Spread Of Plant Viruses Research Articles

Comprehensive Metatranscriptomic Analysis of Plant Viruses in Imported Frozen Cherries and Blueberries.

The possibility of new viruses emerging in various regions worldwide has increased due to a combination of factors, including climate change and the expansion of international trading. Plant viruses spread through various transmission routes, encompassing well-known avenues such as pollen, seeds, and insects. However, research on potential transmission routes beyond these known mechanisms has remained limited. To address this gap, this study employed metatranscriptomic analysis to ascertain the presence of plant viruses in imported frozen fruits, specifically cherries and blueberries. This analysis aimed to identify pathways through which plant viruses may be introduced into countries. Virome analysis revealed the presence of six species of plant viruses in frozen cherries and blueberries: cherry virus A (CVA), prunus necrotic ringspot virus (PNRSV), prune dwarf virus (PDV), prunus virus F (PrVF), blueberry shock virus (BlShV), and blueberry latent virus (BlLV). Identifying these potential transmission routes is crucial for effectively managing and preventing the spread of plant viruses and crop protection. This study highlights the importance of robust quality control measures and monitoring systems for frozen fruits, emphasizing the need for proactive measures to mitigate the risk associated with the potential spread of plant viruses.

Reduction in vertical transmission rate of bean common mosaic virus in bee-pollinated common bean plants

Vertical transmission, the transfer of pathogens across generations, is a critical mechanism for the persistence of plant viruses. The transmission mechanisms are diverse, involving direct invasion through the suspensor and virus entry into developing gametes before achieving symplastic isolation. Despite the progress in understanding vertical virus transmission, the environmental factors influencing this process remain largely unexplored. We investigated the complex interplay between vertical transmission of plant viruses and pollination dynamics, focusing on common bean (Phaseolus vulgaris). The intricate relationship between plants and pollinators, especially bees, is essential for global ecosystems and crop productivity. We explored the impact of virus infection on seed transmission rates, with a particular emphasis on bean common mosaic virus (BCMV), bean common mosaic necrosis virus (BCMNV), and cucumber mosaic virus (CMV). Under controlled growth conditions, BCMNV exhibited the highest seed transmission rate, followed by BCMV and CMV. Notably, in the field, bee-pollinated BCMV-infected plants showed a reduced transmission rate compared to self-pollinated plants. This highlights the influence of pollinators on virus transmission dynamics. The findings demonstrate the virus-specific nature of seed transmission and underscore the importance of considering environmental factors, such as pollination, in understanding and managing plant virus spread.

Activation of peroxymonosulfate by sustainable biomass-based carbon nanotubes for controlling the spread of plant viruses in water environments

With the increasing demand for water in hydroponic systems and agricultural irrigation, viral diseases have seriously affected the yield and quality of crops. By removing plant viruses in water environments, virus transmission can be prevented and agricultural production and ecosystems can be protected. But so far, there have been few reports on the removal of plant viruses in water environments. Herein, in this study, easily recyclable biomass-based carbon nanotubes catalysts were synthesized with varying metal activities to activate peroxymonosulfate (PMS). Among them, the magnetic 0.125Fe@NCNTs-1/PMS system showed the best overall removal performance against pepper mild mottle virus, with a 5.9 log10 removal within 1 min. Notably, the key reactive species in the 0.125Fe@NCNTs-1/PMS system is 1O2, which can maintain good removal effect in real water matrices (river water and tap water). Through RNA fragment analyses and label free analysis, it was found that this system could effectively cleave virus particles, destroy viral proteins and expose their genome. The capsid protein of pepper mild mottle virus was effectively decomposed where serine may be the main attacking sites by 1O2. Long viral RNA fragments (3349 and 1642 nt) were cut into smaller fragments (∼160 nt) and caused their degradation. In summary, this study contributes to controlling the spread of plant viruses in real water environment, which will potentially help protect agricultural production and food safety, and improve the health and sustainability of ecosystems.

Backward bifurcation of a plant virus dynamics model with nonlinear continuous and impulsive control.

Roguing and elimination of vectors are the most commonly seen biological control strategies regarding the spread of plant viruses. It is practically significant to establish the mathematical models of plant virus transmission and regard the effect of removing infected plants as well as eliminating vector strategies on plant virus eradication. We proposed the mathematical models of plant virus transmission with nonlinear continuous and pulse removal of infected plants and vectors. In terms of the nonlinear continuous control strategy, the threshold values of the existence and stability of multiple equilibria have been provided. Moreover, the conditions for the occurrence of backward bifurcation were also provided. Regarding the nonlinear impulsive control strategy, the stability of the disease-free periodic solution and the threshold of the persistence of the disease were given. With the application of the fixed point theory, the conditions for the existence of forward and backward bifurcations of the model were presented. Our results demonstrated that there was a backward bifurcation phenomenon in continuous systems, and there was also a backward bifurcation phenomenon in impulsive control systems. Moreover, we found that removing healthy plants increased the threshold $ R_{1}. $ Finally, numerical simulation was employed to verify our conclusions.

Epidemiology and Management of Plant Viruses Under a Changing Climate.

Plant viruses are an ever-present threat to agricultural production and provide a wide array of symptoms resulting in economic losses throughout the world. Diseases can be transmitted by insect vectors, as well as through pollen, seed, and other means. With the increased globalization of agriculture, the introduction of new viruses from exotic locations and their establishment in new production regions and even new crops is a growing concern. Advancing knowledge of the epidemiology of plant viruses including development of new diagnostic methods, virus surveillance, and modeling, virus ecology and evolution, virus interactions with insect vectors, and other factors are important toward reducing the spread of plant viruses and managing virus diseases.

A viral movement protein co-opts endoplasmic reticulum luminal-binding protein and calreticulin to promote intracellular movement.

Intracellular movement is an important step for the initial spread of virus in plants during infection. This process requires virus-encoded movement proteins (MPs) and their interaction with host factors. Despite the large number of known host factors involved in the movement of different viruses, little is known about host proteins that interact with one of the MPs encoded by potexviruses, the triple-gene-block protein 3 (TGBp3). The main obstacle lies in the relatively low expression level of potexviral TGBp3 in hosts and the weak or transient nature of interactions. Here, we used TurboID-based proximity labeling to identify the network of proteins directly or indirectly interacting with the TGBp3 of a potexvirus, Bamboo mosaic virus (BaMV). Endoplasmic reticulum (ER) luminal-binding protein 4 and calreticulin 3 of Nicotiana benthamiana (NbBiP4 and NbCRT3, respectively) associated with the functional TGBp3-containing BaMV movement complexes, but not the movement-defective mutant, TGBp3M. Fluorescent microscopy revealed that TGBp3 colocalizes with NbBiP4 or NbCRT3 and the complexes move together along ER networks to cell periphery in N. benthamiana. Loss- and gain-of-function experiments revealed that NbBiP4 or NbCRT3 is required for the efficient spread and accumulation of BaMV in infected leaves. In addition, overexpression of NbBiP4 or NbCRT3 enhanced the targeting of BaMV TGBp1 to plasmodesmata (PD), indicating that NbBiP4 and NbCRT3 interact with TGBp3 to promote the intracellular transport of virion cargo to PD that facilitates virus cell-to-cell movement. Our findings revealed additional roles for NbBiP4 and NbCRT3 in BaMV intracellular movement through ER networks or ER-derived vesicles to PD, which enhances the spread of BaMV in N. benthamiana.

Plant-virus-abiotic stress interactions: A complex interplay

Under field conditions, plants are subjected to a wide array of biotic and abiotic stresses. These are detrimental to the survival of plants and adversely affects global crop productivity. Changing climate has led to elevated temperatures and unpredicted whether patterns across the world leading to suboptimal crop performance. This is coupled by the emergence of novel pathogen strains which are resistant to anti-pathogenic agents. The situation is even worse in case of viruses where antiviral agents for controlling viral diseases in plants is lacking. The explosion of international trade has helped in the sharing of surplus resources from one location to the other and benefitted the economy of most countries however, this has also resulted in the spread of viruses and other pathogens. Recent years have seen a paradigm shift in the research methodology with combined stress gaining major attention instead of solitary stress. Viruses influence a plant’s response to various abiotic stresses, similarly, abiotic stress imposition has a great effect on viral disease progression. The recent developments associated with plant-virus-abiotic stress interactions along with the way forward to tackle such stresses has been discussed in the present review. • The interaction between plant, virus and abiotic stresses is less understood. • Viruses tend to show enhanced virulence during higher temperatures. • Plants infected with certain viruses are more tolerant to drought and cold stress. • The global spread of plant viruses along with the rapid climate change demands robust research in this area.

Impact of Temperature and Rainfall Change on Epidemics Caused by Plant Viruses: A Review

Plant virus diseases are one of the limiting factors to crop productivity by diminishing the quantity, quality and responsible for significant economic losses worldwide. The Epidemic of plant virus diseases is the result of interactions between virus, host plant, vector, and environmental factors. Changes in host plants and insect vector dynamics that result from temperature and rainfall change could have an influence on the spread of plant viruses. The rising of temperature and heat stress increase the susceptibility of host plants to virus infection and accelerates the fitness of viruses to cause disease. The increasing temperature also changes insect vector population dynamics by accelerating insect phenology, causing earlier and prolonged colonization because it makes appropriate environmental conditions for the insect vectors. Insect populations of most virus vectors build up more rapidly in areas with high temperatures and high relative humidity and decline at low temperature. In addition, the rising temperatures can increase the efficiency of virus transmission from infected to healthy plants by insect vectors. An increasing frequency of heavy rainfall events is likely to slow the virus prevalence and incidence by washing insect vectors, thus reducing vector density. Flooding within annual crop growing period enhances the subsequent growth of weed and volunteer crop plant which act as reservoirs of insect vectors and the viruses, and its occurrence outside growing seasons increases subsequent growth of such reservoirs. Keywords : Host plant; Vectors; Virus epidemics DOI: 10.7176/JEES/12-1-01 Publication date: January 31 st 2022

Development of a new Collateral Cleavage-independent CRISPR/Cas12a based easy detection system for plant viruses

Plant virus spread through various means, from mechanically to the insect vectors and act as obligate parasite, therefore, are extremely challenging to eradicate. Geminiviruses are an important class of viruses which have reported extensively in last two decades on several new hosts. They infect wide range of annual crops and perineal shrubs, therefore, essentially required to detect them on field and dispose to check their vector transmission to healthy crops. In this study, we have chosen two important begomovirus viz. Mungbean yellow mosaic India virus which infect wide range of leguminous crops while Ageratum enation virus is reported to infect a wide range of crops from weed to opium poppy. Here, we have utilized the binding and cleaving ability of LbaCas12a protein with target to detect the virus infection on field. We proposed here a new Collateral Cleavage Independent CRISPR/Cas12a based detection system (CCI-CRISPR) for plant viruses.

Impact of Temperature and Rainfall Change on Epidemics caused by Plant viruses

Plant virus diseases are one of the limiting factors to crop productivity by diminishing the quantity, quality and responsible for significant economic losses worldwide. The Epidemic of plant virus diseases is the result of interactions between virus, host plant, vector, and environmental factors. Changes in host plants and insect vector dynamics that result from temperature and rainfall change could have an influence on the spread of plant viruses. The rising of temperature and heat stress increase the susceptibility of host plants to virus infection and accelerates the fitness of viruses to cause disease. The increasing temperature also changes insect vector population dynamics by accelerating insect phenology, causing earlier and prolonged colonization because it makes appropriate environmental conditions for the insect vectors. Insect populations of most virus vectors build up more rapidly in areas with high temperatures and high relative humidity and decline at low temperature. In addition, the rising temperatures can increase the efficiency of virus transmission from infected to healthy plants by insect vectors. An increasing frequency of heavy rainfall events is likely to slow the virus prevalence and incidence by washing insect vectors, thus reducing vector density. Flooding within annual crop growing period enhances the subsequent growth of weed and volunteer crop plant which act as reservoirs of insect vectors and the viruses, and its occurrence outside growing seasons increases subsequent growth of such reservoirs. Keywords: Host plant; Vectors; Virus epidemics DOI: 10.7176/JNSR/12-3-05 Publication date: February 28 th 2021

Impact of Abiotic Stresses on Plant Virus Transmission by Aphids.

Plants regularly encounter abiotic constraints, and plant response to stress has been a focus of research for decades. Given increasing global temperatures and elevated atmospheric CO2 levels and the occurrence of water stress episodes driven by climate change, plant biochemistry, in particular, plant defence responses, may be altered significantly. Environmental factors also have a wider impact, shaping viral transmission processes that rely on a complex set of interactions between, at least, the pathogen, the vector, and the host plant. This review considers how abiotic stresses influence the transmission and spread of plant viruses by aphid vectors, mainly through changes in host physiology status, and summarizes the latest findings in this research field. The direct effects of climate change and severe weather events that impact the feeding behaviour of insect vectors as well as the major traits (e.g., within-host accumulation, disease severity and transmission) of viral plant pathogens are discussed. Finally, the intrinsic capacity of viruses to react to environmental cues in planta and how this may influence viral transmission efficiency is summarized. The clear interaction between biotic (virus) and abiotic stresses is a risk that must be accounted for when modelling virus epidemiology under scenarios of climate change.

Comparing the plant virus spread patterns of non-persistently transmitted virus and persistently transmitted virus using an individual-based model

Abstract To compare the spread patterns between two types of plant viruses, non-persistent virus (NPV) and persistent virus (PV), we developed a spatially-explicit individual-based model. Our probability-based model is driven by the actions of insect vectors that are affected by interactions with host plants and plant viruses, considering both biological and behavioral components of their relationship. As a model system, we used potato virus y and potato leafroll virus, respectively for NPV and PV, potato for host plant, and Myzus persicae for the insect vector; empirical results from previous studies were acquired and adjusted to be used as our parameter values. Our simulation results showed that initial infection of PV in the field resulted in over 1.3 times greater number of insect vectors while causing approximately 7 times greater number of virus-infected plants compared to NPV by the end of simulation. Furthermore, spatial analysis showed that PV-infected plants showed greater aggregation in the field, forming larger patches compared to NPV-infected plants. Our results demonstrated the importance of host plant and insect vector manipulation by plant viruses as well as biological properties such as infectious period in the insect on the difference in overall spread pattern.

Comparing patterns and scales of plant virus phylogeography: Rice yellow mottle virus in Madagascar and in continental Africa.

Rice yellow mottle virus (RYMV) in Madagascar Island provides an opportunity to study the spread of a plant virus disease after a relatively recent introduction in a large and isolated country with a heterogeneous host landscape ecology. Here, we take advantage of field survey data on the occurrence of RYMV disease throughout Madagascar dating back to the 1970s, and of virus genetic data from ninety-four isolates collected since 1989 in most regions of the country to reconstruct the epidemic history. We find that the Malagasy isolates belong to a unique recombinant strain that most likely entered Madagascar through a long-distance introduction from the most eastern part of mainland Africa. We infer the spread of RYMV as a continuous process using a Bayesian statistical framework. In order to calibrate the time scale in calendar time units in this analysis, we pool the information about the RYMV evolutionary rate from several geographical partitions. Whereas the field surveys and the phylogeographic reconstructions both point to a rapid southward invasion across hundreds of kilometers throughout Madagascar within three to four decades, they differ on the inferred origin location and time of the epidemic. The phylogeographic reconstructions suggest a lineage displacement and unveil a re-invasion of the northern regions that may have remained unnoticed otherwise. Despite ecological differences that could affect the transmission potential of RYMV in Madagascar and in mainland Africa, we estimate similar invasion and dispersal rates. We could not identify environmental factors that have a relevant impact on the lineage dispersal velocity of RYMV in Madagascar. This study highlights the value and complementarity of (historical) nongenetic and (more contemporaneous) genetic surveillance data for reconstructing the history of spread of plant viruses.

DiRT-qPCR for molecular biological detection of RNA encoded viruses

For propagation of certified horticultural but also agricultural plant material, a phytosanitary virus screening is obligatory in order to avoid the spread of plant viruses regionally but also globally. To date, most high throughput standard virus screenings are still based on the immunological detection method ELISA because of its robustness, high throughput potential and very good cost-benefit ratio. However, in some cases molecular biological applications are compulsorily. For instance in the process of seed potato certification, low virus titres present in seed potatoes require a long virus enrichment phase for adequate virus detection by DAS-ELISA. This time consuming step can be avoided by a change to more sensitive molecular biological techniques. Most nucleic acid based detection protocols are accompanied by high costs for their performance. We introduce a TaqMan® qPCR based one step protocol, named direct reverse transcriptase quantitative PCR (DiRT-qPCR), for the detection of RNA encoded viruses without sophisticated nucleic acid purification at lower costs but with high throughput potential exemplarily on (+)ssRNA Potato leafroll virus (PLRV).

Localized surface plasmon resonance biosensing of tomato yellow leaf curl virus

Current techniques for plant virus detection, such as RT- PCR and ELISA, require multistep procedures and rely on sophisticated equipment. Due to the global spread of plant viruses, the development of simpler, faster and cheaper assay methods is inevitable. Gold nanoparticles (AuNPs) had raised much interest during recent years due to their novel optical properties or diagnostic purposes. The localized surface plasmon resonance (LSPR11LSPR: localized surface plasmon resonance.) of AuNPs had been used in the development of novel colorimetric nano-biosensing systems. The frequency and intensity of the LSPR peak generally depend on the shape, size and the surrounding medium of the AuNPs. In this study, unmodified AuNPs had been used to detect the unamplified Tomato yellow leaf curl virus (TYLCV) genome in infected plants. A specific DNA probe complementary to the coat protein region of virus genome was designed. The extracted total DNA of uninfected and infected plants was mixed with hybridization buffer and the designed probe. The mixture was denatured, annealed and then cooled to room temperature and was followed by AuNPs addition. The color changes in the samples indicating the presence of target virus infections were assessed visually after the addition of salt and confirmed by UV–Vis spectroscopy. The results showed that this strategy allowed for fast and sensitive detection of TYLCV genome and eliminated the need for PCR amplification and detection equipment.

Detecting potato viruses using direct reverse transcription quantitative PCR (DiRT-qPCR) without RNA purification: an alternative to DAS-ELISA

Virus screening is obligatory to avoid the spread of plant viruses regionally and globally. Double-antibody sandwich (DAS)-ELISA is the standard for screening potato viruses owing to its high-throughput potential, robustness, and cost–benefit ratio. However, low virus titers present in dormant potato tubers may not be reliably detected by using DAS-ELISA. Virus enrichment for reliable virus detection by DAS-ELISA assay is time-consuming and can be avoided by switching to more sensitive molecular biological techniques. Therefore, we developed a TaqMan® qPCR-based one-step protocol, termed direct reverse transcription quantitative PCR (DiRT-qPCR) for detection of RNA potato viruses PVY, PLRV and PVS without sophisticated nucleic acid purification and providing a high-throughput potential. Compared with DAS-ELISA, DiRT-qPCR showed up to a 100,000,000-fold higher sensitivity depending on the virus species. We also compared the qualitative results of standard DAS-ELISA used in seed potato certification, performed by sampling leaves of at least 4-weeks-old cultivated tuber eye cuttings, to the 1.5 h long DiRT-qPCR protocol on dormant tubers. The DiRT-qPCR protocol achieved an agreement with the DAS-ELISA procedure of 92.8%, 84.1% and 82.3% for the detection of PLRV, PVY, and PVS, respectively. The investigated different virus species show different multiplication behavior in secondary infected potato tuber eye cuttings, which is assumed to be a reason for the remaining qualitative differences in the outcome of the DiRT-qPCR and DAS-ELISA comparison. In our opinion, DiRT-qPCR protocol can be used as a reliable, work- and resource-saving alternative to DAS-ELISA in qualitative directed virus detection, particularly because no RNA purification is needed and dormant potato tubers can be directly used.

Phytopathogenic fungus hosts a plant virus: A naturally occurring cross-kingdom viral infection

The transmission of viral infections between plant and fungal hosts has been suspected to occur, based on phylogenetic and other findings, but has not been directly observed in nature. Here, we report the discovery of a natural infection of the phytopathogenic fungus Rhizoctonia solani by a plant virus, cucumber mosaic virus (CMV). The CMV-infected R. solani strain was obtained from a potato plant growing in Inner Mongolia Province of China, and CMV infection was stable when this fungal strain was cultured in the laboratory. CMV was horizontally transmitted through hyphal anastomosis but not vertically through basidiospores. By inoculation via protoplast transfection with virions, a reference isolate of CMV replicated in R. solani and another phytopathogenic fungus, suggesting that some fungi can serve as alternative hosts to CMV. Importantly, in fungal inoculation experiments under laboratory conditions, R. solani could acquire CMV from an infected plant, as well as transmit the virus to an uninfected plant. This study presents evidence of the transfer of a virus between plant and fungus, and it further expands our understanding of plant-fungus interactions and the spread of plant viruses.

Modeling the effects of cross-protection control in plant disease with seasonality

Cross-protection in plants has been widely used to control losses caused by virus diseases in the world. Here, a non-autonomous plant-virus disease model was developed including cross-protection. Global dynamics of the model was discussed. Under the quite weak assumptions, integral form conditions were resolved for permanence of the system and extinction of diseases. Furthermore, we looked into the sufficient conditions that plants could be protected against the detrimental effects of infection by an infection with the mild virus isolates. Last, we performed numerical simulations. Our investigations suggested that cross-protection played an important role in controlling the spread of the challenging virus in plants.

The role of plasmodesma-located proteins in tubule-guided virus transport is limited to the plasmodesmata.

Intercellular spread of plant viruses involves passage of the viral genome or virion through a plasmodesma (PD). Some viruses severely modify the PD structure, as they assemble a virion carrying tubule composed of the viral movement protein (MP) inside the PD channel. Successful modulation of the host plant to allow infection requires an intimate interaction between viral proteins and both structural and regulatory host proteins. To date, however, very few host proteins are known to promote virus spread. Plasmodesmata-located proteins (PDLPs) localised in the PD have been shown to contribute to tubule formation in cauliflower mosaic virus and grapevine fanleaf virus infections. In this study, we have investigated the role of PDLPs in intercellular transport of another tubule-forming virus, cowpea mosaic virus. The MP of this virus was found to interact with PDLPs in the PD, as was shown for other tubule-forming viruses. Expression of PDLPs and MPs in protoplasts in the absence of a PD revealed that these proteins do not co-localise at the site of tubule initiation. Furthermore, we show that tubule assembly in protoplasts does not require an interaction with PDLPs at the base of the tubule, as has been observed in planta. These results suggest that a physical interaction between MPs and PDLPs is not required for assembly of the movement tubule and that the beneficial role of PDLPs in virus movement is confined to the structural context of the PD.

Changes in life history parameters of Rhopalosiphum maidis (Homoptera: Aphididae) under four different elevated temperature and CO2 combinations.

Biological characteristics of corn leaf aphid, Rhopalosiphum maidis (Fitch), on barley, Hordeum vulgare L., were examined for two generations under four different elevated temperature and CO2 combinations. The developmental duration for each life stage was significantly reduced under the elevated temperature (+4 degrees C). The elevated CO2 (700-750 microl/liter) reduced only the development time of fourth-instar nymph. The overall duration of nymphal stage was reduced in the second generation. Thus, the temperature was the dominant factor to development duration of corn leaf aphid. The fecundity of corn leaf aphid was significantly increased under the elevated temperature and CO2, as well as in the later generation. Elevated temperature and CO2 increased the number of alate production, which may enhance the aphid migration or dispersal and the spread of plant viruses. Corn leaf aphid had the highest intrinsic rate of increase under the elevated temperature and CO2 combination in the second generation. These results indicate that the combined effects of both elevated temperature and CO2 on aphid biology may exacerbate aphid damage on barley under the climate change in accompany with elevated temperature and CO2 level.