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Verticillium wilt

Verticillium wilt is a destructive soilborne fungal primarily caused by Verticillium dahliae and Verticillium albo-atrum, which infect the vascular tissues of , obstructing water and nutrient transport and leading to characteristic , yellowing, and eventual death of affected branches or entire . The pathogens persist in soil for many years as resilient microsclerotia, entering through root wounds or natural openings, particularly under cool, moist conditions that favor infection. Symptoms typically appear in spring or fall and include sudden wilting of leaves that turn pale green, yellow, or brown, often affecting one side of the plant or scattered branches, with vascular discoloration—such as olive-green to brown streaks in the sapwood—visible upon sectioning stems. The disease impacts over 300 host species worldwide, including deciduous trees like and , shrubs such as lilac and redbud, ornamentals like and , and crops including , , and , though are generally resistant. Young or stressed plants are most susceptible and may succumb in a single season, while mature trees can survive for years with partial recovery under optimal conditions. Transmission occurs mainly through infested soil, contaminated tools, or infected plant debris, with no effective chemical controls available; management relies on cultural practices like proper irrigation, mulching, and pruning infected parts, alongside planting resistant varieties where possible. Accurate diagnosis often requires laboratory confirmation to distinguish it from similar vascular wilts, such as those caused by species.

Causative Agents

Verticillium dahliae

Verticillium dahliae Kleb. is an ascomycete fungus first described in 1913 from infected dahlia plants, named for its association with Dahlia species. It serves as the primary causative agent of Verticillium wilt globally, particularly in temperate and Mediterranean climates where it is widespread. This soilborne pathogen is distinguished from the related V. albo-atrum by its ability to form persistent resting structures. Morphologically, V. dahliae produces , single-celled conidia that are dispersed via water, wind, or plant debris, facilitating infection through root wounds or natural openings. A hallmark feature is the formation of melanized, multicellular microsclerotia, which are dark brown to black resting structures that enable long-term survival in without a host, persisting for up to 14 years. These microsclerotia germinate under favorable conditions to initiate new infection cycles, contributing to the pathogen's durability in agricultural fields. Genetically, V. dahliae is a haploid with a compact of approximately 34 Mb, encoding around 10,000–11,000 protein-coding genes across eight chromosomes. Key factors include effector genes such as Ave1, which promotes pathogenicity on susceptible hosts by contributing to full but is recognized by the tomato immune receptor Ve1, triggering effector-triggered immunity and in resistant plants. This gene-for-gene underscores the pathogen's strategies. The host range of V. dahliae is exceptionally broad, affecting over 200 plant species across diverse families, with particular economic significance in solanaceous crops such as (Solanum lycopersicum) and (Solanum tuberosum), where it causes severe vascular wilt. This wide adaptability, combined with its soil persistence, makes V. dahliae a challenging in global .

Verticillium albo-atrum

Verticillium albo-atrum, first identified as the causal agent of hop wilt in England in the late 1920s and early 1930s, is a soilborne fungal pathogen primarily associated with vascular wilt diseases in temperate regions. It has been reported as a significant issue in northern Europe and parts of North America, particularly in cooler climates where it thrives under lower temperatures compared to related species. Like other Verticillium species, it induces vascular wilt by colonizing plant xylem tissues, though its adaptation to colder conditions distinguishes its ecological niche. Morphologically, V. albo-atrum features dark, melanized resting that enables survival in and plant debris, but it lacks the persistent microsclerotia produced by V. dahliae. Its conidia are (pale or colorless) and single-celled, formed in whorls on verticillate conidiophores, contributing to its in diagnostic settings. Unlike the long-term dormancy of microsclerotia, V. albo-atrum persists in for shorter durations, typically 1-3 years or more under cool conditions (-5°C to 5°C), primarily through melanized hyphae associated with infected material, which limits its long-term soil viability without suitable hosts. Genetically, V. albo-atrum possesses a compact estimated at approximately 30-34 , which supports its specialized pathogenic lifestyle. It deploys secreted effectors to manipulate defenses during , similar to mechanisms observed in related species, though specific effectors like those targeting transcription factors have been more extensively characterized in V. dahliae. The host range of V. albo-atrum is narrower than that of V. dahliae, focusing on cool-season crops such as brassicas (e.g., oilseed rape) and strawberries, where it exhibits moderate aggressiveness adapted to temperate environments. It tends to be less persistent and widespread than V. dahliae due to its reliance on cooler temperatures and shorter survival, resulting in more localized outbreaks rather than broad epidemics.

Symptoms and Diagnosis

General Symptoms

Verticillium wilt manifests through a range of visible and internal symptoms that primarily affect the vascular system and foliage of infected plants, caused by soilborne fungi such as Verticillium dahliae and V. albo-atrum. These symptoms typically begin subtly and progress, often unilaterally, reflecting the fungus's targeted colonization of water-conducting tissues. Early detection relies on recognizing patterns like localized , which distinguishes it from uniform stress. Foliar symptoms are among the most characteristic and usually appear first on lower leaves, starting with or yellowing from the margins, followed by marginal scorching. This progresses upward through the canopy, leading to , browning, and premature defoliation, often confined to one side of the plant or individual branches—a phenomenon known as unilateral . In acute infections, leaves may curl, dry out, or exhibit abnormal reddening before dropping, while cases show slower development with persistent and scorch. Internally, vascular symptoms include brown streaking or discoloration in the tissue, visible upon slicing affected stems or petioles, indicating fungal blockage of water flow. This discoloration varies in intensity but is a hallmark of , extending from roots to branches without rotting the . At the whole-plant level, effects include stunting, branch dieback, and overall reduced vigor, with acute forms causing rapid decline and potential plant death, while chronic infections lead to gradual weakening over multiple seasons. Yield reductions occur due to impaired and , though exact impacts depend on infection timing. Symptom variation is influenced by host susceptibility, with resistant varieties showing milder expressions like limited yellowing or no visible decline, whereas young or stressed plants exhibit exacerbated and faster progression. Environmental factors can further modulate severity, but core symptoms remain consistent across infections.

Diagnostic Methods

Diagnosis of Verticillium wilt typically begins with field observations of characteristic symptoms, such as , , and vascular discoloration in affected plants, which serve as initial indicators but require confirmation to distinguish from other vascular pathogens. To visualize fungal presence in , cross-sections of stems or roots are examined for brown to dark streaking; this is particularly useful in woody hosts like maples, where discoloration appears as olive-green streaks in sapwood. Laboratory provides definitive identification through culturing. Symptomatic , such as 8-12 inch segments from branches at least 1 inch in diameter, is surface-sterilized and plated on selective media like sorbose agar supplemented with to suppress and favor . Incubation at 25°C for 7-14 days yields colonies with verticillate conidiophores bearing hyaline, single-celled conidia (3-7 μm long), and dark microsclerotia (typically 20-100 μm) in V. dahliae or melanized resting mycelia in V. albo-atrum, observable under . This approach, while reliable, can be time-consuming due to slow fungal growth and potential contamination. Molecular methods offer rapid, species-specific detection and quantification. Polymerase chain reaction (PCR) targeting the internal transcribed spacer (ITS) region uses primers such as Vd-F (5'-AGTGCTTGAAGGGGCTTTGT-3') and Vd-R (5'-GAGGTCTCTAGCGGATCATC-3') to amplify V. dahliae DNA from infected tissue or soil, distinguishing it from V. albo-atrum or V. longisporum via fragment size or sequencing. Quantitative PCR (qPCR) enhances sensitivity, quantifying pathogen biomass with ITS1/ITS2 primers for V. longisporum, correlating DNA levels with disease severity in hosts like potato. Enzyme-linked immunosorbent assay (ELISA) detects Verticillium antigens in plant extracts, providing a quicker alternative to culture, though less specific for species differentiation; it matches PCR results in about 60% of cases for oilseed rape infections. Recent advances include metagenomic sequencing to assess loads without prior . High-throughput ITS and 16S rRNA sequencing of microbiomes reveals abundance and shifts, as demonstrated in hop fields where V. dahliae enrichment correlated with wilt incidence post-2020. Emerging non-invasive techniques, such as combined with , enable early detection and severity classification in crops like as of 2025. These culture-independent techniques enable early detection of low-density infections and monitoring of disease-suppressive soils.

Hosts and Impact

Common Hosts

Verticillium wilt affects a broad spectrum of plants, with over 300 susceptible species reported across numerous plant families, including both herbaceous crops and woody ornamentals. Among agricultural crops, solanaceous plants such as (Solanum lycopersicum), (Solanum tuberosum), (Solanum melongena), and (Capsicum spp.) are particularly vulnerable, often experiencing severe vascular blockage leading to wilting. Cruciferous crops like (Brassica oleracea var. capitata) and (Brassica oleracea var. italica) also serve as common hosts, where the pathogen can persist in soil and infect through roots. Other significant crop hosts include (Fragaria × ananassa), (Humulus lupulus), and (Gossypium spp.), which face substantial production challenges in infested fields. Ornamental and tree hosts further highlight the disease's wide host range, with species such as (Acer spp.), (Ulmus spp.), and (Persea americana) frequently impacted in and orchards. , in particular, are among the most susceptible woody hosts, showing unilateral and branch dieback. These examples represent a fraction of the diversity, as the infects plants in a wide range of plant families, spanning annuals, perennials, and . Host specificity varies between the primary causative agents: Verticillium dahliae predominantly affects warm-season crops like and , thriving in temperatures around 25–30°C, while Verticillium albo-atrum targets cool-season hosts such as and certain brassicas, with optimal growth at 17–21°C. This temperature-dependent preference influences disease prevalence in different climates. Recent studies have identified emerging hosts in tropical regions, including (), where V. dahliae causes vascular wilt and has been documented in Central and South American plantations as of 2022. This expansion underscores the 's adaptability to new agricultural systems.

Economic and Ecological Impact

Verticillium wilt imposes substantial agricultural losses worldwide, with yield reductions ranging from 10-50% depending on crop susceptibility, conditions, and density. In tomato production, particularly in , yield losses of up to 25% have been reported in fields infested with virulent races of the , leading to diminished fruit quality and market value. Potato crops in experience 10-15% yield reductions in moderately affected fields and up to 30-50% in severely infested areas, impacting tuber size and overall harvestable yield. In , Verticillium wilt causes annual yield losses exceeding 30% in , with economic damages estimated at $210-280 million USD. In , hop production faces severe setbacks, with outbreaks causing widespread garden abandonment and replacement costs due to the lethal form of the disease. These losses are compounded by trade restrictions on contaminated planting materials and , which limit international movement of susceptible crops like strawberries and ornamentals to prevent spread. A notable historical outbreak occurred in California's strawberry industry during the 1990s, where Verticillium wilt contributed to yield declines of up to 50% in infested fields, necessitating extensive soil fumigation and contributing to millions of dollars in annual losses before resistant varieties were developed. Similar impacts have been observed in perennial systems like almond orchards, where early infections can reduce establishment success and long-term productivity by 20-30%. Ecologically, Verticillium wilt disrupts in perennial cropping systems by causing premature death, which alters structure and reduces understory in affected agroecosystems. Overreliance on fumigants like metam sodium for has led to degradation of , including reduced bacterial and disruption of microbial communities essential for nutrient cycling, exacerbating long-term ecosystem vulnerability. Recent estimates indicate that Verticillium wilt contributes to billions of dollars in global agricultural damages annually, with emerging threats amplified by ; rising temperatures are projected to increase disease susceptibility in crops like and by enhancing in warmer, moist soils. As of 2025, genomic studies have identified key genes like GhAMT2 in for resistance , potentially mitigating future losses.

Disease Cycle

Infection and Colonization

Verticillium wilt pathogens, primarily Verticillium dahliae and V. albo-atrum, initiate through the roots of host plants, where dormant microsclerotia or mycelia in the germinate in response to root exudates and sufficient moisture. The germinated hyphae penetrate the root epidermis, often via wounds, natural openings such as emergence sites, or through the formation of specialized structures like hyphopodia near the zone of root elongation. This entry is facilitated by fungal genes such as Vta1, Vta2, and VdSho1, which regulate adhesion and penetration processes. Once inside the root, the fungus colonizes the cortical tissues inter- and intracellularly, degrading cell walls with secreted enzymes like pectin lyases (VdPEL1) and serine proteases (VdSSP1) to facilitate spread. The hyphae then advance systemically into the vascular , where they grow longitudinally and laterally, producing mycelia that occupy vessel lumens. Colonization leads to vessel occlusion through a combination of fungal mycelial growth, host-produced tyloses (protrusions from cells), and gel-like deposits, which collectively impair water and nutrient transport. Additionally, the pathogens produce phytotoxins, such as host-specific wilt toxins including toxins and extracellular , that induce host and exacerbate vascular dysfunction. The disease progresses through distinct stages following infection. A latent period ensues, lasting several weeks during which the colonizes the asymptomatically, often 2–4 weeks in susceptible annual hosts like or before detectable spread to aerial tissues. Symptom onset then occurs as the reaches the upper and leaves, triggering and due to hydraulic failure. In hosts, the infection can persist chronically, with the remaining viable in for years without immediate lethality. Pathogen-host interactions during colonization involve sophisticated molecular mechanisms to evade or suppress plant immunity. V. dahliae secretes effector proteins, such as VdNEP and PevD1, that interfere with host signaling pathways to inhibit defense responses like production. Notably, the velvet protein Vel1 plays a critical role in suppressing plant defenses by enabling efficient root penetration and conidia formation for xylem distribution; mutants lacking Vel1 show drastically reduced and virulence, with approximately 50% of inoculated plants remaining symptom-free or showing only weak symptoms. This effector-mediated manipulation allows the fungus to establish systemic infection while minimizing early host recognition.

Survival and Dispersal

Verticillium dahliae primarily survives in through the formation of microsclerotia, which are compact clusters of melanized, thick-walled cells that can remain viable for 4 to 15 years under favorable conditions. These structures enable the pathogen to endure periods without a host, resisting and adverse environmental factors. In contrast, Verticillium albo-atrum relies on melanized hyphae or resting for survival, which have a shorter viability, typically lasting from a few months to several years in , depending on moisture and temperature. Dispersal of Verticillium wilt pathogens occurs mainly through contaminated particles moved by machinery, foot traffic, or runoff, as well as infected debris and tools used in . can facilitate long-distance spread by carrying microsclerotia or hyphal fragments from infested fields to new areas. conidia play a limited role in dispersal, as the pathogens are predominantly soilborne and do not rely on for primary . The disease cycle is completed through overwintering of survival structures in crop residues and , allowing reinfection of subsequent host via contact or . Microsclerotia or melanized hyphae persist in decaying material, germinating when conditions favor host proximity. Recent studies have explored the potential for microsclerotia via windblown , highlighting risks of inadvertent across fields or regions, though evidence for significant aerial remains limited.

Environmental Influences

Soil and Microclimate Factors

Verticillium wilt development is favored by neutral to alkaline levels ranging from 6 to 9, with optimal conditions often observed around 6.5 to 7.5, where the exhibits enhanced survival and microsclerotia . Low content in soils exacerbates disease severity by reducing microbial diversity and natural suppression mechanisms, allowing greater persistence of the . Compacted soils further promote susceptibility by restricting expansion and , creating microenvironments conducive to fungal . Microclimatic conditions significantly influence Verticillium wilt progression, with microsclerotia and activation optimally occurring at soil temperatures between 21 and 27°C, aligning with cool-season growth periods for many host plants. Optimal at supports hyphal growth and root infection, while excessive moisture from poor drainage heightens root susceptibility by prolonging wet conditions that stimulate pathogen activity. Soil microbial interactions play a key role in modulating Verticillium wilt, where antagonistic bacteria such as fluorescent pseudomonads (e.g., Pseudomonas fluorescens strains) reduce pathogen load through competition for nutrients, production of antifungal compounds, and induction of plant defenses. These rhizosphere colonizers can suppress microsclerotia viability and limit vascular colonization in hosts like olive and potato. Research from 2023–2024 highlights how soil warming under climate change scenarios can increase the proportion of Verticillium dahliae and enhance pathogen aggressiveness at temperatures within the 20–28°C range, potentially increasing disease incidence in warming agricultural regions.

Geographic Distribution

Verticillium wilt, caused primarily by the soilborne fungi Verticillium dahliae and V. albo-atrum, occurs worldwide but is most problematic in temperate zones with irrigated agriculture. Major hotspots include the United States, where it affects crops across the cotton belt from Virginia to California, as well as the Pacific Northwest; Europe, particularly in the United Kingdom, Germany, and the Mediterranean regions; and China, where it impacts extensive cotton and vegetable production areas. The disease has also emerged in subtropical regions, such as Australia's cotton-growing belts in New South Wales and Queensland, where incidence remains relatively low but poses growing risks to yields. The distribution of the two main Verticillium species reflects climatic preferences: V. dahliae dominates in warmer temperate and subtropical areas due to its higher temperature tolerance, infecting a broad range of hosts in regions like the southern U.S., , , and . In contrast, V. albo-atrum prevails in cooler northern latitudes, such as parts of , the northern U.S., the , and , where it primarily affects crops like potatoes and . These patterns influence regional disease management, with V. dahliae's microsclerotia enabling longer soil persistence in varied climates. The pathogen's spread to new areas often traces to early 20th-century introductions via in infected plant material and seeds; for instance, Verticillium wilt first appeared on Upland in , , in 1918, likely arriving through imported or equipment, and subsequently disseminated across the via contaminated and . Similar pathways introduced it to mint fields in the U.S. Midwest in the , from where it spread westward through plantings. measures have proven challenging due to the fungi's soilborne nature and asymptomatic carriage in seeds or tools, allowing inadvertent long-distance movement despite regulations. Recent trends, including 2023 assessments, point to geographic expansion driven by , which elevates temperatures and favors V. dahliae proliferation, alongside intensified that amplifies inoculum buildup in . These shifts have heightened disease pressure in previously marginal areas.

Management Approaches

Cultural and Preventive Measures

is a primary cultural strategy for managing Verticillium wilt by depleting inoculum levels of the over extended periods. Implementing rotations with non-host crops such as cereals, onions, , corn, sudangrass, , and grass hays (e.g., orchardgrass, fescue, or ) for 4 to 6 years can significantly reduce disease incidence, as these do not support reproduction and allow natural decline of microsclerotia. For solanaceous crops, rotating out for at least 4-5 years is recommended to break the disease cycle. In production, rotations with crops have been shown to lower Verticillium wilt incidence compared to continuous susceptible cropping. Sanitation practices are essential to limit the spread and survival of propagules, targeting and dispersal stages. Effective measures include controlling weeds and volunteer plants that may host the , removing and destroying infected plant debris after harvest to reduce microsclerotia in , and using certified disease-free seedlings or to prevent introduction. Cleaning equipment, tools, vehicles, and footwear between fields—using pressure washers, 10% solutions, or disposable covers—helps avoid mechanical transmission. Additionally, avoiding contaminated is critical, as microsclerotia can persist and spread through reused sources. Prompt removal of diseased plants further prevents local buildup of inoculum. Soil amendments offer non-chemical ways to suppress Verticillium populations by altering the soil environment and promoting antagonistic microbes. Incorporating green manures like sudangrass provides biofumigation effects through the release of compounds during , reducing wilt incidence in subsequent crops such as potatoes; field studies have demonstrated lower rates and higher yields after 2-3 years of sudangrass rotations compared to fallow or other amendments like barley or . Similarly, sorghum-sudangrass green manures suppress the comparably to fumigants in some systems. , achieved by covering moist soil with clear plastic for 4-6 weeks in summer, heats the top 6-18 inches to 90-140°F, killing microsclerotia and providing effective control in warm climates like California's Central Valley. Recent guidelines emphasize combining these cultural practices for high-value crops like , where Verticillium wilt poses significant risks. The 2022 Michigan Hop Management Guide recommends rotations with non-hosts, debris removal, and incorporation as foundational strategies to minimize disease pressure, integrated with to avoid infested fields. In the , similar approaches using cover crops like or sudangrass have reduced wilt effects in hop production areas.

Chemical and Biological Controls

Chemical fumigants, applied pre-planting, represent a primary chemical control strategy for Verticillium wilt, targeting soil-borne propagules of Verticillium dahliae and V. albo-atrum. , often used alone or in mixtures, effectively reduces fungal inoculum density and suppresses disease incidence in crops like strawberries and potatoes by disrupting pathogen survival structures. Metam sodium, applied at rates as low as 373 L/ha, similarly controls Verticillium wilt in potatoes by generating toxic gases that penetrate pores, though efficacy depends on soil temperature and injection depth. However, the phase-out of methyl bromide—a once widely used broad-spectrum fumigant effective against Verticillium in combination with —under the 2005 has limited options, prompting shifts to alternatives like these. Soil-applied or systemic s offer limited efficacy against established infections due to the 's vascular colonization, which restricts penetration. , a demethylation , significantly reduces wilt severity in smoke-tree through interference with in fungal membranes via root , though its protective effects are short-lived and less reliable in perennial crops. Application challenges include regulatory restrictions on fumigants, potential development of resistance in populations, and environmental concerns over non-target effects, necessitating integrated use with cultural practices for sustainable suppression. Biological controls leverage antagonistic microorganisms to suppress Verticillium propagule germination and growth, providing alternatives. species, such as T. harzianum, inhibit Verticillium mycelial growth via mycoparasitism and antibiotic production, reducing wilt incidence in and by 40-60% in field trials. Bacillus subtilis strains, including NCD-2 and HJ5, colonize roots and induce systemic resistance through volatile compounds and competition, effectively lowering disease severity in by enhancing plant defense . Mycoviruses, such as VdOMV2, infect Verticillium isolates to induce hypovirulence, reducing fungal virulence and wilt symptoms in by up to 50% when transmitted via co-culture. Endophytic further contribute to biological management by promoting induced systemic resistance in hosts. In 2021 studies on , Pseudomonas-derived FLiC from endophytic triggered defense responses, decreasing Verticillium wilt disease index by 30-50% across varieties through activation of pathways. Recent advances in 2024 involve nanoparticle-based delivery systems to enhance biocontrol agent efficacy. nanoparticles (ZnO-NPs) applied to roots upregulate immune-related genes and enzymes, conferring resistance to Verticillium wilt by inhibiting growth and reducing the disease index by approximately 36%, while improving targeted delivery of antagonistic microbes. As of 2025, amending with spent substrate has been shown to suppress Verticillium wilt in by enriching beneficial species in the .

Plant Resistance

Susceptible Plants

Verticillium wilt affects a broad range of , with susceptibility varying by species and family, particularly impacting vascular tissues and leading to in affected hosts. Among vegetable crops, those in the family are especially vulnerable, including (Solanum lycopersicum), (Solanum tuberosum), and (Solanum melongena), where the disease can cause severe yield losses through and colonization. These often show symptoms such as unilateral and yellowing leaves, reflecting the pathogen's disruption of . In fruit and field crops, (Fragaria × ananassa) in the family is highly susceptible, with infections leading to and reduced fruit production in infested soils. (Gossypium spp.) experiences significant defoliation and plant decline, while (Mentha piperita) suffers from reduced oil yields and stand density in affected fields. Trees and ornamentals face particular risks, with maple species (Acer spp.) being among the most commonly and severely impacted, often resulting in branch dieback and tree mortality over multiple seasons. Smoke tree (Cotinus coggygria) is highly vulnerable, with infections proving fatal especially in young trees due to extensive vascular blockage. Avocado (Persea americana) also shows susceptibility, with root infections leading to decline in orchards on contaminated sites. The Solanaceae family encompasses numerous susceptible hosts beyond the primary vegetables, such as peppers and okra, where the fungus persists in soil and amplifies disease cycles. In the Rosaceae, while not all members are equally affected, strawberry stands out for its high vulnerability, necessitating careful site selection for cultivation. Overall, over 300 plant species across these categories are known hosts, with severity often heightened in stressed or young plants.

Resistant and Immune Plants

Certain plant species exhibit resistance or immunity to Verticillium wilt, a soilborne fungal caused by Verticillium dahliae and V. albo-atrum, allowing them to grow in infested soils with minimal or no symptoms. Resistance is often genetic and can be constitutive or induced, enabling plants to limit fungal colonization and toxin effects, while immunity implies complete lack of susceptibility, as seen in many gymnosperms. Planting resistant or immune species is a primary strategy for managing the in landscapes and , reducing reliance on chemical controls. Among woody plants, numerous deciduous trees and shrubs demonstrate resistance, tolerating the pathogen without significant vascular discoloration or wilting. Examples include apple, aspen, , , , , crabapple, dogwood, , ginkgo, hackberry, , , , honeylocust, katsura tree, mountain-ash, , , , sweetgum, sycamore, , and . Native trees and shrubs in regions like the southwestern U.S. are generally unaffected, further supporting their use in infested areas. , including pines, spruces, , and other gymnosperms such as ginkgo and cycads, are immune, showing no infection even upon exposure. In herbaceous ornamentals and , resistance varies by crop, with programs developing tolerant varieties that maintain yield in diseased soils. Monocots like grasses and palms are inherently resistant due to physiological barriers against vascular pathogens. For , resistant cultivars include (VFN), Beefmaster (VFN), and Jet Star (VF), which carry the Ve gene for race 1 ; varieties such as Century Russet, , and Ranger Russet show ; and cucurbits like certain cantaloupes and watermelons have available resistant selections. Some cultivars exhibit to Verticillium wilt, such as Irene; others like Classic and Rosa Bianca show and can produce harvests despite infection. Recent (as of 2024) has identified genes from wild species ( spp.) for use in programs. programs, including USDA efforts, have developed Verticillium-resistant lettuce lines, with six new lines registered in 2024-2025 showing low disease severity and stable across races 1, 2, and 3. and also have resistant varieties suited to orchard settings.