Analysis of Whole-Genome facilitates rapid and precise identification of fungal species

被引:3
作者
Qi, Guihong [1 ]
Hao, Lijun [1 ]
Xin, Tianyi [1 ]
Gan, Yutong [1 ]
Lou, Qian [1 ]
Xu, Wenjie [1 ]
Song, Jingyuan [1 ,2 ]
机构
[1] Chinese Acad Med Sci & Peking Union Med Coll, Key Lab Chinese Med Resources Conservat, State Adm Tradit Chinese Med Peoples Republ China, Inst Med Plant Dev, Beijing, Peoples R China
[2] Minist Educ, Engn Res Ctr Chinese Med Resource, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
Analysis of whole GEnome; AGE; fungal species identification; sequencing; genome editing; BIODIVERSITY; BACTERIAL; SEQUENCE; REGION; GENES; ITS2;
D O I
10.3389/fmicb.2024.1336143
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Fungal identification is a cornerstone of fungal research, yet traditional molecular methods struggle with rapid and accurate onsite identification, especially for closely related species. To tackle this challenge, we introduce a universal identification method called Analysis of whole GEnome (AGE). AGE includes two key steps: bioinformatics analysis and experimental practice. Bioinformatics analysis screens candidate target sequences named Targets within the genome of the fungal species and determines specific Targets by comparing them with the genomes of other species. Then, experimental practice using sequencing or non-sequencing technologies would confirm the results of bioinformatics analysis. Accordingly, AGE obtained more than 1,000,000 qualified Targets for each of the 13 fungal species within the phyla Ascomycota and Basidiomycota. Next, the sequencing and genome editing system validated the ultra-specific performance of the specific Targets; especially noteworthy is the first-time demonstration of the identification potential of sequences from unannotated genomic regions. Furthermore, by combining rapid isothermal amplification and phosphorothioate-modified primers with the option of an instrument-free visual fluorescence method, AGE can achieve qualitative species identification within 30 min using a single-tube test. More importantly, AGE holds significant potential for identifying closely related species and differentiating traditional Chinese medicines from their adulterants, especially in the precise detection of contaminants. In summary, AGE opens the door for the development of whole-genome-based fungal species identification while also providing guidance for its application in plant and animal kingdoms.
引用
收藏
页数:14
相关论文
共 47 条
[1]   AutoMLST: an automated web server for generating multi-locus species trees highlighting natural product potential [J].
Alanjary, Mohammad ;
Steinke, Katharina ;
Ziemert, Nadine .
NUCLEIC ACIDS RESEARCH, 2019, 47 (W1) :W276-W282
[2]   ITS1 versus ITS2 as DNA metabarcodes for fungi [J].
Blaalid, R. ;
Kumar, S. ;
Nilsson, R. H. ;
Abarenkov, K. ;
Kirk, P. M. ;
Kauserud, H. .
MOLECULAR ECOLOGY RESOURCES, 2013, 13 (02) :218-224
[3]   A label-free impedance biosensing assay based on CRISPR/Cas12a collateral activity for bacterial DNA detection [J].
Bonini, Andrea ;
Poma, Noemi ;
Vivaldi, Federico ;
Biagini, Denise ;
Bottai, Daria ;
Tavanti, Arianna ;
Di Francesco, Fabio .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2021, 204
[4]   Phosphorothioated Primers Lead to Loop-Mediated Isothermal Amplification at Low Temperatures [J].
Cai, Sheng ;
Jung, Cheulhee ;
Bhadra, Sanchita ;
Ellington, Andrew D. .
ANALYTICAL CHEMISTRY, 2018, 90 (14) :8290-8294
[5]   New and Improved Techniques for the Study of Pathogenic Fungi [J].
Cairns, Timothy C. ;
Studholme, David J. ;
Talbot, Nicholas. J. ;
Haynes, Ken .
TRENDS IN MICROBIOLOGY, 2016, 24 (01) :35-50
[6]   CRISPR-Cas12a target binding unleashes indiscriminate single-stranded DNase activity [J].
Chen, Janice S. ;
Ma, Enbo ;
Harrington, Lucas B. ;
Da Costa, Maria ;
Tian, Xinran ;
Palefsky, Joel M. ;
Doudna, Jennifer A. .
SCIENCE, 2018, 360 (6387) :436-+
[7]   Genome sequence of the model medicinal mushroom Ganoderma lucidum [J].
Chen, Shilin ;
Xu, Jiang ;
Liu, Chang ;
Zhu, Yingjie ;
Nelson, David R. ;
Zhou, Shiguo ;
Li, Chunfang ;
Wang, Lizhi ;
Guo, Xu ;
Sun, Yongzhen ;
Luo, Hongmei ;
Li, Ying ;
Song, Jingyuan ;
Henrissat, Bernard ;
Levasseur, Anthony ;
Qian, Jun ;
Li, Jianqin ;
Luo, Xiang ;
Shi, Linchun ;
He, Liu ;
Xiang, Li ;
Xu, Xiaolan ;
Niu, Yunyun ;
Li, Qiushi ;
Han, Mira V. ;
Yan, Haixia ;
Zhang, Jin ;
Chen, Haimei ;
Lv, Aiping ;
Wang, Zhen ;
Liu, Mingzhu ;
Schwartz, David C. ;
Sun, Chao .
NATURE COMMUNICATIONS, 2012, 3
[8]   Ultrasensitive and visual detection of SARS-CoV-2 using all-in-one dual CRISPR-Cas12a assay [J].
Ding, Xiong ;
Yin, Kun ;
Li, Ziyue ;
Lalla, Rajesh V. ;
Ballesteros, Enrique ;
Sfeir, Maroun M. ;
Liu, Changchun .
NATURE COMMUNICATIONS, 2020, 11 (01)
[9]   Taxonomy of Aspergillus section Flavi and their production of aflatoxins, ochratoxins and other mycotoxins [J].
Frisvad, J. C. ;
Hubka, V. ;
Ezekiel, C. N. ;
Hong, S. -B. ;
Novakova, A. ;
Chen, A. J. ;
Arzanlou, M. ;
Larsen, T. O. ;
Sklenar, F. ;
Mahakarnchanakul, W. ;
Samson, R. A. ;
Houbraken, J. .
STUDIES IN MYCOLOGY, 2019, (93) :1-63
[10]   Application of third-generation sequencing to herbal genomics [J].
Gao, Longlong ;
Xu, Wenjie ;
Xin, Tianyi ;
Song, Jingyuan .
FRONTIERS IN PLANT SCIENCE, 2023, 14