Back

Amplification-free CRISPR/Cas13a-based viroid detection in RNA extracts from infected plants

Le, L. T. T.; Montagud-Martinez, R.; Rodrigo, G.; Daros, J.-A.

2026-07-09 plant biology
10.64898/2026.07.02.736049 bioRxiv
Show abstract

Viroids are plant infectious agents that threaten agricultural production. Current viroid detection methods rely on RT-PCR-based assays, which require specialized laboratory equipment and can sometimes produce false-negative results or non-specific amplification due to the high sequence conservation among closely related viroid species. CRISPR-based diagnostics, particularly Cas12-based systems for DNA detection (DETECTR) and Cas13a-based systems (SHERLOCK) for RNA detection, have emerged as powerful tools for nucleic acid diagnostics. However, most existing workflows still rely on target amplification and, in the case of Cas13a systems, require additional in vitro transcription steps, limiting their simplicity and direct applicability for plant diagnostics. Here, we developed a direct amplification-free Cas13a-based detection platform for viroids using potato spindle tuber viroid (PSTVd) as a model. We optimized CRISPR RNA (crRNA) design, identified inhibitory effects of plant total RNA on readout signal, and employed simplified viroid RNA enrichment workflows enabling robust detection in plant samples. The system further supported both PSTVd-specific and broad-spectrum pospiviroid (genus Pospiviroid) detection and was successfully extended to avocado sunblotch viroid (family Avsunviroidae), demonstrating its adaptability across distinct viroid families. Together, these results establish a practical and modular Cas13a-based platform, not only for viroid diagnostics, but also for broader applications in RNA-derived plant pathogen detection. Graphical abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=68 SRC="FIGDIR/small/736049v1_ufig1.gif" ALT="Figure 1"> View larger version (18K): org.highwire.dtl.DTLVardef@1d04170org.highwire.dtl.DTLVardef@1783aa3org.highwire.dtl.DTLVardef@51baa7org.highwire.dtl.DTLVardef@1b542b9_HPS_FORMAT_FIGEXP M_FIG C_FIG Significance statementA simplified RNA enrichment workflow combined with CRISPR-Cas13a enables direct, amplification-free detection of plant viroids. The assay supports early and reliable diagnosis across different tomato varieties and provides a practical strategy for improving molecular detection of plant pathogens.

Matching journals

The top 7 journals account for 50% of the predicted probability mass.

1
Plant Biotechnology Journal
64 papers in training set
Top 0.1%
18.9%
2
Frontiers in Plant Science
256 papers in training set
Top 0.4%
12.2%
3
ACS Synthetic Biology
287 papers in training set
Top 0.6%
5.6%
4
The Plant Journal
215 papers in training set
Top 1%
5.3%
5
Scientific Reports
3612 papers in training set
Top 22%
4.4%
6
Plant Methods
42 papers in training set
Top 0.2%
3.6%
7
Horticulture Research
47 papers in training set
Top 0.2%
3.6%
50% of probability mass above
8
Journal of Experimental Botany
219 papers in training set
Top 2%
3.6%
9
BMC Genomics
406 papers in training set
Top 3%
2.5%
10
PLOS ONE
5266 papers in training set
Top 42%
2.4%
11
Journal of Virological Methods
37 papers in training set
Top 0.2%
2.4%
12
Plants
43 papers in training set
Top 0.7%
2.2%
13
Plant Communications
36 papers in training set
Top 0.4%
2.2%
14
New Phytologist
346 papers in training set
Top 3%
2.2%
15
Advanced Science
286 papers in training set
Top 4%
1.9%
16
Nature Communications
5641 papers in training set
Top 45%
1.7%
17
eLife
5828 papers in training set
Top 51%
1.5%
18
Nucleic Acids Research
1281 papers in training set
Top 10%
1.4%
19
PLOS Pathogens
820 papers in training set
Top 8%
1.1%
20
Plant Phenomics
18 papers in training set
Top 0.2%
0.9%
21
Biosensors and Bioelectronics
57 papers in training set
Top 0.7%
0.9%
22
Communications Biology
993 papers in training set
Top 29%
0.9%
23
Plant Physiology
238 papers in training set
Top 3%
0.6%
24
Virology Journal
32 papers in training set
Top 1.0%
0.6%
25
Talanta
14 papers in training set
Top 0.4%
0.6%