Analysis of Whole-Genome for Identification of Seven Penicillium Species with Significant Economic Value

被引:1
作者
Huang, Yuanhao [1 ]
Fu, Lianguo [2 ]
Gan, Yutong [1 ]
Qi, Guihong [1 ]
Hao, Lijun [1 ]
Xin, Tianyi [1 ]
Xu, Wenjie [1 ]
Song, Jingyuan [1 ,3 ]
机构
[1] Chinese Acad Med Sci & Peking Union Med Coll, State Key Lab Bioact Subst & Funct Nat Med, Inst Med Plant Dev, Beijing 100193, Peoples R China
[2] Southwest Jiaotong Univ, Sch Life Sci & Engn, Chengdu 610031, Peoples R China
[3] State Adm Tradit Chinese Med Peoples Republ China, Engn Res Ctr Chinese Med Resource, Minist Educ, Key Lab Chinese Med Resources Conservat, Beijing 100193, Peoples R China
关键词
Analysis of whole-GEnome; AGE; bioinformatics analysis; Sanger sequencing; CRISPR-Cas12a; Penicillium species identification; MYCOTOXINS; FUNGI; ROQUEFORTI; AMPLIFICATION; BACTERIAL; REGION; MAIZE; ACID;
D O I
10.3390/ijms25158172
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Penicillium genus exhibits a broad global distribution and holds substantial economic value in sectors including agriculture, industry, and medicine. Particularly in agriculture, Penicillium species significantly impact plants, causing diseases and contamination that adversely affect crop yields and quality. Timely detection of Penicillium species is crucial for controlling disease and preventing mycotoxins from entering the food chain. To tackle this issue, we implement a novel species identification approach called Analysis of whole GEnome (AGE). Here, we initially applied bioinformatics analysis to construct specific target sequence libraries from the whole genomes of seven Penicillium species with significant economic impact: P. canescens, P. citrinum, P. oxalicum, P. polonicum, P. paneum, P. rubens, and P. roqueforti. We successfully identified seven Penicillium species using the target we screened combined with Sanger sequencing and CRISPR-Cas12a technologies. Notably, based on CRISPR-Cas12a technology, AGE can achieve rapid and accurate identification of genomic DNA samples at a concentration as low as 0.01 ng/mu L within 30 min. This method features high sensitivity and portability, making it suitable for on-site detection. This robust molecular approach provides precise fungal species identification with broad implications for agricultural control, industrial production, clinical diagnostics, and food safety.
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页数:15
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