key: cord-0852927-6q3hmo3r
authors: He, Baoye; Hamby, Rachael; Jin, Hailing
title: Plant extracellular vesicles: Trojan horses of cross‐kingdom warfare
date: 2021-06-27
journal: FASEB Bioadv
DOI: 10.1096/fba.2021-00040
sha: 30e72b77821f095b300daa5f7be29c0bd297fa5f
doc_id: 852927
cord_uid: 6q3hmo3r

Plants communicate with their interacting microorganisms through the exchange of functional molecules. This communication is critical for plant immunity, for pathogen virulence, and for establishing and maintaining symbioses. Extracellular vesicles (EVs) are lipid bilayer‐enclosed spheres that are released by both the host and the microbe into the extracellular environment. Emerging evidence has shown that EVs play a prominent role in plant–microbe interactions by safely transporting functional molecules, such as proteins and RNAs to interacting organisms. Recent studies revealed that plant EVs deliver fungal gene‐targeting small RNAs into fungal pathogens to suppress infection via cross‐kingdom RNA interference (RNAi). In this review, we focus on the recent advances in our understanding of plant EVs and their role in plant–microbe interactions.

biogenesis, the role of plant EVs in plant-microbe interactions, the mechanisms of EV sRNA loading, and the potential applications of these discoveries for preventing plant disease.

In mammalian systems, EVs are divided into multiple classes based on their distinct biogenesis pathways and specific protein markers, including exosomes, microvesicles, and apoptotic bodies. 7 Exosomes originate from multivesicular bodies (MVBs), which then fuse with the plasma membrane, to release their intraluminal vesicles (ILVs) into the extracellular space, forming exosomes. 3 Restricted by the size of ILVs, the diameter of exosomes ranges from 30 to 100 nm. 7 Microvesicles originate from the direct outward budding of the plasma membrane. The size of microvesicles ranges from 50 to 1000 nm but can be even larger in some cancer cells. 8 An additional class, apoptotic bodies, arise from blebbing of the apoptotic cell membrane and can be over 1 μm in diameter. 9 In plants, EVs were first observed in the 1960s in chemically fixed carrot cells using electron microscopy. In these initial observations, different sizes of EVs were detected. 10, 11 Now, EVs have been discovered in extracellular fluids of leaves, roots, fruits, and imbibing seeds. 6, [12] [13] [14] In recent years, an increasing number of studies have implied that, like animal cells, there exists a heterogeneous population of EVs in plants ( Figure 1A) .

In mammalian systems, tetraspanin proteins, such as CD9, CD63, CD37, CD81, or CD82, are enriched in the membranes of exosomes and often used as exosome biomarkers. 15 The model plant, Arabidopsis thaliana, has 17 TETRASPANIN (TET)-like genes. Despite their limited amino acid sequence similarity with animal tetraspanin proteins, they share conserved structural hallmarks, including four transmembrane domains (TM1-TM4), a small extracellular loop (ECL1), an intracellular loop (ICL), and a large extracellular loop (ECL2). 16 Two of the Arabidopsis TETs, TET8 and TET9, are specifically induced upon infection by fungal pathogen Botrytis cinerea. 6 Meanwhile, both co-localize with the Arabidopsis MVB-marker Rab5-like GTPase ARA6 inside the cell, and also co-localize in EVs which are enriched at fungal infection sites. 6 These TET8positive EVs were highly enriched in the fraction collected at ultracentrifugation speeds of 100,000 g from leaf apoplastic fluid. 6 In density gradient ultracentrifugation, TET8-positive EVs are enriched in the fractions at the density of 1.12-1.19 g/ml, which is consistent with the density of exosomes in animal systems. 17, 18 Meanwhile, the plant EV-enriched sRNAs and cargo proteins are also present in the same fraction as TET8. 18 These results suggest that TET8-positive EVs can be considered bona fide plant exosomes, and transport sRNAs.

Tetraspanins play a crucial role in EV formation and function in mammalian cells. 15 In plants, the tet8 single mutant or the tet8 tet9 double mutant plants displayed decreased secretion of EVs and sRNAs, and enhanced susceptibility to B. cinerea infection. 6, 18 Further investigation revealed that the amount of an EV-enriched lipid, glycosylinositolphosphoceramides (GIPCs), was dramatically decreased by over fourfold in tet8 total leaf extracts. 19 These results indicate that TET8 mediates the production of EVs in association with GIPCs.

PENETRATION 1(PEN1)-positive EVs represent another class of plant EVs. PEN1 is a plasma membrane-associated plant-specific syntaxin. 20 It was first identified by mutational analysis in Arabidopsis to screen mutants that were disabled in non-host penetration resistance against barley powdery mildew, Blumeria graminis f. sp. Hordei. 21 The secretion of PEN1 depends on an ADP ribosylation factor-GTP exchange factor (ARF-GEF), GNOM, which mediates recycling endosome trafficking rather than MVB pathway. 22 PEN1positive EVs are enriched at a lower ultracentrifugation speed (40,000 g) than TET8-EVs from Arabidopsis leaf apoplastic fluid. 14 Furthermore, PEN1 does not co-localize with MVB marker ARA6 in plant cells and the PEN1-positive EVs are enriched in the gradient fraction of 1.029-1.056 g/ml. 14 Additionally, when TET8-GFP and mCherry-PEN1 were coexpressed in Arabidopsis, distinct GFP-labeled and mCherrylabeled EVs were observed in isolated EVs. 18 These results indicate that TET8-and PEN1-positive EVs represent distinct classes of plant EVs, and likely possess different biogenesis pathways ( Figure 1A) .

EXPO, an exocyst-positive organelle is another source of plant EVs ( Figure 1A ). It is associated with Exo70E2, which is an homolog of the yeast and animal exocyst protein Exo70, in Arabidopsis and tobacco (Nicotiana tabacum) suspension cells. 23 EXPO does not co-localize with any known organelle markers, including markers of the Golgi apparatus, the trans-Golgi network/early endosome, or MVBs in plants. 23 Immunogold labeling of sections cut from high-pressure frozen samples of wild-type Arabidopsis cells and transgenic BY-2 cells expressing Exo70E2-GFP reveals that EXPOs are spherical double-membrane structures. After fusion with the plasma membrane, EXPO releases single-membrane-bound vesicles to the extracellular space. 23 Several arabinogalactan glycosyltransferases involved in arabinogalactan Oglycosylation have been found in the EXPO, indicating that GATLs could be co-secreted to the apoplast via the EXPO. 24 The mechanism of EXPO biogenesis, and whether the cargoes of EXPO are functional is still unclear.

EVs are also present in fruits, such as grapes and coconuts. 25, 26 Exosome-like nanoparticles have been isolated from grape juice using differential centrifugation and sucrose gradient methods. The size of grape EVs is between 50 and 300 nm in diameter, similar to the size of exosomes. They may function in the activation of intestinal stem cell proliferation 660 | HE Et al. and remodeling of intestinal stem cells in response to pathological triggers. 25 Additionally, exosome-like nanoparticles were observed and detected in coconut water by scanning electron microscopy (SEM), fluorescence microscopy, and dynamic light scattering (DLS), although their biological function is unclear. 26 Olive (Olea europaea) pollen grains release nanovesicles during in vitro pollen germination and pollen tube growth, named pollensomes. 27 Electron microscopy analysis has revealed that these pollensomes represent a heterogeneous population of round-shaped nanovesicles. Pollensomes size ranges from 28 to 60 nm in diameter with densities ranging from 1.24 to 1.29 g/ml in a sucrose gradient. Pollensomes may provide an alternative way of protein secretion during the processes of pollen germination and pollen tube growth, which are key steps for successful fertilization in plants. 27 

In order to elucidate the various functions and distinct subclasses of plant EVs, it is critical to develop efficient and effective EV isolation protocols for use in plant systems. Methods for plant EV isolation are based generally on established mammalian EV separation protocols. Differential ultracentrifugation is the most conventional EV isolation method. 28 In this method, large and medium vesicles and membrane structures are eliminated by successive centrifugations (2000 g and 10,000 g) at increasing speeds, which prevents the artificial creation of small vesicles from large ones by direct high-speed centrifugation. 7 Small vesicles are then sedimented by ultracentrifugation at 100,000 g. 7 However, this final ultracentrifugation step only allows for the enrichment of small-sized EVs and cannot distinguish between different subclasses of EVs or protein aggregates of similar size. A more specific method, density gradient ultracentrifugation, enables further separation of membrane-enclosed vesicles from aggregates of proteins, and the separation of similarly sized EVs with different densities. 29 In plants, two gradients, sucrose and iodixanol, have been used to further separate different EVs. 14, 18 Immunoaffinity isolation is the most precise method to isolate specific classes of EVs. It takes advantage of EV surface protein markers such as tetraspanin proteins, CD63, CD9, and CD81. [30] [31] [32] [33] In this method, EV samples isolated by ultracentrifugation are incubated with beads coated with antibodies for EV surface proteins. After washing the beads, only the antibody-specific binding EVs can be isolated. 30, 32 This method can further prevent cytoplasmic protein or RNA from contaminating isolated EVs. In plants, a native antibody that can specifically recognize the ECL2 domain of TET8 has been generated to specifically isolate TET8-positive EVs. 18 The EV-localized sRNA and protein cargos are clearly detectable in immunoaffinity purified TET8-positive EVs. 18 To remove the contaminating RNA and protein molecules that non-specifically attach to the EV surface or co-sediment with EVs, nuclease and protease treatments of EVs are widely performed. 29 Both sRNA and protein cargos contained within EVs are protected from nuclease and protease digestion, unless Triton X-100 is added to rupture the EVs, demonstrating that plant EVs can indeed protect nucleic acid and protein cargos for transportation. 6, 18 This work has established the initial framework for researching plant EVs.

As safe vehicles to deliver functional and regulatory components (such as nucleic acids, lipids, and proteins) to other cells or interacting organisms, EVs play prominent roles in communication between interacting organisms. In animal systems, several parasites have been shown to release EVs into host cells to manipulate host immune responses. 5, [34] [35] [36] Leishmania, the causative agent of tropical and sub-tropical infections termed the leishmaniases, can release exosomes into macrophages. 35 The incubation of macrophages with Leishmania exosomes selectively induced secretion of interleukin-8, which may facilitate the pathogen infection. 35 The gastrointestinal nematode, or helminth, Heligmosomoides polygyrus utilizes exosomes to deliver miRNAs into mouse host cells to suppress inflammation and innate immune responses during infection. 36 Emerging evidence also indicates that plant EVs are critical for communication with their interacting microbes. Specifically, EVs are important for antimicrobial defense. Infection with fungal pathogen B. cinerea or bacterial pathogen Pseudomonas syringae pv tomato DC3000 stimulates the secretion of plant EVs, which indicate the important role of EVs in plant-pathogen interactions. 6, 14 Recently, protein cargos involved in antimicrobial defense, including the glucosinolate transporters PEN3 and NRT1 as well as the myrosinase EPITHIOSPECIFIER MODIFIER1, 26 have been identified inside Arabidopsis EVs. 14 PEN3 is involved in immunity against powdery mildew fungus, Golovinomyces orontii and P. syringae pv tomato DC3000 bacteria, and the plant glucosinolate-myrosinase defensive system is activated only under tissue damage caused by pathogens, insects, or other herbivores. [37] [38] [39] This suggests that plant EVs may function as concentrated packets of antimicrobial molecules and compounds. The plant EV proteome was also enriched in various immunity-related membrane trafficking proteins, such as PEN1 (Syntaxin-121) , Syntaxin-122, and Syntaxin-132, | 661 HE Et al.

further supporting the conclusion that plant EVs are also involved in protein transport during immune signaling. 14 

Based on plant EV sRNA profiling analysis, a specific group of plant sRNAs were detected in EVs, 6 which suggests that a regulatory process for selective loading of sRNAs into EVs exists in plants. Using mass spectrometry (MS) analysis, He et al. identified a group of RNA-binding proteins (RBPs), including Argonaute protein 1 (AGO1), DEAD-box ATP-dependent RNA helicases 11 (RH11), RH37, RH52, Annexin1 (ANN1), and ANN2 in Arabidopsis EVs that isolated at 100,000 g. 18 These RBPs co-localize with TET8positive EVs, and could be detected by Western blot analysis in these TET8-positive exosomes even after trypsin digestion. 18 Among these RBPs, AGO1 and RNA helicase proteins can specifically bind EV-enriched sRNAs in both total RNA extracts and EV fraction. In immunocapture-purified TET8positive exosomes, only the AGO1-, RH11-, and RH37bound sRNAs, but not AGO2-or AGO4-bound sRNAs were detected, suggesting that AGO1 and RH11/37 contribute to selective sRNA loading into exosomes ( Figure 1B) . Annexins bind to sRNAs non-specifically and are not involved in the selective loading process. Moreover, the sRNA levels are reduced in EVs isolated from the ago1 mutant, and the double mutants of both rh11rh37 and ann1ann2, suggesting that all of these RBPs stabilize the sRNAs in EVs. Furthermore, rh11rh37 and ann1ann2 mutants are more susceptible to B. cinerea in comparison to wild-type plants. The expression of fungal virulence-related genes that are targeted by plant secreted sRNAs were de-repressed in B. cinerea that were collected from rh11rh37 and ann1ann2 mutants. 18 These results how that EV-associated RBPs contribute to plant immunity by selective loading and stabilization of sRNAs in plant EVs.

EVs are also involved in arbuscular mycorrhizal symbioses and have been observed in the interface of plants and symbiotic arbuscular mycorrhizal fungus. 13 During the formation and maturation of the arbuscular mycorrhiza, plant MVBs have been observed fusing with the host-derived periarbuscular membrane (PAM) in areas where plant and fungi interact. 13 Whether these EVs contain RNAs cargos, especially sRNAs, remains to be established.

Of the many emerging roles of EVs in plant systems, perhaps the most intriguing one is their critical role in cross-kingdom RNA interference (RNAi). Cross-kingdom RNAi is the transport of sRNAs between interacting organisms, which target and silence genes in the counter party. This communication mechanism was first discovered in the fungal pathogen, B. cinerea, which can deliver sRNAs into multiple plant hosts, including Arabidopsis and tomato. Once inside plant cells, these fungal sRNAs hijack the plant RNAi machinery protein, AGO1 to silence host immune response genes. 40 Soon after this initial discovery, cross-kingdom RNAi was demonstrated to be bidirectional, plants also send sRNAs into B. cinerea in order to target and silence key fungal virulencerelated genes. 6, 41, 42 Since the discovery and characterization of cross-kingdom RNAi, this phenomenon has been observed in a variety of interacting organisms. In addition to fungal pathogens, oomycete pathogen Hyaloperonospora arabidopsidis also transport sRNAs into their plant hosts and utilize host AGO1 to silence plant genes. 43 The parasitic plant, Cuscuta campestris, transports miRNAs into host plants to silence defense response genes. 44 Cross-kingdom RNAi can also function in symbiotic interactions. Plant bacterial symbiont, Rhizobium, although has no conventional RNAi machinery, can generate sRNA-like RNAs from transfer RNA (tRNA) degradation. These tRNA-derived sRNAs are delivered into soybean cells and are loaded into soybean AGO1 to silence soybean genes, which helps to establish the plant-bacteria symbiosis. 45 Outside of plant interaction systems, cross-kingdom RNAi has been observed in animal-pathogen or parasite interactions. For example, the gastrointestinal nematode H. polygyrus sends sRNAs into mammalian gut cells in order to target and silence immunity and inflammation-related genes. 36 The fungal pathogen of mosquito, Beauveria bassiana transfers a miRNA to the host cells and hijacks mosquito AGO1 to silence host immunity gene Toll receptor ligand Spätzle 4. 46 In most cases, the precise mechanisms underlying cross-kingdom RNAi transport remain unclear. However, discoveries in plant-fungal and mammal-parasite interactions both suggest the EVs are a major mechanism of interspecies RNA transport. 6, 36 In 2014, Amy Buck's research group discovered that H. polygyrus packages sRNAs into EVs, specifically exosomes, to deliver sRNAs into mouse intestinal epithelial cells. 36 Following this initial finding, a growing number of papers indicates that other parasites utilize the same strategy for sRNA delivery. 47, 48 In plant systems, Cai et al. discovered that the host plant Arabidopsis packages fungal gene-targeting sRNAs in TET8-positive EVs for delivery into the pathogen B. cinerea. 6 Specifically, Cai et al, found a specific set of plant sRNAs localized in the TET8-associated EVs. 6 To confirm the EV localization of these sRNAs, a series of verification including nuclease treatment of purified EVs, high-speed density gradient ultracentrifugation, and EV immunoaffinity isolation with TET8 antibody were performed. 18 This work clearly demonstrates that sRNAs are located within TET8-positive EVs. Furthermore, these TET8-positive EVs can be efficiently taken up by B. cinerea fungal cells. 6 After taken up by fungal cells, EV delivered sRNAs are released to suppress critical fungal target genes, including vacuolar protein sorting 51 (Vps51), a large subunit of the dynactin complex (DCTN1) and a suppressor of actin-like phosphoinositide phosphatase (SAC1), which coordinates vesicle trafficking and plays important roles in B. cinerea pathogenicity. 27 In PEN1-labeled EVs, a group of "tiny RNAs," which are 10-17 nucleotides in length and derived mainly from the positive strand of mRNA transcripts, have also been found. However, the biological function of these tiny RNAs is still unclear. 49 A similar phenomenon has been discovered between plants and oomycete pathogen Phytophthora capsici. 50 Under infection by P. capsici, Arabidopsis delivers secondary phasiRNAs from PPR gene clusters into the pathogen, likely using EVs, to silence target genes in the P. capsici. 50 Intriguingly, ingested plant EVs can shape the mammalian gut microbiome through cross-kingdom RNAi. Specifically, miRNAs encapsulated in ginger EVs can be taken up by gut microbiota after ingestion, where they target and silence microbe genes, influencing microbiome community composition. 51 However, bacteria do not have conventional RNAi machinery, it is still not clear how host sRNAs manipulate the expression of bacterial genes. Recent discovery of plant AGO1 protein being secreted together with the sRNAs in EVs led us to hypothesize that host AGO proteins may transport and function with associated host sRNAs in silencing bacterial genes. Taken together, these studies suggest that in plants, as well as animals, EVs are a major mechanism of sRNA transport.

The critical role of EVs in cross-kingdom RNAi can be leveraged into innovative plant protection strategies. In one strategy, host-induced gene silencing (HIGS), plants are genetically engineered to express pathogen/pest gene-targeting double-stranded RNAs, which are processed into sRNAs. Subsequently, these sRNAs are transported into the pest/ pathogen where they silence key virulence-related genes to suppress infection. 52, 53 This strategy has been successfully utilized to control both fungal pathogens and insect pests in plants. However, a key drawback with HIGS approaches is that they rely on the generation of transgenic plants, which is still technically challenging in many crop species. Additionally, the cost of overcoming regulatory hurdles necessary for bringing a GMO product to the market further limits the feasibility of the HIGS approach.

An alternative to HIGS, spray-induced gene silencing (SIGS), requires the direct application of pathogen genetargeting RNAs onto plant material, circumventing the need for genetic engineering. Recent discovery of fungal RNA uptake makes SIGS possible to control fungal diseases in crops. 41, 54, 55 SIGS approaches have been successfully used to prevent fungal infections in both monocot and dicot plants, as well as in postharvest materials. 41, 54, 56 Because RNA is already present in most food, these RNAs are likely safe for human consumption. Furthermore, SIGS is an eco-friendly alternative to traditional fungicides, as RNAs degrade within 2 days of soil application. 57 Unfortunately, this rapid degradation is a major hurdle that must be overcome before widespread SIGS applications. One strategy for enhancing RNA stability is to package them within nanoparticles, such as clay nanosheets, which can stabilize RNAs on plant tissue for up to 30 days. 58 In clinical contexts, lipid nanoparticles, which complex with RNAs to form liposomes, can package and stabilize therapeutic RNA treatments in the bloodstream. 59 The recently developed mRNA vaccine of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the virus that causes COVID-19, is also encapsulated in lipid nanoparticles to facilitate the delivery into human cells. 60, 61 This strategy may work particularly well in plant-fungal systems, as the liposome encapsulated RNAs mimics the natural delivery system of plant sRNAs in EVs to fungal pathogens.

Though decades of research have been performed on EVs in animal systems, plant researchers are just beginning to scratch the surface of the multitude of complex roles EVs have in plant systems. Though first observed in the 1960s, plant EVs have garnered little research attention until recently. Indeed, reports of EVs in organisms with thick cell walls have previously been largely overlooked because a mechanism for EVs to cross cell walls was unknown. Recent studies in fungi however, clearly indicate that cell walls are viscoelastic and dynamic in nature, and can stretch and accommodate the passage of large molecules, including EVs. 62 Current methods for EV isolation in plants have largely been adapted from existing EV isolation protocols developed in animals. Using these isolation methods, it has been discovered, that, similar to animals, plants possess a variety of EV subclasses derived from different biogenesis pathways. These EVs are critical for the transport of proteins and small RNAs from plants to their microbe partners and pathogens. Further research into the contents of EVs and their roles in specific plant-pathogen communication mechanisms, such as cross-kingdom RNAi, will play a crucial role in the development of novel plant protection techniques. Beyond the obvious agricultural applications of plant EV research, | 663 HE Et al.

increasing evidence indicates that plant EVs can be used in medical applications. As it has already been demonstrated, dietary EVs can impact microbiome composition. 51 This suggests that it may be possible to package therapeutic sRNAs or medications in plant EVs for transport to target cells in animal systems.

The field of plant EVs is still in its infancy. Early advances have indicated the crucial role of EVs in plantmicrobe interactions, especially in cross-kingdom RNAi. We expect new breakthroughs as this field of research matures. Beyond the basic goal of better understanding both plant physiology and plant-microbe interactions, delving deeper into the world of plant EVs can provide novel solutions to problems in both the agricultural and medical sectors, through innovative crop protection strategies and therapeutic delivery systems.

Small RNAs -big players in plant-microbe interactions

Small RNAs and extracellular vesicles: new mechanisms of cross-species communication and innovative tools for disease control

Shedding light on the cell biology of extracellular vesicles

Extracellular vesicles: unique intercellular delivery vehicles

Exosomes and other extracellular vesicles: the new communicators in parasite infections

Plants send small RNAs in extracellular vesicles to fungal pathogen to silence virulence genes

Biogenesis, secretion, and intercellular interactions of exosomes and other extracellular vesicles

Biology and biogenesis of shed microvesicles

Extracellular vesicles: biology and emerging therapeutic opportunities

Ultrastructural changes during growth and embryogenesis in carrot cell cultures

Occurrence of lomasomes in mesophyll cells of 'Khapli'wheat

Phospholipids are present in extracellular fluids of imbibing sunflower seeds and are modulated by hormonal treatments

Arbuscular cell invasion coincides with extracellular vesicles and membrane tubules

Extracellular vesicles isolated from the leaf apoplast carry stress-response proteins

Tetraspanins in extracellular vesicle formation and function

Arabidopsis tetraspanins are confined to discrete expression domains and cell types in reproductive tissues and form homo-and heterodimers when expressed in yeast

Exosome-mediated transfer of mRNAs and microRNAs is a novel mechanism of genetic exchange between cells

RNA-binding proteins contribute to small RNA loading in plant extracellular vesicles

Lipidomic analysis reveals the importance of GIPCs in Arabidopsis leaf extracellular vesicles

Co-option of a default secretory pathway for plant immune responses

SNAREprotein-mediated disease resistance at the plant cell wall

Arabidopsis ARF-GTP exchange factor, GNOM, mediates transport required for innate immunity and focal accumulation of syntaxin PEN1

EXPO, an exocyst-positive organelle distinct from multivesicular endosomes and autophagosomes, mediates cytosol to cell wall exocytosis in Arabidopsis and tobacco cells

Arabinogalactan glycosyltransferases target to a unique subcellular compartment that may function in unconventional secretion in plants

Grape exosome-like nanoparticles induce intestinal stem cells and protect mice from DSS-induced colitis

Isolation of exosome-like nanoparticles and analysis of microRNAs derived from coconut water based on small RNA high-throughput sequencing

Nanovesicles are secreted during pollen germination and pollen tube growth: a possible role in fertilization

A safe ride in extracellular vesicles -small RNA trafficking between plant hosts and pathogens

Minimal information for studies of extracellular vesicles 2018 (MISEV2018): a position statement of the International Society for Extracellular Vesicles and update of the MISEV2014 guidelines

Proteomic comparison defines novel markers to characterize heterogeneous populations of extracellular vesicle subtypes

Rapid isolation and enrichment of extracellular vesicle preparations using anion exchange chromatography

Highly-purified exosomes and shed microvesicles isolated from the human colon cancer cell line LIM1863 by sequential centrifugal ultrafiltration are biochemically and functionally distinct

Reassessment of exosome composition

An exosomebased secretion pathway is responsible for protein export from Leishmania and communication with macrophages

Leishmania exosomes deliver preemptive strikes to create an environment permissive for early infection

Exosomes secreted by nematode parasites transfer small RNAs to mammalian cells and modulate innate immunity

Induction and suppression of PEN3 focal accumulation during Pseudomonas syringae pv. tomato DC3000 infection of Arabidopsis

Extracellular transport and integration of plant secretory proteins into pathogen-induced cell wall compartments

Biology and biochemistry of glucosinolates

Fungal small RNAs suppress plant immunity by hijacking host RNA interference pathways

Bidirectional cross-kingdom RNAi and fungal uptake of external RNAs confer plant protection

Novel tomato miRNA miR1001 initiates cross-species regulation to suppress the conidiospore germination and infection virulence of Botrytis cinerea in vitro

Oomycete small RNAs bind to the plant RNA-induced silencing complex for virulence. eLife

MicroRNAs from the parasitic plant Cuscuta campestris target host messenger RNAs

Rhizobial tRNA-derived small RNAs are signal molecules regulating plant nodulation

A fungal pathogen deploys a small silencing RNA that attenuates mosquito immunity and facilitates infection

Extracellular vesicle RNA: a universal mediator of microbial communication?

Extracellular vesicles from Heligmosomoides bakeri and Trichuris muris contain distinct mi-croRNA families and small RNAs that could underpin different functions in the host

Plant extracellular vesicles contain diverse small RNA species and are enriched in 10-to 17-nucleotide "tiny

A Phytophthora effector suppresses trans-kingdom RNAi to promote disease susceptibility

Plant-derived exosomal microRNAs shape the gut microbiota

HIGS: host-induced gene silencing in the obligate biotrophic fungal pathogen Blumeria graminis

Host-induced gene silencing: a tool for understanding fungal host interaction and for developing novel disease control strategies

An RNAi-based control of Fusarium graminearum infections through spraying of long dsRNAs involves a plant passage and is controlled by the fungal silencing machinery

Spray-induced gene silencing for disease control is dependent on the efficiency of pathogen RNA uptake

Identification and application of exogenous dsRNA confers plant protection against Sclerotinia sclerotiorum and Botrytis cinerea

Environmental fate of double-stranded RNA in agricultural soils

Clay nanosheets for topical delivery of RNAi for sustained protection against plant viruses

siRNA delivery strategies: a comprehensive review of recent developments

The COVID-19 vaccine development landscape

Safety and efficacy of the BNT162b2 mRNA Covid-19 vaccine

How to cite this article: He B, Hamby R, Jin H. Plant extracellular vesicles: Trojan horses of cross-kingdom warfare

The work in the Jin lab was supported by grants from National Institutes of Health (R01 GM093008 and R35 GM136379-01), National Science Foundation (IOS-1557812