Research Article

Towards Sustainable Paddy Disease Control: Exploring the Potential of Silver Nanoparticles

Roslina Ainna Roslan1, Athirah Marsya Azizul Rashidi1, Nurul Aili Zakaria1, Sharifah Aminah Syed Mohamad1,2 and Norfatimah Mohamed Yunus1*

1School of Biology, Faculty of Applied Sciences, Universiti Teknologi MARA (UiTM), 40450 Shah Alam, Selangor, Malaysia; 2Atta-ur-Rahman Institute for Natural Product Discovery (AuRIns), Level 9, FF3 Building, UiTM Puncak Alam Campus, 42300 Puncak Alam, Selangor, Malaysia.

Abstract | Nanotechnology offers promising solutions for sustainable agriculture, particularly in managing plant diseases. Silver nanoparticles (AgNPs), with their unique properties, have emerged as potent antibacterial agents against various plant pathogens. This review provides an overview of using AgNPs to treat paddy disease, a threat to global food security. The review explores various AgNPs production methods, including chemical reduction, photochemical synthesis, and electrochemical procedures. It delves into the application of AgNPs in combating paddy diseases, highlighting their advantages over conventional chemical treatments. While chemical pesticides and fungicides can effectively control paddy diseases, their overuse leads to pesticide resistance and poses environmental risks. This review demonstrates that AgNPs offer a safer and more sustainable alternative for paddy disease management. Studies have shown the efficacy of AgNPs against major paddy diseases like rice blast and sheath blight. The review discusses challenges and future directions for AgNPs-based treatments, emphasising their potential to develop eco-friendly strategies for global food security.


Received | September 26, 2024; Accepted | June 12, 2025; Published | November 05, 2025

*Correspondence | Norfatimah Mohamed Yunus, School of Biology, Faculty of Applied Sciences, Universiti Teknologi MARA (UiTM), 40450 Shah Alam, Selangor, Malaysia; Email: [email protected]

Citation | Roslan, R.A., A.M.A. Rashidi, N.A. Zakaria, S.A.S. Mohamad and N.M. Yunus. 2025. Towards sustainable paddy disease control: Exploring the potential of silver nanoparticles. Sarhad Journal of Agriculture, 41(4): 1681-1697.

DOI | https://dx.doi.org/10.17582/journal.sja/2025/41.4.1681.1697

Keywords | AgNPs, Biosynthesised nanoparticles, Oryza sativa, Paddy disease, Rice, Silver nanoparticles

Copyright: 2024 by the authors. Licensee ResearchersLinks Ltd, England, UK.

This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).



Introduction

Nanomaterials are substances with at least one spatial dimension measuring less than 100 nanometres. Nanoparticles are applied in fields such as pharmaceuticals, medicine, materials manufacturing, environmental protection, and agriculture (Masum et al., 2019). They include carbon nanotubes, nanorods, nanocapsules, and metallic NPs (Castillo-Henríquez et al., 2020). Among these, silver nanoparticles (AgNPs) are a specific type of NP composed of silver atoms. Silver nanoparticles exhibit distinct physical, chemical, and biological properties compared to bulk silver and other nanoparticle types. Their diminutive size and expansive surface area facilitate heightened reactivity, optical attributes, and antibacterial efficacy.

Silver nanoparticles have been widely used across various industries, including healthcare, consumer products (electronics, optics and cosmetics), and materials and surface treatments (textiles, coatings, paints, and pigments) (Temizel-Sekeryan and Hicks, 2020). In addition to these applications, AgNPs have shown promising results in plant disease management and promoting plant growth (Tariq et al., 2022). The silver nanoparticles have exhibited potent inhibitory activity against a broad spectrum of bacterial strains, including both Gram-positive and Gram-negative species (Al-Sharqi et al., 2019). Recent advances in nanoparticle synthesis have focused on safer and more environmentally friendly approaches compared to traditional chemical methods (Ibrahim et al., 2020). Silver nanoparticles are commonly produced by chemically reducing silver salts, such as silver nitrate, utilising reducing agents like sodium borohydride or sodium citrate. These synthesis procedures occur in the presence of stabilising compounds, including polyvinylpyrrolidone (PVP) or citrate, which help maintain the nanoparticles (Vega-Baudrit et al., 2019). AgNPs can also be synthesised using endophytic bacteria or fungi, where the nanoparticles exhibit both plant growth promotion and antibacterial activity against plant pathogens (Kumar et al., 2020; Zhu et al., 2024).

Despite the potential of AgNPs, there are limited studies on their application for paddy disease management. Rice blast, one of the most severe diseases affecting rice-growing regions, poses a significant threat to global food security. Rice, being a staple food for much of the world, is threatened by diseases such as brown leaf spot, bacterial leaf blight and bacterial panicle blight (Asghar et al., 2019; Datta et al., 2021; Raihanah et al., 2023). Traditional disease management techniques, such as breeding resistant varieties and applying pesticides, are widely used (Li et al., 2018). However, the overuse of pesticides has led to serious environmental issues. A safer alternative is the use of AgNPs, which have been shown to prevent damage from bacterial leaf blight in paddy crops (Chowdhury et al., 2022). Pyricularia oryzae, the fungus responsible for rice blast disease, threatens around 30% of the world’s food grain supply (Parthasarathy et al., 2022).

The challenges faced in paddy production include rising demand, water scarcity, climate change, and disease outbreaks (Ayub et al., 2024). Several major phytopathogens, including blast disease, sheath rot, brown spot, and bacterial blight, are prominent threats to paddy production globally. Accurate diagnosis and effective treatment are crucial for minimising the detrimental effects of these diseases on crop productivity. However, current diagnostic methods for paddy diseases are neither precise nor efficient, often requiring additional equipment. AgNPs, one of the most significant metallic NPs used in agriculture, offer promising potential in addressing these challenges. While AgNPs have been widely used in other crops, their use in paddy disease management remains underexplored.

This review paper’s findings are noteworthy, as they underscore the promising potential of nanoparticles in enhancing crop growth and managing plant diseases. NPs have been employed as treatments in diverse agricultural applications for some time, and researchers continue to explore the most effective NP types for addressing crop diseases. The review provides in-depth insights into how NP-based treatments can improve agricultural productivity and presents a potential environmentally sustainable approach for managing paddy diseases. Consequently, this study makes a vital contribution to advancing future research on paddy disease control strategies.

This review addresses the key issues related to paddy disease, including its causes and the most effective nanoparticle treatments. Additionally, the rationale for selecting AgNPs over organic chemicals is explored. Through these findings, the production of rice could become more stable and less susceptible to disease. Furthermore, the review highlights the properties of AgNPs and examines the advantages and disadvantages of using NPs in agriculture. This research aims to identify common paddy diseases, their causes, and the potential enhancement of treatments using AgNPs. Additionally, it explores the application and challenges of current paddy disease treatments, offering potential improvement solutions.

The overview of paddy (Oryza sativa)

Paddy is a critical food staple in developing nations. Timely and precise assessments of paddy rice cultivation and production can provide valuable insights for government authorities, planners, and policymakers, enabling them to develop effective strategies and policies. In addition to being essential for improving food security, it can create jobs, raise incomes, and decrease poverty. However, the agricultural sector faces complex challenges, including inconsistent production and relatively low yields. Paddy is a man-made ecosystem that is influenced by human activity, including changing cropping patterns, introducing resistant varieties, and applying pesticides. Paddy viral disease epidemics, characterised by fulminant, migratory, and intermittent outbreaks, originated from inappropriate human involvement that made environmental disruption worse (Ma et al., 2022). The prolonged outbreak of rice stripe disease (RSD), first reported in 2000, has served as a model system for advancing research on effective control strategies for plant viral diseases transmitted by insect vectors. Paddy (Oryza sativa L.), a significant cereal crop from the Poaceae family, is a staple food consumed by more than half of the global population, making it one of the world’s most crucial agricultural commodities (Simkhada and Thapa, 2021). Continued inaction will cause a marked reduction in paddy production, with serious implications for global food security and rice-dependent economies.

Paddy disease and the causes

Diseases in paddy crops, predominantly caused by pathogenic bacteria, fungi, and viruses, are a major constraint in rice production. These pathogens significantly reduce both grain yield and quality, posing serious challenges to food security in rice-dependent regions. A comprehensive understanding of the different types of pathogens responsible for these diseases is essential for developing effective management strategies.

Fungal pathogens

Paddy blast is one of the most devastating plant diseases affecting a crucial food staple with significant destructive potential in many developing countries (Simkhada and Thapa, 2021). The causal agent is the filamentous ascomycete fungus Magnaporthe oryzae (anamorphic form Pyricularia oryzae). The most conducive environment for the spread of disease is cloudy, with a relative humidity of 93 to 99%, a low nighttime temperature (15- 20 °C), and a longer dew period. The disease impacts all above-ground plant parts, with leaves, nodes, and panicles exhibiting the most severe symptoms. The affected plant components above the infected nodes are fragmented by irregularly shaped dark lesions encircling the nodes. In studies of neck blast, the fungus Magnaporthe oryzae attacks the peduncle during the flowering stage, leading to brownish-black lesions that result in poor or low grain filling. Additionally, leaf and collar blast caused by Pyricularia oryzae Cavara 1892 (A) can infect paddy tissues at any growth stage, potentially causing complete crop loss. As reported by Asibi et al. (2019), the pathogen infects various plant parts, including the leaves, leaf collars, culms, culm nodes, panicle neck nodes, and panicles, resulting in the development of lesions.

Additionally, the other paddy disease is sheath blight caused by the fungus Rhizoctonia solani. This disease is particularly prevalent from the tilling to heading growth stages (Nadarajah et al., 2014). Initial symptoms manifest as lesions on the lower leaf sheaths during late tiller or early internode elongation, which can then coalesce to encompass the entire leaf sheath and stem (Nadarajah et al., 2014).

Furthermore, brown spot disease caused by the fungus Bipolaris oryzae is prevalent in both upland and rainfed paddy cultivation methods (Laxman et al., 2016; Shaheen et al., 2024). This pathogen can also persist on contaminated paddy straw and stubble. The disease spreads through airborne spores, thriving under optimal conditions of temperatures ranging from 22 °C to 30 °C. This pathogen can also persist on contaminated paddy straw and stubble. The disease spreads through airborne spores, thriving under optimal conditions of temperatures ranging from 22°C to 30°C and relative humidity exceeding 92%. These environmental factors facilitate the development of lesions on the coleoptile, leaf blade, leaf sheath, and glumes, with the leaf blade and glumes exhibiting the most pronounced symptoms. According to Chen et al. (2022), it begins as little brown spots and gradually transforms into shapes ranging from cylindrical to round. The entire leaf dries out as these areas coalesce.

Sheath rot, caused by the fungus Sarocladium oryzae, is particularly detrimental when it manifests during the late booting stage, potentially resulting in significant crop damage (Fetene et al., 2020). The symptoms showed that the uppermost flag leaf sheaths were infected with the pathogen, which, in the boot stage, encircles the budding new particle. Then, another paddy disease is stem rot caused by Sclerotium oryzae, which is a significant soil-borne illness that reduces productivity by roughly 3-45% (Kannan et al., 2021). On paddy leaf sheaths, brownish to black water-soaked lesions without distinct edges were visible (Bashyal et al., 2021).

Bacterial sheath brown rot, caused by the pathogen Pseudomonas fuscovaginae, is a significant disease affecting paddy cultivation. This disease thrives under specific environmental conditions, including low temperatures, high humidity, and elevated altitudes in tropical and subtropical regions. Symptoms of sheath brown rot include grain discolouration, deformities, poorly filled panicles, sheath lesions, and reduced fertility.

Furthermore, Ustilaginoidea virens, the fungus that causes false smut, infects paddy during the reproductive and ripening stages (Song et al., 2021). Individual paddy grains get transformed into a mass of yellow fruiting bodies. Being enclosed in the floral parts, the growth of fuzzy spores can be seen. The immature spores exhibit a slightly flattened, smooth, yellow appearance and are enveloped by a membrane. According to Song et al. (2021), mature spots are orange in colour and turn yellowish-green or greenish black.

On the other side, leaf scald caused by Monographella albescens causes a yield loss in paddy by reducing the photosynthetic area. Leaf scald was first reported in Japan in 1955 and has been identified throughout the world where paddy is the main production (Bueno et al., 2017).

Next, bakanae disease which also known as the “foolish seedling” disease, is caused by the fungus Fusarium fujikuroi Nirenberg. Bakanae disease of paddy is caused by a haploid, heterothallic ascomycete fungus (Volante et al., 2017). Abnormally long seedlings, thin stems, and chlorotic leaves are caused by the high gibberellin secreted by the pathogen (Amr and Abd, 2020). Furthermore, infected plants that are already mature cannot produce normal panicles and grains.

Bacterial pathogens

Panicle blight disease, caused by Burkholderia glumae, affects panicles, turning them straw-colored and causing one or all of their florets to become blighted, often resulting in empty or aborted grains (Figure 1) (Raihanah et al., 2023).

Moreover, bacterial leaf streak (BLS) caused by the Xanthomonas oryzae Pv. oryzicola (Xoc) is a significant bacterial disease affecting paddy crops. Due to a lack of paddy cultivars with strong disease resistance, it is challenging to control (Wu et al., 2019).

 

Additionally, bacterial leaf blight (BLB), caused by the bacterium Xanthomonas oryzae pv. oryzae (Xoo) is a destructive disease affecting paddy crops (Vishakha et al., 2020).

Viral pathogens

Furthermore, Tungro disease, which is transmitted by the green leafhopper vector (Nephotettix virescens) in a semi-persistent manner after feeding on infected plants, is another significant paddy disease (Amelia et al., 2022). The leaf yellowing (chlorosis) process was due to cell proliferation and expansion induced a delay in the intercellular gaps’ development (Na Phatthalung et al., 2022). On young leaves, the yellowish-orange colour is present starting from the tips to the curly leaves, the reduction of tillers number and the plant growth is stunted (Amelia et al., 2022).

Additionally, the rice yellow mottle virus can severely diminish paddy yields. This virus was first identified in sub-Saharan Africa and Madagascar in 1966 and is transmitted to paddy seedlings by biotic vectors, such as Chrysomelidae beetles. (Syed-Ab-Rahman et al., 2020). Paddy yield loss is severely reduced by the rice yellow mottle virus (RYMV). It was first discovered in sub-Saharan Africa and Madagascar in 1966. RYMV is distributed to paddy seedlings via biotic agents like Chrysomelidae beetles. Even a small amount of the virus can cause infection to spread from contaminated soil to healthy transplanted seedlings. The ailment showed mottling, yellowish leaf streaking, shoot stunting, spikelet sterility, and decreased tillering (Sekiya et al., 2022).

Treatment of paddy disease

Various treatments are currently being applied to paddy crops as a means of managing diseases and enhancing overall production. In paddy blast disease caused by Pyricularia oryzae Cav, fungicide application, irrigation control, nutrient fertiliser use, and planting-resistant cultivars are all necessary. Extracts from coffee arabica are said to have a disease-inhibiting effect. It has also been successful to treat Trichoderma viridae seeds with 5 ml/L of water (Simkhada and Thapa, 2021). In addition, paddy blast disease, which results from infected and contaminated paddy seeds, can be treated using seed treatment. Currently, chemical fungicides for seed treatment have numerous drawbacks, including pathogen resistance, environmental harm, and health risk to farmers and consumers (Hashim et al., 2019). These adverse effects have heightened the demand for non-chemical seed treatment alternatives, such as the utilisation of hot water and antimicrobial biological agents. Hot water seed treatment effectively prevents pathogens in various vegetable crops. Microbial seed treatment can protect against soil-borne diseases and reduce seed-borne infections (Hashim et al., 2019). In comparison to untreated seeds, it was shown that seeds treated with Trichoderma asperellum, Bacillus subtilis, and hot water at 50°C for 15 minutes decreased the proportion of infected paddy seeds by 4.3% to 52.7%. Furthermore, the application of B. subtilis as a seed treatment has been shown to reduce the prevalence and severity of paddy blast disease by 10% to 72.4%.

A possible source of key features, such as novel resistance genes to combat pests like sheath blight and blast disease, is the wild Oryza species, which is closely related to cultivated paddy. In the case of bacterial blight and bacterial leaf streak, two mechanisms of resistance have been identified: (i) The qualitative resistance gene locus Xo1 can effectively counteract African Xoc isolates; (ii) The quantitative trait loci (QTL) qBlsr5a (xa5). Next, according to the treatment being applied to the brown spot paddy leaf roller (Cnaphalocrocis medinalis) was infested into the field and was eradicated by Foliar applications of Chlorpyriphos and Cypermethrin.

Conversely, the effect of chemical seed treatment on the paddy false smut control was studied by using 4 types of fungicides with different modes of action. The detection of Ustilaginoidea virens was conducted by taking paddy tissue samples using a Polymerase Chain Reaction (PCR) method at different rice-growing stages. At the maturation stage, the occurrence of false smut in the paddy was investigated. Seed treatment with fungicides is one of the best options for protecting paddy seedlings. Paddy false smut could infect the coleoptile and young root of paddy seedlings, thus causing the abnormal growth of paddy seedlings (Song et al., 2021). Then, in bacterial blight, antibiotics and chemical biocides are used to manage BLB disease in paddy. Streptomycin is mainly used; however, new research has shown that Xoo has a significant level of antibiotic resistance (Vishakha et al., 2020). Additionally, the induced resistance against paddy sheath blight exhibited by strain REB01 is attributed to the modulation of defence enzyme activities, as well as alterations in peroxide and polyphenol oxidase levels (Lin et al., 2021). Additionally, the spread of tungro disease can be addressed through mathematical modelling. Furthermore, the vector-borne model of paddy tungro disease has employed the application of insecticide to infected plants (Amelia et al., 2022).

On the other hand, the fungus Monographella albescens causes leaf scald disease, which harms paddy plants. It could drastically diminish paddy harvests by destroying the leaf surface, sterilising blooms, and degrading seeds, resulting in losses of up to 30%. M. albescens infection reduces CO2 penetration, the rate of carbon dioxide assimilation in the liquid phase, as well as the stomatal conductance to water vapour, are diminished even before the manifestation of leaf scald symptoms. The application of the sequence involving BRM-32113 alongside silicon fertilisers demonstrated a reduction in the severity of leaf scald, shielding the photosynthetic machinery and thereby providing a long-term strategy to mitigate the income losses associated with leaf scald in paddy cultivation (Bueno et al., 2017). Meanwhile, the paddy disease bakanae, commonly called a foolish seedling, is extremely damaging. It is found in practically every area of the planet where paddy is grown (Pathom-aree et al., 2019). To prevent the pathogenic Fusarium from infecting the seeds, nonpathogenic Fusaria are sprayed onto paddy blooms. The pathogen’s hyphal expansion in paddy flowers and seedlings is inhibited by the nonpathogenic Fusaria’s competition with it. F. fujikuroi causes bakanae disease, however, nonpathogenic Fusaria can persist in paddy seeds for at least 6 months, shielding the following generation from the illness (Saito et al., 2021).

Apart from that, sheath rot is treated with the use of resistant varieties because it is much cheaper and does not affect the environment. Based on Fetene et al. (2020), additionally, resistant variants could be developed through selection/screening or crossing (Fetene et al., 2020). Biological control offers an acceptable and prospective substitute for managing disease. Microbial bioagents employ a range of strategies to outcompete and suppress pathogens, including hyperparasitism, competition for resources and spatial dominance, antibiosis, and the stimulation of systemic resistance mechanisms within the host plants (Poveda et al., 2020).

In addition, the efficacy of the emulsion formulation in mitigating bacterial sheath brown rot of paddy has been observed through in vitro plate assays and greenhouse trials. Meanwhile, in rice yellow mottle virus (RYMV), host plant resistance is the most cost-effective and ecologically sustainable method of controlling the RYMV (Suvi et al., 2020). Table 1 summarises the related paddy diseases with their causes and treatments.

Silver nanoparticles and their characteristics

The growing interest in products made of components at the nano size has increased the demand for the manufacture of nanoparticles, especially AgNPs (Długosz and Banach, 2019). AgNPs have the potential for application as antibacterial agents in medical device coatings and wound dressings (Pal et al., 2017). AgNPs exposure may have unfavourable effects that could have unintended consequences. Comparing AgNPs to Ag ions, it is difficult to determine which

 

Table 1: The list of paddy diseases, causes, and treatments.

Paddy disease

Fungus or bacteria caused

Treatment

References

Rice blast

Magnaporthe oryzae

Application of fungicides.

(Simkhada, 2021)

Sheath blight

Rhizoctonia solani.

Novel resistance genes.

(Nadarajah et al., 2014)

Bacterial leaf streak

Xanthomonas oryzae Pv. oryzicola (Xoc).

Gene locus Xo1 and trait loci (QTL) qBlsr5a (xa5).

(Wu et al., 2019)

Blast (leaf and collar)

Pyricularia oryzae

Seed treatment of Pseudomonas fluorence.

(Asibi et al., 2019; Dey, 2022)

Brown spot

Bipolaris oryzae

Rice leaf roller (Cnaphalocrocis medinalis).

(Laxman et al., 2016)

False smut

Ustilaginoidea virens

Chemical seed treatment.

(Song et al., 2021)

Rice grassy stunt and rice ragged stunt

Nilaparvata lugens Stal

Classical miRNA and siRNA- based strategies

(Helina et al., 2020; Lacombe et al., 2021)

Bacterial blight

Xanthomonas oryzae pv. oryzae (Xoo)

Antibiotics and chemical biocides

(Vishakha et al., 2020; Lin et al., 2021)

Tungro

Nephotettix virescens

Mathematical modelling

(Na Phattalung et al., 2022)

Leaf scald

Monographella albescens

BRM- 32113 with Si fertilizers

(Bueno et al., 2017)

Bakanae

Fusarium fujikuroi

Preemptive seed

(Volante et al., 2017)

Sheath rot

Sarocladium oryzae (Sawada)

Usage of resistant varieties

(Fetene et al., 2020)

Stem rot

Sclerotium oryzae

The use of native isolates of Trichoderma as a biocontrol agent to treat rice stem rot

(Kannan et al., 2021; Bashyal et al., 2021)

Bacterial sheath brown rot

Pseudomonas fuscovaginae

Emulsion formulation

(Syed et al., 2020)

Rice stripe disease

Rice stripe virus (RSV)

Insecticides application

(Ma et al., 2022)

Rice yellow mottle virus

Rice yellow mottle virus (RYMV).

Host plant resistance

(Suvi et al., 2020; Sekiya et al., 2022)

 

AgNPs effect is the most notable or what function particle size plays in determining these effects. Engineered nanomaterials (ENMs) were created and developed for a variety of applications in numerous industrial sectors due to their small size within the range of 1 and 100 nm and distinctive chemical and physical properties (Yan and Chen, 2019). Relative to silver in its macroscale state, nanoparticles have exhibited an enhanced surface area to volume ratio and improved functional capacity (Bruna et al., 2021). AgNPs are the most widely used nanomaterial among the many ENMs types. AgNPs are involved in all nanotechnology consumer products, with more than 25%. On the other side, in the agriculture sector, AgNPs were developed as fungicides to prevent fungal infections, plant growth promoters, or agents to accelerate the process of fruit ripening.

Characterisation of silver nanoparticles

Several techniques can be used to characterise the AgNPs. According to Rautela et al. (2019), transmission electron microscopy (TEM) analysis estimated the AgNP size to range between 10 and 30 nm (Rautela et al., 2019). Additionally, scanning electron microscopy (SEM), Energy Dispersive Spectroscopy (EDS), and X-ray diffraction (XRD) were utilised to examine the size, morphology, and confirm the presence of silver in the resultant AgNPs pellets (Ibrahim et al., 2020). For the particle size distribution analysis, the produced AgNPs solution was diluted with Milli-Q water and analysed using a dynamic light scattering particle size analyser. (Chowdhury et al., 2022). Meanwhile, the absorbance between 200 and 800 nm with a resolution of 1 nm was determined using UV-Vis spectroscopy (Ibrahim et al., 2019). The surface plasmon resonance (SPR) properties of the produced AgNPs were represented by a large peak in the UV-Vis spectra of the particles. After 0.5% and 1.0% rice leaf extract reacted with AgNO3 solution, the peak’s strength rose however, the concentration of rice leaf extract at 2% caused the intensity to decline. Therefore, 1% of rice leaf extract was consequently thought to be the ideal concentration to produce AgNPs (Ibrahim et al., 2019).

The synthesis of silver nanoparticles

Several studies showed the production of AgNPs. The production of AgNPs through a biological process is referred to as the biosynthesis of AgNPs. According to Ibrahim et al. (2020), AgNPs were produced by an onion endophytic bacterium (Ibrahim et al., 2020). Endophytic bacteria are a form of bacterium known as an endophyte that dwells inside the tissues of a host plant without harming the host plant. The endophytic bacteria are cultivated using the approach on a nutrient-rich medium, and the filtration is then dissolved in an Ag salt solution. The microbial metabolites facilitate the reduction of silver ions, leading to the synthesis of silver nanoparticles.

Synthesising AgNPs using the biosynthesis of endophytic bacteria is a safe and eco-friendly method (Ibrahim et al., 2019). On the other hand, Magnaporthe oryzae, the cause of the rice blast, was significantly inhibited by the 40 μg/mL concentration of biosynthesised AgNPs, exhibiting an 88% inhibition rate in terms of mycelial growth. Moreover, M. oryzae’s spore germination and appressorium development were markedly reduced by the biosynthesised AgNPs. Therefore, it is inferred that M. oryzae growth is effectively inhibited by the AgNPs produced by onion endophytic bacteria (Ibrahim et al., 2020). Additionally, because biosynthesis uses plant extract, which has benign qualities and supplies natural capping agents, biogenic synthesis is a wonderful method for producing AgNPs (Ibrahim et al., 2019). Compared to other chemical processes, this one is thought to be economical and environmentally beneficial. The result nanoparticles may also possess distinctive properties that render them suitable for diverse applications, including antibacterial agents. Due to their distinctive biological, physicochemical, and antibacterial activity capabilities in controlling plant diseases, biogenic AgNPs have received considerable attention (Ahmed et al., 2020). Otherwise, the sunlight-induced synthesis of AgNPs is a method that uses natural sunlight to prepare AgNPs from easily raw materials. The sunlight’s energy activates the reduction of Ag+ ions to form AgNPs. Following that, the as-prepared AgNPs are analysed under several methods, which are TEM, DLS, XRD, EDS, and UV-vis spectroscopy. This process is regarded as easy, environmentally friendly, and creates no toxic by-products (Rajasekar et al., 2021).

The biosynthesis of silver nanoparticles using Phyllanthus emblica fruit extract was achieved by adding varying concentrations to a 100 ml aqueous solution of 1 mM silver nitrate. The mixture was then boiled for 20 minutes at 65°C and subsequently maintained at room temperature in the dark. The synthesis of AgNPs was confirmed by observing the colour change to dark brown, which is indicative of nanoparticle formation. Further analysis of the AgNPs revealed a UV-visible spectrum with a peak at 430 nm, corresponding to the surface plasmon resonance of the AgNPs produced by the phytochemical agents present in the Phyllanthus emblica fruit extract (Masum et al., 2019).

The effects of silver nanoparticles on paddy

In addition to conventional methods such as chemical treatments, nanoparticles have emerged as promising alternatives for managing paddy diseases. Among these, silver nanoparticles (AgNPs) have gained increasing attention for their application as both biopesticides and nano-fertilizers. This paper focuses specifically on the potential of AgNPs in combating paddy diseases. A total of twelve studies on the application of AgNPs in rice disease management highlighting various rice diseases, their associated phytopathogens, and AgNPs concentrations are summarized in Table 2.

 

Table 2: Overview of silver nanoparticles (AgNPs) applications in rice disease control.

Rice disease

Phytopathogens

Reducing and stabilizing agent

Synthesis condition

Average particle size/ range (nm)

Concentrations of AgNPs

Reference

Rice blast

Magnaporthe oryzae

Bacillus sp.

1 mM AgNO₃ at 30 °C under shaking conditions (200 rpm) for 4 days in the dark

2.00 and 15.00

2 μg mL−1

(Shi et al., 2023)

Rice blast

Magnaporthe oryzae

Bacillus endophyticus

3 mM AgNO3 were shaken at 30oC for 200 rpm. for 3 days in the dark.

4.17 to 26.9

40 µg/mL

(Ibrahim et al., 2020)

Rice bakanae

Fusarium sp.

Azadirachta indica leaf aqueous extract

2 g AiLAE and 1 mM AgNO₃ at a 1:19 extract-to-AgNO₃ ratio, maintained at 85 °C for 4 hours.

4 to 27 nm, average size of 15 nm

17.24 μg/mL

(Akhter et al., 2024)

Rice sheath blight

Rhizoctonia solani

Ipomoea carnea leaf extract

2 mM AgNO₃ at a 1:10 leaf extract-to-AgNO₃ ratio, adjusted to pH 10, and carried out for 30 minutes.

30 to 90

1.5 ppm

(Islam et al., 2024)

Rice sheath blight

Rhizoctonia solani

Pseudomonas fluorescens OKC (Accession number JN128891)

1 mM AgNO₃ at a 3:1 extract to AgNO₃ ratio, maintained at room temperature until a color change was observed.

~74.00

30 ppm

(Lopamudra et al., 2023)

Rice sheath blight

Rhizoctonia solani

rice leaf extract

0.4% rice leaf extract and 0.6 mM AgNO₃, followed by autoclaving at 121 °C and 103 kPa in a domestic pressure cooker for 30 minutes.

~110.80

20 μg/mL

(Kora et al., 2020)

Rice sheath blight

Rhizoctonia solani

N/A

4000 ppm (commercialized AgNPs)

5.00 to 10.00

50 ppm

(Soltani et al., 2017)

Bacterial Leaf Blight

Xanthomonas oryzae pv. oryzae (Xoo)

Bacillus cereus

5 mM AgNO₃ at 28 ± 2 °C under orbital shaking at 150 rpm for 24 hours.

18.00 to 39.00

100 mgL-1

(Ahmed et al., 2020)

Bacterial leaf blight

Xanthomonas oryzae pv. oryzae

Calliblepharis fimbriata aqueous extract

1 mM AgNO3 at a 9:1 aqueous extract was kept at 35 °C, then incubating the mixture in the dark room for 48 hours.

25.00 to 30.00

50 μg/mL

(Thynraj et al., 2021)

Bacterial leaf blight

Xanthomonas oryzae pv. oryzae

Arctium lappa fruit

2 mM AgNO3 and 3 plant extracts were shaken at 30oC for 200 rpm.

20.18

20 µg/mL

(Tian et al., 2022)

Solanum melongena leaves

21.00

Taraxacum mongolicum leaves

40.08

Bacterial leaf blight and bacterial brown stripe

Xanthomonas oryzae pv. oryzae and Acidovorax oryzae

Bacillus siamensis

3 mM aqueous silver nitrate (AgNO3) and incubating at 30oC for 24 hours.

25.00 to 50.00

20 μg mL-1

(Ibrahim et al., 2019)

Rice brown spot

Bipolaris oryzae

NaBH4

1 mmol L-1 AgNO3 were added gradually into 2 mmol L-1 NaBH4. The AgNPs were kept at 4°C in the dark.

~20

10 µmol L-1

(Almeida et al., 2024)

 

Nanoscale silver exhibits distinctive properties, such as a large specific surface area, high target adhesion, robust permeability, and potent bactericidal activity, making it suitable for various applications. These characteristics make it more effective than other substances like streptomycin and copper at penetrating cell membranes or clinging to bacterial surfaces (Rajasekar et al., 2021). Significant growth of the paddy seedlings was aided by the biosynthesised AgNPs. According to Ibrahim et al. (2019), paddy seedlings treated with AgNPs had longer roots, shoots, fresh weight, and dry weight than seedlings treated with water (Ibrahim et al., 2019). Specifically, paddy seedlings treated with silver nanoparticles exhibited enhanced growth characteristics, including root lengths of approximately 7.4 cm, shoot lengths of 11.6 cm, fresh weights of 0.24 g, and dry weights of 0.04 g. In contrast, seedlings treated with water had comparatively shorter root lengths (5.1 cm), shoot lengths (6.5 cm), fresh weights (0.12 g), and dry weights (0.03 g). These findings suggest that the application of AgNPs has a beneficial effect on the growth and development of paddy seedlings.

The research by Ahmed et al. (2020) indicates that silver nanoparticles synthesised by Bacillus cereus SZT1 have been demonstrated to mitigate the damage caused by the paddy leaf blight. Compared to untreated control plants, AgNP suspensions at various concentrations significantly reduced the lesion length associated with bacterial leaf blight (BLB). The maximum inhibition rate was observed in paddy plants treated with an AgNP suspension at a concentration of 25-100 mg L-1. These findings suggest that biogenic AgNPs have significant potential for the biological management of bacterial leaf blight in paddy cultivation. Meanwhile, synthesised AgNPs from Phyllanthus emblica fruit extract exhibited exceptional antimicrobial activity against Acidovorax oryzae strain RS-2, which is the pathogen responsible for paddy bacterial brown stripe disease. The AgNPs prevented bacterial growth and interfered with their capacity to form biofilms and swarm. AgNPs caused cell membrane disruption in strain RS-2, which led to an increase in the release of the effector Hemolysin Coregulated Protein (Hcp). It is a particular class of effector protein that many Gram-negative bacteria produce and is regarded as a distinctive element of the Type VI Secretion System (T6SS). Given the circumstances, AgNPs may be a desirable and environmentally acceptable choice to treat Acidovorax oryzae strain RS-2-induced paddy bacterial illness (Masum et al., 2019).

Mechanisms of antimicrobial action and toxicity of silver nanoparticles

The antimicrobial activity of silver nanoparticles (AgNPs) is attributed to their ability to bind to the cell membrane, which disrupts the phospholipid bilayer structure. This disruption suppresses mycelial growth and inhibits the germination of conidia, causing damage to the cell wall and compromising membrane integrity. Therefore, the cell membrane becomes more permeable, allowing the AgNPs to enter the cells. Once internalised, these nanoparticles interfere with intracellular organelles and the interactions of large molecules, leading to the generation of elevated levels of reactive oxygen species (ROS) and free radicals. This accumulation affects the biological processes within the cells by disrupting signal transduction pathways, metabolic processes, and genetic information processing, ultimately leading to cell death (Shi et al., 2023; Akhter et al., 2024).

Silver nanoparticles exhibit toxicity through various mechanisms, primarily involving the release of silver ions (Ag+), which interact with cellular components and generate reactive oxygen species. ROS cause oxidative stress, damaging cellular structures like DNA, proteins, and lipids, leading to cell death. The physical properties of AgNPs, such as size, shape, and surface coating, also influence their toxicity. Smaller particles exhibit higher toxicity due to their larger surface area to volume ratio, facilitating greater interaction with biological systems (Khan et al., 2023). The overall working mechanism of silver nanoparticles (AgNPs) in disease control, including their antimicrobial action and interaction with phytopathogens, is illustrated in Figure 2.

While AgNPs demonstrate antimicrobial properties even at high concentrations, their toxicity to other organisms raises concerns about environmental and human health risks. Furthermore, the presence of natural organic matter can alter the toxicity of AgNPs by influencing their aggregation and dissolution behaviour. Sulfidation, a process where silver reacts with sulfur-containing compounds, can reduce the toxicity of AgNPs, but its long-term effects are still under investigation (Li et al., 2019).

Determining the allowable max. concentration of AgNPs is complex and depends on numerous factors,

 

including the specific application, the organism being considered, and the exposure route. Regulatory agencies in different countries have established guidelines for silver content in various products, but specific limits for AgNPs are still evolving. For instance, in the phytotoxicity of AgNPs in rice, 1 mg/L of AgNPs will cause a reduction in root elongation, as well as decreases in shoot and root fresh weights, total chlorophyll, and carotenoid contents, reduce the plant biomass and a reduction in sugar content (Pan et al., 2024). Additionally, there was an increase in malondialdehyde, lipid peroxidation and hydrogen peroxide (H2O2) levels in the leaves, shoots, and roots (Pan et al., 2024). At 60 mg/L, the structure and cell morphology will be altered, decreasing in total soluble carbohydrates, causing the production of reactive oxygen species (ROS) and localised root tissue death. At 1000 mg/L, seed germination and seedling growth were impaired, damaging the cell walls and vacuoles of root cells (Yan and Chen, 2019). Further research is needed to establish comprehensive guidelines for safe AgNPs concentrations in different environments and applications. Table 3 provides a comparative overview of the mechanisms of action and nanoparticle-based treatments used in various crops, including tomato, wheat, and paddy, indicating their potential applicability across plant species

Application of silver nanoparticles in plant disease

Various nanoparticles, nanomaterials and nanobiocides have been developed to prevent and treat plant diseases in crops (Vijayreddy et al., 2023). Recent studies have shown that silver nanoparticles have broad antimicrobial activities against bacteria and fungi due to their diverse inhibitory mechanisms. Furthermore, AgNPs have demonstrated fungicidal effects against plant pathogens like Fusarium oxysporum (Huang et al., 2017) and Tritium aestivum (Satti et al., 2021). However, only a few studies have been published on the use of AgNPs to treat plant diseases, notably those brought on by Rhizoctonia solani species that create sclerotia (Kora et al., 2020). In potato plants, R. solani can lead to black scurf and stem canker (Wang and Xu, 2019). Similarly, it can significantly impact canola cultivation, which is predominantly practised in Europe, Canada, Australia, and China. The symptoms observed in affected canola include pre- and post-germination damping-off, seedling root rot, and basal stem rot. The production of canola and rapeseed continues to face a major and ongoingthreat from Sclerotinia stem rot, which is brought on by

 

Table 3: The list of mechanisms of action for other plants.

Plant name

Symptoms mechanism of action

Nanoparticles treatments

References

Tomatoes (Solanum Lycopersicum L.)

Yellowing and wilting will lead to plant death.

Fusarium oxysporum f. sp. lycopersici (FOL) fungus colonizes the vascular tissues at different physiological phases

In vitro assays using copper nanoparticles (CuNPs). CuNPs contain oxidation states that are effective against F.oxysporum

(Huang et al., 2019; Lopez-Lima et al., 2021)

Wheat (Tritium aestivum).

Distinct, elongated, black-brown lesions.

The mycotoxins produced by fungi affect the wheat grains’ overall nutritional value.

Exogenous treatments of TiO2 NPs limit the growth of mycotoxins.

(Satti et al., 2021)

Paddy (Oryza sativa L.)

In infected nodes, irregular black areas encircle the nodes.

Caused by the fungus Pyricularia grisea (Cooke) Sacc. Various fungal races can affect most rice cultivars.

Application of AgNPs to the Magnaphorte grisea culture revealed a dose-dependent decrease in hyphal and the number of colonies produced.

(Elamawi and El-Shafey, 2013; Simkhada, 2021)

 

Sclerotinia sclerotiorum (Zhang et al., 2020). Wheat is similarly harmed by sclerotia. According to Alaoufi et al. (2023), the ergot-causing organism, Claviceps purpurea, is known to infect various grass species, including wheat. The alkaloids synthesised by this pathogen within its mature sclerotial structures result in reduced wheat quality and potential rejection at market (Alaoufi et al., 2023).

Apart from that, it was intended for the current study to synthesise AgNPs using paddy leaf extract as a dual-functional reductant and stabiliser, while also maximising the quantities of extract, silver nitrate, and reaction time (Kora et al., 2020). Paddy leaf extract was applied in combination with a modified version of the process to develop an easy and environmentally friendly way to create AgNPs. Originally, the fresh paddy leaves were collected and cleaned with distilled water. An aqueous extract was prepared by boiling 5 grams of the leaves in 50 millilitres of distilled water, which was then filtered, and the supernatant collected (Chowdhury et al., 2022). Various ratios (0.5%, 1.0%, 2.0%, and 5.0%) of the paddy leaf extract were combined with a 1 mM silver nitrate solution. The mixture’s pH was raised to the alkaline range and then left at room temperature until it turned a yellowish-brown colour, confirming the formation of silver nanoparticles

Advantages and disadvantages of silver nanoparticles

Due to their exceptional antibacterial and catalytic capabilities, AgNPs have generated a significant amount of interest. Instead, the use of microorganisms like fungi, bacteria, and yeast to biosynthesise these nanoparticles has started to gain greater attention as a more straightforward and environmentally acceptable method of their synthesis (Zhao et al., 2022). According to Kale et al. (2021), AgNPs have a high surface area and a high fraction of surface atoms (Kale et al., 2021). Compared to bulk silver, AgNPs have been shown to have a high antimicrobial effect. Additionally, AgNPs are widely known for their anti-inflammatory, anti-viral, anti-bacterial, and anti-fungal effects. Moreover, AgNPs have a variety of effects in both in vivo and in vitro applications. Due to its qualities, ease of use, simplicity, and environmental friendliness, AgNPs synthesis is gaining a lot of interest (Simon et al., 2022). Furthermore, it does not affect living cells, thus making the researcher show a lot of interest in AgNPs.

Despite their potential, silver nanoparticles entail some notable drawbacks. AgNPs synthesis requires considerable space and energy, which raises the ambient temperature around the source material (Simon et al., 2022). Moreover, achieving thermal stability for AgNPs takes a prolonged duration and necessitates substantial power input, often exceeding several kilowatts, as well as extended preheating periods of several minutes to reach a stable operating temperature. Furthermore, according to Zhao et al. (2022), AgNPs preparation involves potentially hazardous reagents like citrate, borohydride, thio-glycerol, and 2-mercaptoethanol, and it is an energy-intensive process, which collectively poses a challenge for their large-scale production (Zhao et al., 2022).

Nanoparticles challenges for paddy disease

The main challenges in using silver nanoparticles to manage paddy diseases are the lack of standardisation across different studies. This makes it difficult to compare findings, as the methods for producing, characterising, and applying AgNPs vary greatly. Additionally, AgNPs tend to aggregate and become unstable, which can reduce their effectiveness and availability in agricultural systems (Lu et al., 2020). To achieve reliable performance, the nanoparticle formulations must be stable and preserve their properties during storage and application.

Furthermore, despite the development of resistance, the efficiency of AgNPs will be reduced over time as a result of pathogens developing resistance with the excessive or continuous use of AgNPs (Huang et al., 2017). It is essential for AgNPs to reach the targeted area, such as particular cells or tissues, to ensure the effectiveness of AgNPs. Nanoparticle size, surface charge, and interactions with biological barriers are a few of the aspects that can make it difficult to achieve targeted distribution. On the other hand, farmers and researchers find it difficult to embrace and implement the technology because there are no clear regulations or guidelines for using AgNPs in agriculture. Regulations and guidelines may apply to the use of nanoparticles in various applications. Testing, registration, and approval procedures might be difficult to manage to comply with these rules.

Conclusions and Recommendations

Nanoparticles are emerging as versatile tools in many fields, with silver nanoparticles showing exceptional promise in agriculture. AgNPs have demonstrated remarkable efficacy in combating plant diseases, effectively inhibiting a broad spectrum of pathogens while simultaneously promoting plant growth. Combined with lower environmental impact, AgNPs offer a promising avenue for safer, more effective treatments for plant diseases, especially in crops like paddy rice.

Paddy rice, a staple food for a massive portion of the global population, is susceptible to a range of devastating diseases, including blast disease caused by Pyricularia oryzae, sheath blight, and bacterial leaf streak. Current disease management strategies often prove inadequate, highlighting the urgent need for more effective and sustainable solutions. This review has highlighted the potential of AgNPs to address this challenge, with research suggesting a possible 30% improvement in disease management through their utilisation.

Despite ongoing challenges in optimising the synthesis, delivery, and understanding the long-term environmental impact of silver nanoparticles, their potential benefits are substantial. Future research should focus on refining AgNPs applications for paddy disease control, exploring their efficacy against a wider range of pathogens, and developing sustainable synthesis methods using biological agents like endophytic bacteria. By addressing these challenges and harnessing the unique properties of AgNPs, we can pave the way for a more sustainable and secure future for paddy rice cultivation and global food security.

Acknowledgements

Upon completing this project, the authors would like to acknowledge the support of the Faculty of Applied Sciences, Universiti Teknologi MARA (UiTM), Shah Alam, Selangor, Malaysia, for providing the facilities and financial support for this research. The authors would like to thank Nur Aatikah Natasha Binti Yusmi for her contribution in illustrating the figure.

Novelty Statement

This review presents a novel examination of biosynthesised silver nanoparticles as a sustainable and environmentally friendly alternative to conventional chemical treatments for paddy disease. It highlights the potential of AgNPs to effectively combat paddy diseases like rice blast and sheath blight, addressing the growing concern of pesticide resistance and environmental harm associated with traditional methods.

Author’s Contribution

Roslina Ainna Roslan, Athirah Marsya Azizul Rashidi and Norfatimah Mohamed Yunus: Collaboratively conceptualised the research review, conducted the literature review, and drafted the manuscript.

Sharifah Aminah Syed Mohammad and Nurul Aili Zakaria: Assisted in the revision of the manuscript.

Conflict of interest

The authors agree that this research was conducted in the absence of any self-benefits, commercial or financial conflicts and declare the absence of conflicting interests with the funders.

References

Amr, A.H. and S.M.A. El-Khalek. 2020. Biochemical and molecular variability of Fusarium fujikuroi isolates and their differential interactions with rice genotypes during infection. Egypt. J. Agric. Res., 98(1). https://doi.org/10.21608/ejar.2020.114848

Ahmed, T., M. Shahid, M. Noman, M.B.K. Niazi, F. Mahmood, I. Manzoor, Y. Zhang, B. Li, Y. Yang, C. Yan and J. Chen. 2020. Silver nanoparticles synthesized by using Bacillus cereus SZT1 ameliorated the damage of bacterial leaf blight pathogen in rice. Pathogens, 9(3): 160. https://doi.org/10.3390/pathogens9030160

Akhter, S., Z. Sultana, Asad Ud-Daula, M. Ashikuzzaman, M.S. Reja, M.M. Rahman, A. Khaton, A.M. Kashem, M.S. Rahman, M.F. Hossain, S.J. Lee and A.T.M.M. Rahman. 2024. Optimization of green silver nanoparticles as nanofungicides for management of rice bakanae disease. Heliyon, 10(6): e27579–e27579. https://doi.org/10.1016/j.heliyon.2024.e27579

Alaoufi, S., A. Friskop and S. Simsek. 2023. Effect of field-applied fungicides on Claviceps purpurea sclerotia and associated toxins in wheat. J. Food Prot., 86(3). https://doi.org/10.1016/j.jfp.2023.100046

Almeida, L.C., A. Sousa, F.L. Mendes, B.F. Duarte, D.R. Santiago, T.R.E. Souza and J.A. Rios. 2024. Silver nanoparticles as potential fungicide against rice brown spot: Physiological and biochemical responses in plants. Trop. Plant Pathol., 49(5): 689–701. https://doi.org/10.1007/s40858-024-00653-5

Al-Sharqi, A., K. Apun, M. Vincent, D. Kanakaraju and L.M. Bilung. 2019. Enhancement of the antibacterial efficiency of silver nanoparticles against gram-positive and gram-negative bacteria using blue laser light. Int. J. Photoenergy, 2019: 1–12. https://doi.org/10.1155/2019/2528490

Amelia, R., N. Anggriani, A.K. Supriatna and N. Istifadah. 2022. A mathematical model for analyzing the dynamics of tungro virus disease in Rice: A systematic literature review. Mathematics, 10(16): 2944. https://doi.org/10.3390/math10162944

Asghar, M., M.M.Q. Baig, S. Chaudhary and M.A. Ali. 2019. Evaluation of difenoconazole along with macronutrients spray for the control of brown leaf spot (Bipolaris oryzae) disease in rice (Oryza sativa) crop. Sarhad J. Agric., 35(1): 1-6. https://doi.org/10.17582/journal.sja/2019/35.1.1.6

Asibi, A.E., Q. Chai and J.A. Coulter. 2019. Rice blast: A disease with implications for global food security. Agronomy, 9(8): 451. https://doi.org/10.3390/agronomy9080451

Ayub, A., A. Ali, S.A. Shah and A.U. Jan. 2024. Climate change impact assessment on net revenue of rice crop in Khyber Pakhtunkhwa: A cross-sectional ricardian rent analysis. Sarhad J. Agric., 40(2). https://doi.org/10.17582/journal.sja/2024/40.2.263.274

Bashyal, B.M., A. Gupta, D. Singh, R. Choudhary and R. Aggarwal. 2021. First report of Sclerotium hydrophilum causing stem rot disease of rice in northeastern plain zone of India. Plant Dis., 105(3): 700. https://doi.org/10.1094/PDIS-07-20-1529-PDN

Bruna, T., F. Maldonado-Bravo, P. Jara and N. Caro. 2021. Silver nanoparticles and their antibacterial applications. Int. J. Mol. Sci., 22(13): 7202. https://doi.org/10.3390/ijms22137202

Bueno, A.C.S.O., G.L.S. De Castro, D.R. Silva, H.A. Pinheiro, M.C.C. De Filippi and G.C. Silva. 2017. Response of photosynthesis and chlorophyll a fluorescence in leaf scald-infected rice under influence of rhizobacteria and silicon fertilizer. Plant Pathol., 66(9): 1487–1495. https://doi.org/10.1111/ppa.12690

Castillo-Henríquez, L., K. Alfaro-Aguilar, J. Ugalde-Álvarez, L. Vega-Fernández, G.M. de Oca-Vásquez and J.R. Vega-Baudrit. 2020. Green synthesis of gold and silver nanoparticles from plant extracts and their possible applications as antimicrobial agents in the agricultural area. Nanomaterials, 10(9): 1763. https://doi.org/10.3390/nano10091763

Chen, J., F. Ran, J. Shi, T. Chen, Z. Zhao, Z. Zhang, L. He, W. Li, B. Wang, X. Chen, W. Wang and Y. Long. 2022. Identification of the causal agent of brown leaf spot on kiwifruit and its sensitivity to different active ingredients of biological fungicides. Pathogens, 11(6): 673. https://doi.org/10.3390/pathogens11060673

Chowdhury, A.R., R. Kumar, A. Mahanty, K. Mukherjee, S. Kumar, K.U. Tribhuvan, R. Sheel, S. Lenka, B.K. Singh, C. Chattopadhyay, T.R. Sharma, V.P. Bhadana and B. Sarkar. 2022. Deciphering the molecular insight behind the inhibitory role of copper and silver nanocomposite on important bacterial and fungal pathogens in rice (Oryza sativa). Res. Square (Research Square). https://doi.org/10.21203/rs.3.rs-2099113/v1

Datta, M.T., C.K. Ghosh and A. Mukherjee. 2021. Dual role of copper nanoparticles in bacterial leaf blight-infected rice: A therapeutic and metabolic approach. ACS Agric. Sci. Technol., 1(3): 160–172. https://doi.org/10.1021/acsagscitech.0c00064

Dey, S.A., J.K. Dey, P. Debbarma and R.K. Saha. 2022. Integrated disease management of rice blast caused by Magnaporthe grisea (T.T. Hebert) Barr in Sepahijala district of Tripura. Pharma Innov. J., 11(12).

Długosz, O. and M. Banach. 2019. Continuous production of silver nanoparticles and process control. J. Cluster Sci., 30(3): 541–552. https://doi.org/10.1007/s10876-019-01505-y

Elamawi, R.M. and R. Elshafey. 2013. Inhibition effects of silver nanoparticles against rice blast disease caused by Magnaporthe grisea. Egypt. J. Agric. Res., 91(4): 1271–1283. https://doi.org/10.21608/ejar.2013.165104

Fetene, D.Y., M. Birhan and T. Zeleke. 2020. Screening of rice germplasms for their resistance against sheath rot disease (Sarocladium oryzae) at Fogera, Ethiopia. J. Plant Pathol. Microbiol., 11(10): 1–7.

Hashim, I.A., D. Mamiro, R.B. Mabagala and T. Tefera. 2019. Reduction of initial occurrence of rice blast (Pyricularia oryzae) inocula on seeds by microbial and hot water seed treatments. Austral. J. Crop Sci., 13(2): 309–314. https://doi.org/10.21475/ajcs.19.13.02.p1474

Helina, S., S. Sulandari, A. Trisyono and S. Hartono. 2020. Assessments of yield losses due to double infection of rice ragged stunt virus and rice grassy stunt virus at different severity in the field, Yogyakarta, Indonesia. Pak. J. Phytopathol., 32(2). https://doi.org/10.33866/phytopathol.030.02.0578

Huang, Q., Y. Liu, Y. Dong, Z. Liu, R. An and P. Li. 2017. Resistance risk assessment of Sclerotinia homoeocarpa to silver nanoparticles. Front. Microbiol., 8: 1244.

Huang, W., M. Xu, H. Duan, Y. Bi and H. Yu. 2018. Inhibition of Fusarium oxysporum by AgNPs biosynthesised using Cinnamomum camphora fruit extract. IET Nanobiotechnol., 13(1): 42–45. https://doi.org/10.1049/iet-nbt.2018.5065

Ibrahim, E.M., H. Fouad, M. Zhang, Y. Zhang, W. Qiu, C. Yan, B. Li, J. Mo and J. Chen. 2019. Biosynthesis of silver nanoparticles using endophytic bacteria and their role in inhibition of rice pathogenic bacteria and plant growth promotion. RSC Adv., 9(50): 29293–29299. https://doi.org/10.1039/C9RA04246F

Ibrahim, E.M., J. Luo, T. Ahmed, W.G. Wu, C. Yan and B. Li. 2020. Biosynthesis of silver nanoparticles using onion endophytic bacterium and its antifungal activity against rice pathogen Magnaporthe oryzae. J. Fungi, 6(4): 294. https://doi.org/10.3390/jof6040294

Islam, S., R. Bhuiyan, R.S. Akter, M. Ashik, S. Akter, M.R. Islam, A. Rahman and M.A. Latif. 2024. Green synthesis and characterization of silver nanoparticles and its efficacy against Rhizoctonia solani, a fungus causing sheath blight disease in rice. PLoS One, 19(6): e0304817–e0304817. https://doi.org/10.1371/journal.pone.0304817

Kale, S.K., G.V. Parishwad and A.S.N.H.S. Patil. 2021. Emerging agriculture applications of silver nanoparticles. ES Food and Agroforestry.

Kannan, C., D. Mishra, A. Miriyala, P. Vellaichamy, B. Kurubar, J. Gompa, S.P. Madamsetty and M. Raman. 2021. Native isolates of Trichoderma as bio-suppressants against sheath blight and stem rot pathogens of rice. Egypt. J. Biol. Pest Contr., 31(1). https://doi.org/10.1186/s41938-020-00356-4

Khan, S., M. Zahoor, R.S. Khan, M. Ikram and N. Islam. 2023. The impact of silver nanoparticles on the growth of plants: The agriculture applications. Heliyon, 9(6): e16928–e16928. https://doi.org/10.1016/j.heliyon.2023.e16928

Kora, A.J., J. Mounika and R. Jagadeeshwar. 2020. Rice leaf extract synthesized silver nanoparticles: An in vitro fungicidal evaluation against Rhizoctonia solani, the causative agent of sheath blight disease in rice. Fungal Biol., 124(7): 671–681. https://doi.org/10.1016/j.funbio.2020.03.012

Kumar, P., V. Pahal, A. Gupta, R. Vadhan, H. Chandra and R.C. Dubey. 2020. Effect of silver nanoparticles and Bacillus cereus LPR2 on the growth of Zea mays. Sci. Rep., 10(1). https://doi.org/10.1038/s41598-020-77460-w

Lacombe, S., M. Bangratz, H.D.K. Ta, T.N. Nguyen, P. Gantet and C. Brugidou. 2021. Optimized RNA-silencing strategies for rice ragged stunt virus resistance in rice. Plants, 10(10): 2008. https://doi.org/10.3390/plants10102008

Laxman, A., G. Bhattarai, A. Subedi, M. Subedi and B. Sah. 2016. Response of rice varieties to brown spot disease of rice at Paklihawa, Rupandehi. Glob. J. Biol. Agric. Health Sci., 5(2): 50–54.

Li, H., J. Huang, F. Lu, Y. Liu, Y. Song, Y. Sun, J. Zhong, Z. Kang, Y. Wang, S. Li, Y. Lifshitz, S. Lee and Z. Kang. 2018. Impacts of carbon dots on rice plants: Boosting the growth and improving the disease resistance. ACS Appl. Bio Mater., 1(3): 663–672. https://doi.org/10.1021/acsabm.8b00345

Li, M., J. Li, J. Sun, Y. He, P. Chen and C. Zhang. 2019. Is sulfidation a true detoxification process for silver nanoparticles? from the perspective of chronic exposure. Environ. Sci. Nano, R. Soc. Chem., 6(12): 3611. https://doi.org/10.1039/C9EN00989B

Lin, Y., S. Shen, C. Wen, T. Chang and S. Chu. 2021. Molecular detection assays for rapid field-detection of rice sheath blight. Front. Plant Sci., 11. https://doi.org/10.3389/fpls.2020.552916

Lopamudra, B., R. Chandra, S. Lenka, A. Mahanty, S. Kumar and P.C. Rath. 2023. Bacterial synthesized silver nanoparticle inhibits Rhizoctonia solani Kuhn, the causal organism for sheath blight disease of rice. ORYZA Int. J. Rice, 60(1): 166–174. https://doi.org/10.35709/ory.2023.60.1.8

López-Lima, D., A. Mtz-Enriquez, G. Carrión, S. Basurto-Cereceda and N. Pariona. 2021. The bifunctional role of copper nanoparticles in tomato: Effective treatment for Fusarium wilt and plant growth promoter. Sci. Hortic., 277: 109810. https://doi.org/10.1016/j.scienta.2020.109810

Lu, J., L. Gao, Y. Cui and Q. Huang. 2020. The challenges and strategies for the application of silver nanoparticles in agriculture and the exacerbated risk of antimicrobial resistance. J. Hazard. Mater., 393: 122384.

Ma, Y., W. Lin, S. Guo, L. Xie, D. He and Z. Cheng. 2022. Human activity played a key role in rice stripe disease epidemics: From an empirical evaluation of over a 10-year period. Agriculture, 12(9): 1484. https://doi.org/10.3390/agriculture12091484

Masum, M.M.I., M.M. Siddiqa, K.A. Ali, Y. Zhang, Y. Abdallah, E.M. Ibrahim, W. Qiu, C. Yan and B. Li. 2019. Biogenic synthesis of silver nanoparticles using Phyllanthus emblica fruit extract and its inhibitory action against the pathogen Acidovorax oryzae strain RS-2 of rice bacterial brown stripe. Front. Microbiol., 10. https://doi.org/10.3389/fmicb.2019.00820

Na Phatthalung, T. and W. Tangkananond. 2022. Interactive effects of rice ragged stunt virus infection in rice and insect vector Nilaparvata lugens. Asia-Pac. J. Sci. Technol., 27(5): APST–27.

Nadarajah, K.K., N.S. Omar, M.M. Rosli and O.S. Tze. 2014. Molecular characterization and screening for sheath blight resistance using Malaysian isolates of Rhizoctonia solani. BioMed. Res. Int., 2014: 1–18. https://doi.org/10.1155/2014/434257

Pal, S., R. Nisi, M. Stoppa and A. Licciulli. 2017. Silver-functionalized bacterial cellulose as antibacterial membrane for wound-healing applications. ACS Omega, 2(7): 3632–3639. https://doi.org/10.1021/acsomega.7b00442

Pan, R., Z. Zhang, Y. Li, S. Zhu, S. Anwar, J. Huang, C. Zhang and L. Yin. 2024. Stage-specific effects of silver nanoparticles on physiology during the early growth stages of rice. https://doi.org/10.3390/plants13233454

Parthasarathy, R., C. Jayabaskaran, A. Manikandan and S. Anusuya. 2022. Synthesis of nickel-chitosan nanoparticles for controlling blast diseases in Asian rice. Res. Square (Research Square). https://doi.org/10.21203/rs.3.rs-564322/v1

Pathom-aree, P., S. Kreawsa, M. Kamjam, S. Tokuyama, S. Yoosathaporn, S. Lumyong and Department of Biology [Chiang Mai University]. 2019. Potential of selected mangrove streptomyces as plant growth promoter and rice bakanae disease control agent. Chiang Mai J. Sci., Retrieved July 4, 2023.

Poveda, J., P. Abril-Urias and C. Escobar. 2020. Biological control of plant-parasitic nematodes by filamentous fungi inducers of resistance: Trichoderma, mycorrhizal and endophytic fungi. Front. Microbiol., 11. https://doi.org/10.3389/fmicb.2020.00992

Raihanah, N., T. Anuar, R. Roslan, L. Watty, Z. Ahmad, R. Kambol, S. Aminah, S. Mohamad, F. Aris, N. Zakaria and N. Yunus. 2023. Molecular detection and analysis of bacterial panicle blight pathogens in rice field in Malaysia. pp. 23–33.

Rajasekar, R., M.S. Samuel, T.N.J.I. Edison and N. Raman. 2021. Sustainable synthesis of silver nanoparticles using Alstonia scholaris for enhanced catalytic degradation of methylene blue. J. Mol. Struct., 1246: 131208. https://doi.org/10.1016/j.molstruc.2021.131208

Rautela, A., J. Rani and M.C. Debnath. 2019. Green synthesis of silver nanoparticles from Tectona grandis seeds extract: Characterization and mechanism of antimicrobial action on different microorganisms. J. Anal. Sci. Technol., 10(1). https://doi.org/10.1186/s40543-018-0163-z

Saito, H., M. Sasaki, N. Yoko, J. Tanaka, T. Tokunaga, A. Kato, T.T. Thuy, L. Van Vang, L.T.C. Tuong, S. Kanematsu, T. Suzuki, K. Kurauchi, N. Fujita, T. Teraoka, K. Komatsu and T. Arie. 2021. Spray application of nonpathogenic fusaria onto rice flowers controls bakanae disease (Caused by Fusarium fujikuroi) in the next plant generation. Appl. Environ. Microbiol., 87(2). https://doi.org/10.1128/AEM.01959-20

Satti, S.H., N.I. Raja, B. Javed, A. Akram, Z.R. Mashwani, M.S. Ahmad and M. Ikram. 2021. Titanium dioxide nanoparticles elicited agro-morphological and physicochemical modifications in wheat plants to control Bipolaris sorokiniana. PLoS One, 16(2). https://doi.org/10.1371/journal.pone.0246880

Sekiya, N., T. Nakajima, N. Oizumi, C. Kurosawa, N. Tibanyendela, M.A. Peter, M. Tomitaka and K.T. Natsuaki. 2022. Agronomic practices preventing local outbreaks of rice yellow mottle virus disease revealed by spatial autoregressive analysis. Agron. Sustain. Dev., 42(2). https://doi.org/10.1007/s13593-022-00757-9

Shaheen, H.M.U., N.A. Rajput, M. Atiq, G.A. Kachelo, H. Ahmad, M. Wahab, M.F. Tahir and A. Hasnain. 2024. Antifungal potential of medicinal plant extracts against brown leaf spot (BLS) disease of rice caused by Bipolaris oryzae. Sarhad J. Agric., 40(2). https://doi.org/10.17582/journal.sja/2024/40.2.603.614

Shi, H., H. Wen, S. Xie, Y. Li, Y. Chen, Z. Liu, N. Jiang, J. Qiu, X. Zhu, F. Lin and Y. Kou. 2023. Antifungal activity and mechanisms of AgNPs and their combination with azoxystrobin against Magnaporthe oryzae. Environ. Sci. Nano, 10(9): 2412–2426. https://doi.org/10.1039/D3EN00168G

Simkhada, K. and R. Thapa. 2021. Rice blast, a major threat to the rice production and its various management techniques. Research Gate. https://doi.org/10.24925/turjaf.v10i2.147-157.4548

Simon, S., N.R.S. Sibuyi, A.O. Fadaka, S. Meyer, J. Josephs, M.O. Onani, M. Meyer and A.M. Madiehe. 2022. Biomedical applications of plant extract-synthesized silver nanoparticles. Biomedicines, 10(11): 2792. https://doi.org/10.3390/biomedicines10112792

Soltani, N.M., G.H.S. Bonjar, M. Khatami, A. Amini and S. Aghighi. 2017. In vitro and in vivo antifungal properties of silver nanoparticles against Rhizoctonia solani, a common agent of rice sheath blight disease. IET Nanobiotechnol., 11(3): 236–240. https://doi.org/10.1049/iet-nbt.2015.0121

Song, J., K. Soytong and S. Kanokmedhakul. 2021. Control of rice blast disease caused by Magnaporthe oryzae by application of antifungal nanomaterials from Emericella nidulans. Plant Prot. Sci., 58(1): 40–48. https://doi.org/10.17221/33/2021-PPS

Suvi, W.T., H. Shimelis, M. Laing, I. Mathew and A. Shayanowako. 2020. Determining the combining ability and gene action for rice yellow mottle virus disease resistance and agronomic traits in rice (Oryza sativa L.). Agronomy, 11(1): 12. https://doi.org/10.3390/agronomy11010012

Syed-Ab-Rahman, S.F., L.C. Carvalhais and D. Omar. 2020. Development of plant-based emulsion formulations to control bacterial leaf blight and sheath brown rot of rice. Heliyon, 6(1): e03151. https://doi.org/10.1016/j.heliyon.2019.e03151

Tariq, M., K. Mohammad, B. Ahmed, M.A. Siddiqui and J. Lee. 2022. Biological synthesis of silver nanoparticles and prospects in plant disease management. Molecules, 27(15): 4754. https://doi.org/10.3390/molecules27154754

Temizel-Sekeryan, S. and A.L. Hicks. 2020. Global environmental impacts of silver nanoparticle production methods supported by life cycle assessment. Resources, Conserv. Recycl., 156: 104676. https://doi.org/10.1016/j.resconrec.2019.104676

Thynraj, A.R., M.P. Sudhakar and A. Kulanthaiyesu. 2021. Synthesis of silver nanoparticle composites using Calliblepharis fimbriata Aqueous extract, phytochemical stimulation, and controlling bacterial blight disease in rice. ACS Agric. Sci. Technol., 1(6): 702–718. https://doi.org/10.1021/acsagscitech.1c00189

Tian, Y., J. Luo, H. Wang, M. Zaki, S. Yu, X. Wang, T. Ahmed, M. Shahid, C. Yan, J. Chen and B. Li. 2022. Bioinspired green synthesis of silver nanoparticles using three plant extracts and their antibacterial activity against rice bacterial leaf blight pathogen Xanthomonas oryzae pv. oryzae. Plants, 11(21): 2892–2892. https://doi.org/10.3390/plants11212892

Vega-Baudrit, J., S.M. Gamboa, E.A.V. Rojas and V.R. Martinez. 2019. Synthesis and characterization of silver nanoparticles and their application as an antibacterial agent. Int. J. Bios. Bioelectron., 5(5). https://doi.org/10.15406/ijbsbe.2019.05.00172

Vijayreddy, D., P. Dutta and K.R.Puzari. 2023. Nanotechnology in plant disease management. Res. Biot., 5(2): 56–62. https://doi.org/10.54083/resbio/5.2.2023/56-62

Vishakha, K., S. Das, S. Banerjee, S. Mondal and A. Ganguli. 2020. Allelochemical catechol comprehensively impedes bacterial blight of rice caused by Xanthomonas oryzae pv. oryzae. Microb. Pathogen., 149: 104559. https://doi.org/10.1016/j.micpath.2020.104559

Volante, A., A. Tondelli, M. Aragona, M.T. Valente, C. Biselli, F. Desiderio, P. Bagnaresi, S. Matic, M.L. Gullino, A. Infantino, D. Spadaro and G. Valè. 2017. Identification of bakanae disease resistance loci in japonica rice through genome wide association study. Rice, 10(1). https://doi.org/10.1186/s12284-017-0168-z

Wang, D. and L. Xu. 2019. The role of Rhizoctonia solani in potato stem canker and black scurf diseases in China. Phytopathol. Res., 1(1): 1-8.

Wu, T., C. Peng, B. Li, W. Wu, L. Kong, F. Li, Z. Chu, F. Liu and X. Ding. 2019. OsPGIP1-mediated resistance to bacterial leaf streak in rice is beyond responsive to the polygalacturonase of Xanthomonas oryzae pv. oryzicola. Rice, 12(1). https://doi.org/10.1186/s12284-019-0352-4

Yan, A. and Z. Chen. 2019. Impacts of silver nanoparticles on plants: A focus on the phytotoxicity and underlying mechanism. Int. J. Mol. Sci., 20(5): 1003. https://doi.org/10.3390/ijms20051003

Zhang, J., D.V. Mavrodi, M. Yang, L.S. Thomashow, O.V. Mavrodi, J. Kelton and D. Weller. 2020. Pseudomonas synxantha 2-79 transformed with pyrrolnitrin biosynthesis genes has improved biocontrol activity against soilborne pathogens of wheat and canola. Phytopathology, 110(5): 1010–1017. https://doi.org/10.1094/PHYTO-09-19-0367-R

Zhao, X., X. Xu, C. Ai, Y. Lu, C. Jiang and J. Shi. 2022. Advantages of silver nanoparticles synthesized by microorganisms in antibacterial activity. Elsevier eBooks, pp. 571–586. https://doi.org/10.1016/B978-0-12-824508-8.00005-8

Zhu, Y., X. Hu, M. Qiao, L. Zhao and C. Dong. 2024. Penicillium polonicum-mediated green synthesis of silver nanoparticles: Unveiling antimicrobial and seed germination advancements. Heliyon, 10: e28971–e28971. https://doi.org/10.1016/j.heliyon.2024.e28971