Selection of Improved Banana Diploid Resistant to Fusarium oxysporum f. sp. cubense Races 1 and Subtropical 4

1. Introduction

Bananas and plantains (Musa spp.) are cultivated in over 150 tropical and subtropical countries, playing a crucial role in the economies of developing nations [1].

Banana cultivation stands as a leading sector in global agricultural production, with India as the largest producer, followed by China, Indonesia, and Brazil [1]. Fusarium wilt, caused by Fusarium oxysporum form specialis f. sp. cubense (Foc), stands out as a primary limitation to banana production, ranking among the top five diseases impacting the economic sector and fruit-producing regions [2,3]. Fusarium wilt is instigated by Foc, a soil-inhabiting fungus with the ability to colonize plants, induce their demise, and employ intricate pathways to suppress plant defenses [4,5].

Isolates of Foc pathogenic to bananas are categorized within the f. sp. cubense, classified into three races based on their infectivity to different cultivars within the species [3,5]. Race 1 (R1) affects Gros Michel (AAA) and Manzano/Silk/Latundan (AAB) sub-groups; Race 2 (R2) targets cultivars susceptible to R1 and those of the Bluggoe subgroup. Race 4 (R4) impacts all cultivars in the Cavendish subgroup (AAA), and those susceptible to R1 and R2 [4,6,7]. R4 has further subdivisions into tropical race 4 (TR4) and subtropical race 4 (ST4). TR4 affects Cavendish in both tropical and subtropical conditions, while Foc ST4 isolates cause disease in Cavendish cultivars in subtropical regions under specific conditions, such as temperature extremes or water deficit [8,9]. The ST4 and TR4 variants can be differentiated by their Vegetative compatibility group (VCGs). Among the 24 known Foc VCGs, VCGs 0120, 01201, 01202, 01209, 01210, 01211, 01215, and 0120/15 are associated with Foc ST4; for Foc TR4, only VCG 01213/16 has been identified [6,9].

Foc TR4 poses a significant threat to banana and plantain cultivation across various regions globally. Apart from its extensive presence in Asia, Africa, and Australia, it has also encroached upon cultivation areas in Latin America and the Caribbean, including Colombia, Peru, and Venezuela [3,10,11]. The escalating concern regarding the damage inflicted on banana cultivation by this threat has redirected research efforts, prompting a worldwide search for new insights based on epidemiological, genetic, and management data. Notably, the absence of a cultivar with sufficient resistance to replace those of the Cavendish subgroup intensifies the urgency of such research [3,6,12,13].

Consequently, genetic improvement programs are actively exploring solutions to mitigate the impacts of Fusarium wilt, along with addressing pest and abiotic stresses affecting banana crops [14,15]. Research institutions worldwide, including the Honduran Foundation for Agricultural Research (FHIA) in Honduras; the African Center for Research on Bananas and Plantains (CARBAP) in Cameroon; the International Institute of Tropical Agriculture (IITA) in Nigeria and Uganda; the Brazilian Agricultural Research Corporation (Embrapa) in Brazil; the National Banana Research Center (NCRB) in India; the National Agricultural Research Organization (NARO) in Uganda; and the International Cooperation Center for Agricultural Research and Development (CIRAD) in France, are collaboratively working towards identifying resistant cultivars [13].

In the exploration of Foc TR4, it was observed that the prevalence of resistant genotypes is linked to diploid genomes. These findings underscore that, currently, resistance sources to Foc TR4 mainly consist of wild or improved diploids, which have not yet been integrated into the development of commercial cultivars through hybridization, unlike Foc R1, benefiting from a broad array of available resistant cultivars [13]. To enhance the genetic diversity of banana cultivars and achieve resistance to Fusarium wilt, researchers globally have been amassing germplasm, including from wild relatives. Despite numerous evaluations conducted in both greenhouse and field conditions, the assessment of resistance to Foc TR4 across a large number of banana genotypes remains notably limited [14,16].

Embrapa employs improved diploids as male parents in crosses with commercial cultivars to develop hybrids. These diploids result from the crossing of different wild diploids, showcasing resistance to key diseases affecting banana cultivation, including yellow Sigatoka, black Sigatoka, and Fusarium wilt. Additionally, they possess other agronomic characteristics of interest for breeding [17]. Notably, the genealogy of some parents of Embrapa's improved diploids, such as Malaccensis, Tjau Lagada, Calcutta 4, and Tuu Gia, includes wild diploids resistant to Foc R1 and black Sigatoka [18]. In Foc R4T research, the parents Calcutta 4 and Tuu Gia emerged as valuable resources for resistance genes, positioning them as promising options for banana breeding and the study of mechanisms resisting Fusarium wilt [5,16,19].

Given the pivotal role of improved diploids in the development of commercial banana hybrids, this study aimed to assess the behavior of 24 improved diploids. The evaluation involves symptomatology analyses post-inoculation with Foc R1 and ST4 in the greenhouse. Additionally, histochemical and histological evaluations were conducted to identify defense responses in the plant-pathogen interaction.

2. Material and Methods

2.1. Fusarium Strains

The isolates belonging to R1 and ST4, identified in the biological collection of the Phytopathology Laboratory of Embrapa and designated as Foc 0801 and Foc 218A, were selected for this study. Foc 0801 serves as a standard for R1, providing a foundational basis for studies [19]. Isolate 218A, collected in the state of São Paulo, induces disease in Nanica (Cavendish), and in previous studies, was characterized as part of VCG 0120, being included as an ST4 isolate [7].

The isolates of Foc R1 and ST4 were multiplied from cultures on plates containing potato dextrose agar, incubated in BODs at a temperature of 25°C with a 12 h photoperiod. After colony growth, the culture medium was prepared, comprising 20 mL of spore suspension and 500 g of autoclaved rice. Incubation occurred in a Biochemical oxygen demand (BOD) at a temperature of 25°C with a 12 h photoperiod. After 20 days, a serial dilution of the infested rice was prepared, and the colony-forming units (CFUs) were counted to adjust concentration and verify spore viability. CFUs were counted using the Neubauer chamber, and the concentration was adjusted to 10⁶ CFU/g of substrate [15,20].

2.2. Plant Materials and Growth

Improved diploids developed by Embrapa were utilized, with the exception of M53 (Jamaica) and SH3263 and SH 3362 (FHIA, Honduras). The rooted plants were transferred to tubes containing substrate and acclimatized in a greenhouse for 30 to 45 days until they reached a height of approximately 15 cm. Twenty-five improved diploids were employed, along with the cultivar Maçã (Silk type), which served as the control. Detailed information on each genotype can be found in Table 1.

2.3. Plant Inoculation

The plants, acclimatized in 3 L pots with a coconut fiber substrate, were individually inoculated with Foc R1 and ST4. For Foc R1 inoculation, infested rice at a concentration of 10⁶ CFU/g was used, distributing a total of 40 g of infested rice in four holes around the plants. In the case of infestation with the ST4 isolate, the experiment was conducted in a greenhouse, utilizing 310 L polyethylene boxes filled with autoclaved soil and infested with the inoculum. Post-rice infestation, soil from the 0 to 20 cm layer of all boxes was collected, and a serial dilution was performed to quantify the concentration, considered ideal at 10⁶ CFU/g.

2.4. Assessment of Symptoms

Internal symptoms were assessed 90 days after infestation (DAI). Measurements associated with internal symptoms were made by crosswise cutting the rhizome and observing discoloration based on the scale proposed by Dita: 1: No symptoms; 2: Initial discoloration; 3: Slight discoloration along the entire vascular system; 4: Most of the internal tissues necrotic; 5: Completely necrotic rhizome [21].

Using the obtained data, the disease severity index (DSI) was estimated following the formula by [22]: DSI = [∑ (disease score × number of plants with the score) × 100] (Number of plants evaluated per genotype × highest score adopted in the scale). Nine plants per treatment (genotype) were used, comprising three replicates for calculating the DSI.

Based on the mean DSI values and the standard deviation of three replicates, the following disease categories were established: highly resistant (HR); resistant (R); moderately resistant (MR); moderately susceptible (MS); susceptible (S); and highly susceptible (HS). Using the internal symptom indices, a hierarchical grouping analysis of the genotypes was conducted based on a heatmap, producing a graphical interpretation where each genotype's data is represented by colors. Shades of green are associated with levels of resistance, while shades of red indicate susceptibility. The statistical package used for the analysis was gplots in the R software [23].

Utilizing the "Performance Analytics" package in R, a Pearson correlation analysis was performed between the DSIs related to Foc R1, Foc ST4, and between the average DSIs of both breeds.

2.5. Histological and Histochemical Analysis

2.5.1. Whitening and Staining of Fungal Structures in Roots

At 90 days after inoculation (DAI), plants were evaluated, and root fragments were collected and immediately immersed in formaldehyde-acetic acid-alcohol solution. Root clarification and staining of fungal structures were carried out according to a method described by Phillips [24] with modifications. For clarification, roots were immersed in a 10% potassium hydroxide solution at room temperature for 48 h and then in a 1% HCl solution for 30 min. Trypan blue dye in a 0.05% solution (lactic acid 2:1:1: glycerol: water) was applied for 1 h to stain the structures. After staining, slides were prepared, and fragments were microphotographed under a light microscope (Olympus Latin America Inc., Tokyo, Japan).

2.5.2. Histochemical Analysis

At 90 DAI, small root fragments were collected and immersed in Karnovsky solution [25]. Fragments remained in the Karnovsky solution for 48 h; they were then dehydrated in an increasing ethanol series at intervals of 3 h each (30–100%). They were infiltrated and embedded with historesin (hydroxyethyl methacrylate, Leica Heidelberg, Germany). After the historesin polymerization process, histological sections (8 μm) were obtained using a Leitz 1516 microtome. The slides were then assembled with the cuts and stained with aniline blue dye [26] to assess the presence of callosity. The histological sections were analyzed and photographed using a B x S1 fluorescence microscope (Olympus Latin America Inc., Tokyo, Japan).

2.5.3. Scanning Electron Microscopy

Root samples were collected at 90 DAI. In the initial steps, the samples underwent dehydration in a series of ethanol and were dried in a critical point apparatus (Leica EM CPD 030) using liquid CO₂. Following this, they were affixed to a metal support (stubs) with double-sided carbon adhesive tape and metallized with gold in a JEOL Smart Coater DII-29010SCTR device. After metallization, micrographs were captured using a JEOL JSM-6390LV scanning electron microscope in the electron microscopy laboratory of the Gonçalo Moniz Institute, FIOCRUZ, Salvador-BA, Brazil.

3. Results

3.1. Screening for Resistance to Foc R1

After 3 months of inoculation, based on cutting the pseudostem close to the rhizome, genotypes were classified regarding the presence of typical symptoms of Foc R1. Improved diploids 013004-04, M53, 050012-02, SH3263, SH3362, 013019-01, CNPMF 0496, 050012-02, CNPMF 0513, CNPMF 0534 showed complete resistance to Foc, exhibiting no symptoms of the pathogen (Figure 1). Improved diploids 058054-03, CNPMF 0993, 001016-01, CNPMF 0542, CNPMF 0557, CNPMF 1323, 013018-02, CNPMF 0612, CNPMF 0731, and CNPF 0998 displayed spots or discoloration around the xylem, classified as resistant. Genotypes with slight discoloration of the rhizome in the vascular system, namely, 013018-01, CNPMF 0536, 086094-20, and 013018-01, were classified as moderately resistant. The genotype 042085-02 with discoloration around the rhizome in the vascular system was characterized as moderately susceptible, while the diploid CNPMF 0519 was characterized as susceptible. The control cultivar, Maçã (Silk type), exhibited over 50% discoloration of the rhizome, categorizing it as highly susceptible to Foc R1.

3.2. Screening for Resistance to Foc ST4

Three improved diploids, 001016-01, CNPMF 0534, and CNPMF 0536, demonstrated complete resistance to Foc ST4, displaying no internal symptoms of the disease (Figure 2). fourteen other genotypes were classified as resistant due to some spots or discoloration around the xylem. Diploids 013004-04, 013018-01, CNPMF 0612, exhibited slight discoloration of the rhizome along with the entire vascular system, categorized as moderately resistant. Regarding susceptibility to Foc ST4, diploids, 013018-02, 086094-20, and 042085-02, were moderately susceptible, the diploid CNPMF 0519 was classified as susceptible, and the cultivar Silk was highly susceptible, following the grading scale used in the evaluation.

3.3. Cluster Analysis between Diploids for Responses to Foc R1 and Foc ST4

The cluster analysis, depicted in the heat map (Figure 3A), considers disease indices per genotype for evaluations of resistance to Foc R1 and Foc ST4. CNPMF 0534 exhibited high resistance to both Foc R1 and ST4, while M53, 050012-02, SH3362, 013019-01, CNPMF 0496, SH3263, CNPMF 0513, and 042085-02 were classified as resistant. Thirteen other diploids fell into the moderately resistant category. Diploids 086094-20 and CNPMF 0519 were grouped as susceptible, and the cultivar Maçã (Silk type) formed an exclusive group as highly susceptible, aligning with expectations. Correlation analysis (Figure 3B) showed a high correlation between evaluations of Foc R1 and ST4 (0.77), Foc R1 and the average of IDs (0.92), and Foc ST4 and the average (0.96), indicating similar responses to the two races.

3.4 Histological and Histochemical Analyses

Irrespective of diploid behavior, whether resistant or susceptible, pathogen structures were observed in the roots of most evaluated genotypes. Notably, the highly resistant CNPMF 0534 exhibited Foc R1 microconidia in the roots, similar to observations in the cultivar Maçã (Silk type). Conversely, for Foc ST4, no Foc structures were detected in the roots of CNPMF 0534, possibly due to either fungus non-penetration or incapacity to colonize tissues post-penetration (Figure 4). In diploid M53, fungal hyphae and spores were observed in interaction with Foc R1, while only spores were seen with Foc ST4. Diploid 013018-01, classified as moderately resistant, displayed the presence of spores and hyphae in the tissues. The cultivar Maçã (Silk type) exhibited an abundance of spores in interaction with both isolates (Figure 4).

Upon staining root tissues with aniline blue dye to assess callose production, blue-white fluorescence indicated the presence of this mechanism. CNPMF 0534 exhibited pronounced fluorescence when inoculated with isolates Foc R1 and ST4 after 90 DAI (Figure 5). The resistant diploid M53 also displayed fluorescence, indicating callose presence (Figure 5). Diploid 013018-01, moderately resistant, showed less callose emission. The cultivar Maçã (Silk type), when inoculated with isolates R1 and ST4, displayed slight fluorescence, indicating low levels of callose.

The scanning electron microscopy (SEM) study examined the interaction between genotypes contrasting in susceptibility or resistance to Foc R1 and ST4 at 90 DAI. In both cases, variability in structures and tissue reactions was observed, including abundant calcium oxalate crystals, varying in quantity and shape, and signs of tissue obstruction by gums and fungal structures such as mycelium, hyphae, and spores.

The highly resistant CNPMF 0534 diploid produced calcium oxalate crystals in the tissue (Figure 7.A1), as well as gums (Figure 7.A2) and vessel occlusion (Figure 7.A3). Resistant diploid M53 showed a significant deposition of calcium oxalate crystals on the vessels and spores of the pathogen on the tissue (Figure 7.B1, B2). Moderately resistant diploid 013018-01 exhibited intense infection by Foc R1, with concentrated spores in the tissues and the presence of some calcium oxalate crystals (Figure 7.C1, C2, C3). In the cultivar Maçã, the study revealed the growth of hyphae, fungal mycelium, and obstruction of conducting vessels (Figure 7. D1, D2, D3).

In the interaction between genotypes and Foc ST4, diploid CNPMF 0534 exhibited intense production of calcium oxalate crystals in the form of a druse (Figure 8.A1). No vessel occlusions were observed; instead, scattered spores throughout the tissue were seen, still in the process of germination, indicating delayed fungal growth, considering the analysis at 90 DAI (Figure 8.A2, A3). Resistant diploid M53 showed minimal vessel occlusion; however, mycelial growth was observed in some spaces where occlusion occurred (Figure 8.B2). Moderately resistant diploid 013018-01 displayed vessel occlusion, hyphae growth (Figure 8.C2), and the presence of calcium oxalate crystals. The cultivar Maçã (Silk type) showed spores, calcium oxalate crystal production in the form of a druse similar to a needle (Figure 8.D3), and thylose deposition (Figure 8.D1), characterized as the physiological process of xylem occlusion.

4. Discussion

In this study, we assessed 24 improved banana diploid hybrids for resistance to Foc R1 and ST4 in a greenhouse setting. The diploids were categorized as highly resistant, resistant, moderately resistant, moderately susceptible, susceptible, and highly susceptible based on the mean values of rhizome discoloration index. Selected for further analysis were CNPMF0534 (highly resistant), M53 (resistant), 013018-01 (moderately resistant), and the cultivar Maçã - Silk type (highly susceptible) as a control. Among these, only the diploid hybrid CNPMF0534 exhibited resistance to both races, displaying no characteristic vascular bundle discoloration in the rhizome, with all nine plants scoring one.

By averaging the scores and calculating the standard deviation from 10 repetitions for the diploid response profiles to both races, we observed that 10 genotypes were grouped in the highly resistant category against Foc R1. In contrast, only three were grouped in this category when evaluated against Foc ST4 (Figure 1 and Figure 2). Notably, differences between categories emerged, as two diploids were classified in the interaction with Foc ST4, whereas none received this classification in the interaction with Foc R1.

These findings are linked to the known virulence and aggressiveness of ST4 isolates in environmental conditions featuring temperature extremes, such as intense cold prevalent in certain regions of Brazil [8,27]. The data underscore the importance of using appropriate Foc isolates and methods that exert the necessary selection pressure to draw accurate conclusions about resistance, both in the greenhouse and subsequently in the field, as practiced in other studies [5,16,28].

In a cluster and correlation analysis, utilizing estimated Foc R1 and Foc ST4 IDs, we demonstrated that hybrids are classified in the same categories for both races. There is a positive correlation between evaluations of Foc R1 and ST4 IDs, as well as the average of both (Figure 3B). To our knowledge, this is the first report correlating resistance profiles to Foc R1 and ST4 based on disease index estimates. These data reinforce the accuracy of the selection method adopted by the Embrapa breeding program in Brazil for over twenty years and suggest that all plant materials that have been selected and indicated as resistant to Foc R1 over these years may also be resistant to Foc ST4 and possibly to Foc TR4, such as the hybrids BRS Platina (Prata type, AAAB) and BRS Princesa (Silk type, AAAB), already widespread in the Brazilian market.

Previous studies by Gonçalves et al. [18] described the resistance capacity of improved diploids developed by Embrapa to Foc R1 under field conditions. The diploids CNPMF 1323, CNPMF 0612, CNPMF 0534, CNPMF 0998, CNPMF 0731, and CNPMF 0542 exhibited resistance to Foc R1, aligning with the results of the present work. These improved diploids have parents such as Calcutta 4, M53, Malaccensis, Tjau Lagada, M61, and Tuu Gia, all confirmed to be resistant to R1 and ST4 [16,18,19,29].

From our histological analyses, we have observed no distinction between highly resistant and susceptible genotypes concerning the presence of Foc R1 within tissues post-bleaching and staining with Trypan blue. This reaffirms that penetration occurs in both cases, suggesting that defense strategies distinguishing resistant from susceptible genotypes manifest after the penetration process. This aligns with findings by Li et al [30], Rocha et al [7] Rocha et al [27]; and Ferreira et al [15]. Conversely, in the interaction with Foc ST4, a notable difference was observed in the CNPMF 0534 diploid. This diploid, considered highly resistant, did not exhibit pathogen structures inside the tissue, possibly associated with the absence of penetration or advancement in colonization. SEM analysis confirms this observation, revealing only calcium oxalate crystals inside the tissue, and the spores were still in the process of germination, indicating a delay in infection (Figure 8.A1, A3).

These findings parallel those obtained in a study of genotypic interaction with Foc ST4, aiming to select and evaluate resistant banana somaclones. The absence of pathogen structures in root tissues suggests that resistant somaclones may have developed physical and/or chemical barriers to impede pathogen penetration [15,31].

In SEM analyses, we consistently observed the presence of calcium oxalate crystals, with quantity and distribution in the tissue seemingly associated with genotypes classified as resistant. While specific data on the direct influence of these crystals on resistance are lacking, studies have documented their varied forms and functions across more than 215 plant families. Other research suggests that these crystals play a crucial role, as their degradation can produce reactive oxygen species linked to the response to pathogen infection and the inhibition of such infections [32,33].

Our results align with previous findings indicating abundant calcium oxalate crystals in the cultivar BRS Platina, a tetraploid banana hybrid of the Prata subgroup, inoculated with Foc ST4. These crystals may play vital roles in resistance [27]. Furthermore, we emphasize the importance of conducting additional studies to investigate the role of calcium oxalate crystals not only in the resistance of banana genotypes to Fusarium wilt but also their role and differences in wild diploid genotypes. These wild diploids form the basis for genetic improvement and are the primary source of genetic variability in Musa spp.

In the histochemical analyses, evaluating plants' response to fungal attack through the production of chemical compounds, callose was assessed. All genotypes exhibited fluorescence, indicating the presence of this compound. However, in the diploid CNPMF 0534, identified as highly resistant, notably high levels of fluorescence were observed, suggesting a potential increase in production during interactions with both Foc R1 and Foc ST4 (Figure 5). This could be linked to the fact that callose deposition is induced by various factors, particularly biotic and abiotic stresses, such as pathogen attacks, exposure to heavy metals, and wounds [34]. The formation of callose, gels, and tyloses in infested vessels has been reported in resistant banana plants as a mechanism to immobilize spores, preventing their invasion during the pathogen-host interaction [35,36].

The improved diploids M53, 013004-04, 013018-01, 013018-02, 013019-01, CNPMF0542, CNPMF0612, and CNPMF1323 result from crosses with wild diploids like Malaccensis, Pahang, Calcutta-4, Pisang Lilin, and Tuu Gia, which are part of their genealogy. These diploids have been previously reported for their resistance to Foc TR4 [13]. The Malaccensis diploid stands out as a promising candidate for crosses with elite cultivars to transfer resistance alleles to Foc, given its relevant breeding characteristics. The resistance of this diploid can be further explored by isolating a resistance gene (R) of the putative nucleotide-binding and leucine-rich repeat type from Musa acuminata ssp. Malaccensis, which has been utilized in transgenic experiments [37,38].

Besides the Malaccensis diploid, 10 genotypes, including four wild diploids (Jaran, Birmanie, Pipit) and a tetraploid hybrid of the Silk type developed by Embrapa named BRS Princesa (from the cross between Yangambi Nº2 - AAB, and the M53 diploid - AA), were classified as resistant to Fusarium wilt. The Pahang diploid, extensively studied, has demonstrated resistance to Foc TR4 in both greenhouse and field experiments [16,39,40] In a study by Zuo et al [16] 129 accessions from the germplasm bank were evaluated for resistance to Foc TR4 in both greenhouse and field conditions, identifying DH Phang, Tuu Gia, Calcutta 4, and Borneo as highly resistant. These genotypes also contribute to the genealogy of some improved diploids assessed in this study, such as 013019-01, CNPMF 0557, CNPMF 0496, and CNPMF 0731, all characterized as resistant to both Foc R1 and ST4. Based on the genealogy of the diploids under study, a potential resistance to TR4 in these hybrids can be hypothesized, warranting confirmation under natural or artificially induced pathogen infestation conditions.

The comprehensive analyses conducted in this study suggest that the resistance observed, particularly to Foc ST4, in some of the evaluated improved diploids may be inherited from their parent genotypes. Notably, diploids CNPMF 0534 and CNPMF 0536, classified as highly resistant to Foc ST4, have Calcutta 4 in their genealogy, while those grouped as resistant have Malaccensis and Tuu Gia. These wild relatives of edible bananas are recognized as valuable sources of resistance genes to Foc TR4 [13,16,30]. Furthermore, diploid hybrids 001016-01, CNPMF 0534, and CNPMF 0536, displaying total resistance to black Sigatoka, hold potential for crosses with susceptible commercial cultivars to transfer resistance alleles to commercial germplasm [18]. The diploid M53, used as a parent in crosses for generating commercially relevant cultivars, has been identified as resistant to Foc R1 [18,29], with previous reports confirming its resistance to Foc TR4 in a heavily infested field in Australia [42].

Consequently, the results discussed herein can significantly contribute to banana breeding programs. The improved diploids identified as resistant have the potential for use in crosses with commercial cultivars, particularly 001016-01, CNPMF 0534, and CNPMF 0536, exhibiting high resistance to Foc ST4, and 013004-04, M53, 050012-02, SH3263, SH3362, 013019-01, CNPMF 0496, CNPMF 0513, and CNPMF 0534, displaying high resistance to Foc R1. Moreover, the diploid hybrids evaluated as resistant or moderately resistant for both races, with low Fusarium wilt symptom scores, can be considered quantitatively resistant. These hybrids are valuable for transferring genes with minor effects, easily selectable, and efficient in cultivation systems based on integrated management.

5. Conclusion

The screening conducted in this study, under the specified conditions, facilitated the selection of diploid hybrids 001016-01, CNPMF 0534, and CNPMF 0536, highly resistant to Foc ST4, and 013004-04, M53, 050012-02, SH3263, SH3362, 013019-01, CNPMF 0496, CNPMF 0513, and CNPMF 0534, highly resistant to Foc R1, exhibiting no symptoms of Fusarium wilt in the greenhouse. Remarkably, diploid CNPMF0534 demonstrated complete resistance to both evaluated races, with its resistance to Foc ST4 possibly attributed to impeding fungal penetration.