| Literature DB >> 36134297 |
Zheng Li1,2, Tao Yu2, Rajesh Paul2, Jingyuan Fan3, Yuming Yang4, Qingshan Wei2,5.
Abstract
Crop diseases caused by pathogenic microorganisms pose severe threats to the global food supply. Effective diagnostic tools for timely determination of plant diseases become essential to the assurance of agricultural sustainability and global food security. Nucleic acid- and antibody-based molecular assays are gold-standard methodologies for the diagnosis of plant diseases, but the analyzing procedures are complex and laborious. The prominent physical or chemical properties of nanomaterials have enabled their use as innovative and high-performance diagnostic tools for numerous plant pathogens and other important disease biomarkers. Engineered nanomaterials have been incorporated into traditional laboratory molecular assays or sequencing technologies that offer notable enhancement in sensitivity and selectivity. Meanwhile, nanostructure-supported noninvasive detection tools combined with portable imaging devices (e.g., smartphones) have paved the way for fast and on-site diagnosis of plant diseases and long-term monitoring of plant health conditions, especially in resource-poor settings. This journal is © The Royal Society of Chemistry.Entities:
Year: 2020 PMID: 36134297 PMCID: PMC9417629 DOI: 10.1039/c9na00724e
Source DB: PubMed Journal: Nanoscale Adv ISSN: 2516-0230
Fig. 1Methods for plant biotic stress monitoring. (a) Categories of different direct or indirect techniques for plant disease detection. (b) Chronological advances in nanoscale tools for plant disease diagnosis.
Fig. 2Microneedle-based plant DNA extraction and nanopore sequencing platform. (a) Photograph of a polymeric microneedle patch. (b) Illustration of plant pathogen DNA (Phytophthora infestans) extraction by applying MN patches on plant leaves. The microneedles can penetrate the leaf tissue and absorbs DNA on the surface of tips. (c) Principle of the handheld nanopore sequencing device (MinION) developed by Oxford Nanopore Technologies. (d) Alignment of reads produced by MinION from Prunus persica (peach) datasets to the total viral genomes using nanopore sequencing of whole transcriptome amplification. The target viruses are plum pox virus (PPV) and Candidatus Liberibacter asiaticus, two major viral pathogens of stone fruits. The inset shows the number of total viral reads versus the number of reads mapping to the P. persica genome. Figure panels reproduced from ref. 36 with permission from American Chemical Society, copyright 2019; ref. 47 with permission from American Phytopathological Society, copyright 2018.
Fig. 3Wearable sensors for the monitoring of plant health. (a) A photograph of the graphene-based relative humidity (RH) sensor for the detection of water movement from the roots to the lower and upper leaves within the plant. (b) Schematic illustration of the construction and detection mechanism of the RH sensor (upper figure). The lower figure shows the resistance measurement of this sensor as a function of RH. (c) Optical image and real image (inset) of a flexible polyimide-based plant drought sensor. (d) The drought stress responses over time on the Nicotiana tabacum leaf. The blue arrow points to normal conditions, while a red arrow points to drought. Figure panels reproduced from ref. 49 with permission from Wiley, copyright 2017; ref. 51 with permission from MDPI, copyright 2018.
Summary of nanoparticle-based sensors for plant pathogen or disease marker detection
| Target | Sensor component | Sensor Fabrication | Detection mechanism | Sensitivity | Specificity | Toxicity | Ref. |
|---|---|---|---|---|---|---|---|
|
| Au NP | Nanoparticle functionalization and DNA hybridization | Electrochemistry | 214 pM | Unresponsive to | Low |
|
|
| Ag NP-ssDNA | Nanoparticle functionalization and DNA hybridization | SERS | N/A | Unresponsive to | Low |
|
| Aflatoxins | Ag NR | Surface functionalization | SERS | 5 × 10−5 M for Aflatoxin B1 | Discriminable among Aflatoxin B1, B1, G1 and G2 | Low |
|
|
| Pt NP-IgG | Surface immunological functionalization | MALDI-TOF MS | ∼102 CFU | Discriminable between two bacteria | Low |
|
|
| Si NP-Rubpy-IgG | Surface immunological functionalization | Fluorescence quenching | 3 × 102 CFU | N/A | Moderate |
|
|
| Au NP-ssDNA | Surface functionalization | Colorimetry | 7.5 ng | No specific band revealed by PCR | Low |
|
|
| CdSe/ZnS-MPA | Surface functionalization | Fluorescence | 25 μg mL−1 | N/A | High |
|
|
| CdSe-PEI | Surface functionalization | Fluorescence | 10 μg mL−1 | N/A | High |
|
|
| CD | Surface functionalization | Fluorescence | pH range of 2.13–9.34 | No interference from ions | Low |
|
|
| CD | Surface functionalization | Fluorescence | N/A | Discriminable between | Low |
|
| 3′-Diphosphate-5′-diphosphate | Tb( | Metal ligation | Fluorescent ratiometry | 50 nM | Unresponsive to analogues including ATP, CTP, and UTP | Moderate |
|
|
| CdTe QD-CD | Surface immunological functionalization | FRET | 520 ng mL−1 | N/A | High |
|
|
| CdTe QD-Rd | Surface immunological functionalization | FRET | 220 ng mL−1 | N/A | High |
|
|
| TiO2 and SnO2 NP | Surface functionalization | Electrochemistry | 35–62 nM | Slightly responsive to | Low |
|
| Ethylene | Cu( | Ball-milling | Chemiresistor | 0.5 ppm | Unresponsive to common solvents except acetonitrile, THF, and acetaldehyde | Low |
|
| Ethylene | Pd( | Ultrasonic spray pyrolysis | Colorimetry | 0.17 ppm | Unresponsive to alcohols or esters | Moderate |
|
| Terpene vapor | Au NP@sol–gel | One-pot hydrolysis | LSPR | N/A | Discriminable among | Low |
|
| Various VOCs | Au NR-cysteine and nanoporous dyes | Surface functionalization | LSPR | 0.4–1.7 ppm for hexenal; 1.8–5.2 ppm for phenol | Discriminable among over ten VOCs | Low |
|
Nanoparticle.
Surface-enhanced Raman spectroscopy.
Tris(bipyridine)ruthenium(ii) chloride.
Immunoglobulin G.
Matrix-assisted laser desorption/ionization-time of flight mass spectroscopy.
3-Mercaptopropionic acid.
Quantum dot.
Polyethylenimine.
Carbon dot.
Förster resonance energy transfer.
Rhodamine 123.
Single-walled carbon nanotube.
Volatile organic compounds.
Fig. 4Metallic nanoparticles as nanobiosensors in plant pathogen detection. (a) Fluorescence microscopy to verify the functionality of the hybridization assay on an Ag nanoparticle-based SERS substrate. Top: hybridization of P. ramorum target DNA with matching P. ramorum capture probes; bottom: absence of signals for P. ramorum target DNA with non-matching P. lateralis capture probes. (b) Workflow chart showing procedures of Pt nanoparticle-assisted MALDI MS analysis of plant-associated bacteria from soil and root samples. Figure panels reproduced from ref. 68 with permission from Royal Society of Chemistry, copyright 2015; ref. 71 with permission from Elsevier, copyright 2012.
Fig. 5QDs used in the plant system. (a) Fluorescence imaging of the uptake and transport of QDs in Arabidopsis thaliana. (b) Schematic illustration of specific CTV biosensor based on FRET. (c) ZnO QDs were used to conjugate KAS for the controlled release of pesticides for the plant system. Figure panels reproduced from ref. 79 with permission from American Chemical Society, copyright 2015; ref. 89 with permission from International Frequency Sensor Association Publishing, copyright 2017; ref. 90 with permission from Elsevier, copyright 2019.
Fig. 6Different array-based nanosensor platforms for plant monitoring. (a) Schematic of AuNPs@MISG-coated Au nanoislands for selective detection of terpenes. (b) VOC sampling and detection of tomato late blight enabled by a 10-element nanostructured colorimetric sensor array using a smartphone-based detector. Early infection can be detected by the smartphone platform 2 days after inoculation. Figure panels reproduced from ref. 106 with permission from American Chemical Society, copyright 2018; ref. 107 with permission from Springer, copyright 2019.