Next Article in Journal
The Role of Pseudomonas aeruginosa ExoY in an Acute Mouse Lung Infection Model
Next Article in Special Issue
Multi-Mycotoxin Occurrence in Dairy Cattle Feeds from the Gauteng Province of South Africa: A Pilot Study Using UHPLC-QTOF-MS/MS
Previous Article in Journal
Zearalenone Promotes Cell Proliferation or Causes Cell Death?
Previous Article in Special Issue
Comparison of Anorectic Potencies of Type A Trichothecenes T-2 Toxin, HT-2 Toxin, Diacetoxyscirpenol, and Neosolaniol
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Toxins
Volume 10
Issue 5
10.3390/toxins10050089
toxins-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Current Status of Mycotoxin Contamination of Food Commodities in Zimbabwe

by
Nancy Nleya
1,2,*,
Modupeade Christianah Adetunji
1,3 and
Mulunda Mwanza
1
1
Department of Animal Health, Northwest University, Mafikeng, Private Bag X2046, Mmabatho 2735, South Africa
2
Department of Applied Biology and Biochemistry, National University of Science and Technology, P.O. Box AC 939 Ascot, Bulawayo, Zimbabwe
3
Department of Biological Sciences, McPherson University, Seriki Sotayo, Ogun State, Abeokuta P.M.B. 2094, Ogun State, Nigeria
*
Author to whom correspondence should be addressed.
Toxins 2018, 10(5), 89; https://doi.org/10.3390/toxins10050089
Submission received: 18 April 2018 / Revised: 27 April 2018 / Accepted: 30 April 2018 / Published: 3 May 2018
(This article belongs to the Collection Understanding Mycotoxin Occurrence in Food and Feed Chains)
Browse Figure
Versions Notes

Abstract

:
Agricultural products, especially cereal grains, serve as staple foods in sub-Saharan Africa. However, climatic conditions in this region can lead to contamination of these commodities by moulds, with subsequent production of mycotoxins posing health risks to both humans and animals. There is limited documentation on the occurrence of mycotoxins in sub-Saharan African countries, leading to the exposure of their populations to a wide variety of mycotoxins through consumption of contaminated foods. This review aims at highlighting the current status of mycotoxin contamination of food products in Zimbabwe and recommended strategies of reducing this problem. Zimbabwe is one of the African countries with very little information with regards to mycotoxin contamination of its food commodities, both on the market and at household levels. Even though evidence of multitoxin occurrence in some food commodities such as maize and other staple foods exist, available published research focuses only on Aspergillus and Fusarium mycotoxins, namely aflatoxins, deoxynivalenol (DON), trichothecenes, fumonisins, and zearalenone (ZEA). Occurrence of mycotoxins in the food chain has been mainly associated with poor agricultural practices. Analysis of mycotoxins has been done mainly using chromatographic and immunological methods. Zimbabwe has adopted European standards, but the legislation is quite flexible, with testing for mycotoxin contamination in food commodities being done voluntarily or upon request. Therefore, the country needs to tighten its legislation as well as adopt stricter standards that will improve the food safety and security of the masses.
Keywords:
mycotoxins; legislation; Zimbabwe; food; feed; standards; analysis
Key Contribution: This review has shown that there is very limited published research on mycotoxin contamination of food commodities in Zimbabwe. The little information available focused on Aspergillus and Fusarium mycotoxins, although the population may be exposed to an array of other mycotoxins. Therefore, this study serves as a baseline indicating which areas of mycotoxin research need to be looked at in Zimbabwe.

Graphical Abstract

1. Introduction

Mycotoxins are secondary metabolites produced mainly by moulds belonging to the genera Aspergillus, Fusarium, and Penicillium [1] that contaminate food commodities worldwide, with developing countries being most affected [2]. Different fungal species produce different mycotoxins [3] which are named on the basis of the mould that produces them; for example, aflatoxins are produced by Aspergillus, whereas fumonisins are produced by Fusarium. More than 300 mycotoxins have been identified [4], but those of significant toxicological importance are aflatoxins, zearalenone, trichothecenes, fumonisins, and ochratoxins [5,6,7,8], as they possess carcinogenic and immunosuppressive properties and can also retard growth in both humans and animals, thereby affecting productivity [9].
Mycotoxins are very stable, and their contamination in agricultural commodities can be pre-harvest, during harvest, and post-harvest [7,10,11], resulting in the classification of the mycotoxin-producing fungi as field and storage fungi. Mycotoxin production is affected by several conditions which can be biological, chemical, and physiological [12]. However, some of these factors are beyond human control, especially ecological and environmental factors such as temperature, nutrient content of substrate, and relative humidity, which play important roles in toxin production. Most mycotoxins are produced in hot and humid climates, mainly the tropical countries [4], most of which are African countries [6].
Humans are exposed to mycotoxins through consumption of foods of plant origin that may be contaminated with toxins or as mycotoxin metabolites which are carried over into animal food products [4]. Ingestion of mycotoxins results in a disease known as mycotoxicosis in animals and humans [4,11,13]. The toxicity of mycotoxins on specific tissues and organs depends on the toxin involved, concentration of the toxin, and the age and nutritional status of the individual [3,13]. Some mycotoxins affect the nervous system, some cause liver and kidney damage, and others even cause vomiting in some animal species, with clinical implications ranging from chronic disease to death.
Biodiversity of mycotoxin-producing fungi in the environment results in a wide range of mycotoxins being present in some agricultural commodities, known as multitoxin occurrence [14], with moulds being capable of producing multiple mycotoxins [4]. Multitoxin contamination of food commodities results in more severe effects when compared to single toxin contamination due to synergism [15]. This review focused on research that has been done in Zimbabwe on mycotoxins from their discovery to date.

2. Methods

The review was done under Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines [16] in order to gather information on mycotoxin contamination of foods and feeds in Zimbabwe. Key words/phrases used to access information were: mycotoxin, aflatoxin, food, stock feed, feed ration, cereal grains, oil seeds, legumes, legislation, analysis, tolerance limits, maize, sorghum, mealie-meal, groundnuts, silage, milk, livestock, poultry, cattle, Aspergillus, Zimbabwe, and sub-Saharan Africa. Papers with relevant information were downloaded and analysed. A total of 81 papers were identified and 31 of these had information relevant to the review.

3. Occurrence of Toxigenic Fungi in Foods and Feeds in Zimbabwe

Little information is available on the typical range of mycotoxins in foods that are mainly consumed in Zimbabwe [1,17]. However, considerable work on mycotoxins has been done in Zimbabwe. Research has revealed the presence of mycotoxin-producing moulds on maize, the staple food of Zimbabwe which constitutes about 70% of the diet, and other cereal crops such as wheat, finger millet, millet, and sorghum [6,17,18,19,20,21,22,23]. The most common genera that were isolated are Aspergillus and Fusarium [22,23], which are known to produce mycotoxins of concern to animal and human health, namely aflatoxins, zearalenone, trichothecenes, fumonisins, and ochratoxins [24]. Colonisation of the grains by the moulds is mainly due to infection of the cobs in the field by insects such as the maize stalk borer (Busseola fusca), inadequate drying of crops, as well as the primitive methods used during the shelling of maize and other grains [1,19,25].
Other researchers have worked on groundnuts, beans, cowpeas, and Bambara nuts, where they also isolated Aspergillus and Fusarium [21,26,27]; whereas in another study [2], Aspergillus flavus (A. flavus) and Aspergillus parasiticus (A. parasiticus) were isolated from peanut butter samples from Zimbabwe and Botswana. This suggests that the temperature of 160 °C used for roasting in commercial peanut butter production [28] is not high enough to destroy the vegetative cells and spores, not to mention the temperatures used in homemade peanut butter, which are not even monitored [2]. This increases the chances of continual aflatoxin production in the peanut butter during storage.
A 120-day storage trial carried out by Titterton [29] to assess the effects of different storage conditions on the nutritional value of maize and sorghum stovers showed a positive effect of storage on the nutritional values. In addition, several potential mycotoxin-producing moulds belonging to the genera Fusarium, Phoma, Altenaria, Penicilium, and Aspergillus were also isolated from the stovers [30]. Aspergillus and Penicillium species were detected in both freshly harvested and stored samples. During the dry season, farmers face the challenge of feed shortage [29], hence the use of supplements such as plant stovers. The presence of mycotoxigenic fungi in the stovers is of concern as this may expose the livestock to mycotoxin poisoning and can also be carried over into foods of animal origin, followed by subsequent transfer along the food chain to humans, causing harm [31].

4. Aflatoxins

A lot of attention has been given to aflatoxins due to their effect on animal and human health [7], which ranges from gastroenteritis to cancers in acute and chronic aflatoxicosis, respectively. Aflatoxins are produced by moulds belonging to the genus Aspergillus, dominated by A flavus, A parasiticus, and A nomius. There are four naturally occurring aflatoxins in food and feed, namely aflatoxin (AF) B1, B2, G1, and G2, depending on the fluorescence colour under ultraviolet light at 365 nm [32,33,34]. AFB1 is the most toxic of them all and is produced by almost all aflatoxigenic Aspergillus species, whereas there are some species that cannot produce the G series, such as A flavus (produces B1 and B2 only) [35,36,37,38]. When consumed, aflatoxins cause liver cancer and stunted growth as well as suppressing immunity. In the body, aflatoxins are biotransformed predominantly in the liver, and the by-products or metabolites are eventually excreted mainly through renal flux [39]. When lactating cows and other mammals ingest aflatoxins in contaminated feed, toxic metabolites can be formed and found in milk due to the biotransformation of AFB1 and AFB2 by the hepatic microsomal mixed-function oxidase system to a hydroxylated metabolite known as “milk toxin” or aflatoxin M1 (AFM1) and AFM2, respectively, which is excreted in the milk and urine [40]. It has been shown that AFM1 retains some carcinogenicity, thus exposing humans to chronic toxicity, and thus making milk a source of aflatoxin contamination in humans [41].

5. Aflatoxins in Food and Feed

Research on aflatoxins in Zimbabwe was initiated by disease outbreaks on farms, particularly in poultry. One such particular incident was the death of 70 ostriches on a farm. Analysis of the feed showed contamination by aflatoxin of 11 µg/kg. Samples from other feed batches were also tested and gave results as high as 129 µg/kg. However, no action was taken as there are no limits for ostrich feed [42]. The presence of determinants of aflatoxin exposure in the Zimbabwean population has been used as indicators of the people’s exposure to aflatoxin poisoning [43]. This has been revealed by the presence of AFM1 in urine and breast milk of the rural populations [43,44,45].
Analysis of some food commodities and their products showed the presence of aflatoxins [2,27,28]. Foods that have been analysed include maize, groundnuts, peanut butter, beans, Bambara nuts, and cowpeas, among others, as shown in Table 1. Probst et al. [46] analysed maize samples from African countries including Zimbabwe, and all the samples tested positive for aflatoxin contamination, ranging from 9–123 µg/kg, which is above the Codex Alimentarius Commission permissible limit of 5 µg/kg for maize intended for human consumption [47]. Siwela [48] also analysed maize and maize meal samples intended for human consumption, and 35% of the samples were above the Zimbabwean 20 µg/kg limit, with one sample having a concentration of 1391 µg/kg.
The presence of both Aspergillus and aflatoxins in peanut butter is of great concern as it is considered a highly nutritious food recommended for infants [53]. Infants are more susceptible to the effects of mycotoxins [54]. Aflatoxin presence in the peanut butter could be attributed to their high melting points, which range from 237 °C to 289 °C [55]. The temperatures used during peanut roasting are not high enough to destroy them, hence their presence in the final product. This was shown by the presence of aflatoxins in peanut butter at levels that were above the 4 µg/kg European Union (EU) limit and some above the Zimbabwean legislation of 15 µg/kg for total aflatoxin [2,48,56].
All four major aflatoxins were detected in groundnuts, Bambara nuts, beans, and cowpeas in research done by Maringe and others [27]. Groundnuts and other legumes are important protein supplements in animal feeds [57,58,59] as well as the human population [48]. Traces of aflatoxins may remain in the seedcake, which is usually used as feed [42]. Therefore, it is of paramount importance to assess the levels of aflatoxin contamination of these seeds so as to avoid or reduce carryover into foods of animal origin such as milk, eggs, and meat, among others.
There is only one published study with regards to aflatoxin contamination of milk (AFM1) in Zimbabwe, carried out by Choga et al. [50]. Milk and dairy products, as important constituents in the human diet, may be the major way for entrance of aflatoxins into humans if not monitored [60]. Crop residues have been used as alternative animal feeds [61], and research has indicated the presence of aflatoxigenic moulds with potential to produce mycotoxins which can be carried over into foods of animal origin such as milk. Findings by Morton and coworkers [52] on the effects of post-harvest practices on the production and nutritive value of maize residues in Zimbabwe indicated the presence of AFB1 in the maize stovers used to feed dairy cows in the Silozwi Communal Area area south of Bulawayo, although the concentrations were low. Milk is consumed mainly by infants, especially during the weaning period, thus the growth of infants and young children could be impaired by the presence of AFM1 in milk [43]. Nevertheless, there are no reports on mycotoxin contamination of milk products.

6. Fusarium Mycotoxins

The major mycotoxins produced by Fusarium species are trichothecenes, zearalenone (ZEA), and fumonisins [8,62], and can cause several acute and chronic mycotoxicosis in humans [63]. Fusarium species are classified under field fungi as they tend to contaminate food crops before harvest [64,65].
Fumonisins are toxic compounds produced predominantly by F. verticillioides, previously known as F moniliforme and F. proliferatum, and other toxigenic Fusarium species [17,21,64]. They have been associated with oesophageal cancer in South Africa [66]. Fumonisin B1 (FB1), the most toxic of the fumonisins, has been shown to interfere with folate uptake, resulting in congenital disorders in human babies such as neural tube defects [4].
Work done on Fusarium mycotoxins on Zimbabwean foods is shown in Table 2. Other researchers [17] reported on fumonisin contamination on all the 388 samples of maize grain collected from households in Shamva and Makoni rural areas. Even though the concentrations were below the 1000 µg/kg European Community (EC) limit, there is still the risk of the development of chronic ailments such as cancer in these populations. Research by Mubatanhema and others [19] revealed coproduction of zearalenone, moniliformin, and fumonisin B1 by Fusarium isolates from maize samples collected from nine grain marketing board (GMB) centres in Zimbabwe. There has been limited research in Zimbabwe on other Fusarium toxins such as trichothecenes and zearalenone, which has also been the case with other countries [8]. Multitoxin production by mycotoxigenic fungi in Zimbabwean food samples was also demonstrated by Gehesquière and collegues [20] and Murashiki and coworkers [17]. Fumonisins were also shown to be the prevalent mycotoxin in the maize stovers used as feed during the dry season [52].

7. Mycotoxin Analysis

Mycotoxin poisoning can occur even after consumption of very small quantities of the toxin, therefore there is a need to use sensitive methods for their analysis and quantification [69,70]. The most common methods for mycotoxin analysis are chromatographic, such as thin-layer chromatography (TLC), high-performance liquid chromatography (HPLC), and immunoassays (radioimmunoassays, RDIs, and enzyme immunoassays, EIAs) [69]. Chromatographic methods combined with mass spectrometry have also been recently used in the detection and quantification of mycotoxins [71], and are capable of multitoxin detection [69,72] and even that of masked mycotoxins. Analysis of food and feed matrices from Zimbabwe has been carried out using some of these methods as shown in Table 3.

8. Legislation

Many countries are recognising the importance of aflatoxins and have generated regulations governing permissible concentrations of aflatoxins in food depending on the intended use of the particular food involved. These limits are, however, guided by the food regulating bodies such as the Food and Agriculture Organization (FAO), World Health Organization (WHO), and EU. The limits for individual countries range from 4–20 µg/kg [7] for foods intended for human consumption; whereas for milk and milk products, the range is 0.05–1.0 µg/kg. The strictest standards are those for the EU, which are 2 µg/kg for AFB1 for human consumption and 5 µg/kg for lactating cows’ feed, 4 µg/kg for total aflatoxin, and 0.05 µg/kg for AFM1. There are no regulatory limits set for mycotoxin level in food and feed in Zimbabwe, except for aflatoxins [74], which are not even considered when farmers come to deliver their produce as well as when food producers buy the raw materials [64]. This is the same for most developing countries in Southern Africa, mainly due to the shortage of resources for mycotoxin testing making it difficult to enforce laws on mycotoxin regulation [7]. Zimbabwe initially adopted the 5–25 µg/kg limit for AFB1 in food intended for human consumption in 1971; however, it was revised in 1990 to 20 µg/kg [42]. Politics and economic crisis have made it tough to come up with an up-to-date and effective food control system [75]. When the GMB was responsible for handling agricultural commodities, it was easy to control the movement of produces. No grain would be released before being tested for aflatoxins, either for export or local consumption. However, with the liberalisation and indigenisation of the economy, farmers and manufacturers trade without government interference [42]. This has made the country the only one in the region with a twofold system of food standards, including the voluntary one and the controlled one [76]; one where the processor makes a choice on whether they want the raw commodity tested for contaminants or not, and one where the analysis of produce is mandatory. Zimbabwe has been affected by droughts which caused food shortages, and coupled with economic hardships, its citizens now worry about having food on the table, without being concerned too much about quality. In the case of livestock poisoning, there are no rules regarding aflatoxin limits in feed, and this has seen these cases settled out of court between the feed manufacturer and the farmer [42].

9. Discussion

This review has shown that the Zimbabwean population and livestock are exposed to a wide range of mycotoxins, as evidenced by multitoxin occurrence in some of the foods and feeds [19,20,52], which exposes the populations to more severe toxicity and immune suppression as compared to single mycotoxin contamination [63]. Work done by Siwela [48] showed that the aflatoxin contamination in 69% of the samples were within the limit of 20 µg/kg, with the remaining 31% above the limit. These results concur with those that were reported in Kenya, where 96% of the groundnut samples were contaminated with <4 µg/kg of AFB1, while 4% were above the national regulatory limit of 20 µg/kg [77]. Although most of the samples are within the limits, the population is still at risk of chronic aflatoxicosis, which could lead to cancer development later in life and immunosuppression, as well as stunted growth in children and animals [78]. However, a study in the Democratic Republic of Congo showed that a greater percentage of the groundnut samples analysed (70%) had aflatoxin contamination of ˃5 µg/kg [79]. Foods such as groundnuts and legumes are used as alternative protein sources [53] and their contamination by aflatoxins is of great concern, especially to children and vegetarians. Research on maize showed that the most common mycotoxins are aflatoxins and fumonisin B1 [67], as the maize crop is known to be susceptible to fumonisin B-producing moulds. The EU maximum limit for fumonisins in food intended for human consumption is 1000 µg/kg [80], and most of the samples that were analysed had figures above this limit (Table 2). Gehesquière and others [20] showed that the levels of mycotoxins increase mainly during storage compared to pre-harvest. This was supported by Mubatanhema and coworkers [19], who attributed mould infection of maize as being a result of primitive methods used when shelling the grain which damage the kernels, paving the way for fungal infection. Therefore, there is need for the use of storage facilities that result in minimal growth of mycotoxigenic species. However, for groundnuts, contamination was mainly before harvest, with no significant change during storage [28]. Very little relevant research has been done on milk, even though it is an important component of the diet, especially used for weaning of children. The limited information on contamination levels of AFM1 in milk and milk products means that the country is still very far from dealing with stunted growth in children, as mycotoxins have been associated with growth suppression [43,54,81].
The bulk of the research on mycotoxins in Zimbabwe was conducted between 1980 and the early 1990s, and most of the samples analysed were taken from the GMB. This might not have given a true reflection on the extent of food contamination, as farmers have a tendency of sending the best produce to the GMB so that they can earn more money, whereas what would remain for their consumption will be of compromised quality. The majority of research done after 2000 has been conducted outside the country, due to limited funds and equipment making it difficult for the authorities involved in policy formulation to access this information. Also, most journals with high impact factors would not publish research done in most developing countries, as they lag behind in technological advancement in terms of analytical methods. In addition, most researchers from developing countries cannot afford the exorbitant publication fees charged by most journals. This means that most of the research findings remain unpublished or get published after several years.

10. Conclusions

Most of the work done in Zimbabwe has been focused on Aspergillus and Fusarium mycotoxins and has shown the presence of these mycotoxins in foods and feeds. Therefore, there is a need to come up with strategies that will help reduce and manage levels of the mycotoxins in foods. Zimbabwe does not have legislation on the maximum levels of mycotoxins, but adopts European legislation [20]. This is a cause of concern, especially with regards to maize as it is used as an animal feed in Europe, whereas in Zimbabwe it is the staple food. Zimbabwe should come up with its own standards which cater for the nation’s own diet. For legumes, there are no limits on the level of mycotoxins, making it difficult to enforce law [27]. There is also a need for researchers to share their findings with the general population. A study by Loreen and Moses [82] revealed that most of the people of Dora village in Mutare did not know anything about aflatoxins, except for the agricultural extension officers, meaning that these officers are not passing on information to the farmers. Research has also indicated that mycotoxin contamination of smaller grains is lower compared to that of the large grains, with some having no mycotoxins at all [21,22,23], so growing smaller grains could be one of the options in trying to reduce the mycotoxin burden; a replacing grains that are highly susceptible to mycotoxin contamination (such as maize) with grains that are less susceptible (such as sorghum or finger millet) could be another option. This will in turn reduce the rate of exposure of consumers to mycotoxins in their diet, especially for children. Improvement on the methods of harvest as well as sorting of the grains before storage will also help in reducing and managing mycotoxins in the granaries [20]. Dehulling, although not nutritionally recommended [83], has been proven as one of the ways of reducing mycotoxin contamination in grains [73,84].

Author Contributions

M.M. premeditated the idea. N.N. gathered information, analysed data and wrote the paper. M.C.A. reviewed and edited the paper.

Acknowledgments

This work was supported by funds from National Research Foundation (NRF) Grant number 105882 and the Research Board, NUST (Grant number RB No. 43/16).

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Misihairabgwi, J.; Ezekiel, C.; Sulyok, M.; Shephard, G.; Krska, R. Mycotoxin contamination of foods in Southern Africa: A 10-year review (2007–2016). Crit. Rev. Food Sci. Nutr. 2017, 1–16. [Google Scholar] [CrossRef] [PubMed]
  2. Mupunga, I.; Lebelo, S.L.; Mngqawa, P.; Rheeder, J.; Katerere, D. Natural occurrence of aflatoxins in peanuts and peanut butter from Bulawayo, Zimbabwe. J. Food Prot. 2014, 77, 1814–1818. [Google Scholar] [CrossRef] [PubMed]
  3. Datsugwai, M.S.S.; Ezekiel, B.; Audu, Y.; Legbo, M.I.; Azeh, Y.; Gogo, M.R. Mycotoxins: Toxigenic fungal compounds—A review. ARPN J. Sci. Technol. 2013, 3, 687–692. [Google Scholar]
  4. Zain, M.E. Impact of mycotoxins on humans and animals. J. Saudi Chem. Soc. 2011, 15, 129–144. [Google Scholar] [CrossRef]
  5. Guchi, E. Implication of aflatoxin contamination in agricultural products. Am. J. Food Nutr. 2015, 3, 12–20. [Google Scholar]
  6. Darwish, W.S.; Ikenaka, Y.; Nakayama, S.M.; Ishizuka, M. An overview on mycotoxin contamination of foods in Africa. J. Vet. Med. Sci. 2014, 76, 789–797. [Google Scholar] [CrossRef] [PubMed]
  7. Udomkun, P.; Wiredu, A.N.; Nagle, M.; Bandyopadhyay, R.; Müller, J.; Vanlauwe, B. Mycotoxins in sub-Saharan Africa: Present situation, socio-economic impact, awareness, and outlook. Food Control 2017, 72, 110–122. [Google Scholar] [CrossRef]
  8. Wagacha, J.M.; Muthomi, J.W. Mycotoxin problem in Africa: Current status, implications to food safety and health and possible management strategies. Int. J. Food Microbiol. 2008, 124, 1–12. [Google Scholar] [CrossRef] [PubMed]
  9. Wild, C.P.; Gong, Y.Y. Mycotoxins and human disease: A largely ignored global health issue. Carcinogenesis 2009, 31, 71–82. [Google Scholar] [CrossRef] [PubMed]
  10. Songsermsakul, P. Mycotoxins contamination of food in Thailand (2000–2010): Food safety concerns for the world food exporter. Int. Food Res. J. 2015, 22, 426–434. [Google Scholar]
  11. Gallo, A.; Giuberti, G.; Frisvad, J.C.; Bertuzzi, T.; Nielsen, K.F. Review on mycotoxin issues in ruminants: Occurrence in forages, effects of mycotoxin ingestion on health status and animal performance and practical strategies to counteract their negative effects. Toxins 2015, 7, 3057–3111. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Afsah-Hejri, L.; Jinap, S.; Hajeb, P.; Radu, S.; Shakibazadeh, S. A review on mycotoxins in food and feed: Malaysia case study. Compr. Rev. Food Sci. Food Saf. 2013, 12, 629–651. [Google Scholar] [CrossRef]
  13. Pessu, P.; Agoda, S.; Isong, I.; Adekalu, O.; Echendu, M.; Falade, T. Fungi and mycotoxins in stored foods. Afr. J. Microbiol. Res. 2011, 5, 4373–4382. [Google Scholar]
  14. Mansfield, M.; Kuldau, G. Microbiological and molecular determination of mycobiota in fresh and ensiled maize silage. Mycologia 2007, 99, 269–278. [Google Scholar] [CrossRef] [PubMed]
  15. Zaki, M.M.; El-Midany, S.; Shaheen, H.; Rizzi, L. Mycotoxins in animals: Occurrence, effects, prevention and management. J. Toxicol. Environ. Health Sci. 2012, 4, 13–28. [Google Scholar] [CrossRef]
  16. Hutton, B.; Salanti, G.; Caldwell, D.M.; Chaimani, A.; Schmid, C.H.; Cameron, C.; Ioannidis, J.P.; Straus, S.; Thorlund, K.; Jansen, J.P. The prisma extension statement for reporting of systematic reviews incorporating network meta-analyses of health care interventions: Checklist and explanations. Ann. Intern. Med. 2015, 162, 777–784. [Google Scholar] [CrossRef] [PubMed]
  17. Murashiki, T.C.; Chidewe, C.; Benhura, M.A.; Maringe, D.T.; Dembedza, M.P.; Manema, L.R.; Mvumi, B.M.; Nyanga, L.K. Levels and daily intake estimates of aflatoxin B1 and fumonisin B1 in maize consumed by rural households in Shamva and Makoni districts of Zimbabwe. Food Control 2017, 72, 105–109. [Google Scholar] [CrossRef]
  18. Dangwa, N.; Mwenje, E.; Dhlamini, Z.; Siwela, A. Molecular characterization of aflatoxigenic Aspergillus species in dried traditional foods in Zimbabwe. Adv. Biores. 2014, 5, 29–36. [Google Scholar]
  19. Mubatanhema, W.; Moss, M.O.; Frank, M.J.; Wilson, D.M. Prevalence of Fusarium species of the liseola section on Zimbabwean corn and their ability to produce the mycotoxins zearalenone, moniliformin and fumonisin B1. Mycopathologia 1999, 148, 157–163. [Google Scholar] [CrossRef] [PubMed]
  20. Gehesquière, S.; De Saeger, P.D.; Hove, M.; Haesaert, G. The Effect of Time on Mycotoxins in Subsistence Farmed Maize from Zimbabwe. Master’s Thesis, Ghent University, Ghent, Belgium, 16 August 2016. [Google Scholar]
  21. Gamanya, R.; Sibanda, L. Survey of Fusarium moniliforme (F. verticillioides) and production of fumonisin B1 in cereal grains and oilseeds in Zimbabwe. Int. J. Food Microbiol. 2001, 71, 145–149. [Google Scholar] [CrossRef]
  22. Onyike, N.B.; Nelson, P.E. Fusarium species associated with sorghum grain from Nigeria, Lesotho, and Zimbabwe. Mycologia 1992, 84, 452–458. [Google Scholar] [CrossRef]
  23. Onyike, N.B.; Nelson, P.E.; Marasas, W. Fusarium species associated with millet grain from Nigeria, Lesotho, and Zimbabwe. Mycologia 1991, 83, 708–712. [Google Scholar] [CrossRef]
  24. Ibáñez-Vea, M.; González-Peñas, E.; Lizarraga, E.; De Cerain, A.L. Co-occurrence of aflatoxins, ochratoxin a and zearalenone in barley from a northern region of Spain. Food Chem. 2012, 132, 35–42. [Google Scholar] [CrossRef] [PubMed]
  25. Nleya, N.; Nyararai, Y.; Mawanza, M.; Mlalazi, F. Colonization of stem borer damaged maize plants by aflatoxigenic Aspergillus species in Zimbabwe. Trop. Plant Res. 2017, 4, 109–114. [Google Scholar] [CrossRef]
  26. Dube, M.; Maphosa, M. Prevalence of aflatoxigenic Aspergillus spp and groundnut resistance in Zimbabwe. IOSR J. Agric. Vet. Sci. 2014, 7, 8–12. [Google Scholar] [CrossRef]
  27. Maringe, D.T.; Chidewe, C.; Benhura, M.A.; Mvumi, B.M.; Murashiki, T.C.; Dembedza, M.P.; Siziba, L.; Nyanga, L.K. Natural postharvest aflatoxin occurrence in food legumes in the smallholder farming sector of Zimbabwe. Food Add. Contam. Part B 2017, 10, 21–26. [Google Scholar] [CrossRef] [PubMed]
  28. Siwela, A.H.; Caley, A. Aflatoxin contamination of stored groundnuts in Zimbabwe. In International Proceedings of the International Crops Research Institute Workshop, 6–9 Octomber 1987, ICRISAT for the Semi-Arid Tropics); ICRISAT Center: Patancheru, India, 1989. [Google Scholar]
  29. Titterton, M. Forage Production and Conservation for Dry Season Feeding of Dairy Cattle in the Semi-Arid Region of Zimbabwe: A Review and Report on Recent Work for a DFID Project; Department for International Development: London, UK, 2001.
  30. Panigrahi, S. Final Technical Report: The Effects of Storage of Fibrous Feeds on Ruminant Livestock in Developing Countries; Natural Resources Institute (NRI): Warwickshire, UK, 1996; p. 50. [Google Scholar]
  31. Atherstone, C.; Grace, D.; Lindahl, J.; Kang’ethe, E.; Nelson, F. Assessing the impact of aflatoxin consumption on animal health and productivity. Afr. J. Food Agric. Nutr. Dev. 2016, 16, 10949–10966. [Google Scholar] [CrossRef]
  32. Baranyi, N.; Kocsubé, S.; Vágvölgyi, C.; Varga, J. Current trends in aflatoxin research. Acta Biol. Szeged. 2013, 57, 95–107. [Google Scholar]
  33. Arapcheska, M.; Jovanovska, V.; Jankuloski, Z.; Musliu, Z.; Uzunov, R. Impact of aflatoxins on animal and human health. Int. J. Innov. Sci. Eng. Technol. 2015, 2, 156–161. [Google Scholar]
  34. Reid, C.X.; Sparks, D.L.; Williams, W.P.; Brown, A.E. Single corn kernel aflatoxin b1 extraction and analysis method. Nat. Res. 2016, 7, 405. [Google Scholar]
  35. Donner, M.; Lichtemberg, P.S.; Doster, M.; Picot, A.; Cotty, P.J.; Puckett, R.D.; Michailides, T.J. Community structure of Aspergillus flavus and A. parasiticus in major almond-producing areas of California, United States. Plant Dis. 2015, 99, 1161–1169. [Google Scholar] [CrossRef]
  36. Yu, J.; Fedorova, N.D.; Montalbano, B.G.; Bhatnagar, D.; Cleveland, T.E.; Bennett, J.W.; Nierman, W.C. Tight control of mycotoxin biosynthesis gene expression in Aspergillus flavus by temperature as revealed by RNA-seq. FEMS Microbiol. Lett. 2011, 322, 145–149. [Google Scholar] [CrossRef] [PubMed]
  37. Dhanasekaran, D.; Shanmugapriya, S.; Thajuddin, N.; Panneerselvam, A. Aflatoxins and aflatoxicosis in human and animals. In Aflatoxins-Biochemistry and Molecular Biology; InTech: Houston, TX, USA, 2011; pp. 221–254. [Google Scholar]
  38. Abdel-Hadi, A.; Schmidt-Heydt, M.; Parra, R.; Geisen, R.; Magan, N. A systems approach to model the relationship between aflatoxin gene cluster expression, environmental factors, growth and toxin production by Aspergillus flavus. J. R. Soc. Interface 2011. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  39. Bbosa, G.S.; Kitya, D.; Odda, J.; Ogwal-Okeng, J. Aflatoxins metabolism, effects on epigenetic mechanisms and their role in carcinogenesis. Health 2013, 5, 14. [Google Scholar] [CrossRef]
  40. Jawaid, S.; Talpur, F.N.; Nizamani, S.M.; Afridi, H.I. Contamination profile of aflatoxin m1 residues in milk supply chain of Sindh. Toxicol. Rep. 2015, 2, 1418–1422. [Google Scholar] [CrossRef] [PubMed]
  41. Mohammadi, H. A review of aflatoxin m1, milk, and milk products. In Aflatoxins-Biochemistry and Molecular Biology; InTech: Houston, TX, USA, 2011; pp. 397–414. [Google Scholar]
  42. Siwela, A.H.; Nziramasanga, N. Regulatory aspects of aflatoxin control in Zimbabwe—A review. J. Appl. Sci. South. Afr. 1999, 5, 141–147. [Google Scholar] [CrossRef]
  43. Smith, L.E.; Mbuya, M.N.; Prendergast, A.J.; Turner, P.C.; Ruboko, S.; Humphrey, J.H.; Nelson, R.J.; Chigumira, A.; Kembo, G.; Stoltzfus, R.J. Determinants of recent aflatoxin exposure among pregnant women in rural Zimbabwe. Mol. Nutr. Food Res. 2017, 61. [Google Scholar] [CrossRef] [PubMed]
  44. Nyathi, C.B.; Mutiro, C.F.; Hasler, J.A.; Chetsanga, C.J. A survey of urinary aflatoxin in Zimbabwe. Int. J. Epidemiol. 1987, 16, 516–519. [Google Scholar] [CrossRef] [PubMed]
  45. Wild, C.P.; Pionneau, F.A.; Montesano, R.; Mutiro, C.F.; Chetsanga, C.J. Aflatoxin detected in human breast milk by immunoassay. Int. J. Cancer 1987, 40, 328–333. [Google Scholar] [CrossRef] [PubMed]
  46. Probst, C.; Bandyopadhyay, R.; Cotty, P. Diversity of aflatoxin-producing fungi and their impact on food safety in sub-Saharan Africa. Int. J. Food Microbiol. 2014, 174, 113–122. [Google Scholar] [CrossRef] [PubMed]
  47. Matsiko, F.; Kanyange, C.; Ingabire, G.; Dusingizimana, T.; Vasanthakaalam, H.; Kimonyo, A. Detection and quantification of aflatoxin in cassava and maize flour sold in Kigali open markets, Rwanda. Int. Food Res. J. 2017, 24, 459–464. [Google Scholar]
  48. Siwela, A.H. Combined use of phenyl-bonded phase clean-up and hplc for the determination of aflatoxins. Trop. Sci. 1996, 36, 197–200. [Google Scholar]
  49. Musundire, R.; Osuga, I.M.; Cheseto, X.; Irungu, J.; Torto, B. Aflatoxin contamination detected in nutrient and anti-oxidant rich edible stink bug stored in recycled grain containers. PLoS ONE 2016, 11, e0145914. [Google Scholar] [CrossRef] [PubMed]
  50. Choga, R.J.S.O.; Chiriseri, B.; Pfukenyi, D.M. Detection and levels of aflatoxin m₁ in raw milk of dairy cows from selected small scale and commercial farms in harare, Zimbabwe. Zimb. Vet. J. 2016, 34, 1–6. [Google Scholar]
  51. Hove, M.; De Boevre, M.; Lachat, C.; Jacxsens, L.; Nyanga, L.; De Saeger, S. Occurrence and risk assessment of mycotoxins in subsistence farmed maize from Zimbabwe. Food Control 2016, 69, 36–44. [Google Scholar] [CrossRef]
  52. Morton, J.; Wood, C.; Ncube, S.; Coker, R.; Nyoni, N.; Thomas, D.; Nagler, M. Effects of Post-Harvest Practices on the Production and Nutritive Value of Maize Residues in Zimbabwe; Final Technical Report; Annexes: Herndon, VA, USA, 2000. [Google Scholar]
  53. Mupunga, I.; Mngqawa, P.; Katerere, D.R. Peanuts, aflatoxins and undernutrition in children in sub-Saharan Africa. Nutrients 2017, 9, 1287. [Google Scholar] [CrossRef] [PubMed]
  54. Ghiasian, S.; Maghsood, A. Infants’ exposure to aflatoxin M1 from mother’s breast milk in Iran. Iran. J. Public Health 2012, 41, 119. [Google Scholar] [PubMed]
  55. Siwela, A.H.; Mukaro, K.J.; Nziramasanga, N. Aflatoxin carryover during large scale peanut butter production. Food Nutr. Sci. 2011, 2, 103–108. [Google Scholar] [CrossRef]
  56. Njoroge, S.M.; Matumba, L.; Kanenga, K.; Siambi, M.; Waliyar, F.; Maruwo, J.; Monyo, E.S. A case for regular aflatoxin monitoring in peanut butter in sub-Saharan Africa: Lessons from a 3-year survey in Zambia. J. Food Prot. 2016, 79, 795–800. [Google Scholar] [CrossRef] [PubMed]
  57. Ramin, M.; Höjer, A.; Hetta, M. The effects of legume seeds on the lactation performance of dairy cows fed grass silage-based diets. Agric. Food Sci. 2017, 26, 129–137. [Google Scholar] [CrossRef]
  58. Moog, F. Forage and legumes as protein supplements for pasture based systems. In Feeding Dairy Cows in the Tropics, Proceedings of the FAO Expert Consultation, Bangkok, Thailand, 7–11 July 1989; FAO: Rome, Italy, 1989. [Google Scholar]
  59. Batterham, E.; Egan, A. Utilization of food legumes as feed. In Food Legume Improvement for Asian Farming Systems; ACIAR: Canberra, Australia, 1986; pp. 193–200. [Google Scholar]
  60. Oluwafemi, F.; Lawal, S. Hygienic status of cow milk and wara from local Fulani herdsmen in two western states of Nigeria. Br. Microbiol. Res. J. 2015, 5, 389. [Google Scholar] [CrossRef]
  61. Tajkarimi, M.; Aliabadi-Sh, F.; Nejad, A.S.; Poursoltani, H.; Motallebi, A.; Mahdavi, H. Aflatoxin M1 contamination in winter and summer milk in 14 states in Iran. Food Control 2008, 19, 1033–1036. [Google Scholar] [CrossRef]
  62. D’mello, J.; Placinta, C.; Macdonald, A. Fusarium mycotoxins: A review of global implications for animal health, welfare and productivity. Anim. Feed Sci. Technol. 1999, 80, 183–205. [Google Scholar] [CrossRef]
  63. Antonissen, G.; Martel, A.; Pasmans, F.; Ducatelle, R.; Verbrugghe, E.; Vandenbroucke, V.; Li, S.; Haesebrouck, F.; Van Immerseel, F.; Croubels, S. The impact of Fusarium mycotoxins on human and animal host susceptibility to infectious diseases. Toxins 2014, 6, 430–452. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  64. Tembo, E. Mycotoxigenic Fungi Associated with Ear-Rots in Zimbabwe: Identification and Inheritance of Resistance in Southern and West African Maize Inbred Lines. Ph.D. Thesis, University of the Free State, Bloemfontein, South Africa, 2015. [Google Scholar]
  65. Chilaka, C.A.; De Boevre, M.; Atanda, O.O.; De Saeger, S. The status of Fusarium mycotoxins in sub-Saharan Africa: A review of emerging trends and post-harvest mitigation strategies towards food control. Toxins 2017, 9, 19. [Google Scholar] [CrossRef] [PubMed]
  66. Marasas, W. Discovery and occurrence of the fumonisins: A historical perspective. Environ. Health Perspect. 2001, 109, 239. [Google Scholar] [CrossRef] [PubMed]
  67. Hove, M.; Van Poucke, C.; Njumbe-Ediage, E.; Nyanga, L.; De Saeger, S. Review on the natural co-occurrence of afb1 and fb1 in maize and the combined toxicity of AFB1 and FB1. Food Control 2016, 59, 675–682. [Google Scholar] [CrossRef]
  68. Mupunga, I. A Comparative Study of Natural Contamination with Aflatoxins and Fumonisins in Selected Food Commodities from Botswana and Zimbabwe. Master’s Thesis, University of South Africa, Pretoria, South Africa, 2013. [Google Scholar]
  69. Rahmani, A.; Jinap, S.; Soleimany, F. Qualitative and quantitative analysis of mycotoxins. Compr. Rev. Food Sci. Food Saf. 2009, 8, 202–251. [Google Scholar] [CrossRef]
  70. Sinha, K.K. Testing methods for aflatoxins in foods. Food Nutr. Bull. 1999, 20, 458–464. [Google Scholar] [CrossRef]
  71. Wacoo, A.P.; Wendiro, D.; Vuzi, P.C.; Hawumba, J.F. Methods for detection of aflatoxins in agricultural food crops. J. Appl. Chem. 2014, 2014. [Google Scholar] [CrossRef]
  72. Roseanu, A.; Jecu, L.; Badea, M.; Evans, R.W. Mycotoxins: An overview on their quantification methods. Rom. J. Biochem. 2010, 47, 79–86. [Google Scholar]
  73. Siwela, A.H.; Siwela, M.; Matindi, G.; Dube, S.; Nziramasanga, N. Decontamination of aflatoxin-contaminated maize by dehulling. J. Sci. Food Agric. 2005, 85, 2535–2538. [Google Scholar] [CrossRef]
  74. Mazumder, P.M.; Sasmal, D. Mycotoxins-limits and regulations. Anc. Sci. Life 2001, 20, 1. [Google Scholar] [PubMed]
  75. Pswarayi, F.; Mutukumira, A.N.; Chipurura, B.; Gabi, B.; Jukes, D.J. Food control in Zimbabwe: A situational analysis. Food Control 2014, 46, 143–151. [Google Scholar] [CrossRef]
  76. Mutukumira, A.; Jukes, D.J. The Development of National Food Safety Control Systems in Sub-Saharan Africa-Issues and Opportunities. Available online: http://citeseerx.ist.psu.edu/viewdoc/download?doi=10.1.1.543.4408&rep=rep1&type=pdf (accessed on 14 April 2018).
  77. Mutegi, C.; Wagacha, M.; Kimani, J.; Otieno, G.; Wanyama, R.; Hell, K.; Christie, M.E. Incidence of aflatoxin in peanuts (Arachis hypogaea linnaeus) from markets in western, Nyanza and Nairobi provinces of Kenya and related market traits. J. Stored Prod. Res. 2013, 52, 118–127. [Google Scholar] [CrossRef]
  78. Ogodo, A.C.; Ugbogu, O.C. Public health significance of aflatoxin in food industry—A review. Eur. J. Clin. Biom. Sci. 2016, 2, 51–58. [Google Scholar]
  79. Kamika, I.; Takoy, L.L. Natural occurrence of aflatoxin B1 in peanut collected from Kinshasa, Democratic Republic of Congo. Food Control 2011, 22, 1760–1764. [Google Scholar] [CrossRef]
  80. Dall’Asta, C.; Galaverna, G.; Mangia, M.; Sforza, S.; Dossena, A.; Marchelli, R. Free and bound fumonisins in gluten-free food products. Mol. Nutr. Food Res. 2009, 53, 492–499. [Google Scholar] [CrossRef] [PubMed]
  81. Katerere, D.R.; Shephard, G.S.; Faber, M. Infant malnutrition and chronic aflatoxicosis in southern Africa: Is there a link? Int. J. Food Saf. Nutr. Public Health 2008, 1, 127–136. [Google Scholar] [CrossRef]
  82. Loreen, D.; Moses, M. Assessment of aflatoxin awareness by players in groundnut value chain: The case of Dora in Mutare, Zimbabwe. Int. J. Innov. Res. Dev. 2015, 4, 90–99. [Google Scholar]
  83. Ezeokeke, C.T.; Onuoha, A.B. Nutrient composition of cereal (maize), legume (soybean) and fruit (banana) as a complementary food for older infants and their sensory assessment. J. Food Sci. Eng 2016, 6, 139–148. [Google Scholar]
  84. Fandohan, P.; Ahouansou, R.; Houssou, P.; Hell, K.; Marasas, W.; Wingfield, M. Impact of mechanical shelling and dehulling on Fusarium infection and fumonisin contamination in maize. Food Add. Contam. 2006, 23, 415–421. [Google Scholar] [CrossRef] [PubMed]
Table
Table 1. Occurrence of aflatoxins in foods and feeds in Zimbabwe.
Table 1. Occurrence of aflatoxins in foods and feeds in Zimbabwe.
Food/FeedMycotoxinSample SourceConcentration Range (µg/kg)Analytical MethodReference
GroundnutTotal AFFood and feed companies˂1–394HPLC[48]
Peanut butterTotal AFFood and feed companies˂1–213HPLC
CowpeasTotal AFFood and feed companies˂1–20HPLC
MaizeTotal AFFood and feed companies˂1–1391HPLC
Stock feedTotal AFFood and feed companies˂1–30HPLC
CornstarchTotal AFFood and feed companies˂1HPLC
Beans Total AFFood and feed companies˂1–30HPLC
GroundnutsAFB1Grain marketing board˂5–250TLC[28]
AFG1Grain marketing board˂4–200TLC
GroundnutsTotal AFRetail shops and vendors6.6–622.1HPLC[2]
Peanut butterTotal AFRetail shops and vendors6.1–247HPLC
GroundnutsAFB1Makoni District0.7–108.3HPLC[27]
AFB1Shamva District3.1–175.9HPLC
AFB2Makoni District1.3–320HPLC
AFB2Shamva District1.3–320HPLC
AFG1Makoni District20.9–271.6HPLC
AFG1Shamva District20.9–271.6HPLC
AFG2Makoni District29.1–377.8HPLC
AFG2Shamva District29.1–377.8HPLC
Total AFMakoni District9.2–697.8HPLC
Total AFShamva District9.2–697.8HPLC
BeansTotal AFShamva District27.3HPLC[27]
Total AFMakoni District70.9HPLC
CowpeasTotal AFMakoni District1.4–103.4HPLC
Total AFShamva District2.3HPLC
Bambara nutsTotal AFMakoni District8.6–53.5HPLC
Stink bugsAFB1Bikita District0.5–0.59LC-QtoF-MS[49]
MilkAFM1Harare590–4510 *HPLC[50]
MaizeTotal AFZimbabwe˂1–123ELISA[46]
MaizeAFB1Zimbabwe˂1–11LC-MS/MS[51]
MaizeAFB1Shamva District0.65–26.65ELISA[17]
Makoni District0.57–9.22ELISA
MaizeAFG1Manicaland and Mashonaland Provincesnd–23.7HPLC [20]
Maize stoversAFB1Silozwi Communal Area0.8–1.6HPLC[52]
* Milk concentration is given in µg/L. HPLC: high-performance liquid chromatography; AF: aflatoxin; TLC: thin-layer chromatography; nd: not detected
Table
Table 2. Occurrence of Fusarium mycotoxins in foods and feeds in Zimbabwe.
Table 2. Occurrence of Fusarium mycotoxins in foods and feeds in Zimbabwe.
Food/FeedMycotoxinSample SourceConcentration Range (µg/kg)Analytical MethodReference
MaizeFumonisinsZimbabwe36,000–159,000ELISA[46]
DONnd–12,000ELISA
MaizeFB1Zimbabwend–1106LC-MS/MS[67]
DONnd–492LC-MS/MS
SorghumFumonisinsZimbabwe8–187HPLC[68]
MaizeFB1Shamva District108.35–337.14ELISA[17]
Makoni District15.65–579.6ELISA
Maize mealFB1Shamva District10.43–432.32ELISA
Makoni District13.84–606.64ELISA
Maize (preharvest)DONMainacland and Mashonaland West Provincesnd–220.6HPLC[20]
ZEAnd–44.6HPLC
FB1nd–3865.99HPLC
FB2nd–819.01HPLC
FB3nd–472.20HPLC
Maize (at harvest)DONMainacland and Mashonaland West Provincesnd–184HPLC
ZEAnd–16.3HPLC
FB1nd–3866HPLC
FB2nd–431HPLC
FB3nd–472 HPLC
Maize (3 months in storage)DONMainacland and Mashonaland West Provincesnd–147HPLC[20]
ZEAnd–30.8HPLC
FB1nd–2842HPLC
FB2nd–819HPLC
FB3nd–275HPLC
Maize (6 months in storage)DONMainacland and Mashonaland West Provincesnd–115HPLC
ZEAnd–44.6HPLC
FB1nd–2709HPLC
FB2nd–424HPLC
FB3nd–121HPLC
Maize stovers (beginning of storage)FB1Silozwi Communal Area109–752HPLC[52]
ZEAnd–73
Maize stovers (end of storage, i.e., 4 months later)FB1Silozwi Communal Areand–38HPLC
ZEA: zearalenone; DON: deoxynivalenol; nd: not detected
Table
Table 3. Mycotoxin analysis and quantification methods.
Table 3. Mycotoxin analysis and quantification methods.
SampleMycotoxinAnalytical MethodReferences
GroundnutsTotal AflatoxinTLC[28]
HPLC[27]
MaizeFumonisinsHPLC[21,73]
AFB1HPLC[20]
AFB2LC-MS/MS
AFG1LC-MS/MS
AFG2LC-MS/MS
FB1LC-MS/MS
FB2LC-MS/MS
FB3LC-MS/MS
ZEALC-MS/MS
DONLC-MS/MS
OTALC-MS/MS[17]
AFB1HPLC
FB1ELISA
UrineAFM1ELISA[43]
TLC, HPLC[44]
Peanut butterTotal aflatoxinHPLC[55]
BeansTotal Aflatoxin HPLC[27]
CowpeasTotal AflatoxinHPLC
Bambara nutsTotal AflatoxinHPLC
MilkAFM1HPLC[50]
OTA: Ochratoxin A.

Share and Cite

MDPI and ACS Style

Nleya, N.; Adetunji, M.C.; Mwanza, M. Current Status of Mycotoxin Contamination of Food Commodities in Zimbabwe. Toxins 2018, 10, 89. https://doi.org/10.3390/toxins10050089

AMA Style

Nleya N, Adetunji MC, Mwanza M. Current Status of Mycotoxin Contamination of Food Commodities in Zimbabwe. Toxins. 2018; 10(5):89. https://doi.org/10.3390/toxins10050089

Chicago/Turabian Style

Nleya, Nancy, Modupeade Christianah Adetunji, and Mulunda Mwanza. 2018. "Current Status of Mycotoxin Contamination of Food Commodities in Zimbabwe" Toxins 10, no. 5: 89. https://doi.org/10.3390/toxins10050089

APA Style

Nleya, N., Adetunji, M. C., & Mwanza, M. (2018). Current Status of Mycotoxin Contamination of Food Commodities in Zimbabwe. Toxins, 10(5), 89. https://doi.org/10.3390/toxins10050089

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