An interactive dashboard for global reports on the Ralstonia solanacearum species complex

The Ralstonia solanacearum species complex (RSSC) is a globally distributed group of gram-negative, soil-borne bacteria that cause wilt diseases on a broad range of hosts. Due to these pathogens’ impact on economically important plant species, there is a need for consolidated and visualized information on RSSC pathogen isolation data. We developed an interactive dashboard designed to allow users to explore the diversity and biogeography of the RSSC. The dashboard visualizes data in the form of maps, charts, and tables with a variety of user-interactive filters for taxonomic, geographic, and host of isolation specifications. This Ralstonia Wilt Dashboard will aid in communicating knowledge to researchers, regulatory scientists, and other stakeholders to improve disease control and regulation. This report highlights the deployment of the Ralstonia Wilt Dashboard and provides four case studies that address focused scientific questions (https://ralstoniadashboard.shinyapps.io/RalstoniaWiltDashboard/).

Mexico produces more than four million tons of tomato fruits and ranks tenth worldwide. In February 2022, tomato plants in a greenhouse in Culiacan, Sinaloa State, were affected by wilt diseases with an incidence of 20% and irreversible wilt and death of the infected plants (severity up 70%). When cut stems from affected plants, a reddish to brown discoloration of the vascular system was observed and these were disinfected with 1% NaClO for 5 min and then placed in a humid chamber. Characteristic milky-white exudate was obtained. From that exudate, irregular, mucoid, and white colonies with pink centres were obtained on casamino peptone glucose (CPG) plates supplemented with 1% 2,3,5-triphenyl 15 tetrazolium chloride (TZC); these characteristics are typical of the Ralstonia solanacearum species complex (RSSC) (Garcia et al., 2019). Identification of the pathogen was done by PCR using specific primer pairs reported by Paudel et al. (2022), RssC-wF3 (5'-TATATATCCTCGACTTTTCCATGAAGCTGTG-3') - RssCwR3 (5'-CTATATATATACCCCACTTGTTGAGGAACTG-3') and Rpseu-wF5 (5'-TTTTATTTTTTTGGTGTCCGGGCCAAGATAG-3') - Rpseu-wR5 (5'- TTATATTACTCGAACGTGCTGCAAAACCACT-3'), which amplified fragments of 162 and 251 bp for RSSC and Ralstonia pseudosolanacearum, respectively. Additionally, 759 (5'-GTCGCCGTCAACTCACTTTCC-3') - 760 (5'-GTCGCCGTCAGCAATGCGGAATCG-3') (Opina, et al., 1997) and Nmult21:1F (5'-CGTTGATGAGGCGCGCAATTT-3') - Nmult22:RR (5'- TCGCTTGACCCTATAACGAGTA-3') (Fegan and Prior, 2005) were used to generate 282 and 144 bp amplicons for RSSC and phylotype I, respectively. Subsequen to making the specific detection, the representative strain ClnMx was used to generate a sequence for the endoglucanase (egl) gene for separation into sequevars by using the primers Endo-F (5'- ATGCATGCCGCTGGTCGCCGC-3') and Endo-R (5'-GCGTTGCCCGGCACGAACACC-3'), which amplified a fragment of 750 bp (Fegan et al., 1998). The egl sequence (GenBank Access ON542479) showed 100% identity with the well-defined R. pseudosolanacearum sequevar 14, which was isolated from tomato plants from Senegal (UW763, I-14 GenBank Access CP051174) (Steidl et al., 2021), as well as, the strain MAFF 301070 (GenBank Access AB508612) from Japanese tomato. For pathogenicity tests, four 1-month-old tomato plants were infected using an insulin syringe that contained a pure bacterial suspension with approximately 2x108 CFU/mL. For each plant, 20 µL was infiltrated into the axil of the third upper leaf, and for untreated controls, tomato plants were infiltrated with sterile water. All plants were kept at 28°C under greenhouse conditions. Symptoms resembling those observed in the field were observed in inoculated plants six days after inoculation, and the plant pathogen was recovered on TZC medium. To confirm the bacteria identification a PCR using the specific primer pairs mentioned early was carried out. In contrast, water-treated control plants remained healthy. Koch's postulates were carried out twice with similar results. Ralstonia solanacearum species complex (RSSC) causes severe economic losses in many countries of the world because of their capability to infect a wide range of host plants, including potato, tomato, eggplant, tobacco, and, banana, among others. Ralstonia pseudosolanacearum has been reported to cause tomato wilt disease mainly on the Afro-Eurasian continent in areas such as Senegal, Cambodia, and Japan (Klass et al., 2019). To our knowledge, this is the first report of R. pseudosolanacearum causing bacterial wilt diseases in tomato plants from Mexico and because, the control of this bacteria is a challenge by the long survival time in soil, water, and infected plant tissues, the identification of this important pathogen could provide relevant information for developing management strategies.

Ginger (Zingiber officinale) is an herbaceous perennial in the Zingiberaceae family grown primarily in tropical to subtropical biomes as a culinary spice, a traditional medicine, and a landscaping plant. While ginger grows at soil temperatures above 20°C, several farmers in the upper Midwestern US farmers grows short-season ginger in high tunnels. In 2023 and 2024, growers in southeastern Minnesota reported a new disease of ginger. USDA traced the origin of the ginger rhizomes imported by these growers to Peru (Soto-Heredia et al., 2024). Plants exhibited wilting, chlorosis, pseudostem collapse, and plant death. Rhizomes were squishy with a fetid, rotting odor. Disease incidence ranged from scattered plants to 50% of the crop. Symptomatic samples tested positive for Ralstonia solanacearum species complex (RSSC) using AgDia ImmunoStrips. Rhizome tissue extracts plated onto CPG + 1% tetrazolium chloride agar and mSMSA agar produced irregular, round-to-fluidal white colonies with pink centers after 48 h of incubation at 28°C (Kelman 1954; Engelbrecht 1994). Diagnostic RSSC phylotype-specific multiplex PCR primers Nmult21:1F, Nmult21:2F, Nmult23:AF, Nmult22:InF, Nmult22:RR, and 759f/760r confirmed isolate identity; two isolates (UMN24-1, UMN24-2) yielded bands at 280 bp and 144 bp, identifying them as RSSC and phylotype I respectively (Fegan and Prior 2005; Opina et al. 1997). Additionally, 16S rRNA PCR of these isolates was sequenced using primers 27F (5'-AGAGTTTGATCMTGGCTCAG-3')/1492R (5'-TACGGYTACCTTGTTACGACTT-3') and shared >99% identity (isolate UMN24-1: 99.00% 27F, 99.53% 1492R; UMN24-2: 99.32% 1492R) with R. pseudosolanacearum (Rps) strain Gj707 (GenBank CP104497.1). Eight ginger plants in individual pots were grown in a Conviron growth chamber (28°C, 250 μmol/m2/s, 16 h photoperiod) and inoculated at the six-leaf stage (6 weeks old) by pipetting 109 CFU of the isolate, UMN24-1, suspended in sterile water into a 30°angled 1 cm incision on the pseudostem. We scored disease incidence based on wilted leaves per total leaves on each plant for 14 days post inoculation (dpi). While control plants remained healthy, inoculated plants showed symptoms (wilting, vascular discoloration, chlorosis) at 4 dpi, were 100% wilted by 6 dpi, and all pseudostems completely collapsed by 11 dpi (Fig. S1). Bacteria recovered from the inoculated plants matched the original isolate in appearance and positively identified as RSSC phylotype I using the PCR analyses described above. To confirm taxonomic identification of UMN24-1, the complete genome of this isolate was sequenced using hybrid Illumina and Oxford Nanopore sequencing (NCBI BioProject ID PRJNA1178296, release date upon publication) (Fig. S2). Average nucleotide identity (ANI) analysis of UMN24-1 using KBase's FastANI app reported 99.8% identity shared with Japanese RSSC phylotype I strain MAFF311693 (GenBank GCF 015698385.1). We also sequenced UMN24-2, and its phylogenetic analysis revealed that the two isolates are clonal (Fig. S2). Hence, we did not submit its sequence to the NCBI. This marks the first documented case of Rps in ginger in the United States. Similar to bacterial wilt in ginger closely related crop like turmeric has been repeatedly reported in northern Europe in recent years (EPPO 2024). While RSSC phylotype I is geographically limited by its minimal cold tolerance, the emergence of a pathogen with a potentially broad host range has worrying implications in a changing climate.

Ralstonia solanacearum species complex (RSSC) contains a group of destructive plant pathogenic bacteria, causing bacterial wilt of >200 species of crops and trees, such as Casuarina equisetifolia, worldwide. RSSC can survive in the soil environment for a long time and start infection after activation by host plants. This study conducted a transcriptome analysis on the expression pattern of the pathogenicity-related genes of a new isolated RSSC strain YQ (Ralstonia pseudosolanacearum phylotype I-16) in response to C. equisetifolia cladophyll (a branch of a stem that resembles and functions as a leaf) and root debris under invitro culture. The cladophyll debris induced more genes up-regulated than the root debris, including pathogenicity-related genes involved in motility, effectors, type III secretion systems, quorum sensing, and plant cell wall degradation. Besides, many differentially expressed genes were related to transcriptional regulator such as cyclic dimeric guanosine monophosphate. Moreover, the cultures with cladophyll debris induced a faster wilting in bioassays, and the cell swimming was enhanced by cladophyll exudate. C. equisetifolia cladophylls could activate the expression of pathogenicity-related genes of strain YQ and accelerate infection. Our findings suggest that litterfall management in C. equisetifolia forests, or even other plantations, should receive attention to prevent the induction of bacterial wilt disease caused by RSSC.

Ralstonia solanacearum species complex (RSSC) includes soilborne bacterial plant pathogens with worldwide distribution and wide host ranges. Virulence factors are regulated via four hierarchically organized cell-cell contact independent quorum-sensing (QS) signalling systems: the Phc, which uses as signals (R)-methyl 3-hydroxypalmitate [(R)-3-OH PAME] or (R)-methyl 3-hydroxymyristate [(R)-3-OH MAME], the N-acyl homoserine lactone (AHL)-dependent RasI/R and SolI/R systems, and the recently identified anthranilic acid-dependent system. The unique Phc QS system has been extensively studied; however, the role of the two AHL QS systems has only recently been addressed. In this microreview, we present and discuss current data of the SolI/R and RasI/R QS systems in the RSSC. We also present the distribution and frequency of these AHL QS systems in the RSSC, discuss possible ecological roles and evolutive implications. The complex QS hierarchical networks emphasizes the crucial role of cell-cell signalling in the virulence of the RSSC.

The Ralstonia solanacearum species complex (RSSC) can be divided into four phylotypes, and includes phenotypically diverse bacterial strains that cause bacterial wilt on various host plants. This study used 93 RSSC isolates responsible for potato bacterial wilt in Korea, and investigated their phylogenetic relatedness based on the analysis of phylotype, biovar, and host range. Of the 93 isolates, twenty-two were identified as biovar 2, eight as biovar 3, and sixty-three as biovar 4. Applied to the phylotype scheme, biovar 3 and 4 isolates belonged to phylotype I, and biovar 2 isolates belonged to phylotype IV. This classification was consistent with phylogenetic trees based on 16S rRNA and egl gene sequences, in which biovar 3 and 4 isolates clustered to phylotype I, and biovar 2 isolates clustered to phylotype IV. Korean biovar 2 isolates were distinct from biovar 3 and 4 isolates pathologically as well as genetically - all biovar 2 isolates were nonpathogenic to peppers. Additionally, in host-determining assays, we found uncommon strains among biovar 2 of phylotype IV, which were the tomato-nonpathogenic strains. Since tomatoes are known to be highly susceptible to RSSC, to the best of our knowledge this is the first report of tomato-nonpathogenic potato strains. These results imply the potential prevalence of greater RSSC diversity in terms of host range than would be predicted based on phylogenetic analysis.

Bacterial wilt (BW) is caused by Ralstonia solanacearum species complex (RSSC) and can lead to severe losses in a wide range of crops, including many traditional African vegetables (TAV). Given the critical role of TAV in African food security, investigations of BW incidence, distribution, and effective breeding strategies are needed to support public and private TAV breeding programs. In this review, we address key questions related to the diversity of BW pathogens, susceptible TAV hosts, distribution, incidence, breeding strategies, sources of resistance, and gaps in the development of resistant TAV varieties in Africa. We also discuss the potential of multiomics integration to enhance our understanding of the host plant defense system against BW in Solanaceae crops. We curated BW strain databases obtained from several online platforms, representing a total of 948 BW strains. Using a refined database, we highlighted the diversity of RSSC and TAV crops affected by RSSC in different regions of Africa. Out of 29 species documented to be affected by BW in Africa, ten are TAV, including widely consumed TAV such as Amaranths and nightshades. In addition, phylotypes I and III are reported to affect TAV, and the incidence can reach up to 72.4% in farmers’ fields. An overview of the first reports revealed that the disease has become a serious threat to TAV in the past decade. Finally, this review proposes a schematic map of possible avenues for successful breeding of BW-resistant TAV using Gboma eggplant as a case study.

Ralstonia solanacearum species complex is a devastating group of phytopathogens with an unusually wide host range and broad geographical distribution. R. solanacearum isolates may differ considerably in various properties including host range and pathogenicity, but the underlying genetic bases remain vague. Here, we conducted the genome sequencing of strain EP1 isolated from Guangdong Province of China, which belongs to phylotype I and is highly virulent to a range of solanaceous crops. Its complete genome contains a 3.95-Mb chromosome and a 2.05-Mb mega-plasmid, which is considerably bigger than reported genomes of other R. solanacearum strains. Both the chromosome and the mega-plasmid have essential house-keeping genes and many virulence genes. Comparative analysis of strain EP1 with other 3 phylotype I and 3 phylotype II, III, IV strains unveiled substantial genome rearrangements, insertions and deletions. Genome sequences are relatively conserved among the 4 phylotype I strains, but more divergent among strains of different phylotypes. Moreover, the strains exhibited considerable variations in their key virulence genes, including those encoding secretion systems and type III effectors. Our results provide valuable information for further elucidation of the genetic basis of diversified virulences and host range of R. solanacearum species.

Ralstonia solanacearum species complex (RSSC) is the main pathogen causing bacterial wilt disease in tomatoes. This study applied the colony polymerase chain reaction (PCR) technique to rapidly screen and select RSSC strains from isolated bacteria of diseased tomatoes. This method directly used bacterial colonies on the Petri plate as templates to amplify with RSSC’s specific and multiplex primers. The results showed that the Vietnamese isolates were identified as R. pseudosolanacearum, phylotype I. Phylogenetic analysis of the 16S-23S rDNA sequencing also confirmed these results. Therefore, this is the first report to recognize R. pseudosolanacearum phylotype I as the cause of bacterial wilt disease in tomatoes from Danang.

The Ralstonia solanacearum species complex (RSSC) causes bacterial wilt diseases, which affect a wide range of plant hosts, including Solanaceae, and is of major economic importance. Point-of-care (POC) techniques such as loop-mediated isothermal amplification (LAMP) enable the rapid and sensitive detection of plant pathogens and can be deployed directly in the field. For fast and reliable diagnosis on site, we optimized an RSSC-LAMP assay and developed a real-time LAMP assay targeting the phylotype I. Both LAMPs were highly specific, yielding negative results for a wide collection of nontarget strains and positive results for all target strains, except for two particular mulberry strains for the phylotype I assay. These results were supported by an extensive in silico analysis performed on 6,105 genomes of Burkholderiaceae. The two LAMP assays displayed high sensitivity on pure suspensions, with a detection limit at 103 and 104 CFU/ml for phylotype I and the RSSC, respectively. These thresholds correspond to theoretical quantities of as low as 5 and 50 CFU per reaction. Two simplified extraction methods were successfully used to detect the pathogen from different Solanaceae samples. We demonstrated that LAMP assays were operable on solanaceous crops during field surveys and varietal evaluation trials as rapid POC diagnostics tools, which can improve the disease management and control of the RSSC. [Formula: see text] Copyright © 2023 The Author(s). This is an open access article distributed under the CC BY-NC-ND 4.0 International license .

Ralstonia solanacearum species complex (RSSC) is a diverse group of plant pathogens that attack a wide range of hosts and cause devastating losses worldwide. In this study, we conducted a comprehensive analysis of 131 RSSC strains to detect their genetic diversity, pathogenicity, and evolution dynamics. Average nucleotide identity analysis was performed to explore the genomic relatedness among these strains, and finally obtained an open pangenome with 32,961 gene families. To better understand the diverse evolution and pathogenicity, we also conducted a series of analyses of virulence factors (VFs) and horizontal gene transfer (HGT) in the pangenome and at the single genome level. The distribution of VFs and mobile genetic elements (MGEs) showed significant differences among different groups and strains, which were consistent with the new nomenclatures of the RSSC with three distinct species. Further functional analysis showed that most HGT events conferred from Burkholderiales and played a great role in shaping the genomic plasticity and genetic diversity of RSSC genomes. Our work provides insights into the genetic polymorphism, evolution dynamics, and pathogenetic variety of RSSC and provides strong supports for the new taxonomic classification, as well as abundant resources for studying host specificity and pathogen emergence.

Bacterial wilt caused by the Ralstonia solanacearum species complex (RSSC) is among the most important plant diseases worldwide, severely affecting a high number of crops and ornamental plants in tropical regions. Only a limited number of phages infecting R. solanacearum have been isolated over the years, despite the importance of this bacterium and the associated plant disease. The antibacterial effect or morphological traits of these R. solanacearum viruses have been well studied, but not their genomic features, which need deeper consideration. This study reports the full genome of 23 new phages infecting RSSC isolated from agricultural samples collected in Mauritius and Reunion islands, particularly affected by this plant bacterial pathogen and considered biodiversity hotspots in the Southwest Indian Ocean. The complete genomic information and phylogenetic classification is provided, revealing high genetic diversity between them and weak similarities with previous related phages. The results support our proposal of 13 new species and seven new genera of R. solanacearum phages. Our findings highlight the wide prevalence of phages of RSSC in infected agricultural settings and the underlying genetic diversity. Discoveries of this kind lead more insight into the diversity of phages in general and to optimizing their use as biocontrol agents of bacterial diseases of plants in agriculture.

In September 2023, symptoms of bacterial wilt were observed in ginger (Zingiber officinale) plants in two greenhouses in Zreče, Savinjska region, Slovenia. Affected plants exhibited symptoms such as leaf yellowing, wilting, and stem browning, eventually progressing to dieback. Rhizomes exhibited brown vascular discoloration, with tissue softening and maceration, and milky-white exudates. In one greenhouse, an incidence of up to 80% of the plants was observed. Bulk samples (three plants per greenhouse) were surface disinfected with 70% ethanol. Extracts were prepared separately from rhizomes and stems, plated on a modified SMSA medium (mSMSA; Elphinstone et al., 1996) and incubated at 28 °C for three days. Colonies characteristic of the Ralstonia solanacearum species complex (RSSC) on mSMSA were isolated from all samples. Four isolates were purified and characterized on mSMSA, TSBA (BD Difco ™ , Cat. No. 211768), and SPA (Hayward, 1960) media. Real-time PCR (Vreeburg et al., 2016) was employed to confirm the identity of the strain as RSSC, and conventional PCR using primers Rs-1-F/Rs-3-R (Pastrik et al., 2002) was used to identify the pathogen as Ralstonia pseudosolanacearum Safni et al., 2014. Sequevar determination using egl gene sequencing (EPPO, 2021) showed 100% identity with 100% coverage to strain RUN 6824 from ginger in Germany (GenBank OQ753212), confirming phylotype I, sequevar 30 (Cellier et al., 2023). The sequences were deposited in GenBank (accessions: PV358607–PV358610). The pathogenicity of two selected ginger isolates was assessed by inoculating five tomato (Solanum lycopersicum cv. Moneymaker) plants per isolate. The stems were pricked with a sterile needle dipped in 24-h-old cultures grown on CPG medium (Schaad et al., 2001). Positive controls (R. solanacearum NCPPB 4156 and R. pseudosolanacearum GBBC 1112 (ILVO Plant Clinic, Merelbeke, Belgium) and a negative control (sterile needle) were included in the study. Wilting symptoms appeared within 2 days. Ginger isolates caused partial to complete wilting by 14 days post-inoculation. Plants were incubated in a growth chamber at 28°C (day), 25°C (night), and 80% humidity. Ginger isolates NIB Z 3683 and NIB Z 3685, from this study, initially induced more severe wilting than positive controls. Fourteen days post inoculation (pricking) positive controls caused plant death, while ginger isolates led to partial or complete wilting, affecting most leaves except the top parts of the inoculated plants. The negative control remained asymptomatic. The pathogen was successfully reisolated from infected plants and identified by real-time PCR (Vreeburg et al., 2016). This is the first report of R. pseudosolanacearum causing bacterial wilt of ginger in Slovenia. Traceability analysis suggests indirect introduction via imported rhizomes from Peru. Official eradication measures were taken, including destruction of all plants, disinfection, and a three-year host-plant ban. Ongoing annual monitoring is conducted in and around the affected area. As the cultivation of ginger is constantly increasing in Europe, this report underscores the need for vigilant monitoring and phytosanitary control of imported rhizomes to prevent further spread of this regulated pathogen.

The Ralstonia solanacearum species complex (Rssc) encompasses strains that are highly destructive on a wide host range, and some are listed as quarantine organisms in Europe, the United States, and many other countries. This soil-borne bacterial plant pathogen invades the roots and colonizes the xylem vessels, causing a bacterial wilt (BW) disease. Strains are distributed into four phylogenetic groups (phylotypes) linked to their geographical origin of evolution: phylotype I (Asia), phylotype II (America), phylotype III (Africa), and phylotype IV (Australia - Indonesia - Japan). Phylotypes are subdivided into sequevars, encompassing strains that share high homology on the endoglucanase gene partial sequence (750 bp) (Fegan and Prior 2005). Rodrigues is part of the Mascarene Islands in the Southwest Indian Ocean. In February 2016, a survey was conducted to identify the causal agent of BW, encountered for years on this island. Typical BW disease symptoms, including leaf epinasty and browning vessels, were observed on tomato (Solanum lycopersicum L.) in Terre Rouge and on chili pepper (Capsicum frutescens L.) in Nouvelle Découverte and Montagne Malgache. Seventy-eight stem sections were collected, surface disinfected with 70% ethanol, and crushed into 2 ml of Tris-buffer, then processed for bacterial isolation by plating 50 µl on SM-1 medium (Granada and Sequeira 1983). Among all of the collected stems, typical Ralstonia pseudosolanacearum colonies grew on the semiselective medium from 51 of the 78 samples. Corresponding strains were subcultured and typed as R. pseudosolanacearum phylotype I (Safni et al. 2014), based on the PMX-PCR (Fegan and Prior 2005). A subset of six strains, two from each location, was selected for sequevar identification (Fegan et al. 1998). Strains CFBP8472 and CFBP8465 (Terre Rouge) were identified as sequevar I-31 (GenBank KX242311 and KX242312), but strains CFBP8467 and CFBP8468 (Montagne Malgache) along with CFBP8469 and CFBP8466 (Nouvelle Découverte) were identified as sequevar I-33 (KX242313 to KX242316). This subset of strains was inoculated on five plants per strain by soil drenching on the susceptible tomato cultivar L390 (Lebeau et al. 2011) with 5 ml of a calibrated suspension (108 CFU/ml in Tris-buffer). Plants were grown in a fully controlled environment at day/night temperatures of 30/25°C ± 1°C under high relative humidity (∼90%). Sterile Tris-buffer inoculated negative controls were grown with the same parameters. Typical BW symptoms were observed within 6 days postinoculation and strains were reisolated and characterized using the same protocol as for the strains that were inoculated, fulfilling Koch's postulates. No symptoms were observed and no Rssc strains could be isolated from negative controls. To our knowledge, this is the first report of R. pseudosolanacearum phylotype I strains causing bacterial wilt on tomato and pepper on Rodrigues. Further studies need to be conducted on the prevalence and diversity of the Rssc strains causing the BW disease, in order to implement adapted control measures, such as the use of local and adapted resistant cultivars. Further surveys on other Southwest Indian Ocean islands such as Mauritius, Réunion, and Seychelles should be achieved to determine the potential origin of the R. pseudosolanacearum phylotype I strains isolated on Rodrigues island. (Texte intégral)

We share whole genome sequences of six strains from the Ralstonia solanacearum species complex, a diverse group of Betaproteobacteria that cause plant vascular wilt diseases. Using single-molecule real-time technology, we sequenced and assembled full genomes of Rs5 and UW700, two phylotype IA-sequevar 7 (IIA-7) strains from the southeastern United States that are closely related to the R. solanacearum species type strain, K60, but were isolated >50 years later. Four sequenced strains from Africa include a soil isolate from Nigeria (UW386, III-23), a tomato isolate from Senegal (UW763, I-14), and two potato isolates from the Madagascar highlands (RUN2474, III-19 and RUN2279, III-60). This resource will support studies of the genetic diversity, ecology, virulence, and microevolution of this globally distributed group of high-impact plant pathogens.[Formula: see text] Copyright © 2021 The Author(s). This is an open access article distributed under the CC BY-NC-ND 4.0 International license.