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一种用于快速检测与香蕉枯萎病生物防治活性相关遗传标记表达的实时荧光逆转录定量PCR检测方法

A Real-Time Fluorescent Reverse Transcription Quantitative PCR Assay for Rapid Detection of Genetic Markers' Expression Associated with Fusarium Wilt of Banana Biocontrol Activities in .

作者信息

Li Shu, He Ping, Fan Huacai, Liu Lina, Yin Kesuo, Yang Baoming, Li Yongping, Huang Su-Mei, Li Xundong, Zheng Si-Jun

机构信息

Yunnan Key Laboratory of Green Prevention and Control of Agricultural Transboundary Pests, Agricultural Environment and Resources Institute, Yunnan Academy of Agricultural Sciences, Kunming 650205, China.

State Key Laboratory for Conservation and Utilization of Bio-Resources in Yunnan, Ministry of Education Key Laboratory of Agriculture Biodiversity for Plant Disease Management, College of Plant Protection, Yunnan Agricultural University, Kunming 650201, China.

出版信息

J Fungi (Basel). 2021 Apr 30;7(5):353. doi: 10.3390/jof7050353.

DOI:10.3390/jof7050353
PMID:33946404
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8147159/
Abstract

Fusarium wilt of banana, caused by f. sp. (), especially Tropical Race 4 (TR4), seriously threatens banana production worldwide. There is no single effective control measure, although certain strains secrete antibiotics as promising disease-biocontrol agents. This study identified five strains displaying strong antibiotic activity against TR4, using a systemic assessment for presence/absence of genetic markers at genome level, and expression profiles at transcriptome level. A conventional PCR with 13 specific primer pairs detected biocontrol-related genes. An accurate, quantitative real-time PCR protocol with novel designed specific primers was developed to characterise strain-specific gene expression, that optimises strain-culturing and RNA-isolation methodologies. Six genes responsible for synthesising non-ribosomal peptide synthetase biocontrol metabolites were detected in all five strains. Three genes were involved in synthesising three Polyketide synthetase metabolites in all five strains, but the macrolactin synthase gene was only detected in WBN06 and YN1282-2. All five strains have the genes and , essential for synthesising bacillibactin and biotin. However, the gene involved in subtilisin synthesis, is absent in all five strains. These genes' expression patterns were significantly different among these strains, suggesting different mechanisms involved in TR4 biocontrol. Results will help elucidate functional genes' biocontrol mechanisms.

摘要

香蕉枯萎病由尖孢镰刀菌古巴专化型(Fusarium oxysporum f. sp. cubense)引起,尤其是热带4号小种(TR4),严重威胁着全球香蕉生产。尽管某些菌株能分泌抗生素,有望成为病害生物防治剂,但目前尚无单一有效的防治措施。本研究通过对基因组水平上遗传标记的有无以及转录组水平上的表达谱进行系统评估,鉴定出5株对TR4具有较强抗生素活性的菌株。使用13对特异性引物进行常规PCR检测生物防治相关基因。开发了一种采用新设计的特异性引物的准确、定量实时PCR方法来表征菌株特异性基因表达,该方法优化了菌株培养和RNA分离方法。在所有5株菌株中均检测到6个负责合成非核糖体肽合成酶生物防治代谢产物的基因。在所有5株菌株中,有3个基因参与合成3种聚酮合酶代谢产物,但大环内酯合成酶基因仅在WBN06和YN1282 - 2中检测到。所有5株菌株都具有合成杆菌肽和生物素所必需的基因 和 。然而,参与枯草杆菌蛋白酶合成的基因 在所有5株菌株中均不存在。这些基因在这些菌株中的表达模式存在显著差异,表明在TR4生物防治中涉及不同的机制。研究结果将有助于阐明功能基因的生物防治机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68b9/8147159/a92a9f1663ec/jof-07-00353-g007a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68b9/8147159/635b2e623bae/jof-07-00353-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68b9/8147159/e5310cf2fafc/jof-07-00353-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68b9/8147159/36de9547b05a/jof-07-00353-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68b9/8147159/edf841b8be76/jof-07-00353-g005a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68b9/8147159/5d0f48cb7371/jof-07-00353-g006a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68b9/8147159/a92a9f1663ec/jof-07-00353-g007a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68b9/8147159/635b2e623bae/jof-07-00353-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68b9/8147159/0e85d1d9eb50/jof-07-00353-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68b9/8147159/e5310cf2fafc/jof-07-00353-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68b9/8147159/36de9547b05a/jof-07-00353-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68b9/8147159/edf841b8be76/jof-07-00353-g005a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68b9/8147159/5d0f48cb7371/jof-07-00353-g006a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68b9/8147159/a92a9f1663ec/jof-07-00353-g007a.jpg

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