Genetic Diversity and Pathogenicity of Rhizoctonia spp. Isolates Associated with Red Cabbage in Samsun (Turkey)

A total of 132 Rhizoctonia isolates were recovered from red cabbage plants with root rot and wirestem symptoms in the province of Samsun (Turkey) between 2018 and 2019. Based on the sequence analysis of the internal transcribed spacer (ITS) region located between the 18S and 28S ribosomal RNA genes and including nuclear staining, these 124 isolates were assigned to multinucleate Rhizoctonia solani, and eight were binucleate Rhizoctonia. The most prevalent anastomosis group (AG) was AG 4 (84%), which was subdivided into AG 4 HG-I (81%) and AG 4 HG-III (3%), followed by AG 5 (10%) and AG-A (6%), respectively. The unweighted pair group method phylogenetic tree resulting from the data of 68 isolates with the inter-PBS amplification DNA profiling method based on interspersed retrotransposon element sequences confirmed the differentiation of AGs with a higher resolution. In the greenhouse experiment with representative isolates (n = 24) from AGs on red cabbage (cv. Rondale), the disease severity index was between 3.33 and 4.0 for multinucleate AG isolates and ranged from 2.5 to 3.17 for AG-A isolates. In the pathogenicity assay of six red cabbage cultivars, one isolate for each AG was tested using a similar method, and all cultivars were susceptible to AG 4 HG-I and AG 4 HG-III isolates. Redriver and Remale were moderately susceptible, while Rescue, Travero, Integro, and Rondale were susceptible to the AG 5 isolate. The results indicate that the most prevalent and aggressive AGs of Rhizoctonia are devastating pathogens to red cabbage, which means that rotation with nonhost-crops for these AGs may be the most effective control strategy. This is the first comprehensive study of Rhizoctonia isolates in red cabbage using a molecular approach to assess genetic diversity using iPBS-amplified DNA profiling.


Introduction
Turkey is the world's fourth-largest vegetable producer with approximately one million hectares of cultivation area and an annual yield of 24.1 million tons [1]. Brassicas is a family of vegetables, including important and highly diverse crops that are widely grown due to their contribution to the human diet and other health benefits [2,3].
The most common cultivated species of the brassicas are broccoli (Brassica oleracea var. italica), Brussels sprouts (B. oleracea var. gemmifera), cauliflower (B. oleracea var. botrytis), Chinese cabbage (B. pekinensis), kale (B. oleracea var. acephala), radish (Raphanus sativus), red cabbage (B. oleracea var. capitata f. rubra), and white head cabbage (B. oleracea var. capitata f. alba), which are responsible for 4.5% of total vegetable production in Turkey. Red cabbage in Samsun province has about 52.266 da of a total cultivation area and 192.219 tons of annual production, accounting for 57% of the country's total production [4]. Cruciferous vegetables in the family of Brassicaceae are cultivated throughout the world; however, they suffer from various bacterial, fungal, protozoan, and viral diseases [5]. Rhizoctonia spp. is an important and difficult-to-treat group among the myriad of fungal pathogens and associated with damping off, root rot, wirestem, foot rot, and the head rot disease complex of brassicas, which result in economic yield losses [5][6][7][8][9][10][11]. This phytopathogen as a complex group shows significant differences in cultural, molecular, and biochemical properties, and pathogenicity.
Rhizoctonia isolates can be classified into the groups of multinucleate Rhizoctonia (MNR) binucleate Rhizoctonia (BNR), and uninucleate Rhizoctonia (UNR), taking into account the average number of nuclei per young vegetative hyphal cell of the isolates [6]. Isolates of Rhizoctonia spp. are further divided into numerous anastomosis groups (AGs) on the basis of interactions of isolates with hyphal anastomosis that differed in genotypic and phenotypic properties. Thirteen AGs designated as AG1-AG13 and AG-BI have been assigned within MNR, Rhizoctonia solani J.G. Kuhn, whilst 19 AGs of BNR, referred to as AG A-AG W, have been designated based on hyphal fusion [12][13][14][15][16]. Some multinucleate AGs are further clustered into distinct subgroups [12,17].
The internal transcribed spacer (ITS) between the 18S and 28S ribosomal RNA genes, including ITS1, 5.8S rRNA, and ITS2, has been widely employed to evaluate genetic variation and characterize AG groups of Rhizoctonia isolates [13]. The resolution of hyphal anastomosis analysis is insufficient to distinguish subgroups within AG 1, AG 2, and AG 4, because anastomosis reaction occurs between isolates of various subgroups in the same group [12,18]. The analysis of the ITS sequences is a critical tool to overcome this bottleneck.
However, the genetic conservationism of the internal transcribed spacer sequences for a particular species makes the study of these sequences for intraspecific diversity unsuitable. Ideal and simple approaches that may correspond to the assessment of genetic intraspecific diversity are based on DNA profiling methods. Such DNA profiling methods include all PCR-based DNA fingerprinting method variants of the Random Amplified Polymorphic DNA (RAPD) method, such as Inter Simple Sequence Repeat (ISSR), and others [27].
Fundamental components of all eukaryote genomes include mobile genetic elements and other interspersed repeats that can activate under stress conditions and indirectly promote survival under environmental stresses. Various PCR-based DNA fingerprinting methods are used to detect chromosomal changes related to recombination processes of mobile genetic elements [28][29][30]. These methods are based on interspersed repeat sequences and are an effective approach to assess the biological diversity of hosts and their variability. The assessment of genetic intraspecific diversity using mobile genetic elements or other interspersed repeats is simple and accessible as RAPD. Most disseminated repeats with one other during inter-and intrachromosomal recombination, which leads to the formation of inverted repeats that are close to one other and allow PCR amplification [27,31]. These interspersed repeat sequences arise from various families of long-terminal repeat (LTR) retrotransposons that have replicated through RNA reverse transcription and integration of resultant cDNA into another locus [32]. Highly conserved repeat sequences for these retrotransposons include the tRNA priming binding site (PBS) when initializing retrotransposon replication. Sequences of the PBS region are complementary to at least 12 nucleotides of the tRNA sequences, which are sufficient for use as PCR primers [33]. As retrotransposon sequences are frequently near one other in inverted orientation, PBS sequences are accessible when used for DNA amplification for most eukaryotic species with large genomes, such as plants and animals [28].
Genetic differences in the AGs and their subgroups were genetically evaluated using DNA profiling PCR methods based on a single-primer complementary to the PBS region downstream of the 5 LTR for retrotransposons [33]. This DNA marker system based on retrotransposons, the Inter Primer Binding Site (iPBS) amplification technique, is ideal for the assessment of the genetic intraspecific diversity of all eukaryotes [33,34]. This PCR-based DNA fingerprinting method has permitted the genetic differentiation between mold and yeast at intraspecies levels, as well as the identification of the AGs of Rhizoctonia spp. [35][36][37][38][39][40]. Genetic differences in hypertension and their subgroups have been phylogenetically assessed using PCR-based DNA fingerprint techniques even in the absence of prior knowledge of the sequences [34,[41][42][43][44]. Several studies have reported that Rhizoctonia isolates within many AGs have caused diseases in important crops in Turkey to date [11,[45][46][47][48][49]; however, there are no detailed reports identifying the AGs and their subgroups of Rhizoctonia isolates causing the root rot and wirestem of red cabbage in Turkey.
No information is available about the aggressiveness of the red cabbage isolates to red cabbage cultivars commonly cultivated in the country. The aims of this study were the following: (i) to conduct the molecular characterization of AGs and their subgroups of Rhizoctonia isolates recovered from diseased red cabbage plants showing root rot and wirestem symptoms; (ii) to apply DNA-profiling PCR methods based on iPBS amplification to discriminate AGs of Rhizoctonia spp.; (iii) to determine the pathogenicity of the isolates belonging to AGs determined in this study in red cabbage cv. Rondale; and (iv) to reveal the resistance status of six red cabbage cultivars against different AGs under greenhouse conditions.

Sample Collection and Isolation of Rhizoctonia Isolates
During the 2018 and 2019 growing seasons, diseased plants with typical symptoms of root rot and wirestem were sampled from 79 randomly selected commercial red cabbage fields in Samsun province between July and October. For each field, three diseased plants were quickly collected onto Whatman filter paper and shipped at room temperature to the laboratory.
Necrotic basal stem and root tissues were washed under tap water, rinsed in sterile distilled water, and cut into 1-2 cm sections. These segments were surface sterilized in 1% NaClO solution for 2 min, blotted-dry on sterile filter papers, and placed on 2% acidified water agar (pH 4.5) with 10% lactic acid. The plates were incubated at 23 • C in the dark for two days. Following two-day incubation, the hyphae of fungal colonies recovered from the sections were examined under a CX31 compound microscope (Olympus, Tokyo, Japan) at a magnification of 200×. Colonies showing Rhizoctonia-like growth [50] were subjected to a second transfer to potato dextrose agar (PDA; 213400, BD Difco, Sparks, MD, USA) and incubated at 23 • C for one week in the dark. The isolates were maintained at 4 • C on PDA slants.
To specify the number of nuclei per hyphal cell of Rhizoctonia isolates, the 2-day-old hyphal tips of each isolate were stained with 0.5% safranin O and 3% KOH solution as described by Bandoni [51] and observed immediately at 400× by the CX31 microscope.

DNA Extraction
The mycelial discs from the solid culture of isolates were transferred to 250 mL Erlenmeyer flasks each containing 80 mL potato dextrose broth (254920, BD Difco, Sparks, MD, USA) placed on a shaking incubator at 180 rpm and 23 • C for three days. Mycelia were harvested by filtration, washed three-times with sterile distilled water, blotted dry, and ground to a powder in liquid nitrogen. Approximately 50-100 mg of the mycelial powder for each isolate was subjected to genomic DNA extraction with the CTAB method, as described in [52]. The DNA pellets were dissolved in 1 × TE buffer (1 mM EDTA, 10 mM Tris-HCl, pH 8.0). DNA concentration was measured using a nanospectrophotometer (DS-11 FX+, Denovix Inc., Wilmington, DE, USA). The resultant DNA for each isolate was diluted with 1 × TE solution to 10 ng/µL and used as a template for PCR experiments.

ITS Sequencing
To amplify the ITS of genomic rDNA from Rhizoctonia isolates, the primer pair ITS1/ITS4 [53]  Nucleotide sequence comparisons were conducted using the National Center for Biotechnology Information (NCBI) Basic Local Alignment Search Tool (BLAST) network services with ITS sequences as a query to determine the closest available reference sequences of various AGs in the complete NCBI nucleotide library.
The alignment of the sequences of the isolates derived in this study and representative Rhizoctonia isolates retrieved from GenBank (AG 4 HG-I: AB000012, HQ636466, AY387544; AG 4 HG-III: AF354077, JF701709, HQ185372; AG 5: HQ185737, MF070670, KJ170355; AG-A: AY927330, DQ102411, FR734301) was implemented in MEGA X [54] with the CLUSTAL W alignment method [55]. A Maximum Likelihood (ML) tree was constructed in a maximum parsimony (MP) analysis starting tree automatically generated by the software, and the robustness of phylogeny was assessed using 1000 bootstraps [56].

iPBS Amplification Analyses
A total of 7 PBS primers were selected for the assessment of genetic intraspecific diversity based on DNA profiling methods for 68 Rhizoctonia isolates belonging to different AGs (Table 1). The iPBS-amplification PCR was carried out in a 25 µL reaction volume containing 12.5 µL DreamTaq PCR Master Mix (2×), 0.04 unit of Pfu DNA Polymerase (Thermo Fischer Scientific, Waltham, MA, USA), 0.8 µM of primer, and 10 ng template DNA. The reaction program was set at 95 • C for 3 min, followed by 32 cycles of 30 s at 95 • C, 30 s at 50-62 • C (depending on primers), and 1 min at 72 • C, with a final extension at 72 • C for 5 min. The amplified DNA fragments were analyzed on 1.4% agarose gel using 1 × TAE buffer at 70 V for 5 h and staining with ethidium bromide. PCR products were visualized and imaged under ultraviolet (UV-B) light in the G: BOX F3 gel documentation system (Syngene, Synoptics Ltd., Cambridge, UK). The PCR reaction was conducted twice for each primer to ensure the reproducibility of the results. Ta ( • C), annealing temperature; TB, total band; PB, polymorphic band; PIC, polymorphism information content; RP, resolving power.
A binary matrix was obtained reporting each specific iPBS fragment present (1) or absent (0). The values of polymorphism information content (PIC) and resolving power (RP) were estimated to assess the performance of iPBS markers according to Roldán-Ruiz et al. [57] and Prevost and Wilkinson [58], respectively. Estimates of similarity based on Jaccard's similarity coefficient were created using the NTSYS-pc version 2.10e program [59]. The similarity matrix was then analyzed using the unweighted pair group method using the arithmetic average (UPGMA) clustering method. The R software package vegan ver. 2.4.4 [60] was used to construct Principal coordinate analyses (PCoA).
The population structure analysis of 68 Rhizoctonia isolates with 106 loci was inferred by Bayesian model-based clustering implemented in the program Structure v.2.3.4 [61]. The algorithm was run using a mixed model of 14 independent values (K) from 2 to 15 assumed groups, using 100,000 Markov chain Monte Carlo (MCMC) repetitions after a 100,000 burn-in period. The delta K (∆K) model and the estimated likelihood values were used to estimate the most probable number of the clusters using STRUCTURE HARVESTER [62].

Pathogenicity Assays
Of 24 isolates, 14 belonged to AG 4 HG-I, 2 to AG 4 HG-III, 4 to AG 5, and 4 to AG-A of Rhizoctonia spp., selected on the basis of AGs, and geographical origin was tested for aggressiveness on red cabbage cv. Rondale under greenhouse conditions. The inoculum of each isolate was prepared on wheat seeds using the seed-colonization method of Brayford [63]. The seeds of red cabbage were superficially disinfected in 1% NaOCl solution for 3 min, washed twice with sterilized distilled water, and air-dried on sterile tissue paper in a laminar flow. Each single seed was sown in plastic pots (7 cm in length, 6.5 cm in diameter) filled with a sterilized peat:perlite (2:1, v:v) mixture. The pots were maintained at 20-25 • C with a 16 h photoperiod in a greenhouse.
Six-week-old seedlings at the three true leaf stage were singly transplanted into 10 cm diameter plastic pots (250 mL) containing a sterilized mixture of sandy loam soil:manure:washed sand (2:2:1, v:v:v), and inoculated with 5 g of colonized wheat seeds by placing into the pit dispersedly and surrounded seedling roots at the same time. Controls were inoculated with sterile wheat seeds. Plants were kept in the greenhouse at 20-25 • C. Six replicates were employed for each isolate, with an equal number of control plants. After inoculation, plants were kept in the greenhouse. Twenty-one days after inoculation, plants were gently uprooted, washed with tap water for 5 min, and evaluated for the disease. The disease severity index (DSI) was assessed by evaluating seedling/root symptoms using a slightly modified 1-4 disease severity scale: 1 = no symptom; 2 = basal rot on part of the stem; 3 = basal rot girdled stem superficially, but plants did not wilt; 4 = basal rot deeply girdled stem, stem base was constricted, roots were sometimes detached from stem, and plants wilted [9]. The values of plant height, shoot and root dry weights, and root length were also recorded for each plant. The experimental set-up was a completely randomized design with six red cabbage seedlings per treatment, and the experiment was repeated once. The isolates tested were re-isolated from the symptomatic tissues of the seedlings.

Resistance Response Classification
The reactions of six red cabbage cultivars (Rescue, Travero, Integro, Remale, Redriver, and Rondale) grown commonly in Turkey were estimated using the method described in the pathogenicity experiment against Rhizoctonia spp. The isolates of Rs-RC-20 (AG 4 HG-I), Rs-RC-109 (AG 4 HG-III), Rs-RC-118 (AG 5), and R-RC-131 (AG-A) representing each AG were selected for this experiment. The cultivars were grouped according to disease severity on stems and roots. The cultivars were considered resistant (R) if the mean disease severity was ≤1.50, moderately resistant (MR) if the mean disease severity ranged between 1.51 and 2.25, moderately susceptible (MS) if the mean disease severity ranged between 2.26 and 3.00, and susceptible (S) if the mean disease severity was ≥3.01.

Statistical Analysis
All data obtained from pathogenicity tests was subjected to Box-Cox transformation before statistical analyses, since they failed to meet the assumptions of normal distribution (Shapiro-Wilk test) and variance homogeneity (Levene's test). Each plant growth parameter was separated individually at a probability level of p < 0.05 by Fisher's least significant difference (LSD) test based on the transformed data. On the other hand, due to the nonnormal distribution of disease severity data, analysis was performed with the Dunn-test based on the rank sums using the Kruskal-Wallis pairwise multiple comparisons. To assess the effect of the isolate, cultivar, and isolate-cultivar on disease severity, a nonparametric test of two-way ANOVA, the Scheirer-Ray-Hare (SRH) test, was performed using R software. All other analyses were conducted using the XLSTAT program version 18.07 (Addinsoft Company, New York, NY, USA).

Rhizoctonia Species and AGs on Red Cabbage
Altogether, 132 isolates of Rhizoctonia spp. associated with dark lesions of underground parts of red cabbage plants were obtained from the fields planted in sixteen locations of Samsun province. Using the nuclear staining method, 124 of 132 isolates were classified as MNR, while the remaining isolates (n = 8) were BNR ( Table 2).    The BLAST service at the NCBI website was used for analysis of ITS sequences. The BLAST analysis revealed that 107 isolates were MNR AG 4 HG-I, the most prevalent group (81%) in the investigated area, followed by AG 5, AG 4 HG-III, and BNR AG-A with 13 (10%), 4 (3%), and 8 (6%) isolates, respectively. No polymorphism was observed among the nucleotide sequences of isolates within the same AG. The ITS fragments amplified using primers ITS1 and ITS4 showed 100% similarity with those of the corresponding isolates belonging to different AGs from GenBank. The accession numbers provided by GenBank for the sequences obtained in this study are shown in Table 2. The Maximum Likelihood tree generated with the ITS sequences showed a clear clustering among anastomosis groups (Figure 1). All isolates obtained in this study and the known AGs retrieved from GenBank clustered into two major groups with strong bootstrap values (99-100%) according to their nuclei number within vegetative cells. Group I comprised multinucleate isolates, which were further grouped into three subgroups according to their anastomosis groups, whereas the isolates of AG-A formed Group II as the most diverse group. Figure 1. The Maximum Likelihood tree was generated using the ITS sequences of Rhizoctonia isolates from this study (bold) and reference isolates representing AGs from GenBank. The percentage of replicate trees in which the associated taxa clustered together in the bootstrap test (1000 replicates) is shown next to the branches.

iPBS Amplification Analysis
The seven PBS primers in iPBS-amplification profiling generated 106 scorable and reproducible fragments to evaluate the extent of genetic variation between Rhizoctonia isolates. Ninety-six of those fragments (90%) were polymorphic. The number of fragments amplified with the primers varied between 11 (2219/2237) and 30 (2395), with a mean of 15 fragments per PBS primer. The values of the PIC and RP index estimated for the markers are listed in Table 1. The range of PIC was 0.37 (2219)-0.14 (2239), averaging 0.18 ( Figure 2). The mean of the RP values, a parameter that indicates the discriminatory potential of the primers chosen, was 3.15 for all primers. The highest RP value of 5.32 was obtained from 2395, while the lowest RP value was recorded as 1.94 for 2239. The UPGMA dendrogram produced using the Jaccard's similarity coefficient for iPBS profiling methods clustered distinctly 68 Rhizoctonia isolates into four major groups, which were completely conserved among isolates within the same AG assignment (Figure 3). Group I comprised 58 AG 4 HG-I isolates, and Group 2, 3, and 4 were composed of AG 4 HG-III (3), AG 5 (4), and AG-A (3) isolates, respectively. The groups were further clustered into subgroups at different similarity degrees. In addition, UPGMA cluster analysis based on iPBS-amplification profiling data supported the grouping of isolates based on ITS sequences. The PcoA analysis distinguished Rhizoctonia isolates according to their anastomosis groups and plotted the isolates to four major groups, which confirmed the UPGMA pattern ( Figure 4). Structure runs were conducted for K = 2 to 15 based on the iPBS data. Ln values increased sharply at K = 3, after which the increase was slow without reaching the plateau ( Figure 5). The highest peak was detected at K = 3, which implies that the isolates could be distributed into three separated clusters according to the ΔK criteria of Evanno et al. [64].

iPBS Amplification Analysis
The seven PBS primers in iPBS-amplification profiling generated 106 scorable and reproducible fragments to evaluate the extent of genetic variation between Rhizoctonia isolates. Ninety-six of those fragments (90%) were polymorphic. The number of fragments amplified with the primers varied between 11 (2219/2237) and 30 (2395), with a mean of 15 fragments per PBS primer. The values of the PIC and RP index estimated for the markers are listed in Table 1. The range of PIC was 0.37 (2219)-0.14 (2239), averaging 0.18 ( Figure 2). The mean of the RP values, a parameter that indicates the discriminatory potential of the primers chosen, was 3.15 for all primers. The highest RP value of 5.32 was obtained from 2395, while the lowest RP value was recorded as 1.94 for 2239. The UPGMA dendrogram produced using the Jaccard's similarity coefficient for iPBS profiling methods clustered distinctly 68 Rhizoctonia isolates into four major groups, which were completely conserved among isolates within the same AG assignment (Figure 3). Group I comprised 58 AG 4 HG-I isolates, and Group 2, 3, and 4 were composed of AG 4 HG-III (3), AG 5 (4), and AG-A (3) isolates, respectively. The groups were further clustered into subgroups at different similarity degrees. In addition, UPGMA cluster analysis based on iPBS-amplification profiling data supported the grouping of isolates based on ITS sequences. The PcoA analysis distinguished Rhizoctonia isolates according to their anastomosis groups and plotted the isolates to four major groups, which confirmed the UPGMA pattern ( Figure 4). Structure runs were conducted for K = 2 to 15 based on the iPBS data. Ln values increased sharply at K = 3, after which the increase was slow without reaching the plateau ( Figure 5). The highest peak was detected at K = 3, which implies that the isolates could be distributed into three separated clusters according to the ∆K criteria of Evanno et al. [64].

Virulence of the Isolates
The results of the pathogenicity test on seedlings of red cabbage cv. Rondale revealed a significant difference in virulence between the isolates tested (Kruskal-Wallis ANOVA, H 24,125 = 106.81, p < 0.0001) ( Figure 6). Disease symptoms developed in inoculated red cabbage seedlings were scored after twenty-one days of inoculation (Figure 7). The disease severity index (DSI) varied from 3.33 to 4.0 for all R. solani isolates. In particular, almost all AG 4 HG-I isolates, and isolate Rs-RC-122 of AG 5, caused severe necrosis symptoms in the seedlings, resulting in damping off. All AG-A isolates had a lower virulence ranging from 2.5 to 3.17. All isolates caused a significant reduction in the dry weight of shoots and roots compared to control plants (ANOVA, F 24,125 = 7.002, p < 0.0001; F 24,125 = 3.369, p < 0.0001, respectively) ( Table 3). Compared to the control, some R. solani isolates and all AG-A isolates were found to have no adverse effects on root length or/and plant height (ANOVA F 24,125 = 2.554, p < 0.0004; F 24,125 = 4.051, p < 0.0001, respectively).

Host Response of Some Commercial Cultivars to Different AGs of Rhizoctonia
A statistically significant difference was observed among different AGs (AG 4 HG-I, -HG-III, and 5) of Rhizoctonia isolates in the severity of root rot in the cultivars (Rescue, Travero, Integro, Remale, Redriver, and Rondale) of red cabbage (SRH test: isolates: H4 = 135.85, p < 0.0001; cultivars: H5 = 11.45, p < 0.0432, respectively) ( Table 4). In general, the AG-A isolate caused low disease severity in all cultivars, but R. solani isolates led to the development of severe root rot resulting in high disease severity values ranging from 2.5 Figure 6. Pathogenicity of Rhizoctonia spp. isolates obtained from red cabbage to seedlings of the cv. Rondale twenty-one days after inoculation. Seedling/root symptoms were evaluated 21 days after inoculation based on the following scale: 1 = no symptom; 4 = basal rot deeply girdled stem, stem base was constricted, roots were sometimes detached from stem, and plants wilted. Values followed by the same letter are not significantly different according to Dunn-test based on the rank sums using the Kruskal-Wallis (p < 0.0001).
J . Fungi 2021, 7, 234 15 of 21 Figure 6. Pathogenicity of Rhizoctonia spp. isolates obtained from red cabbage to seedlings of the cv. Rondale twenty-one days after inoculation. Seedling/root symptoms were evaluated 21 days after inoculation based on the following scale: 1 = no symptom; 4 = basal rot deeply girdled stem, stem base was constricted, roots were sometimes detached from stem, and plants wilted. Values followed by the same letter are not significantly different according to Dunn-test based on the rank sums using the Kruskal-Wallis (p < 0.0001).

Host Response of Some Commercial Cultivars to Different AGs of Rhizoctonia
A statistically significant difference was observed among different AGs (AG 4 HG-I, -HG-III, and 5) of Rhizoctonia isolates in the severity of root rot in the cultivars (Rescue, Travero, Integro, Remale, Redriver, and Rondale) of red cabbage (SRH test: isolates: H4 =

Host Response of Some Commercial Cultivars to Different AGs of Rhizoctonia
A statistically significant difference was observed among different AGs (AG 4 HG-I, -HG-III, and 5) of Rhizoctonia isolates in the severity of root rot in the cultivars (Rescue, Travero, Integro, Remale, Redriver, and Rondale) of red cabbage (SRH test: isolates: H 4 = 135.85, p < 0.0001; cultivars: H 5 = 11.45, p < 0.0432, respectively) ( Table 4). In general, the AG-A isolate caused low disease severity in all cultivars, but R. solani isolates led to the development of severe root rot resulting in high disease severity values ranging from 2.5 to 4. All cultivars were susceptible to AG 4 HG-I and HG-III isolates of R. solani. Redriver and Remale to the AG 5 isolate were moderately susceptible, while Rescue, Travero, Integro, and Rondale were susceptible. On the other hand, Redriver was moderately resistant to AG-A; Remale, Rescue, and Travero were moderately susceptible; and Integro and Rondale were susceptible. No significant isolate-cultivar interaction was observed for root rot severity on red cabbages (SRH test: isolates:cultivars H 20 = 15.09, p < 0.7712).

Discussion
This is the first characterization of Rhizoctonia isolates obtained from red cabbage growing areas in Turkey. To the best of our knowledge, no reports about the pathogenicity of Rhizoctonia spp. in red cabbage plants have been recorded in the world. The majority of the Rhizoctonia isolates were MNR AG 4 (84%). The sequence analysis of the ITS allowed further division of the 111 isolates belonging to MNR AG 4 into two subgroups, AG 4 HG-I (n = 107) and AG 4 HG-III (n = 4). The remaining isolates were classified into AG 5 (8 isolates) and BNR AG-A (13 isolates).
As indicated in the previous reports, both BNR and MNR isolates cause disease in Brassica crops, including white cabbage, kale, broccoli, cauliflower, oilseed rape, and canola in several countries in the world [7][8][9][10][11]18,20,22,23,26,65]. The most prevalent and damaging R. solani AGs were AG 2-1 and AG 4 among AGs determined for brassicas [19,24,25,66,67]. Recently, Türkkan, Kılıçoglu and Erper [11] determined that 37% (11 isolates) of limited Rhizoctonia isolates (30 isolates) obtained from kale growing areas in Ordu province, Black Sea region of Turkey, belong to AG 2-1, followed by AG-A with 20% (9 isolates), and AG 4 HG-I with 10% (3 isolates). They isolated Rhizoctonia isolates during November-April when temperatures ranged from 7-16 • C. However, in the present study, surveys were conducted between July and October when the weather was warmer (25-33 • C). Previous studies have shown that the abundance of each AG may depend on the climate. For example, it has been reported in several studies that AG 4 HG-I is dominant in warmer periods, while AG 2-1, AG 1-IB, and AG-BI are dominant during colder periods [68][69][70]. Moreover, Yitbarek et al. [71] observed that AG 4 caused severe root rot in B. napus seedlings at temperatures varying between 26 and 35 • C, whereas the pathogenic activity of AG 2-1 was considerably reduced at these temperatures. The relationship between AG and temperature is probably the same for isolates in this study and may explain why we commonly isolate R. solani AG 4 HG-I during warmer periods. In addition, previous studies have reported that it is the most common pathogen on cucumber, winter squash, bean, and soybean in the Samsun province of Turkey, where brassicas (cauliflower, white cabbage, and red cabbage) are used as an effective rotational crop [47,72,73]. Given that the pathogen is polyphagous, these alternative hosts likely contributed to the prevalence of Rhizoctonia root rot in the fields, which is consistent with Keinath's findings [74]. Cubeta and Vilgalys [75], and Sharon et al. [76] noted that DNA fingerprinting techniques for studying the genetic variation of Rhizoctonia are most suitable at the individual level rather than for the determination of AGs or subgroups within an AG. There is a lack of evidence, however, to support this hypothesis, since no DNA marker system has been tested in grouping a large number of Rhizoctonia isolates of different AGs. In the present study, the retrotransposon-based iPBS amplification DNA profiling method differentiated the isolates according to their anastomosis groups, including AG 4 HG-I, HG-III, AG 5, and AG-A, via phylogenetic analysis. A more detailed sub-grouping was observed among the isolates within each AG group formed in the phylogenetic tree, especially among AG 4 HG-I isolates. This is in accordance with other researchers who have grouped Rhizoctonia spp. isolates using these markers [35,36]. Pourmahdi and Taheri [35] showed the efficacy of this molecular marker system to determine the AGs of R. solani isolates from tomato as a novel universal molecular marker system. iPBS-amplification markers have also been successfully employed for the characterization of several other fungi and yeast [36][37][38][39][40]77,78]. To the best of our knowledge, this study is the first characterization of various Rhizoctonia spp. isolates belonging to different AGs obtained from red cabbage using the retrotransposon marker system for DNA fingerprinting.
The pathogenicity studies on red cabbage seedlings showed that the disease severity index (DSI) used in the evaluation of the aggressiveness of Rhizoctonia isolates varied widely between 2.5 and 4.0. In the MNR isolates, AG 4 HG-I isolates had the highest index value (DSI: 4.0) on the seedlings, with exceptions of the RS-RC-28, -76, and -82 isolates, and Rs-RC-122 isolate of AG 5. The AG 4 HG-I isolates caused wirestem symptoms by severe necrosis of the stem and root tissues. AG 4 HG-III and AG 5 isolates were more aggressive than isolates of BNR AG-A. Pannecoucque, Van Beneden, and Höfte [20] found that cauliflower plants were more susceptible to AG 1-IC, AG 2-1, AG 2-1 subset Nt, AG 2-2, and AG 4 HG-II isolates than AG 1-IB and AG 5 isolates. None of the AG-A isolates caused symptoms on Chinese and white cabbage, but AG-Fc isolates caused severe lesions [8]. Türkkan, Kılıçoglu, and Erper [11] noted that except for several isolates within AG 2-1, AG 2-1 and AG 4 HG-I caused severe symptoms and deaths on seedlings of kale cv. Arzuman, but the isolates in AG 5, AG-E, AG-Fb, and AG-K were of relatively low and moderate virulence.
The results of pathogen-cultivar interactions in the current study are consistent with those of Keinath and Farnham [24], who found no cultivar by isolate interaction when testing cultivars for root rot resistance against AG 4 and AG 2-1 of R. solani. They also determined that AG 4 caused severe wirestem rot in the seedlings of 12 brassica cultivars (3 each of broccoli, cauliflower, cabbage, and collard) in all experiments, while AG 2-1 caused less root rot in the growth chamber but no root rot in the field. Chinese cabbage and white cabbage seedlings were highly susceptible to R. solani AG 4 HG-I in both in vitro and in vivo bioassays conducted by Hua, Bertier, Soltaninejad, and Hofte [8]. Türkkan et al. [11] reported that R. solani AG 2-1 and AG 4 HG-I isolates generally caused more severe root rot in the seedlings of kale cv. Arzuman. The present study revealed that the Redriver cultivar was moderately resistant to Rhizoctonia AG-A, although no cultivars tested were resistant to AGs of R. solani.
In conclusion, the Rhizoctonia spp. isolates, whether MNR or BNR, cause devastating diseases in many crops, resulting in economic crop losses. The AG classification of Rhizoctonia isolates is a critical approach to characterize the various groups that cause plant diseases. The iPBS-amplification DNA profiling analysis is a simple, effective, and powerful tool to identify AG subgroups. Further studies with other isolates belonging to more AGs are needed to comprehensively investigate the association between grouping within Rhizoctonia spp. isolates and iPBS-amplification DNA profiling.
In this study, we confirmed the presence of some virulent Rhizoctonia isolates associated with root rot and wirestem in red cabbage. Due to the persistence of Rhizoctonia in the soil for several years and the presence of different AGs that are aggressive in various host plants [6], crop rotational strategies alone are insufficient to control Rhizoctonia in the fields surveyed. The isolates of AG 4 HG-I cause problems for several crops cultivated in the agricultural areas of the Black Sea region, including the province of Samsun [10,11]. AG 4 HG-I, therefore, has the potential to damage Brassica crops. Although the use of chemical fungicides is environmentally undesirable, the most common method for protecting crops against Rhizoctonia isolates is the use of fungicides worldwide [79]. In Turkey, several fungicides are used to control Rhizoctonia species on different crops as seed or seedling treatments. An approach of integrated management of plant disease including applying chemical and biological fungicides, crop rotation, and breeding varieties with resistance is needed for the efficient control of the root rot and wirestem of red cabbage.