Abstract
This article provides a comprehensive and in-depth examination of the microbial diversity inherent in African food and beverages, with a particular emphasis on fermented products. It identifies and characterizes the dominant microorganisms, including both prokaryotes and yeasts, prevalent in these foods, and furthermore, critically analyzes the health benefits of these microbial strains, especially their probiotic properties, which could potentially improve digestion and contribute to human health. Notably, it underscores the vital role these microorganisms play in bolstering food security across Africa by enhancing and preserving food quality and safety. It also delves into the potential applications of microbial products, such as metabolites, in the food industry, suggesting their possible use in food processing and preservation. Conclusively, with a summarization of the key findings, emphasizing the importance of gaining a deep understanding of microbial diversity in African beverages and foods. Such knowledge is crucial not only in promoting food security but also in advancing public health.
Graphical Abstract
Similar content being viewed by others
Avoid common mistakes on your manuscript.
Introduction
This article is an exploration of the pivotal role microbial diversity plays in food security and human health on the African continent. Boasting a diverse array of microorganisms, Africa's rich reservoir serves numerous functions, including food preservation, nutritional enhancement, boosting food production, and even acting as a food source itself [1, 2].
A significant aspect of the African diet is the age-old tradition of consuming fermented foods [2]. This process, driven by microorganisms that convert carbohydrates into organic acids, alcohols, or other easily digestible products, not only enriches the food's flavor but also enhances nutritional value and extends shelf life [3]. Fermented foods in Africa are largely grouped into non-alcoholic fermented cereals, starchy root crops, vegetable proteins, animal proteins, and alcoholic beverages. Each of these fermented food types plays a pivotal role in the African diet due to the wide range of substances that can be fermented [4]. Most fermented foods and beverages worldwide, including those in Africa, are naturally fermented by a combination of cultivable and non-cultivable microorganisms, primarily sourced from raw materials and processing facilities [5].
In addition, the study of the microbial ecology of natural food fermentations can assist in identifying biomarkers for assessing fermented food quality and aid in the development of optimal starter cultures [6]. Microbial ecology is the study of microorganisms in their natural environments [7]. In the context of food, this involves the study of the various bacteria, yeasts, and molds that play a role in the fermentation process. Identifying biomarkers, which are measurable indicators of some biological state or condition, can help assess the quality of fermented foods. For example, certain microbial metabolites, enzymes, and proteins can be used as biomarkers to determine whether a food product has been properly fermented or if it contains harmful microorganisms [8].
Furthermore, the article investigates the probiotic properties of the dominant strains of microorganisms found in African foods and beverages. Probiotics, live microorganisms that confer health benefits to the host when consumed in adequate amounts, present a vast potential for new probiotic strain discovery due to Africa's microbial diversity. These strains could provide numerous health benefits, including improved digestion, enhanced immunity, and potential protection against certain diseases [9]. This exploration holds significant potential for both the health of the African population and global health applications.
This article also explores deeper into the significance of microbial proteins in the food industry, their role in producing a wide array of products, and their contribution to food security. Finally, the critical role microorganisms play in ensuring food securty is emphasized. The increasing global population and the subsequent demand for food necessitate sustainable food production methods. Microorganisms can play a crucial role in addressing food security issues. This is particularly relevant in Africa, where food insecurity is a pressing issue. Efficient utilization of microbial resources could significantly contribute to sustainable food production and security. This paper aims to illuminate these aspects, revealing the potential of microbial diversity in Africa's food and beverage industry. This article concludes by highlighting the existing knowledge gaps and potential areas for future research.
Microorganisms Commonly Used in African Foods and Beverages and Their Probiotic Properties
Traditional fermented foods play an important part in African food regime, as far as fermentation process facilitates food preservation, increases the shelf life, and promotes the nutritional value of the food products. One the most important aspects of any fermentation process is the associated food microbiota and the studies on African fermented foods and beverages have revealed the presence of diverse microbial populations in which most of them have technological, fundamental commercial importance [2, 10, 11]. According to these indicated studies, African fermented foods are categorized as non-alcoholic fermented cereals (millet, sorghum, and maize), starchy root crops (cassava), vegetable proteins (oilseeds and legumes), animal proteins (dairy), and alcoholic beverages (sap, fruits, honey, or cereals). The microbial consortium is multifaceted and consists of numerous distinct microorganisms that coexist and interact in different ways. Some organisms are killed or inactivated during the fermentation process, while strains better suited to fermentation are activated and undergo rapid growth [12]. The entire competitive microbial activities result in spontaneous fermentation. During fermentation, the lactic acid bacteria that survives make a synergistic correlation with some yeasts. Table 1 lists the microbial flora of drinks and fermented food in Africa, the continent of original and natural substrates.
Prokaryotes
The early stages of fermentation are dominated by lactic acid bacteria, following which yeasts increase and participate [13]. This is due to lactic acid bacteria relatively rapid growth rate. Lactobacillus, Lactococcus, Leuconostoc, and Pedicoccus are the four most common genera. Saccharomyces cerevisiae (eukaryotes), Streptococcus, and Corynebacterium are additional organisms (Table 1). Penicillum, Aspergillus, Cladosporium, and Fusarium are mold, which may also be present. In many traditional African fermentations, L. plantarum and L, fermentum strains dominate [14,15,16].
Diaz et al. [2] used 16S rRNA gene amplicon sequencing to examine the bacterial microflora of African fermented foods produced from various raw materials. In all of the samples, Lactobacillus was abundant, with the exception of those produced in laboratories. Fermentations of cereal, dairy, and cassava was dominated by genera in the order Lactobacillales. Lactobacillus and Bacillus were the most common genera in locust bean, while Zymomonas, Bacillus, and members of the order Lactobacillales were the most common in alcoholic beverages. This was the first observation of the genus Zymomonas in alcoholic fermentations [2].
Most studies describing on microbial communities of fermented foods from Africa agree that the dominant species are L. plantarum and L. fermentum. In some fermented cereal and dairy samples, other genera, like Acetobacter, are present in relatively high numbers. Also, numerous cereal and dairy samples contained potentially pathogenic genera such as Clostridium and Escherichia [17, 18].
Lactobacillus, Streptococcus, Zymomonas, Leuconostoc, and Bacillus are the most plentiful genera in alcoholic samples. Lactobacillus and Leuconostoc are the main groups present in palm wine [19, 20]. The process of fermenting locust bean is alkaline and typically involves Lactobacillus and other genera in the Lactobacillales order. Bacillus is responsible for fermenting the beans. Thus, high concentrations of this genus is expected and has been reported [21]. Bacteria like B. subtilis, B. circulans, and B. megaterium, which break down protein, are found in fermented condiments. Among these species, Bacillus subtilis is the most dominant and best suited for fermentation [22, 23]. According to Oguntoyinbo et al. [24], B. subtilis is the key factor affecting the production of mucilage, because of the high production of amylase, protease, and polyglutamic acid [24]. The fermentation of foods is also associated with microorganisms from other genera. Pediococcus, Proteus, Escherichia, Micrococcus, Streptococcus, Staphylococcus, Pseudomonas, Alcaligenes, Enterococcus, and Corynebacterium are some of the species that fall under this category [25, 26]. The bionetwork of fermented plant protein, particularly in the beginning of production, has been linked to members of the Enterobacteriaceae family [27, 28]. According to Ogueke and Aririatu (2004), the altered environment is probably the reason why these species do not flourished until the fermentation is complete [29]. As seen in African matured food sources, fermentation is initially started by various microorganisms, which eventually favors Gram-positive bacteria [12].
The phenotypic approach has been used frequently to identify the microorganisms in African fermented foods, but has inherent flaws and fails, to isolate and recognize non-cultivable microorganisms. Culture independent techniques such as amplicon sequencing can be used to study microorganisms of fermented food [30, 31]. However, not many studies have focussed on African food varieties [32, 33]. The latest research on the safety and processing methods of ugba, a fermented food condiment from Nigeria utilized both molecular and phenotypic approaches. The clone library technique identified new bacterial species of Arthrobacter, Brevibacterium, Providencia, Empedobacter, Acinetobacter Elizabethkingia, Proteobacterium, Burkholderiales, Dysgomonas, Wautersiella, Flavobacterium, and Zymomonas. These findings, subsequently, highlight the advantages of molecular techniques in the assessment of microbial flora. The microbial structure described for these products might be more complex than what is currently known.
Yeasts
The role of yeasts in the fermentation of spontaneously fermented beverages and foods is crucial. Studies have shown that the diversity and succession of yeast species during fermentation are influenced by factors, such as commensal microorganisms, raw materials, hygiene, and processing techniques. Successions occur at species and strain levels according to intrinsic and extrinsic growth factors, which are constantly changing. Yeasts are necessary for flavor development and affect shelf life and nutritional value. Practical properties of yeasts in fermentation of food and beverages include fermentation of carbohydrates, formation of flavor compounds, stimulation of lactic acid bacteria, corruption of cyanogenic glycosides, development of proteins that debase tissues, the binding as well as degrading of mycotoxins, and probiotic properties[34, 35].
Many sub-Saharan African foods and beverages have been studied for the incidence of yeasts. Yeasts are vital in the processing of African fermented food and beverages, and the related data are exceptionally disorganized. This makes it difficult to outline their incidence, identity, effects, and interactions. The current review assembles current information on yeasts in African fermented food and beverages, concentrating on the species and strain.
Saccharomyces cerevisiae is the predominant yeast isolated from the majority of fermented products, followed by Pichia kudriavzevii, Candida tropicalis, and Kluyveromyces marxianus [36]. S. cerevisiae dominated the fermentation of solid foods kenkey and mawè, as well as ogi (non/low-alcoholic drink) [37]. S. cerevisiae was surmised to be the primary fermenting agent for 93% of African alcoholic drinks, which are mostly derived from cereal crops. Other types of alcoholic drinks, such as palm wine made from sap [19, 38], fermented dairy products like Nunu [39, 40], rob, and suusac [41] also had S. cerevisiae as the predominant species.
Low concentrations of S. cerevisiae have been recorded in indigenous African fermented products such as fufu [42], lafun [15], and adjuevan, non/low-alcoholic drinks such as bushera [43] and togwa [44], and some of the fermented dairy products such as amabere amaruranu [45], kefir [46], amasi [47], nyarmie [48], mashita [49],and sethemi [50].
Probiotic Properties of Strains
Live microorganisms are administered to improve the health of the host. These microorganisms are commonly referred to as probiotics. The genera Lactobacillus, Bifidobacterium, Lactococcus, Enterococcus, Leuconostoc, and Streptococcus comprise the probiotic lactic acid bacteria. Yogurt, fermented milk, and fermented foods are all sources of probiotics [106]. Several potentially nutritious and health-promoting components (mainly microorganisms) are found in fermented African foods. However, despite the growing interest in lactic acid bacteria as a probiotic, available data on novel applications as a probiotic are rare, particularly from Africa. Only a few probiotic products have made it past clinical trials due to stringent international regulations. There is a lack of data on the probiotics market share in Africa compared to the rest of the world. In South Africa, the market for fortified foods (especially baby cereals), supplements, and fermented dairy products appears to be fairly established.
It is expected that lactic acid bacteria members, including those found in fermented condiments such as Iru, Ugba, and Ogiri, and fermented milk products such as Nunu and yoghurt Wara have been the focus of research from a microbiological perspective. These include Lactobacillus, Lactococcus, Pediococcus, and Weissella species, with particular emphasis on the presence of the last two in fermented cereal-based foods such as Ogi [107, 108]. Table 2 summarizes research into the probiotic potential of strains found in traditional African food products. The term "potentially" is used when indications of health benefits do not meet the necessary criteria for the usage of the term "probiotic." Before the term "probiotic" could be used to describe these microorganisms, additional research, including clinical trials, is required.
Lei and Jacobsen investigated the main lactic acid bacteria present in koko and koko sour water from different locations in Ghana, with regard to their genotype, fermentation patterns, tolerance to low pH and bile salts, and antimicrobial properties [109]. The presence of oxgall bile had no effect on the growth of any of the lactic acid bacteria isolates. In pH 2.5 media, the strains survived, but were unable to grow. The strains were tolerant to acid and bile with antimicrobial activity in fresh koko sour water at levels of 108 colony-forming units/mL. Pinto et al. investigated lactic acid bacteria in African fermented millet, including diversity, naming, and as a possible as a probiotic for the local community. Additionally, the probiotic properties of Lactobacillus strains and human intestinal isolates from traditional African fermented milk products were examined. The researchers found that the survival rate of the strains was influenced by factors, such as acidic conditions (pH 2.5), pepsin, lysozyme, and milk. Under simulated gastrointestinal conditions, five strains were identified as L. plantarum and two as L. johnsonii survived well. Antimicrobial activity was also demonstrated by these strains, probably because of the production of organic acids. Bile salt hydrolase activity was present in all strains, but β-galactosidase activity was only present in L. plantarum strains. An investigation into how various dietary treatments affect the permeability of the intestinal wall during acute diarrhea was performed on 87 hospitalized children aged 6 to 25 months in Tanzania. According to [110], fermented porridge performed better than conventional porridge or porridge digested with amylase in the treatment of intestinal permeability.
Mensah et al. (1995) included mothers from Ghana and Nigeria to compare fermented and non-fermented maize–soybean porridges with conventionally fermented maize-only porridges [111]. According to their findings, infants who consumed fermented porridges had significantly higher daily nutrient intakes than those who ate regular porridge. In many areas of Nigeria, Ogi liquor, which is water made from fermented cereal pulp, is given to infants by nursing mothers, to cure their illness. Adebolu et al. found that the ogi liquor, which included Lactobacillus species among others, inhibited pathogens (common diarrhoeal bacteria) in southwest Nigeria. Zakpaa et al. reported that Ghanaian fermented meats have lactic acid bacteria species, Staphylococcus spp., Streptococcus spp., and Micrococcus spp. in their microbial flora [112].
The species of Staphylococcus are identified as pathogenic, along with Streptococcus spp. and lactic acid bacteria species as probiotics. Based on these findings, robust probiotic starter culture to improve the quality of fermented meats by preventing the growth of potentially pathogenic organisms could be beneficial.
Since the term "probiotic" may be unfamiliar to a number of African communities, any mention of such products must coincide with an educational campaign. Few studies have been conducted to determine whether microorganism in African fermented foods meets the requirements to be termed probiotics. As a result, it is necessary to train people and develop technologies to improve the production processes, starting with accurate strain-level characterization of probiotic organisms found in fermented foods.
Role of Microorganisms in Improving Food Security in Africa
Although Africa has a vast amount of uncultivated and fertile land, it continues to face food security challenges despite the potential to feed its growing population and more. Approximately 240 million individuals in sub-Saharan Africa do not have access to enough food to maintain an active and healthy lifestyle. [118]. One possible approach to tackle this problem involves utilizing microorganisms in different ways to maintain food quality, enhance its nutritional value, increase food output, or even provide food as a resource.
Fermented foods have been subjected to enzymatic actions of microorganisms [119]. Fermentation is a centuries-old way of preserving surplus vegetables, fruit, meats, and grains and can enhance the overall flavor of the meal. Fermentation produces acids that avert the growth of spoilage-causing pathogens, making food safer and increasing its shelf life, especially when refrigeration or other forms of food processing are unavailable. Additionally, fermentation enhances the food's sensory properties, improves its nutritional value, and may also improve digestibility [120, 121].
Limiting the expansion of destructive microorganisms can lower the chances of pathogenic diarrhea, which is a primary reason for the death of infants in sub-Saharan Africa. Raw sorghum flour has more than 2,400 colony-forming units per gram (cfu/g) of Escherichia coli, whereas the count is notably lower in fermented dough [102]. Moreover, the fermented dough does not contain any Salmonella spp., which were present in different sorghum varieties. [122].
Several types of fermented food are commonly consumed in Nigeria, including gari and fufu, which are two popular types of fermented cassava. Other examples of fermented products ogi (maize), dawadawa (African locust beans), ogiri (castor oil seeds), ugba (African oil beans), kunu zaki (maize drink), shekete (palm wine), and traditionally fermented milk and cheese. The microorganisms responsible for most of these fermentations are yeasts and lactic acid bacteria [123].
Microorganisms are used to improve food security globally and can play a significant role in food security in Africa. Therefore, to increase the effectiveness of food production systems and counteract the negative impacts of agricultural production, including meat production, innovative technologies are crucial. While the practice of utilizing microorganisms to ferment food has been around for centuries, the concept of using microorganisms as a source of food has only gained widespread acceptance in recent times [124]. The utilization of microbial biomass as a food or feed source is known as "microbial protein" or MP. Around 75% of the dry biomass of MP comprised protein, including all the essential amino acids. In addition, MP is a good source of vitamins, minerals, and other nutrients [125].
Bioreactors, depicted in Fig. 1, are closed systems that can generate MP. The design and operation of these systems vary to create ideal conditions based on the organism's characteristics, such as being a phototroph or chemotroph, as well as an autotroph or heterotroph. Bioreactors are much more effective than growing crops in open fields or keeping livestock, because the growth parameters can be kept stable, nutrients are used with near 100% efficiency (nutrients can be added to match demand precisely), the footprint for water and land use is small, and there is no need for pesticides, antibiotics or vaccines [124]. Examples of methane-oxidizing bacteria are Methylococcus capsulatus and Methylomonas methanica [126]. Examples of hydrogen-oxidizing bacteria are Alcaligenes eutrophus, Seliberia carboxydohydrogena, and Ralstonia eutropha [127]. Microfungi, notably Fusarium venenatum, and microalgae have also been used.
Another advantage of microbial protein is that it can be produced in a variety of forms such as powders, flakes, or bars. This makes it versatile and easy to use in a wide range of food products, from traditional dishes to modern food products such as protein bars, protein shakes, and meat alternatives.
Usefulness of Microbial Products (Metabolites)
Food-processing technologies modify raw materials to obtain products with desirable quality characteristics, which meet nutritional and functional needs. The process of food fermentation involves the use of microbial growth technology to transform raw food materials into a variety of value-added products on various substrates. [79, 102]. This is one of the traditional methods of food processing and preservation in Africa, where there is a rich history of fermented foods. Africa is believed to be the origin of humankind, and its long-standing food-processing techniques, including fermentation, have been passed down through generations for centuries. Additionally, there are both modern and basic food-processing technologies, with simple techniques such as drying, salting, smoking, and fermentation [118, 128, 129].
Traditional fermented dairy products that have been consumed for centuries. These products continue to be important sources of essential nutrients and income for local populations [72, 130]. The type of fermented dairy products varies in different African countries. The fermented foods produced in African countries include non-alcoholic and alcoholic beverages like wine and pito. Fermented dairy products also include yogurt, yogurt-like foods, and beverages [131]. These fermented foods are made from animal sources such as cow milk, camel milk, buffalo milk, goats’ milk, ewe milk, meat, and fish as well as plant-based raw materials such as starchy vegetable proteins, root crops, fruits, and leaves [132, 133].
Milk has had a substantial economic and nutritional impact in African countries, predominantly those that rely on cattle-keeping. These regions comprise North Africa, the Sudanian Savanna (Burkina Faso, Gambia, Senegal, and Southern Mali), as well as northern countries such as Ghana, Côte d'Ivoire, Togo, Benin, Guinea, and Nigeria, and the highlands of East Africa [134]. Generally, African fermented dairy products are enriched in nutrients, micronutrients, delivering high-quality proteins, vitamins, and energy-containing fats [135, 136], but notably vitamins. The eight vitamins in African beers, for instance, are well documented. African fermented dairy products can be categorized into three functional groups, staples, beverages, and the relishes and sauces [132, 137].
The production of African fermented dairy products involves two methods. The first is spontaneous fermentation, which occurs at household level and produces yogurt-like products [138, 139]. These products have a diverse microbial community consisting of lactic acid bacteria and yeasts and are rich in nutrients. African fermented dairy products also provide benefits such as inhibiting harmful microorganisms and improving digestion and nutritional value. Second, a few products as Madila in Botswana and Amasi in South Africa are produced commercially [131, 140]. A list of fermented milk products is shown in Table 1. These fermented milk products such as Amabere, Amasi, Ergo, Fene, Gariss, Ititu, Kefir, Kindirmou, Kiviguto, Kule-naoto, Kwerionik, Leben (lben), Mabisi, Madila, Mafi, Makamo, Masse, Mursik, Nunu, Nyarmie, Omashikawa, Pendidaam, Rob, Suusac, and Zabady are made from good quality raw milk [130]. A significant aspect of African pastoral societies is the importance of milk, not only as a source of sustenance but also plays a crucial role in their social, economic, and cultural practices. Milk plays a vital role in the organization of society, trade, eating habits, technological advancements, and cultural heritage. According to Mattiello and colleagues [72], dairy products are classified into five groups based on production method and type, fresh cheese, ripened cheese, fermented milk, butter, and dairy by-products [72].
The significance of fermented milk in Africa should be highlighted. It plays a crucial socio-economic role and is widely used [91]. There are several traditional fermented milk products in Africa (Table 1). The production methods for these products vary depending on the local microbiota, which is influenced by the climate of each area. The consumption of traditional fermented milk products has health benefits, such as potential probiotic properties of some lactic acid bacteria. Probiotics refer to live microorganisms that offer health advantages to the host if consumed in proper amounts [141]. The presence of live bacteria in fermented milk can impede the growth and spread of harmful microorganisms responsible for causing food-related illnesses such as diarrhea [142, 143]. L. acidophilus, L. bulgaricus, B. bifidum, and S. thermophilus are among the lactic acid bacteria that impede colonizing pathogens in the gastrointestinal tract [143].
Microbial Biomarkers for Assessing Food Quality
Biomarkers, including proteins and metabolites, play a crucial role in assessing the quality of food. By measuring specific molecules present in food samples, scientists and food industry professionals can gain valuable insights into its safety, nutritional content, and overall quality. Therefore, exploring the significance of biomarkers in food quality assessment and highlighting their potential applications are essentially important [144]. They provide objective measurements that can help in determining the freshness, nutritional value, and potential hazards associated with food products. One of the key implications of biomarkers is in the food industry for determining the freshness of perishable products. As food undergoes spoilage, certain biomolecules undergo changes that can be detected and measured. For example, the degradation of proteins or the production of volatile compounds can indicate the presence of spoilage bacteria. By monitoring these biomarkers, food manufacturers and distributors can assess the quality of their products and make informed decisions regarding their shelf life [145]. Analyzing biomarkers data requires a systematic and rigorous approach. From data quality control and preprocessing to statistical analysis and interpretation, each step plays a crucial role in extracting meaningful insights from the biomarker data. By following these steps, food scientists can make informed decisions regarding food safety, quality control, and regulatory compliance [146, 147].
Protein Biomarkers in Food Quality Assessment
Proteins are fundamental components of food and essential macromolecules found in all living organisms. They are not only indicators of nutritional content but also play a vital role in determining the authenticity and safety of food products. By analyzing the presence, quantity, or modifications of specific proteins, researchers can detect adulteration, contamination, or the presence of allergens in food. Specific protein biomarkers can indicate the presence of allergens, pathogens, or spoilage in food products. For instance, the detection of allergenic proteins in processed foods helps in identifying the potential health risks for individuals with allergies. Similarly, specific pathogen-related proteins can indicate contamination, aiding in rapid response and preventing foodborne illnesses. Similarly, the presence of gluten proteins can help in identifying products that are gluten-free, ensuring the safety of consumers with gluten intolerance [148, 149].
Metabolite Biomarkers in Food Quality Assessment
Metabolites, small molecules produced during metabolic processes, are also involved in various biochemical processes within living organisms. They can serve as valuable biomarkers for assessing food quality due to their sensitivity to changes caused by processing, storage, or contamination. By analyzing the levels and profiles of specific metabolites, scientists can evaluate the freshness, nutritional value, and potential hazards of food products [150]. In brief, various analytical techniques are employed to analyze the levels and profiles of specific metabolites in food. These techniques can be broadly categorized into targeted and untargeted metabolomics approaches. Targeted metabolomics focuses on the quantification of specific known metabolites. This approach utilizes analytical techniques such as gas chromatography (GC), liquid chromatography (LC), or mass spectrometry (MS) to identify and quantify the predetermined metabolites. Targeted metabolomics offers high sensitivity, specificity, and reproducibility, making it suitable for analyzing specific metabolites of interest. Untargeted metabolomics involves the comprehensive analysis of all detectable metabolites present in a sample. This approach utilizes advanced analytical techniques, such as nuclear magnetic resonance (NMR) spectroscopy and high-resolution mass spectrometry (HRMS), to identify and quantify various metabolites. Untargeted metabolomics allows for a holistic understanding of food metabolite composition, enabling the discovery of novel metabolites and metabolic pathways [151]. After obtaining the analytical data, the analysis of metabolites in food involves data processing, statistical analysis, and interpretation. Advanced computational tools and software are employed to process the vast amount of data generated by analytical techniques. Statistical analysis helps to identify the significant differences in metabolite levels between samples and provides insights into the relationships and interactions between metabolites. The interpretation of the data allows researchers to draw meaningful conclusions about the metabolite profiles and their potential implications for food quality, nutritional value, and health benefits [152].
Furthermore, they can provide insights into food products' nutritional content, flavor, and freshness. Metabolite profiling can help identify the changes in food composition due to storage conditions, processing methods, or adulteration. For example, the analysis of volatile metabolites can reveal the degradation of fats and oils, indicating rancidity and the potential loss of nutritional value. Besides, the presence of specific metabolites can indicate the presence of microbial contamination (determining the presence or absent of their metabolites(, helping to prevent foodborne illnesses [153].
Other Biomarkers
Apart from proteins and metabolites, various other biomarkers, such as DNA, RNA, enzymes, and volatile compounds, can be utilized to assess the quality of food. DNA-based biomarkers are specific DNA sequences that can distinguish between different species or origins. These biomarkers are unique to each organism and can be used to determine the presence or absence of a particular species in a given food product. DNA-based biomarkers, such as mitochondrial DNA (mtDNA), nuclear DNA (nDNA), and single-nucleotide polymorphisms (SNPs), can be used to identify the species or origin of food products, ensuring their authenticity [154]. On the other hand, RNA biomarkers can provide insights into gene expression changes during food processing or storage, help in monitoring its quality, while enzymes can be used to assess the freshness of food products by measuring their activity levels. Additionally, volatile compounds can serve as indicators of flavor, aroma, and spoilage, enabling sensory quality evaluation [155].
Applications of Biomarkers in Food Quality Assessment
-
a.
Shelf life determination: Biomarkers, such as volatile organic compounds (VOCs), enzymes, proteins, and DNA fragments, can assist in predicting the shelf life of food products. By monitoring the changes in these biomarkers, manufacturers can gain valuable insights into the degradation and spoilage processes of their products, establish appropriate storage conditions, and ensure consumer safety.
-
b.
Quality control: Analysis of biomarkers allow to detect contaminants, adulterants, and other quality-related issues in food, facilitating effective quality control measures.
-
c.
Nutritional profiling: Biomarkers can provide insights into the nutritional composition of food, inform consumer to make their specific choices about their diet.
-
d.
Authentication and traceability: Biomarkers can be used to verify the origin, authenticity, and traceability of food products, ensuring adherence to label regulations [146, 156].
The use of biomarkers, such as proteins, metabolites, and other molecular indicators, have revolutionized the assessment of food quality. Their measurement and analysis enable food scientists and industry professionals to make suitable decisions regarding safety, composition, nutritional content, the authenticity of food products, and overall quality of food products. Additionally, this assessment also aid in the development of quality control measures [144, 157]. By analyzing the presence, quantity, or modifications of these biomarkers, scientists and food regulators can ensure the production of safe and nutritious food for consumers. Biomarker analysis techniques continue to improve, which has tremendous potential for improving food quality evaluation. On the other hand, by leveraging biomarker-based approaches, the food industry can enhance consumer trust, ensure regulatory compliance, and improve overall food safety and quality [157].
Future Perspectives and Opportunities
In future studies on the microbial diversity of African food and drinks, the identification and characterization of microorganisms found in traditional fermented products should be prioritized, and their effects on food safety and nutrition were evaluated. Research should examine the potential of microorganisms to produce fermented food and new food products. Additionally, exploring methods to improve storage and preservation of food and ways to enhance their nutritional content would be beneficial. One potential research area is exploring the health advantages in consuming fermented food and drink, and how these benefits might differ depending on the population and region. Therefore, it is crucial to investigate how alterations in food processing, production, and distribution methods might affect the safety and variety of fermented foods and beverages in Africa. There is a significant chance to enhance food security by encouraging the utilization of biofertilizers and boosting the creation and consumption of microbial protein.
Conclusion
Understanding the microbial diversity of African foods and beverages is essential for promoting food security and human health, particularly in Africa. This is due to the numerous benefits that these microorganisms provide, ranging from probiotic properties that improve human health to metabolites that have potential in the food industry. African fermented foods are made from a variety of raw materials and provide many health benefits. Knowledge of the microbial ecology of natural fermentations can identify the biomarkers to evaluate the quality of fermented foods and optimal starter cultures for food production. With more research into the microbial diversity of African foods and beverages, food security and human health can be improved. Additionally, microbial proteins are useful in the food industry and future research should continue to explore their role as a food source to improve in food security.
References
Panizzon JP, Pilz Júnior HL, Knaak N, Ramos RC, Ziegler DR, Fiuza LM (2015) Microbial diversity: relevance and relationship between environmental conservation and human health. Braz Arch Biol Technol 58(1):137–145. https://doi.org/10.1590/S1516-8913201502821
Diaz M, Kellingray L, Akinyemi N, Adefiranye OO, Olaonipekun AB, Bayili GR, Ibezim J, du Plessis AS, Houngbédji M, Kamya D, Mukisa IM, Mulaw G, Manthi Josiah S, Onyango Chienjo W, Atter A, Agbemafle E, Annan T, Bernice Ackah N, Buys EM, Joseph Hounhouigan D, Muyanja C, Nakavuma J, Odeny DA, Sawadogo-Lingani H, Tesfaye Tefera A, Amoa-Awua W, Obodai M, Mayer MJ, Oguntoyinbo FA, Narbad A (2019) Comparison of the microbial composition of African fermented foods using amplicon sequencing. Sci Rep 9(1):13863–13863. https://doi.org/10.1038/s41598-019-50190-4
Adebo OA (2020) African sorghum-based fermented foods: past, current and future prospects. Nutrients 12(4):1111. https://doi.org/10.3390/nu12041111
Franz C, Huch M, Mathara J, Abriouel H, El Bakali N, Reid G, Gálvez A (2014) African fermented foods and probiotics. Int J Food Microbiol 190:84–96. https://doi.org/10.1016/j.ijfoodmicro.2014.08.033
Tamang JP, Watanabe K, Holzapfel WH (2016) Review: diversity of microorganisms in global fermented foods and beverages. Front Microbiol 7:377. https://doi.org/10.3389/fmicb.2016.00377
Rezac S, Kok CR, Heermann M, Hutkins R (2018) Fermented foods as a dietary source of live organisms. Front Microbiol 9:1785. https://doi.org/10.3389/fmicb.2018.01785
Schaechter M (2009) Encyclopedia of microbiology. Elsevier, Amsterdam
Afzaal M, Saeed F, Hussain M, Shahid F, Siddeeg A, Al-Farga A (2022) Proteomics as a promising biomarker in food authentication, quality and safety: a review. Food Sci Nutr 10(7):2333–2346. https://doi.org/10.1002/fsn3.2842
Kechagia M, Basoulis D, Konstantopoulou S, Dimitriadi D, Gyftopoulou K, Skarmoutsou N, Fakiri EM (2013) Health benefits of probiotics: a review. ISRN Nutr 2013:481651. https://doi.org/10.5402/2013/481651
Walsh AM, Crispie F, Daari K, O’Sullivan O, Martin JC, Arthur CT, Claesson MJ, Scott KP, Cotter PD (2017) Strain-level metagenomic analysis of the fermented dairy beverage nunu highlights potential food safety risks. Appl Environ Microbiol 83(16):e01144-e1117. https://doi.org/10.1128/AEM.01144-17
Braide W, Azuwike C, Adeleye S (2018). The role of microorganisms in the production of some indigenous fermented foods in Nigeria. https://doi.org/10.22192/ijarbs
Odunfa SA, Oyewole OB (1998) African fermented foods. Microbiology of fermented foods. Springer, US, pp 713–752
Holzapfel WH (2002) Appropriate starter culture technologies for small-scale fermentation in developing countries. Int J Food Microbiol 75(3):197–212. https://doi.org/10.1016/s0168-1605(01)00707-3
Kostinek M, Specht I, Edward VA, Schillinger U, Hertel C, Holzapfel WH, Franz CMAP (2005) Diversity and technological properties of predominant lactic acid bacteria from fermented cassava used for the preparation of Gari, a traditional African food. Syst Appl Microbiol 28(6):527–540. https://doi.org/10.1016/j.syapm.2005.03.001
Padonou SW, Hounhouigan JD, Nago MC (2009) Physical, chemical and microbiological characteristics of lafun produced in Benin. Afr J Biotechnol 8(14):3320–3325
Owusu-Kwarteng J, Akabanda F, Nielsen DS, Tano-Debrah K, Glover RLK, Jespersen L (2012) Identification of lactic acid bacteria isolated during traditional fura processing in Ghana. Food Microbiol 32(1):72–78. https://doi.org/10.1016/j.fm.2012.04.010
Ahaotu NN, Anyogu A, Obioha P, Aririatu L, Ibekwe VI, Oranusi S, Sutherland JP, Ouoba LII (2017) Influence of soy fortification on microbial diversity during cassava fermentation and subsequent physicochemical characteristics of garri. Food Microbiol 66:165–172. https://doi.org/10.1016/j.fm.2017.04.019
Mukisa IM, Porcellato D, Byaruhanga YB, Muyanja CMBK, Rudi K, Langsrud T, Narvhus JA (2012) The dominant microbial community associated with fermentation of Obushera (sorghum and millet beverages) determined by culture-dependent and culture-independent methods. Int J Food Microbiol 160(1):1–10. https://doi.org/10.1016/j.ijfoodmicro.2012.09.023
Amoa-Awua WK, Sampson E, Tano-Debrah K (2007) Growth of yeasts, lactic and acetic acid bacteria in palm wine during tapping and fermentation from felled oil palm (Elaeis guineensis) in Ghana. J Appl Microbiol 102(2):599–606. https://doi.org/10.1111/j.1365-2672.2006.03074.x
Ouoba LII, Kando C, Parkouda C, Sawadogo-Lingani H, Diawara B, Sutherland JP (2012) The microbiology of Bandji, palm wine of <i>Borassus akeassii</i> from Burkina Faso: identification and genotypic diversity of yeasts, lactic acid and acetic acid bacteria. J Appl Microbiol 113(6):1428–1441. https://doi.org/10.1111/jam.12014
Adedeji BS, Ezeokoli OT, Ezekiel CN, Obadina AO, Somorin YM, Sulyok M, Adeleke RA, Warth B, Nwangburuka CC, Omemu AM, Oyewole OB, Krska R (2017) Bacterial species and mycotoxin contamination associated with locust bean, melon and their fermented products in south-western Nigeria. Int J Food Microbiol 258:73–80. https://doi.org/10.1016/j.ijfoodmicro.2017.07.014
Isu NR, Ofuya CO (2000) Improvement of the traditional processing and fermentation of African oil bean (Pentaclethra macrophylla Bentham) into a food snack – ‘ugba.’ Int J Food Microbiol 59(3):235–239. https://doi.org/10.1016/s0168-1605(00)00318-4
Obeta JAN (1983) A note on the micro-organisms associated with the fermentation of seeds of the African oil bean tree (<i>Pentaclethra macrophylla</i>). J Appl Bacteriol 54(3):433–435. https://doi.org/10.1111/j.1365-2672.1983.tb02639.x
Oguntoyinbo FA, Sanni AI, Franz CMAP, Holzapfel WH (2007) In vitro fermentation studies for selection and evaluation of Bacillus strains as starter cultures for the production of okpehe, a traditional African fermented condiment. Int J Food Microbiol 113(2):208–218. https://doi.org/10.1016/j.ijfoodmicro.2006.07.006
Anyanwu N, Okonkwo O, Iheanacho C, Ajide B (2016) Microbiological and Nutritional Qualities of Fermented Ugba (Pentaclethra macrophylla, Bentham) Sold in Mbaise, Imo State, Nigeria. Annual Research & Review in Biology 9(4):1–8. https://doi.org/10.9734/arrb/2016/23610
Ogbadu L, Okagbue RN (1988) Bacterial fermentation of soya bean for ‘daddawa’ production. J Appl Bacteriol 65(5):353–356. https://doi.org/10.1111/j.1365-2672.1988.tb01902.x
Achi OK (1992) Microorganisms associated with natural fermentation ofProsopis africana seeds for the production of okpiye. Plant Foods Hum Nutr 42(4):297–304. https://doi.org/10.1007/bf02194090
Mulyowidarso RK, Fleet GH, Buckle KA (1989) The microbial ecology of soybean soaking for tempe production. Int J Food Microbiol 8(1):35–46. https://doi.org/10.1016/0168-1605(89)90078-0
Ogueke CC, Aririatu LE (2005) Microbial and organoleptic changes associated with “ugba” stored at ambient temperature. Nigerian Food Journal. https://doi.org/10.4314/nifoj.v22i1.33578
Ghosh S (2015) Metagenomic screening of cell wall hydrolases, their anti-fungal activities and potential role in wine fermentation.
Ghosh S, Divol B, Setati ME (2021) A shotgun metagenomic sequencing exploration of cabernet sauvignon grape must reveals yeast hydrolytic enzymes. S Afr J Enol Vitic 42(2):213–223. https://doi.org/10.2148/42-2-4724
Ezekiel CN, Ayeni KI, Ezeokoli OT, Sulyok M, van Wyk DAB, Oyedele OA, Akinyemi OM, Chibuzor-Onyema IE, Adeleke RA, Nwangburuka CC, Hajšlová J, Elliott CT, Krska R (2019) High-throughput sequence analyses of bacterial communities and multi-mycotoxin profiling during processing of different formulations of kunu, a traditional fermented beverage. Front Microbiol 9:3282–3282. https://doi.org/10.3389/fmicb.2018.03282
Parker M, Zobrist S, Donahue C, Edick C, Mansen K, Hassan Zade Nadjari M, Heerikhuisen M, Sybesma W, Molenaar D, Diallo AM, Milani P, Kort R (2018) Naturally fermented milk from northern senegal: bacterial community composition and probiotic enrichment with Lactobacillus rhamnosus. Front Microbiol 9:2218–2218. https://doi.org/10.3389/fmicb.2018.02218
Jespersen L (2003) Occurrence and taxonomic characteristics of strains of predominant in African indigenous fermented foods and beverages. FEMS Yeast Res 3(2):191–200. https://doi.org/10.1016/s1567-1356(02)00185-x
Tamang J, Samuel D (2010) Dietary Cultures and Antiquity of Fermented Foods and Beverages. Fermented Foods and Beverages of the World. CRC Press, Boca Raton, pp 1–40
Halm M, Lillie A, Sørensen AK, Jakobsen M (1993) Microbiological and aromatic characteristics of fermented maize doughs for kenkey production in Ghana. Int J Food Microbiol 19(2):135–143. https://doi.org/10.1016/0168-1605(93)90179-k
Omemu AM, Oyewole OB, Bankole MO (2007) Significance of yeasts in the fermentation of maize for ogi production. Food Microbiol 24(6):571–576. https://doi.org/10.1016/j.fm.2007.01.006
Ezeronye OU, Legras JL (2009) Genetic analysis ofSaccharomyces cerevisiaestrains isolated from palm wine in eastern Nigeria. Comparison with other African strains. J Appl Microbiol 106(5):1569–1578. https://doi.org/10.1111/j.1365-2672.2008.04118.x
Akabanda F, Owusu-Kwarteng J, Glover RLK, Tano-Debrah K Microbiological characteristics of ghanaian traditional fermented milk product, Nunu.
Akabanda F, Owusu-Kwarteng J, Tano-Debrah K, Glover RL, Nielsen DS, Jespersen L (2013) Taxonomic and molecular characterization of lactic acid bacteria and yeasts in nunu, a Ghanaian fermented milk product. Food Microbiol 34(2):277–283. https://doi.org/10.1016/j.fm.2012.09.025
Njage P, Dolci S, Jans C, Wangoh J, Lacroix C, Meile L (2011) Characterization of yeasts associated with camel milk using phenotypic and molecular identification techniques. Res J Microbiol 6(9):678. https://doi.org/10.3923/jm.2011.678.692
Oyewole OB (2001) Characteristics and significance of yeasts’ involvement in cassava fermentation for ‘fufu’ production. Int J Food Microbiol 65(3):213–218. https://doi.org/10.1016/s0168-1605(01)00431-7
Mukisa IM, Byaruhanga YB, Muyanja CMBK, Langsrud T, Narvhus JA (2016) Production of organic flavor compounds by dominant lactic acid bacteria and yeasts from Obushera, a traditional sorghum malt fermented beverage. Food Sci Nutr 5(3):702–712. https://doi.org/10.1002/fsn3.450
Mugula JK, Narvhus JA, Sørhaug T (2003) Use of starter cultures of lactic acid bacteria and yeasts in the preparation of togwa, a Tanzanian fermented food. Int J Food Microbiol 83(3):307–318. https://doi.org/10.1016/s0168-1605(02)00386-0
Nyambane B, Thari WM, Wangoh J, Njage PM (2014) Lactic acid bacteria and yeasts involved in the fermentation of amabere amaruranu, a Kenyan fermented milk. Food Sci Nutr 2(6):692–699. https://doi.org/10.1002/fsn3.162
Witthuhn RC, Schoeman T, Britz TJ (2004) Isolation and characterization of the microbial population of different South African kefir grains. Int J Dairy Technol 57(1):33–37. https://doi.org/10.1111/j.1471-0307.2004.00126.x
Gadaga T (1999) A review of traditional fermented foods and beverages of Zimbabwe. Int J Food Microbiol 53(1):1–11. https://doi.org/10.1016/s0168-1605(99)00154-3
Obodai M, Dodd C (2006) Characterization of dominant microbiota of a Ghanaian fermented milk product, nyarmie, by culture-and nonculture-based methods. J Appl Microbiol 100(6):1355–1363. https://doi.org/10.1111/j.1365-2672.2006.02895.x
Ongol MP, Asano K (2009) Main microorganisms involved in the fermentation of Ugandan ghee. Int J Food Microbiol 133(3):286–291. https://doi.org/10.1016/j.ijfoodmicro.2009.06.003
Kebede A, Viljoen BC, Gadaga TH, Narvhus JA, Lourens-Hattingh A (2007) The effect of container type on the growth of yeast and lactic acid bacteria during production of Sethemi, South African spontaneously fermented milk. Food Res Int 40(1):33–38. https://doi.org/10.1016/j.foodres.2006.07.012
Jain C, Rodriguez-R LM, Phillippy AM, Konstantinidis KT, Aluru S (2018) High throughput ANI analysis of 90K prokaryotic genomes reveals clear species boundaries. Nat Commun 9(1):5114–5114. https://doi.org/10.1038/s41467-018-07641-9
Olasupo N, Odunfa S, Obayori O (2010) Ethnic African Fermented Foods. Fermented foods and beverages of the world. CRC Press, Boca Raton, pp 323–352
Odunfa SA (1988) African fermented foods: from art to science MIRCEN. J Appl Microbiol Biotechnol 4(3):259–273. https://doi.org/10.1007/bf01096132
Bauer R, du Toit M, Kossmann J (2010) Influence of environmental parameters on production of the acrolein precursor 3-hydroxypropionaldehyde by Lactobacillus reuteri DSMZ 20016 and its accumulation by wine lactobacilli. Int J Food Microbiol 137(1):28–31. https://doi.org/10.1016/j.ijfoodmicro.2009.10.012
El-Baradei G, Delacroix-Buchet A, Ogier J-C (2008) Bacterial biodiversity of traditional Zabady fermented milk. Int J Food Microbiol 121(3):295–301. https://doi.org/10.1016/j.ijfoodmicro.2007.11.014
Bacha K, McHari T, Ashenafi M (1999) Microbiology of the fermentation of shamita, a traditional Ethiopian fermented beverage. SINET: Ethiop J Sci. https://doi.org/10.4314/sinet.v22i1.18137
El-Sadek GM, Zawahry MR, Mahmoud SA, El-Motteleb LA (1958) Chemical composition of Egyptian Kishk. Indian J Dairy Sci 11:67–75
Mangia NP, Garau G, Murgia MA, Bennani A, Deiana P (2014) Influence of autochthonous lactic acid bacteria and enzymatic yeast extracts on the microbiological, biochemical and sensorial properties of Lben generic products. J Dairy Res 81(2):193–201. https://doi.org/10.1017/S0022029914000119
Bensalah F, Delorme C, Renault P (2009) Characterisation of thermotolerant cocci from indigenous flora of ‘leben’in algerian arid area and DNA identification of atypical Lactococcus lactis strains. Curr Microbiol 59(2):139–146. https://doi.org/10.1007/s00284-009-9411-1
Steinkraus KH (1983) Fermented foods, feeds and beverages. Biotechnol Adv 1(1):31–46. https://doi.org/10.1016/0734-9750(83)90299-9
Muyanja CMBK, Narvhus JA, Treimo J, Langsrud T (2003) Isolation, characterisation and identification of lactic acid bacteria from bushera: a Ugandan traditional fermented beverage. Int J Food Microbiol 80(3):201–210. https://doi.org/10.1016/s0168-1605(02)00148-4
Coppock D, Holden S, O'Connor C (1991) Milk processing and peri-urban dairy marketing in semi-arid Ethiopia and prospects for development intervention.
Mathara JM (1999) Studies on lactic acid producing microflora in mursik and kule naoto, traditional fermented milks from Nandi and Masai communities in Kenya. University of Nairobi
Mathara JM, Schillinger U, Kutima PM, Mbugua SK, Holzapfel WH (2004) Isolation, identification and characterisation of the dominant microorganisms of kule naoto: the Maasai traditional fermented milk in Kenya. Int J Food Microbiol 94(3):269–278. https://doi.org/10.1016/j.ijfoodmicro.2004.01.008
Nieminen MT, Novak-Frazer L, Collins R, Dawsey SP, Dawsey SM, Abnet CC, White RE, Freedman ND, Mwachiro M, Bowyer P (2013) Alcohol and acetaldehyde in african fermented milk mursik—a possible etiologic factor for high incidence of esophageal cancer in western kenya. Cancer Epidemiol Prev Biomark 22(1):69–75. https://doi.org/10.1158/1055-9965.EPI-12-0908
Owusu-Kwarteng J, Akabanda F, Agyei D, Jespersen L (2020) Microbial safety of milk production and fermented dairy products in Africa. Microorganisms 8(5):752. https://doi.org/10.3390/microorganisms8050752
Mlotha V, Mwangwela AM, Kasapila W, Siyame EWP, Masamba K (2016) Glycemic responses to maize flour stiff porridges prepared using local recipes in Malawi. Food Sci Nutr 4(2):322–328. https://doi.org/10.1002/fsn3.293
Gonfa A, Fite A, Urga K, Gashe BA (1999) Microbiological aspects of Ergo (Ititu) fermentation. SINET Ethiop J Sci 22(2):283–290
Anyogu A, Olukorede A, Anumudu C, Onyeaka H, Areo E, Adewale O, Odimba JN, Nwaiwu O (2021) Microorganisms and food safety risks associated with indigenous fermented foods from Africa. Food Control 129:108227. https://doi.org/10.1016/j.foodcont.2021.108227
Wedajo Lemi B (2020) Microbiology of ethiopian traditionally fermented beverages and condiments. Int J Microbiol 2020:1478536–1478536. https://doi.org/10.1155/2020/1478536
Mugula JK, Nnko SAM, Narvhus JA, Sørhaug T (2003) Microbiological and fermentation characteristics of togwa, a Tanzanian fermented food. Int J Food Microbiol 80(3):187–199. https://doi.org/10.1016/s0168-1605(02)00141-1
Mattiello S, Caroprese M, Matteo CG, Fortina R, Martini A, Martini M, Parisi G, Russo C, Zecchini M, Projects” ACAPiDC (2018) Typical dairy products in Africa from local animal resources. Ital J Anim Sci 17(3):740–754. https://doi.org/10.1080/1828051X.2017.1401910
Kassaye T, Simpson B, Smith J, O’connor C (1991) Chemical and microbiological characteristics of Ititu. Milchwissenschaft 46(10):649–653
Abdelgadir WS, Ahmed TK, Dirar HA (1998) The traditional fermented milk products of the Sudan. Int J Food Microbiol 44(1–2):1–13. https://doi.org/10.1016/s0168-1605(98)00090-7
Jans C, Bugnard J, Njage PMK, Lacroix C, Meile L (2012) Lactic acid bacteria diversity of African raw and fermented camel milk products reveals a highly competitive, potentially health-threatening predominant microflora. Lwt-Food Sci Technol 47(2):371–379. https://doi.org/10.1016/j.lwt.2012.01.034
Nakavuma J, Møller P, Jakobsen M, Salimo P (2012) Afr J Biomed Sci 7(2):82–93
Schutte LM (2013) Isolation and identification of the microbial consortium present in fermented milks from sub-Saharan Africa. Stellenbosch University, Stellenbosch
Agyei D, Owusu-Kwarteng J, Akabanda F, Akomea-Frempong S (2020) Indigenous African fermented dairy products: Processing technology, microbiology and health benefits. Crit Rev Food Sci Nutr 60(6):991–1006. https://doi.org/10.1080/10408398.2018.1555133
Owusu-Kwarteng J, Akabanda F, Johansen P, Jespersen L, Nielsen DS (2017) Nunu, a West African fermented yogurt-like milk product Yogurt in health and disease prevention. Elsevier, Amsterdam, pp 275–283
Jiwoua C, Milliere J (1990) Lactic flora and enterococci of fermented [zebu] milk (pindidam) produced in Adamaoua (Cameroun). Lait (France)
Mbawala A, Mahbou P, Mouafo H, Tatsadjieu L (2013) Antibacterial activity of some lactic acid bacteria isolated from a local fermented milk product (pendidam) in Ngaoundere. Cameroon J Anim Plant Sci 23(1):157–166
Libouga D, Ngang J, Halilou H (2005) Quality of some Cameroonian fermented milk. Sci Aliment 25(1):53–66. https://doi.org/10.3166/sda.25.53-66
Wullschleger S, Lacroix C, Bonfoh B, Sissoko-Thiam A, Hugenschmidt S, Romanens E, Baumgartner S, Traoré I, Yaffee M, Jans C (2013) Analysis of lactic acid bacteria communities and their seasonal variations in a spontaneously fermented dairy product (Malian fènè) by applying a cultivation/genotype-based binary model. Int Dairy J 29(1):28–35. https://doi.org/10.1016/j.idairyj.2012.08.001
Shiferaw Terefe N, Augustin MA (2019) Fermentation for tailoring the technological and health related functionality of food products. Crit Rev Food Sci Nutr 60(17):2887–2913. https://doi.org/10.1080/10408398.2019.1666250
Owusu-Kwarteng J, Tano-Debrah K, Akabanda F, Nielsen DS, Jespersen L (2013) Partial characterization of bacteriocins produced by lactobacillus reuteri 2–20b and pediococcus acidilactici 0–11a isolated from fura, a millet-based fermented food in ghana. J Food Res 2(1):50. https://doi.org/10.5539/jfr.v2n1p50
Mashau ME, Maliwichi LL, Jideani AIO (2021) Non-alcoholic fermentation of maize (Zea mays) in Sub-Saharan Africa. Fermentation-Basel 7(3):158. https://doi.org/10.3390/fermentation7030158
Blandino A, Al-Aseeri ME, Pandiella SS, Cantero D, Webb C (2003) Cereal-based fermented foods and beverages. Food Res Int 36(6):527–543. https://doi.org/10.1016/s0963-9969(03)00009-7
Odunfa SA (1981) Microorganisms associated with fermentation of African locust bean (<i>Parkia filicoidea</i>) during <i>iru</i> preparation. J Plant Foods 3(4):245–250. https://doi.org/10.1080/0142968x.1981.11904236
Vieira-Dalodé G, Jespersen L, Hounhouigan J, Moller PL, Nago CM, Jakobsen M (2007) Lactic acid bacteria and yeasts associated with gowé production from sorghum in Bénin. J Appl Microbiol 103(2):342–349. https://doi.org/10.1111/j.1365-2672.2006.03252.x
Okafor UI, Omemu AM, Obadina AO, Bankole MO, Adeyeye SAO (2018) Nutritional composition and antinutritional properties of maize ogi cofermented with pigeon pea. Food Sci Nutr 6(2):424–439. https://doi.org/10.1002/fsn3.571
Odunfa SA, Oyeyiola GF (1985) Microbiological study of the fermentation of <i>Ugba</i>, a nigerian indigenous fermented food flavour. J Plant Foods 6(3):155–163. https://doi.org/10.1080/0142968x.1985.11904309
Sanni A, A O, I F, S O, R A, (2002) Selection of starter cultures for the production of ugba, a fermented soup condiment. Eur Food Res Technol 215(2):176–180. https://doi.org/10.1007/s00217-002-0520-3
Kayode A, Vieira-Dalodé G, Linnemann A, Kotchoni S, Hounhouigan A, Van Boekel M, Nout M (2011) Diversity of yeasts involved in the fermentation of tchoukoutou, an opaque sorghum beer from Benin. Afr J Microbiol Res 5(18):2737–2742. https://doi.org/10.5897/AJMR11.546
Odunfa SA, Oyewole OB (1986) Identification of Bacillus species from ‘iru’, a fermented African locust bean product. J Basic Microb 26(2):101–108. https://doi.org/10.1002/jobm.3620260212
Parkouda C, Nielsen DS, Azokpota P, Ivette Irène Ouoba L, Amoa-Awua WK, Thorsen L, Hounhouigan JD, Jensen JS, Tano-Debrah K, Diawara B, Jakobsen M (2009) The microbiology of alkaline-fermentation of indigenous seeds used as food condiments in Africa and Asia. Crit Rev Microbiol 35(2):139–156. https://doi.org/10.1080/10408410902793056
Ayeloja AA, Jimoh WA (2022) Fermented Fish Products in Sub-Saharan Africa. African Fermented Food Products- New Trends. Springer, Berlin, pp 251–263
Osvik R, Sperstad S, Breines E, Hareide E, Godfroid J, Zhou Z, Ren P, Geoghegan C, Ringoe E (2013) Bacterial diversity of aMasi, a South African fermented milk product, determined by clone library and denaturing gradient gel electrophoresis analysis. Afr J Microbiol Res 7:4146–4158. https://doi.org/10.5897/AJMR12.2317
Abdelgadir W, Nielsen DS, Hamad S, Jakobsen M (2008) A traditional Sudanese fermented camel's milk product, Gariss, as a habitat of Streptococcus infantarius subsp. infantarius. International journal of food microbiology 127(3):215–219. https://doi.org/10.1016/j.ijfoodmicro.2008.07.008
Schoustra SE, Kasase C, Toarta C, Kassen R, Poulain AJ (2013) Microbial community structure of three traditional zambian fermented products: mabisi, chibwantu and munkoyo. PLoS ONE 8(5):e63948–e63948. https://doi.org/10.1371/journal.pone.0063948
Chelule P, Mokoena M, Gqaleni N (2010) Advantages of traditional lactic acid bacteria fermentation of food in Africa. Current Research, Technology and Education Topics in Applied Microbiology and Microbial Biotechnology 2
Vardjan T, Lorbeg PM, Rogelj I, Majhenič AČ (2013) Characterization and stability of lactobacilli and yeast microbiota in kefir grains. J Dairy Sci 96(5):2729–2736. https://doi.org/10.3168/jds.2012-5829
MacDonald R, Reitmeier C (2017) Understanding food systems: agriculture, food science, and nutrition in the United States. Academic Press, London
Beukes EM, Bester BH, Mostert JF (2001) The microbiology of South African traditional fermented milks. Int J Food Microbiol 63(3):189–197. https://doi.org/10.1016/s0168-1605(00)00417-7
Ohenhen R, Imarenezor E, Kihuha A (2013) Microbiome of madila-a southern-african fermented milk product. Int J Basic Appl Sci 2(2):170. https://doi.org/10.1419/ijbas.v2i2.639
Nicholas J The Microbial Succession in Indigenous Fermented Maize Products.
Holzapfel WH, Haberer P, Geisen R, Björkroth J, Schillinger U (2001) Taxonomy and important features of probiotic microorganisms in food and nutrition. Am J Clin Nutr 73(2):365s–373s. https://doi.org/10.1093/ajcn/73.2.365s
Besselink MGH, Timmerman HM, Buskens E, Nieuwenhuijs VB, Akkermans LMA, Gooszen HG, Dutch Acute Pancreatitis Study G (2004) Probiotic prophylaxis in patients with predicted severe acute pancreatitis (PROPATRIA): design and rationale of a double-blind, placebo-controlled randomised multicenter trial [ISRCTN38327949]. BMC Surg 4:12–12. https://doi.org/10.1186/1471-2482-4-12
Besselink MGH, van Santvoort HC, Buskens E, Boermeester MA, van Goor H, Timmerman HM, Nieuwenhuijs VB, Bollen TL, van Ramshorst B, Witteman BJM, Rosman C, Ploeg RJ, Brink MA, Schaapherder AFM, Dejong CHC, Wahab PJ, van Laarhoven CJHM, van der Harst E, van Eijck CHJ, Cuesta MA, Akkermans LMA, Gooszen HG (2008) Probiotic prophylaxis in predicted severe acute pancreatitis: a randomised, double-blind, placebo-controlled trial. The Lancet 371(9613):651–659. https://doi.org/10.1016/s0140-6736(08)60207-x
Lei V, Jakobsen M (2004) Microbiological characterization and probiotic potential of koko and koko sour water, African spontaneously fermented millet porridge and drink. J Appl Microbiol 96(2):384–397. https://doi.org/10.1046/j.1365-2672.2004.02162.x
Darling JC, Kitundu JA, Kingamkono RR, Msengi AE, Mduma B, Sullivan KR, Tomkins AM (1995) Improved energy intakes using amylase-digested weaning foods in tanzanian children with acute diarrhea. J Pediatr Gastroenterol Nutr 21(1):73–81. https://doi.org/10.1097/00005176-199507000-00013
Mensah P, Ndiokwelu CI, Uwaegbute A, Ablordey A, van Boxtel AMGA, Brinkman C, Nout MJR, Ngoddy PO (1995) Feeding of lactic acid-fermented high nutrient density weaning formula in paediatric settings in Ghana and Nigeria: acceptance by mother and infant and performance during recovery from acute diarrhoea. Int J Food Sci Nutr 46(4):353–362. https://doi.org/10.3109/09637489509012567
Zakpaa H, Imbeah C, Mak-Mensah E (2009) Microbial characterization of fermented meat products on some selected markets in the Kumasi metropolis, Ghana. Afr J Food Sci 3:340–346
Banwo K, Sanni A, Tan H (2012) Technological properties and probiotic potential of Enterococcus faecium strains isolated from cow milk. J Appl Microbiol 114(1):229–241. https://doi.org/10.1111/jam.12031
Jacobsen CN, Rosenfeldt Nielsen V, Hayford AE, Møller PL, Michaelsen KF, Paerregaard A, Sandström B, Tvede M, Jakobsen M (1999) Screening of probiotic activities of forty-seven strains of Lactobacillus spp by in vitro techniques and evaluation of the colonization ability of five selected strains in humans. Appl Environ Microbiol 65(11):4949–4956. https://doi.org/10.1128/AEM.65.11.4949-4956.1999
Turpin W, Humblot C, Guyot J-P (2011) Genetic screening of functional properties of lactic acid bacteria in a fermented pearl millet slurry and in the metagenome of fermented starchy foods. Appl Environ Microbiol 77(24):8722–8734. https://doi.org/10.1128/AEM.05988-11
Njeru P, Rösch N, Ghadimi D, Geis A, Bockelmann W, de Vrese M, Schrezenmeir J, Heller K (2010) Identification and characterisation of lactobacilli isolated from<i>Kimere</i>, a spontaneously fermented pearl millet dough from Mbeere, Kenya (East Africa). Benef Microbes 1(3):243–252. https://doi.org/10.3920/bm2010.0019
Mathara J, Schillinger U, Guigas C, Franz C, Kutima P, Mbugua S, Shin H, Holzapfel W (2008) Functional characteristics of Lactobacillus spp from traditional Maasai fermented milk products in Kenya. Int J Food Microbiol 126(1–2):57–64. https://doi.org/10.1016/j.ijfoodmicro.2008.04.027
Okoye J, Oni K (2017) Promotion of indigenous food preservation and processing knowledge and the challenge of food security in Africa. Journal of food security 5(3):75–87. https://doi.org/10.12691/jfs-5-3-3
Klingenberg P (1989) G. Campbell-Platt: Fermented Foods of the World. A Dictionary and Guide. 291 Seiten. Butterworth, London, Boston, Durban u. a (1987) Preis: 35,— £ (hardcover). Food / Nahrung 33(3):304–304. https://doi.org/10.1002/food.19890330322
Barbosa-Cánovas GV, Food, Agriculture Organization of the United N (2003) Handling and preservation of fruits and vegetables by combined methods for rural areas : technical manual/by Gustavo V. Barbosa-Cánovas [and others]. Rome : Food and Agriculture Organization of the United Nations,
Motarjemi Y (2002) Impact of small scale fermentation technology on food safety in developing countries. Int J Food Microbiol 75(3):213–229. https://doi.org/10.1016/s0168-1605(01)00709-7
Suleiman AME, Gadir WSA (2009) Effect of fermentation on the nutritional and microbiological quality of dough of different sorghum varieties. J Sci Technol 10:109–119
Cooke RD, Twiddy DR, Alan Reilly PJ (1987) Lactic-acid fermentation as a low-cost means of food preservation in tropical countries. Fems Microbiol Lett 46(3):369–379. https://doi.org/10.1016/0378-1097(87)90120-0
Ciani M, Lippolis A, Fava F, Rodolfi L, Niccolai A, Tredici MR (2021) Microbes: food for the future. Foods 10(5):971. https://doi.org/10.3390/foods10050971
Matassa S, Boon N, Pikaar I, Verstraete W (2016) Microbial protein: future sustainable food supply route with low environmental footprint. Microb Biotechnol 9(5):568–575. https://doi.org/10.1111/1751-7915.12369
Acosta N, Sakarika M, Kerckhof F-M, Law CKY, De Vrieze J, Rabaey K (2020) Microbial protein production from methane via electrochemical biogas upgrading. Chem Eng J 391:123625. https://doi.org/10.1016/j.cej.2019.123625
Volova TG, Barashkov VA (2010) Characteristics of proteins synthesized by hydrogen-oxidizing microorganisms. Prikl Biokhim Mikrobiol 46(6):624–629. https://doi.org/10.1134/S0003683810060037
Clark JD (1975) African origins of man the toolmaker.
Nduko JM, Matofari JW, Nandi ZO, Sichangi MB (2017) Spontaneously fermented Kenyan milk products: a review of the current state and future perspectives. Afr J Food Sci 11(1):1–11. https://doi.org/10.5897/AJFS2016.1516
Akinyemi MO, Ayeni KI, Ogunremi OR, Adeleke RA, Oguntoyinbo FA, Warth B, Ezekiel CN (2021) A review of microbes and chemical contaminants in dairy products in sub-Saharan Africa. Comprehens Rev Food Sci Food Saf 20(2):1188–1220. https://doi.org/10.1111/1541-4337.12712
Maleke M, Adefisoye MA, Doorsamy W, Adebo OA (2021) Processing, nutritional composition and microbiology of amasi: A Southern African fermented milk product. Sci Afr 12:e00795. https://doi.org/10.1016/j.sciaf.2021.e00795
Jans C, Meile L, Kaindi DWM, Kogi-Makau W, Lamuka P, Renault P, Kreikemeyer B, Lacroix C, Hattendorf J, Zinsstag J (2017) African fermented dairy products–overview of predominant technologically important microorganisms focusing on African Streptococcus infantarius variants and potential future applications for enhanced food safety and security. Int J Food Microbiol 250:27–36. https://doi.org/10.1016/j.ijfoodmicro.2017.03.012
Tamang JP, Kailasapathy K (2010) Fermented foods and beverages of the world. CRC Press
Swelum AA, El-Saadony MT, Abdo M, Ombarak RA, Hussein EO, Suliman G, Alhimaidi AR, Ammari AA, Ba-Awadh H, Taha AE (2021) Nutritional, antimicrobial and medicinal properties of Camel’s milk: A review. Saudi J Biol Sci 28(5):3126–3136. https://doi.org/10.1016/j.sjbs.2021.02.057
Schönfeldt HC, Hall NG (2012) Dietary protein quality and malnutrition in Africa. Br J Nutr 108(S2):S69–S76. https://doi.org/10.1017/S0007114512002553
Wuehler SE, Hess SY, Brown KH (2011) Accelerating improvements in nutritional and health status of young children in the Sahel region of Sub-Saharan Africa: review of international guidelines on infant and young child feeding and nutrition. Matern Child Nutr 7(Suppl 1):6–34. https://doi.org/10.1111/j.1740-8709.2010.00306.x
Johansen PG, Owusu-Kwarteng J, Parkouda C, Padonou SW, Jespersen L (2019) Occurrence and importance of yeasts in indigenous fermented food and beverages produced in sub-Saharan Africa. Front Microbiol 10:1789. https://doi.org/10.3389/fmicb.2019.01789
Hadj Saadoun J, Bertani G, Levante A, Vezzosi F, Ricci A, Bernini V, Lazzi C (2021) Fermentation of agri-food waste: A promising route for the production of aroma compounds. Foods 10(4):707. https://doi.org/10.3390/foods10040707
Jay JM, Loessner M, Golden D (2021) Modern food microbiology. Chapman Hall. https://doi.org/10.1007/BF03174975
GEREMU T, WOGI L, FEYISSA S (2021) SOIL FERTILITY AND MICRONUTRIENT STATUS IN TISSUES OF MAIZE IN DARO LABU DISTRICT, WEST HARARGHE ZONE, EASTERN ETHIOPIA. Asian Journal of Advances in Research. 32–53
Fijan S (2014) Microorganisms with claimed probiotic properties: an overview of recent literature. Int J Environ Res Public Health 11(5):4745–4767. https://doi.org/10.3390/ijerph110504745
Gandhi D (2000) Fermented dairy products and their role in controlling food borne diseases. Food Processing: Biotechnological Applications, Asiatech Publishers Inc, New Delhi:209–220
Marco ML, Sanders ME, Gänzle M, Arrieta MC, Cotter PD, De Vuyst L, Hill C, Holzapfel W, Lebeer S, Merenstein D (2021) The International Scientific Association for Probiotics and Prebiotics (ISAPP) consensus statement on fermented foods. Nat Rev Gastroenterol Hepatol 18(3):1–13. https://doi.org/10.1038/s41575-020-00390-5
Agrawal GK, Timperio AM, Zolla L, Bansal V, Shukla R, Rakwal R (2013) Biomarker discovery and applications for foods and beverages: proteomics to nanoproteomics. J Proteomics 93:74–92. https://doi.org/10.1016/j.jprot.2013.04.014
More AS, Ranadheera CS, Fang ZX, Warner R, Ajlouni S (2020) Biomarkers associated with quality and safety of fresh-cut produce. Food Biosci 34:100524. https://doi.org/10.1016/j.fbio.2019.100524
Dragsted LO, Gao Q, Scalbert A, Vergeres G, Kolehmainen M, Manach C, Brennan L, Afman LA, Wishart DS, Andres Lacueva C, Garcia-Aloy M, Verhagen H, Feskens EJM, Pratico G (2018) Validation of biomarkers of food intake-critical assessment of candidate biomarkers. Genes Nutr 13:14. https://doi.org/10.1186/s12263-018-0603-9
Dragsted LO, Gao Q, Pratico G, Manach C, Wishart DS, Scalbert A, Feskens EJM (2017) Dietary and health biomarkers-time for an update. Genes Nutr. https://doi.org/10.1186/s12263-017-0578-y
Prentice RL, Mossavar-Rahmani Y, Huang Y, Van Horn L, Beresford SAA, Caan B, Tinker L, Schoeller D, Bingham S, Eaton CB, Thomson C, Johnson KC, Ockene J, Sarto G, Heiss G, Neuhouser ML (2011) Evaluation and comparison of food records, recalls, and frequencies for energy and protein assessment by using recovery biomarkers. Am J Epidemiol 174(5):591–603. https://doi.org/10.1093/aje/kwr140
Kumar V, Sinha AK, Uka A, Antonacci A, Scognamiglio V, Mazzaracchio V, Cinti S, Arduini F (2020) Multi-potential biomarkers for seafood quality assessment: Global wide implication for human health monitoring. Trac-Trend Anal Chem. https://doi.org/10.1016/j.trac.2020.116056
Sébédio JL (2017) Metabolomics, nutrition, and potential biomarkers of food quality, intake, and health status. Adv Food Nutr Res 82:83–116. https://doi.org/10.1016/bs.afnr.2017.01.001
Selamat J, Rozani NAA, Murugesu S (2021) Application of the metabolomics approach in food authentication. Molecules 26(24):7565
Hong E, Lee SY, Jeong JY, Park JM, Kim BH, Kwon K, Chun HS (2017) Modern analytical methods for the detection of food fraud and adulteration by food category. J Sci Food Agr 97(12):3877–3896. https://doi.org/10.1002/jsfa.8364
Shibutami E, Ishii R, Harada S, Kurihara A, Kuwabara K, Kato S, Iida M, Akiyama M, Sugiyama D, Hirayama A, Sato A, Amano K, Sugimoto M, Soga T, Tomita M, Takebayashi T (2021) Charged metabolite biomarkers of food intake assessed via plasma metabolomics in a population-based observational study in Japan. PLoS ONE. https://doi.org/10.1371/journal.pone.0246456
Sajali N, Wong SC, Abu Bakar S, Mokhtar NFK, Manaf YN, Yuswan MH, Desa MNM (2021) Analytical approaches of meat authentication in food. Int J Food Sci Tech 56(4):1535–1543. https://doi.org/10.1111/ijfs.14797
Sundramoorthy AK, Gunasekaran S (2014) Applications of graphene in quality assurance and safety of food. Trac-Trend Anal Chem 60:36–53. https://doi.org/10.1016/j.trac.2014.04.015
Wild CP, Andersson C, O’Brien NM, Wilson L, Woods JA (2001) A critical evaluation of the application of biomarkers in epidemiological studies on diet and health. British J Nutr 86:S37–S53. https://doi.org/10.1079/Bjn2001338
Nelis JLD, Bose U, Broadbent JA, Hughes J, Sikes A, Anderson A, Caron K, Schmoelzl S, Colgrave ML (2022) Biomarkers and biosensors for the diagnosis of noncompliant pH, dark cutting beef predisposition, and welfare in cattle. Comprehens Rev Food Sci Food Saf 21(3):2391–2432. https://doi.org/10.1111/1541-4337.12935
Acknowledgements
We would like to extend our heartfelt gratitude to the Wood-Whelan Research Fellowships for their generous support and for awarding the fellowship to Maryam Meskini. This funding has been instrumental in advancing our research and enabling us to pursue our scientific endeavors. The Wood-Whelan Research Fellowships provide a crucial platform for aspiring researchers to explore new horizons and make meaningful contributions to the scientific community. We are sincerely thankful for the trust and investment they have placed in Maryam Meskini's research, which has significantly contributed to the success of this project. We are also thankful to Dr. Swagata Ghosh, Assistant Professor of English, Symbiosis Institute of Technology, Symbiosis International University, Pune, India, for editing this manuscript.
Funding
Open access funding provided by University of the Free State. This research did not receive any specific grants from funding agencies in the public, commercial, or non-profit sectors.
Author information
Authors and Affiliations
Contributions
SG conceptualized the idea. SG along with CB, MM, and MJ collected, analyzed the data and drafted the manuscript. All the authors read, edited, and approved the manuscript for publication.
Corresponding author
Ethics declarations
Conflict of interest
The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Ghosh, S., Bornman, C., Meskini, M. et al. Microbial Diversity in African Foods and Beverages: A Systematic Assessment. Curr Microbiol 81, 19 (2024). https://doi.org/10.1007/s00284-023-03481-z
Received:
Accepted:
Published:
DOI: https://doi.org/10.1007/s00284-023-03481-z