Haitian Yu1,2*
Feng Yang1Chaoqin Hu1Xin Yang1Aiqing Zheng1Yubao Wang1Yongsheng Tang3Yuhua He1*Meiyuan Lv1*- 1Institute of Food Crops, Yunnan Academy of Agricultural Science, Kunming, Yunnan, China
- 2Department of Agricultural, Food and Nutritional Science, University of Alberta, Edmonton, AB, Canada
- 3Qujing Academy of Agricultural Sciences, Qujing, Yunnan, China
China is the largest producer of faba bean with a total harvested area of 8.11×105 ha and a total production of 1.69 ×106 tons (dry beans) in 2020, accounting for 30% of the world production. Faba bean is grown in China for both fresh pods and dry seed. East China cultivates large seed cultivars for food processing and fresh vegetables, while northwestern and southwestern China grow cultivars for dry seeds, with an increased production of fresh green pods. Most of the faba bean is consumed domestically, with limited exports. The absence of unified quality control measures and simple traditional cultivation practices contributes to the lower competitiveness of the faba bean industry in international markets. Recently, new cultivation methods have emerged with improved weed control, as well as better water and drainage management, resulting in higher quality and income for producers. Root rot disease in faba bean is caused by multiple pathogens, including Fusarium spp., Rhizoctonia spp., and Pythium spp. Fusarium spp. is the most prevalent species causing root rot in faba bean crops and is responsible for severe yield loss, with different species causing the disease in different regions in China. The yield loss ranges from 5% to 30%, up to 100% in severely infected fields. The management of faba bean root rot disease in China involves a combination of physical, chemical, and bio-control methods, including intercropping with non-host crops, applying rational nitrogen, and treating seeds with chemical or bio-seed treatments. However, the effectiveness of these methods is limited due to the high cost, the broad host range of the pathogens, and potential negative impacts on the environment and non-targeted soil organisms. Intercropping is the most widely utilized and economically friendly control method to date. This review provides an overview of the current status of faba bean production in China, the challenges faced by the industry due to root rot disease, and the progress in identifying and managing this disease. This information is critical for developing integrated management strategies to effectively control root rot in faba bean cultivation and facilitating the high-quality development of the faba bean industry.
1 Introduction
Faba bean (Vicia faba L.), native to the Mediterranean and Central Asia, is an important legume crop that can be used as food for human consumption and as livestock feed (Crépon et al., 2010). The characteristics of high protein content in seed and straw, the high efficacy of root-rhizobia in nitrogen fixation, the good potential in soil quality improvement (Duchene et al., 2017), and the good adaptation in different habitats (Singh et al., 2013) make it well recognized and widely cultivated in the world.
While the production of primary crops such as wheat, rice, maize, and sugarcane has increased 52% from 2000 to 2021 (9.3 billion tons) (FAOSTAT, 2022), the challenges posed by climate change and loss of quality and area of arable land are limiting crop production (Döös, 2002; Shi et al., 2016; Snowdon et al., 2021). Additionally, global water stress and rising hunger (Alcamo et al., 2007; Oxford Analytica, 2019), with most of the undernourished population living in Asia and Africa, are increasing stress on agricultural production. To meet the food needs of the rapidly growing world population, a 70% increase in food production by 2050 is suggested by the FAO (Food and Agriculture Organization of the United Nations) (Kuttibai et al., 2022). The overuse of chemical fertilizers and pesticides to achieve high yield, although to a lesser extent, also impairs agricultural sustainability and human health (Liu and Wu, 2022). As reported by the FAO, over 200 million tons of fertilizers, with 56% nitrogen, were applied in 2020 and pesticide use has increased by 30% since 2000. These factors emphasize the importance of increasing the cultivation and utilization of legume crops in agriculture, which will diversify the agroecosystem, reduce pest stress, lower nitrogen fertilizer inputs, improve soil quality, and increase the availability of legume protein for nourishing the needy population (Costanzo and Bàrberi, 2014; Duchene et al., 2017; Blesh, 2019; Zhang et al., 2019).
The production of legume crops, including faba bean, is crucial to alleviate the increasing challenges in crop production such as global food stress, land degradation, and overuse of chemicals. However, various abiotic and biotic factors can hamper legume productivity (Varshney et al., 2009). Root rot disease associated with Fusarium wilt is considered as one of the major constraints on legume production (Liebenberg, 2002; Infantino et al., 2006; Singh and Schwartz, 2010) and has been reported to cause severe disease in faba bean (Sillero et al., 2010; Hou et al., 2011; Paul and Gupta, 2021). In faba bean production in China, root rot and wilt disease caused by various fungi including Fusarium spp., Rhizoctonia solani, and Pythium debaryanum are a major challenge, leading to yield losses of 5%–30% and even up to 100% under favorable environmental conditions (Dong et al., 2014a; Zhang et al., 2018). Charcoal rot caused by Macrophomina phaseolina has also been recently reported in Yunnan province (Sun et al., 2019; Yu et al., 2021). This review summarizes the status of faba bean production in China and the research advancement on root rot and wilt diseases, providing crucial information for future strategies in the development of the faba bean industry and integrated disease management.
2 Status of faba bean production of China
According to data from the FAO from 2001 to 2020, China led the world in faba bean production, with total harvested area and production of dry bean both accounting for more than 30% of the total global amount. In 2020, China and the world produced 1.69×106 and 5.68×107 metric tons of faba beans, respectively, with total harvested areas of 8.11×105 and 2.66×106 ha, respectively (dry beans), followed by Ethiopia, Australia, and the UK (FAOSTAT, 2022). In the past 20 years in China (Figures 1, 2), the lowest area harvested and the resulting production of faba bean was seen in 2014, which then reached a relatively stable level between 2016 and 2020. Compared to 2001, the harvested area and production of faba bean have decreased by 37.62% and 11.61%, respectively, by 2020. The shift in land use in Yunnan province from faba bean cultivation to vegetable cultivation, due to the desire for higher income crops, contributed to the decrease (Yu et al., 2019a). Despite the reduction in the harvested area and production, the increase in average yield of faba bean, from 1.47 tons·ha−1 to 2.12 tons·ha−1 (FAOSTAT, 2022), has helped compensate for the losses. Furthermore, there is still a huge potential for improvement, as the yield of faba bean in the regional trials in Yunnan was more than 3.0 tons·ha−1. In China, most of the fresh beans and over 90% of the dry products were consumed domestically. However, importation of fresh beans has not been reported since 1961 and imports of dry beans, from 2014 to 2020, was limited to a few hundred kilograms, with most of the faba bean imported from ICARDA and used as germplasm for research purposes. Furthermore, the quantity of dry seeds exported out of China accounted for only 0.5%–2.5% of the total production in China and 0.66%–8.24% of the total production in the world (Figures 3, 4). The trend of decreased exports has lasted for more than 10 years (FAOSTAT, 2022). The low level of importation suggests a high degree of self-sufficiency, and a low level of export is attributed to the low consistency and quality of the faba bean product. Conversely, Australia, the third leading producer of faba bean, is the leading exporter (Johnson et al., 2021; Dhull et al., 2022) and is highly competitive in international markets because of consistent, high-quality commodity production (AEGIC, 2019).
Figure 1 Harvested area of faba bean of china and the World from 2001 to 2020.
Figure 2 Production of faba bean of China and the World from 2001 to 2020.
Figure 3 Exporting quantity of faba bean of China and the world from 2001 to 2020.
Figure 4 Proportion of Exporting quantity of faba bean in total production of China from 2001 to 2020.
Faba bean is traditionally cultivated in most parts of China, except for the northeast provinces of Heilongjiang, Jilin, and Changchun (Ye et al., 2003). The cultivation region of faba bean crosses large latitudinal and longitudinal ranges. The ecotype of faba bean was classified into the winter ecotype (between 21°N and 35°N latitude), basically sown between August and December and harvested from March to May of the next year, and the spring ecotype (between 31°N and 53°N latitude), sown between February and May and maturing in the fall season (Ye et al., 2003; Wang et al., 2012; Yu et al., 2019a). Typically, the northern and northwestern provinces are the regions for the spring ecotype, whereas the central, east, and southwest areas of China normally cultivate the winter faba bean (Lang et al., 1993; Wang et al., 2012). All parts of the faba bean plant, fresh or dry, were well utilized in China, usually eaten as a vegetable (fresh seed, pods, and plant shoots), used as food (dry seed), used in livestock (all parts), and used as a natural nitrogen resource for the agricultural system (all parts) (Ye et al., 2003; Yu et al., 2020), with dry beans being the major product. Cultivation of faba bean in China (Table 1) and the intended market is determined by seed size (Ye et al., 2003). Different cultivars have been developed for various purposes, with big seed cultivars [(hundred seed weight (HSW) > 120 g] used for both food processing and fresh vegetable use, while medium (70 g ≤ HSW ≤ 120 g) and small (HSW < 70 g) seed cultivars are mainly used for food processing and as fodder. The traditional landraces have been replaced by newly bred cultivars, which were developed by different agricultural science academies (Bao et al., 2008; Wang et al., 2020a; Xiang et al., 2022; Yu et al., 2019a). Besides the use of traditional cultivars, breeding and testing new germplasm, and breeding cultivars for special use are emerging purposes (Du, 2021; Yu et al., 2019b). For example, in Chongqing, there is a registered cultivar of faba bean that is used both as an ornamental plant, due to its pink color and defined inflorescence, and as a source of dry seed. This makes it unique when compared to other faba bean cultivars that are primarily grown for their pods or seed (Du, 2021).
Table 1 Harvested area of faba bean in the main producing province or autonomous region in China.
In East China, production of fresh green pods of faba bean has been commercially well-developed (Zhou et al., 2022). The cultivars of Tongcanxian series and Qidou series, the landraces Cixidabaican and Haimendaqingpi, and the introduced cultivar Lingxiyicun are commonly grown in East China, with a harvested area of approximately 7–8×104 ha. In the northwestern part of China, particularly the provinces of Qinghai, Gansu, Ningxia, and Xinjiang, faba bean is typically harvested for dry seed upon reaching maturity. The Qingdou and Lincan series cultivars are commonly grown in this region, with a harvested area of 2.4–3.0 ×104 ha and 7 × 104 ha, respectively. The cultivation area of faba bean in Gansu alone accounts for over 60% of the total spring faba bean cultivation area in China (Li and Nan, 2000; Hou et al., 2011). In the top-producing region of faba bean, located in southwest China, the crop is predominantly grown for dry seed with an increasing area for fresh green pods production (Yu et al., 2019a; Zhou et al., 2022). Yunnan and Sichuan are the first and second largest producers of faba bean in China, respectively, with more than 30% of faba bean cultivated in Yunnan (Yu et al., 2020). In Sichuan, approximately 1.4× 105 ha of faba bean were harvested in 2022 for both fresh and dry pods, with most of the dry faba bean processed into paste (Xiang et al., 2022).
The cultivation of faba bean in these regions usually involves crop rotation with paddy rice, wheat, oil crops, and other spring crops. In some southwest provinces, such as the mountainous region of Yunnan, early autumn and summer season cultivation is becoming more recognized as a special production of fresh faba bean at an altitude of 2,000 m above the sea level (Yu et al., 2019a). Additionally, Yunnan has a distinct advantage over other production regions, as it has a very diverse agricultural ecosystem at altitudes between 1,500 and 3,000 m above sea level that allows for the production of faba bean in multiple seasons, extending the marketing time (Bao, 2016; Yu et al., 2019a). Traditionally, farmers in Yunnan used broadcast sowing with surface soil tillage and crop rotation with dry land crops as well as direct seeding after rice (Oryza sativa) harvest. These methods were widely used due to their cost-effectiveness and high efficiency in nitrogen utilization for the succeeding crop. Recently, new cultivation patterns have been developed in Yunnan, including intercropping with perennial fruit trees such as grape, kiwi, date, and berry, as well as mulching-film side seeding, early autumn seeding, and off-season planting methods. These new methods have been recognized for their advantages, such as improved weed control, better capacity in providing or maintaining water and improving drainage, combined with higher quality and income for producers. Compared to traditional methods, these new patterns are more intensive and suitable for commercial and large-scale production of green beans, and have expanded the plantation region to cooler and higher elevation areas (Bao, 2016; Yu et al., 2018; Yu et al., 2019a).
In China, diverse habitats for cultivation provide a strong foundation for the high-quality and high-yield development of the faba bean industry. Over the past two centuries, based on the national developed research system, significant efforts have been made in cultivar breeding and improving cultural practices. However, the cultivation of faba bean in China is still challenged by the varying environmental conditions in different regions. Further research is necessary to enhance cultural practices that are tailored to the specific needs of each region and production purpose. This will contribute to the goal of achieving high-quality and high-yield production of faba bean. In addition, implementing a standardized quality testing system is critical to the growth and development of the faba bean industry in China.
3 Identification of root rot disease in China
The root rot disease of faba bean can be caused by a number of different pathogens, including Fusarium spp., Rhizoctonia spp., Pythium spp., Phoma spp., and Aphanomyces spp. (Rubiales and Khazaei, 2022). The group of pathogens is often referred to as the root rot complex, with Fusarium spp. being the most commonly identified species causing foot and root rot, as well as wilt diseases, in faba bean in China (Table 2).
Table 2 Disease incidence and yield losses caused by Fusarium spp. in a major producing province or autonomous region in China.
In Qinghai province, Fusarium spp. was responsible for severe yield loss, which caused wilt disease in the field with disease incidence ranging from 44% to 68% (Chen, 1999). Fusarium wilt, caused by Fusarium oxysporum, has been reported, but root rot caused by Fusarium solani is considered the major constraint on faba bean production in Qinghai (Wang et al., 2006). In the cold and humid regions of Gansu province, root rot disease caused by Fusarium spp. is a major constraint on faba bean production. The disease can result in yield losses of up to 90% under favorable conditions. Fusarium solani is the dominant species, followed by Fusarium semitectum and Fusarium dimerum (Hou et al., 2011). In addition, Fusarium avenaceum was also a commonly identified species causing root rot in faba bean crops. Other pathogens, including Gliocladium roseum, F. oxysporum, Phoma spp., Pythium spp., Alternaria spp., and R. solani, were also identified (Li and Nan, 1996). In Zhejiang province, located in the eastern part of China, the most significant pathogens causing root rot in faba bean were identified as Fusarium acuminatum, F. oxysporum, Fusarium moniliforme, F. moniliforme var. subglutinans, and F. solani. These species were determined based on their frequency of occurrence and pathogenicity index. Additionally, F. semitectum and Fusarium tricinctum were also confirmed (Bao et al., 1992). In Fujian province, the frequency of stem wilt disease caused by F. oxysporum increased since 2010, resulting in yield losses of 5% to 12% in 2013, and over 85% of the faba bean fields were infected (Wang, 2013). In Jiangsu province, a large amount of root and stem rot diseases were observed in the field, with 10% to 30% of plants dying and up to 40% in fields with severe infection. Fusarium spp. was identified as the major causal agent, the top four isolated species being F. oxysporum, F. avenaceum, F. moniliforme, and Fusarium equiseti. All the four species showed high virulence on faba bean (Ren et al., 2003).
In Yunnan province, wilt disease, stem rot, and root rot usually occurred in faba bean simultaneously (Figure 5), with major pathogens including F. oxysporum, F. avenaceum, F. solani, R. solani, and P. debaryanum Hesee (Wang et al., 2002a). Furthermore, after treatment with the secondary metabolite of F. oxysporum, the wilting symptom was also clearly observed on pea (Pisum sativum), common bean (Phaseolus vulgaris), cowpea (Vigna unguiculata), and maize (Wang et al., 2002b), which suggested the non-specific toxicity of the pathogen. Fusarium oxysporum is dominant at the seedling stage, causing stem rot, while F. avenaceum is more commonly associated with stem rot and wilt in mature plants (Wang et al., 1988). Based on a provincial survey on faba bean, Fusarium spp. is the main genus causing seedling root rot, with F. oxysporum and F. avenaceum being the most frequently isolated species. Rhizoctonia solani was identified as having the highest virulence among all the isolates, followed by F. oxysporum and Fusarium sporotrichioides (Ruan et al., 1986). Host range studies showed that F. avenaceum, isolated from the stem of faba bean, caused severe stem and root rot on faba bean and pea, and induced wilt and necrosis symptoms on the leaf of vetch (Vicia cracce). However, no infection was found on wheat, maize, common bean, or 35 other crops from 11 different genera (Ruan et al., 1982). Charcoal rot caused by M. phaseolina (Tassi) Goid has recently been reported as a problem for faba bean in Yunnan, causing serious yield losses due to root rot, leaf chlorosis, and wilting; eventually, plant death occurred with the necrosis leaf attached (Sun et al., 2019; Yu et al., 2021).
Figure 5 Root rot and wilt symptoms in faba bean in the field of Yunnan.
In Xinjiang province, root rot disease on faba bean has been a significant problem since 2009, leading to yield losses of nearly 100% in severely infected fields. The top three prevalent pathogens were identified as Fusarium spp., Rhizoctonia spp., and Alternaria spp. through molecular and morphological characterization (Duan, 2021). Additionally, Fusarium chlamydosporum var. fuscum was reported to cause severe root and basal stem rot diseases (Chu et al., 2019). In Hubei province, Fusarium proliferatum was reported as a causal agent of faba bean root rot (Zhao et al., 2011).
Generally, root rot and wilt diseases are prevalent in faba bean cultivation regions across China, which can cause 100% yield loss under severe conditions. The predominant causative agent of these diseases is the genus Fusarium, with different species dominating in different regions. Similarly, Fusarium spp. has been reported as the most common pathogen causing foot and root rot in faba bean globally (Sillero et al., 2010; Šišić et al., 2020). However, the characterization of Fusarium spp. at diverse taxonomic levels and the impact of the pathogens on the disease development have been investigated to a lesser extent in China and worldwide, although it is crucial for the development of resistant varieties and integrated management strategies. Additionally, most of the studies conducted in China were carried out many years ago, highlighting the need for more recent studies to obtain more accurate information on the causal agents.
4 Management of root rot disease in China
Management strategies for root rot have included fungicide treatments, crop rotation, and variety selection, with the most cost-effective strategy being the use of resistant varieties (Marburger et al., 2014; Dolatabadian et al., 2022). However, the availability of resistance to root rot is limited (Rubiales and Khazaei, 2022). Crop rotation can also be an effective strategy but is limited by the broad host range of the pathogens (Bullock, 1992; Cook, 2006; Hwang et al., 2009; Marburger et al., 2014). Fungicide seed treatments are widely used but their efficacy varies depending on the specific species of Fusarium and may also have negative impacts on soil organisms and the environment (Munkvold and O’Mara, 2002; Broders et al., 2007; Ellis et al., 2011; Esker and Conley, 2012; Chang et al., 2014).
The management of faba bean root rot disease in China involves various methods, including physical, chemical, and bio-control approaches. One widely used strategy is intercropping with non-host crops, such as wheat, which has been shown to increase the diversity of rhizosphere fungi, reduce the incidence of faba bean root rot disease, and decrease the presence of Fusarium spp. in the soil (Luo et al., 2012). Intercropping with wheat has also been reported to decrease the content of citric and malic acid in the rhizosphere, resulting in reduced incidence and severity of Fusarium wilt disease caused by F. oxysporum (Xiao, 2013). Moreover, intercropping with wheat has been shown to increase the diversity of the rhizosphere microorganism, promote plant tissue integrity and growth, suppress the cinnamic acid-induced stress, alleviate the autotoxicity of faba bean, and increase the gene copy number of Bacillus brevis, which can alleviate the effects of Fusarium wilt on the faba bean crop (Dong et al., 2013a; Dong et al., 2017; Lv et al., 2020; Wang et al., 2020b; Guo et al., 2021; Zhang et al., 2023). Furthermore, intercropping faba bean with different wheat cultivars, such as Yunmai 42 and Yunmai 47, has been shown to significantly reduce the disease index of Fusarium wilt and improve rhizosphere microbial activity and diversity. The significant increase in the total content of organic acids and reduction in the levels of soluble sugar and free amino acids in the root exudates of Yunmai 42 and Yunmai 47 were identified as the main reason for the reduction in Fusarium wilt disease (Yang et al., 2014). In field conditions in Gansu, intercropping faba bean with potato in a 2:2 row ratio reduced Fusarium wilt incidence by 5.66% and disease index by 1.6 (Zhang et al., 2020). Faba bean density was also tested, with results showing that 12×105 plants per hectare had the lowest disease incidence and index, and the highest hundred seed weight and yield (Zhang et al., 2018). Under controlled environmental conditions, faba bean grown in soil collected from diseased fields had the lowest plant death rate at 50% water holding capacity (WHC), while growth parameters were significantly better at 50% WHC than at 30% or 70% WHC (Li and Nan, 2000).
The application of nitrogen has been found to be an effective method to control Fusarium wilt in faba bean by altering the composition and metabolic function of the rhizospheric microbial community and reducing the density of F. oxysporum (Dong et al., 2013b). In Zhejiang, a field study was conducted to investigate the effect of a 3% plant activator protein extracted from Alternaria spp. on root rot caused by F. solani. The results showed that leaf application of a 1,000-times diluted plant activator protein at the seedling stage reduced the disease index by 85.5% compared to the non-treated control (Wu et al., 2006). Similarly, the use of root exudates from different faba bean cultivars can increase resistance to Fusarium wilt by reducing the total content of free amino acids and soluble sugar and increasing organic acids (Dong et al., 2014b).
Inoculation of faba bean with arbuscular mycorrhizal fungi (AMF) species has also been found to enhance the plant’s ability to resist Fusarium wilt and improve microbial carbon metabolic activity in the rhizosphere soil (Dong et al., 2019). Additionally, some rhizobacteria and Bacillus subtilis strains have been shown to inhibit the growth of F. oxysporum and F. chlamydosporum var. fuscum, respectively, which are known to cause root rot in faba bean (Wang et al., 2018; Chu et al., 2019). In Xinjiang, the use of bio-control agents, either as seed treatment, root irrigation, or applied at the time of seeding, showed a significant reduction in disease incidence and an increase in yield (Duan, 2014). The results of a study conducted in Qinghai indicated that the use of two biological pesticides, Paenibacillus polymyxa and Trichoderma harzianum, was effective in reducing the disease index of Fusarium wilt in faba bean. Application of 1 billion cfu·g−1 of P. polymyxa reduced the disease index by 74.23%, while application of ≥200 million live spores·g−1 of T. harzianum reduced it by 71.01% (Zhang et al., 2022).
A 2-year field study on faba bean root rot control found that applying triadimefon (0.01 g·kg−1 seed) showed the best efficacy, reducing disease index by 51.5% and death rate of mature plants by 31.9%–36%, while increasing seed yield by 19.6%–97.6% (Nan et al., 2002). In vitro tests demonstrated that tebuconazole and prochloraz were the most effective fungicides in inhibiting the growth of Fusarium spp. and the germination of conidia spores. In field trials, the best seed or root treatment was found to be a combination of prochloraz and B. subtilis at a ratio of 1:1 (v:v), with concentrations of 104 μg·ml−1 and 2×1010 cfu·ml−1, respectively. This treatment reduced the disease index by 44.67%–52.21% across several field sites (Ren, 2002).
In China, a few cultivars with moderate to high resistance to F. oxysporum have been mentioned (Dong et al., 2014b), but the genetic basis of resistance has yet to be explored. Similarly, in Egypt, sources of resistance to F. oxysporum and F. solani were reported in faba bean, mostly moderate resistance, but no further studies were conducted to explore the genetic mechanisms (Ali et al., 2019; Mahmoud and Abd El-Fatah, 2020).
In summary, various methods have been found to be effective in reducing the incidence of root rot and wilt disease in faba bean in China. Most of the research has focused on the pathogen F. oxysporum, and control of other Fusarium species and other pathogens has been less investigated. In Egypt, intercropping faba bean with garlic, as well as with onion and caraway, along with AMF inoculation can reduce root rot disease and enhance profitability and sustainable production (Abdel-Monaim and Abo-Elyousr, 2012; Mousa and El-Sayed, 2016; El-Mehy et al., 2022). Bio-control agents, such as Paenibacillus spp., Bacillus spp., and Trichoderma spp., all exhibited good potential in suppressing root-related disease in faba bean (Alfauomy and Atwa, 2020). Although biological control has shown promising results on the control of root rot disease, it has not been widely applied in faba bean production because of its cost. Chemical control is widely used, but the timing of application is crucial, as it can be difficult to control the disease once it has already started in the field. While resistance to stem, foot, and root rots has been reported in some germplasms of faba bean, no genetic information was reported. Understanding the genetic mechanism of resistance to Fusarium species and pathogens from other genera is essential for the development of effective disease control strategies, including resistance breeding. Developing an integrated management strategy that takes into account multiple factors and adopts a holistic approach is crucial to effectively controlling root rot disease in faba bean in China.
5 Conclusion
As a leading country, China plays an irreplaceable role in faba bean production worldwide. The long history of cultivation and diverse habitats across the country allow year-round and multipurpose production to meet domestic needs. However, the lack of standard criteria for quality control, as well as traditional extensive cultural practices, lowers the competitiveness of faba bean products in international markets. Root rot and wilt disease pose another threat to the development of the faba bean industry. Studies on the identification and control of these diseases are still in the primary stage, with little systemic understanding of exploiting the diversity of the causal agents to integrated disease management strategies. To facilitate the faba bean industry development domestically or internationally, it is extremely important to set unified standards for agricultural products, change cultural practices to more intensive methods, and conduct systemic projects to explore knowledge regarding the characteristics of the pathogens involved in root-related diseases and the integrated disease control methods for a specific single pathogen or for a pathogen complex.
Author contributions
HY: drafting the manuscript. FY, CH, and XY: analysis and/or interpretation of data. AZ, YT, and YW: acquisition of data. AS: revising the manuscript. HY, YH, and ML: revising the manuscript critically for important intellectual content and approval of the version of the manuscript to be published. All authors contributed to the article and approved the submitted version.
Funding
This work was supported by the Natural Science Foundation of Yunnan Province (202001AT070011), the International Plan of Talented Young Scientist Program (Egypt-19-046), and the Yunnan Key R&D Program (202202AE090003).
Acknowledgments
We thank members of the Innovation Team of Food Legume from the Food Crop Institute, Yunnan Academy of Agricultural Science for helpful discussion.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
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References
Abdel-Monaim, M. F., Abo-Elyousr, K. A. (2012). Effect of preceding and intercropping crops on suppression of lentil damping-off and root rot disease in new valley-Egypt. Crop Protection. 32, 41–46. doi: 10.1016/j.cropro.2011.10.011
AEGIC (2019) Australian Pulses: quality, versatility, nutrition. Available at: https://www.aegic.org.au (Accessed 6 February 2019).
Alcamo, J., Flörke, M., Märker, M. (2007). Future long-term changes in global water resources driven by socio-economic and climatic changes. Hydrological Sci. J. 52 (2), 247–275. doi: 10.1623/hysj.52.2.247
Alfauomy, G. A., Atwa, M. A. (2020). Influences of biological control on damping off diseases of faba beans as well as physico-chemical and technological properties. Middle East J. Agric. Res. 9 (4), 812–827. doi: 10.36632/mejar/2020.9.4.64
Ali, M. B., Haridy, A. G., Mahmoud, A. F. (2019). Evaluation of faba bean genotypes for yield and resistance to fusarium root rot under greenhouse and field conditions. Int. J. Biosciences. 14 (2), 374–385. doi: 10.12692/ijb/14.2.374-385
Bao, S., He, Y., Zong, X., Wang, L., Li, L., Enneking, D., et al. (2008). Collection of pea (Pisum sativum) and faba bean (Vicia faba) germplasm in yunnan. Plant Genet. Resour. Newsletter. 156, 11–22.
Bao, J. R., Wang, G. C., Ye, C. M. (1992). Analysis on Fusarium pathogens on faba bean in zhejiang province. Acta Agriculturae Universitatis Zhejiangensis. 18 (3), 61–64.
Blesh, J. (2019). Feedbacks between nitrogen fixation and soil organic matter increase ecosystem functions in diversified agroecosystems. Ecol. Applications: a Publ. Ecol. Soc. America. 29 (8), e01986. doi: 10.1002/eap.1986
Broders, K. D., Lipps, P. E., Paul, P. A., Dorrance, A. E. (2007). Evaluation of Fusarium graminearum associated with corn and soybean seed and seedling disease in Ohio. Plant Disease. 91, 1155–1160. doi: 10.1094/PDIS-91-9-1155
Bullock, D. G. (1992). Crop rotation. Crit. Rev. Plant Sci. 11 (4), 309–326. doi: 10.1080/07352689209382349
Chang, K. F., Conner, R. L., Hwang, S. F., Ahmed, H. U., McLaren, D. L., Gossen, B. D., et al. (2014). Effects of seed treatments and inoculum density of Fusarium avenaceum and Rhizoctonia solani on seedling blight and root rot of faba bean. Can. J. Plant Sci. 94 (4), 693–700. doi: 10.4141/cjps2013-339
Chen, Z. Q. (1999). Investigation and research on the incidence and harm of broad bean wilt disease in the main production areas of qinghai province. Qinghai Agric. Forestry Sci. Technology. 03, 14–17.
Chu, M., Gu, M. Y., Tang, Q. Y., Zhu, J., Hao, X. Y., Zhang, Z. D. (2019). Identification of pathogenic fungi causing the root rot disease of dabancheng faba bean and analysis of antagonistic effect by the biocontrol bacteria. Xinjiang Agric. Sci. 56 (10), 1904–1911. doi: 10.6048/j.issn.001-4330.2019.010.016
Cook, R. J. (2006). Toward cropping systems that enhance productivity and sustainability. Proc. Natl. Acad. Sci. 103 (49), 18389–18394. doi: 10.1073/pnas.0605946103
Costanzo, A., Bàrberi, P. (2014). Functional agrobiodiversity and agroecosystem services in sustainable wheat production. a review. Agron. Sustain. Dev. 34 (2), 327–348. doi: 10.1007/s13593-013-0178-1
Crépon, K., Marget, P., Peyronnet, C., Carrouee, B., Arese, P., Duc, G. (2010). Nutritional value of faba bean (Vicia faba l.) seeds for feed and food. Field Crops Res. 115 (3), 329–339. doi: 10.1016/j.fcr.2009.09.016
Dhull, S. B., Kidwai, M. K., Noor, R., Chawla, P., Rose, P. K. (2022). A review of nutritional profile and processing of faba bean (Vicia faba l.). Legume Science. 4 (3), e129. doi: 10.1002/leg3.129
Dolatabadian, A. R., Cornelsen, J., Huang, S. H., Zou, Z., Fernando, W. D. (2022). Sustainability on the farm: breeding for resistance and management of major canola diseases in Canada contributing towards an IPM approach. Can. J. Plant Pathology. 44 (2), 157–190. doi: 10.1080/07060661.2021.1991480
Dong, Y., Dong, K., Tang, L., Zheng, Y., Yang, Z. X., Xiao, J. X., et al. (2013a). Relationship between rhizosphere microbial community functional diversity and faba bean fusarium wilt occurrence in wheat and faba bean intercropping system. Acta Ecologica Sinica. 33 (23), 7445–7454. doi: 10.5846/stxb201208281214
Dong, Y., Dong, K., Yang, Z. X., Zhu, J. H., Tang, L., Zheng, Y. (2017). Effect of cinnamic acid on incidence of faba bean fusarium wilt and incidence-mitigating mechanisms of wheat and faba bean intercropping. Acta Pedologica Sinica. 54 (02), 503–515. doi: 10.11766/trxb201605030043
Dong, Y., Dong, K., Zheng, Y., Tang, L., Yang, Z. X. (2014a). Faba bean fusarium wilt (Fusarium oxysporum) control and its mechanismin different wheat varieties and faba bean intercropping system. Chin. J. Appl. Ecology. 25 (7), 1979–1987. doi: 10.13287/j.1001-9332.20140505.001
Dong, Y., Dong, K., Zheng, Y., Yang, Z. X., Tang, L., Xiao, J. X. (2014b). Allelopathic effects and components analysis of root exudates of faba bean cultivars with different degrees of resistance to Fusarium oxysporum. Chinese journal of eco-agriculture 22, 3, 292–299. doi: 10.3724/SP.J.1011.2014.31020
Dong, Y., Yang, Z. X., Dong, K., Tang, L., Zheng, Y., Hu, G. B. (2013b). Effects of nitrogen application rate on faba bean fusarium wilt and rhizospheric microbial metabolic functional diversity. Chin. J. Appl. Ecology. 24 (4), 1101–1108. doi: 10.13287/j.1001-9332.2013.0265
Dong, Y., Zhao, S., Lv, J. X., Dong, K. (2019). Synergistic effects of intercropping with wheat and inoculation with arbuscular mycorrhizal fungi on improvement of anti-fusarium wilt and rhizosphere microbial carbon metabolic activity of faba bean. J. Plant Nutr. Fertilizers. 25 (10), 1646–1656. doi: 10.11674/zwyf.18400
Döös, B. R. (2002). Population growth and loss of arable land. Global Environ. Change. 12 (4), 303–311. doi: 10.1016/S0959-3780(02)00043-2
Du, C. Z. (2021) A breakthrough in the breeding of new varieties of broad beans Available at: http://www.moa.gov.cn/xw/qg/202104/t20210429_6366977.htm
Duan, X. D. (2014). Evaluation of three biocontrol agents for managing root rot in faba bean. Rural Sci. Technology. 10, 26–27. doi: 10.3969/j.issn.1002-6193.2014.10.015
Duan, X. D. (2021). Isolation and identification of several broad bean root rot pathogens. Heilongjiang Agric. Sci. 6, 59–66. doi: 10.11942/j.issn1002-2767.2021.06.0059
Duchene, O., Vian, J. F., Celette, F. (2017). Intercropping with legume for agroecological cropping systems: complementarity and facilitation processes and the importance of soil microorganisms. a review. Agriculture Ecosyst. Environment. 240, 148–161. doi: 10.1016/j.agee.2017.02.019
Ellis, M. L., Broders, K. D., Paul, P. A., Dorrance, A. E. (2011). Infection of soybean seed by Fusarium graminearum and effect of seed treatments on disease under controlled conditions. Plant Disease. 95 (4), 401–407. doi: 10.1094/PDIS-05-10-0317
El-Mehy, A. A., El-Gendy, H. M., Aioub, A. A., Mahmoud, S. F., Abdel-Gawad, S., Elesawy, A. E., et al. (2022). Response of faba bean to intercropping, biological and chemical control against broomrape and root rot diseases. Saudi J. Biol. Sci. 29 (5), 3482–3493. doi: 10.1016/j.sjbs.2022.02.032
Esker, P. D., Conley, S. P. (2012). Probability of yield response and breaking even for soybean seed treatments. Crop Science. 52 (1), 351–359. doi: 10.2135/cropsci2011.06.0311
FAO (2016). Available at: http://www.fao.org/pulses-2016/en/ (Accessed April 11, 2016).
FAOSTAT (2022) Statistics database of the food and agriculture organization of the united nations. Available at: http://www.fao.org/statistics/databases/en/ (Accessed 26 May 2022).
Guo, Y., Lv, J., Dong, Y., Dong, K. (2021). Exploration of the potential mechanism of faba bean–wheat intercropping to control faba bean fusarium wilt due to allelopathic plant extracts. ACS omega. 6 (24), 15590–15600. doi: 10.1021/acsomega.0c06120
He, Z. B. (2019). Study on the nutrient release pattern and allelopathic mechanism of faba bean green manure in chongqing (China: Southwest University).
Hou, S. W., Li, M. ,. Q., Yang, X. M., Yang, F. R. (2011). Identification of fusarium pathogens for root rot of Vicia faba l. at seedling stage in the cold and humid regions of gansu. Hunan Agric. Sci. 15, 97–100. doi: 10.3969/j.issn.1006-060X.2011.15.030
Hwang, S. F., Ahmed, H., Gossen, B. D., Kutcher, H., Brandt, S., Strelkov, S. E., et al. (2009). Effect of crop rotation on the soil pathogen population dynamics and canola seedling establishment. Plant Pathol. J. 8 (3), 106–112. doi: 10.3923/ppj.2009.106.112
Infantino, A., Kharrat, M., Riccioni, L., Coyne, C.J., McPhee, K.E., Grünwald, N.J. (2006). Screening techniques and sources of resistance to root diseases in cool season food legumes. Euphytica 147, 201–221. doi: 10.1007/s10681-006-6963-z
Johnson, J. B., Skylas, D. J., Mani, J. S., Xiang, J., Walsh, K. B., Naiker, M. (2021). Phenolic profiles of ten Australian faba bean varieties. Molecules. 26, 4642. doi: 10.3390/molecules26154642
Kuttibai, T. G. J., Bhagavathi, M. S., Prakash, V. (2022). Smart farming: future of agriculture. Res. Highlights Agric. Sci. 6, 64–72. doi: 10.9734/bpi/rhas/v6/3951E
Lang, L. J., Yu, Z. H., Zheng, Z., Xu, M., Ying, H. Q. (1993). Faba bean in China: state-of-the-art review (Aleppo, Syria: ICARDA), 4–7.
Li, L., Guo, Y. P., Yang, S. H. (2018). Breeding of spring faba bean cultivar lincan 12 and the cultivation technic. China Seed Industry. 9, 88–89. doi: 10.19462/j.cnki.1671-895x.20180829.015
Li, C. J., Nan, Z. B. (1996). Investigation of the incidence and effect of root rot on spring faba bean in linxia area. Plant Protection. 22 (06), 25–26.
Li, C. J., Nan, Z. B. (2000). Effects of soil moisture contents on root rot and growth of faba bean. Acta Phytopathologica Sinica. 30 (3), 245–249. doi: 10.3321/j.issn:0412-0914.2000.03.010
Liebenberg, A. J. (2002) Dry bean production. printed and published by department of agriculture, resource centre, directorate agricultural information services, private bag X. Available at: https://archive.org/details/liebenberg-2002-dry-bean-production.
Liu, T., Wu, G. (2022). Does agricultural cooperative membership help reduce the overuse of chemical fertilizers and pesticides? Evidence Rural China. Environ. Sci. pollut. Res. 29 (5), 7972–7983. doi: 10.1007/s11356-021-16277-0
Luo, Y. T., Tang, L., Zheng, Y., Dong, Y. (2012). Effects of wheat-faba bean intercropping on the yield and rhizosphere pathogen in different n application rates. Chin. J. Soil Science. 43 (4), 826–831. doi: 10.19336/j.cnki.trtb.2012.04.011
Lv, J., Dong, Y., Dong, K., Zhao, Q., Yang, Z., Chen, L. (2020). Intercropping with wheat suppressed fusarium wilt in faba bean and modulated the composition of root exudates. Plant Soil. 448, 153–164. doi: 10.1007/s11104-019-04413-2
Mahmoud, A. F., Abd El-Fatah, B. E. S. (2020). Genetic diversity studies and identification of molecular and biochemical markers associated with fusarium wilt resistance in cultivated faba bean (Vicia faba). Plant Pathol. J. 36 (1), 11–28. doi: 10.5423/PPJ.OA.04.2019.0119
Marburger, D., Venkateshwaran, M., Conley, S., Esker, P., Lauer, J., Ane, J.-M. (2014). Crop rotation and management effect on fusarium spp. populations. Crop Science. 55, 1–12. doi: 10.2135/cropsci2014.03.0199
Minor Grain Crops (2018). Available at: http://www.mgcic.com/content/4378 (Accessed December 12, 2018).
Mousa, A. M., El-Sayed, S. A. (2016). Effect of intercropping and phosphorus fertilizer treatments on incidence of Rhizoctonia root-rot disease of faba bean. Int. J. Curr. Microbiol. Appl. Sci. 5 (4), 850–863. doi: 10.20546/ijcmas.2016.504.097
Munkvold, G. P., O’Mara, J. K. (2002). Laboratory and growth chamber evaluation of fungicidal seed treatments for maize seedling blight caused by Fusarium species. Plant Disease. 86 (2), 143–150. doi: 10.1094/PDIS.2002.86.2.143
Nan, Z. B., Ge, G. Z., Li, C. J. (2002). Effect of pesticides on field-controlling root rot of Vicia faba. Chinese journal of applied ecology 13, 8, 943–947. doi: 10.13287/j.1001-9332.2002.0220
Oxford Analytica (2019). World hunger is likely to rise as 2030 UN target nears. Expert Briefings. doi: 10.1108/OXAN-DB246018
Paul, S. K., Gupta, D. R. (2021). Faba bean (Vicia faba l.), a promising grain legume crop of Bangladesh: a review. Agric. Rev. 42 (3), 292–299. doi: 10.18805/ag.R-203
Ren, H. Y. (2002). Study on the pathogen of faba bean fusarium wilt and their control in changshu of jiangsu province (Nanjing, China: Nanjing Agricultural University).
Ren, H. Y., Chen, Z. Y., Xu, Z. G., Lu, J. Y., Xu, Y. C. (2003). Study on main species and virulence of faba bean fusarium wilt in changshu area. Plant Protection. 04, 30–32. doi: 10.3969/j.issn.0529-1542.2003.04.009
Ruan, X. Y., Jiang, Y. C., Luo, W. F., Wang, J. H. (1982). Two new forms of Fusarium avenaceum (FR) sacc. -the pathogens of broad bean stem-end rot. Acta Phytopathologica Sinica. 02, 27–34.
Ruan, X. Y., Wang, J. H., Tang, J. Y., Gu, S. (1986). Analysis on the mycoflora and their dominant species of the pathogen which caused seedling root disease of faba bean. J. Yunnan Agric. University. 01, 15–22.
Rubiales, D., Khazaei, H. (2022). Advances in disease and pest resistance in faba bean. Theor. Appl. Genet. 135 (11), 3735–3756. doi: 10.1007/s00122-021-04022-7
Shi, K., Chen, Y., Yu, B., Xu, T., Li, L., Huang, C., et al. (2016). Urban expansion and agricultural land loss in China: a multiscale perspective. Sustainability. 8 (8), 790. doi: 10.3390/su8080790
Sillero, J. C., Villegas-Fernández, A. M., Thomas, J., Rojas-Molina, M. M., Emeran, A. A., Fernández-Aparicio, M., et al. (2010). Faba bean breeding for disease resistance. Field Crops Res. 115 (3), 297–307. doi: 10.1016/j.fcr.2009.09.012
Singh, A. K., Bharati, R. C., Manibhushan, N. C., Pedpati, A. (2013). An assessment of faba bean (Vicia faba l.) current status and future prospect. Afr. J. Agric. Res. 8 (50), 6634–6641. doi: 10.5897/AJAR2013.7335
Singh, S. P., Schwartz, H. F. (2010). Breeding common bean for resistance to diseases: a review. Crop Science. 50 (6), 2199–2223. doi: 10.2135/cropsci2009.03.0163
Šišić, A., Baćanović-Šišić, J., Schmidt, H., Finckh, M. R. (2020). “Root pathogens occurring on pea (Pisum sativum) and faba bean (Vicia faba) in Germany,” in 30th Scientific-Experts Conference of Agriculture and Food Industry: Answers for Forthcoming Challenges in Modern Agriculture. 69–75. (Springer International Publishing).
Snowdon, R. J., Wittkop, B., Chen, T. W., Stahl, A. (2021). Crop adaptation to climate change as a consequence of long-term breeding. Theor. Appl. Genet. 134 (6), 1613–1623. doi: 10.1007/s00122-020-03729-3
Sun, S. L., Zhu, Z. D., Duan, C. X., Zhao, P., Sun, F., Deng, D., et al. (2019). First report of charcoal rot caused by Macrophomina phaseolina on faba bean in China. Plant Disease. 103 (6), 1415. doi: 10.1111/jph.12413
Varshney, R. K., Close, T. J., Singh, N. K., Hoisington, D. A., Cook, D. R. (2009). Orphan legume crops enter the genomics era! Curr. Opin. Plant Biol. 12, 202–210. doi: 10.1016/j.pbi.2008.12.004
Wang, H. Z. (2013). Occurrence and control for stem wilt (Fusarium avenaceum) of broad beans. Fujian Agric. Sci. Technology. 10, 45–46. doi: 10.3969/j.issn.0253-2301.2013.10.020
Wang, J. H., Nie, Z. L., Xu, Y. Q., Zheng, Y. (2018). The inoculation effect of rhizobia on Vicia faba growth and its disease resistance with root rot. J. Southwest Forestry University. 38 (4), 94–99. doi: 10.11929/j.issn.2095-1914.2018.04.015
Wang, Y. Y., Ren, J. B., Zhang, Y., Zheng, Y., Tang, L. (2020b). Effect of wheat and faba bean intercropping on improving rhizosphere microflora and reducing fusarium wilt of faba bean. Chin. J. Soil Sci. 51 (05), 127–1133. doi: 10.19336/j.cnki.trtb.2020.05.16
Wang, J. H., Tang, J. Y., Ruan, X. Y. (1988). Study on the correlation of root-disease incidence between seedling and adult stage of faba bean. J. Yunnan Agric. University. 02, 119–124.
Wang, J. H., Wang, C. D. (2002a). Outbreak characters of broad bean blight and complex infection by pathogens in yunnan, China. J. Yunnan Agric. University. 04, 449. doi: 10.3969/j.issn.1004-390X.2002.04.062
Wang, J. H., Wang, C. D., Lu, N. (2002b). Toxic effects of Fusarium oxysporum extracts on broad bean seed germination and seedling growth. J. Yunnan Agric. Univ. 04, 395–396+399. doi: 10.3969/j.issn.1004-390X.2002.04.028
Wang, L. P., Yu, H. T., Lv, M. Y., He, Y. H. (2020a). Superior varieties of food legume and cultivation technologies in yunnan (Yunnan: Yunnan Technology Press).
Wang, X. O., Zhu, Z. D., Leur, J. V., Bretag, T., Bayaa, B., Kumari, S., et al. (2006). “Predictive forecasting and integrated control,” in Proceedings of the 2006 Academic Conference of the Chinese Society of Plant Pathology, Status of disease of faba bean and pea in Qinghai province. (Changsha, China: Chinese Agricultural Science and Technology Press). 363–368.
Wang, H. F., Zong, X. X., Guan, J. P., Yang, T., Sun, X. L., Ma, Y., et al. (2012). Genetic diversity and relationship of global faba bean (Vicia faba l.) germplasm revealed by ISSR markers. Theor. Appl. Genet. 124 (5), 789–797. doi: 10.1007/s00122-011-1750-1
Wu, Q., Yang, X., Qiu, D. (2006). 3% plant activating protein induced antibiotic resistance in broad bean. Plant Prot. 06, 149–152. doi: 10.3969/j.issn.0529-1542.2006.06.045
Xiang, et al. (2022). Available at: http://www.chinawestagr.com/homepage/showcontent.asp?id=50272.
Xiao, J. X. (2013). Characteristics of root exudates and its reaction to faba bean fusarium wilt in wheat and faba bean intercropping (China: Yunnan Agricultural University).
Yang, Z. X., Tang, L., Zheng, Y., Dong, K., Dong, Y. (2014). Effects of different wheat cultivars intercropped with faba bean on faba bean fusarium wilt, root exudates and rhizosphere microbial community functional diversity. J. Plant Nutr. Fertilizer. 20 (3), 570–579. doi: 10.11674/zwyf.2014.0307
Ye, Y., Lang, L., Xia, M., Tu, J. (2003). Faba bean in China (Beijing: China Agriculture Press), 1–15.
Yu, H. T., Wang, L. P., Lv, M. Y., Yang, F., Tang, Y. S., Ding, M. L., et al. (2020). Correlation and path analysis of major agronomic traits to fresh yield of early-mature and autumn-sowing faba bean (Vicia faba l.). Southwest China J. Agric. Sci. 33 (4), 711–717. doi: 10.16213/j.cnki.scjas.2020.4.005
Yu, H. T., Wang, L. P., Lv, M. Y., Yang, F., Yan, H. B., Wang, Q. F., et al. (2019a). Analysis of status and development of food legumes industry in yunnan province. Southwest China J. Agric. Sci. 32 (supp.), 80–85.
Yu, H. T., Wang, L. P., Yang, F., He, Y. H., Lv, M. Y. (2021). Complete mitochondrial genome of the important phytopathogenic fungus Macrophomina phaseolina (Botryosphaeriales, ascomycota). Mitochondrial DNA. Part B Resources. 6 (10), 2972–2974. doi: 10.1080/23802359.2021.1975505
Yu, H. T., Wang, L. P., Yang, F., Lv, M. Y., Zong, X. X., Yang, T., et al. (2019b). Identification and utilization of short wing petal broad bean (Vicia faba l.) germplasm. J. Plant Genet. Resource 20 (5), 1334–1339+1348. doi: 10.13430/j.cnki.jpgr.20181212001
Yu, H. T., Yang, F., Wang, L. P., Lv, M. Y., Hu, C. Q., Yang, X., et al. (2018). Highly efficient cultivation model of fresh edible autumn-sown early-maturing faba bean in yunnan-using mulching-film side seeding. Liaoning Agric. Sci. 6, 87–88. doi: 10.3969/j.issn.1002-1728.2018.06024
Yuan, T. T., Dong, Y., Zhao, Q. (2020). Effects of benzoic acid on pathogenicity of Fusarium oxysporum f. sp. fabae and tissue structure resistance of faba bean root. Plant Physiol. J. 56 (3), 441–454. doi: 10.13592/j.cnki.ppj.2019.0411
Zhang, Y., Bai, X. J., Fan, J. X., Guo, Y. P., Liu, Y., Xia, Z. L. (2020). Effects of different intercropping modes on root rot and crop growth of broad bean. Agric. Sci. Technol. Communication. 1, 128–131. doi: 10.3969/j.issn.1000-6400.2020.01.045
Zhang, C., Dong, Y., Tang, L., Zheng, Y., Makowski, D., Yu, Y., et al. (2019). Intercropping cereals with faba bean reduces plant disease incidence regardless of fertilizer input; a meta-analysis. Eur. J. Plant Pathology. 154 (4), 931–942. doi: 10.1007/s10658-019-01711-4
Zhang, Y., Li, L., Guo, Y. P., Shao, Y. (2018). Impact of different planting densities on root rot and crop growth of faba bean in intercropping systems. Anhui Agric. Sci. Bullet. 24 (18), 60–61. doi: 10.16377/j.cnki.issn1007-7731.2018.18.028
Zhang, L. Y., Liu, Y., Chen, P. Q., Weng, H., Ma, Z. Q. (2022). Control efficacy of several biological pesticides on the main diseases and pests of broad bean in qinghai. Chin. J. Biol. Control. 38 (6), 1377–1384. doi: 10.16409/j.cnki.2095-039x.2022.01.019
Zhang, Z., Yang, W., Li, Y., Zhao, Q., Dong, Y. (2023). Wheat-faba bean intercropping can control fusarium wilt in faba bean under F.commune and ferulic acid stress as revealed by histopathological analysis. Physiol. Mol. Plant Pathology. 124, 101965. doi: 10.1016/j.pmpp.2023.101965
Zhao, Z. Y., Xiao, Y. N., Zhu, Z. D. (2011). “Identification and biological characteristics of the pathogen Fusarium proliferatum isolated from root rot tissue of broad bean,” in Proceedings of the 2011 Academic Conference of the Chinese Society of Plant Pathology. 1. (Yichang, China: China Agricultural Science and Technology Press).
Keywords: Vicia faba, production, root rot, identification, management
Citation: Yu H, Yang F, Hu C, Yang X, Zheng A, Wang Y, Tang Y, He Y and Lv M (2023) Production status and research advancement on root rot disease of faba bean (Vicia faba L.) in China. Front. Plant Sci. 14:1165658. doi: 10.3389/fpls.2023.1165658
Received: 14 February 2023; Accepted: 03 May 2023;
Published: 02 June 2023.
Edited by:
Marie-Laure Pilet-Nayel, INRAE Bretagne Normandie, FranceReviewed by:
Jiban Shrestha, Nepal Agricultural Research Council, NepalRobyne Davidson, Lakeland College, Canada
Copyright © 2023 Yu, Yang, Hu, Yang, Zheng, Wang, Tang, He and Lv. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Haitian Yu, haitian7@ualberta.ca/haitianlegume@outlook.com; Yuhua He, hyhyaas@163.com; Meiyuan Lv, lvmeiyang01@163.com