Next Article in Journal
Coir, an Alternative to Peat—Effects on Plant Growth, Phytochemical Accumulation, and Antioxidant Power of Spinach
Next Article in Special Issue
The Impact of Salt Stress on Plant Growth, Mineral Composition, and Antioxidant Activity in Tetragonia decumbens Mill.: An Underutilized Edible Halophyte in South Africa
Previous Article in Journal
Physiological and Biochemical Characterization of the GABA Shunt Pathway in Pea (Pisum sativum L.) Seedlings under Drought Stress
Previous Article in Special Issue
Genetic Diversity and Population Differentiation of Pinus koraiensis in China
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Solanum aethiopicum: The Nutrient-Rich Vegetable Crop with Great Economic, Genetic Biodiversity and Pharmaceutical Potential

1
Co-Innovation Center for Sustainable Forestry in Southern China, College of Biology and the Environment, Nanjing Forestry University, Nanjing 210037, China
2
Department of Crop and Soil Sciences, Kwame Nkrumah University of Science and Technology, Kumasi AK-449, Ghana
3
Key Laboratory of State Forestry Administration on Subtropical Forest Biodiversity Conservation, Nanjing Forestry University, Nanjing 210037, China
*
Author to whom correspondence should be addressed.
Horticulturae 2021, 7(6), 126; https://doi.org/10.3390/horticulturae7060126
Submission received: 1 May 2021 / Revised: 22 May 2021 / Accepted: 26 May 2021 / Published: 28 May 2021

Abstract

:
Solanum aethiopicum is a very important vegetable for both rural and urban communities in Africa. The crop is rich in both macro- and micronutrients compared with other vegetables and is suitable for ensuring food and nutritional security. It also possesses several medicinal properties and is currently employed in the treatment of high blood pressure, diabetes, cholera, uterine complaints as well as skin infections in humans. The crop is predominantly cultivated by traditional farmers and plays an important role in the subsistence and economy of poor farmers and consumers throughout the developing world. It also holds potential for dietary diversification, greater genetic biodiversity and sustainable production in Africa. Despite the numerous benefits the crop presents, it remains neglected and underutilized due to the world’s over-dependence on a few plant species, as well as the little attention in research and development it has received over the years. This review highlights the importance of S. aethiopicum, its role in crop diversification, reducing hidden hunger, the potential for nutritive and medicinal benefits, agricultural sustainability and future thrusts for breeding and genetic improvement of the plant species.

1. Introduction

Solanum aethiopicum is a horticultural crop species consumed in Africa and it contains a great amount of nutrients [1]. The crop is an important food source for many people. The fruits and leaves are employed in the preparation of stews and soups. It is used to treat certain diseases because of the phytochemicals it contains and serves as a rich source of important macro and micronutrients [2]. It is thus a potential curative to hidden hunger [3,4,5]. The crop is one of the most widely grown vegetables in Africa and was brought to Brazil through the slave trade. The crop belongs to the Solanaceae family with a chromosome number of 24. It is commonly called African eggplant, scarlet eggplant, garden eggs and bitter tomato. The species is believed to have originated from Africa and was domesticated from the wild Solanum anguivi Lam., via the semi-domesticated Solanum distichum Schumach. & Thonn., both of which are found throughout tropical Africa [6,7]. The crop is cultivated in the humid zones of West Africa for its immature fruit, in the savanna area frequently for both its leaves and immature fruits (often called ‘djakattou’), and in East Africa, especially Uganda, mainly as a leaf vegetable (called ‘nakati’). African eggplant is a good and reliable crop as it yields a harvest of about 25 tons per hectare [8]. The species Solanum melongena and Solanum macrocarpon are the close relatives of S. aethiopicum and both species are commonly grown in Africa. Mwinuka et al. describe this crop as a neglected and underutilized horticultural species, despite possessing the ability to significantly contribute to nutrition and food security. It has been overlooked as there is limited knowledge on the plant and research efforts about it are limited, especially in terms of climate adaptation and sustainable agricultural growth in Africa and particularly in East Africa [9].
Although African eggplants possess several important properties, knowledge on the genetic improvement potential, possibility of providing medicinal or nutritional benefits, such as disease prevention and treatment and its potential for agricultural sustainability is still limited. This is because the crop has not received adequate research attention for years. There is therefore a need to promote the dynamic use, documentation, conservation and evaluation of genetic resources of this important but neglected crop [10]. Additionally, due to the overdependence on the three major food crops (wheat, maize and rice) and their subsequent shortages, the conservation, improvement and utilization of underutilized plant species such as African eggplant is of utmost importance. The cultivation of underutilized crops provides greater genetic biodiversity, and can potentially improve food security [11]. The purpose of this review is to give an overview of research carried out on S. aethiopicum for the detection of avenues that will contribute to promoting the plant species, mainly in its potential for biodiversity, nutritive and medicinal benefits, and agricultural sustainability.

2. Physiological and Genetic Properties of S. aethiopicum

2.1. Characterization and Ecophysiology

S. aethiopicum grows to about 2.5 m in height and is an often a branched deciduous shrub. On the stems, the leaves are alternately arranged and have smooth or lobed margins. Leaf-blades can reach a length of up to 30 cm and a width of 21 cm. The leaves’ petioles are oval or elliptical, reaching a length of up to 11 cm [12]. The species is hermaphrodite (has both male and female organs) and mainly self-pollinated, but insect pollinators complement self-pollination as they provide cross-pollen, which augments gene exchange and hybrids in natural population and lessens inbreeding depression. The inflorescence is a five-flowered lateral, racemose cyme [13]; peduncle often short or even absent, rachis short to long. The flowers develop into egg- or spindle-shaped berries, which are red to orange in color with a smooth or grooved surface depending on the variety. The crop becomes ready for harvesting from 100 to 120 days after planting and the fruit should be plucked before it changes color from white to pale yellow. African eggplant seeds are flattened, 2–5 mm in diameter, lenticular to reinformed and pale brown or yellow in color. Germination is epigeal with cotyledons being thin and leafy [14]. Multiplication of the species is carried out mainly through the seeds.
S. aethiopicum is a complex species consisting of groups that are very distinct morphologically and were formerly regarded as four separate species [15] (Figure 1). It is also described to be a hypervariable species as it is made up of many forms and types that differ morphologically, with hundreds of local varieties [16]. The species S. aethiopicum can be classified with respect to its use into four distinct groups. They are the Gilo, Shum, Kumba and Aculeatum group [17]. The Gilo group gives rise to several differently shaped edible fruit (ranging from a spherically depressed form to elliptic in outline); the Kumba group possess a stout main stem with large hairless leaves that can be picked as a green vegetable, and later produces very large grooved fruit that is picked green or even red; the Shum group is a short much-branched plant with small hairless leaves and shoots that are plucked frequently as a leafy green vegetable but the small (1.5 cm across) very bitter fruits are not eaten; the Aculeatum group produces flat-shaped fruit [18]. The plant is also sometimes grown as an ornamental one.
Being a tropical plant species, the African eggplant is intolerant to low temperatures and very cold or water-logged conditions. Some level of tolerance to irrigation-induced salinity has been reported from Senegal [19]. The edible groups of African eggplant (Gilo, Kumba and Shum) are adapted to diverse areas depending on the climate. The Gilo group is commonly found in humid areas all over tropical Africa where its members grow best at the full sun of woodland savanna on fairly deep and well-drained soils of pH 5.5–6.8, with 25–35 °C and 20–27 °C day and night temperatures, respectively [20]. The Kumba group, which is cultivated chiefly in semi-arid areas from Occidental Sahel to the north of Nigeria, is able to put up with environments that are hotter than normal (even to 45 °C day temperature) with an occasionally low air humidity of about 20%, especially after irrigation [20]. The Shum group is typically seen to shed its leaves during plant water loss under the warm, humid conditions. In Africa, the group is found at high altitude and very humid areas mainly in Uganda and the southeast of Nigeria [20]. In Uganda, it is grown in swamps during the dry season [21,22].
The hybrids emanating from the cross between S. aethiopicum and S. anguivi Lam (wild ancestor) are fertile [23]. Characterization of a plant species gives a description of its germplasm and determines the expression of highly heritable traits ranging from morphological or agronomical features to seed proteins or molecular markers. The characterization of cultivated eggplants and their wild relatives has commonly been analyzed by employing conventional morphological descriptors that are highly heritable and simple to assess [15,24]. Studies on the morphological characterization of scarlet eggplant have shown it to be a highly variable crop. The most extensive research was performed by Lester in 1986 [16]. The authors characterized 108 accessions of the scarlet eggplant complex using morphological and taxonomically relevant characters (e.g., fruit size, number of locules, number of flowers per inflorescence, prickliness) and observed that the four cultivar groups could be differentiated by a set of traits (including leaf shape, fruit shape, prickly leaves and stem, bitter taste) detected in a single group. A number of the accessions were also observed to be intermediate between S. anguivi and S. aethiopicum. According to Osei et al. [25], a wide variation exists among species S. aethiopicum, S. anguivi and S. macrocarpon. They also observed a lot of similarities between the lines of S. aethiopicum and S. anguivi.

2.2. Propagation, Cultivation Techniques and Systems

The African eggplant is often grown as an annual, but generally a perennial, plant with stems that become more or less woody and persist. It grows well in deep, well-drained soils. Cultivation of African eggplant is mainly dependent on the rain, but irrigation can be applied during the dry seasons. The African eggplant requires a pH of 5.5–6.8, and thrives well at daytime temperatures ranging between 20–30 °C, but it can tolerate 10–40 °C. It cannot tolerate very cold or water-logged conditions [26]. It is more prudent to grow the crop on a minimum to low salinity soil to promote maximum growth and development, since salinity plays a part in disturbing the anatomical and morphological features of the crop [27]. S. aethiopicum is propagated by seed. The seeds for planting are obtained from fully ripe fruits that should not be exposed to direct sunlight. Seeds remain viable for a long time when stored in a cool, dry place. Seeds also store well inside air-dried fruits, which is the traditional form of seed storage by farmers. The 1000-seed weight of African eggplant is 2–4 g. Its germination takes 5–9 days for the Gilo and Shum groups, but only 3–5 days for the Kumba group, although the latter may express seed dormancy and end up having few seeds per fruit. Seeds are sown in sandy soil in nursery beds or containers. The seedlings are transplanted to the field after 30–35 days, when they have 5–7 leaves and are 15–20 cm tall. Plants of the Kumba group grown in dry savanna regions are often planted at a distance of 1 m × 1 m, whereas those of the Gilo group can be spaced at 50–100 cm in the row and 75–100 cm between rows, depending on the cultivar [14]. They can be grown either on flat land or ridges. The cultivation of Shum Group is somewhat different. Cultivars of the Shum group are grown for their young shoots, which are frequently harvested, and the crop can thus be spaced at 20–30 cm in the row and 60–75 cm between rows. An alternative is to broadcast seeds of Shum group, for thinned plants to be used as the first harvest. Seeds are sometimes broadcast together with amaranths (Amaranthus spp.) and spider plant (Cleome gynandra L.), where the latter two crops are harvested early by uprooting and the plants of S. aethiopicum Shum group remain.
Production of African eggplant is created using a range of cultivation techniques. These techniques are aimed at the preservation and modification of the physical and chemical characteristics of the soil (soil preparation and tillage, irrigation, fertilization), while improving plant production (training, pruning, fruiting, production and pesticide treatments). Some examples of cultivation techniques employed by farmers include intercropping, mixed cultures and monocultures. On the farm, it can be intercropped with crops such as cowpea, sorghum, Ziziphus mauritiana Lam, Solanum lycopersicum, Capsicum annuum, Corchorus olitorius and Abelmoschus esculentus [28,29]. In mixed cultures, African eggplant is the main crop, whereas Zea mays and Manihot esculenta are grown as secondary crops. Monoculture is also practiced where an optimal crop density is cultivated on the farm and sometimes under irrigation during the dry season. Most of the farmers in Africa cultivate using conventional and organic systems. From the study of Aguessy et al., the majority of the farmers who were interviewed acknowledged the use of NPK and urea fertilizers a few days before transplanting as compensation for soil deficiency conditions. The other proportions of farmers are into the use of organic manures [30]. Animal manure and compost are being employed in the cultivation of African eggplant. They are helpful in soil amendment due to the needed organic matter and sequester carbon they add, as well as the reduced reliance on chemical pesticides and fertilizers. Compost from false yam (Icacina oliviformis) tuber was applied to a field planted with African eggplant and it showed support for plant growth and yield characteristics [31].
Efforts are also underway to optimize the yield of African eggplant. Mwinuka and others in a recent report assessed how irrigation water and nitrogen affects the growth parameters of African eggplant, as well as the yield, fruit quality, water use efficiency (WUE) and nitrogen use efficiency (NUE). They observed that the African eggplant growth variables (plant height and Leaf Area Index) correlated well with fruit yield, and when 100% water was added to a 75% (187 kg/ha) nitrogen treatment, the quality of the fruit was at maximum. Superlative WUE and NUE were obtained at 80% and 100% water supply, respectively, in addition to a nitrogen concentration of 75%. It was further suggested that in soils with a mixture of sand, clay and loam, under sub humid circumstances that are tropical, the optimal application for African eggplant will likely be about 80% of the total irrigation requirement and 75% of the nitrogen requirement, in order to minimize the rate of exchange between the various indicators [9].
The crop is affected by several diseases and pests. Common diseases of African eggplant include Chilli veinal mottle virus (ChiVMV) borne by the vector green peach aphid (Myzus persicae) [32], Stemphylium disease caused by Stemphylium solani and other soil-borne severe diseases such as wilt caused by Ralstonia solanacearum, collar rot and wilting caused by Sclerotium rolfsii and Verticillium dahliae, and root-knot nematodes (Meloidogyne spp.) [33]. Pests of the plant include green peach aphid Myzus persicae, grasshoppers (Zonocerus sp.), fruit and flower borers (Leucinodes and Scrobipalpa), leafhopper (Jacobiasca lybica) and caterpillars (Selepa docilis) [34]. Spider mites (Hemitarsonemus and Tetranychus) are a serious problem in drier regions; acaricide sprays can normally control them [35].

2.3. Biodiversity and Conservation

Today, the production of crops is based on just a small circle of plant species [36]. Despite this fact, several undermined crops are grown and collected, thereby adding to biodiversity [37]. Although S. aethiopicum is one of the less recognized crops, it shows a distinct diversity in the cultivated types of varieties in Ghana. As well as contributing to biodiversity intraspecifically, it also helps to maintain a wide intraspecies biodiversity through local cultivation. Limited scale producers keep up the genetic diversity of this crop. Not only is there scattering of cultivars across locations, their naming is often also set differently. Moreover, the cultivars could be equivalent, yet exhibit differences in their phenotype due to diverse biotic and abiotic factors. S. aethiopicum has noticeable qualities such as taste, size, color, shape and others, but these attributes differ widely. For instance, its color could be deep green, green, white, cream, or even yellow and this could be used as the basis of freshness. The sizes range from small to big with a massive demand for the latter. The shape could be round, elongated, with ridged or smooth surfaces. Taste is additionally a significant quality property pursued by buyers and very frequently identified with the shape. Most often than not, the bitter ones are the round shaped ones, and this characteristic is genotype-specific but environmental factors could also play a part in it [37]. In Ghana, research scope to determine the reason for this diversity is very little, though not for lack of diversity in African eggplant germplasm, and due to this myopic research level, to our knowledge, nothing has been implemented to conserve diversity.
Accurate information on the analysis of genetic diversity, which is expressed as variants in a linear sequence of nucleotides in DNA, is relevant to know which genes are responsible for which trait expressed in S. aethiopicum. African eggplant differs severely when it comes to agronomic traits, some of which include time of flowering, fruit yield, fruit maturity, branching habits [25]. Taking the physiology, morphology and biochemical properties of the eggplant’s related species and wild types into consideration, there exists a wide diversity morphologically [38,39]. For any breeding program to be effective, the detail in the genetic magnitude of diversity within the crop species is dire. This is because informed knowledge on genetic diversity could go a long way in sustaining selection gain in the long term [40]. From Sharma and Jana’s [41] point of view, a priority for starting an efficient breeding program is the assessment of how species vary genetically, since it gives a platform for cutting desirable genes to size. Additionally, knowing how genetically diverse a huge population of African eggplant germplasm is aids in the decision-making of breeding techniques and management schedules for current and future use [42]. The study of genetic diversity allows for the selection of African eggplant parents that are genetically diverse to obtain in the segregating generations, recombinants that are desirable [43]. This choice of parental selection using biodiversity studies is valuable because it showcases how useful variations can be expressed in later offspring. Thus, with African eggplant, diversity studies at their early stages would amount to the creation of cultivars and varieties that are shared across the board and known for their stability and adaptability in terms of performance (consistency in tolerance of harsh weather conditions and disease resistance) based on evidential characteristics.
Since there is a lack of large genomic resources for conservation, this implies that S. aethiopicum breeding is lagging behind other vegetable crops, especially of the same species. It is thus highly important to evaluate and safeguard S. aethiopicum, as it is highly underrepresented in the global conservation system of plant genetic resources and may have hidden genes that are of relevance when it comes to tolerance or resistance of biotic or abiotic stresses [8]. The World Vegetable Center (WorldVeg) secures some amount of public germplasm collection of eggplant, which includes the major cultivated species (S. melongena, S. aethiopicum and S. macrocarpon), and more than 30 eggplant wild relatives, with more than 3200 accessions collected from 90 countries of which S. aethiopicum is included and considered as important. Over the last 15 years, more than 10,000 seed samples from the Center’s eggplant collection have been shared with public and private sector entities, including other genebanks. An analysis of the global occurrences and genebank holdings of cultivated eggplants and their wild relatives reveals that the WorldVeg genebank holds the world’s most extensive public collection of the three cultivated eggplant species with S. aethiopicum being the third. However, comparing this with other vegetable crops (with huge genomic resources for conservation), there is still a significant deficiency in the conservation of S. aethiopicum. The main cluster of S. aethiopicum is in West Africa, with a total of 1288 occurrences based on the literature of previous studies and characterization data available at the WorldVeg [8]. From 1981–1986, the International Plant Genetic Resources Institute (IPGRI) performed a collection of genetic resources of African eggplant. In 2001, efforts were made to regenerate and evaluate the collections as part of the EGGNET project, an international project for managing the genetic resources of eggplant. A rich germplasm collection is maintained at INRA in Montfavet, France. A collection is kept at AVRDC in Arusha, Tanzania, and plant breeders in Ghana, Côte d’Ivoire, Nigeria, Senegal and elsewhere in Africa also maintain some accessions of African eggplant [14].

2.4. Genetics and Breeding

The breeding of African eggplant has received little attention, although germplasm collections of it exist. Most of the cultivated species came about as a result of selection by farmers and consumers’ preference for fruit size, color and taste (sweet or bitter), skin toughness, shelf life, as well as yield potential, disease resistance, earliness and duration of the harvest season, plant architecture and fruit location, and in the case of the Shum group, ease of leaf harvest. S. aethiopicum for a long time has been neglected by formal programs involved in the improvement of crops except in breeding programs where some of its specific traits are exploited to improve the resistance of S. melongena to diseases. Domesticated and wild relatives of African eggplant possess important traits that remain to be explored. S. aethiopicum has been reported to express low susceptibility to pests and diseases than S. melongena [44], leading to the selection of S. aethiopicum (Aculeatum group) in Japan as a rootstock for tomato and garden egg due to its resistance to wilt. It also shows a higher level of tolerance to drought and heat than tomato and eggplant in the field. Ano et al. [45] reported on S. aethiopicum in a breeding program used as a source of the disease resistance gene. From this study, S. melongena was crossed with S. aethiopicum and the hybrids subsequently backcrossed to S. melongena. It was likely to derive families with a high resistance level to bacterial wilt from the second backcross, as well as vast differences in the shape and fruit color. Studies into the molecular mechanism underlying double fertilization between self-crossed S. melongena and that hybridized with S. aethiopicum have been carried out using comparative transcriptome analysis. A number of differentially expression genes (DEGs) were found which are involved in plant hormone transduction, cell senescence, metabolism, and biosynthesis pathways. The findings of this study provide insights into the regulatory mechanisms underlying variations between ovaries of self-crossed and hybrid eggplants and a basis for future studies of crossbreeding Solanum [46].
In a study by Hamidou et al. [47], 12 scarlet eggplant accessions were assessed via morphological and cytomolecular characterization. This study established the genetic closeness of S. aethiopicum and S. melongena not only in terms of their chromosome number but also in terms of their genome size. Similarities and contrasts among the 12 scarlet eggplant accessions were observed for 27 quantitative descriptors. The cluster analysis was able to classify the accessions into four distinct groups. A great deal of variability was found among the 12 scarlet eggplants accessions, most of which was associated with flower and fruit-related traits. However, no significant differences among the accessions for the GC content, for seedling and stomatal traits evaluated were found. Additionally, there was no significant difference (α = 0.05), with the exception of one accession (PI 420226), among the scarlet eggplants evaluated for their nuclear DNA content.
Availability of the genome information of a neglected crop such as S. aethiopicum will hasten a more productive and exact selection of exceptional accessions of the crop and breeding of it, as well as other crops within the Solanaceae family. A recently published draft genome sequence of the African eggplant has afforded some insights into disease resistance, drought tolerance, and the evolution of the genome [48]. The 1.02 Gb draft genome assembly of S. aethiopicum contained largely repetitive sequences (78.9%). Gene models were annotated including 34,906 protein-coding genes. Expansion of disease resistance genes was found through two rounds of amplification of long terminal repeat retrotransposons, which may have happened ∼1.25 and 3.5 million years ago. The resequencing of S. aethiopicum and S. anguivi genotypes resulted in identification of 18,614,838 single-nucleotide polymorphisms (SNPs), of which 34,171 were positioned within disease resistance genes [48]. Furthermore, the investigation into the domestication and demographic history showed active selection in both the Gilo and Shum groups for genes involved in drought tolerance. A pan-genome of S. aethiopicum was generated containing 51,351 protein-coding genes, 7069 of which were missing from the reference genome [48].
More recently, few researchers have focused their attention on improving the agronomic characters of farmer’s selection. In Senegal, very hairy, mite-resistant cultivars of the Kumba group have been bred. Some promising cultivars for high yield were obtained when S. anguivi was crossed with ‘Dwomo’, a cultivar whose fruits resembles an egg in its size and shape. This was achieved by collaboration between the Crops Research Institute in Ghana and the Natural Resources Institute (United Kingdom) [49]. A seed company in Senegal (Technisem Seed Company) is into the commercialization of improved cultivars of African eggplant. The most popular cultivars of the Kumba group are ‘Ndrowa’ (flat, ribbed, green-yellow fruits of 70–80 g, diameter 5 cm, with a mild taste, plant height 60–100 cm, harvestable 50–70 days after planting, yield potential 25 t/ha, resistant to mites), ‘Ngalam’ (flat, strongly ribbed, pale green to white fruits of 120–180 g, diameter 7 cm, slightly bitter taste, plant height 60 cm, harvestable 50–60 days after planting, yield potential 10 fruits per plant, resistant to mites) and ‘Jaxatu Soxna’ (flat, ribbed, pale green to white fruits of 40–50 g, diameter 5–6 cm, bitter taste, plant height 50 cm, harvestable 40–60 days after planting, yield 20–25 fruits per plant or 30 t/ha, or used as a leafy vegetable, resistant to mites, drought, high rainfall and high temperatures).
The inheritance of some important traits in S. aethiopicum has also been studied intensively. Most wild-type characters such as prickles, stellate hairs and long racemose cymes are often dominant. Imperfect morphogenesis, indicating loss of genetic regulation, was involved in many of the recessive domesticated traits. The F1 hybrids between cultivars (S. anguivi and S. aethiopicum) also showed significant heterosis and are recommended for crop production [23]. Research for yield of fruit and yield component traits on the mode of inheritance, genetic control, heritability and heterosis has been implemented. Traits such as fruits per cluster, the cluster per plant and length and width, are the parameters of fruit yield in fruit vegetable. Out of the components of fruit yield studied in an experiment for S. aethiopicum, fruit length and fruit clusters per plant were both affected by the additive gene action, while on the other hand, diameter and fruits per cluster required the dominance gene action when it comes to their inheritance. Dominance and dominance by dominance digenic interaction expressed the duplicate type of epistasis for fruit clusters per plant [50]. This genetic information is very imperative for efficient breeding strategy and development of hybrids and open-pollinated varieties.
In vitro regeneration from cotyledonary and true leaf explants (direct organogenesis) of S. aethiopicum and S. macrocarpon have been reported by Carmina et al. [51]. A higher level of regeneration and the average of shoots per explant has been demonstrated by using low concentrations (0.1 and 0.2 µM) of thidiazuron (TDZ) in the media. The success allows for further genetic transformation and improvement of S. aethiopicum through in vitro techniques. Somaclonal variation occurring in tissue culture media has proven to be a potential source of variability for crop improvement [52,53]. Studies have shown that in vitro regeneration of plants through indirect organogenesis (i.e., via callus phase) could induce more variants as compared to direct organogenesis. Hence, tissue culture avenues could be exploited to induce somaclonal variants of African eggplant, so as to broaden the genetic base of the crop for future breeding programs. Mutants of African eggplant demonstrate differences in traits that are agro-morphological and yield attributes with varying doses of Gamma irradiation. The effect of the mutagen on S. aethiopicum is assessed in terms of its influence on growth improvement by inducing changes in cells and tissues of the plant that are cytological, genetical, biochemical, physiological and morphogenetic. Low doses of gamma irradiation (40 Gy and 60 Gy) caused significant variation in some traits that are agro-morphological, like plant height, leaf characteristics, days to first flowering, number of leaves per plant and number of branches per plant in S. aethiopicum [54]. Therefore, mutation breeding by gamma irradiation and other mutagens can be employed as an effective means of inducing genetic variability in African eggplant to improve and select desirable mutants for breeding purposes.

2.5. Phytochemical and Pharmacological Activities

The African eggplant fruits are usually used in the preparation of soups, in stews as a vegetable, and they can sometimes be eaten raw. It is also possible to eat the shoots and leaves in a cooked form. African eggplant contains many protein, minerals, vitamins, carbohydrate, fat, crude fiber, ash and water substances that are relevant and massively helpful in nutrient supplement and health promotion. The fruits mostly possess high moisture content and low dry matter [55]. Several fundamental mineral elements, including calcium, magnesium, potassium, sodium, manganese, iron, copper, zinc and phosphorus are also contained in the fruits of S. aethiopicum. These minerals are involved in functions such as maintenance of heart rhythm, muscle contractility, formation of bones and teeth, acid-base balance, regulation of cellular metabolism and enzymatic reactions [56]. Moreover, S. aethiopicum has been shown to be rich in vitamins (such as vitamin A, B, C, D and E) [57]. Analysis of the nutritional and mineral composition of the fruits and leaves of S. aethiopicum brought to light that the crop is rich in major and minor nutrients and all the nutrients are known to be vital for the proper functioning of the body [1]. Of note, the exocarp of both ripe and unripe S. aethiopicum fruit bears no incidence of toxic metals (e.g., chromium, cadmium, lead, etc.), which makes it a better source of health products. The nutrient, mineral and vitamin composition of S. aethiopicum fruits is presented in Table 1 as adopted from previous studies [55,56,57]. Chinedu et al. in their study on the proximate and phytochemical analyses of the fruits of S. aethiopicum also identified nutrients and mineral elements [58] that had similar values to the ones presented above.
Phytochemical screening of the crop showed a copious presence of alkaloids, flavonoids, phytosterols, saponins and vitamin C, moderate presence of cardiac glycosides, steroids and tannins, and a trace amount of terpenoids in the fruits [55,58]. Alkaloidal extracts of Solanum species have been reported to express analgesic effects and central nervous system depression [59]. The presence of alkaloids, mainly glycoalkaloids, gives the bitterness in eggplants and the relative bitterness determines to a great extent their edibility or otherwise. The incidence of toxic glycoalkaloids leads to poisoning in some Solanum species by causing diarrhea or carcinogenic glycosides which bring about excessive deposition of calcium in tissues. Researchers have cautioned that care should be taken when using the fruit and insist that its consumption should be in small quantities [60]. African eggplant is of great medicinal importance and thus has many functional food properties. Its saponins are important dietary supplements and nutraceuticals. They possess antimicrobial properties and protect plants from microbial pathogens. Reports have shown that saponins present in traditional medicine preparations cause hydrolysis of glycosides from terpenoids which avert the toxicity associated with the intact molecule [61,62]. Ascorbic acid and flavonoids have been found to be present in the fruits and stalk of the plant, which contain high antioxidant potential [63,64,65]. Traditionally, many tropical African countries use the fruits of bitter cultivars as medicine to cure certain ailments [66]. The roots and fruits of African eggplant are used as a carminative and sedative, and to treat colic and high blood pressure; leaf juice as a sedative to treat uterine complaints; an alcoholic extract of leaves as a sedative, anxiolytic, anti-emetic and to treat tetanus after an abortion [67,68]. The crushed and softened fruits are also used as a purgative. The juice of boiled roots is used to treat hookworms, while the crushed leaves are used for gastric ailments [19]. Several parts of the plant are used, as powder or ash, to treat diseases such as diabetes, otitis, cholera, toothache, bronchitis, skin infections, dysuria, asthenia, dysentery and haemorrhoids in decoction. Moreover, antiviral, anticancer, anticonvulsant and anti-infective effects have been reported in eggplants due to the phytochemicals they contain. Narcotic, anti-asthmatic and antirheumatic effects are also ascribed to eggplants [69].
A previous study identified four groups of phenolic acids in the fruit of S. aethiopicum. Group 1 comprised chlorogenic acid isomers and 3-O-trans, 5-O-trans, 5-O-cis isomers of caffeoylquinic acid (3CQA, neochlorogenic acid; 5-CQA, chlorogenic acid; 4-CQA, cryptochlorogenic acid and 5-(Z)-CQA, cis-chlorogenic acid). Chlorogenic acid was the predominant compound in Group 1, with average levels 176-, 28.9-, and 92.5-fold higher than levels of neochlorogenic acid, cryptochlorogenic acid and cis-chlorogenic acid, respectively. Group 2 consisted of two phenolics: 3,5-diCQA and 4,5-diCQA. Group 3 comprised four compounds: N,N′-dicaffeoylspermidine (predominated); N-caffeoylputrescine and their isomers; and Group 4 comprised 3-O-actyl-5-O-caffeoylquinic acid (3-acetyl-5CQA), 3-O-actyl-4-O-caffeoylquinic acid (3-actetyl-4-CQA) [70]. The leaves of African eggplant possess oxalate and alkaloids such as solasodine, with reported glycocorticoid effects [14]. Its characteristic bitter taste is a result of the furostanol glycosides [44,67].
Anosike et al. [71] in their study reported that S. aethiopicum fruit had anti-inflammatory properties. Compared to the control group, the fruit extract substantially reduced the fresh egg albumin-15-mediated rat paw oedema and reduced the granuloma tissue formation in the fruit treated groups. According to Tunwagun et al. [72], phytochemicals such as alkaloids, saponin, tannin, volatile oil, phenol and flavonoids can be found in different anatomical parts of ripe African eggplant fruits. The presence of these phytochemicals in the different parts of the fruit indicates that the fruit might be pharmacologically active against a number of diseases. Another study by Emiloju and Chinedu [73] observed a dose-dependent, weight-reducing effect on rats in their study of the effects of dietary supplements of S. aethiopicum and S. macrocarpon on weight gain and glucose metabolism in rats. They further concluded that these underutilized crops may be used to alleviate the challenge of obesity.

2.6. Postharvest Factors Affecting their End-Use Quality

African eggplant production is characterized by poor post-harvest handling practices, a short shelf life of approximately three to four days and fruit spoilage losses estimated at 25% depending on the fruit harvesting stage and storage environment [37,74]. The lack of adequate management practices for post-harvest storage is estimated to cause up to 50 percent of vegetable crop yield losses between harvesting and consumption [75]. The most critical issue affecting the quantity, quality and thus the market value of fruits is poor harvesting and storage practices [76]. It is estimated that about 40–50% of horticultural crops produced are lost even before consumption in developing countries, mainly due to poor post-harvest handling which results in bruising, water loss and eventual decay during post-harvest handling [77]. A number of factors will lead to a reduction in the quality of fruits after harvest when not properly handled. Postharvest factors influencing postharvest quality of fruits include maturity stage, method of harvesting, time of harvesting, sorting and grading, packaging and packaging materials, storage, type of storage, temperature and relative humidity during storage.
The maturity stage at harvest is an essential factor that influences flavor and shelf-life qualities of fruits [78]. Failure to harvest fruits on time causes them to over-mature and ripen while still on the plant. On the other hand, harvesting fruits at the immaturity stage gives rise to increased shriveling and fruits susceptible to mechanical damages [79]. In Tanzania, African eggplant fruits are harvested by farmers based on their size and regularly comprise immature, mature and over-mature fruits. It is reported that cultivating the fruits at the immature level (fruits with non-shiny peel) is suitable for increasing yield in number of fruits per hectare and increasing vitamins and minerals content while harvesting at the mature fruits stage (by fruits with shinny peel) is recommended for increasing fruit beta carotene content, carbohydrate and fiber content [80]. An appropriate harvesting method is necessary to prevent bruises or injuries during harvesting as they may later express black or brown patches that make them unattractive. Injury to the peel may serve as an entry point for microorganisms, causing rotting. In Africa, harvesting of S. aethiopicum is carried out primarily with the hand by pulling or twisting the fruit pedicel or harvesting individual fruits or fruit bunch with the help of fruit clippers/secateurs/scissors. Time for harvesting also influences quality. Fruits harvested and transported early in the morning for sorting, grading, and packing at the packing house are long-lasting and of better quality. To minimize the risk of heat injury and sunburn, it is advisable that the fruits be harvested during the cooler periods of the day [81]. Harvesting fruits early in the morning facilitates faster pre-cooling and yields better quality.
Sorting and grading after harvest are one of the most critical postharvest practices. This is carried out mainly to remove diseased and defective fruits from the lot. This activity is conducted in a pack house or farmer’s field and an assurance of a quality produce depends on a proper sorting and grading. Currently, grading is performed manually by farmers, but mechanical graders can also be employed. Most farmers and traders in Africa neither grade nor sort their produce after harvest. According to Apolot et al. [81], 16.6% of traders in Uganda are generally involved with sorting and grading of their vegetables as against 83.4% who are not. Packaging of fruits is needed in order to protect them from mechanical injuries. The packages should be well-ventilated and care should also be taken to prevent compression damages on the fruit during storage and transportation. A previous report revealed that storing fruits in perforated polyethylene bags reduced water loss and had the longest shelf life, although they faced the highest incidence of decay [82]. In Africa, the most commonly used storage facilities are air-cooled storage houses which rely on natural cold air. Proper management of temperature, ventilation and relative humidity are the key factors that affect the postharvest quality and storage life of horticultural product. Presently, mechanical refrigerators are employed in the storage of African eggplant, but they are energy intensive, unaffordable for local farmers and require constant supplies of electricity which is unavailable in many rural parts of Africa. In a study by Sekulya et al. [83], the shelf life of Shum (leafy vegetable) saw an increase (from one day to four days) when it was submerged into portable water intermittently for 2 to 3 s after every one hour during the day for sample in ambient storage both with roots intact and with roots cut-off. Samples stored in perforated polyethylene and meshed perforated polyethylene maintained more moisture and showed a minimal percentage of weight loss with the highest chlorophyll content when stored in the charcoal cooler, making it the best-tested packaging material.
The most efficient way to preserve quality has been found to be proper temperature control between the time of harvesting and consumption [84]. Since the fruits are alive after harvesting, all physiological processes, such as respiration and transpiration (water loss), begin after harvesting, and the supply of nutrients and water is not possible since the product is no longer attached to the parent plant. Respiration leads to product deterioration, including loss of nutritional value, changes in texture and taste, and weight loss through transpiration. Storing harvested fruits at low temperatures of approximately 20 °C can slow down many metabolic activities that lead to ripening, hence allowing more time for all postharvest handling. The loss of water from the harvested fruit product is primarily due to the amount of humidity present in the ambient air, expressed as relative humidity [85]. Harvested fruits at high levels of relative humidity retain their nutritional quality, weight, appearance and flavor, while reducing the rate at which wilting, softening and juiciness takes place. Fruits of African eggplant are vulnerable to shrinkage after harvest so any small loss of moisture and fruit shrinkage will become apparent. Enzymes are vital in the postharvest degradation of fruits of African eggplant. In order to avoid their degradation, enzymatic activities responsible for hydrolysis and oxidation activities in the fruits have been studied. Out of the enzymatic activities experimented, phosphatases, N’Acethylglucosaminidase, dopamineoxydase and pyrocatecholoxydase were the principal enzymatic proteins. Being able to control the activities of these enzymes will be very helpful in the postharvest preservation of the fruits of S. aethiopicum [86].

3. Product and Process Innovations

African eggplant is very beneficial to human health, but due to the short shelf life of about three to five days, it results in postharvest losses when the harvesting season is at its peak. Since in its fresh state, it has a relatively limited postharvest life, African eggplant can be changed through processing to forms that are shelf-stable [87]. African eggplant would usually require cold chain systems for the process following harvesting (handling, transport and distribution) to maintain its quality. Unluckily, these facilities are not enough and even sourly established in developing countries where this crop is predominantly located. One of the most recent innovations has been in drying of S. aethiopicum as a processing technology [88]. Certain initiatives for the processing of African eggplant, such as canning, have also been put underway. With the drying technology, a plausible way of producing food products that are shelf-stable is assured.
Drying technology for S. aethiopicum is simple, safe and easy to learn. Water activity that promotes microbial activities is reduced with this technology thereby reducing its weight and volume, effectively making packaging and transportation costs minimal [89]. The most reliable drying methods include osmotic, freeze, vacuum, Ohmic, solar, hot air, and microwave [90]. But Sagar and Kumar [91] reported in their review that, freeze-drying, osmotic dehydration and vacuum drying are too expensive for a broad-scale production of African eggplant. The freeze-drying technique is crucial in water removal as it stops deterioration activities due to enzyme and microbial activity, thus generating the highest quality of the final product [91]. According to Mbondo [92], drying of S. aethiopicum using freeze-drying retains a high amount of phenolics and beta carotene after the process. The drying of African eggplant through sun drying and hot air cabinet drying has been reported [88]. Another study recommended slicing the vegetable, dipping them in plain water and drying using a cabinet dryer as the best method for producing dried S. aethiopicum powder [88]. Osmotic dehydration of African eggplant using sodium chloride (NaCl) solution can be employed after harvest to preserve the fruits by reducing the water activity of the fruits [93]. Processing of S. aethiopicum for the purpose of export is being carried out by the Food Processing International as well as the Nsawam Cannery Company in Ghana. This is a practicable and achievable attempt to deal with its poor shelf life [94]. It could be seen by private initiatives as a means of positive return if they invest, which in turn could encourage further research [37].

4. Landscape Protection and Restoration

African eggplant is well known for its ability to yield so much from limited spaces. They can produce a worthwhile harvest while being grown on the tiniest of plots or even in garden pots. This characteristic partiality for small spaces of the crop enables it to be used for city gardens squeezed in modern structures like factories, roads, train tracks, high-rise buildings and factories, allowing for conservation of soil fertility while maximizing landscape spaces. Known also for its aesthetic property, African eggplant can turn many eyes just with their looks. As a result, it is a very eligible crop for ornamental and beautification purposes [95]. Due to its tendency to tolerate shade, the crop is usually employed to cover bare soil found between main crops grown on the farm, to promote soil conservation activities (nutrients and moisture), thus keeping the soil enriched and fertile. This makes them likely candidates for infertile and complex soils, thereby putting to use and reducing the numerous agricultural wastelands present. Moreover, despite its profuse branching, this propensity allows the crop to shade out unwanted competitors as it makes weeding difficult [95].
National Research Council suggested that, the crops’ resistance to diseases that are soil-borne and caused by pathogens such as Fusarium oxysporum and Verticillium dahlia gives the potential for it to curb soil sickness. It has also been claimed that the crop hosts several commercial crop-affecting pests, bacteria and fungi. Hence, it can be used as bait to lure these pests and pathogens away from the main crops. In addition, the crop has also shown some molluscicidal abilities, making it beneficial in the control of garden snails, slugs and schistosomiasis parasite-harboring water snails.

5. Conclusions

S. aethiopicum, although an underutilized crop species, is a very important vegetable that can contribute to improving food security and provide sustainable productions. Since fruits are culinarily and aesthetically attractive, farmers can export dried or canned fruits to European or Asian countries as an alternative food or garnish. Alongside its agricultural importance and ornamental value, African eggplant also has pharmaceutical uses. The crop is dense in secondary metabolites, which can be used in medicine and in crop protection. Cultivating this plant species should be a better business for local farmers to sell these products to a chemical company that can start investigations on natural medicines and pesticide. In order to increase the consumption and cultivation of this vegetable, the vital genetic resource should receive much research attention and improvement. In vitro and ex situ conservation of the plant’s genetic resource should be maintained, as well as a genomic resource database created to store the crop’s sequenced genome information. Currently, the crop faces huge postharvest losses due to its short shelf life. Fruits are not durable, therefore, they should be quickly dried or processed. Solar drying could be employed as the cheapest drying method, and one can use UV filters if necessary, to protect those precious compounds in the fruits. Breeding regimes for African eggplant should develop fruits that stay longer on the shelf. Furthermore, promoting the use of this vegetable will stimulate dietary diversification among the people in Africa.

Author Contributions

K.N.O. gathered the information and prepared the initial draft of the manuscript. M.H. and T.S. developed the concept and revised the final draft of the manuscript. N.A.B.B. assisted with literature search and proofreading of the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the National Natural Science Foundation of China (NSFC), grant number (31870589; 31700525); the Scientific Research Foundation for High-Level Talents of Nanjing Forestry University (SRFNFU) (GXL2017011; GXL2017012); the Priority Academic Program Development of Jiangsu Higher Education Institutions.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Data sharing not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Kamga, R.T.; Kouamé, C.; Atangana, A.R.; Chagomoka, T.; Ndango, R. Nutritional Evaluation of Five African Indigenous Vegetables. J. Hortic. Res. 2013, 21, 99–106. [Google Scholar] [CrossRef]
  2. Hossein Aminifard, M.; Aroiee, H.; Fatemi, H.; Ameri, A.; Karimpour, S. Responses of eggplant (Solanum melongena L.) to different rates of nitrogen under field conditions. J. Cent. Eur. Agric. 2010, 11, 453–458. [Google Scholar] [CrossRef] [Green Version]
  3. Bisamaza, M.; Banadda, N. Solar drying and sun drying as processing techniques to enhance the availability of selected African indigenous vegetables, Solanum aethiopicum and Amaranthus lividus for nutrition and food security in Uganda. Afr. J. Food Sci. Technol. 2017, 8, 1–6. [Google Scholar] [CrossRef]
  4. Padulosi, S.; Thompson, J.; Rudebjer, P. Fighting Poverty, Hunger and Malnutrition with Neglected and Underutilized Species (NUS): Needs, Challenges and the Way Forward; Biodiversity International: Rome, Italy, 2013. [Google Scholar]
  5. Cernansky, R. The rise of Africa’s super vegetables. Nature 2015, 522, 146–148. [Google Scholar] [CrossRef] [PubMed]
  6. Anaso, H.U. Comparative cytological study of Solanum aethiopicum Gilo group, Solanum aethiopicum Shum group and Solanum anguivi. Euphytica 1991, 53, 81–85. [Google Scholar] [CrossRef]
  7. Lester, R.N. Genetic resources of capsicum and eggplants. In Proceedings of Xth Meeting on Genetics and Breeding of Capsicum and Eggplant, Avignon, France, 7–11 September 1998; Palloix, A., Daunay, M.C., Eds.; Eucarpia: Wageningen, The Netherlands, 1998; pp. 25–30. [Google Scholar]
  8. Taher, D.; Solberg, S.Ø.; Prohens, J.; Chou, Y.; Rakha, M.; Wu, T. World Vegetable Center Eggplant Collection: Origin, Composition, Seed Dissemination and Utilization in Breeding. Front. Plant Sci. 2017, 8, 1484. [Google Scholar] [CrossRef] [PubMed]
  9. Mwinuka, P.R.; Mbilinyi, B.P.; Mbungu, W.B.; Mourice, S.K.; Mahoo, H.F.; Schmitter, P. Optimizing water and nitrogen application for neglected horticultural species in tropical sub-humid climate areas: A case of African eggplant (Solanum aethiopicum L.). Sci. Hortic. 2021, 276, 109756. [Google Scholar] [CrossRef]
  10. Padulosi, S.; Hodgkin, T.; Williams, J.T. Underutilized crops: Trends, challenges and opportunities in the 21st Century. In Managing Plant Genetic Resources; Engels, J.M.M., Ramanatha Rao, V., Brown, A.H.D., Jackson, M.T., Eds.; CAB International: Wallingford, UK; IPGRI: Rome, Italy, 2002; pp. 323–338. [Google Scholar] [CrossRef]
  11. Ebert, A.W. Potential of Underutilized Traditional Vegetables and Legume Crops to Contribute to Food and Nutritional Security, Income and More Sustainable Production Systems. Sustainability 2014, 6, 319–335. [Google Scholar] [CrossRef] [Green Version]
  12. Bukenya, Z.R.; Carasco, J.F. Ethnobotanical aspects of Solanum L. (Solanaceae) in Uganda. In Solanaceae IV: Advances in Biology and Utilization; Royal Botanic Gardens: Kew, UK, 1999; pp. 345–360. [Google Scholar]
  13. Prasad, D.N.; Prakash, R. Floral biology of brinjal (Solanum melongena L.). Indian J. Agric. Sci. 1968, 38, 1053. [Google Scholar]
  14. Lester, R.N.; Seck, A. Solanum aethiopicum L. In Plant Resources of Tropical Africa/Ressources Végétales de l’Afrique Tropicale; Grubben, G.J.H., Denton, O.A., Eds.; Backhuys Publishers: Wageningen, The Netherlands, 2004; pp. 530–536. [Google Scholar]
  15. Polignano, G.; Uggenti, P.; Bisignano, V.; Gatta, C. Della Genetic divergence analysis in eggplant (Solanum melongena L.) and allied species. Genet. Res. Crop Evol. 2010, 57, 171–181. [Google Scholar] [CrossRef]
  16. Lester, R.N. Taxonomy of Scarlet Eggplants, Solanum aethiopicum L. Acta Hort. 1986, 182, 125–132. [Google Scholar] [CrossRef]
  17. Lester, R.N.; Daunay, M.C. Diversity of African vegetable Solanum species and its implications for a better understanding of plant domestication. Schr. Genet. Ressour. 2003, 22, 137–152. [Google Scholar]
  18. Plazas, M.; Andújar, I.; Vilanova, S.; Gramazio, P.; Herraiz, F.J.; Prohens, J. Conventional and phenomics characterization provides insight into the diversity and relationships of hypervariable scarlet (Solanum aethiopicum L.) and gboma (S. macrocarpon L.) eggplant complexes. Front. Plant Sci. 2014, 5, 1–13. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  19. Lim, T.K. Edible medicinal and non medicinal plants. Springer 2015, 6, 310–317. [Google Scholar] [CrossRef] [Green Version]
  20. Kouassi, A.; Béli-Sika, E.; Tian-Bi, T.Y.-N.; Alla-N’Nan, O.; Kouassi, A.; N’Zi, J.-C.; N’Guetta, A.S.-P.; Tio-Touré, B. Identification of Three Distinct Eggplant Subgroups within the Solanum aethiopicum Gilo Group from Côte d’Ivoire by Morpho-Agronomic Characterization. Agriculture 2014, 4, 260–273. [Google Scholar] [CrossRef] [Green Version]
  21. Schippers, R.R. African Indigenous Vegetables: An Overview of the Cultivated Species; Natural Resources Institute: Chatham, UK, 2000; p. 221. [Google Scholar]
  22. Nyadanu, D.; Lowor, S.T. Promoting competitiveness of neglected and underutilized crop species: Comparative analysis of nutritional composition of indigenous and exotic leafy and fruit vegetables in Ghana. Genet. Resour. Crop Evol. 2015, 62, 131–140. [Google Scholar] [CrossRef]
  23. Lester, R.N.; Thitai, G.N.W. Inheritance in Solanum aethiopicum, the scarlet eggplant. Euphytica 1989, 40, 67–74. [Google Scholar]
  24. Prohens, J.; Plazas, M.; Raigón, M.D.; Seguí-Simarro, J.M.; Stommel, J.R.; Vilanova, S. Characterization of interspecific hybrids and backcross generations from crosses between two cultivated eggplants (Solanum melongena and S. aethiopicum Kumba group) and implications for eggplant breeding. Euphytica 2012, 186, 517–538. [Google Scholar] [CrossRef]
  25. Osei, M.K.; Banful, B.; Osei, C.K.; Oluoch, M.O. Characterization of African eggplant for morphological characteristics. J. Agric. Sci. Tech. 2010, 4, 33–37. [Google Scholar]
  26. James, B.; Atcha-Ahowe, C.; Godonou, I.; Baimey, H.; Goergen, G.; Sikirou, R.; Toko, M. Integrated Pest Management in Vegetable Production: A Guide for Extension Workers in West Africa; International Institute of Tropical Agriculture (IITA): Ibadan, Nigeria, 2010; p. 120. [Google Scholar]
  27. Mensah, S.I.; Ekeke, C.; Udom, M. Effect of Salinity on the Growth Characteristics of Solanum aethiopicum L. (Solanaceae). Asian Res. J. Agric. 2020, 12, 17–22. [Google Scholar] [CrossRef]
  28. Ofori, K.; Gamedoagbao, D.K. Yield of scarlet eggplant (Solanum aethiopicum L.) as influenced by planting date of companion cowpea. Sci. Hortic. 2005, 105, 305–312. [Google Scholar] [CrossRef]
  29. Sidibé, D.; Sanou, H.; Bayala, J.; Teklehaimanot, Z. Yield and biomass production by African eggplant (Solanum aethiopicum) and sorghum (Sorghum bicolor) intercropped with planted Ber (Ziziphus mauritiana) in Mali (West Africa). Agrofor. Syst. 2017, 91, 1031–1042. [Google Scholar] [CrossRef]
  30. Aguessy, S.; Laura, Y.; Loko, E. Ethnobotanical Characterization of Scarlet Eggplant (Solanum aethiopicum L.) Varieties Cultivated in Benin Republic. Res. Sq. 2021, 1–27, pre-print. [Google Scholar] [CrossRef]
  31. Agyapong, R.B.; Quainoo, A.K. Effects of False yam (Icacina oliviformis) tuber compost manure on the growth performance of garden eggs (Solanum aethiopicum L.). Ghana J. Sci. Tech. Dev. 2021, 7, 20–28. [Google Scholar] [CrossRef]
  32. Ahabwe, S. Role of Seed and Aphid Vectors in Proliferation of Tomato Virus Diseases on Small Holder Farms in Kasese District, Uganda. Master’s Dissertation, Makerere University, Kampala, Uganda, June 2019. [Google Scholar]
  33. Sabatino, L.; Iapichino, G.; D’Anna, F.; Palazzolo, E.; Mennella, G.; Rotino, G.L. Hybrids and allied species as potential rootstocks for eggplant: Effect of grafting on vigour, yield and overall fruit quality traits. Sci. Hortic. 2018, 228, 81–90. [Google Scholar] [CrossRef]
  34. Amengor, N.E.; Boamah, E.D.; Akrofi, S.; Gamedoagbao, D.K.; Egbadzor, K.F.; Davis, H.E.; Owusu, E.O.; Kotey, D.A. Reconnaissance Study of Insect-Pests Infestation of Garden Eggs in the Volta Region of Ghana. Int. J. Agric. Ext. 2017, 5, 1–10. [Google Scholar]
  35. Taher, D.; Schafleitner, R. Sources of Resistance for Two-spotted Spider Mite (Tetranychus urticae) in Scarlet (Solanum aethiopicum L.) and Gboma (S. macrocarpon L.) Eggplant Germplasms. Hort. Sci. 2019, 54, 240–245. [Google Scholar] [CrossRef] [Green Version]
  36. Prescott-Allen, R.; Prescott-Allen, C. How Many Plants Feed the World? Conserv. Biol. 1990, 4, 365–374. [Google Scholar] [CrossRef]
  37. Horna, D.; Gruère, G. Marketing Underutilized Crops for Biodiversity: The Case of African Garden Egg (Solanum ethiopicum) in Ghana; Global Facilitation Unit for Underutilized Species (GFU): Rome, Italy, 2007. [Google Scholar]
  38. Daunay, M.C.; Lester, R.N.; Laterrot, H. The Use of Wild Species for the Genetic Improvement of Brinjal Egg-Plant (Solanum melongena) and Tomato (Lycopersicon esculentum); The Royal Botanic Gardens: Kew, UK, 1991. [Google Scholar]
  39. Collonnier, C.; Fock, I.; Kashyap, V.; Rotino, G.L.; Daunay, M.C.; Lian, Y.; MariskaI, K.; Rajam, M.V.; Servaes, A.; Ducreux, G.; et al. Applications of biotechnology in eggplant. Plant CellTissue Organ Cult. 2001, 65, 91–107. [Google Scholar] [CrossRef]
  40. Chowdhury, M.A.; Vandenberg, B.; Warkentin, T. Cultivar identification and genetic relationship among selected breeding lines and cultivars in chickpea (Cicer arietinum L.). Euphytica 2002, 127, 317–325. [Google Scholar] [CrossRef]
  41. Sharma, T.R.; Jana, S. Random amplified polymorphic DNA (RAPD) variation in Fagopyrum tataricum Gaertn. accessions from China and the Himalayan region. Euphytica 2002, 127, 327–333. [Google Scholar] [CrossRef]
  42. Kumar, R.; Venuprasad, R.; Atlin, G.N. Genetic analysis of rainfed lowland rice drought tolerance under naturally-occurring stress in eastern India: Heritability and QTL effects. Field Crop. Res. 2007, 103, 42–52. [Google Scholar] [CrossRef]
  43. Kubie, L.D. Evaluation of Genetic Diversity in Garden Egg (Solanum aethiopicum) Germplasm in Ghana. Doctoral Dissertation, University of Ghana, Accra, Ghana, July 2013. [Google Scholar]
  44. Lock, M.; Grubben, G.J.H.; Denton, O.A. Plant Resources of Tropical Africa 2. Vegetables. Kew Bull. 2004, 59, 650. [Google Scholar] [CrossRef] [Green Version]
  45. Ano, G.; Hebert, Y.; Prior, P.; Messiaen, C. A new source of resistance to bacterial wilt of eggplants obtained from a cross: Solanum aethiopicum L. × Solanum melongena L. Agronomie 1991, 11, 555–560. [Google Scholar] [CrossRef] [Green Version]
  46. Li, D.; Li, S.; Li, W.; Liu, A.; Jiang, Y.; Gan, G.; Li, W.; Liang, X.; Yu, N.; Chen, R.; et al. Comparative transcriptome analysis provides insights into the molecular mechanism underlying double fertilization between self- crossed Solanum melongena and that hybridized with Solanum aethiopicum. PLoS ONE 2020, 15, 1–20. [Google Scholar] [CrossRef] [PubMed]
  47. Sakhanokho, H.F.; Islam-faridi, M.N.; Blythe, E.K.; Smith, B.J.; Rajasekaran, K.; Majid, M.A. Morphological and Cytomolecular Assessment of Intraspecific Variability in Scarlet Eggplant (Solanum aethiopicum L.). J. Crop Improv. 2014, 28, 437–453. [Google Scholar] [CrossRef]
  48. Song, B.; Song, Y.; Fu, Y.; Kizito, B.; Kamenya, S.N.; Kabod, P.N.; Liu, H.; Muthemba, S.; Kariba, R.; Njuguna, J.; et al. Draft genome sequence of Solanum aethiopicum provides insights into disease resistance, drought tolerance, and the evolution of the genome. GigaScience 2019, 8, 1–16. [Google Scholar] [CrossRef] [Green Version]
  49. Grubben, G.J.H. Plant Resources of Tropical Africa 2. Vegetables; PROTA Foundation: Wageningen, The Netherlands; Backhuys Publishers: Leiden: The Netherlands; CTA: Wageningen, The Netherlands, 2004; p. 668. [Google Scholar]
  50. Adeniji, O.T.; Kusolwa, P.M.; Reuben, S.W.O.M. Quantitative analysis of fruit size and fruit number in Solanum aethiopicum group. AGRIEAST 2019, 13, 27. [Google Scholar] [CrossRef]
  51. Gisbert, C.; Prohens, J.; Nuez, F. Efficient regeneration in two potential new crops for subtropical climates, the scarlet (Solanum aethiopicum) and gboma (S. macrocarpon) eggplants. N. Z. J. Crop Hortic. Sci. 2006, 34, 55–62. [Google Scholar] [CrossRef]
  52. Larkin, P.J.; Scowcroft, W.R. Somaclonal variation—A novel source of variability from cell cultures for plant improvement. Theor. Appl. Genet. 1981, 60, 197–214. [Google Scholar] [CrossRef]
  53. Anil, V.S.; Lobo, S.; Bennur, S. Somaclonal variations for crop improvement: Selection for disease resistant variants in vitro. Plant Sci. Today 2018, 5, 44–54. [Google Scholar] [CrossRef]
  54. Titus, S.D.; Falusi, O.A.; Abdulhakeem, A.; Liman, M. Effects of gamma irradiation on the agro-morphological traits of selected Nigerian eggplant (Solanum aethiopicum L.) accessions. GSC Biol. Pharm. Sci. 2018, 2, 23–30. [Google Scholar] [CrossRef]
  55. Eletta, O.A.A.; Orimolade, B.O.; Oluwaniyi, O.O.; Dosumu, O.O. Evaluation of proximate and antioxidant activities of Ethiopian eggplant (Solanum aethiopicum L.) and Gboma Eggplant (Solanum macrocarpon L.). J. Appl. Sci. Environ. Manag. 2017, 21, 967–972. [Google Scholar] [CrossRef]
  56. Michael, U.; Banji, A.; Abimbola, A.; David, J.; Oluwatosin, S.; Aderiike, A.; Ayodele, O.; Adebayo, O. Assessment of variation in mineral content of ripe and unripe African eggplant fruit (Solanum aethiopicum L.) Exocarps. J. Pharmacog. Phytochem. 2017, 6, 2548–2551. [Google Scholar]
  57. Offor, C.E.; Igwe, S.U. Comparative Analysis of the Vitamin Composition of Two Different Species of Garden Egg (Solanum aethiopicum and Solanum macrocarpon). World J. Med. Sci. 2015, 12, 274–276. [Google Scholar] [CrossRef]
  58. Chinedu, S.N.; Olasumbo, A.C.; Eboji, O.K.; Emiloju, O.C.; Olajumoke, K.; Dania, D.I. Proximate and Phytochemical Analyses of Solanum aethiopicum L. and Solanum macrocarpon L. Fruits. Res. J. Chem. Sci. 2011, 1, 65–71. [Google Scholar]
  59. Vohora, S.B.; Kumar, I.; Khan, M.S.Y. Effect of alkaloids of Solanum melongena on the central nervous system. J. Ethnopharmacol. 1984, 11, 331–336. [Google Scholar] [CrossRef]
  60. Bello, S.O.; Muhammad, B.Y.; Gammaniel, K.S.; Abdu-Aguye, I.; Ahmed, H.; Njoku, C.H.; Pindiga, U.H.; Salka, A.M. Preliminary Evaluation of the Toxicity and Some Pharmacological Properties of the Aqueous Crude Extract of Solanum melongena. Res. J. Agric. Biol. Sci. 2005, 1, 1–9. [Google Scholar]
  61. Xu, R.; Zhao, W.; Xu, J.; Shao, B.; Qin, G. Studies on Bioactive Saponins from Chinese Medicinal Plants. Adv. Exp. Med. Biol. 1996, 404, 371–382. [Google Scholar] [CrossRef] [PubMed]
  62. Asl, M.N.; Hosseinzadeh, H. Review of Pharmacological Effects of Glycyrrhiza sp. and its Bioactive Compounds. Phytother. Res. 2008, 22, 709–724. [Google Scholar] [CrossRef] [PubMed]
  63. Vinson, J.A.; Hao, Y.; Su, X.; Zubik, L. Phenol Antioxidant Quantity and Quality in Foods: Vegetables. J. Agric. Food Chem. 1998, 46, 3630–3634. [Google Scholar] [CrossRef]
  64. Bagchi, M.; Milnes, M.; Williams, C.; Balmoori, J.; Ye, X.; Stohs, S.; Bagchi, D. Acute and chronic stress-induced oxidative gastrointestinal injury in rats, and the protective ability of a novel grape seed proanthocyanidin extract. Nutr. Res. 1999, 19, 1189–1199. [Google Scholar] [CrossRef]
  65. Diatta, K.; Diatta, W.; Fall, A.D.; Ibra, S.; Dieng, M.; Mbaye, A.I.; Sarr, A.; Adegbindin, M.A. Evaluation of the Antioxidant Activity of Stalk and Fruit of Solanum aethiopicum L. (Solanaceae). Asian J. Res. Biochem. 2020, 6, 6–12. [Google Scholar] [CrossRef]
  66. Sodipo, O.A.; Abdulrahman, F.I.; Alemika, T.E.; Gulani, I.A. Chemical Composition and Biological Properties of the Petroleum Ether Extract of Solanum macrocarpum L. (Local Name: Gorongo). Br. J. Pharm. Res. 2012, 2, 108–128. [Google Scholar] [CrossRef]
  67. Tchoupang, E.N.; Reder, C.; Ateba, S.B.; Zehl, M.; Kählig, H.; Njamen, D.; Holler, F.; Glasi-Tazreiter, S.; Krenn, L. Acetylated Furostene Glycosides from Solanum gilo Fruits. Planta Med. 2017, 83, 1227–1232. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  68. Abubakar, A.R.; Sani, I.H.; Malami, S.; Yaro, A.H. Anxiolytic and Sedative Activities of Methanol Extract of Solanum aethiopicum (Linn.) Fruits in Swiss Mice. Trop. J. Nat. Prod. Res. 2021; 5, 353–358. [Google Scholar] [CrossRef]
  69. Yang, R.-Y.; Ojiewo, C. African Nightshades and African Eggplants: Taxonomy, Crop Management, Utilization, and Phytonutrients. In African Natural Plant Products: Discoveries and Challenges in Chemistry, Health, and Nutrition; Juliani, H.R., Simon, J.E., Ho, C.-T., Eds.; ACS Symposium Series; American Chemical Society: Washington, DC, USA, 2013; Volume 2, pp. 137–165. [Google Scholar] [CrossRef]
  70. Stommel, J.R.; Whitaker, B.D. Phenolic Acid Content and Composition of Eggplant Fruit in a Germplasm Core Subset. J. Am. Soc. Hortic. Sci. 2003, 128, 704–710. [Google Scholar] [CrossRef]
  71. Anosike, C.A.; Obidoa, O.; Ezeanyika, L.U.S. egg albumin-induced oedema and granuloma tissue formation in rats. Asian Pac. J. Trop. Med. 2012, 5, 62–66. [Google Scholar] [CrossRef] [Green Version]
  72. Tunwagun, D.A.; Akinyemi, O.A.; Ayoade, T.E.; Oyelere, S.F. Qualitative Analysis of the Phytochemical Contents of Different Anatomical Parts of Ripe Solanum aethiopicum Linneaus Fruits. J. Complement. Altern. Med. Res. 2020, 9, 14–22. [Google Scholar] [CrossRef]
  73. Emiloju, O.C.; Chinedu, S.N. Effect of Solanum aethiopicum and Solanum macrocarpon Fruits on Weight Gain, Blood Glucose and Liver Glycogen of Wistar Rats. World 2016, 4, 1–4. [Google Scholar] [CrossRef]
  74. Chadha, M.L. AVRDC’s Experiences within Marketing of Indigenous Vegetables–A Case Study on Commercialization of African Eggplant; AVRDC-Regional Center for Africa Duluti: Arusha, Tanzania, 2003. [Google Scholar]
  75. Lumpkin, T.A. A Perspective from the World Vegetable Center. Acta Hortic. 2009, 841, 245–248. [Google Scholar] [CrossRef]
  76. Bachmann, J.; Earles, R. Postharvest Handling of Fruits and Vegetables; ATTRA: Ozark Mountains, University of Arkansas, Fayetteville, NC, USA, 2000; pp. 1–19. [Google Scholar]
  77. Ray, R.C.; Ravi, V. Post-Harvest Spoilage of Sweet potato in Tropics and Control Measures. Crit. Rev. Food Sci. Nutr. 2005, 45, 623–644. [Google Scholar] [CrossRef]
  78. Kader, A.A. Flavor quality of fruits and vegetables. J. Sci. Food Agric. 2008, 88, 1863–1868. [Google Scholar] [CrossRef]
  79. Kader, A.A. Fruit Maturity, Ripening, and Quality Relationships. Acta Hortic. 1999, 485, 203–208. [Google Scholar] [CrossRef]
  80. Msogoya, T.J.; Majubwa, R.O.; Maerere, A.P. Effects of harvesting stages on yield and nutritional quality of African eggplant (Solanum aethiopicum L.) fruits. J. Appl. Biosci. 2014, 78, 6590–6599. [Google Scholar] [CrossRef] [Green Version]
  81. Apolot, M.G.; Acham, H.; Ssozi, J.; Namutebi, A.; Masanza, M.; Kizito, E.; Jagwe, J.; Kasharu, A.; Deborah, R. Postharvest practices along supply chains of Solanum aethiopicum (shum) and Amaranthus lividus (linn) leafy vegetables in Wakiso and Kampala Districts, Uganda. Afr. J. Food Agric. Nutr. Dev. 2020, 20, 15978–15991. [Google Scholar] [CrossRef]
  82. Majubwa, R.O.; Msogoya, T.J.; Maerere, A.P. Effects of local storage practices on deterioration of African eggplant (Solanum aethiopicum L.) fruits. Tanzan. J. Agric. Sci. 2015, 14, 106–111. [Google Scholar]
  83. Sekulya, S.; Nandutu, A.; Namutebi, A.; Ssozi, J.; Masanza, M.; Jagwe, J.N.; Kasharu, A.; Rees, D.; Kizito, E.B.; Acham, H. Effect of Post-Harvest Handling Practices, Storage Technologies and Packaging Material on Post-Harvest Quality and Antioxidant Potential of Solanum aethiopicum (Shum) Leafy Vegetable. Am. J. Food Technol. 2018, 6, 167–180. [Google Scholar] [CrossRef]
  84. Kitinoja, L.; AlHassan, H.Y. Identification of Appropriate Postharvest Technologies for Small Scale Horticultural Farmers and Marketers in Sub-Saharan Africa and South Asia—Part 1. Postharvest Losses and Quality Assessments. Acta Hortic. 2012, 934, 31–40. [Google Scholar] [CrossRef] [Green Version]
  85. Hong, M.N.; Lee, B.C.; Mendonca, S.; Grossmann, M.V.E.; Verhe, R. Effect of infiltrated calcium on ripening of tomato fruits. LWT J. Food Sci. 1999, 33, 2–8. [Google Scholar]
  86. Bedel, F.J.; Yolande, A.; Yves, D.; Alban, N.K.; Lucien, K. Screening of some catalytic activities of mature berries of Solanum aethiopicum cultivar “Klongbo”. Magna Sci. Adv. Biol. Pharm. 2021, 1, 35–41. [Google Scholar] [CrossRef]
  87. Vincente, A.R.; Manganaris, G.A.; Ortiz, C.M.; Sozzi, G.O.; Crisosto, C.H. Nutritional Quality of Fruits and Vegetables. In Postharvest Handling; Academic Press: Cambridge, MA, USA, 2014; pp. 69–122. [Google Scholar] [CrossRef]
  88. Sam, A.; Hedwig, A.; Gaston, T.; Namutebi, A.; Masanza, M.; Jagwe, J.N.; Apolo, K.; Kizito, B.E.; Rees, D. Effect of different processing conditions on proximate and bioactive contents of Solanum aethiopicum (Shum) powders, and acceptability for cottage scale production. Am. J. Food Nutr. 2018, 6, 46–54. [Google Scholar]
  89. Swanson, M.A.; McCurdy, S.M. Drying Fruits & Vegetables; A Pacific Northwest Extension Publication: Moscow, ID, USA; Corvallis, OR, USA; Pullman, DC, USA, 2009. [Google Scholar]
  90. George, S.D.; Cenkowski, S.; Muir, W.E. A review of drying technologies for the preservation of nutritional compounds in waxy skinned fruit. In Proceedings of the 2004 North Central ASAE/CSAE Conference, Winnipeg, MB, Canada, 24–25 September 2004; pp. 4–104. [Google Scholar]
  91. Sagar, V.R.; Suresh Kumar, P. Recent advances in drying and dehydration of fruits and vegetables: A review. J. Food Sci. Technol. 2010, 47, 15–26. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  92. Mbondo, N.N. Characteristic Effects of Drying Processes on Bioactive Compounds in African Eggplant (Solanum aethiopicum L.). Master’s Dissertation, Jomo Kenyatta University of Agriculture and Technology, Juja, Kenya, 2019. [Google Scholar]
  93. Adekeye, D.K.; Aremu, O.; Popoola, O.K.; Fadunmade, E.O.; Adedotun, I.S.; Araromi, A.A. Osmotic Dehydration of Garden Egg (Solanum aethiopicum): The Shrinkage and Mass Transfer Phenomena. J. Anal. Tech. Res. 2020, 2, 1–17. [Google Scholar] [CrossRef]
  94. Danquah-Jones, A. Variation and Correlation among Agronomic Traits in Garden Egg (Solanum gilo Radii). Master’s Dissertation, University of Ghana, Legon, Ghana, 2000. [Google Scholar]
  95. National Research Council. Lost Crops of Africa: Volume II: Vegetables; National Academies Press: Washinton, DC, USA, 2006; pp. 1–352. [Google Scholar] [CrossRef]
Figure 1. Fruit vegetable pictures for (a) Kumba, (b) Aculeatum, (c) Shum and (d) Gilo group of Solanum aethiopicum.
Figure 1. Fruit vegetable pictures for (a) Kumba, (b) Aculeatum, (c) Shum and (d) Gilo group of Solanum aethiopicum.
Horticulturae 07 00126 g001
Table 1. Proximate composition of Solanum aethiopicum L. fruits.
Table 1. Proximate composition of Solanum aethiopicum L. fruits.
NutrientComposition (per 100 g of Fresh Fruit)
Moisture content91.20 ± 0.34%
Crude protein1.07 ± 0.01%
Crude fat0.38 ± 0.03%
Crude fiber2.44 ± 0.04%
Ash content0.73 ± 0.03%
Carbohydrate4.18 ± 0.08%
Dry matter8.80 ± 0.19%
Mineral ElementConcentration (mg/g Dry Weight Basis)
Calcium0.310~0.360
Magnesium0.595~0.625
Iron0.025~1.125
Potassium4.475~9.525
Sodium0.865~1.005
Manganese0.005
Copper0.007~0.008
Zinc0.077~2.938
Phosphorus1.091~1.245
VitaminsContent (mg/100 g Fresh Fruit)
Vitamin A (retinol)53.550 ± 0.55
Vitamin B1 (thiamine).0.037 ± 0.00
Vitamin B2 (riboflavin)0.034 ± 0.00
Vitamin B (niacin)0.700 ± 0.00
Vitamin C (ascorbic acid)2.300 ± 0.00
Vitamins D (calciferol)0.010 ± 0.00
Vitamin E (tocopherol)0.310 ± 0.00
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Han, M.; Opoku, K.N.; Bissah, N.A.B.; Su, T. Solanum aethiopicum: The Nutrient-Rich Vegetable Crop with Great Economic, Genetic Biodiversity and Pharmaceutical Potential. Horticulturae 2021, 7, 126. https://doi.org/10.3390/horticulturae7060126

AMA Style

Han M, Opoku KN, Bissah NAB, Su T. Solanum aethiopicum: The Nutrient-Rich Vegetable Crop with Great Economic, Genetic Biodiversity and Pharmaceutical Potential. Horticulturae. 2021; 7(6):126. https://doi.org/10.3390/horticulturae7060126

Chicago/Turabian Style

Han, Mei, Kwadwo N. Opoku, Nana A. B. Bissah, and Tao Su. 2021. "Solanum aethiopicum: The Nutrient-Rich Vegetable Crop with Great Economic, Genetic Biodiversity and Pharmaceutical Potential" Horticulturae 7, no. 6: 126. https://doi.org/10.3390/horticulturae7060126

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop