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Reaction of Grafted Cashew Genotypes to Powdery Mildew Disease in the Western Province of Zambia

  • L. Chisengele
  • A. Uaciquete
  • P. W. Kachapulula
  • 970-975
  • Aug 20, 2024
  • Agriculture

Reaction of Grafted Cashew Genotypes to Powdery Mildew Disease in the Western Province of Zambia

L. Chisengele1, A. Uaciquete2, P. W. Kachapulula1

1Department of Plant Science, School of Agricultural Sciences, University of Zambia, Lusaka.

2Instituto de Amêndoas de Moçambique, Serviços de Investigação. Maputo.

DOI: https://doi.org/10.51244/IJRSI.2024.1107076

Received: 03 July 2024; Accepted: 09 July 2024; Published: 20 August 2024

ABSTRACT

Cashew powdery mildew disease (CPMD), caused by the fungus Pseudoidium anarcadii, has become an economically significant disease of cashew trees in the Western Province of Zambia and many tropical parts of the world. The disease causes significant yield losses of 70 to 100 %. The most effective, sustainable, and environmentally friendly approach to the management of CPMD elsewhere has been through the use of resistant genotypes. Nevertheless, in Zambia, information on the reaction of existing cashew genotypes to CPMD still needs to be discovered. Therefore, this study aimed to evaluate the reaction of cashew genotypes to CPMD in Western Zambia. 90-day-old seedlings from seven cashew genotypes from the ZARI collections were planted and artificially inoculated with cashew powdery mildew spore suspension in a completely randomized design with 15 plant replicates. The experiment was conducted in a screenhouse at Simulumbe Agricultural research station in the Mongu district of Zambia from 20th June to 30th July 2020. Disease incidence and severity were evaluated weekly. Results indicated high variability in the response of the genotypes to powdery mildew disease (P<0.05). Genotype Mab/J/T01 was highly tolerant, while genotype Mab/T117 and Itufa/T01 were moderately tolerant, and genotypes KK/T139 and KK/T65 had low tolerance to CPMD. The rest were highly susceptible. The identified tolerant cashew genotypes are recommended for further direct utilization or incorporation into breeding programs to develop resistant varieties against CPMD in Zambia.

Keywords: Powdery Mildew disease, resistance, genotypes, Anarcadium occidentale, Dwarf, giant cashew type

INTRODUCTION

The Cashew industry has become the primary source of employment for more than 60,000 smallholder farmers in Zambia’s Western Province (Chisengele et al., 2022). It is a significant source of household income, nutrition, and employment for the local communities. Cashew is the only tree crop other than Mango that has successfully adapted to the conditions of Western Province since its introduction in the 1950s (Isimwaa, 1993). Despite its acceptability and economic advantages, significant crop damage has been observed worldwide in most cashew plantations and farmer’s fields, with qualitative and quantitative losses caused mainly by fungi (Cardoso et al., 2017; Freire et al., 2002).

Cashew powdery mildew caused by Pseudoidium anarcadii first reported in Zambia in 1979 (Uaciquete et al., 2013), has recently become a vital cashew disease in Zambia (Chisengele et al., 2022). Powdery mildew in Tanzania has been associated with crop losses ranging from 70 to 100% (Sijaona et al., 2001; Wonni, 2017). The disease affects all young parts of the shoot, including leaves, inflorescences, apples, and nuts, reducing the quality and yield of cashew apples and nuts (Lima et al., 2019; Pinto et al., 2018). The disease is effectively controlled with sulfur powder applications (Martin et al., 1997; Nathaniels et al., 2003; Swart, 2004). However, chemical control is associated with legal, practical, and environmental problems, including the need for legislative approval by environmental agencies, application equipment acquisition, and labour costs (Pinto et al., 2018). Therefore, genetic resistance is a perfect option for long-term economic and environmental strategies to control powdery mildew disease (Pinto et al., 2018). Early studies have suggested the potential use of resistance genotypes for integration into disease management (Nathaniels et al., 1996; Waller et al., 2008). The main constraints of disease evaluation methods include the irregularity in budding time among different genotypes and differences in environmental conditions at the plant’s vulnerability to infection, which makes comparisons among cashew genotypes subject to errors (Freire et al., 2002; Pinto et al., 2018). In addition, studies by Sijaona et al. (2001) revealed that powdery mildew disease developed on inoculated young leaves 48 h after inoculation; however, mature leaves were immune to infection. Despite these limitations, several methods for assessing the reaction of cashew genotypes to CPMD under laboratory and field conditions have been studied (Nathaniels, 1996; Sijaona et al., 2001). These include pathogen inoculation on detached leaves, disease development on plants and flower comparison, and the infection of seedlings also proved successful under field conditions (Sijaona et al., 2001). Currently, more than 80 cashew genotypes are available for growers in Zambia, but no scientific report is available on their reaction to CPMD. As a result, hardly any commercial cultivars have been identified that are either tolerant or resistant to the disease. Therefore, this study’s objective was to evaluate seven cashew nut genotypes for resistance against powdery mildew disease in the Western Province of Zambia, thereby selecting promising genotypes for inclusion in crop improvement programs for disease control.

MATERIALS AND METHODS

Preparation of Plant Materials

Cashew Seedlings raised to 50 cm in height were softwood grafted using scions from seven cashew genotypes pre-selected by Zambia Agricultural Research Institute (ZARI) in 2018 following the Nursery Operators’ guidelines manual (Chisengele et al., 2022) at Simulumbe Research Station, ZARI in Western province. The seedlings were planted in the greenhouse and cared for routinely, and fifteen (15) seedlings per genotype with similar height and girth and without visible attacks of any disease and pest were selected when they had grown to 50 cm tall.

Preparation of Inoculum

Diseased plant leaves were collected from farmers’ fields in Nalolo, Mongu districts, and Simulumbe Research Station. First, the conidia were dislodged from infected leaves by brushing fungal materials into water containing 20% tween. Then, using a haemocytometer, the conidial suspension was adjusted to a concentration of 1 x 105 conidia/ml (Rizhsky et al., 2002).

Inoculation and Disease Evaluation

Inoculation was done by spraying the spore suspension onto 90-day-old seedlings arranged in a completely randomized design with fifteen (15) replications in a greenhouse. The control consisted of uninoculated cashew seedlings to monitor the eventual development of the disease from natural infection and was replicated 15 times. After inoculation, the greenhouse was maintained at 27 ± 20C and a relative humidity of 80 to 90 %. Disease severity was done according to Nathaniels (1990). Briefly, the number and size of lesions on the leaves were rated on a five-scale rapid disease screening technique, with a score of one implying powdery mildew fungus covering less than 5% of the leaf and a score of five standing for powdery mildew fungus covering more than 35% of the leaf. The lesions were scaled based on their size.

Table 1. A five-scale rapid disease screening technique by ( Nathaniels & Kennedy, 1996) Nathaniels (1990)

Infection scale Infection Index
0 No lesions visually detectable
1 Powdery mildew fungus covering less than 5% of the leaf
2 Powdery mildew fungus covering 5- 15% of the leaf
3 Powdery mildew fungus covering 15 – 25% of the leaf
4 Powdery mildew fungus covering 25 – 35% of the leaf
5 Powdery mildew fungus covering more than 35% of the leaf

The Infection index was calculated using the formula

DSI (%) = [sum (class frequency × score of rating class)]/[(total number of plants) × (maximal disease index)] × 100

Where DSI =Infection index; xi = Infection scale; ni = number of leaves suffering corresponding infection scale; I = Different scales of infection; N = Total number of leaves under observation and Severity values∑(yi+yi+1)/2 x dti, where yi+yi+1 are the values observed in two consecutive evaluations and the dti is the interval between the evaluations. Nathaniel’s scale is associated with genotype degree susceptibility as follows:

Table 2. PMD genotype reaction scale adapted from Nathaniels (1990)

Infection scale Tolerance Scale (%)
1 Not tolerant (infection scale ≥ 35)
3 Low tolerant (25 ≤ infection scale < 35)
5 Moderately tolerant (15 ≤ infection scale < 25)
7 Highly tolerant (5 ≤ infection index < 15)
9 Very highly tolerant (infection index < 5)

Un-inoculated plants showed no symptoms of disease development. Therefore, the assessed disease development resulted from the inoculation effected in this trial. There were significant differences (P < 0.001) in the response of the seven cashew genotypes (Table 3) studied to powdery mildew disease. One genotype was highly tolerant, two (2) were moderately tolerant, two had low tolerance, and the other two were highly susceptible to powdery mildew disease (Table 4.0). The most tolerant genotype was Mab/ptn/ Jumbo (9.78%), while KK/Kas/T136, with a PMD severity of (42.47%) (Table 4.0), was the most susceptible.

Table 3. Analysis of the variation table showing the reaction of the seven cashew genotypes seedlings to powdery mildew disease

Source of variation d.f s.s m.s v.r F pr
Genotype 6 12619.15 2103.19*** 120.79 <.001
Error 98 1706.39 17.41
Total 104 14325.54

***Data significant at P=0.05, PMD-Powdery mildew incidence severity; sum of squares (ss); mean square (ms).

Table 4. Mean CPMD Severity among cashew genotype

S/N Genotype Tree type DSI Resistance Criteria
1 Mab/ptn/ Jumbo Dwarf 9.78a Highly Tolerant
2 Mab/ptn/ T117 Dwarf 19.19b Moderately Tolerant
3 Itufa – 01 Giant 20.74b Moderately Tolerant
4 MS/K/KK/T139 Dwarf 32.83c Low Tolerance
5 MS/K/KK/T65 Dwarf 33.47c Low Tolerance
6 Itufa-T05 Giant 38.80d Susceptible
7 KK/Kas/T136 Giant 42.47e Very Susceptible

Means with the same letter (s) in the same column are not significantly different following Boniferroni Test (P ≤ 0.05). DSI-Disease Severity Index Means.

DISCUSSION

In this study, seven (7) selected cashew genotypes planted at the study sites between 1985 and 2014 (Chisengele et al., 2022; Eijnatten et al., 1984; Isimwaa, 1993) were assessed for CPMD incidence and severity. The results showed that none of the genotypes exhibited complete resistance to CPMD, but the tolerance levels differed. This agrees with early publications involving different cashew genotypes (Sijaona et al., 2001; Sijaona & Mansfield, 2001). Thus, one of the genotypes was very tolerant, two moderately tolerant, two low tolerance to CPMD, and the other very susceptible. Genotypic variations in cashew tree reactions to CPMD were previously reported by Faenza et al. (1982) as cited by Majune et al (2018) on cashew trees in Tanzania. Similar findings were also reported by (Martin et al. 1997; Masawe, 2016; Agboton et al., 2013). The ability of the cashew genotypes to tolerate infection by the CPMD-causing fungi has been attributed to their inherent genetic tolerance (Sijaona & Mansfield, 2001). All the genotypes evaluated are of foreign origin and were introduced in Zambia between 1988 and 1990 for the common giants and 1990 to 1992 for the dwarf genotypes and were introduced for experimental purposes and multiplication (Chisengele et al., 2022; Eijnatten et al., 1984; Isimwaa, 1993). The dwarf genotypes were imported from Brazil, while the common giants were imported from Mozambique and Tanzania (Chisengele et al., 2022).

In the Zambian collection of elite mother trees, dwarf genotypes were more tolerant to the disease than the common giant trees. Furthermore, these dwarf genotypes are said to have been sourced from Brazil (Chisengele et al., 2022), which agrees with the studies carried out by (Pinto et al., 2018), who evaluated the response of commercial cashew nut cultivars to powdery mildew by monitoring the disease during three disease epidemic cycles. The authors’ findings showed partial resistance of cashew cultivars to powdery mildew that was Dwarf (Pinto et al., 2018). According to these authors, some of the imported planting materials had genetic resistance to the disease, and the environment may not have affected their reaction to the disease. Other related studies in Tanzania (Masawe, 1994; Nathaniels, 1990, 1996; Sijaona et al., 2001), Mozambique (Uaciquete, 2013) and Brazil (Lima et al., 2019) reported similar findings. For all these authors, resistant cashew genotypes could be integrated into the disease management programmes of cashews, in screening disease susceptibility trials as check genotypes, and in breeding resistant varieties.

Efforts to address the CPMD by initiating cashew breeding programmes are in preparation in Zambia. The starting step is identifying elite mother trees as planting material and genetic resources for breeding at ZARI Simulumbe (unpublished). Therefore, the presence of tolerant cashew genotypes in Zambia is an excellent opportunity for a young cashew industry already struggling with powdery mildew disease to immediately commence breeding of even more tolerant varieties and quickly integrate these genotypes into disease control programmes. Currently, CPMD in Zambia is controlled by chemical spraying using hexaconazole (Chisengele et al., 2022). It is not only environmentally unfriendly to natural pollinators but also raises public health concerns, and it is not sustainable for resource-limited cashew farmers (Pinto et al., 2018). As suggested, tolerant genotypes are the most natural and sustainable way of managing CPMD in Zambia (Pinto et al., 2018). In the Western province of Zambia, the cashew industry represents a significant proportion of employment and income for more than 60,000 smallholder farmers (Chisengele et al., 2022). Therefore, proper disease management will safeguard the farmers’ livelihoods.

Furthermore, using resistant cashew genotypes could be the most feasible and sustainable approach to managing CPMD and avoiding long-term breeding programmes, as Pinto et al. (2018) suggested. Unfortunately, such genotypes were not found in our experimental lot. The Dwarf genotypes and Common Giants are the cashew trees that are in existence in Zambia, but to date, no commercial varieties have been bred. Currently, genetic and phenotypic characterization is being conducted by the Zambia Agricultural Institute (ZARI) to study the genetic diversity of cashew germplasm in Zambia.

This is the first scientific study on the response of cashew genotypes to powdery mildew disease in Zambia. The results presented here provide valuable information for cashew growers, policymakers, and researchers involved in breeding cashew plants and studying the response to the most severe cashew disease nationwide. Given the widespread CPMD epidemic in Zambia, this investigation contributes to further studies that will elucidate the genetic basis of resistance. The results also indicate a highly diverse cashew population in response to the CPMD, indicating the polygenic nature of resistance (Ponomareva et al., 2022), which is an excellent source of genes for a successful breeding programme.

CONCLUSION AND RECOMMENDATIONS

The present study has identified five out of seven cashew genotypes exhibiting varying levels of tolerance to the disease, while the rest were very susceptible. Of the five (5) tolerant genotypes, Mab/ptn/Jumbo, Mab/ptn/T117, Itufa-01, MS/K/KK/T139 and MS/K/KK/T65 are recommended for immediate integration into national breeding programmes and distribution to the cashew farmers in the province. In the Zambian collection of genotypes context, the number of dwarfs tolerant to CPMD was generally higher than that of the common giants. Therefore, it can be stated that the likelihood of finding tolerant genotypes is higher among dwarfs compared to common cashew populations. The presence of tolerant cashew genotypes in Zambia is an excellent opportunity for a young cashew industry already struggling with powdery mildew disease to immediately commence breeding of even more tolerant varieties and integrate these genotypes into disease control programmes. In the current study, none of the genotypes showed complete resistance, which is known to be fragile under high disease pressure due to its single gene dependence.

It is recommended that a study should investigate the reaction of other cashew populations under Zambian conditions.

REFERENCES

  1. Agboton, B. V., Salifu, D., Seguni, Z., Sijaona, M. E., Shomari, S., Ekesi, S., & Maniania, N. K. (2013). Bioecology of some key cashew insect pests and diseases in diverse habitats and landscapes in Tanzania. Journal of Applied Entomology, 137(10). https://doi.org/10.1111/jen.12069
  2. Cardoso, J. E., Viana, F. M. P., Ootani, M. A., Martins, M. V. V., & Araújo, F. S. A. (2017). First report of Erysiphe quercicola causing powdery mildew on cashew in Brazil. Plant Disease, 101(7), 1327. https://doi.org/10.1094/PDIS-11-16-1658-PDN
  3. Chisengele, L., Uaciquete, A., & Kachapulula, P. W. (2022). Prevalence of Cashew Powdery Mildew Disease in Western Province of Zambia. International Journal of Environment, Agriculture and Biotechnology, 7(5), 181–187. https://doi.org/10.22161/ijeab.75.18
  4. Eijnatten, C. L. M. van, Akushanga, L., & Moonga, G. H. (1984). Selection for the productivity of cashew trees in western province, Zambia. Selection for Productivity of Cashew Trees in Western Province, Zambia.
  5. Freire, F., Cardoso, J. E., Marto, F., Viana, P., Pinto, F. M., Freire, F. C. O., Cardoso, J. E., Santos, A. A. Dos, & Viana, F. M. P. (2002). Diseases of cashew nut plants (Anacardium occidentale L.) in Brazil. Elsevier, 21, 489–494. https://doi.org/10.1016/S0261-2194(01)00138-7
  6. Isimwaa, M. (1993). Cashew agroforestry in the context of the natural resources of the western province of Zambia. https://mspace.lib.umanitoba.ca/bitstream/handle/1993/22547/Isimwaa Cashew agroforestry.pdf?sequence=1
  7. Lima, J. S., Martins, M. V. V. V. V., Cardoso, J. E., Wonni, I., Sijaona, M. E. R. R., Mansfield, J. W., Clewer, A., Maddison, A., Mansfield, J. W., Pinto, O. R. de O. R. O., Cardoso, J. E., Maia, A. H. N., Pinto, C. M., Lima, J. S., Viana, F. M. P., Martins, M. V. V. V. V., Majune, D. J., Masawe, P. A. L. P. A., Mbega, E. R., … Wingfield, M. J. (2019). The powdery mildews: A review of the world’s most familiar (yet poorly known) plant pathogens. Mycoscience, 49(1), 27–51. https://doi.org/10.1146/annurev.phyto.46.081407.104740
  8. Majune, D. J., Masawe, P. A., & Mbega, E. R. (2018). Status and Management of Cashew Disease in Tanzania. International Journal of Environment, Agriculture and Biotechnology, 3(5), 1590–1597. https://doi.org/10.22161/ijeab/3.5.4
  9. Martin, P. J., Topper, C. P., Bashiru, R. A., Boma, F., De Waal, D., Harries, H. C., Kasuga, L. J., Katanila, N., Kikoka, L. P., Lamboll, R., Maddison, A. C., Majule, A. E., Masawe, P. A., Millanzi, K. J., Nathaniels, N. Q., Shomari, S. H., Sijaona, M. E., & Stathers, T. (1997). Cashew nut production in Tanzania: Constraints and progress through integrated crop management. Crop Protection, 16(1), 5–14. https://doi.org/10.1016/S0261-2194(96)00067-1
  10. Masawe, P. (1994). Aspects of breeding and selecting improved cashew genotypes (Anacardium occidentale L.). https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.386973
  11. Masawe, P. A. L. (2016). Cashew Research Innovations. A Decade of Transformation: ACA World Cashew Festival & Expo, 1–44.
  12. Nathaniels, N. Q.R. & Kennedy, R. (1996). Variation in severity of cashew powdery mildew (Oidium anacardii Noack) disease in Tanzania: Implications for research and extension. International Journal of Pest Management. https://doi.org/10.1080/09670879609371991
  13. Nathaniels, Nicholas Q.R., Sijaona, M. E. R., Katinila, N., & Shoo, J. A. E. (2003). IPM for control of cashew powdery mildew in Tanzania. I: Farmers’ crop protection practices, perceptions and sources of information. International Journal of Pest Management, 49(1), 25–36. https://doi.org/10.1080/713867836
  14. Pinto, O. R. O., Cardoso, J. E., Maia, A. H. N., Pinto, C. M., Lima, J. S., Viana, F. M. P., & Martins, M. V. V. (2018). Reaction of commercial clones of cashew to powdery mildew in northeastern Brazil. Crop Protection, 112, 282–287. https://doi.org/10.1016/j.cropro.2018.06.016
  15. Ponomareva, M., Gorshkov, V., Ponomarev, S., Mannapova, G., Askhadullin, D., Askhadullin, D., Gogoleva, O., Meshcherov, A., & Korzun, V. (2022). Resistance to Snow Mold as a Target Trait for Rye Breeding. Mdpi.Com. https://doi.org/10.3390/plants11192516
  16. Rizhsky, L., Liang, H., & Mittler, R. (2002). The combined effect of drought stress and heat shock on gene expression in tobacco. Plant Physiology, 130(3), 1143–1151. https://doi.org/10.1104/pp.006858
  17. Sijaona, M. E. R., Clewer, A., Maddison, A., & Mansfield, W. (2001). Comparative analysis of powdery mildew development on leaves, seedlings and flower panicles of different genotypes of cashew. Plant Pathology. https://doi.org/10.1046/j.1365-3059.2001.00544.x
  18. Swart, W. J. (2004). First Report of Powdery Mildew of Cashew Caused by Oidium anacardii in South Africa . Plant Disease. https://doi.org/10.1094/pdis.2004.88.11.1284a
  19. Uaciquete, A., Korsten, L., & Van der Waals, J. E. (2013). Epidemiology of cashew anthracnose (Colletotrichum gloeosporioides Penz.) in Mozambique. Crop Protection, 49, 66–72. https://doi.org/10.1016/j.cropro.2013.02.016
  20. Waller, J. M., Nathaniels, N., Sijoana, M. E. R., & Shomari, S. H. (2008). Cashew powdery mildew (Oidium anacardii Noack) in Tanzania. Http://Dx.Doi.Org/10.1080/09670879209371675, 38(2), 160–163. https://doi.org/10.1080/09670879209371675
  21. Wonni, I. (2017). Diseases of Cashew Nut Plants (Anacardium Occidentale L.) in Burkina Faso. Advances in Plants & Agriculture Research, 6(3). https://doi.org/10.15406/apar.2017.06.00216

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