Identification of stem rust resistance genes in wheat cultivars in China using molecular markers.

Wheat stem rust caused by Puccinia graminis f. sp. tritici Eriks. & E. Henn. (Pgt), is a major disease that has been effectively controlled using resistance genes. The appearance and spread of Pgt races such as Ug99, TKTTF, and TTTTF, which are virulent to most stem rust-resistant genes currently deployed in wheat breeding programs, renewed the interest in breeding cultivars resistant to wheat stem rust. It is therefore important to investigate the levels of resistance or vulnerability of wheat cultivars to Pgt races. Resistance to Pgt races 21C3CTHQM, 34MKGQM, and 34C3RTGQM was evaluated in 136 Chinese wheat cultivars at the seedling stage. A total of 124 cultivars (91.2%) were resistant to the three races. Resistance genes Sr2, Sr24, Sr25, Sr26, Sr31, and Sr38 were analyzed using molecular markers closely linked to them, and 63 of the 136 wheat cultivars carried at least one of these genes: 21, 25, and 28 wheat cultivars likely carried Sr2, Sr31, and Sr38, respectively. Cultivars "Kehan 3" and "Jimai 22" likely carried Sr25. None of the cultivars carried Sr24 or Sr26. These cultivars with known stem rust resistance genes provide valuable genetic material for breeding resistant wheat cultivars.

Introduction

Wheat stem rust caused by Puccinia graminis Per. f. sp. tritici Eriks. & E. Henn. (Pgt) is a devastating disease that has caused severe yield losses worldwide. Since the deployment of stem rust-resistant wheat cultivars in the second half of the 20th century, stem rust has been successfully controlled in most wheat cultivating areas (Chen et al., 2015). However, a new race of the stem rust pathogen (Ug99), identified in Uganda in 1999 and highly virulent to resistance gene Sr31, was designated as TTKSK under the North American nomenclature system (Pretorius et al., 2000). Within a few years, virulence of TTKSK to other important stem rust resistance genes (e.g., Sr24, Sr36, Sr9h, Sr31 + Sr24, Sr31 + Sr36, and Sr31 + SrTmp) was detected (BGRI, 2017; Jin et al., 2008, 2009; Pretorius et al., 2012; Rouse et al., 2014), and 13 variants of Ug99 have now been documented across wheat growing regions in 13 countries (Food and Agriculture Organization of the United Nations (FAO), 2017). Realizing the disastrous threat on world food security posed by the Ug99 race group, Nobel Peace Prize laureate Norman Borlaug called for a coordinated global campaign to reduce wheat rust epidemics and mitigate the potential impact on food security. The resistance of worldwide wheat accessions (over 200,000) to the Ug99 group was screened in Kenya (He, Xia & Chen, 2008). The results indicated that only 5–15% of the wheat accessions grown globally were resistant to Ug99, and only two of the 118 Chinese wheat cultivars (“Jimai 20” and “Linmai 6”) were resistant to Ug99. The high susceptibility (85–95%) of wheat lines to Ug99 highlighted the potential threat of this group to wheat production worldwide. Furthermore, other broadly virulent Pgt races caused wheat stem rust epidemics in recent years. The new race TKTTF (from a genetic lineage distinct from that of Ug99) virulent to the widely grown wheat cultivar “Digalu,” caused yield losses close to 100% in Southern Ethiopia during 2013–2014 (Olivera et al., 2015). In 2016, a new and unusually devastating strain of Pgt named TTTTF (virulent to Sr9e and Sr13) caused the largest outbreak and epidemics of wheat stem rust in Sicily since the 1950s (Bhattacharya, 2017), as tens of thousands of hectares of both durum wheat and bread wheat were infected. Thus, wheat stem rust seems to have returned.

The most effective way to control wheat stem rust is by using resistant genes against this disease to breed and propagate resistant varieties (Pathan & Park, 2007). However, an important issue in the use of resistant varieties is that the simplification of the resistance source may be overcome by variation in the pathogen, resulting in the loss of resistance. Understanding resistance gene content of wheat varieties can effectively avoid this situation, and provide a basis for the reasonable distribution of varieties. Moreover, it is also helpful to discover new genes, enriching the gene pool, and for breeding resistant varieties. Nevertheless, the spread of new Pgt races and their variants threatens the safety of wheat production in China (Li et al., 2016). If the conditions are suitable, there is the possibility of wheat stem rust becoming a significant disease. Because the resistance of Chinese wheat varieties to the new races Ug99, TKTTF, and TTTTF is very poor, if these races spread into China they will cause massive losses in wheat production (Cao et al., 2007). We should therefore make full use of wheat cultivar resources to screen for resistant materials. Given the importance of understanding disease resistance genes, those against Ug99, TKTTF, and TTTTF races have been screened and identified worldwide since these races were reported.

In our previous study, the prevalence of Sr2, Sr24, Sr25, Sr26, Sr31, and Sr38 in wheat cultivars from Gansu and Yunnan Province has been finished (Li et al., 2016; Xu et al., 2017), and based on it, this study was carried out. We collected 136 wheat cultivars from two different localities presenting epidemic patterns of wheat stem rust to examine their resistance level to the predominant races of Pgt in China. Resistance genes Sr2, Sr24, Sr25, Sr26, Sr31, and Sr38 were detected using molecular markers aiming to screen and identify cultivars that are potentially resistant to emerging races (especially to Ug99, TKTTF, and TTTTF) and map the distribution of those genes in wheat regions based on wheat cultivars’ resistance level to predominant races of Pgt. Thus far, our team have identified and characterized these resistant genes in four wheat-producing regions of China (Fig. 1), which will contribute to the deployment of wheat stem rust resistance genes and control of large-scale epidemics of this disease. Additionally, this information will be important for developing potentially durable combinations of stem rust resistance genes in wheat cultivars.

Figure 1

Epidemic patterns of wheat stem rust in four wheat-producing regions in China.

Materials and Methods

Wheat cultivars (lines) and Pgt races

A total of 136 wheat cultivars (lines) were collected from the largest wheat growing regions in China: the Northeastern spring-wheat growing provinces and the lower-middle Yangtze River basin and central winter-wheat growing provinces. All wheat accessions were provided by researchers from Heilongjiang, Inner Mongolia, Shandong, Shanxi, Anhui, Jiangsu, Beijing, and Ningxia Academies of Agricultural Sciences. A total of six monogenic wheat lines carrying individual Sr genes (Sr2, Sr24, Sr25, Sr26, Sr31, and Sr38), and 29 differentials for Pgt, including the original four Stakman differentials (Little Club, Reliance, Einkorn, and Vernal), five Chinese differentials (Mianzi 52, Huadong 6, Mini 2761, Orofen, and Rulofen), and 20 single Sr-gene lines from North America (Sr5, Sr21, Sr9e, Sr7b, Sr11, Sr6, Sr8a, Sr9g, Sr36, Sr9b, Sr30, Sr17, Sr9a, Sr9d, Sr10, SrTmp, Sr24, Sr31, Sr38, and SrMcN) used worldwide, were provided by the Plant Immunity Institute, Shenyang Agricultural University, China.

Races 21C3CTHQM (Pgt isolate Ab3), 34MKGQM (Pgt isolate H31), and 34C3RTGQM (Pgt isolate XN11) (a new race identified from the alternative host Berberis sp.) were used for evaluating seedling stem rust response in the tested cultivars. These races were isolated and identified by the Plant Immunity Institute, Shenyang Agricultural University, China. The names, virulence/avirulence spectrums, and urediniospores produced method of races were described by Li et al. (2016) and Xu et al. (2017).

Seedling infection types

The 136 wheat accessions were planted in 10-cm diameter porcelain pots (each pot contained one cultivar represented by eight to 10 seedlings). A mixture of urediniospores and dried talc (1 g), in a ratio of 1:20 (v:v), was sprayed onto the fully expanded primary leaves of seedling (seven to eight days old) moistened with 0.05% Tween-20. The detail inoculation and cultivation methods followed Xu et al. (2017). Three replicates of the seedling assays were performed for each Pgt race. Infection types (ITs) were assessed two weeks after inoculation using the 0–4 IT scale, as described by Stakman, Stewart & Loegering (1962).

DNA extraction

DNA was extracted from the young leaves of seven-day old seedlings grown to the one-leaf stage, using a DNA extraction kit (Sangon Biotech, Shanghai, China). PCR amplifications were followed Xu et al. (2017). Primers were synthesized by Sangon Biotech (China) (Table 1), and PCR amplification conditions were as described in previous studies (Table 1). Fragments of the targeted genes were detected by electrophoresis using 2% (W/V) agarose gels and then gels were observed under UV light.

Table 1

PCR primers and conditions for the amplification of the tested markers.

Marker	Primers	PCR conditions
		Temperature (°C)/time	Number of cycles cycle
Xgwm533	5′-GTTGCTTTAGGGGAAAAGCC5′-AAGGCGAATCAAACGGAATA	92/3 min	One
		92/30 s; 62/30 s; 72/30 s	1 °C Reducing/cycle for seven cycles
		92/30 s; 62/30 s; 72/30 s	47
Sr24#12	5′-CACCCGTGACATGCTCGTA5′-AACAGGAAATGAGCAACGATGT	94/3 min	One
		94/30 s; 65/30 s; 72/40 s	1 °C Reducing/cycle for seven cycles
		94/30 s; 58/30 s; 72/40 s	30
		20/1 min	One
Gb	5′-CATCCTTGGGGACCTC5′-CCAGCTCGCATACATCCA	94/3 min	One
		94/30 s; 60/30 s; 72/40 s	30
		20/1 min	One
Sr26#43	5′-AATCGTCCACATTGGCTTCT5′-CGCAACAAAATCATGCACTA	94/3 min	One
		94/30 s; 56/30 s; 72/40 s	30
		20/1 min	One
SCSS30.2576	5′-GTCCGACAATACGAACGATT5′-CCGACAATACGAACGCCTTG	95/5 min; 60/1 min; 72/30 s	One
		95/1 min; 60/1 min; 72/30 s	35
		72/10 min	One
Iag 95	5′-CTCTGTGGATAGTTACTTGATCGA5′-CCTAGAACATGCATGGCTGTTACA	94/3 min	One
		94/30 s; 55/60 s; 72/70 s	30
		25/60 s	One
VENTRIUP-LN2	5′-AGGGGCTACTGACCAAGGCT5′-TGCAGCTACAGCAGTATGTACACAAAA	94/45 s	One
		94/45 s; 65/30 s; 72/7 min	30
		72/1 min	One

Results

Wheat seedling resistance

The ITs produced by wheat cultivars to races 21C3CTHQM, 34MKGQM, and 34C3RTGQM are listed in Table 2. A total of 124 (91.2%) wheat cultivars were resistant to the three races (ITs 2, 1+, or lower) while the remaining 12 were susceptible (ITs 3-, 3, 3+, and 4) (Fig. 2). A total of 48 wheat cultivars (35.3%) showed IT 0 to all tested races (Fig. 2) and 127 showed resistance to the new race 34C3RTGQM.

Table 2

Seedling infection types and resistance genes.

Cultivars	Province	Pedigree	Infection typesa			Sr2	Sr24	Sr25	Sr26	Sr31		Sr38
			21C3CTHQM	34MKGQM	34C3RTGQM	Xgwm533	Sr24#12	Gb	Sr26#43	SCSS30.2576	Iag95	VENTRIUP-LN2
Xinkehan 9	Heilongjiang	Kefeng 2/Ke74F3-249-3	;1	1	;	−b	−	−	−	−	−	−
Kehan 2	Heilongjiang	Jiusan 80 jian 119/Nongda75-65533	;1	1	1	−	−	−	−	−	−	+
Kehan 3	Heilongjiang	Ke 61F3-199/Agropyron glaucum	0	0	0	−	−	+	−	−	−	−
Kehan 4	Heilongjiang	Kezhen/Kehong	;1	1	1+	−	−	−	−	−	−	+
Kehan 8	Heilongjiang	Ke65F2-196-7/Rulofen	;	0	0	−	−	−	−	−	−	−
Kehan 9	Heilongjiang	Kefeng 2/Ke 74F3-249-3	;	0	0	−	−	−	−	−	−	−
Kehan 10	Heilongjiang	Kefeng 2//T808/Ke 69-513	;	1	0	−	−	−	−	−	−	−
Kehan 11	Heilongjiang	Ke 73-402/Bei 74-205	;	0	0	+	−	−	−	−	−	−
Kehan 12	Heilongjiang	Ke 68-88/Ke 68-585-13	;	1	1	−	−	−	−	−	−	+
Kehan 13	Heilongjiang	Kefeng 3/Kehan 8	;1	0	0	−	−	−	−	−	−	−
Kehan 14	Heilongjiang	Ke 80-10-1/Ke 81 hou 88-0-1	;	1−	1	−	−	−	−	−	−	+
Kehan 15	Heilongjiang	Ke 86F2-172/Ke 86F5-325-3	0	0	0	−	−	−	−	−	−	−
Kehan 16	Heilongjiang	Jiusan 79F5-541/Ke 80 yuan 229//Ke 76-750/76F4-779-5//Ke76-413	0	0	0	−	−	−	−	−	−	+
Kehan 18	Heilongjiang	Jiusan 1989/Kefeng 5	0	0	0	−	−	−	−	−	−	−
Kehan 19	Heilongjiang	Ke 90-99/MY4490	1	0	0	−	−	−	−	−	−	+
Kehan 20	Heilongjiang	Ke 89-46/Cundo	;1	0	0	−	−	−	−	−	−	+
Kehan 21	Heilongjiang	Ke89F6 nan-2/Ke 89F1-1237	1	2	1	−	−	−	−	−	−	−
Kefeng 6	Heilongjiang	Ke 85-869/Ke 85-784	;1	;	0	−	−	−	−	−	−	−
Kefeng 7	Heilongjiang	Ke 84F5-250-1/84F5-668	;	;	0	−	−	−	−	−	−	−
Kefeng 8	Heilongjiang	Kehan 12/Ke 82-371	0	1	;	−	−	−	−	−	−	−
Longfu 1	Heilongjiang	Xinshuguang 3/Liaochun 8	0	1	;	−	−	−	−	−	−	−
Longfu 2	Heilongjiang	Longxi 35/Ke 250	;1	1	;	−	−	−	−	−	−	−
Longfu 3	Heilongjiang	Longfu 77-4096/S-A-25	0	0	0	−	−	−	−	−	−	−
Longfu 4	Heilongjiang	Heiza 266/Ke 79F3-392	;	1	1	−	−	−	−	−	−	−
Longfu 5	Heilongjiang	Jiusan B29-/32P	0	0	0	−	−	−	−	−	−	−
Longfu 6	Heilongjiang	Longfu 2108/Haishu	0	0	0	−	−	−	−	−	−	−
Longfu 7	Heilongjiang	Longfu 3/Gang 98-446	;	0	0	−	−	−	−	−	−	−
Longfu 8	Heilongjiang	K202 60Coγ 1000 Rad	0	0	0	−	−	−	−	−	−	−
Longfu 9	Heilongjiang	Kejian 23 60Coγ180Gy	0	0	0	−	−	−	−	−	−	−
Longfu 10	Heilongjiang	Ke 87-183 γ1.1 kRad	0	0	0	−	−	−	−	−	−	−
Longfu 11	Heilongjiang	Longfu 81-8106 60 Coγ 1.1 kRad	0	0	0	−	−	−	−	−	−	+
Longfu 12	Heilongjiang	Jia 5 60 Coγ	;	;	0	−	−	−	−	−	−	−
Longfu 13	Heilongjiang	Unknown	2	1	1	−	−	−	−	−	−	−
Longfu 14	Heilongjiang	F0 (Ke 86F6-545/Hei 85-1584) γ1.0 Rad	1	0	1	−	−	−	−	−	−	−
Longfu 16	Heilongjiang	Unknown	0	0	;1	−	−	−	−	−	−	−
Longfu 18	Heilongjiang	Long 94-4083 mutagenesis	;	0	;	+	−	−	−	−	−	−
Longfu 19	Heilongjiang	SP4/Longmai 26	0	0	0	−	−	−	−	−	−	−
Longfu 20	Heilongjiang	Xiaoyan 6/Long 94-4083	1−	1	0	−	−	−	−	−	−	−
Longmai 10	Heilongjiang	Dongnong 101/Yuanzhong 3908	0	0	0	−	−	−	−	−	−	−
Longmai 15	Heilongjiang	Ke 76-686/Tieling 3	1	1+	;	−	−	−	−	−	−	−
Longmai 20	Heilongjiang	Unknown	0	0	;	−	−	−	−	−	−	−
Longmai 23	Heilongjiang	Unknown	0	0	0	−	−	−	−	−	−	−
Longmai 24	Heilongjiang	Unknown	0	0	0	−	−	−	−	−	−	−
Longmai 26	Heilongjiang	Long 87-7129/Ke 88F22060	;1	0	0	+	−	−	−	−	−	+
Longmai 27	Heilongjiang	Unknown	;1	1	0	−	−	−	−	+	+	−
Longmai 30	Heilongjiang	Long 90?05098/Long 90?06351	1	0	1	−	−	−	−	−	−	+
Longmai 31	Heilongjiang	Longmai 20/PSN/BOW//Longmai 206	0	0	0	−	−	−	−	−	−	−
Longmai 32	Heilongjiang	Long 94-4018/Ke 88F2165-3	0	0	0	−	−	−	−	−	−	−
Longmai 33	Heilongjiang	Longmai 26/Jiusan 3u92	;	;	0	+	−	−	−	−	−	−
Longmai 34	Heilongjiang	F1 (Zhong B054-3/2*Longmai 15//97 Chanjian489/3) /Longmai 26	;	;	;	+	−	−	−	−	−	−
Longmai 35	Heilongjiang	Ke 90-513/Longmai 26	1−	0	0	−	−	−	−	−	−	+
Longmai 36	Heilongjiang	Ke 92-387/Long 99F3-6725-1	0	0	1−	−	−	−	−	−	−	−
Longmai 37	Heilongjiang	Long 2003M8059-3/Long 01D1572-2	;	1	0	+	−	−	−	−	−	−
Longmai 39	Heilongjiang	Long 03F3-6519/Longfu 20-378	2	2	0	+	−	−	−	−	−	−
Kefeng 2	Heilongjiang	Kehan 7/Ke 68F4-585-13	0	1−	1	+	−	−	−	−	−	−
Kefeng 3	Heilongjiang	Kehan 8/Kehong/Kezheng//Nadadoles	;	1−	;	−	−	−	−	−	−	−
Kefeng 4	Heilongjiang	Ke 71F4-370-7/Moyi 66	0	0	;	−	−	−	−	−	−	−
Kefeng 5	Heilongjiang	Ke 76-250/Ke 76F_4-799-5	1	0	0	−	−	−	−	−	−	−
Kefeng 6	Heilongjiang	Ke 85-869/Ke 85-784	;1	2	1−	−	−	−	−	−	−	+
Kefeng 10	Heilongjiang	Kehan 12/Ke 89RF6287	0	0	;	−	−	−	−	−	−	−
Kenda 4	Heilongjiang	82-5621/Ke 79-369	0	0	0	−	−	−	−	−	−	−
Kenda 5	Heilongjiang	Longfu 5009/Nongda 84-838	0	0	0	−	−	−	−	−	−	−
Kenda 6	Heilongjiang	Nongda 89-2729/Bei 89-22	0	1−	0	−	−	−	−	−	−	−
Kenda 7	Heilongjiang	Nongda 89-2729/Bei 89-22	0	0	0	−	−	−	−	−	−	−
Kenda 8	Heilongjiang	Nongda 89-2729/Bei 86-1701	0	0	0	−	−	−	−	−	−	−
Kenda 9	Heilongjiang	Nongda 88-1116-8/Bei88-26	2	1	1−	−	−	−	−	−	−	−
Kenda 10	Heilongjiang	Nongda 94-3537/Bei 90-1201	1	1	1	−	−	−	−	−	−	−
Kenda 11	Heilongjiang	Jiusan 93u92/Ke 90-514	0	0	0	−	−	−	−	−	−	−
Kenda 12	Heilongjiang	Jiadongmai 19/Nongda 96-2543	0	1	1−	−	−	−	−	−	−	−
Kenda 13	Heilongjiang	Unknown	0	0	0	+	−	−	−	−	−	−
Kenjiu 9	Heilongjiang	Xiyin 1/Jiusan 80-41123-7-3	0	0	0	−	−	−	−	+	+	−
Kenjiu 10	Heilongjiang	Jiusan 84-7251/Jiusan 87148//Ke	0	0	1−	−	−	−	−	−	−	+
Kechun 2	Heilongjiang	Ke 90-514/Ke 93RF6-128//Ke 90-514	;	1	1−	+	−	−	−	−	−	+
Kechun 5	Heilongjiang	Ke 99F2-33-3/Jiusan 94-9178	0	0	0	−	−	−	−	+	+
Kechun 8	Heilongjiang	Ke 99F2-33-3/Jiusan 94-9178	0	0	0	−	−	−	−	+	+	+
Kechun 9	Heilongjiang	Ke 99F2-33-3/Jiusan 94-9178	0	1+	2	−	−	−	−	+	+	−
Xiaobing 33	Heilongjiang	A. glaucum/Triticum aestivum	0	0	0	−	−	−	−	−	−	−
Beimai 6	Heilongjiang	Jiusan 93-3U92/Ke 90-514	0	2	0	−	−	−	−	−	−	+
Beimai 9	Heilongjiang	Jiusan 97F4-1057/Jiusan 97F4-255F1/119-54-4-Ⅱ-3	2	1	1	−	−	−	−	−	−	+
Longken 402	Heilongjiang	Unknown	1	1	0	−	−	−	−	−	−	−
2010j159	Heilongjiang	Unknown	0	0	2	+	−	−	−	+	+	−
Norstar	Heilongjiang	Unknown	1	2	1+	+	−	−	−	−	−	+
Dongnong 125	Heilongjiang	Unknown	;1	0	2	−	−	−	−	−	−	+
Nongmai 850	Beijing	Unknown	1	0	0	+	−	−	−	+	+	−
Zhongmai 8	Beijing	Hehua 971-3/Ji Z76	1+	1	0	−	−	−	−	−	−	+
Jingdong 8	Beijing	Afuleer 5238-016/Hongliang 4//Jingnong 79-106	2	0	1	−	−	−	−	+	+	−
Zhongmai 895	Beijing	Zhoumai 16/Liken 4	1	0	1	−	−	−	−	+	+	−
Chimai 2	Inner Mongolia	Wenge 7/Kehan 6	1	0	1	−	−	−	−	−	−	−
Chimai 5	Inner Mongolia	Wenge 1/Ke 76 tiao 295	;1	1	1−	−	−	−	−	−	−	−
Chimai 7	Inner Mongolia	Ke 76 tiao 295/Wenge 1	2	1	1	−	−	−	−	−	−	−
Ba 13p51	Inner Mongolia	Unknown	;1−	0	1	+	−	−	−	+	+	−
Shannong 22	Shandong	PH82-2-2/954072	2	1+	2	−	−	−	−	−	−	−
Shannong 23	Shandong	Tal (Ms2) recurrent selection	2	2	2	−	−	−	−	+	+	−
Shannong 24	Shandong	Tal (Ms2) recurrent selection	1−	0	2	−	−	−	−	+	+	−
Jimai 19	Shandong	Lunai 13/Linfen 5064	4	4	4	−	−	−	−	−	−	−
Jimai 20	Shandong	Lunai 14/Lu 884187	;	0	0	+	−	−	−	−	−	+
Jimai 21	Shandong	865186/Chuannongda 84-1109/Ji 84-5418	3	4	4	−	−	−	−	−	−	−
Jimai 22	Shandong	935024/935106	0	0	1	−	−	+	−	−	−	+
Jimai 44	Shandong	Jinan 17/954027	2	;	2	+	−	−	−	−	−	+
Yannong 19	Shandong	Yan 1933/Shan 82-29	;1	;	;	−	−	−	−	−	−	+
Yannong 21	Shandong	Heyan 1933/Shan 8229	3−	2	1	−	−	−	−	−	−	−
Yannong 23	Shandong	Yan 1061/Lumai 14	3	4	3	−	−	−	−	−	−	−
Tainong 18	Shandong	Laizhou 137/Yan 369-7	2	0	1	−	−	−	−	−	−	−
Taishan 23	Shandong	876161/881414	1+	0	1−	−	−	−	−	+	+	−
Taishan 24	Shandong	904017/Zhenzhou 8329	3	4	3−	−	−	−	−	−	−	−
Luyuan 502	Shandong	9940168/Jimai 19	;	0	0	−	−	−	−	+	+	−
Tanmai 98	Shandong	Jining 13/942	4	3	2	−	−	−	−	−	−	−
Lumai 21	Shandong	Yanzhong 144/Baofeng 7228	3+	4	4	−	−	−	−	−	−	−
Jinan 17	Shandong	Linfen 5064/Lumai 13	4	4	4	−	−	−	−	−	−	−
Liangxing 66	Shandong	Ji91102/Ji 935031	2	3	1	−	−	−	−	−	−	−
Liangxing 99	Shandong	Ji 91102/Lumai14//PH85-16	3−	4	0	−	−	−	−	−	−	−
Zhoumai 28	Henan	Zhoumai 18/Zhoumai 22//Zhou 2168	1	;	;	−	−	−	−	+	+	−
Zhumai 762	Henan	Unknown	2	;	;	−	−	−	−	+	+	+
Luomai 6010	Henan	Yuanyang /Luo152/82C6/M	2	;1	2	−	−	−	−	−	−	−
Guomai 301	Henan	G883/Pumai 9	2	0	2	−	−	−	−	−	−	+
Zhoumai 27	Henan	Zhoumai 16/Aikang 58	1	0	;	−	−	−	−	+	+	−
Xumai 33	Henan	Neixiang 991/Zhoumai 16	0	1	0	−	−	−	−	+	+	−
Xinmai 29	Henan	Yanzhan 4110/Zhoumai 16	4	4	4	−	−	−	−	−	−	−
Annong 0711	Henan	Yannong 19/Aanong 0016	2	1	2	−	−	−	−	−	−	−
Anke 157	Henan	Taishan 241/Xinong 1718	2	3	4	−	−	−	−	−	−	−
Pumai 053	Henan	Bainong AK58/Zhoumai 18	1	1	0	−	−	−	−	+	+	−
Kaimai 22	Henan	Zhoumai 18/ Bainong AK58	1−	1	0	−	−	−	−	+	+	−
Zhenmai 1860	Henan	Unknown	1	;	;	−	−	−	−	+	+	−
Womai 9	Henan	Laizhou 953/Bainong AK58	1	1	1	−	−	−	−	+	+	−
Ning 52	Ningxia	Yong 403/Yongliang 15//Yong 1147/230	0	0	0	+	−	−	−	+	+	−
Ning 39	Ningxia	Yong 833/Ningchun 4	;	0	0	+	−	−	−	−	−	−
Ningchun 4	Ningxia	Suonuola 64/Hongtu	0	0	0	−	−	−	−	−	−	−
Ning 51	Ningxia	Yong 3002/Ningchun 4	0	0	0	+	−	−	−	−	−	−
Ningchun 53	Ningxia	Ningchun 39/Moxige M7021	0	0	0	+	−	−	−	−	−	−
Ningdong 11	Ningxia	RENAN//Beinong 2/Beijing 841	1+	0	0	−	−	−	−	+	+	+
Linfeng 3	Shanxi	Linyuan 86-7065/Linyuan 81-5011	2	0	;	−	−	−	−	−	−	−
Jinmai 90	Shanxi	Jinmai 47/02L013	4	4	4	−	−	−	−	−	−	−
Wanmai 38	Jiangsu	Yanzhong 114/85-15-9	1+	0	2	−	−	−	−	−	−	+
Wansu 0217	Jiangsu	Unknown	2	2	1	−	−	−	−	−	−	−
Huaimai 4064	Jiangsu	Unknown	1	1	1	−	−	−	−	+	+	−
Wanmai 1643	Jiangsu	Unknown	0	0	0	+	−	−	−	−	−	−

Notes:

Seedling infection types produced by three races of P. graminis f. sp. tritici and molecular detection of resistance genes Sr2, Sr24, Sr25, Sr26, Sr31, and Sr38 in the 136 wheat cultivars (lines).

Infection types (ITs): are based on a 0–4 scale where ITs of 0, ;, 1, and 2 are indicative of a resistant (low) response and ITs of 3 or 4 of a susceptible (high) response; Symbols + and − indicate slightly larger and smaller pustule sizes, respectively (Stakman, Stewart & Loegering, 1962).

Symbol “+” indicates the cultivar (line) carry the tested genes; “−” indicates the cultivar (line) don’t carry the tested genes.

Figure 2

Screening for resistance genes against three Pgt races in wheat seedlings.

Seedling infection type (IT) scores have been converted to letters to facilitate reading: a, 0; b, −1; c, 1; d, 1+; e, 2; f, 3−; g, 3; h, 3+; i, 4.

Detection of stem rust resistance genes using molecular markers

Sr2 screening

The adult plant resistant gene Sr2, which provides a durable broad-spectrum to Pgt is difficult to screen under field conditions (Hayden, Kuchel & Chalmers, 2004). However, the Sr2-closely linked microsatellite marker Xgwm533, developed by Hayden, Kuchel & Chalmers (2004), typically amplifies a 120-bp fragment from wheat lines known to carry Sr2. In the present study, we used this marker to detect Sr2 and 21 of the 136 wheat varieties showed the Sr2 fragment (Fig. 1A; Table 2), suggesting that those wheat varieties carry Sr2.

Sr24 screening

Gene Sr24 is effective against some Pgt races in China and it was derived from Thinopyrum ponticum. It is widely used in wheat breeding though it has become susceptible to some Ug99 variants (Jin et al., 2008). Mago et al. (2005) reported that marker Sr24#12, linked to Sr24, was associated with the 3Ag/1BS Amigo-type translocation, and this marker can amplify a 500-bp fragment in the wheat variety “Westonia/Sr24.” Using a diverse collection of wheat germplasm, Yu et al. (2010) showed that this 500-bp PCR fragment was amplified in wheat germplasm carrying Sr24. In the present study, 500-bp fragments were amplified in the wheat line “LcSr24Ag,” suggesting it carries Sr24 (Fig. 3B) but no fragment was amplified in the other tested varieties (Table 2).

Figure 3

Amplification results for some of the wheat cultivars tested using six markers.

A, Xgwm533; B, Sr24#12; C, Gb; D, Sr26#43; E, SCSS30.2576; F, VENTRIUP-LN2. Lanes A1 to F1 are results of Hope, LcSr24Ag, Agatha/9*LMPG, Eagle, Sr31/6*LMPG, and Trident cultivars. Lanes 2–14 are Kenda 9, Kechun 8, Nongmai 850, Longfu 18, Kenjiu 9, Ningdong 11, Jimai 22, Yannong 19, Taishan 23, Ning 39, Ning 52, Wanmai 38, and Zhumai 762 cultivars. M is the DNA ladder used to identify the specific sequences of each molecular marker.

Sr25 and Sr26 screening

Ug99-effective-genes Sr25 and Sr26 were transferred into wheat from T. ponticum. These two genes were firstly backcrossed into Australian wheat, and some old varieties may carry these genes in China (Cao et al., 1994; Knott, 1961). We used markers Gb (amplifies a 130-bp fragment) and Sr26#43 (amplifies a 207-bp fragment), which are closely linked to genes Sr25 and Sr26, respectively (Liu et al., 2010), to screen these genes in the 136 accessions. The 130-bp fragment was only amplified in Kehan 3 and Jimai 22 (Fig. 3C; Table 2), indicating that only these two wheat varieties carry Sr25; the other tested wheat varieties lack Sr25 and Sr26 (Fig. 3D; Table 2).

Sr31 and Sr38 screening

The effective resistance of Sr31 and Sr38 to Pgt was overcome by Ug99, as no race with virulence to these genes had been found in China (Li et al., 2016). Genes Sr31 and Sr38 were widely used in wheat programs. Markers SCSS30.2 (amplifies a 576-bp fragment) and Iag95 (amplifies a 1,100-bp fragment) linked to Sr31, and the 2NS-specific primer VENTRIUP-LN2 (amplifies a 262-bp fragment), linked to the rust resistance gene cluster Lr37-Sr38-Yr17, were used in the present study to screen Sr31 and Sr38. Fragment sizes consistent with the presence of both resistant genes were amplified in 25 wheat cultivars and in the positive control Sr31/6*LMPG using markers SCSS30.2 and Iag95, and in 28 wheat cultivars using marker VENTRIUP-LN2.

Discussion

It is reported that the resistance of wheat cultivars to Pgt is higher in the northern rather than in the southern wheat region, especially in varieties from North China where stem rust is prone to occur. Results obtained in the present study are similar to that previously reported. In total, 124 (91.2%) wheat cultivars were resistant to the three Pgt races (ITs 2, 1+, or lower), and the resistance level of the accessions from Heilongjiang was higher than that of accessions from other provinces. All wheat cultivars from Heilongjiang Province were resistant to races 21C3CTHQM, 34MKGQM, and 34C3RTGQM, as wheat lines must be resistant to Pgt for being registered in Heilongjiang. In addition, the resistance level of wheat lines from Heilongjiang is tested by the Plant Immunity Institute, Shenyang Agricultural University, every year using the 21C3 and 34 Pgt race groups. Therefore, all registered cultivars registered in Heilongjiang should present ITs below 3, which was confirmed in the present study (0, 1, 1-, and 2 ITs were found; Table 2). Wheat cultivars from the lower-middle Yangtze River basin and central winter-wheat growing provinces were also highly resistant (73.9%) to the tested Pgt races.

Gene Sr2, originated from Triticum dicoccum Schronk, was transferred into North American and International Maize and Wheat Improvement Center (CIMMYT) wheat breeding programs in 1925, and since then it has been extensively used in many regions worldwide (Borlaug, 1968). In the present study, marker Xgwm533, which was used to detect Sr2, revealed that only 21 of the 136 wheat varieties were likely to carry this gene. Such cultivars might be resistant to Ug99, as the high resistance of Jimai 20 to Ug99 tested in Kenya in 2006 has been attributed to the Sr2 gene carried by this cultivar (He, Xia & Chen, 2008). But it is difficult to conclude that these 21 wheat varieties carry Sr2, because many North American, Australian and CIMMYT lines which predicted not carry this gene can amplified a 120-bp fragment (Jemanesh et al., 2013; Mago et al., 2011).

The wheat stem rust gene Sr24, derived from T. ponticum, is effective against most Pgt races, including race TTKSK (i.e., Ug99). Races virulent to Sr24 are rare in the Pgt population in North America (Jin et al., 2008). This gene has been used as a differential in North America and worldwide race surveys, but a new variant of race TTKSK with Sr24 virulence has arisen in Kenya, South Africa, Tanzania, Ethiopia, Mozambique, and Uganda (BGRI, 2017). Leaf rust gene Lr24 in association with Sr24 provides resistance to all Pgt isolates. Thus, we used marker Sr24#12, completely linked to Sr24 (Mago et al., 2005), to screen for Sr24/Lr24 genes in the 136 wheat accessions. None of the tested cultivars carried Sr24, although previous research using postulated gene presence based on marker data showed that some Chinese wheat cultivars might be carrying this gene (Cao et al., 2007). On the other hand, the study conducted by Zhang et al. (2008) supports our result as none of the 23 wheat cultivars they screened using molecular markers linked to Lr24 carried this gene. Thus, more races and molecular markers should be used to confirm whether Chinese wheat cultivars carry Sr24 or not.

Genes Sr25 and Sr26, derived from T. ponticum, are effective against Ug99 and all Pgt races in China, and their use is increasing based on their resistance to Ug99 (Bariana et al., 2007). Novel genetic tools based on molecular marker technologies were developed to tag the presence of those genes (Mago et al., 2005; Liu et al., 2010). In the present study, we used molecular markers Gb, linked with Sr25, and Sr26#43, linked with Sr26, to identify these genes. Two wheat cultivars, “Kehan 3” (Ke61F3-199/Agropyronglaucum) and “Jimai 22” (935024/935106) are likely to carry Sr25. Pedigree tracking indicated that “Kehan 3” parents contained A. glaucum, but Sr25 is derived from T. ponticum, so the result obtained for this cultivar might not be accurate. Expectedly, none of the wheat varieties carried Sr26, as this gene is not widely used in breeding programs in China (Li et al., 2016). Results obtained here are similar to those of previous studies; for example, using marker Sr26#43, Li et al. (2016) detected that none of the 119 wheat materials examined carried Sr26.

Gene Sr31, derived from “Petkus” rye, is located on 1BL/1RS. It is distributed in wheat cultivars worldwide, but was transferred into Chinese wheat backgrounds from the Soviet Union and Romania in the 1960s (Jiang et al., 2007). Since then, the wheat cultivars “Alondra S,” “Aftab LeEr,” “Kavkaz,” and “Luofulin” lines carrying Sr31 have been released in wheat growing regions in China. Although, this gene is susceptible to Ug99, it is effective against TKTTF and TTTTF and all Pgt races in China (Pretorius et al., 2000; Olivera et al., 2015; Bhattacharya, 2017; Li et al., 2016). Markers Iag95 and SCSS30.2, which were used to screen the gene Sr31 in the present study, revealed that 25 wheat cultivars contained Sr31, and pedigree information and low ITs supported these results. Thus, Sr31 should be used in breeding programs in China in combination with other genes resistant to Ug99 to ensure that Chinese wheat cultivars are resistant to Chinese Pgt races and to Ug99.

Gene Sr38, originated from T. ventricosum, is widely used due to its association with the stripe rust gene Yr17 and the leaf rust gene Lr37 that confer resistance to the three species of wheat rust pathogens (Delibes et al., 1993; Dyck & Lukow, 1988). Genes Yr17 and Lr37 were reported from wheat cultivars in China using molecular markers linked to them (Peng et al., 2013; Xue et al., 2014). In the present study, the marker VENTRIUP-LN2, which is linked with the Sr38-Yr17-Lr37 cluster of rust resistance genes, was used and the specific PCR fragment for this marker was detected in 28 of the 136 wheat cultivars examined. These 28 cultivars presented low ITs indicating they carry Sr38. Gene Sr38 is susceptible to Ug99, similar to gene Sr31, but resistant to all Pgt races in China (Cao et al., 2007). Therefore, in China, it should be used in combination with genes resistant to Ug99 through gene pyramiding.

Molecular markers linked to resistance genes are an alternative to gene postulation and may allow breeders to identify resistance genes rapidly and accurately (Goutam et al., 2013). Combining molecular markers with pedigree information of the tested varieties can greatly increase the success of gene postulation (Yu et al., 2010). Due to the rapid development of molecular markers and to the great importance of the new Pgt races, molecular markers closely linked to resistance genes against such races have been frequently reported, and many have been converted to simple sequence repeat (Mago et al., 2013; Tsilo, Jin & Anderson, 2007), sequence tagged site/cleaved amplified polymorphic sequence (Helguera et al., 2003; Mago et al., 2011), sequence tagged site (Mago et al., 2005; Bansal et al., 2014), and simple sequence repeats/amplified fragment length polymorphism markers (Periyannan et al., 2014). This approach overcomes gene interactions and plant stage-dependent gene expression problems associated with traditional gene postulation.

Conclusion

In the present study, we used molecular markers to determine if Sr2, Sr24, Sr25, Sr26, Sr31, and Sr38 were present in the 136 wheat cultivars examined. Overall, genes Sr31, and Sr38 were differently distributed across wheat regions in China and none of the wheat cultivars contained Sr24 and Sr26. Additional studies will be needed to verify the gene postulations for Sr2 and Sr25. These cultivars comprising stem rust resistance genes are valuable genetic materials for future wheat-breeding plans.

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