Scientia Agricultura Sinica ›› 2020, Vol. 53 ›› Issue (3): 527-538.doi: 10.3864/j.issn.0578-1752.2020.03.006

• PLANT PROTECTION • Previous Articles     Next Articles

Establishment and Application of a Multiple PCR Method to Detect Mating Types of Exserohilum turcicum and Bipolaris maydis

DAI YuLi1,GAN Lin1,TENG ZhenYong2,YANG JingMin3,QI YueYue4,SHI NiuNiu1,CHEN FuRu1,YANG XiuJuan1()   

  1. 1 Institute of Plant Protection, Fujian Academy of Agricultural Sciences/Fujian Key Laboratory for Monitoring and Integrated Management of Crop Pests, Fuzhou 350013
    2 Fujian Seed Management Station, Fuzhou 350001
    3 Jianou Municipal Bureau of Agriculture and Rural Affairs, Jianou 353100, Fujian
    4 Zhejiang Tianfeng Biological Science Co. Ltd, Jinhua 321000, Zhejiang
  • Received:2019-08-13 Accepted:2019-09-18 Online:2020-02-01 Published:2020-02-13
  • Contact: XiuJuan YANG E-mail:yxjzb@126.com

Abstract:

【Objective】 Northern corn leaf blight (NCLB) and southern corn leaf blight (SCLB), caused by Exserohilum turcicum and Bipolaris maydis, respectively, are the most important foliar fungal diseases affecting maize production. The objective of this study is to establish a multiple PCR method to detect mating types of E. turcicum and B. maydis, and to provide a technical method for the study of mating type distribution in the field and sexual reproduction of E. turcicum and B. maydis. 【Method】 Mating type-specific primers for the two pathogens were designed on the basis of mating type gene sequences of E. turcicum (accession numbers: GU997138 for MAT1-1; GU997137 for MAT1-2) and B. maydis (accession numbers: X68399 for MAT1-1; X68398 for MAT1-2) obtained from GenBank, and the important parameters of primer annealing temperatures, extension times and amplification cycles in the amplification program were optimized using the single factor method. A multiple PCR method was established to detect mating types of E. turcicum and B. maydis, and the sensitivity and specificity of the multiple PCR were also assessed. Meanwhile, the mating types of 129 strains of E. turcicum and 194 strains of B. maydis from field-collections were detected by the multiple PCR to determine the adaptability of the established method.【Result】The expected 816, 132 bp (E. turcicum), and 490, 136 bp (B. maydis) target fragments were amplified specifically using the multiple PCR with mating type-specific primers of StMAT01-2F/R, StMAT02-3F/R, and ChMAT01-3F/R, ChMAT02-2F/R from MAT1-1 and MAT1-2 strains, respectively. A 25 μL PCR reaction system consisted of 12.5 μL 2×Multiplex PCR Mix, 10 pmol each primer, and 100 ng DNA template. The annealing temperatures for E. turcicum and B. maydis were 57.2℃ and 55.0℃, respectively, and the number of amplification cycles was 35. The multiple PCR method could reliably detect mating types of E. turcicum at 0.1 ng genomic DNA for MAT1-1 or 0.01 ng DNA for MAT1-2 from single-spore strains, while the sensitivity of the multiple PCR to detect mating types of B. maydis was 0.1 ng genomic DNA for both MAT1-1 and MAT1-2 from pure culture strains. The method exhibited specificity in differentiating mating types of E. turcicum and B. maydis from their closely-related species, as well as 14 other fungal genera. The results of mating types detection of E. turcicum and B. maydis strains from different geographical origins indicated that the multiple PCR could reliably detect mating types of 129 and 194 strains of E. turcicum and B. maydis, respectively. These results were consistent with the verification results of laboratorial cross assays with random selected strains from different locations.【Conclusion】The established multiple PCR method for mating types detection of E. turcicum and B. maydis in this study was characterized as high sensitivity, specificity and user-friendly control, it could accurately and rapidly detect mating types of E. turcicum and B. maydis. This study provides a reliable technique and approach for the study of distribution and monitoring of mating types in the field and sexual reproduction of E. turcicum and B. maydis.

Key words: Exserohilum turcicum, Bipolaris maydis, mating type, multiple PCR, sensitivity, specificity

Table 1

Information of tested strains"

菌株编号
Code of strains
学名
Scientific name
菌株来源
Source of strains
采集年份
Year of collection
交配型
Mating type
1 玉米大斑病菌E. turcicum 福建建瓯 Jianou, Fujian 2018 MAT1-2
2 玉米大斑病菌E. turcicum 福建建瓯 Jianou, Fujian 2018 MAT1-2
3 玉米大斑病菌E. turcicum 福建南靖 Nanjing, Fujian 2018 MAT1-1
4 玉米大斑病菌E. turcicum 福建南靖 Nanjing, Fujian 2018 MAT1-1
5 玉米大斑病菌E. turcicum 福建松溪 Songxi, Fujian 2018 MAT1-1
6 玉米大斑病菌E. turcicum 福建松溪 Songxi, Fujian 2018 MAT1-2
7 玉米大斑病菌E. turcicum 福建南靖 Nanjing, Fujian 2019 MAT1-2
8 玉米大斑病菌E. turcicum 福建建瓯 Jianou, Fujian 2019 MAT1-1
9 玉米大斑病菌E. turcicum 福建屏南 Pingnan, Fujian 2016 MAT1-2
10 玉米大斑病菌E. turcicum 福建屏南 Pingnan, Fujian 2016 MAT1-2
11 玉米大斑病菌E. turcicum 福建建瓯 Jianou, Fujian 2019 MAT1-2
12 玉米大斑病菌E. turcicum 福建建瓯 Jianou, Fujian 2019 MAT1-1
13 玉米小斑病菌B. maydis 福建武夷山 Wuyishan, Fujian 2015 MAT1-2
14 玉米小斑病菌B. maydis 福建建阳 Jianyang, Fujian 2014 MAT1-2
15 玉米小斑病菌B. maydis 福建建阳 Jianyang, Fujian 2014 MAT1-2
16 玉米小斑病菌B. maydis 福建建瓯 Jianou, Fujian 2016 MAT1-2
17 玉米小斑病菌B. maydis 福建屏南 Pingnan, Fujian 2016 MAT1-2
18 玉米小斑病菌B. maydis 福建建瓯 Jianou, Fujian 2016 MAT1-1
19 玉米小斑病菌B. maydis 安徽霍邱 Huoqiu, Anhui 2017 MAT1-2
20 玉米小斑病菌B. maydis 海南三亚 Sanya, Hainan 2018 MAT1-2
21 玉米小斑病菌B. maydis 浙江泰顺 Taishun, Zhejiang 2017 MAT1-2
22 玉米小斑病菌B. maydis 福建屏南 Pingnan, Fujian 2016 MAT1-1
23 玉米小斑病菌B. maydis 福建屏南 Pingnan, Fujian 2016 MAT1-1
24 玉米小斑病菌B. maydis 广东惠州 Huizhou, Guangdong 2018 MAT1-2
近缘种及其他真菌Closely related and other fungal species
25 參子凸脐蠕孢Exserohilum frumentacei CGMCC 2009 ND
26 小柄凸脐蠕孢Exserohilum pedicellatum CGMCC 2009 ND
27 芦苇凸脐蠕孢Exserohilum phragmitis CGMCC 2009 ND
28 突脐蠕孢属Exserohilum sp. 广东广州 Guangzhou, Guangdong 2016 ND
29 水稻胡麻斑病菌Bipolaris oryzae 福建建瓯 Jianou, Fujian 2017 ND
30 双色平脐蠕孢Bipolaris bicolor 福建建瓯 Jianou, Fujian 2017 ND
31 玉米圆斑病菌Bipolaris zeicola 四川 Sichuan ND ND
32 麦根腐平脐蠕孢Bipolaris sorokiniana 安徽 Anhui ND ND
33 玉米弯孢叶斑病菌Curvularia lunata 福建霞浦 Xiapu, Fujian 2016 ND
34 玉米画眉草弯孢叶斑病菌Curvularia eragrostidis 福建莆田 Putian, Fujian 2016 ND
35 番茄早疫病菌Alternaria solani 福建 Fujian ND ND
36 稻曲病菌Ustilaginoidea virens 福建 Fujian 2016 ND
37 胶孢炭疽菌Colletotrichum gloeosporioides 福建福州 Fuzhou, Fujian 2017 ND
38 尖镰孢Fusarium oxysporum 福建漳州 Zhangzhou, Fujian 2014 ND
39 桃褐腐病菌Monilinia laxa 福建Fujian ND ND
40 柑橘酸腐病菌Oospora citriaurantii 福建 Fujian ND ND
41 玉米纹枯病菌Rhizoctonia solani 福建 Fujian 2017 ND
42 油菜菌核病菌Sclerotinia sclerotiorum 安徽宁国 Ningguo, Anhui 2004 ND
43 柑橘疮痂病菌Sphaceloma fawcetti 福建 Fujian ND ND
44 哈茨木霉Trichoderma harzianum 福建 Fujian ND ND
45 稻瘟病菌Magnaporthe oryzae 福建 Fujian ND ND
46 苹果红粉病菌Trichothecium roseum 福建 Fujian ND ND

Fig. 1

Results of multiple sequence alignment of mating type sequences of E. turcicum and B. maydis and the mating type-specific primer binding locations The red and blue boxes and arrows show the primer binding locations of E. turcicum (A) and B. maydis (B) mating type of MAT1-1 and MAT1-2, respectively"

Table 2

Specific primers for multiple PCR to detect mating types of E. turcicum and B. maydis"

引物名称
Primer name
引物序列
Primer sequence (5′→3′)
退火温度
Tm (℃)
产物大小
Size (bp)
目标基因
Target gene
StMAT01-2 F: TGCCTTTGTTGGATTTCG 57.2 816 E. turcicum MAT1-1
R: CATCGTTCTGGCTGTGGG
StMAT02-3 F: TACACCAAACAACATCGCTCCT 57.2 132 E. turcicum MAT1-2
R: TCGGCGTCGTAGAACAAG
ChMAT01-3 F: ACCACGAGACAACATACGC 55.0 490 B. maydis MAT1-1
R: GTTTGAGGTGAGGGCAGA
ChMAT02-2 F: GGCGAAGTTTGTGGGTTT 55.0 136 B. maydis MAT1-2
R: GCGATGTCTGGGCTGATT

Fig. 2

Validation of the multiple PCR to detect mating types of E. turcicum and B. maydis Twelve known mating type strains of E. turcicum (A) and B. maydis (B) listed in Table 1"

Fig. 3

Sensitivity test of the multiple PCR to detect mating types of E. turcicum and B. maydis"

Fig. 4

Specificity of the multiple PCR to detect mating types of E. turcicum and B. maydis"

Table 3

Multiple PCR and hybridization detection of mating types of E. turcicum and B. maydis strains from different geographic origins"

菌株来源
Source of strains
病原菌
Pathogen
菌株数量
Strain numbers a
交配型的多重PCR和杂交检测结果
Results of mating type detection using multiple PCR and cross assay b
MAT1-1 MAT1-2
福建建瓯Jianou, Fujian 玉米大斑病菌E. turcicum 64 (10) + (2) + (8)
玉米小斑病菌B. maydis 12 (5) + + (5)
福建松溪Songxi, Fujian 玉米大斑病菌E. turcicum 20 (8) + (1) + (7)
福建屏南Pingnan, Fujian 玉米大斑病菌E. turcicum 15 (5) + + (5)
玉米小斑病菌B. maydis 24 (10) + (3) + (7)
福建福州Fuzhou, Fujian 玉米小斑病菌B. maydis 20 (8) + (2) + (6)
福建莆田Putian, Fujian 玉米大斑病菌E. turcicum 1 ND +
玉米小斑病菌B. maydis 8 (5) + + (5)
福建南靖Nanjing, Fujian 玉米大斑病菌E. turcicum 20 (10) + (1) + (9)
玉米小斑病菌B. maydis 11 (5) + + (5)
福建龙岩Longyan, Fujian 玉米大斑病菌E. turcicum 8 (5) + + (5)
玉米小斑病菌B. maydis 9 (5) + (1) + (4)
安徽霍邱Huoqiu, Anhui 玉米小斑病菌B. maydis 26 (8) + (1) + (7)
海南三亚Sanya, Hainan 玉米大斑病菌E. turcicum 1 ND +
玉米小斑病菌B. maydis 24 (6) + (2) + (4)
浙江泰顺Taishun, Zhejiang 玉米小斑病菌B. maydis 27 (8) + (3) + (5)
广东Guangdong 玉米小斑病菌B. maydis 33 (10) + (4) + (6)
总计 Total 玉米大斑病菌E. turcicum 129 (38) + (4) + (34)
玉米小斑病菌B. maydis 194 (70) + (16) + (54)
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