinia graminis f. sp. tritici) Races in Ethiopia. Am. J. Plant Biol. 2025, 10(4), 121-132. doi: 10.11648/j.ajpb.20251004.16

    Copy | Download

    AMA Style

    Mideksa T, Eshetu Z. Evaluation of Adult Plant Resistance in Bread Wheat (Triticum aestivum L.) Genotypes to Wheat Stem Rust (Puccinia graminis f. sp. tritici) Races in Ethiopia. Am J Plant Biol. 2025;10(4):121-132. doi: 10.11648/j.ajpb.20251004.16

    Copy | Download

  • @article{10.11648/j.ajpb.20251004.16,
      author = {Tamene Mideksa and Zerihun Eshetu},
      title = {Evaluation of Adult Plant Resistance in Bread Wheat (Triticum aestivum L.) Genotypes to Wheat Stem Rust (Puccinia graminis f. sp. tritici) Races in Ethiopia},
      journal = {American Journal of Plant Biology},
      volume = {10},
      number = {4},
      pages = {121-132},
      doi = {10.11648/j.ajpb.20251004.16},
      url = {https://doi.org/10.11648/j.ajpb.20251004.16},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ajpb.20251004.16},
      abstract = {A field experiment was conducted during the 2021 main cropping season using an augmented design to evaluate adult plant resistance in bread wheat genotypes against wheat stem rust (Puccinia graminis f. sp. tritici) in Ethiopia. Final rust severity (FRS), coefficient of infection (CI), and relative area under the disease progress curve (rAUDPC) were used to identify slow rusting genotypes. These parameters proved reliable for assessing resistance. Eleven Pgt races were tested on 20 near-isogenic lines carrying single stem rust resistance genes. Greenhouse results showed seven lines were resistant to all races. Genotypes were grouped based on infection types: Group I (e.g., genotypes 40 and 56) showed low infection types (ITs); Group II (e.g., genotypes 2, 3, 12, 13, 43, 91, 98) showed high ITs; Group III included 68 lines with variable reactions. TTKTF and TKPTF caused the highest ITs, while TTKTT showed the lowest. Thirty slow rusting genotypes were identified based on field FRS (Trace MS to 25 MS) and seedling ITs (2+ to 4). These cultivars offer valuable genetic resources for wheat improvement programs targeting durable resistance to stem rust. These findings demonstrate the importance of combining field-based slow rusting parameters with greenhouse race-specific evaluations to obtain a comprehensive understanding of resistance. The identification of genotypes with stable resistance across multiple environments provides a strong foundation for breeding programs aimed at durable stem rust resistance. Such cultivars are particularly valuable in Ethiopia, where stem rust epidemics pose a recurring threat to wheat production and national food security. This study contributes to the global effort of developing improved wheat varieties by offering genetic resources that can be integrated into international breeding pipelines. By highlighting both race-specific and slow rusting resistance, the research underscores the need for continuous monitoring of pathogen variability and the deployment of diverse resistance genes to ensure long-term effectiveness.},
     year = {2025}
    }
    

    Copy | Download

  • TY  - JOUR
    T1  - Evaluation of Adult Plant Resistance in Bread Wheat (Triticum aestivum L.) Genotypes to Wheat Stem Rust (Puccinia graminis f. sp. tritici) Races in Ethiopia
    AU  - Tamene Mideksa
    AU  - Zerihun Eshetu
    Y1  - 2025/12/29
    PY  - 2025
    N1  - https://doi.org/10.11648/j.ajpb.20251004.16
    DO  - 10.11648/j.ajpb.20251004.16
    T2  - American Journal of Plant Biology
    JF  - American Journal of Plant Biology
    JO  - American Journal of Plant Biology
    SP  - 121
    EP  - 132
    PB  - Science Publishing Group
    SN  - 2578-8337
    UR  - https://doi.org/10.11648/j.ajpb.20251004.16
    AB  - A field experiment was conducted during the 2021 main cropping season using an augmented design to evaluate adult plant resistance in bread wheat genotypes against wheat stem rust (Puccinia graminis f. sp. tritici) in Ethiopia. Final rust severity (FRS), coefficient of infection (CI), and relative area under the disease progress curve (rAUDPC) were used to identify slow rusting genotypes. These parameters proved reliable for assessing resistance. Eleven Pgt races were tested on 20 near-isogenic lines carrying single stem rust resistance genes. Greenhouse results showed seven lines were resistant to all races. Genotypes were grouped based on infection types: Group I (e.g., genotypes 40 and 56) showed low infection types (ITs); Group II (e.g., genotypes 2, 3, 12, 13, 43, 91, 98) showed high ITs; Group III included 68 lines with variable reactions. TTKTF and TKPTF caused the highest ITs, while TTKTT showed the lowest. Thirty slow rusting genotypes were identified based on field FRS (Trace MS to 25 MS) and seedling ITs (2+ to 4). These cultivars offer valuable genetic resources for wheat improvement programs targeting durable resistance to stem rust. These findings demonstrate the importance of combining field-based slow rusting parameters with greenhouse race-specific evaluations to obtain a comprehensive understanding of resistance. The identification of genotypes with stable resistance across multiple environments provides a strong foundation for breeding programs aimed at durable stem rust resistance. Such cultivars are particularly valuable in Ethiopia, where stem rust epidemics pose a recurring threat to wheat production and national food security. This study contributes to the global effort of developing improved wheat varieties by offering genetic resources that can be integrated into international breeding pipelines. By highlighting both race-specific and slow rusting resistance, the research underscores the need for continuous monitoring of pathogen variability and the deployment of diverse resistance genes to ensure long-term effectiveness.
    VL  - 10
    IS  - 4
    ER  - 

    Copy | Download

Author Information
  • Abstract
  • Keywords
  • Document Sections

    1. 1. Introduction
    2. 2. Materials and Methods
    3. 3. Results and Discussion
    4. 4. Conclusion and Recommendations
    Show Full Outline
  • Abbreviations
  • Acknowledgments
  • Author Contributions
  • Conflicts of Interest
  • Appendix
  • References
  • Cite This Article
  • Author Information