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RNAi Crop Protection
RNAi technology is a versatile, effective, safe, and eco-friendly alternative for crop protection. There is plenty of evidence of its use through host-induced gene silencing (HIGS) and emerging evidence that spray-induced gene silencing (SIGS) techniques can work as well to control viruses, bacteria, fungi, insects, and nematodes. For SIGS, its most significant challenge is achieving stability and avoiding premature degradation of RNAi in the environment or during its absorption by the target organism.
The world is moving toward a more sustainable crop production system that requires specific and efficient tools to battle plant pathogens. RNAi can be used for such purposes. The molecule is used in nature, degrades quickly, can disrupt the pathogen at a genetically specific level, and can complement the current agronomic crop protection practices used for organic, conventional, ecological, or technological production . The reader may be familiar with the concept of DNA and genes located in the nucleus of eukaryote cells, containing the instructions to create organic molecules, mainly proteins. RNA messenger works as an intermediator, carrying the nucleus’s message to the cytoplasm to be read by the ribosomes to assemble the protein. The RNAi eukaryotic machinery is a complex system for virus defense and gene expression control, sometimes called post transcriptional gene silencing (PTGS). The system can be triggered by external specific dsRNA, resulting in its RNA messenger being blocked before it gets to the ribosome, leaving the organism, such as a pathogen, disarmed . The extravesical delivery of dsRNA to disarm the expression system was proven to be natural and bidirectional from plant to fungal pathogens and vice versa cross-kingdom communication .
Consequently, RNAi represents an opportunity to emulate or improve the natural plant pathogen control system by providing well-designed external dsRNA . Here, we aimed to present advantages in crop protection mediated by RNAi. There are two RNAi plant-based technologies: host-induced gene silencing (HIGS) since the 1990s and emerging spray-induced gene silencing (SIGS). Both can provide sustainable solutions to control pathogens, such as insects, viruses, and fungi. We will focus on SIGS because it is becoming an emerging affordable option with a cost reduction of approximately USD 0.5–1 per gram ; the small amount of dsRNA necessary seems to be near 2–10 g per hectare; it is safe; and it has fast environmental degradation . When dsRNA is applied externally to plants, one proposed mechanism is that plant cells can take it and use it directly to tackle the pathogen through secreted vesicles containing the RNA at the site of the infection and plasmodesmata . The amount of sprayed RNA may vary depending on the target species’ sensitivity to RNAi, the capacity to trigger the defense system, and the efficiency of the delivery method. Other challenges for this technology are the need for science-based risk assessment procedures for topical RNAi applications within existing plant protection product legislation, regulatory approaches , and strategies to use more than one target sequence to avoid resistance of uptake .
2. How it Works
3. Potential Targets
The potential targets of RNAi can be viruses, fungi, bacteria, nematodes, and endogenous genes. Next, we describe a general table ( Table 1 ) containing several targets to demonstrate that the technology is flexible enough to start exploring other plagues, and broader reviews exist in case of interest by the reader . Out of these possibilities, we would like to remark on the potential of using SIGS to produce a new generation of crop protection-specific products.
Table 1. Potential targets for spray-induced gene silencing (SIGS) in plants.
|Target||Experimental Evidence||Target Genes||Reference|
|Virus||dsRNA + clay resulted in BCMV virus resistance for 20 d||Nib and CP genes of BCMV|||
|TMV Tobacco virus resistance for 7–20 d||CP, P126, RP of TMV|||
|Fungi||Inhibits Botrytis cinerea disease||DCL1, DCL2 of Botrytis cinerea|||
|Efficiently inhibited Fusarium graminearum||CYP51A, CYP51B, CYP51C of F. graminearum|||
|Sclerotinia sclerotiorum/Botrytis cinerea||mRNA splicing, ribosome biogenesis, protein disulfide oxidoreductase, peroxisomal protein|||
|Fusarium asiaticum, Botrytis cinerea, Magnaporthe oryzae, Colletotrichum truncatum||β2-tubulin|||
|Fusarium oxysporum f. sp. cubense and Mycosphaerella fijiensi, Fusarium||adenylate cyclase, DNA polymerase alpha subunit/delta subunit/CYP51|||
|Nematodes||Caenorhabditis elegans, Radopholus similis, Meloidogyne artiellia, Meloidogyne incognita, Globodera pallida||Several genes such as 16D10 peptide, chitin synthase, xylanase, glutathione-S- transferase, FMRF-like peptides|||
|Insects||Coleopterans are highly sensitive, Hemiptera, Orthoptera, Diptera, Hymenoptera, and Lepidoptera have different responses.||Several genes such as salivary protein C002, 16D10, αCOP, Cytochrome P450, Acetylcholinesterase, ABC transporter, β-actin, chitin synthase B|||
|Endogenous plant genes||Arabidopsis, Tobacco, poplar, rice||Transgenes/CHS/EPSPS/STM/WER/MYB1/WRKY23|||
4. Encapsulation Technology to Improve Efficiency
|Encapsulation System||Potential Crop Protection
2-(aminoethyl) methacrylate (AEMA)/dsRNA polyplex nanoparticles.
|Insecticide induces decreased feeding in Lepidopteran larvae (Spodoptera exigua), then promoting weight loss, developmental halt, and mortality.||Increases RNAi efficiency in targeting the essential gene chitin synthase B (ChSB), while preventing the degradation of dsRNA in the alkaline gut of insects and enhancing its cellular uptake in midgut cells.|||
|poly-[N-(3-guanidinopropyl) methacrylamide] (pGPMA)/dsRNA interpolyelectrolyte nanocomplex.||Ingestion insecticide regulates gene silencing in Lepidopteran larvae (Spodoptera frugiperda), increasing mortality from starvation and growth stunting.||Increased internalization and protection of dsRNA in insect cells, decreasing the accumulation of target mRNA due to the knockdown of genes related to vital functions such as nutrient absorption (sfVATPase), intracellular transport (sfKIF), and cell division (sfCDC27).|||
|Nematicide can homogeneously enter the nematode’s body (Caenorhabditis elegans) through noncanonical endocytotic pathways and attack specific genes. The combined effect decreases the development of the nematode by the action of the chitosan vehicle.||Increases RNAi efficiency of gene knockdown throughout the whole body of the nematode by introducing intact dsRNA through the Clathrin-mediated endocytosis pathway, which is different from the canonical pathway (sid-1 and sid-2) in the study model. Furthermore, chitosan was shown to effectively decrease myosin gene expression, which is critical for the growth and reproduction of the model nematode.|||
|Insecticide against Lepidopteran larvae (Spodoptera frugiperda) acts on genes related to the apoptosis pathway, inducing growth impairment and larval mortality.||Improves RNAi efficiency through the protection of dsRNA from degradation by intracellular and intercellular RNases. It also reduces the accumulation of dsRNA in the endosome while favoring its transport to the cytoplasm, where the formation of siRNAs is promoted, producing knockdown of apoptosis-related genes (iap).|||
|Layered double hydroxide (LDH) clay nanosheets/dsRNA||Develop a topical product that induces viral resistance in plants (against PMMoV and CMV) using dsRNA absorption technology in clay nanosheets (Bio-Clay).||Increased persistence of the topical treatment due to strong adhesion of dsRNA in the vehicle (LDH) and with the leaves. It also allows the controlled release of the biomolecule and confers protection against environmental degradation while favoring the internalization of dsRNA in the plant.|||
|Lipofectamine 2000 liposomes/dsRNA.||Insecticide against Diptera of the genus Drosophila (D. melanogaster, D. sechellia, D. yakuba, and D. pseudoobscura) acting by ingestion. It attacks essential genes of development through knockdown management.||Promotion of dsRNA internalization in insects through encapsulation protection, increasing silencing efficiency by promoting more significant RNAi accumulation in larvae. Knockdown of the genes of the VATPase (gut lumen pH stabilizer associated with nutrient uptake) and gTub23C (mitosis-related g-tubulin protein, essential for microtubule organization).|||
|Lipofectamine 2000 liposomes/dsRNA.||Specific insecticide against larvae and adults of Drosophila suzukii combining synergic effect of multiple gene knockdown. Oral administration route.||It facilitates uptake in the insect’s gut. It causes significant mortality in larvae and adults by the reduction in transcript levels of essential genes rps13 (housekeeping), alpha COP (coatomer subunit for trans-organelles transport), and vha26 (subunit of the vacuolar ATPase). The synergistic action of knockdown of the rps13 and alpha COP genes significantly increases mortality in the insect.|||
|Liposomes/dsRNA||Oral insecticide for the control of nymphs of Euschistus heros (hemiptera: pentatomidae), which is one of the main soybean pests in the field.||Protection of dsRNA against degradation promoted by the ribonuclease action of insect saliva. Enhanced silencing activity of target genes vATPaseA (V-type proton ATPase catalytic subunit A) and act-2 (muscle actin).|||
|Recombinant Flock House Virus FHV/dsRNA||Recombinant insecticide based on a viral vehicle transporting dsRNA silencers of essential genes in Drosophila melanogaster. For potential massive application in other species susceptible to FHV infection.||Use of the insect cell machinery to assemble infective recombinant FHV virions that carry target sequences for the production of dsRNA when replicating in cells. Thus, virions protect the sequences responsible for silencing the rps13 (housekeeping), alpha COP (coatomer subunit for trans-organelle transport), and vha26 (subunit of the vacuolar ATPase) genes while at the same time favoring dispersal in insects. It simulates natural viral infection.|||
|Virus-Like Particles (VLP)/dsRNA||Oral insecticide for the control of ants of several genera (Solenopsis invicta (fire ants), Camponotus pennsylvanicus and Camponotus floridanus (carpenter ants), Linepithema humile (Argentine ants), Tapinoma sessile (odorous ants), Tetramorium caespitum (pavementom ants), and Monstrous ants) pharaonis (pharaoh ants); inducing the silencing of physiological genes required for the survival of the colony.||Recombinant production in E. coli, which through specific plasmids manufactures capsid proteins of bacteriophages Qß and MS2 and inducible RNAi precursor sequences. The packaging of dsRNAs in VLPs protects them from degradation by nonspecific environmental organisms and the intestinal RNases of the target organism. It also favors its absorption by lining the gut cells. The silenced genes are related to the viability of the colony, for example, the induction of sterility and individual mortality. VLP carrying dsRNA is sprayed on the ground for spot application or incorporated into the bait. Target genes include VgR (vitellogenin receptor protein), TVXl (telomerase variant XI protein), PBAN (pheromone biosynthesis activating neuropeptide), PBANR (pheromone biosynthetic activating neuropeptide receptor), WLS (wntless protein), MEGF10 (multiple epidermal growth factor-like domain proteins 10), CHCP (clatherin heavy chain protein), CDC7 (cell division cycle 7-related protein), Cep89 (centrosomal protein 89 kdal), PSMBl (beta subunit of the type-1 proteosome), A5C (actin 5C protein), ATPSD (ATP synthase delta subunit); as well others related with anamorsin, beta actin, and Csp9 proteins||
WO2017/136353Al for APSE RNA Containers (ARCs)
|Ribonucleoprotein particle (RNP)/dsRNA||Insecticide for control of cotton boll weevil (Anthonomus grandis) adults.||Developing a protection and stability system for dsRNA avoids degradation by nucleases in the insect’s gut and favors rapid cellular incorporation. The above is based on a chimeric protein PTD-DRBD (peptide transduction domain–dsRNA binding domain) combined with dsRNA. This type of resulting protein is known as cell-penetrating peptide (CPP).|||
According to the data available in the references, we identified four principal encapsulation systems: the formation of liposomes, virus-like particles, polyplex nanoparticles, and bioclay. As mentioned in Table 2, these systems coincide in the biodegradability of the materials, the ability to improve the stability of RNAi, and its synergistic effect to induce control. Figure 2 presents a diagram of the most reported systems.
Figure 2. Primary encapsulation system for RNAi delivery.
Liposomes are spherical artificial vesicles synthesized from cholesterol and nontoxic natural phospholipids. They present hydrophilic and hydrophobic characteristics (amphiphilic molecules) that facilitate their interaction in multiple chemical environments .
The hydrophobic part consists of two fatty acid chains (10–24 carbon atoms and 0–6 double bonds in each chain), while the hydrophilic section is mainly phosphoric acid bound to a water-soluble molecule . They are made up of at least one phospholipid layer. The type of lipid defines properties such as surface charge, solubility, and size of the vesicles; therefore, it is critical in the functionality of the particle. For example, unsaturated phosphatidylcholine lipids form much more permeable but less stable bilayers, while saturated phospholipids with long acyl chains form more rigid and waterproof structures. According to their size, they are classified as very small (0.025 m) or large (2.5 m) vesicles . Multiple types of lipids are used as raw materials, the most frequent in the literature being phosphatidylglycerol (PG), phosphatidylcholine (PC), distearoylphosphatidylcholine (DSPC), dipalmitoylphosphatidylcholine (DPPC), dicetylphosphate, cholesterol (CH) stearylamine, or their mixture .
One advantage of this type of particle is its semipermeable character that simulates biological membranes, allowing smart delivery of the compounds it carries due to its cellular penetration capacity . Additionally, its low solubility in hydrophilic environments is an advantage when looking for a slow-release mechanism, which helps immobilize compounds and facilitate their environmental biodegradation. However, this technology also has some technical disadvantages, such as a short half-life due to oxidation and hydrolysis of phospholipids, vulnerability to temperature, and others related to its cost of production . The most cited synthesis methods are injection, electroformation, reversephase evaporation, hydration or thin-film hydration (Bangham method), microfluidics, freeze drying of double emulsions, heated membrane extrusion, detergent depletion, and supercritical fluid preparation. The challenge of the methods is to achieve stable vesicles with controlled and functional sizes .
The applications of liposomes are very versatile; for example, in the case of human and animal cells, they include a vast inventory of drug delivery systems to treat multiple diseases by reducing collateral damage in nontarget tissues and excessive doses . In food science, they are used for the protection and controlled delivery of enzymes, vitamins, functional compounds, antibiotics, and metabolites to improve the properties of food . In plants, in addition to the reports in Table 2 for RNAi delivery, they are used as carriers of CRISPR/Cas gene-editing systems, proteins, DNA, or mRNA . Additionally, lipofection (liposome-mediated DNA delivery) in protoplasts  and nutrient
transport/internalization are cited .
4.2. Virus Like-Particles (VLPs)
Virus-like particles (VLPs) are defined as supramolecular self-assemblies of proteins of approximately 10–200 nm in diameter, presenting the same or similar structure as that of native virions. VLPs are not infectious since they lack infective genetic material . In addition to being nanocarriers, VLPs can be functionalized on the surface by ligand proteins, exhibiting additional properties such as immunological and labeling reactivity to changes in the chemical environment .
VLPs can be produced by heterologous expression systems such as baculovirus, bacteria, yeast, plants, and animal cells (insects, mammals, etc.). The expression vector to be used must be selected depending on the type of the desired protein and the target organism since the system’s success may depend on post-translational modifications. According to the type of virus from which they are derived, VLPs are classified as single-stranded RNA positive-sense viruses, single-stranded RNA negative-sense viruses, double-1 stranded RNA viruses, and single- and double-1 stranded DNA viruses. Additionally, VLPs can be produced in crude protein extracts (cell-free system), mainly when heterologous expression implies the production of toxic compounds for the vector . Furthermore, the expression systems have different yields and are generally more efficient in viral and bacterial vectors.
VLP surface conjugation can be covalent and noncovalent; the first option is to functionalize VLPs with large molecules, even complete proteins. This type of conjugation is frequent through bacteriophage expression systems (MS2 and Q-beta) . Regarding noncovalent conjugation, a biotinylation process is required, which needs a linking agent such as streptavidin to ensure surface fixation .
Some of the advantages of VLPs are self-assembly, repetitive structural stability, and the resulting polydispersity systems. This improves uptake by target cells compared to that of naked molecules . Using cell recognition proteins represents lower barriers to biointeraction . However, its production is not exempt from limitations related to vectors and strategic aspects in terms of system complexity, speed of expression, performance, scalability, and regulation .
The main application of this technology is for prophylactic vaccines; however, their valuable properties allow them to be used as nanocarriers in drug and gene therapy, as scaffolds for bioimaging, and for the synthesis of bionanomaterials . Regarding its uses in plants and plant cells, in addition to being vehicles for the transport of RNAi, it is used to carry the CRISPR/Cas complex as a DNA-free gene editing system .
4.3. Polyplex Nanoparticles
The term polyplex nanoparticles refers to the encapsulation of genetic material in polymeric particles. The polymers used are polycations that electrostatically interact with negatively charged nucleic acid molecules. Thus, neutralization of charges (phosphodiester groups) and the consequent compaction in a colloidal complex occur. It is also stabilized by hydrogen bonding interactions between the components . The final properties of the polyplex depend on the physicochemical characteristics of the pristine polymers and the resulting nanoparticle features: size, surface charge, polydispersion, and hydrophilicity .
There is a large number of polymers used for the manufacturing of polyplexes, and a limited list of the most commonly used polymers includes poly(ethyleneimine) (PEI) , poly-L-lysine (PLL), poly(amidoesters) (PAE) , polyamidoamine (PAMAM), poly(2-dimethylaminoethyl methacrylate) (PDMAEMA) , polyethylene glycol (PEG), and chitosan , as well as copolymeric combinations such as phosphorylcholine-modified polyethyleneimine (PEI) PEGylated PEI-based, PEGylated poly(dimethylaminomethyl methacrylate) containing folate, PEI-grafted , -poly(N-3-hydroxypropyl)-DL-aspartamide, galactose-modified trimethyl chitosan-cysteine-based, and others . Theoretically, any
positively charged polymer could form a polyplex, of particular interest being biodegradable polymers such as PEG, poly(glutamic acid) (PGA), poly(caprolactone) (PCL), poly(D,Llactide- coglycolide) (PLGA), poly(lactic acid) (PLA), N-(2-hydroxypropyl)-methacrylate copolymers (HPMA), polystyrene-maleic anhydride copolymer, and poly(amino acids) (PAAs) . Polycations can also be synthesized by ring-opening polymerization controlling the resulting charge .
The synthesis methods of polyplexes are very diverse, defined by the raw material and the application. There are promising methodologies, such as the three-dimensional hydrodynamic focusing (3D-HF) technique supported by microfluidic devices. It seeks to optimize the properties and the resulting system’s effectiveness; since conventional methods can become a limitation since some of them involve an organic-aqueous interface, shear stress, or pH and temperature levels that can damage the genetic material .
Another limitation is the reduced biocompatibility and biodegradability of some polymers, as well as their cytotoxicity, requiring the production of derivatives to cope with these disadvantages . Nevertheless, they are a widely used transport mechanism for genetic material because they manage to prevent the degradation of genetic material caused by extracellular enzymes and precisely direct the load to the target cells, increasing the effectiveness of gene expression systems . Nanoparticle uptake occurs by endocytosis involving interactions with cell membrane glycoproteins and the formation of the endosome, followed by its release into the cell cytoplasm and further translocation to the target organelles .
Its main application is as a nonviral vector for DNA transfer in gene therapy, including regenerative medicine , AIDS, cancer, and hereditary disorder treatments . It has also been used for transfection and editing of genomes in plants , as well as for the gene silencing systems mentioned above aimed at disease and pest control .
Bioclay systems are based on 10–100 nm nanoclay particles able to transport selected compounds such as nucleic acids. Nanoclays are stratified aluminosilicates of a single (0.7 nm thick) or double layer (1 nm thick) with variable plasticity and swelling capacity. Its chemical formula is (Ca, Na, H) (Al, Mg, Fe, Zn)2(Si, Al)4O10(OH)2-xH2O. There are both natural and synthetic materials, and their structures consist of alternating tetrahedral SiO2 and octahedral AlO6 sheets with varying ratios .
Its properties depend on the nature of the atoms on the surface and the exchangeable cations between layers. Clays are negatively charged due to the substitution of Al3+ or Mg2+ ions by Si. Consequently, the surface of the nanolayer is hydrophobic due to Si-O covalent bonds; however, the addition of exchangeable hydrophilic cations can change the charge to positive . The most commonly used raw materials are bentonite, hectorite, montmorillonite, kaolinite, laponite, halloysite, laponite, sepiolite, saponite, and vermiculite. They are low-cost, nontoxic, and charge versatile vehicles .
Surface functionalization is frequently performed to adapt them to specific applications. Processes such as silylation prevent the aggregation of clays through covalent modification of the surface. For example, modified montmorillonite shows improvement in the polymer mechanical performance as well as in water absorption, cationic exchange, and ionic retention capacities. Other clays, such as sepiolite, are functionalized by grafting organosilane due to its many silanol groups on the surface, making them excellent heavy metal removers. Halloysite is modified mainly by covalent grafting of organosilane via condensation with hydroxyl groups . Synthetic clays, such as Laponite® (phyllosilicate composed of layered synthetic silicate), are obtained from inorganic mineral salts and are superficially modified by ion exchange or covalent linkage . Their applications mainly cover materials science, chemistry, physics, and biology, where they become strategic materials for developing smart nanoarchitectures. Among the most documented uses are drug delivery, environmental remediation, wastewater treatment, and food packaging . Plant biotechnology has also been used for the manufacture of nanocomposites to improve resistance properties in wood , vehicles for the controlled dosage of nutrients, and regulating soil properties . It is relevant to mention the transformation of desert soils into cultivable fields through liquid nanoclay .
5. Regulatory Approaches
The time and cost associated with obtaining the data for a registry of a biomolecule such as dsRNA can be low compared with that of a conventional pesticide of 4 versus 12 years and USD 3–7 million versus USD 280 . An important consideration is that dsRNA generally has low environmental persistence in soil, sediment, and water .
The biomolecule shows a record of safe consumption of short and long RNAs in the diet from food and lacks oral immunostimulation . Another positive input when regulating this technology is the technical discussion that has occurred over the last decade, where the USEPA and OECD (Organization for Economic Co-operation and Development) proposed using and adapting the existing plant protection product norms and procedures as described next. The United States Environmental Protection Agency (EPA) has analyzed addressing this technology based on problem formulation for human health and ecological risk assessment. At the same time, OECD proposed using risk assessment to evaluate the toxicity profile and exposure of the molecule by adapting the current regulatory framework for small-molecule agrochemicals as a general framework for dsRNA-based agricultural products and proposed taking into consideration the experience gained through the review
of dsRNA-based GE crops. The EFSA literature review on GM plants is a document to be taken into consideration as well. A summary is presented next in Table 3.
Table 3. Regulatory approaches.
Propose using Problem Formulation-
European Food Safety Authority (EFSA)
Do not directly address the spray products, but a literature review focused on RNAi-based GM plants and Risk Assessment
Proposed using risk assessment to evaluate the toxicity profile and exposure by using the current regulatory framework for small molecule agrochemicals as a general framework for dsRNA-based agricultural products. Proposed using the experience with the review of dsRNA-based GE crops
6. Conclusions and Future Perspectives
RNAi technology is a powerful and versatile alternative for pest and disease control in crops. Its use in the agricultural field extends to viruses, bacteria, fungi, insects, nematodes, and plants. It grows steadily with other complementary technologies, such as the recombinant production of RNAi in vectors, transgenesis, and micro/nanoencapsulation of candidate si/dsRNA. The main issue preventing its adoption in the past was the cost of production and stability. The cost of production is getting lower with the development of new technologies, while stability encapsulation strategies provide a solution to avoid degradation.
Together with the positive approaches to regulation, the emergence of more interdisciplinary alternatives that combine gene silencing by RNAi is also expected. For instance, the induction of resistance in crops by elicitation and metabolic control methods, using the strengths of both. Following this approach, we are developing a technology that uses elicitor nanoparticles made of natural polymers to induce defense in plants, which will also carry a double control mechanism based on RNAi to unblock inhibitors of systemic defense against systemic defense pathogenic species of the genus Fusarium. There is also interest in the scientific community to produce multiple knockdowns that protect systemically against a consortium of pathogens under the same application. Another challenge for this technology is to keep reducing production costs, for which biotechnology is emerging as one of the main allies to improve profitably on a large scale.
This entry is adapted from 10.3390/ijms222212148
- Hernández-Soto, A.; Echeverría-Beirute, F.; Guzmán-Hernández, T. The RNAi as a tool to control tropical pathogens. Agron. Mesoam. 2021, 32, 326–337.
- Yogindran, S.; Rajam, M.V. RNAi for Crop Improvement Sneha. In Plant Biology and Biotechnology; Bahadur, B., Rajam, M.V., Sahijram, L., Krishnamurthy, K.V., Eds.; Springer: New Delhi, India, 2015; Volume II, pp. 623–637.
- Wang, M.; Weiberg, A.; Lin, F.-M.; Thomma, B.P.H.J.; Huang, H.-D.; Jin, H. Bidirectional cross-kingdom RNAi and fungal uptake of external RNAs confer plant protection. Nat. Plants 2016, 2, 1–10.
- Cai, Q.; He, B.; Kogel, K.-H.; Jin, H. Cross-kingdom RNA trafficking and environmental RNAi—Nature’s blueprint for modern crop protection strategies. Curr. Opin. Microbiol. 2018, 46, 58–64.
- Castillo-González, C.; Zhang, X. The Trojan Horse of the Plant Kingdom. Cell Host Microbe 2018, 24, 1–3.
- Zhao, Y.; Liang, X.; Zhou, J.-M. Small RNA trafficking at the forefront of plant–pathogen interactions. F1000Research 2018, 7, 1633.
- Cai, Q.; Qiao, L.; Wang, M.; He, B.; Lin, F.-M.; Palmquist, J.; Huang, S.-D.; Jin, H. Plants send small RNAs in extracellular vesicles to fungal pathogen to silence virulence genes. Science 2018, 360, 1126–1129.
- Weiberg, A.; Wang, M.; Lin, F.-M.; Zhao, H.; Zhang, Z.; Kaloshian, I.; Huang, H.-D.; Jin, H. Fungal Small RNAs Suppress Plant Immunity by Hijacking Host RNA Interference Pathways. Science 2013, 342, 118–123.
- Giudice, G.; Moffa, L.; Varotto, S.; Cardone, M.F.; Bergamini, C.; De Lorenzis, G.; Velasco, R.; Nerva, L.; Chitarra, W. Novel and emerging biotechnological crop protection approaches. Plant Biotechnol. J. 2021, 19, 1495–1510.
- Taning, C.N.T.; Arpaia, S.; Christiaens, O.; Dietz-Pfeilstetter, A.; Jones, H.; Mezzetti, B.; Sabbadini, S.; Sorteberg, H.; Sweet, J.; Ventura, V.; et al. RNA-based biocontrol compounds: Current status and perspectives to reach the market. Pest Manag. Sci. 2020, 76, 841–845.
- Rodrigues, T.B.; Petrick, J.S. Safety Considerations for Humans and Other Vertebrates Regarding Agricultural Uses of Externally Applied RNA Molecules. Front. Plant Sci. 2020, 11, 407.
- Zotti, M.; dos Santos, E.A.; Cagliari, D.; Christiaens, O.; Taning, C.N.T.; Smagghe, G. RNA interference technology in crop protection against arthropod pests, pathogens and nematodes. Pest Manag. Sci. 2018, 74, 1239–1250.
- Mezzetti, B.; Smagghe, G.; Arpaia, S.; Christiaens, O.; Dietz-Pfeilstetter, A.; Jones, H.; Kostov, K.; Sabbadini, S.; Opsahl-Sorteberg, H.-G.; Ventura, V.; et al. RNAi: What is its position in agriculture? J. Pest Sci. 2020, 93, 1125–1130.
- Rutter, B.; Innes, R.W. Extracellular vesicles as key mediators of plant–microbe interactions. Curr. Opin. Plant Biol. 2018, 44, 16–22.
- Song, X.-S.; Gu, K.-X.; Duan, X.-X.; Xiao, X.-M.; Hou, Y.-P.; Duan, Y.-B.; Wang, J.-X.; Yu, N.; Zhou, M.-G. Secondary amplification of siRNA machinery limits the application of spray-induced gene silencing. Mol. Plant Pathol. 2018, 19, 2543–2560.
- Reagan, B.C.; Ganusova, E.E.; Fernandez, J.C.; McCray, T.N.; Burch-Smith, T.M. RNA on the move: The plasmodesmata perspective. Plant Sci. 2018, 275, 1–10.
- Wytinck, N.; Manchur, C.L.; Li, V.H.; Whyard, S.; Belmonte, M.F. dsRNA Uptake in Plant Pests and Pathogens: Insights into RNAi-Based Insect and Fungal Control Technology. Plants 2020, 9, 1780.
- Fire, A.; Xu, S.; Montgomery, M.K.; Kostas, S.A.; Driver, S.E.; Mello, C.C. Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans. Nature 1998, 391, 806–811.
- Wilson, R.C.; Doudna, J.A. Molecular Mechanisms of RNA Interference. Annu. Rev. Biophys. 2013, 42, 217–239.
- Axtell, M.J. Classification and Comparison of Small RNAs from Plants. Annu. Rev. Plant Biol. 2013, 64, 137–159.
- Muthamilarasan, M.; Prasad, M. Plant innate immunity: An updated insight into defense mechanism. J. Biosci. 2013, 38, 433–449.
- Lichtenberg, S.S.; Tsyusko, O.V.; Palli, S.R.; Unrine, J.M. Uptake and Bioactivity of Chitosan/Double-Stranded RNA Polyplex Nanoparticles in Caenorhabditis elegans. Environ. Sci. Technol. 2019, 53, 3832–3840.
- Rosa, C.; Kuo, Y.-W.; Yan, Z.; Falk, B.W. RNA Interference Mechanisms and Applications in Plant Pathology. Annu. Rev. Phytopathol. 2018, 56, 581–610.
- Worrall, E.; Bravo-Cazar, A.; Nilon, A.T.; Fletcher, S.J.; Robinson, K.E.; Carr, J.; Mitter, N. Exogenous Application of RNAi-Inducing Double-Stranded RNA Inhibits Aphid-Mediated Transmission of a Plant Virus. Front. Plant Sci. 2019, 10, 265.
- Konakalla, N.C.; Kaldis, A.; Berbati, M.; Masarapu, H.; Voloudakis, A.E. Exogenous application of double-stranded RNA molecules from TMV p126 and CP genes confers resistance against TMV in tobacco. Planta 2016, 244, 961–969.
- Niehl, A.; Soininen, M.; Poranen, M.M.; Heinlein, M. Synthetic biology approach for plant protection using dsRNA. Plant Biotechnol. J. 2018, 16, 1679–1687.
- McLoughlin, A.G.; Wytinck, N.; Walker, P.L.; Girard, I.J.; Rashid, K.Y.; De Kievit, T.; Fernando, W.G.D.; Whyard, S.; Belmonte, M.F. Identification and application of exogenous dsRNA confers plant protection against Sclerotinia sclerotiorum and Botrytis cinerea. Sci. Rep. 2018, 8, 1–14.
- Koch, A.; Biedenkopf, D.; Furch, A.; Weber, L.; Rossbach, O.; Abdellatef, E.; Linicus, L.; Johannsmeier, J.; Jelonek, L.; Goesmann, A.; et al. An RNAi-Based Control of Fusarium graminearum Infections through Spraying of Long dsRNAs Involves a Plant Passage and Is Controlled by the Fungal Silencing Machinery. PLoS Pathog. 2016, 12, e1005901.
- Gu, K.-X.; Song, X.-S.; Xiao, X.-M.; Duan, X.-X.; Wang, J.-X.; Duan, Y.-B.; Hou, Y.-P.; Zhou, M.-G. A β-tubulin dsRNA derived from Fusarium asiaticum confers plant resistance to multiple phytopathogens and reduces fungicide resistance. Pestic. Biochem. Physiol. 2019, 153, 36–46.
- Mumbanza, F.M.; Kiggundu, A.; Tusiime, G.; Tushemereirwe, W.K.; Niblett, C.; Bailey, A. In vitro antifungal activity of synthetic dsRNA molecules against two pathogens of banana, Fusarium oxysporumf. sp. cubense and Mycosphaerella fijiensis. Pest Manag. Sci. 2013, 69, 1155–1162.
- Höfle, L.; Biedenkopf, D.; Werner, B.T.; Shrestha, A.; Jelonek, L.; Koch, A. Study on the efficiency of dsRNAs with increasing length in RNA-based silencing of the Fusarium CYP51 genes. RNA Biol. 2020, 17, 463–473.
- Banerjee, S.; Banerjee, A.; Gill, S.; Gupta, O.; Dahuja, A.; Jain, P.K.; Sirohi, A. RNA Interference: A Novel Source of Resistance to Combat Plant Parasitic Nematodes. Front. Plant Sci. 2017, 8, 834.
- Iqbal, S.; Jones, M.G.K.; Fosu-Nyarko, J. RNA interference of an orthologue of Dicer of Meloidogyne incognita alludes to the gene’s importance in nematode development. Sci. Rep. 2021, 11, 1–12.
- Lilley, C.J.; Davies, L.J.; Urwin, P.E. RNA interference in plant parasitic nematodes: A summary of the current status. Parasitology 2012, 139, 630–640.
- Fanelli, E.; Di Vito, M.; Jones, J.; De Giorgi, C. Analysis of chitin synthase function in a plant parasitic nematode, Meloidogyne artiellia, using RNAi. Gene 2005, 349, 87–95.
- Kimber, M.J.; McKinney, S.; McMaster, S.; Day, T.A.; Fleming, C.C.; Maule, A.G. flp gene disruption in a parasitic nematode reveals motor dysfunction and unusual neuronal sensitivity to RNA interference. FASEB J. 2007, 21, 1233–1243.
- Christiaens, O.; Whyard, S.; Vélez, A.M.; Smagghe, G. Double-Stranded RNA Technology to Control Insect Pests: Current Status and Challenges. Front. Plant Sci. 2020, 11, 451.
- Knorr, E.; Fishilevich, E.; Tenbusch, L.; Frey, M.L.F.; Rangasamy, M.; Billion, A.; Worden, S.E.; Gandra, P.; Arora, K.; Lo, W.; et al. Gene silencing in Tribolium castaneum as a tool for the targeted identification of candidate RNAi targets in crop pests. Sci. Rep. 2018, 8, 1–15.
- Willow, J.; Soonvald, L.; Sulg, S.; Kaasik, R.; Silva, A.; Taning, C.; Christiaens, O.; Smagghe, G.; Veromann, E. First Evidence of Bud Feeding-Induced RNAi in a Crop Pest via Exogenous Application of dsRNA. Insects 2020, 11, 769.
- Willow, J.; Soonvald, L.; Sulg, S.; Kaasik, R.; Silva, A.I.; Taning, C.N.T.; Christiaens, O.; Smagghe, G.; Veromann, E. RNAi efficacy is enhanced by chronic dsRNA feeding in pollen beetle. Commun. Biol. 2021, 4, 1–8.
- Nitnavare, R.B.; Bhattacharya, J.; Singh, S.; Kour, A.; Hawkesford, M.J.; Arora, N. Next Generation dsRNA-Based Insect Control: Success So Far and Challenges. Front. Plant Sci. 2021, 12, 673576.
- Mutti, N.S.; Park, Y.; Reese, J.C.; Reeck, G.R. RNAi Knockdown of a Salivary Transcript Leading to Lethality in the Pea Aphid, Acyrthosiphon pisum. J. Insect Sci. 2006, 6, 1–7.
- Dubrovina, A.S.; Kiselev, K.V. Exogenous RNAs for Gene Regulation and Plant Resistance. Int. J. Mol. Sci. 2019, 20, 2282.
- Mitter, N.; Worrall, E.; Robinson, K.E.; Li, P.; Jain, R.G.; Taochy, C.; Fletcher, S.J.; Carroll, B.; Lu, G.; Xu, Z.P. Clay nanosheets for topical delivery of RNAi for sustained protection against plant viruses. Nat. Plants 2017, 3, 16207.
- Gurusamy, D.; Mogilicherla, K.; Palli, S.R. Chitosan nanoparticles help double-stranded RNA escape from endosomes and improve RNA interference in the fall armyworm, Spodoptera frugiperda. Arch. Insect Biochem. Physiol. 2020, 104, 1–15.
- Killmer, J.; Kumar, A.; McLaughlin, P.D.; Humberto, J.P. Methods and Compositions for Controlling Pests. Patent Application No PCT/US2017/015861, 31 January 2017.
- Christiaens, O.; Tardajos, M.G.; Reyna, Z.L.M.; Dash, M.; Dubruel, P.; Smagghe, G. Increased RNAi Efficacy in Spodoptera exigua via the Formulation of dsRNA With Guanylated Polymers. Front. Physiol. 2018, 9, 1–13.
- Wang, K.; Peng, Y.; Pu, J.; Fu, W.; Wang, J.; Han, Z. Variation in RNAi efficacy among insect species is attributable to dsRNA degradation in vivo. Insect Biochem. Mol. Biol. 2016, 77, 1–9.
- Ivashuta, S.; Zhang, Y.; Wiggins, B.E.; Ramaseshadri, P.; Segers, G.C.; Johnson, S.; Meyer, S.E.; Kerstetter, R.A.; McNulty, B.C.; Bolognesi, R.; et al. Environmental RNAi in herbivorous insects. RNA 2015, 21, 840–850.
- Kolliopoulou, A.; Taning, C.N.T.; Smagghe, G.; Swevers, L. Viral Delivery of dsRNA for Control of Insect Agricultural Pests and Vectors of Human Disease: Prospects and Challenges. Front. Physiol. 2017, 8, 1–24.
- Gillet, F.-X.; Garcia, R.A.; Macedo, L.L.P.; Albuquerque, E.; Silva, M.C.M.; Grossi-De-Sa, M.F. Investigating Engineered Ribonucleoprotein Particles to Improve Oral RNAi Delivery in Crop Insect Pests. Front. Physiol. 2017, 8, 1–14.
- Parsons, K.H.; Mondal, M.; McCormick, C.L.; Flynt, A.S. Guanidinium-Functionalized Interpolyelectrolyte Complexes Enabling RNAi in Resistant Insect Pests. Biomacromolecules 2018, 19, 1111–1117.
- Taning, C.N.T.; Christiaens, O.; Berkvens, N.; Casteels, H.; Maes, M.; Smagghe, G. Oral RNAi to control Drosophila suzukii: Laboratory testing against larval and adult stages. J. Pest Sci. 2016, 89, 803–814.
- Taning, C.N.T.; Christiaens, O.; Li, X.; Swevers, L.; Casteels, H.; Maes, M.; Smagghe, G. Engineered Flock House Virus for Targeted Gene Suppression Through RNAi in Fruit Flies (Drosophila melanogaster) In Vitro and In Vivo. Front. Physiol. 2018, 9, 1–13.
- Whyard, S.; Singh, A.D.; Wong, S. Ingested double-stranded RNAs can act as species-specific insecticides. Insect Biochem. Mol. Biol. 2009, 39, 824–832.
- Castellanos, N.L.; Smagghe, G.; Sharma, R.; E Oliveira, E.; Christiaens, O. Liposome encapsulation and EDTA formulation of dsRNA targeting essential genes increase oral RNAi-caused mortality in the Neotropical stink bug Euschistus heros. Pest Manag. Sci. 2019, 75, 537–548.
- Akbarzadeh, A.; Rezaei-Sadabady, R.; Davaran, S.; Joo, S.W.; Zarghami, N.; Hanifehpour, Y.; Samiei, M.; Kouhi, M.; Nejati-Koshki, K. Liposome: Classification, preparation, and applications. Nanoscale Res. Lett. 2013, 8, 1.
- Yadav, D.; Sandeep, K.; Pandey, D.; Dutta, R.K. Liposomes for Drug Delivery. J. Biotechnol. Biomater. 2017, 7, 1–8.
- Maja, L.; Željko, K.; Mateja, P. Sustainable technologies for liposome preparation. J. Supercrit. Fluids 2020, 165, 104984.
- Temidayo, O.B.; Olusanya, I.D.; Ahmad, R.R.H.; Ibegbu, D.M.; Smith, J.R.; Elkordy, A.A. Liposomal drug delivery systems and anticancer drugs. Molecules 2018, 23, 907.
- Wagner, A.; Vorauer-Uhl, K. Liposome Technology for Industrial Purposes. J. Drug Deliv. 2011, 2011, 1–9.
- Maherani, B.; Arab-Tehrany, E.; Mozafari, M.R.; Gaiani, C.; Linder, M. Liposomes: A Review of Manufacturing Techniques and Targeting Strategies. Curr. Nanosci. 2011, 7, 436–452.
- Alghuthaymi, M.; Ahmad, A.; Khan, Z.; Khan, S.; Ahmed, F.; Faiz, S.; Nepovimova, E.; Kuča, K.; Abd-Elsalam, K. Exosome/Liposome-like Nanoparticles: New Carriers for CRISPR Genome Editing in Plants. Int. J. Mol. Sci. 2021, 22, 7456.
- Ortiz-Matamoros, M.F.; A Villanueva, M.; Islas-Flores, T. Genetic transformation of cell-walled plant and algae cells: Delivering DNA through the cell wall. Briefings Funct. Genom. 2018, 17, 26–33.
- Karny, A.; Zinger, A.; Kajal, A.; Shainsky-Roitman, J.; Schroeder, A. Therapeutic nanoparticles penetrate leaves and deliver nutrients to agricultural crops. Sci. Rep. 2018, 8, 1–10.
- Zepeda-Cervantes, J.; Ramírez-Jarquín, J.O.; Vaca, L. Interaction Between Virus-Like Particles (VLPs) and Pattern Recognition Receptors (PRRs) From Dendritic Cells (DCs): Toward Better Engineering of VLPs. Front. Immunol. 2020, 11, 1100.
- Tagliamonte, M.; Tornesello, M.L.; Buonaguro, F.M.; Buonaguro, L. Virus-Like Particles. In Micro and Nanotechnology: Micro and Nanotechnology in Vaccine Development: Chapter 11; Skwarczynski, M., Toth, I., Eds.; William Andrew Publishing: Oxford, UK, 2017; pp. 205–219.
- Biabanikhankahdani, R.; Alitheen, N.B.M.; Ho, K.L.; Tan, W.S. pH-responsive Virus-like Nanoparticles with Enhanced Tumour-targeting Ligands for Cancer Drug Delivery. Sci. Rep. 2016, 6, 37891.
- Zeltins, A. Construction and Characterization of Virus-Like Particles: A Review. Mol. Biotechnol. 2012, 53, 92–107.
- Chackerian, B. Virus-like particles: Flexible platforms for vaccine development. Expert Rev. Vaccines 2007, 6, 381–390.
- Karandikar, S.; Mirani, A.; Waybhase, V.; Patravale, V.B.; Patankar, S. Nanovaccines for Oral Delivery-Formulation Strategies and Challenges. In Micro and Nanotechnology: Nanostructures for Oral Medicine: Chapter 10; Andronescu, E., Mihai, A.v., Eds.; Elsevier Inc.: Amsterdam, The Netherlands, 2017; pp. 263–293.
- Domingo-Espin, J.; Unzueta, U.; Saccardo, P.; Rodríguez-Carmona, E.; Corchero, J.L.; Vazquez, E.; Ferrer-Miralles, N. Engineered Biological Entities for Drug Delivery and Gene Therapy. Eng. Biol. Entities Drug Deliv. Gene Ther. Protein Nanoparticles 2011, 104, 247–298.
- Le, D.; Müller, K. In Vitro Assembly of Virus-Like Particles and Their Applications. Life 2021, 11, 334.
- Yan, D.; Wei, Y.-Q.; Guo, H.-C.; Sun, S.-Q. The application of virus-like particles as vaccines and biological vehicles. Appl. Microbiol. Biotechnol. 2015, 99, 10415–10432.
- Tsanova, T.; Stefanova, L.; Topalova, L.; Atanasov, A.; Pantchev, I. DNA-free gene editing in plants: A brief overview. Biotechnol. Biotechnol. Equip. 2021, 35, 131–138.
- Reineke, T.M.; Davis, M.E. Nucleic Acid Delivery via Polymer Vehicles. In Polymer Science: A Comprehensive Reference: Volumen 09: Polymers in Biology and Medicine; Matyjaszewski, K., Möller, M.v., Eds.; Elsevier B.V.: Amsterdam, The Netherlands, 2012; Volume 09, pp. 497–527.
- Rosenkranz, A.; Sobolev, A.S. Polyethylenimine-based polyplex nanoparticles and features of their behavior in cells and tissues. Russ. Chem. Bull. 2015, 64, 2749–2755.
- Wirth, T.; Ylä-Herttuala, S. Gene transfer vectors (DNA vehicles) and their incorporation into biomaterials for bone repair. Biomater. Bone Regen. Novel Tech. Appl. 2014, 374–405.
- Aggarwal, R.; Targhotra, M.; Kumar, B.; Sahoo, P.; Chauhan, M.K. Polyplex: A Promising Gene Delivery System. Int. J. Pharm. Sci. Nanotechnol. 2019, 12, 4681–4686.
- Lin, W.J.; Hsu, W.Y. Pegylation effect of chitosan based polyplex on DNA transfection. Carbohydr. Polym. 2015, 120, 7–14.
- Vasile, C. Polymeric Nanomaterials: Recent Developments, Properties and Medical Applications. In Micro and Nano Technologies: Polymeric Nanomaterials In Nanotherapeutics: Chapter 01; Vasile, C., Ed.; Elsevier Inc.: Amsterdam, The Netherlands, 2018; pp. 1–66.
- Zhang, Q.-F.; Yi, W.-J.; Wang, B.; Zhang, J.; Ren, L.; Chen, Q.-M.; Guo, L.; Yu, X.-Q. Linear polycations by ring-opening polymerization as non-viral gene delivery vectors. Biomaterials 2013, 34, 5391–5401.
- Hall, A.; Lächelt, U.; Bartek, J.; Wagner, E.; Moghimi, S.M. Polyplex Evolution: Understanding Biology, Optimizing Performance. Mol. Ther. 2017, 25, 1476–1490.
- Firoozi, B.; Nasser, Z.; Sofalian, O.; Sheikhzade-Mosadegh, P. Enhancement of the transfection efficiency of DNA into Crocus sativus L. cells via PEI nanoparticles. J. Integr. Agric. 2018, 17, 1768–1778.
- Zolghadrnasab, M.; Mousavi, A.; Farmany, A.; Arpanaei, A. Ultrasound-mediated gene delivery into suspended plant cells using polyethyleneimine-coated mesoporous silica nanoparticles. Ultrason. Sonochemistry 2021, 73, 105507.
- Christiaens, O.; Dzhambazova, T.; Kostov, K.; Arpaia, S.; Joga, M.R.; Urru, I.; Sweet, J.; Smagghe, G. Literature review of baseline information on RNAi to support the environmental risk assessment of RNAi-based GM plants. EFSA Support. Publ. 2018, 15, 173.
- Dhandapani, R.K.; Gurusamy, D.; Howell, J.L.; Palli, S.R. Development of CS-TPP-dsRNA nanoparticles to enhance RNAi efficiency in the yellow fever mosquito, Aedes aegypti. Sci. Rep. 2019, 9, 1–11.
- Kausar, A. Flame Retardant Potential of Clay Nanoparticles. In Micro and Nano Technologies: Clay Nanoparticles: Properties and Applications: Chapter 07; Cavallaro, G., Fakhrullin, R., Pasbakhsh, P., Eds.; Elsevier Inc.: Amsterdam, The Netherlands, 2020; pp. 169–184.
- Peña-Parás, L.; Sánchez-Fernández, J.A.; Vidaltamayo, R. Nanoclays for Biomedical Applications. In Handbook of Ecomaterials: Volumen 05; Martínez, L., Kharissova, O., Kharisov, B., Eds.; Springer Nature: Cham, Switzerland, 2019; pp. 3453–3471.
- Villanova-de-Benavent, C. Geological Overview of Clay Nanoparticles. In Micro and Nano Technologies: Clay Nanoparticles: Properties and Applications: Chapter 01; Cavallaro, G., Fakhrullin, R., Pasbakhsh, P., Eds.; Elsevier Inc.: Amsterdam, The Netherlands, 2020; pp. 3–36.
- Massaro, M.; Cavallaro, G.; Lazzara, G.; Riela, S. Covalently Modified Nanoclays: Synthesis, Properties and Applications. In Micro and Nano Technologies: Clay Nanoparticles: Properties and Applications: Chapter 13; Cavallaro, G., Fakhrullin, R., Pasbakhsh, P., Eds.; Elsevier Inc.: Amsterdam, The Netherlands, 2020; pp. 305–333.
- Cavallaro, G.; Lazzara, G.; Rozhina, E.; Konnova, S.; Kryuchkova, M.; Khaertdinov, N.; Fakhrullin, R. Organic-nanoclay composite materials as removal agents for environmental decontamination. RSC Adv. 2019, 9, 40553–40564.
- Lisuzzo, L.; Cavallaro, G.; Parisi, F.; Riela, S.; Milioto, S.; Lazzara, G. Colloidal Stability and Self-Assembling Behavior of Nanoclays. In Micro and Nano Technologies: Clay Nanoparticles: Properties and Applications: Chapter 04; Cavallaro, G., Fakhrullin, R., Pasbakhsh, P., Eds.; Elsevier Inc.: Amsterdam, The Netherlands, 2020; pp. 95–116.
- Hazarika, A.; Maji, T.K. Strain sensing behavior and dynamic mechanical properties of carbon nanotubes/nanoclay reinforced wood polymer nanocomposite. Chem. Eng. J. 2014, 247, 33–41.
- Mandal, M.; Halim, Z.; Maji, T.K. Mechanical, moisture absorption, biodegradation and physical properties of nanoclay-reinforced wood/plant oil composites. SN Appl. Sci. 2020, 2, 250.
- Guo, H.; White, J.C.; Wang, Z.; Xing, B. Nano-enabled fertilizers to control the release and use efficiency of nutrients. Curr. Opin. Environ. Sci. Health 2018, 6, 77–83.
- Bernardo, M.P.; Guimarães, G.G.F.; Majaron, V.F.; Ribeiro, C. Controlled Release of Phosphate from Layered Double Hydroxide Structures: Dynamics in Soil and Application as Smart Fertilizer. ACS Sustain. Chem. Eng. 2018, 6, 5152–5161.
- Songkhum, P.; Wuttikhun, T.; Chanlek, N.; Khemthong, P.; Laohhasurayotin, K. Controlled release studies of boron and zinc from layered double hydroxides as the micronutrient hosts for agricultural application. Appl. Clay Sci. 2018, 152, 311–322.
- Nourizadeh, H.; Bakhshayesh, A. Nanoclay-Based Products Across Global Markets. In StatNano Applied and Industrial Series: Nanoclay-Based Products Across Global Markets: Applications and Properties; Nourizadeh, H., Bakhshayesh, A., Eds.; StatNano Publications: Lund, Sweden, 2020; pp. 3–33.
- Parker, K.M.; Borrero, V.B.; Van Leeuwen, D.M.; Lever, M.A.; Mateescu, B.; Sander, M. Environmental Fate of RNA Interference Pesticides: Adsorption and Degradation of Double-Stranded RNA Molecules in Agricultural Soils. Environ. Sci. Technol. 2019, 53, 3027–3036.
- Bachman, P.; Fischer, J.; Song, Z.; Urbanczyk-Wochniak, E.; Watson, G. Environmental Fate and Dissipation of Applied dsRNA in Soil, Aquatic Systems, and Plants. Front. Plant Sci. 2020, 11, 11.