Skip to main content

MINI REVIEW article

Front. Plant Sci., 12 December 2024
Sec. Plant Nutrition
This article is part of the Research Topic Enhancing Plant Health Through Silicon Supplementation Under Nutritional Stress View all 3 articles

Unlocking the role of silicon against biotic stress in plants

Krishan K. Verma&#x;Krishan K. Verma1†Xiu-Peng Song*Xiu-Peng Song1*Qiang LiangQiang Liang1Hai-Rong HuangHai-Rong Huang1Rajan BhattRajan Bhatt2Lin XuLin Xu1Gan-Lin Chen,,,&#x;Gan-Lin Chen3,4,5,6†Yang-Rui Li*&#x;Yang-Rui Li1*†
  • 1Sugarcane Research Institute, Guangxi Academy of Agricultural Sciences/Key Laboratory of Sugarcane Biotechnology and Genetic Improvement, Ministry of Agriculture and Rural Affairs/Guangxi Key Laboratory of Sugarcane Genetic Improvement, Nanning, Guangxi, China
  • 2Punjab Agricultural University (PAU)-Krishi Vigyan Kendra Amritsar, Punjab, India
  • 3Guangxi Subtropical Crops Research Institute, Guangxi Academy of Agricultural Sciences, Nanning, Guangxi, China
  • 4Guangxi Key Laboratory of Quality and Safety Control for Subtropical Fruits, Ministry of Agriculture and Rural Affairs, Nanning, Guangxi, China
  • 5Key Laboratory of Quality and Safety Control for Subtropical Fruit and Vegetable, Ministry of Agriculture and Rural Affairs, Nanning, Guangxi, China
  • 6School of Chemistry and Chemical Engineering, Guangxi Minzu University, Nanning, Guangxi, China

The requirement for agricultural crops continues to enhance with the continuous growth of the human population globally. Plant pathogenic diseases outbreaks are enhancing and threatening food security and safety for the vulnerable in different regions worldwide. Silicon (Si) is considered a non-essential element for plant growth. It regulates the biological functions, plant development and productivity, and balance the defense mechanism in response to fungal, bacterial and pest attacks. The optimum crop yield can be achieved by applying Si in agricultural systems through different methods to replace or minimize the use of synthetic fertilizers. This approach can be effective on crop production during limited resources, extreme climates, pests and diseases, and environmental pollution. Silicon can be applied as foliar spray, priming of seeds, soil water irrigation, soil amendment and soilless medium (hydroponic) to enhance plant performance and stress tolerance capacity during stress conditions. This article summarized the effective roles of Si and the ability to perform in agroecosystems for better crop production, food security and safety for sustainable agriculture in the future.

Introduction

Silicon (Si) has a brittle crystalline structure with enormous application in biological sciences. Si finds a second position in the abundance of the earth’s crust (Verma et al., 2023a, b). Due to its affinity towards oxygen (Verma et al., 2019), Si forms two oxides, silica (SiO2) and silicon monoxide (SiO), as the SiO bond is unusually strong. The average Si content in normal soil is very high, i.e., 28% (weight basis). Soil carries silicon dioxide, silicate minerals, and alumino-silicates are not available to plants through their uptake process. The uptake and accumulation of Si depends on the variety of crop plants, soil properties, sources and concentration of Si in planta. Si content can vary from 0.1 to 10% (dry weight basis) near the detection limit (Coskun et al., 2019; Verma et al., 2020a, b; 2023a). Monosilicic acid is soluble in water and adsorbed by plant roots (Matichenkov and Calvert, 2002; Verma et al., 2020c; Paton, 2023).

Interestingly, the concentration of plant-accessible Si exceeds the phosphorus in the soil solution. Different factors, including pH, water status, temperature, and accompanying ions, influence Si availability in the rhizospheric soil (Bityutskii et al., 2019; Verma et al., 2020d, e). Specific soil types, such as extensively weathered acidic soil and calcareous paddy soil, may experience Si deficiency. Si can be detected in nearly all land-dwelling plant species but in different concentrations range. Some plant species have optimum Si accumulation capacity, while most have relatively low levels (Verma et al., 2020f; Hernandez-Apaolaza, 2022).

Plant diseases negatively impact plants’ growth, development and food grain quality. It is a severe problem for sustainable agriculture and food security. Unsuitable agricultural approaches are degrading the atmospheric environmental variables and facing population pressure due to less crop productivity as required (Verma et al., 2021a, b). Si was reported to enhance the defense system against biotic stresses occurring in the form of plant pathogens, such as fungi, insects, weeds, bacteria and viruses or animals, i.e., vertebrates and arthropod herbivores. The deposition of Si upregulated the abrasiveness of plant tissues and thus reduced palatability and digestibility for herbivores (Massey and Hartley, 2009; Luyckx et al., 2017). The physical strength of the leaf resulting from the accumulation of Si can afford mechanical protection and control the frequency and severity of the infection (Zhang et al., 2013; Ning et al., 2014; Song et al., 2021). The postulation of potential physical obstruction formation is based on the type of Si deposition in foliage, especially in the cell wall. Si in the plant cell wall and apoplast protects pathogen penetration (Luyckx et al., 2017; Gulzar et al., 2021). Recent demonstrations have shown that the biochemical mechanisms of Si compared to physical mechanisms play a significant role in enhancing plant tolerance efficiency during pathogenic diseases (Song et al., 2016, 2021).

The current global scenario presents humanity with an alarming level of hunger, primarily driven by rapid population pressure. Unfortunately, the limited availability of inadequate resources is incapable to fulfilling the demand of food (Verma et al., 2021c, d). The era of climate change is a significant obstacle to achieving sustainable agricultural productivity (Verma et al., 2024). However, biotic stress adds to the challenges faced by plant production systems worldwide, and a transition towards environmentally friendly approaches is necessary (Kumari et al., 2022; 2023; Verma et al., 2022a, b, c). Si offers a natural defense system against various insects and pathogens by strengthening plant tissues, inducing the production of defense compounds, and activating systemic defense responses. Si significantly reduce the reliance on synthetic pesticides, i.e., nematicides (Santos et al., 2022).

This review thoroughly discussed how Si mitigates biotic stress in plants. It provides technical and theoretical knowledge, and action of defense mechanisms on Si-based strategies to enhance plant resilience and productivity in adverse climatic conditions. It aims to understand how plants acquire and allocate Si in plant parts during biotic stress.

Impact of biotic stress on plant development

Pathogenic diseases have significant implications for plant growth, development and crop protection. Fungal pathogens invade plant tissues, causing diseases, such as rust and powdery mildew, which cause wilting and reduce crop productivity and quality. Similarly, bacterial and viral pathogens release toxins that induce symptoms like wilting and rotting, disrupting plant cell processes, impeding nutrient absorption, and stunting plant growth (Muthu et al., 2022). Insects and pests damage plant tissues and downregulate plant growth and photosynthetic CO2 assimilation rate. These biotic stresses compromise photosynthesis, nutrient absorption, and plant defense mechanisms, making plants more vulnerable to secondary infections. Different plant species possess some specific action mechanisms for the uptake and accumulation of Si in other plant parts during stress conditions.

Role of Si on insects, pests, and weeds infection

In natural ecosystems, plant communities coexist with plant-feeding insects. However, agricultural productivity is directly damaged in agricultural systems by attacks from pathogens, pests, and weeds (Al-Gaashani et al., 2023). The impact of pest attacks on plants is observed by their effect on yield, which refers to the amount of economically viable product per unit area. Insect pests pose a significant threat to crops for human and animal consumption, directly damaging plants. In agri-systems, direct losses caused by pathogens and weeds account for a significant portion of the reduction in global crop production (Sharma et al., 2017; El-Ramady et al., 2022). Wheat and cotton were particularly susceptible, with potential losses exceeding 80%. Rice is affected by more than 800 insect species, resulting in actual losses of nearly 40% worldwide. In India, yield loss (21-50%) was observed in the rice by insect pests attack (Fahad et al., 2019). In wheat, actual losses of more than 30% worldwide (Jasrotia et al., 2021). Substantial yield loss was also observed in sorghum by pest challenges, such as Atherigona soccata Rondani and stem borer (Table 1).

Table 1
www.frontiersin.org

Table 1. Potential of Si against biotic stress mitigation strategies.

Rapeseed-mustard crops damage from pests, like mustard aphids, leading to yield losses (35-73%) in India (Tyczewska et al., 2018). Leguminous crops, like chickpeas and pigeon peas are affected by various pests, which result in considerable yield losses. Forage leguminous plants such as berseem, alfalfa, and Persian clover encounter challenges from the pod borer, H. armigera, leading to substantial losses in seed yield. Cotton plants require the optimum amounts of insecticides compared to other crop plants. Insecticides account for a significant portion of the total expenditure in cotton production (15-42%). Cotton accounts for nearly 23% of the worldwide insecticide use (Shahrajabian et al., 2020). Various insect pests, including whiteflies, bollworms, aphids, and various sucking pests, cause yield losses (up to 82%). Bollworms have triggered yield losses before 20 years (Lashari et al., 2022).

Pest insects pose a significant damage to global food production. Much more research is available to support the idea that Si application on plants can boost resistance to insects, pests, and diseases, leading to increased crop yield (Song et al., 2021). Si deposits in monocots can act as a “mechanical barrier against insects,” and their active role in biological resistance is now acknowledged. Si is a promoter in triggering biological resistance by generating compounds like tannic and phenolic chemicals (Tayade et al., 2022). Application of Si exhibits resistance to stalk borer damage. It was demonstrated that applying Si to maize plants reduces larval survival of the borer. Increasing the silica content and lowered larva survival efficiency (Rajput et al., 2021). An association of notable significance was discovered between the resistance of maize to the subsequent generation of Ostrinia nubilalis Hübnera and the Si concentration present within the sheath and collar tissues. Si in the epidermis of plant leaves can dislodge young borer larvae, hindering their establishment in the stem. It is well known that Si increases plant tissue toughness, interfering with insect larval boring and feeding. High Si content in rice plants damages the mandibles of rice stem borer larvae (Juma et al., 2015; Cabrera-Ponce et al., 2019). The physical arrangement of Si along the sheath of leaves could cause varietal resistance to the insects. When plants attack, signaling cascades are triggered, regulating target genes by entering proteins into the nucleus. The soluble Si protects cucumbers against fungal diseases (Song et al., 2021; El-Ramady et al., 2022).

By developing physical barrier, Si deposition under leaf cuticles enhances plants’ resistance to insect pests. It makes the tissue rigid and abrasive, reducing palatability and digestibility for herbivores (Nikpay et al., 2023). Differences in epidermal Si deposition among cultivars contribute to variations in resistance. Leaf abrasiveness and digestibility are influenced by spine and phytolith morphology. Si upregulates the gene expression associated with defense systems and promotes the accumulation of defensive compounds. It improves pest resistance in wheat and cucumber, and upregulates the activities of defensive enzymes. In response to pathogen infection, Si-mediated defense includes forming papilla, developing callose, and accumulating phenolic compounds. Si hinders fungal ET production, preventing suppression of the innate immune system and enhancing resistance against brown spot disease in rice plants (Akhtar et al., 2018) (Table 2). The cell wall of fungi consists of the carbohydrates chitin and β-1,3-glucan, Si-induced chitinases, and β-1,3-glucanases enzymes can hydrolyze these compounds to oligosaccharides and, as a result, the plant’s defense responses are elicited (Cruz et al., 2013). Si-enhanced tolerance to fungal diseases, there is limited information is available on the Si and bacterial disease interaction in plants (Song et al., 2016).

Table 2
www.frontiersin.org

Table 2. Plant pathogens and insects reported to be suppressed by Si application.

Silicon nanoparticles (SiNPs) have shown efficacy as pesticides with the interactive application of commercial pesticides. SiNPs are assimilated into the cuticular lipids, resulting in the physical mortality of insects (Mittal et al., 2020). Applied SiNPs with garlic essential oil has successfully managed agricultural insect pests. SiNPs can act as nano-pesticides or nanocarriers, enhancing the effectiveness of commercial pesticides. SiNPs can lead to insect mortality through desiccation and damage to the digestive system. The effects of SiNPs on pests have primarily been studied in laboratory conditions, focusing on specific pests and applied concentration. Weeds exert a harmful influence on the crop yield loss. A nano-herbicide formulation has been developed to combat weeds. It enhances the accumulation of Si in plant tissues. Nanoparticles assist for better customization, facilitating improved penetration through the plant’s protective cuticle and targeted release of active ingredients. The loss in herbivore populations is notably noted in Si-accumulating and non-accumulating plants (Mathur and Srivastava, 2022; Sarraf et al., 2022; Verma et al., 2023a).

Biochemical and molecular mechanisms of Si on plants to biotic stress

Si effectively mitigates biotic stresses in plants, serving as a key player in their adaptation and survival under unfavorable plant growth conditions. Si exerts its protective effects through various biochemical mechanisms, enabling plants to combat stresses effectively (Khan et al., 2024). It enhances the biochemical activities, i.e., peroxidase (POD), catalase (CAT), and superoxide dismutase (SOD). The generation of reactive oxygen species (ROS) and antioxidant metabolism have been linked with bacterial and fungal infection, and in response to damage from chewing and sucking insects (Debona et al., 2014; Yang et al., 2017; Frew et al., 2018). ROS played significant roles in different signaling pathways with plant hormones (Glazebrook, 2005; Torres, 2010). However, ROS can activate plant defense genes and the associated accumulation of defense metabolites, such as phytoalexins and allelochemicals (Thoma et al., 2003).

Si plays a significant role during the uptake and translocation of nutritional elements. It enhances the absorption of essential nutrients from the rhizospheric soil, i.e., nitrogen, phosphorus, potassium, and calcium. It affects the action of nutrient transporters and balances the nutritional efficiency. It influences hormonal signaling pathways in plants, contributing to their ability to respond to stress. It involves the synthesis, transport, and signaling of phytohormones. Si induces the production of ABA, stress hormone implied in regulating stomatal closure and stress responses (Mukarram et al., 2022; Chen et al., 2024). Si also activates JA signaling pathways for plant defense mechanisms in response to biotic stresses (Figure 1).

Figure 1
www.frontiersin.org

Figure 1. The outline of the major mitigation effects of Si on biotic stresses and some of the progressively more fundamental proximate and underlying phenomena associated with the mitigation of stress. The stress responsive genes associated with metabolic processes with variation in the response of transcription factors in response to Si. The essential Si transporter genes for the uptake of Si in plants are as Lsi1, Lsi2, Lsi6 (Frew et al., 2018). Arrows shows linkages for which there is significant support and potential interactions.

Biochemical and molecular functions are also induced or reinforced by Si, allowing the plant to enhance stress tolerance efficiency and include defensive compounds, i.e., phenolics, phytoalexins and momilactons, but also activate the enzymatic defensive system, like polyphenol oxidase (PPO), lipoxygenase (LPO) and phenylalanine ammonia-lyase (PAL) (Remus-Borel et al., 2005; Rahman et al., 2015; Verma et al., 2021d). Applied Si can upregulate transcript levels corresponding to defensive-related genes during stressed conditions. Si also attracts predators or parasitoids to plants in response to herbivore attacks. However, soluble Si enhances herbivore-induced plant volatiles to upregulate or maintain predator attraction by pest-infected plants. The insect’s life cycle phenology is also downregulated in Si-applied plants, making it more prone to predation (Cai et al., 2008; Reynolds et al., 2016).

Si can control the stress-responsive gene expression, activating pathways that enhance plant tolerance efficiency. It upregulates stress-responsive transcription factors (SRTFs), heat shock proteins (HSPs), and pathogenesis-related proteins (Song et al., 2021; Mir et al., 2022). The modulation of gene expression, Si plays a significant role in triggering stress signaling pathways, facilitating the establishment of stress tolerance in plants (Figure 1). It promotes the accumulation of osmoprotectants, which are organic compounds that help to maintain cellular osmotic balance and protect against osmotic stress (Shomali et al., 2022, 2024). Subsequent solutes, such as sugars, proline, betaine, and glycine, accumulate in higher concentrations in Si-treated plants. These osmolytes act as osmoprotectants, maintaining cell turgor and stabilizing macromolecules, ultimately contributing to stress resilience (Song et al., 2021).

The application of transcriptomic strategies, i.e., microarrays alongside more targeted assays such as real-time quantitative PCR (qPCR) are critical in developing an understanding of how Si impacts the expression of plant genes. The pathogenic infection enhanced defense genes and reduced primary metabolism genes, but following the use of Si reduced genes were not as severely impacted, while they found limited information to suggest an impact of Si without pathogen stress (Fauteux et al., 2006). The application of Si nearly eradicated the effects of pathogen stress on the plant transcriptome. Some transcriptomic research work has been reported, limited research has assessed the impact of Si on enhanced plant resistance efficiency to insect herbivores. However, further studies on the interactions of Si with the transcriptome of a variety of crop plants varying in their Si uptake and accumulation ability, like accumulators, non-accumulators under different forms of insect herbivory, such as chewers, suckers should provide valuable insight into how Si changes plant gene expression in response to insect stressors (Chain et al., 2009; Bockhaven et al., 2015) (Figure 1).

Mitigation of pathogenic bacteria, fungi, and viral diseases by Si application

Applying Si formulation open a new window in plant-pathogen interaction and management strategies. Si enhances resistance against diverse fungal pathogens in different plant-pathogen interactions. It effectively reduces plant diseases, such as black point in barley (Alternaria spp (Al-Sadi, 2021), leaf and glume blotch in wheat (Septoria nodorum), root rot in cucumber (Pythium ultimum and Pythium aphanidermatum) (Sun et al., 2022), damping off and stem rots in maize (Pythium aphanidermatum) (Haq et al., 2021), ascochyta blight in pea (Mycosphaerella pinodes), cercospora leaf spot in coffee (Cercospora coffeicola), blue mold decay and brown rot decay in cherry (Penicillium expansum and Monilinia fructicola), root rot in melon (Pythium aphanidermatum) (Sakr, 2018), wilt in potato (Fusarium sulphureum), black sigatoka in banana (Mycosphaerella fijiensis), and gray mold in strawberry (Botrytis cinerea). Foliar application of Si significantly reduces Fusarium crown and root rot in tomato plants. Si also reduces the intensity of hemibiotrophic fungal pathogens in different pathosystems, such as black spot in rose (Diplocarpon rosae), phytophthora blight in bell pepper (Phytophthora capsici), anthracnose in sorghum (Colletotrichum sublineolum), anthracnose in bean, and blast in wheat (Pyricularia oryzae). Si application reduces powdery mildew disease in wheat, cucumber, muskmelon, grape, arabidopsis, pearl millet, sugarcane, bean, strawberry, soybean, coffee, and rose, as well as powdery mildew in melon caused by Podosphaera xanthii (Farhat et al., 2018).

Si application upregulates plants’ efficiency for epiphytic and endophytic bacterial pathogens in mango plants where bacterial apical necrosis was reduced (Etesami et al., 2020; Verma et al., 2023b). Si treatments have also controlled bacterial wilt on tomato (Jiang et al., 2019), bacterial spot-on Passiflora edulis, bacterial streak on wheat, angular leaf spot on cotton, bacterial wilt on sweet pepper, and bacterial blight on rice. Applied calcium silicate in soil (1.41 g Si kg−1) defense against Acidovorax citrulli in melon plants (Bakhat et al., 2018). Different research groups’ demonstrations have confirmed the suppressive effects of Si application on viral pathogens. For instance, Si treatments have effectively reduced the incidence of Cucumber mosaic virus and Papaya ring spot virus on cucumbers. Applied Si in tobacco plants (0.1 mM) showed no systemic symptoms caused by the Tobacco ring spot virus than control plants, and higher Si rates slowed reduce the development of virus systemic symptoms. Si-mediated biotic stress tolerance by promoting various functions as shown in Figure 1 and summarized in Tables 1, 2.

Conclusion and future prospects

Si can influence the ecophysiology and cellular metabolism of plants. It stimulates antioxidant mechanisms and photosynthetic apparatus, maintain nutritional balance, regulates nutrients’ uptake and accumulation, promotes the production of secondary metabolites, ROS, and toxic metal chelation, changes plant cell walls, and regulates stress resistance proteins. However, the most significant effect of Si is the reduction in the intensities and frequencies of different plant diseases caused by biotrophic, hemibiotrophic, and necrotrophic plant pathogens causing seed-borne, soilborne, and foliar diseases in a variety of crops of great economic importance. The plant responses during pathogen infection and pest attack at the physio-biochemical and molecular levels are remarkably similar when Si is taken up by the plant roots and translocated to shoots, indicating an active role played by this element in one or more plant defense signaling pathways. The regulatory functions of Si during stressed conditions discussed how Si tolerates stress efficiency. While Si is associated with various plant proteins, it is unclear which other transcription factors and signaling proteins interact with Si to enhance plant stress. It will be very interesting to discover the functional role of signaling pathways and interactions with phytohormones at the cellular level to understand better how plants react during biotic stress with Si application. However, upcoming research demonstrations should focus on deciphering the role of Si in crop plants at field trials rather than laboratory conditions. The CRISPR/Cas system should be explored to Si-encoding proteins to enhance the stress resistance capacity in response to pathogenic diseases in major crop plants.

Author contributions

KV: Writing – original draft, Software, Resources, Methodology, Investigation, Formal analysis, Data curation. X-PS: Writing – review & editing, Visualization, Validation, Supervision, Project administration, Investigation, Funding acquisition, Conceptualization. QL: Writing – review & editing, Supervision, Software, Resources, Data curation. H-RH: Writing – review & editing, Software, Resources, Methodology, Formal analysis, Data curation. RB: Writing – review & editing, Software, Resources, Methodology, Formal analysis, Data curation. LX: Writing – review & editing, Software, Resources, Formal analysis, Data curation. G-LC: Writing – review & editing, Validation, Supervision, Resources. Y-RL: Writing – review & editing, Visualization, Validation, Supervision, Project administration, Methodology, Investigation, Funding acquisition, Conceptualization.

Funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This research was financially supported by the Guangxi Natural Science Foundation (2021GXNSFAA220022; 2023GXNSFAA026459; 2023GXNSFAA026460), Guangxi Innovation Teams of Modern Agriculture Technology (nycytxgxcxtd-2021-03), Guangxi Characteristic Crop Experimental Station (GTS2022022), National Key Research and Development Project (2022YFD2301102-07), The National Natural Science Foundation of China (31760415; 32060468), Fund of Guangxi Academy of Agricultural Sciences (2021YT011), Science and Technology Major Project of Guangxi (Guike AA22117002-1), Fundamental Research Fund of Guangxi Academy of Agriculture Sciences (2023YM55), and Key Research and Development Program of Nanning (20232060), and Guangxi key Laboratory of Sugarcane Genetic Improvement Project (21-238-16-K-03-09).

Acknowledgments

The authors would like to thank the Guangxi Academy of Agricultural Sciences, Nanning, Guangxi, China, for providing the necessary facilities for this study.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

Abbai, R., Kim, Y., Mohanan, P., Mathiyalagan, R., Yang, D., Rangaraj, S., et al. (2019). Silicon confers protective effect against ginseng root rot by regulating sugar efflux into apoplast. Sci. Rep. 9, 1–10. doi: 10.1038/s41598-019-54678-x

PubMed Abstract | Crossref Full Text | Google Scholar

Ahmad, F., Jabeen, K., Iqbal, S., Umar, A., Ameen, F., Gancarz, M., et al. (2023). Influence of silicon nanoparticles on Avena sativa L. To alleviate the biotic stress of Rhizoctonia solani. Sci. Rep. 13, 1–15. doi: 10.1038/s41598-023-41699-w

PubMed Abstract | Crossref Full Text | Google Scholar

Akhtar, N., Chandra, R., Mazhar, Z. (2018). Silicon based defence mechanism in plants. Trends Biosci. 11 (32), 3663–3674.

Google Scholar

Al-Gaashani, M. S., Samee, N. A., Alnashwan, R., Khayyat, M., Muthanna, M. S. A. (2023). Using a resnet50 with a kernel attention mechanism for rice disease diagnosis. Life 13, 1277. doi: 10.3390/life13061277

PubMed Abstract | Crossref Full Text | Google Scholar

Al-Sadi, A. M. (2021). Bipolaris sorokiniana-induced black point, common root rot, and spot blotch diseases of wheat: A review. Front. Cell Infect. Microbiol. 11. doi: 10.3389/fcimb.2021.584899

PubMed Abstract | Crossref Full Text | Google Scholar

Alves, A. L., Costa, A. C. T., Mottin, M. C., Pietrowiski, V., Junior, J. B. D., Nunes, M. (2018). Evaluation of the insect pest population dynamics in common bean cultivars in relation to the foliar fertilisation with potassium silicate. J. Exp. Agric. Int. 27, 1–12. doi: 10.9734/jeai/2018/44031

Crossref Full Text | Google Scholar

Alves, A. O., Santos, M. M. B., Souza, L. J. N., Souza, E. B., Mariano, R. L. R. (2015). Use of silicon for reducing the severity of bacterial wilt of sweet pepper. J. Plant Pathol. 97, 419–429. doi: 10.4454/JPP.V97I3.002

Crossref Full Text | Google Scholar

Andrade, C. C. L., Resende, R. S., Rodrigues, F. A., Ferraz, H. G. M., Moreira, W. R., Oliveira, J. R., et al. (2013). Silicon reduces bacterial speck development on tomato leaves. Trop. Plant Pathol. 38, 436–442. doi: 10.1590/S1982-56762013005000021

Crossref Full Text | Google Scholar

Bakhat, H. F., Bibi, N., Zia, Z., Abbas, S., Hammad, H. M., Fahad, S., et al. (2018). Silicon mitigates biotic stresses in crop plants: A review. J. Crop Prot. 104, 21–34. doi: 10.1016/j.cropro.2017.10.008

Crossref Full Text | Google Scholar

Basagli, M. A. B., Moraes, J. C., Carvalho, G. A., Ecole, C. C., Gonçalves-Gervásio, R., de, C. R. (2003). Efeito da aplicação de silicato de sódio na resistência de plantas de trigo ao pulgão-verde schizaphis graminum (Rond.) (Hemiptera: Aphididae). Neotrop. Entomol. 32, 659–663. doi: 10.1590/S1519-566X2003000400017

Crossref Full Text | Google Scholar

Bityutskii, N. P., Yakkonen, K. L., Petrova, A. I., Lukina, K. A., Shavarda, A. L. (2019). Calcium carbonate reduces the effectiveness of soil-added monosilicic acid in cucumber plants. J. Soil Sci. Plant Nutr. 19, 660–670. doi: 10.1007/s42729-019-00066-3

Crossref Full Text | Google Scholar

Bockhaven, J. V., Steppe, K., Bauweraerts, I., Kikuchi, S., Asano, T., Hofte, M., et al. (2015). Primary metabolism plays a central role in moulding silicon-inducible brown spot resistance in rice. Mol. Plant Pathol. 16, 811–824. doi: 10.1111/mpp.12236

PubMed Abstract | Crossref Full Text | Google Scholar

Boer, C. A., Sampaio, M. V., Pereira, H. S. (2019). Silicon-mediated and constitutive resistance to Rhopalosiphum maidis (Hemiptera: Aphididae) in corn hybrids. Bull. Entomol. Res. 109, 356–364. doi: 10.1017/S0007485318000585

PubMed Abstract | Crossref Full Text | Google Scholar

Cabrera-Ponce, J. L., Valencia-Lozano, E., Trejo-Saavedra, D. L. (2019). “Genetic modifications of corn,” in Corn, 3rd ed. (AACC International Press, Oxford). doi: 10.1016/B978-0-12-811971-6.00003-6

Crossref Full Text | Google Scholar

Cai, K., Gao, D., Luo, S., Zeng, R., Yang, J., Zhu, X. (2008). Physiological and cytological mechanisms of silicon-induced resistance in rice against blast disease. Physiol. Plant 134, 324–333. doi: 10.1111/j.1399-3054.2008.01140.x

PubMed Abstract | Crossref Full Text | Google Scholar

Carre-Missio, V., Rodrigues, F. A., Schurt, D. A., Resende, R. S., Souza, F. A., Rezende, D. C., et al. (2014). Effect of foliar-applied potassium silicate on coffee leaf infection by Hemileia vastatrix. Ann. Appl. Biol. 164, 396–403. doi: 10.1111/aab.12109

Crossref Full Text | Google Scholar

Chain, F., Côté-Beaulieu, C., Belzile, F., Menzies, J. G., Bélanger, R. R. (2009). A comprehensive transcriptomic analysis of the effect of silicon on wheat plants under control and pathogen stress conditions. Mol. Plant Microbe Int. 22, 1323–1330. doi: 10.1094/MPMI-22-11-1323

PubMed Abstract | Crossref Full Text | Google Scholar

Chen, D., Li, C., Wu, K., Xun, G., Yuan, S., Shen, Q., et al. (2015). A phcA– marker-free mutant of Ralstonia solanacearum as potential biocontrol agent of tomato bacterial wilt. Biol. Contr. 80, 96–102. doi: 10.1016/j.biocontrol.2014.09.005

Crossref Full Text | Google Scholar

Chen, J., Li, Y., Zeng, Z., Zhao, X., Zhang, Y., Li, X., et al. (2024). Silicon induces ROS scavengers, hormone signalling, antifungal metabolites, and silicon deposition against brown stripe disease in sugarcane. Physiol. Plant 176, e14313. doi: 10.1111/ppl.14313

PubMed Abstract | Crossref Full Text | Google Scholar

Chen, Y., Liu, M., Wang, L., Lin, W., Fan, X., Cai, K. (2014). Proteomic characterization of silicon-mediated resistance against Ralstonia solanacearum in tomato. Plant Soil 387, 425–440. doi: 10.1007/s11104-014-2293-4

Crossref Full Text | Google Scholar

Conceiaco, C. S., Felix, K. C. S., Mariano, R. L., Medeiros, E. V., Souza, E. B. (2014). Combined effect of yeast and silicon on the control of bacterial fruit blotch in melon. Sci. Horticult. 174, 164–170. doi: 10.1016/j.scienta.2014.05.027

Crossref Full Text | Google Scholar

Correa, R. S. B., Moraes, J. C., Auad, A. M., Carvalho, G. A. (2005). Silício e acibenzolar-s-methyl como indutores de resistência em pepino, à mosca-branca Bemisia tabaci (Gennadius) (Hemiptera: Aleyrodidae) Biótipo B. Neotrop. Entomol. 34, 429–433. doi: 10.1590/S1519-566X2005000300011

Crossref Full Text | Google Scholar

Coskun, D., Deshmukh, R., Sonah, H., Menzies, J. G., Reynolds, O., Ma, J. F., et al. (2019). The controversies of silicon's role in plant biology. New Phytol. 221, 67–85. doi: 10.1111/nph.15343

PubMed Abstract | Crossref Full Text | Google Scholar

Cruz, M., Rodrigues, F. A., Polanco, L. R., Curvelo, C. R. D. S., Nascimento, K. J. T., Moreira, M. A., et al. (2013). Inducers of resistance and silicon on the activity of defense enzymes in the soybean-Phakopsora pachyrhizi interaction. Bragantia 72, 162–172. doi: 10.1590/S0006-87052013005000025

Crossref Full Text | Google Scholar

Dallagnol, L. J., Rodrigues, F. A., Tanaka, F. A., Amorim, L., Camargo, L. E. (2012). Effect of potassium silicate on epidemic components of powdery mildew on melon. Plant Pathol. 61, 323–330. doi: 10.1111/j.1365-3059.2011.02518.x

Crossref Full Text | Google Scholar

De Almeida, G. D., Pratissoli, D., Zanuncio, J. C., Vicentini, V. B., Holtz, A. M., Serrão, J. E. (2008). Calcium silicate and organic mineral fertilizer applications reduce phytophagy by Thrips palmi Karny (Thysanoptera: Thripidae) on eggplants (Solanum melongena L.). Interciencia 33, 835–838.

Google Scholar

Debona, D., Rodrigues, F. A., Rios, J. A., Nascimento, K. J. T., Silva, L. C. (2014). The effect of silicon on antioxidant metabolism of wheat leaves infected by Pyricularia oryzae. Plant Pathol. 6, 581–589. doi: 10.1111/ppa.2014.63.issue-3

Crossref Full Text | Google Scholar

Dias, P. A. S., Sampaio, M. V., Rodrigues, M. P., Korndörfer, A. P., Oliveira, R. S., Ferreira, S. E., et al. (2014). Induction of resistance by silicon in wheat plants to alate and apterous morphs of Sitobion avenae (Hemiptera: Aphididae). Environ. Entomol. 43, 949–956. doi: 10.1603/en13234

PubMed Abstract | Crossref Full Text | Google Scholar

Dorneles, K. R., Dallagnol, L. J., Pazdiora, P. C., Rodrigues, F. A., Deuner, S. (2017). Silicon potentiates biochemical defense responses of wheat against tan spot. Physiol. Mol. Plant Pathol. 97, 69–78. doi: 10.1016/j.pmpp.2017.01.001

Crossref Full Text | Google Scholar

dos Santos, M. C., Junqueira, M. R., de Sá, V. M., Zanúncio, J. C., Serrão, J. E. (2015). Effect of silicon on the morphology of the midgut and mandible of tomato leaf miner Tuta absoluta (Lepidoptera: gelechiidae) larvae. Invertebr. Surviv. J. 12, 158–165.

Google Scholar

Dugui-Es, C., Pedroche, N., Villanueva, L., Galeng, J., De, D. W. (2010). Management of root knot nematode,Meloidogyne incognitain cucumber (Cucumis sativus) using silicon. Commun. Agric. Appl. Biol. Sci. 75, 497–505. doi: 10.3390/plants8060148

PubMed Abstract | Crossref Full Text | Google Scholar

El-Ramady, H. R., Verma, K. K., Rajput, V. D., Minkina, T., Elbehiry, F., Elbasiouny, H. Y., et al. (2022). “Sources of silicon and nano-silicon in soil and plants,” in book: silicon and nano-silicon in environmental stress management and crop quality improvement: progress and prospects (United Kingdom: Academic Press, Elsevier). doi: 10.1016/B978-0-323-91225-9.00003-0

Crossref Full Text | Google Scholar

Etesami, H., Jeong, B. R., Rizwan, M. (2020). “The use of silicon in stressed agriculture management,” in Metalloids in plants (Wiley Online Library, Hoboken). doi: 10.1002/9781119487210.ch19

Crossref Full Text | Google Scholar

Fahad, S., Adnan, M., Noor, M., Arif, M., Alam, M., Khan, I. A., et al. (2019). “Major constraints for global rice production,” in Advances in rice research for abiotic stress tolerance (Woodhead Publishing, Sawston). doi: 10.1016/B978-0-12-814332-2.00001-0

Crossref Full Text | Google Scholar

Farhat, M., Haggag, W., Thabet, M., Mosa, A. (2018). Efficacy of silicon and titanium nanoparticles biosynthesis by some antagonistic fungi and bacteria for controlling powdery mildew disease of wheat plants. Technol. 14, 661–674. Available at: https://www.thaiscience.info/Journals/Article/IJAT/10992391.pdf.

Google Scholar

Fauteux, F., Chain, F., Belzile, F., Menzies, J. G., Bélanger, R. R. (2006). The protective role of silicon in the Arabidopsis-powdery mildew pathosystem. Proc. Natl. Acad. Sci. U. S. A. 103, 17554–17559. doi: 10.1073/pnas.0606330103

PubMed Abstract | Crossref Full Text | Google Scholar

Ferreira, H. A., do Nascimento, C. W. A., Datnoff, L. E., de Sousa Nunes, G. H., Preston, W., de Souza, E. B., et al. (2015). Effects of silicon on resistance to bacterial fruit blotch and growth of melon. Crop Protect. 78, 277–283. doi: 10.1016/j.cropro.2015.09.025

Crossref Full Text | Google Scholar

Ferreira, R. S., Moraes, J. C. (2011). Silicon influence on resistance induction against Bemisia tabaci biotype B (Genn.) (Hemiptera: aleyrodidae) and on vegetative development in two soybean cultivars. Neotrop. Entomol. 40, 495–500. doi: 10.1590/S1519-566X2011000400014

PubMed Abstract | Crossref Full Text | Google Scholar

Fortunato, A. A., da Silva, W. L., Rodrigues, F. A. (2014). Phenylpropanoid pathway is potentiated by silicon in the roots of banana plants during the infection process of Fusarium oxysporum f. sp. cubense. Phytopathol. 104, 597–603. doi: 10.1094/PHYTO-07-13-0203-R

PubMed Abstract | Crossref Full Text | Google Scholar

Fortunato, A. A., Debona, D., Bernardeli, A. M. A., Rodrigues, F. A. (2015). Defence-related enzymes in soybean resistance to target spot. J. Phytopathol. 163, 731–742. doi: 10.1111/jph.12370

Crossref Full Text | Google Scholar

French-Monar, R. D., Rodrigues, F. A., Korndörfer, G. H., Datnoff, L. E. (2010). Silicon suppresses phytophthora blight development on bell pepper. J. Phytopathol. 158, 554–560. doi: 10.1111/j.1439-0434.2009.01665.x

Crossref Full Text | Google Scholar

Frew, A., Weston, L. A., Reynolds, O. L., Gurr, G. M. (2018). The role of silicon in plant biology: a paradigm shift in research approach. Ann. Bot. 121, 1265–1273. doi: 10.1093/aob/mcy009

PubMed Abstract | Crossref Full Text | Google Scholar

Gatarayiha, M. C., Laing, M. D., Miller, R. M. (2010). Combining applications of potassium silicate and Beauveria bassiana to four crops to control two spotted spider mite, Tetranychus urticae Koch. Int. J. Pest Manage. 56, 291–297. doi: 10.1080/09670874.2010.495794

Crossref Full Text | Google Scholar

Gbongue, L.-R., Lalaymia, I., Zeze, A., Delvaux, B., Declerck, S. (2019). Increased Silicon Acquisition in Bananas Colonized by Rhizophagus irregularis MUCL 41833 reduces the incidence of Pseudocercospora Fijiensis. Front. Plant Sci. 9, 1977. doi: 10.3389/fpls.2018.01977

PubMed Abstract | Crossref Full Text | Google Scholar

Ghanmi, D., McNally, D. J., Benhamou, N., Menzies, J. G., Belanger, R. R. (2004). Powdery mildew of Arabidopsis thaliana: A pathosystem for exploring the role of silicon in plant–microbe interactions. Physiol. Mol. Plant Pathol. 64, 189–199. doi: 10.1016/j.pmpp.2004.07.005

Crossref Full Text | Google Scholar

Ghareeb, H., Bozsó, Z., Ott, P. G., Repenning, C., Stahl, F., Wydra, K. (2011). Transcriptome of silicon-induced resistance against Ralstonia solanacearum in the silicon non-accumulator tomato implicates priming effect. Physiol. Mol. Plant Pathol. 75, 83–89. doi: 10.1016/j.pmpp.2010.11.004

Crossref Full Text | Google Scholar

Glazebrook, J. (2005). Contrasting mechanisms of defense against biotrophic and necrotrophic pathogens. Ann. Rev. Phytopathol. 43, 205–227. doi: 10.1146/annurev.phyto.43.040204.135923

PubMed Abstract | Crossref Full Text | Google Scholar

Goussain, M. M., Prado, E., Moraes, J. C. (2005). Efeito do silício, aplicado em plantas de trigo, na biologia e comportamento alimentar do pulgão-verde Schizaphis graminum (Rond.) (Hemiptera: Aphididae). Neotrop. Entomol. 34, 807–813. doi: 10.1590/S1519-566X2005000500013

Crossref Full Text | Google Scholar

Guerin, V., Lebreton, A., Cogliati, E. E., Hartley, S. E., Belzile, F., Menzies, J. G., et al. (2014). A zoospore inoculation method with Phytophthora Sojae to assess the prophylactic role of silicon on soybean cultivars. Plant Dis. 98, 1632–1638. doi: 10.1094/PDIS-01-14-0102-RE

PubMed Abstract | Crossref Full Text | Google Scholar

Gulzar, N., Kamili, A. N., Shah, M. A. (2021). Silicon, the multifunctional element in reducing biotic and abiotic stress in plants. Int. Res. J. Plant Sci. 12, 1–9. doi: 10.14303/irjps.2021.20

Crossref Full Text | Google Scholar

Gutiérrez-Barranquero, J. A., Arrebola, E., Bonilla, N., Sarmiento, D., Cazorla, F. M., De Vicente, A. (2012). Environmentally friendly treatment alternatives to Bordeaux mixture for controlling bacterial apical necrosis (BAN) of mango. Plant Pathol. 61, 665–676. doi: 10.1111/j.1365-3059.2011.02559.x

Crossref Full Text | Google Scholar

Han, Y., Lei, W., Wen, L., Hou, M. (2015). Silicon-mediated resistance in a susceptible rice variety to the rice leaf folder, Cnaphalocrocis medinalis Guenée (Lepidoptera: Pyralidae). PloS One. 10 (4), e0120557. doi: 10.1371/journal.pone.0120557

PubMed Abstract | Crossref Full Text | Google Scholar

Han, Y.-Q., Wen, J.-H., Peng, Z.-P., Zhang, D.-Y., Hou, M.-L. (2018). Effects of silicon amendment on the occurrence of rice insect pests and diseases in a field test. J. Integr. Agric. 17, 2172–2181. doi: 10.1016/S2095-3119(18)62035-0

Crossref Full Text | Google Scholar

Haq, I. U., Khurshid, A., Inayat, R., Zhang, K., Liu, C., Ali, S., et al. (2021). Silicon-based induced resistance in maize against fall armyworm [Spodoptera frugiperda (Lepidoptera: Noctuidae). PloS One 16, e0259749. doi: 10.1371/journal.pone.0259749

PubMed Abstract | Crossref Full Text | Google Scholar

Hernandez-Apaolaza, L. (2022). Priming with silicon: a review of a promising tool to improve micronutrient deficiency symptoms. Front. Plant Sci. 13. doi: 10.3389/fpls.2022.840770

PubMed Abstract | Crossref Full Text | Google Scholar

Hou, M., Han, Y. (2010). Silicon-mediated rice plant resistance to the asiatic rice borer (Lepidoptera: Crambidae): effects of silicon amendment and rice varietal resistance. J. Econ. Entomol. 103, 1412–1419. doi: 10.1603/ec09341

PubMed Abstract | Crossref Full Text | Google Scholar

Inbar, M., Gerling, D. (2008). Plant-mediated interactions between whiteflies, herbivores, and natural enemies. Annu. Rev. Entomol. 53, 431–448. doi: 10.1146/annurev.ento.53.032107.122456

PubMed Abstract | Crossref Full Text | Google Scholar

Jadhao, K. R., Bansal, A., Rout, G. R. (2020). Silicon amendment induces synergistic plant defense mechanism against pink stem borer (Sesamia inferens Walker.) in finger millet (Eleusine coracana Gaertn.). Sci. Rep. 10, 1–15. doi: 10.1038/s41598-020-61182-0

PubMed Abstract | Crossref Full Text | Google Scholar

Jasrotia, P., Bhardwaj, A. K., Katare, S., Yadav, J., Kashyap, P. L., Kumar, S., et al. (2021). Tillage intensity influences insect-pest and predator dynamics of wheat crop grown under different conservation agriculture practices in rice-wheat cropping system of indo-Gangetic plain. Agron. 11, 1087. doi: 10.3390/agronomy11061087

Crossref Full Text | Google Scholar

Jayawardana, H. A. R. K., Weerahewa, H. L. D., Saparamadu, M. D. J. S. (2015). Enhanced resistance to anthracnose disease in chili pepper (Capsicum annuum L.) by amendment of the nutrient solution with silicon. J. Hortic. Sci. Biotechnol. 90, 557–562. doi: 10.1080/14620316.2015.11668714

Crossref Full Text | Google Scholar

Jayawardana, H. A. R. K., Weerahewa, H. L. D., Saparamadu, M. D. J. S. (2016). The mechanisms underlying the anthracnose disease reduction by rice hull as a silicon source in capsicum (Capsicum annuum L.) grown in simplified hydroponics. Proc. Food Sci. 6, 147–150. doi: 10.1016/j.profoo.2016.02.035

Crossref Full Text | Google Scholar

Jeer, M., Telugu, U. M., Voleti, S. R., Padmakumari, A. P. (2017). Soil application of silicon reduces yellow stem borer, Scirpophaga incertulas (Walker) damage in rice. J. Appl. Entomol. 141, 189–201. doi: 10.1111/jen.12324

Crossref Full Text | Google Scholar

Jiang, N., Fan, X., Lin, W., Wang, G., Cai, K. (2019). Transcriptome analysis reveals new insights into the bacterial wilt resistance mechanism mediated by silicon in tomato. Int. J. Mol. Sci. 20, 761. doi: 10.3390/ijms20030761

PubMed Abstract | Crossref Full Text | Google Scholar

Juma, G., Ahuya, P., Ong'amo, G., Ru, B., Magoma, G., Silvain, J.-F., et al. (2015). Influence of plant silicon in Busseola fusca (Lepidoptera: Noctuidae) larvae–Poaceae interactions. Bull. Entom. Res. 105, 253–258. doi: 10.1017/S000748531500005X

PubMed Abstract | Crossref Full Text | Google Scholar

Kablan, L., Lagauche, A., Delvaux, B., Legrève, A. (2012). Silicon reduces black Sigatoka development in banana. Plant Dis. 96, 273–278. doi: 10.1094/PDIS-04-11-0274

PubMed Abstract | Crossref Full Text | Google Scholar

Keeping, M. G., Meyer, J. H. (2002). Calcium silicate enhances resistance of sugarcane to the African stalk borer Eldana saccharina Walker (Lepidoptera: Pyralidae). Agric. For. Entomol. 4, 265–274. doi: 10.1046/j.1461-9563.2002.00150.x

Crossref Full Text | Google Scholar

Keeping, M. G., Meyer, J. H. (2006). Silicon-mediated resistance of sugarcane to Eldana saccharina Walker (Lepidoptera: Pyralidae): Effects of silicon source and cultivar. J. Appl. Entomol. 130, 410–420. doi: 10.1111/j.1439-0418.2006.01081.x

Crossref Full Text | Google Scholar

Khan, S. R., Ahmad, Z., Khan, Z., Khan, U., Asad, M., Shah, T. (2024). Synergistic effect of silicon and arbuscular mycorrhizal fungi reduces cadmium accumulation by regulating hormonal transduction and lignin accumulation in maize. Chemosphere 346, 140507. doi: 10.1016/j.chemosphere.2023.140507

PubMed Abstract | Crossref Full Text | Google Scholar

Korth, K. L., Doege, S. J., Park, S. H., Goggin, F. L., Wang, Q., Gomez, S. K., et al. (2006). Medicago truncatula mutants demonstrate the role of plant calcium oxalate crystals as an effective defense against chewing insects. Plant Physiol. 141, 188–195. doi: 10.1104/pp.106.076737

PubMed Abstract | Crossref Full Text | Google Scholar

Kumari, A., Dash, M., Singh, S. K., Jagadesh, M., Mathpal, B., Mishra, P. K., et al. (2023). Soil microbes: a natural solution for mitigating the impact of climate change. Environ. Monit. Assess. 195, 1436. doi: 10.1007/s10661-023-11988-y

PubMed Abstract | Crossref Full Text | Google Scholar

Kumari, A., Lakshmi, G. A., Krishna, G. K., Patni, B., Prakash, S., Bhattacharyya, M., et al. (2022). Climate change and its impact on crops: A comprehensive investigation for sustainable agriculture. Agronomy 12, 3008. doi: 10.3390/agronomy12123008

Crossref Full Text | Google Scholar

Lashari, A. A., Korai, S. K., Nizamani, I. A., Qureshi, K. H., Lodhi, A. M., Korai, A. K., et al. (2022). Monitoring of sucking pest on mustard crop through different colours sticky traps. Pak. J. Zool. 54, 801–808. doi: 10.17582/journal.pjz/20200427210427

Crossref Full Text | Google Scholar

Lepolu Torlon, J., Heckman, J. R., Simon, J. E., Wyenandt, C. A. (2016). Silicon soil amendments for suppressing powdery mildew on pumpkin. Sustainability 8, 293. doi: 10.3390/su8040293

Crossref Full Text | Google Scholar

Liu, J., Zhu, J., Zhang, P., Han, L., Reynolds, O. L., Zeng, R., et al. (2017). Silicon supplementation alters the composition of herbivore induced plant volatiles and enhances attraction of parasitoids to infested rice plants. Front. Plant Sci. 8. doi: 10.3389/fpls.2017.01265

PubMed Abstract | Crossref Full Text | Google Scholar

Luyckx, M., Hausman, J. F., Lutts, S., Guerriero, G. (2017). Silicon and plants: current knowledge and technological perspectives. Front. Plant Sci. 8. doi: 10.3389/fpls.2017.00411

PubMed Abstract | Crossref Full Text | Google Scholar

Massey, F. P., Ennos, A. R., Hartley, S. E. (2006). Silica in grasses as a defence against insect herbivores: Contrasting effects on folivores and a phloem feeder. J. Anim. Ecol. 75, 595–603. doi: 10.1111/j.1365-2656.2006.01082.x

PubMed Abstract | Crossref Full Text | Google Scholar

Massey, F. P., Hartley, S. E. (2009). Physical defences wear you down: progressive and irreversible impacts of silica on insect herbivores. J. Anim. Ecol. 78, 281–291. doi: 10.1111/j.1365-2656.2008.01472.x

PubMed Abstract | Crossref Full Text | Google Scholar

Mathur, P. G. J., Srivastava, N. (2022). Silica nanoparticles as novel sustainable approach for plant growth and crop protection. Heliyon 8, e09908. doi: 10.1016/j.heliyon.2022.e09908

PubMed Abstract | Crossref Full Text | Google Scholar

Matichenkov, V. V., Calvert, D. V. (2002). Silicon as a beneficial element for sugarcane. J. Am. Soc Sug. Technol. 22, 21–30.

Google Scholar

Mburu, K., Oduor, R., Mgutu, A., Tripathi, L. (2016). Silicon application enhances resistance to xanthomonas wilt disease in banana. Plant Pathol. 65, 807–818. doi: 10.1111/ppa.12468

Crossref Full Text | Google Scholar

Meyer, J. H., Keeping, M. G. (2001). Chapter 16 Past, present and future research of the role of silicon for sugarcane in southern Africa. Stud. Plant Sci. 8, 257–275. doi: 10.1016/S0928-3420(01)80020-3

Crossref Full Text | Google Scholar

Mir, R. A., Bhat, B. A., Yousuf, H., Islam, S. T., Raza, A., Rizvi, M. A., et al. (2022). Multidimensional role of silicon to activate resilient plant growth and to mitigate abiotic stress. Front. Plant Sci. 13. doi: 10.3389/fpls.2022.819658

PubMed Abstract | Crossref Full Text | Google Scholar

Mittal, D., Kaur, G., Singh, P., Yadav, K., Ali, S. A. (2020). Nanoparticle-based sustainable agriculture and food science: Recent advances and future outlook. Front. Nanotechnol. 2. doi: 10.3389/fnano.2020.579954

Crossref Full Text | Google Scholar

Moraes, J. C., Goussain, M. M., Carvalho, G. A., Costa, R. R. (2005). Feeding non-preference of the corn leaf aphid Rhopalosiphum maidis (Fitc) (Hemiptera: Aphididae) to corn plants (Zea mays L.) treated with silicon. Ciec. e Agrotecnologia 29, 761–766. doi: 10.1590/s1413-70542005000400007

Crossref Full Text | Google Scholar

Mukarram, M., Petrik, P., Mushtaq, Z., Khan, M. M. A., Gulfishan, M., Lux, A. (2022). Silicon nanoparticles in higher plants: Uptake, action, stress tolerance, and crosstalk with phytohormones, antioxidants, and other signalling molecules. Environ. pollut. 310, 119855. doi: 10.1016/j.envpol.2022.119855

PubMed Abstract | Crossref Full Text | Google Scholar

Muthu, N. M., Ahmad, N., Shivanand, P., Metali, F. (2022). The role of endophytes in combating fungal-and bacterial-induced stress in plants. Molecules 27, 6549. doi: 10.3390/molecules27196549

PubMed Abstract | Crossref Full Text | Google Scholar

Nikpay, A., Tiwari, A. K., Vejar-Cota, G., Ziaee, M., Wilson, B., Srivastava, S., et al. (2023). “Biotic stresses in sugarcane plants and its management,” in Agro-industrial perspectives on sugarcane production under environmental stress (Springer, Singapore). doi: 10.1007/978-981-19-3955-6_15

Crossref Full Text | Google Scholar

Ning, D., Song, A., Fan, F., Li, Z., Liang, Y. (2014). Effects of slag-based silicon fertilizer on rice growth and brown-spot resistance. PloS One 9, e102681. doi: 10.1371/journal.pone.0102681

PubMed Abstract | Crossref Full Text | Google Scholar

Oliveira, J. C., Albuquerque, G. M. R., Mariano, R. L. R., Gondim, D. M. F., Oliveira, J. T. A., Souza, E. B. (2012). Reduction of the severity of angular leaf spot of cotton mediated by silicon. J. Plant Pathol. 94, 297–304.

Google Scholar

Paton, T. R. (2023). Soils: a new global view (London: CRC Press). doi: 10.1201/9781003420361

Crossref Full Text | Google Scholar

Pazdiora, P. C., da Rosa Dorneles, K., Forcelini, C. A., Del Ponte, E. M., Dallagnol, L. J. (2018). Silicon suppresses tan spot development on wheat infected by Pyrenophora tritici-repentis. Eur. J. Plant Pathol. 150, 49–56. doi: 10.1007/s10658-017-1251-4

Crossref Full Text | Google Scholar

Rahman, A., Wallis, C. M., Uddin, W. (2015). Silicon-induced systemic defense responses in perennial ryegrass against infection by Magnaporthe oryzae. Phytopathol. 105, 748–757. doi: 10.1094/PHYTO-12-14-0378-R

PubMed Abstract | Crossref Full Text | Google Scholar

Rajput, V. D., Minkina, T., Feizi, M., Kumari, A., Khan, M., Mandzhieva, S., et al. (2021). Effects of silicon and silicon-based nanoparticles on rhizosphere microbiome, plant stress and growth. Biology 10, 791. doi: 10.3390/biology10080791

PubMed Abstract | Crossref Full Text | Google Scholar

Ramirez-Godoy, A., Puentes-Pérez, G., Restrepo-Díaz, H. (2018). An evaluation of the use of calcium, potassium and silicon for the management of Diaphorina citri populations in Tahiti lime trees. Not. Bot. Horti Agrobot. Cluj-Napoca 46, 546–552. doi: 10.15835/nbha46211152

Crossref Full Text | Google Scholar

Ranger, C. M., Singh, A. P., Frantz, J. M., Cañas, L., Locke, J. C., Reding, M. E., et al. (2009). Influence of Silicon on Resistance of Zinnia elegans to Myzus persicae (Hemiptera: Aphididae). Environ. Entomol. 38, 129–136. doi: 10.1603/022.038.0116

PubMed Abstract | Crossref Full Text | Google Scholar

Rasoolizadeh, A., Labbé, C., Sonah, H., Deshmukh, R. K., Belzile, F., Menzies, J. G., et al. (2018). Silicon protects soybean plants against Phytophthora sojae by interfering with effector-receptor expression. BMC Plant Biol. 18, 97. doi: 10.1186/s12870-018-1312-7

PubMed Abstract | Crossref Full Text | Google Scholar

Ratnayake, R.M.R.N.K., Daundasekera, W. A. M., Ariyarathne, H. M., Ganehenege, M. Y. U. (2016). Some biochemical defense responses enhanced by soluble silicon in bitter gourd-powdery mildew pathosystem. Australas. Plant Pathol. 45, 425–433. doi: 10.1007/s13313-016-0429-0

Crossref Full Text | Google Scholar

Remus-Borel, W., Menzies, J. G., Bélanger, R. R. (2005). Silicon induces antifungal compounds in powdery mildew-infected wheat. Physiol. Mol. Plant Pathol. 66, 108–115. doi: 10.1016/j.pmpp.2005.05.006

Crossref Full Text | Google Scholar

Reynolds, O. L., Padula, M. P., Zeng, R., Gurr, G. M. (2016). Silicon: potential to promote direct and indirect effects on plant defence against arthropod pests in agriculture. Front. Plant Sci. 7. doi: 10.3389/fpls.2016.00744

PubMed Abstract | Crossref Full Text | Google Scholar

Rodrigues, F.Á., Duarte, H. S. S., Rezende, D. C., Wordell Filho, J. A., Korndorfer, G. H., Zambolim, L. (2010). Foliar spray of potassium silicate on the control of angular leaf spot on beans. J. Plant Nutr. 33, 2082–2093. doi: 10.1080/01904167.2010.519082

Crossref Full Text | Google Scholar

Sakr, N. (2018). Silicon-enhanced resistance of plants to biotic stresses review article. Acta Phytopathol. Entomol. Hung. 53, 125–141. doi: 10.1556/038.53.2018.005

Crossref Full Text | Google Scholar

Santos, L. B., de Souza Junior, J. P., de Mello Prado, R., Junior, R. F., de Souza, V. F., dos Santos Sarah, M. M., et al. (2022). Silicon allows halving Cadusafos dose to control Meloidogyne incognita and increase cotton development. Silicon 14, 3809–3816. doi: 10.1007/s12633-021-01126-z

Crossref Full Text | Google Scholar

Sarraf, M., Vishwakarma, K., Kumar, V., Arif, N., Das, S., Johnson, R., et al. (2022). Metal/metalloid-based nanomaterials for plant abiotic stress tolerance: An overview of the mechanisms. Plants 11, 316. doi: 10.3390/plants11030316

PubMed Abstract | Crossref Full Text | Google Scholar

Shahrajabian, M. H., Sun, W., Cheng, Q. (2020). Considering white gold, cotton, for its fiber, seed oil, traditional and modern health benefits. J. Biol. Environ. Sci. 14, 25–39.

Google Scholar

Sharma, S., Kooner, R., Arora, R. (2017). “Insect pests and crop losses,” in Breeding insect resistant crops for sustainable agriculture (Springer, Singapore). doi: 10.1007/978-981-10-6056-4_2

Crossref Full Text | Google Scholar

Shoaib, A., Elabasy, A., Waqas, M., Lin, L., Cheng, X., Zhang, Q., et al. (2018). Entomotoxic effect of silicon dioxide nanoparticles on Plutella xylostella (L.) (Lepidoptera: Plutellidae) under laboratory conditions. Toxicol. Environ. Chem. 100, 80–91. doi: 10.1080/02772248.2017.1387786

Crossref Full Text | Google Scholar

Shomali, A., Das, S., Arif, N., Sarraf, M., Zahra, N., Yadav, V., et al. (2022). Diverse physiological roles of flavonoids in plant environmental stress responses and tolerance. Plants 11, 3158. doi: 10.3390/plants11223158

PubMed Abstract | Crossref Full Text | Google Scholar

Shomali, A., Das, S., Sarraf, M., Johnson, R., Janeeshma, E., Kumar, V., et al. (2024). Modulation of plant photosynthetic processes during metal and metalloid stress, and strategies for manipulating photosynthesis-related traits. Plant Physiol. Biochem. 206, 108211. doi: 10.1016/j.plaphy.2023.108211

PubMed Abstract | Crossref Full Text | Google Scholar

Siddiqui, Z. A., Hashmi, A., Khan, M. R., Parveen, A. (2020). Management of bacteria Pectobacterium carotovorum, Xanthomonas campestris pv. carotae, and fungi Rhizoctonia solani, Fusarium solani and Alternaria dauci with silicon dioxide nanoparticles on carrot. Int. J. Vegetable Sci. 26, 547–557. doi: 10.1080/19315260.2019.1675843

Crossref Full Text | Google Scholar

Silva, R. V., Oliveira, R. D. L., Nascimento, K. J. T., Rodrigues, F. A. (2010b). Biochemical responses of coffee resistance against Meloidogyne exigua mediated by silicon. Plant Pathol. 59, 586–593. doi: 10.1111/j.1365-3059.2009.02228.x

Crossref Full Text | Google Scholar

Silva, I. T., Rodrigues, F.Á., Oliveira, J. R., Pereira, S. C., Andrade, C. C. L., Silveira, P. R., et al. (2010a). Wheat resistance to bacterial leaf streak mediated by Silicon. J. Phytopathol. 158, 253–262. doi: 10.1111/j.1439-0434.2009.01610.x

Crossref Full Text | Google Scholar

Somapala, K., Weerahewa, H. L. D., Thrikawala, S. (2015). Silicon rich rice hull amended soil enhances anthracnose resistance in tomato. Proc. Food Sci. 6, 190–193. doi: 10.1016/j.profoo.2016.02.046

Crossref Full Text | Google Scholar

Song, X. P., Verma, K. K., Tian, D. D., Zhang, X. Q., Liang, Y. J., Huang, X., et al. (2021). Exploration of silicon functions to integrate with biotic stress tolerance and crop improvement. Biol. Res. 54, 19. doi: 10.1186/s40659-021-00344-4

PubMed Abstract | Crossref Full Text | Google Scholar

Song, A., Xue, G., Cui, P., Fan, F., Liu, H., Yin, C., et al. (2016). The role of silicon in enhancing resistance to bacterial blight of hydroponic- and soil-cultured rice. Sci. Rep. 6 (1), 1–13. doi: 10.1038/srep24640

PubMed Abstract | Crossref Full Text | Google Scholar

Sun, S., Yang, Z., Song, Z., Wang, N., Guo, N., Niu, J., et al. (2022). Silicon enhances plant resistance to Fusarium wilt by promoting antioxidant potential and photosynthetic capacity in cucumber (Cucumis sativus L.). Front. Plant Sci. 13. doi: 10.3389/fpls.2022.1011859

PubMed Abstract | Crossref Full Text | Google Scholar

Tayade, R., Ghimire, A., Khan, W., Lay, L., Attipoe, J. Q., Kim, Y. (2022). Silicon as a smart fertilizer for sustainability and crop improvement. Biomol. 12, 1027. doi: 10.3390/biom12081027

PubMed Abstract | Crossref Full Text | Google Scholar

Thoma, I., Loeffler, C., Sinha, A. K., Gupta, M., Krischke, M., Steffan, B., et al. (2003). Cyclopentenone isoprostanes induced by reactive oxygen species trigger defense gene activation and phytoalexin accumulation in plants. Plant J. 34, 363–375. doi: 10.1046/j.1365-313X.2003.01730.x

PubMed Abstract | Crossref Full Text | Google Scholar

Torres, M. A. (2010). ROS in biotic interactions. Physiol. Plant 138, 414–429. doi: 10.1111/j.1399-3054.2009.01326.x

PubMed Abstract | Crossref Full Text | Google Scholar

Tyczewska, A., Woźniak, E., Gracz, J., Kuczyński, J., Twardowski, T. (2018). Towards food security: current state and future prospects of agrobiotechnology. Trends Biotechnol. 36, 1219–1229. doi: 10.1016/j.tibtech.2018.07.008

PubMed Abstract | Crossref Full Text | Google Scholar

Verma, K. K., Anas, M., Chen, Z., Rajput, V. D., Malviya, M. K., Verma, C. L., et al. (2020a). Silicon supply improves leaf gas exchange, antioxidant defense system and growth in sugarcane responsive to water limitation. Plants 9, 1032. doi: 10.3390/plants9081032

PubMed Abstract | Crossref Full Text | Google Scholar

Verma, K. K., Li, D. M., Singh, M., Rajput, V. D., Malviya, M. K., Minkina, T., et al. (2020b). Interactive role of silicon and plant-rhizobacteria mitigating abiotic stresses: A new approach for sustainable agriculture and climate change. Plants 9, 1055. doi: 10.3390/plants9091055

PubMed Abstract | Crossref Full Text | Google Scholar

Verma, K. K., Liu, X.-H., Wu, K.-C., Singh, R. K., Song, Q. Q., Malviya, M. K., et al. (2020f). The impact of silicon on photosynthetic and biochemical responses of sugarcane under different soil moisture levels. Silicon 12, 1355–1367. doi: 10.1007/s12633-019-00228-z

Crossref Full Text | Google Scholar

Verma, K. K., Singh, P., Song, X.-P., Malviya, M. K., Singh, R. K., Chen, G.-L., et al. (2020c). Mitigating climate change for sugarcane improvement: role of silicon in alleviating abiotic stresses. Sugar Tech. 22, 741–749. doi: 10.1007/s12355-020-00831-0

Crossref Full Text | Google Scholar

Verma, K. K., Singh, R. K., Song, Q. Q., Singh, P., Zhang, B.-Q., Song, X.-P., et al. (2019). Silicon alleviates drought stress of sugarcane plants by improving antioxidant responses. Biomed. J. Sci. Tech. Res. 17 (1), 2019. doi: 10.26717/BJSTR.2019.17.002957

Crossref Full Text | Google Scholar

Verma, K. K., Song, X. P., Budeguer, F., Nikpay, A., Enrique, R., Singh, M., et al. (2022a). Genetic engineering: an efficient approach to mitigating biotic and abiotic stresses in sugarcane cultivation. Plant Signaling Behav. 17, e2108253. doi: 10.1080/15592324.2022.2108253

PubMed Abstract | Crossref Full Text | Google Scholar

Verma, K. K., Song, X. P., Joshi, A., Tian, D. D., Rajput, V. D., Singh, M., et al. (2022c). Recent trends in nano-fertilizer for advancing sustainable agriculture under the era of climate change to ensure food security for future generations. Nanomaterials 12, 173. doi: 10.3390/nano12010173

PubMed Abstract | Crossref Full Text | Google Scholar

Verma, K. K., Song, P., Kumari, A., Jagadesh, M., Singh, S. K., Bhatt, R., et al. (2024). Climate change adaptation: Challenges for agricultural sustainability. Plant Cell Environ. doi: 10.1111/pce.15078

PubMed Abstract | Crossref Full Text | Google Scholar

Verma, K. K., Song, X. P., Li, D. M., Singh, M., Wu, J. M., Singh, R. K., et al. (2022b). Silicon and soil microorganisms improves rhizospheric soil health with bacterial community, plant growth, performance and yield. Plant Signaling Behav. 17, e2104004. doi: 10.1080/15592324.2022.2104004

PubMed Abstract | Crossref Full Text | Google Scholar

Verma, K. K., Song, X. P., Lin, B., Guo, D. J., Singh, M., Rajput, V. D., et al. (2021a). Silicon induced drought tolerance in crop plants: physiological adaptation strategies. Silicon 14 (6), 2473–2487. doi: 10.1007/s12633-021-01071-x

Crossref Full Text | Google Scholar

Verma, K. K., Song, X. P., Singh, M., Tian, D. D., Rajput, V. D., Minkina, T., et al. (2023a). Association of silicon and soil microorganisms induces stress mitigation, increasing plant productivity. Benefits Silicon Nutr. Plants pp, 299–328. doi: 10.1007/978-3-031-26673-7_17

Crossref Full Text | Google Scholar

Verma, K. K., Song, X., Tian, D. D., Guo, D., Chen, Z., Zhong, C., et al. (2021d). Influence of silicon on biocontrol strategies to manage biotic stress for crop protection, performance, and improvement. Plants 10, 2163. doi: 10.3390/plants10102163

PubMed Abstract | Crossref Full Text | Google Scholar

Verma, K. K., Song, X. P., Tian, D. D., Singh, M., Verma, C. L., Rajput, V. D., et al. (2021b). Investigation of defensive role of silicon during drought stress induced by irrigation capacity in sugarcane: physiological and biochemical characteristics. ACS Omega 6, 19811–19821. doi: 10.1021/acsomega.1c02519

PubMed Abstract | Crossref Full Text | Google Scholar

Verma, K. K., Song, X., Verma, C. L., Huang, H., Singh, M., Xu, L., et al. (2023b). Mathematical modeling of climate and fluoride effects on sugarcane photosynthesis with silicon nanoparticles. Plant Physiol. Biochem. 204, 108089. doi: 10.1016/j.plaphy.2023.108089

PubMed Abstract | Crossref Full Text | Google Scholar

Verma, K. K., Song, X. P., Zeng, Y., Guo, D. J., Singh, M., Rajput, V. D., et al. (2021c). Foliar application of silicon boosts growth, photosynthetic leaf gas exchange, antioxidative response and resistance to limited water irrigation in sugarcane (Saccharum officinarum L.). Plant Physiol. Biochem. 166, 582–592. doi: 10.1016/j.plaphy.2021.06.032

PubMed Abstract | Crossref Full Text | Google Scholar

Verma, K. K., Song, X. P., Zeng, Y., Li, D. M., Guo, D. J., Rajput, V. D., et al. (2020d). Characteristics and correlation of leaf stomata and its relationship with photosynthesis on. Saccharum under different irrigation silicon application. ACS Omega 5, 24145–24153. doi: 10.1021/acsomega.0c03820

PubMed Abstract | Crossref Full Text | Google Scholar

Verma, K. K., Wu, K. C., Verma, C. L., Li, D. M., Malviya, M. K., Singh, R. K., et al. (2020e). Developing mathematical model for diurnal dynamics on photosynthetic responses in sugarcane responsive to different irrigation and silicon application. PeerJ 8, e10154. doi: 10.7717/peerj.10154

PubMed Abstract | Crossref Full Text | Google Scholar

Vermeire, M. L., Kablan, L., Dorel, M., Delvaux, B., Risède, J. M., Legrève, A. (2011). Protective role of silicon in the banana-Cylindrocladium spathiphylli pathosystem. Eur. J. Plant Pathol. 131, 621–630. doi: 10.1007/s10658-011-9835-x

Crossref Full Text | Google Scholar

Vivancos, J., Labbe, C., Menzies, J. G., Belanger, R. R. (2015). Silicon-mediated resistance of Arabidopsis against powdery mildew involves mechanisms other than the salicylic acid (SA)- dependent defence pathway. Mol. Plant Pathol. 16, 572–582. doi: 10.1111/mpp.12213

PubMed Abstract | Crossref Full Text | Google Scholar

Wang, L., Cai, K., Chen, Y., Wang, G. (2013). Silicon-mediated tomato resistance against Ralstonia solanacearumis associated with modification of soil microbial community structure and activity. Biol. Trace Elem. Res. 152, 275–283. doi: 10.1007/s12011-013-9611-1

PubMed Abstract | Crossref Full Text | Google Scholar

Whan, J. A., Dann, E. K., Aitken, E. A. (2016). Effects of silicon treatment and inoculation with Fusarium oxysporum f. sp. vasinfectum on cellular defences in root tissues of two cotton cultivars. Ann. Bot. 118, 219–226. doi: 10.1093/aob/mcw095

PubMed Abstract | Crossref Full Text | Google Scholar

Wiese, J., Wiese, H., Schwartz, J., Schubert, S. (2005). Osmotic stress and silicon act additively in enhancing pathogen resistance in barley against barley powdery mildew. J. Plant Nutr. Soil Sci. 168, 269–274. doi: 10.1002/jpln.200420490

Crossref Full Text | Google Scholar

Yang, L., Han, Y., Li, P., Li, F., Ali, S., Hou, M. (2017). Silicon amendment is involved in the induction of plant defense responses to a phloem feeder. Sci. Rep. 7, 4232. doi: 10.1038/s41598-017-04571-2

PubMed Abstract | Crossref Full Text | Google Scholar

Yang, L., Li, P., Li, F., Ali, S., Sun, X., Hou, M. (2018). Silicon amendment to rice plants contributes to reduced feeding in a phloem-sucking insect through modulation of callose deposition. Ecol. Evol. 8, 631–637. doi: 10.1002/ece3.3653

PubMed Abstract | Crossref Full Text | Google Scholar

Ye, M., Song, Y., Long, J., Wang, R., Baerson, S. R., Pan, Z., et al. (2013). Priming of jasmonate-mediated antiherbivore defense responses in rice by silicon. Proc. Natl. Acad. Sci. U.S.A. 110, E3631–E3639. doi: 10.1073/pnas.1305848110

PubMed Abstract | Crossref Full Text | Google Scholar

Zellner, W., Frantz, J., Leisner, S. (2011). Silicon delays Tobacco ringspot virus systemic symptoms in Nicotiana tabacum. J. Plant Physiol. 168, 1866–1869. doi: 10.1016/j.jplph.2011.04.002

PubMed Abstract | Crossref Full Text | Google Scholar

Zhan, L. P., Peng, D. L., Wang, X. L., Kong, L. A., Peng, H., Liu, S. M., et al. (2018). Priming effect of root-applied silicon on the enhancement of induced resistance to the root-knot nematode Meloidogyne graminicola in rice. BMC Plant Biol. 18, 50. doi: 10.1186/s12870-018-1266-9

PubMed Abstract | Crossref Full Text | Google Scholar

Zhang, Q., Fry, J., Lowe, K., Tisserat, N. (2006). Evaluation of calcium silicate for brown patch and dollar spot suppression on turfgrasses. Crop Sci. 46, 1635–1643. doi: 10.2135/cropsci2005.04-0002

Crossref Full Text | Google Scholar

Zhang, C., Wang, L., Zhang, W., Zhang, F. (2013). Do lignification and silicification of the cell wall precede silicon deposition in the silica cell of the rice (Oryza sativa L.) leaf epidermis? Plant Soil 372, 137–149. doi: 10.1007/s11104-013-1723-z

Crossref Full Text | Google Scholar

Keywords: pathogenic diseases, disease tolerance efficiency and management, crop productivity, plant nutrition, silicon

Citation: Verma KK, Song X-P, Liang Q, Huang H-R, Bhatt R, Xu L, Chen G-L and Li Y-R (2024) Unlocking the role of silicon against biotic stress in plants. Front. Plant Sci. 15:1430804. doi: 10.3389/fpls.2024.1430804

Received: 10 May 2024; Accepted: 25 November 2024;
Published: 12 December 2024.

Edited by:

Dilier Olivera Viciedo, Universidad de O’Higgins, Chile

Reviewed by:

Rodolfo Lizcano Toledo, Tolima University, Colombia
Jonas Pereira De Souza Júnior, University of Florida, United States

Copyright © 2024 Verma, Song, Liang, Huang, Bhatt, Xu, Chen and Li. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Xiu-Peng Song, eGl1cGVuZ3NvbmdAZ3hhYXMubmV0; Yang-Rui Li, bGl5ckBneGFhcy5uZXQ=

ORCID: Yang-Rui Li, orcid.org/0000-0002-7559-9244
Krishan K. Verma, orcid.org/0000-0002-5501-7905
Gan-Lin Chen, orcid.org/0000-0003-0076-5268

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.