Rapeseed black shank specific sequence and lamp detection primers and application

A technology for blackleg bacteria and rape, which is applied to the field of blackleg bacteria specific sequences and LAMP detection primers, can solve problems such as the specificity variation of amplification, and achieve the effects of controlling false positives, good specificity, and avoiding false positives

Active Publication Date: 2021-09-07
HUAZHONG AGRI UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Sometimes the addition of loop primers will make the specificity of amplification worse

Method used

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  • Rapeseed black shank specific sequence and lamp detection primers and application
  • Rapeseed black shank specific sequence and lamp detection primers and application
  • Rapeseed black shank specific sequence and lamp detection primers and application

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0030] Application of rapeseed blackleg pathogen specific sequence (SEQ ID NO.1) or primers designed for the sequence in the preparation of rapeseed blackleg pathogen (L.biglobosa) detection reagent:

[0031] For the sequence shown in SEQ ID NO.1, LAMP primers were designed as follows:

[0032] F3:TAGGTGAACCTGCGGAAG

[0033] B3:GTTACTGACGCTGACTGC

[0034] FIP: GGAAAGGGACAGAAATTAAGCCAAAATTACCCTTCTATCAGGGGAT

[0035] BIP: TCTGATTCTACCCATGTTTTTTGCGAATTACAAGTGGTTTGAATTGTC

[0036] LB: GTGGGCTTGCCTGCCAAAA.

[0037] The LAMP amplification system is as follows:

[0038]

[0039] Bst 2.0 WarmStart DNA Polymerase was purchased from New England Biolabs.

[0040] The LAMP amplification procedure is as follows:

[0041] React at 65°C for 40 minutes; inactivate at 80°C for 5 minutes

[0042] 1000×SYBR Green I was added to the reaction product, and the positive reaction showed fluorescent green, indicating the presence of L.biglobosa; the negative control remained orange.

Embodiment 2

[0044] Specific detection and sensitivity detection of LAMP primers for L.biglobosa:

[0045] Specific detection of LAMP primers for L.biglobosa:

[0046] Using the method described in Example 1, the applicant has carried out LAMP detection to the bacterial strains described in Table 1, and the bacterial strains in Table 1 include 21 strains of L.biglobosa (including subspecies L.biglobosa 'brassicae' and L.biglobosa 'canadensis '), 2 strains of related bacteria L.maculans (including subspecies L.maculans'brassicae') and 10 strains of pathogenic fungi isolated from rapeseed (such as: Phoma sp, Phoma macrostoma, Phoma glomerata, Phoma herbarum, Botrytiscinerea, Sclerotinia sclerotiorum, Colletotrichum sp, Alternaria alternata, Chaetomium globosum,)

[0047] Table 1

[0048]

[0049]

[0050] Sensitivity detection of LAMP primers for rapeseed black shank

[0051] Genomic DNA of Rapeseed Blackleg Germ (HGHCT2-2) was diluted in a 10-fold concentration gradient, and its se...

Embodiment 3

[0052] Example 3: Field Application of LAMP-specific Detection Primers for Rapeseed Blackleg Germ

[0053] The stalks of rapeseed were collected from winter rapeseed production areas in China (Chibi, Hubei, Nanjing, Jiangsu, Qujing, Yunnan, Chengdu, Sichuan, Xinyang, Henan, Huizhou, Anhui, Hanzhong, Shaanxi, Huaihua, Hunan, Ningbo, Zhejiang, Guiyang, Guizhou, etc.) and randomly selected 7 The stalks of rapeseed with black shank and 6 rapeseeds with no symptoms, DNA was extracted from the diseased tissues, and the LAMP primers provided by the invention were used for LAMP detection. The results showed that all 7 rapeseed stalks with diseased Rapeseed black shank was detected, and 5 rape stalks also had the presence of rapeseed black shank on 6 rape stalks without symptoms, and only 1 strain did not detect the existence of the pathogen ( image 3 ), cultured 5 rapeseed stalks with no symptoms and tested positive in a moist environment at 25°C, and observed brown lesions typical o...

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PUM

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Abstract

The invention belongs to the technical field of plant protection, and discloses the specific sequence of blackleg pathogen of rapeseed, LAMP detection primers and applications. The invention provides a specific detection target of L.biglobosa, and the target has good specificity, strong stability and high sensitivity. characteristics, it can distinguish the closely related species of Brassica napus with higher homology, avoiding the generation of false positives. The LAMP primers designed for this target can detect 112 fg / μL of L.biglobosa genomic DNA, which provides a good tool for field detection of Brassica napus and rapid high-throughput inspection and quarantine at ports.

Description

technical field [0001] The invention belongs to the technical field of plant protection, and in particular relates to the specific sequence of blackleg pathogen of rapeseed, a LAMP detection primer and application thereof. Background technique [0002] Rapeseed blackleg (Blackleg) is a worldwide disease of rapeseed. According to reports, in each rapeseed production season, the global economic loss is as high as 900 million U.S. dollars (Fernando et al., 2016). The pathogen is the fungus of the genus Micrococcomus, which can seriously damage Brassicaceae plants such as rapeseed. Leptosphaeria fungi include two closely related species: Leptosp haeria maculans and L. biglobosa (Shoemaker and Brun., 2001) (Kaczmarek., 2009). The former is mainly distributed in Canada, Australia, Europe and other places, and the infection site is at the base of the rapeseed stem, which will cause the stem base to rot and cause the stem to fall, causing serious damage to rapeseed production and c...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C12Q1/6844C12Q1/6895C12Q1/04C12N15/11
CPCC12Q1/6844C12Q1/6895C12Q2531/119
Inventor 李国庆杜然杨龙张静吴明德
Owner HUAZHONG AGRI UNIV
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