Quantitative and rapid on-site identification of multi-species toxic mushrooms with a portable sample-to-answer platform

Mushroom poisoning presents significant food safety and public health risks. The rapid, accurate point-of-care testing is critical for detoxification and saving lives. However, traditional toxin-based assays require costly instrumentation and specialized operators, making them unsuitable for rapid on-site testing of poisonous mushrooms. Thus, we developed a portable multiplex qPCR platform featuring a novel nucleic acid release rubbing tube that enables integrated sample-to-answer molecular diagnosis. This mechanically assisted nucleic acid release concept eliminates the need for chemical lysis or centrifugation. The cost-effective platform detects as few as 0.5 copies µL -1 (830.5 zM or 1.54 ag/μL) and simultaneously tests 6 samples / 12 species in 38 minutes—nearly half the time of standard commercial mushroom qPCR assays. Assay specificity was validated using 8 primer/probe sets derived from database-scale internal transcribed spacer (ITS) regions design workflow. Moreover, we successfully tested 24 toxic mushroom samples under raw, cooked, and digested conditions, demonstrating robust adaptability across real-world matrices. Beyond mushroom toxins, this modular, field-deployable qPCR architecture provides a prospective framework for universal on-site pathogen detection, environmental surveillance, and resource-limited diagnostic applications. • Portable qPCR multiplex platform for on-site detection of toxic mushrooms. • Three-minute, one-step DNA release with rubbing tubes, no centrifugation required. • Database-scale eight species-specific primers design validated against 26 species. • Robust and high sensitivity/specificity in raw, cooked, and digested samples.

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Publication Details

Journal
Journal of Food Composition and Analysis
Published
2026-01-29
DOI
https://doi.org/10.1016/j.jfca.2026.108950
Primary Topic
Silymarin and Mushroom Poisoning
Type
article
Field-Weighted Citation Impact
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article

Quantitative and rapid on-site identification of multi-species toxic mushrooms with a portable sample-to-answer platform

Zhengying Si, Q.H. Wang, Liping Guo, Yang Yu et al.
Journal of Food Composition and Analysis
Silymarin and Mushroom Poisoning
article

Quantitative and rapid on-site identification of multi-species toxic mushrooms with a portable sample-to-answer platform

Zhengying Si, Q.H. Wang, Liping Guo, Yang Yu, Fan Jiang, Jiayao He, Qiu S, Feng Chen, Shanshan Yu, Enjing Tian, Zhao Li, Guangsheng Liang
article en

Abstract

Mushroom poisoning presents significant food safety and public health risks. The rapid, accurate point-of-care testing is critical for detoxification and saving lives. However, traditional toxin-based assays require costly instrumentation and specialized operators, making them unsuitable for rapid on-site testing of poisonous mushrooms. Thus, we developed a portable multiplex qPCR platform featuring a novel nucleic acid release rubbing tube that enables integrated sample-to-answer molecular diagnosis. This mechanically assisted nucleic acid release concept eliminates the need for chemical lysis or centrifugation. The cost-effective platform detects as few as 0.5 copies µL -1 (830.5 zM or 1.54 ag/μL) and simultaneously tests 6 samples / 12 species in 38 minutes—nearly half the time of standard commercial mushroom qPCR assays. Assay specificity was validated using 8 primer/probe sets derived from database-scale internal transcribed spacer (ITS) regions design workflow. Moreover, we successfully tested 24 toxic mushroom samples under raw, cooked, and digested conditions, demonstrating robust adaptability across real-world matrices. Beyond mushroom toxins, this modular, field-deployable qPCR architecture provides a prospective framework for universal on-site pathogen detection, environmental surveillance, and resource-limited diagnostic applications. • Portable qPCR multiplex platform for on-site detection of toxic mushrooms. • Three-minute, one-step DNA release with rubbing tubes, no centrifugation required. • Database-scale eight species-specific primers design validated against 26 species. • Robust and high sensitivity/specificity in raw, cooked, and digested samples.

Journal of Food Composition and AnalysisVol. 151
North China Electric Power University (CN), Chinese Academy of Sciences (CN), Chinese Academy of Inspection and Quarantine (CN), Institute of Semiconductors (CN), Jilin Agricultural University (CN), University of Chinese Academy of Sciences (CN)
Openalex Percentile: Top 74%
Silymarin and Mushroom Poisoning
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