ABSTRACT
Pumpkins (Cucurbita pepo) are grown all around the world for a variety of reasons ranging from agricultural purposes to commercial and ornamental sales. The pathogens causing the rot of pumpkin in the world include fungi, bacteria, and viruses. Three hundred and sixty-six (366) fruits of pumpkins were studied in Pela, Gaya and Kulinyi districts of Hong Local Government Area of Adamawa State. The diseased samples (fruits) were randomly purchased. Of all the districts visited, Kulinyi has the highest percentage of disease samples (43.82%) while the least is Gaya district with 21.35%. Potato Dextrose Agar (PDA) was used for the isolation of pathogens and these gave Rhizopus stolonifer, Aspergillus niger, Aspergillus flavus, and Phytophthora capsici. All the fungal isolates exhibited different degree of pathogenic effect on the pumpkin fruits. The pathogens are susceptible to treatment both in-vitro and in-vivo control trials with wood ash and mango leaf at p ≤ 0.05. Inhibition improved with increased in concentration of the wood ash and mango leaf. Rice chaff treatment equally proved worthwhile with significant inhibition compared to the control at p ≤ 0.05.
Key word: Pumpkin fruit, pathogens, ash, mango leaf, rice chaff.
Pumpkin, one of the common names for flowering plants that belong to the Curcubitaceae family with four genera which include Curcubita maxima, Curcubita pepo, Curcubita moschata and Cucurbita mixta. They are characterized by spreading vines with showy yellow-orange flowers, large lobed leaves, long twisting tendrils and thick shell which contain the seeds and pulp (Neel et al., 2017). They are grown all around the world for a variety of reasons ranging from agricultural purposes (such as animal feed) to commercial and ornamental purposes (Wolford and Banks, 2008).
In Nigeria, it is a traditional vegetable crop, grown mainly for its leaves, fruits, and seeds and, consumed either by boiling the leaves and fruits or by baking the seed (Facciola, 1990). In Hong Local Government of Adamawa State, there was a huge production of pumpkins, but the crops suffer from many diseases which destroy both the crops and fruits during harvest and storage resulting to economy loss.
Postharvest diseases destroy 10 to 30% of the total yield of crops and in some perishable crops especially in developing countries; they destroy more than 30% of the
crop yield (Agrios, 2005; Kader, 2002). The marketability and the nutritional value of infected pumpkin are highly reduced and they are usually being thrown away as useless (Davis et al., 2008). Fungi are the most important and prevalent pathogens, infecting a wide range of host plants and causing destructive and economically important losses of most fresh fruits and vegetables during storage and transportation (Sommer, 1985). Crop losses due to the soil borne fungus like oomycete Phytophthora capsici (Leonian) have been well documented (Hausbeck and Lamour, 2004; Erwin and Ribeiro, 1996). P. capsici affects a wide range of solanaceous and cucurbit hosts worldwide (Erwin and Ribeiro, 1996). Fusarium crown and foot rot of squash and pumpkin is caused by Fusarium solani f. sp. cucurbitae. The pathogen exhibits host specificity for all cucurbits (Thomas, 1998). Bacterial wilt can be a serious disease in pumpkin plantings if striped or spotted cucumber beetles are present when plants first emerge from the soil. Mosaic viruses can cause problems on pumpkin plantings in the home garden.
Pumpkin disease management begins with cultural and preventative controls such as proper site selection, field preparation and the use of resistant varieties, and by remembering that excess water is the enemy of your pumpkin planting. Ijato (2011) reported that plant parts, powder of plant, ash, aqueous extracts which are environmentally non-hazardous, locally available and can be cheaply maintained are suitable alternatives to the expensive synthetic fungicide. Bristone et al. (2011) reported that when tubers of sweet potatoes were treated with wood ash, rot caused by Rhizopus stolonifer and Penicillium expansum was reduced to minimal level. Extract of many higher plants have been reported to exhibit antibacterial, antifungal and insecticidal properties under laboratory trails (Bonaldo et al., 2004; Rodrigues et al., 2007). Aisha et al. (2013) reported the use of guinea corn chaff on Solenoslemon rotundifolius. Muhammed et al. (2001) observed that rice product like rice husks composted soil reduced the incidence of wilting of Parkia biglobosa caused by F. solani in the range of 31.4 to 70.3%. This study will be useful in providing knowledge on the fungal pathogens of pumpkin diseases during storage, as well as on control measures of pumpkin diseases using wood ash, mango leaf and rice chaff, thereby helping in reducing losses of the crops during storage.
Study areas and samples collection
The study of pathogens associated with pumpkins fruit was conducted in three districts (Kulinyi, Gaya and Pella) in Hong local government of Adamawa state. In each district, 122 fruits were inspected and collected from market for further studies. The experimental design was Complete Randomized Design (CRD) arranged in three replicates.
Survey of rot pumpkin
Pumpkin that had been harvested from three out of the six districts of Hong Local Government which has been stored for commercial purposes were observed and every fruit with a rot was recorded. The incidence of fruit spoilage/rot was expressed in percentage using the adopted method of Anjili et al. (2015):
Isolation and identification of isolates
The isolation and identification from diseased pumpkin fruit was carried out using the methods of Fawole and Oso (1995) and Robert et al. (1996).
Determination of severity during the pathogenicity analysis
The pathogenecity test was carried using the method of Chukwuka et al. (2010) and the severity of rot was measured and recorded after seven days of incubation.
In-vitro effect of mango leaf extracts and ash on fungi growth
The approach of Ijato (2011) and Nene and Thapilyal (2000) were used to evaluate the effects of the extract on fungal growth in-vitro by introducing 0.5, 1.0, and 1.5 ml of plant extract into the Petri-dish containing equal amount of PDA media (food poisoned method) and swirled to mix. Each plate was inoculated with 2 mm diameter plug of the isolate and incubated at 31±2°C and the control plates contained only the PDA media. Mycelia growth diameter of each isolates was measured and recorded when the growths of the isolates were completed in the control treatment. Similarly, different grams of sterilize ash were tested (0 g for control, 5, 10, and 40 g). The set up was completely randomised design in three replicates, incubated at 31±2°C for 7 days. The data recorded was analysed using SAS version 7.
In-vivo effect of mango leaf extracts, ash and rice chaff on fungi growth
The methods of Bristone (2004) and Anjili et al. (2016) were used for in-vivo control trail by inoculating the fruits with spores’ suspension of the isolated pathogens then 20, 30 and 40 g of ash, mango leaf, respectively were sprinkled separately on the bore samples in three replicates. A control was set with ash free. It was incubated at 31±2°C for 7 days.
Similarly, healthy pumpkins were sterilized, punctured with sterilized 5 mm diameter cork-borer and inoculated with the isolated fungi. It was placed in-between rice chaff, and the control set up was without rice chaff. The set up was replicated thrice. It was kept for 7 days and after which the level of rot was measured with thread and ruler. The data recorded was analysed using SAS version 7.
Statistical analysis
Data collected were analysed using statistical tool ‘Statistical Analysis System (SAS)’ for analysis of variance (ANOVA) and the means were separated using the least significant difference (LSD) at 95% probability level (P≤0.05).
Pumpkin fruits were observed to show different types of rot symptoms. A total number of 366 harvested pumpkin fruit were inspected in the three districts from the studied area, 89 diseased pumpkins were recorded during the survey (Table 1). Kulinyi district had the highest disease fruits with 39, followed by Pella district with 31 and Gaya district had the least with 19. The major infection was black rot and water-soaked lesions. They were well spread and extensively prevalent in all the three districts of the studied area. Tsado et al. (2013) also reported fruit rots of pumpkin in markets and farms in Minna, Niger State of Nigeria. The highest incidence of disease fruit was however, more prominent in Kulinyi areas than in the other areas. This may not be unconnected with the number of farming activities. Tsado et al. (2013) also suggested that the presence of many pathogens in soils may be major sources of microorganisms present on many vegetables. Mapanda et al. (2005) also shared the same view that pathogens existing in soils or water can be the source of both pre- and post-harvest contamination of several vegetables. Amadioha and Obi (1999) have shown how most of the vegetables consumed are not produced by highly knowledgeable people therefore, liable to be unsafe for consumption.
The isolated fungi from the pumpkin fruit in Hong Adamawa State were identified as Rhizopus stolonifer, Aspergillus niger, Aspergillus flavus, and Phytophthora capsici.
R. stolonifer was the most prevalent in Kulinyi compared to the other districts, while P. capsici was the lowest isolated pathogen and it was observed only in Pella district (Table 2).
All the fungal isolates exhibited different degree of pathogenic effect on the pumpkin fruits. They were able not only to grow on the fruits but also were able to induce some level of rot indicating their virulence. However, there is no growth evident or rot formation within the first 24 h after inoculation in all cases. Rots caused by this fungus occurred on all pumpkin fruits. The lesions started as water-soaked, sometimes sunken, and light to dark spots which often exuded watery ooze. Older lesions were dried and cracked, and fruiting bodies of the fungus were common seen on the surface and deep when it was cut. The rots were characterised by a water-soaked appearance and infected fruit often collapsed completely in the time between inspections. Internally, the tissue was spongy and sometimes dried out, with the mycelium of the fungus clearly visible. The analysis of variance to determine the level of severity at p<0.05 showed to be highly significant among all the pathogens with control. R. stolonifer had the highest severity mean of 121.67 mm, followed by A. niger with 19.85 mm, A. flavus (8.71 mm), while P. capsici had the least mean of 2.71 mm (Table 3). Zakari et al. (2015) reported similar observation on the degree of pathogenicity though on pepper fruits a different vegetable where he also found Aspergillus species more virulence than P. capsici. The differences in severity of the fungi isolated might be due to their ability to overcome the natural defense mechanism of the fruit or their ability to induce resistance in the fruit when infected (Brian and Gwyn, 2008). On the Phytophthora rot, Babadoost (2012) further maintained that P. capsici can infect pumpkin fruit at any stage of development (during transit, and in storage). Hausbeck et al. (2008) also reported P. capsici has been found to associate with postharvest rot of some vegetables viz., taro (Colocasia esculenta (L.) Schott), bottle gourd (Lagenaria siceraria (Molina) Standley), eggplant (Solanum melongena L.), common bean (Phaseolus vulgaris L.), sponge gourd (Luffa aegyptiaca Mill.) and tomato (Lycopersicon esculentum Mill.).
![](/app/webroot/files/images/AJPS/2019/September/Kazi%202.png)
The phytochemical characteristics of mango leaves investigated revealed the presence of medicinally active constituents and secondary metabolites, these includes tannins, flavanoids, saponins, terpenoids, alkaloid, glycoside, steroids and phenols (Table 4) and the phytoconstituents in the leaf extracts may be responsible for the antifungal (Jamuna et al., 2013) and antibacterial activity of the plant (Marjorie, 1999).
The effects of mango leaves, ash and rice chaff on isolated organism
Mango leave extracts both in-vivo and in-vitro produced a significant difference between the mango leave extract and the control at p ≤ 0.05 with retardation of vegetative growth of the fungi when compared with the control. Treatment with mango leaf extract on organisms differs significantly with the quantity of the extracts applied and among the isolates treated. It has been documented that different solvents and quantities have diverse solubility capacities for different phytoconstituents. Jigna and Sumitra (2006) report the difference in activities may be associated with the presence of oils, wax, resins, fatty acids or pigments, which had been reported capable of blocking the active ingredients in the plant extracts, thus, preventing the plant extract from accessing the fungal cell wall. Of all the fungi tested the P. capsici was slightly more susceptible to the extracts than the Aspergillus species and R. stolonifer. The finding agreed with earlier reports that P. capsisi are more susceptible to extracts from Tridax procumbens, Vernonia amygdalina, and Azadirachta indica than other Aspergillus species among other fungi isolated from pepper in Yola (Zakari et al., 2015) (Tables 5 and 7).
Ash treatment in both in-vitro and in-vivo produced a significant difference between ash treatment and the control at p ≤0.05. Treatment also differs significantly with the quantity of the ash applied and this was also reported by Anjili et al. (2016) and Mark et al. (2015) who worked on fungi isolated from date palm fruits and cowpea blotch respectively. Channya and Chimbekujwo (2002) reported that wood ash effectively controlled fungal rot of plantains (Musa parasidiaca L.). Bristone et al. (2011) reported that when tubers of sweet potatoes were treated with wood ash, rot caused by R. stolonifer and P. expansum was reduced to minimal level. Oguntade and Adekunle (2010) also reported that wood ashes proved effective in preserving stored crops against pest and microbes (Tables 6 and 8).
![](/files/images/AJPS/2019/September/Kazi 3.png)
The control using rice chaff produced a significant difference between rice chaff and the control at p ≤ 0.05. Muhammed et al. (2001) in their studies observed that rice product like rice husks composted soil reduced the incidence of wilting of P. biglobosa caused by F. solani. According to Aliyu et al. (2011) amending cowpea with rice husk showed considerable less susceptibility to the virus pathogen infecting cowpea compared to the non-amended plants. He further showed that the rate and time of application of the Rice-husk powder was a key factor in the ameliorative effect of this organic amendment in the suppression of the viral inoculums. Muhammed et al. (2013) reported a significant effect of guinea corn chaff on S. rotundifolius microbes. These clearly show why fungi isolated from pumpkin responded differently with different amendment (Table 9).
R. stolonifer, A. niger, A. flavus, and P. capsici are some of the pathogenic fungi which cause rots of pumpkin in the studied area. The pathogenicity test result indicated that the isolated fungi are pathogenic and attributed to rots of pumpkin in Hong L.G.A. The activities of these fungi can affect the market value of fruits. Of all the treatments, wood ash which is alkaline shows to be more promising than other treatments. Therefore, there is need to assess the phytochemical properties of the fruits in order to determine the level of nutritional loss as a result of the activities of pathogens.
The authors have not declared any conflict of interests.
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