Review Article

Precision Agriculture Science and Technology. 30 September 2025. 200-215
https://doi.org/10.22765/pastj.20250015

ABSTRACT


MAIN

  • Introduction

  •   Effects of mycotoxins

  •   Aflatoxins

  •   Fumonisins

  •   Ochratoxins (OTA)

  •   Pre-Harvest Interventions

  •   Resistant varieties

  •   Biocontrol

  •   Good agricultural practices (GAP)

  •   Analytical approach to mycotoxins

  • Conclusion

Introduction

Mycotoxins are the toxic secondary metabolites produced by certain fungi that can contaminate food and feed, posing health risks to humans and animals. These mycotoxins are produced by toxigenic mold and cause potent effects on human health and economic development (Petrović et al., 2023). An estimated 25% of the world’s food crops are believed to be contaminated by mycotoxins, which cause significant losses in trade and agricultural productivity (Alshannaq and Yu, 2017; Pandey et al., 2023).

Occasionally, several mycotoxins appear simultaneously, raising the risk for users (Awuchi et al., 2021). The three genera Aspergillus, Fusarium, and Penicillium are home to the most prevalent mycotoxin-producing fungi (Ismaiel and Papenbrock, 2015) (Fig. 1). Aspergillus produces aflatoxins (AFs), especially B1 and B2, which cause significant economic losses in agriculture and healthcare, and pose serious health risks, including liver cancer and other severe health issues. (Sultan et al., 2024). Fusarium produces deoxynivalenol (DON), fumonisins (FUMs), and zearalenone (ZEN), affecting agricultural products (Adetunji et al., 2014) such as wheat, maize, and barley (Muthomi et al., 2008). For example, research has demonstrated that the coexistence of AFs, FUMs, and DON can increase health hazards since the ways in which these toxins interact are not entirely understood (Abdullah et al., 2025; Ezekiel et al., 2021). The possibility of synergistic interactions between various mycotoxins adds complexity to risk assessments, emphasizing the importance of thorough monitoring and strict regulation (Eskola et al., 2020). Prolonged exposure to low concentrations of mycotoxins, such as AFs, can cause liver cancer, while other mycotoxins have been linked to kidney damage and weakened immune function (Mafe and Büsselberg, 2024; Mamo et al., 2020). Pregnant women in rural Bangladesh consumed certain mycotoxins, including citrinin (CIT), at levels that pose a public health concern (Kyei et al., 2022). Studies in the Netherlands and France have shown that exposure to low levels of mycotoxins could pose health risks to children (Pustjens et al., 2022). The transfer of mycotoxins across the placenta to the developing foetus highlights the critical need to tackle mycotoxin contamination in the food supply (Kyei et al., 2022).

Ensuring food and feed safety is essential, as contamination from physical, chemical, and biological sources can cause diseases (Mader et al., 2023). Microorganisms like viruses, fungi, and bacteria thrive in conditions with moisture, oxygen, and high temperatures, impacting food from cultivation to processing (Karanth et al., 2023). Fig. 1 summarizes the most common mycotoxin-producing fungi with their associated mycotoxins and effects to crops.

https://cdn.apub.kr/journalsite/sites/kspa/2025-007-03/N0570070303/images/kspa_2025_073_200_F1.jpg
Fig. 1.

The most common mycotoxin-producing fungi with their associated mycotoxins.

The prevalence of mycotoxins in agriculture is a global concern and is directly related to the environmental conditions in which moulds can be viable (Khan et al., 2024). Temperature, Carbon dioxide levels, and rainfall variations greatly influence to their growth in agriculture (Zingales et al., 2022). Aspergillus flavus and Fusarium verticillioides thrive between 15-30°C, with optimal growth at 30°C, emphasizing the role of climate conditions (Leggieri et al., 2019). Also, agricultural practices and storage methods for the products influence the prevalence (Omotayo et al., 2019) as they accelerate fungal growth and mycotoxin formation (Oluwakayode et al., 2024). The climate condition is the main driving factor in the production, as are other factors such as awareness, farming systems, regulatory limits, and detection techniques (Ngum et al., 2022). Sub-Saharan Africa is facing a significant mycotoxin problem, starting in the field and intensifying during storage as the environment promotes mould development (Adetunji et al., 2014). Both developing and developed countries are facing serious mycotoxin issues (Petrović et al., 2023). In Europe, the same situation is happening as illustrated by (Loi et al., 2023). Again, mycotoxin analysis performed in America, Asia, Oceania, and Europe showed that 81% of the 21,781 feed samples were found to contain at least one mycotoxin (Rodrigues and Naehrer, 2012).

This review paper aims to enlighten the pre-harvest practices that will contribute to the mitigation of mycotoxin contamination in food and feeds, thereby protecting and nourishing the well-being of humans and animals. Good agricultural practices (GAP) refer to a collection of guidelines, norms, and procedures designed to guarantee the production of sustainable, safe, and healthy agricultural products. It covers all stages of food production, from planting and growing to harvesting, processing, and distribution. GAP, resistant seed varieties, and biocontrol are the interventions that help in mitigating the mycotoxin contamination. GAP such as crop rotation help in breaking the life cycle of infectious micro-organisms. On the other hand, the resistant seed varieties help to reduce plant stress, which often accelerates the accumulation of mycotoxins. Biocontrol has shown a promising sign of mitigating mycotoxins by using endemic atoxigenic strains of counterpart toxic strains. For efficient and effective alleviations of mycotoxin contamination, these three interventions are more effective when used jointly.

Effects of mycotoxins

Due to the high severity of mycotoxins and their types, effective strategies must be implemented to reduce human exposure and protect both human health and animal feed from contamination (Fig. 2). Exposure to AFs during pregnancy can impact fetal development and is linked to perinatal mortality and a higher risk of liver cancer (Kościelecka et al., 2023). In addition, recent studies have indicated that AFs will account for 4.6-28.2% of global hepatocellular carcinogenesis (Syafinatunnajah et al., 2023), the third leading cause of cancer-related deaths worldwide (Haque et al., 2020).

https://cdn.apub.kr/journalsite/sites/kspa/2025-007-03/N0570070303/images/kspa_2025_073_200_F2.jpg
Fig. 2.

The potential mycotoxin contamination cycle, which has a thin boundary in the ecosystem.

Mycotoxins are associated with contaminating 25% of the global food, as pointed out in a report of the Food and Agriculture Organization (Moretti et al., 2017). This causes the food losses mostly in cereals such as wheat, corn, rice, barley, oat, rye, and millet (El-Sayed et al., 2022). The losses are accelerated due to the employment of poor agricultural practices in all stages of crops, from the cropping stage to storage (Andriani et al., 2024). Animals that eat tainted feed develop poisons in their cells, which infect humans who eat animal-derived foods like meat, milk, etc. (Kępińska-Pacelik and Biel, 2021). Fungal species like Fusarium spp., Penicilium spp., have significant effects on human health and life-threatening diseases (Al-Falih, 2024). Kenya experienced several incidences of acute poisoning from mycotoxicosis in 1981 after the consumption of contaminated maize (Kibugu et al., 2022). Again in 2004, 500 outbreaks were recorded, with 400 cases of infestation and 200 deaths (Mahuku et al., 2019). Table 1 organizes the types of mycotoxins that frequently occur in the pre-and post-harvest stages of cereal grains.

Table 1.

The most associated mycotoxins with cereal grains following pre- and post-harvest contamination (Bryden, 2012).

Cereals Pre-Harvest Post-Harvest
Barley DON, NIV, ZEN, HT, HT-2, T-2 OTA, Afla, Cit
Maize DON, Fum, ZEN ZEN, Afla
Oats DON, NIV, HT-2, T-2 OTA, Cit
Rice Afla, Sterig, OTA
Rye Ergot OTA
Sorghum Ergot Afla
Wheat DON, NIV, ZEN, Ergot OTA, Afla, Cit

Note: Afla : Aflatoxins; Cit : Citrinin; DON : Deoxynivalenol; Ergot : Ergotamine; HT-2 : HT-2 toxin, T-2 : T-2 toxin, NIV : Nivalenol; OTA : Ochratoxin A; Sterig : Sterigmatocystin; ZEN : Zearalenone.

The regulation of mycotoxin levels is crucial for the safety of food and feed to protect the health of humans and animals (Milićević et al., 2010). Regulatory agencies like the FDA, WHO, FAO, and EFSA set limits on mycotoxin levels in food and feed to ensure consumer safety (Agriopoulou et al., 2020), Several analytical techniques are employed by the FDA mycotoxin program to identify distinct mycotoxins (Khan et al., 2024); however, each technique focusses on a single mycotoxin or class of mycotoxins (Cai et al., 2020). African countries in the East African Community (EAC), COMESA, and ECOWAS have been focused on reducing mycotoxin levels to ensure food safety (Ortega-Beltran and Bandyopadhyay, 2021). As awareness of mycotoxins like AFs increased, the African Union Commission issued directives and established an African working group under the Comprehensive Africa Agriculture Development Programme (CAADP) in 2011 to tackle AFs control. (Chilaka et al., 2017). Ongoing research and awareness efforts aim to develop strategies to mitigate the prevalence of mycotoxins and ensure the safety of global food supplies (Ortega-Beltran and Bandyopadhyay, 2021).

Aflatoxins

AFs are the secondary metabolites that belong to the class of organic compounds called furanocoumarins. four major types of AFs, aflatoxins G1 (AFG1), aflatoxins G2 (AFG2), aflatoxins B1 (AFB1) and aflatoxins B2 (AFB2). Due to their highest level of toxicity, numerous studies have been done looking for mitigation measures since their discovery in 1960. They are the most well-known mycotoxins and are produced naturally by certain Fungi, such as Aspergillus parasiticus, Aspergillus nomius, and Aspergillus flavus. AFs are found in food and feeds and are produced by fungi in humid and warm conditions.

AFs pose serious health issues to human beings and animals compared to other forms of mycotoxins (Agriopoulou et al., 2020). Variables such as animal type, age, health, species, breed, dosage, and exposure duration significantly influence the severity of AFs infections. AF exposure for at least 8 hours through skin contact, ingestion, or inhalation can cause carcinogenic, teratogenic, hepatotoxic, and mutagenic effects (Wen et al., 2014). Research conducted worldwide, including in China, Kenya, Malaysia, and India, shows that AFs can cause acute aflatoxicosis (Bisrat, 2024), leading to symptoms such as vomiting, edema, and abdominal pain (Liew and Mohd-Redzwan, 2018). It can also result in chronic aflatoxicosis, which may lead to hepatocellular cancer (Bisrat, 2024). Furthermore, AFs can lead to lung cancer, gastrointestinal tract, and kidney damage in bovines (Li et al., 2019). Poor food storage and drying methods pose a risk to over 5 billion people, especially in tropical and subtropical regions with high humidity and temperatures (Alp and Bulantekin, 2021).

Fumonisins

Fumonisins (FUM) are mycotoxins found in food and animal feeds, produced by Fusarium species such as Fusarium verticillioides and Fusarium proliferatum (Marin et al., 2013). They share structural similarities with sphinganine and sphingolipids (Kim et al., 2020). Fusarium verticilloides produces FUM type B1 and B2, where B1 has carcinogenic effects such as tumour and edema to rodents (Anumudu et al., 2025). Fusarium verticillioides, found in all maize species, significantly affects corn samples, living within plant tissues without causing illness (Omotayo et al., 2019). Hot climate, insect damage, and temperature stress can accelerate FUM in maize, leading to blight, stalk, and ear rot (Roucou et al., 2021). A case study in Nigeria found mycotoxins in maize, rice, cocoa, and cocoa-based powder beverages, indicating a high prevalence of FUM in these food products (Imade et al., 2021). Contaminated maize grains in South-Africa, China, and Italy have led to esophageal cancer in humans and animals (Chilaka et al., 2017). The ingestion of FUM-contaminated maize in China, Italy, and along the Texas-Mexico border causes abnormalities that cause neural tube defects in developing infants during pregnancy (Ortiz et al., 2015).

Ochratoxins (OTA)

OTA, which is among the mycotoxins, has been shown to be teratogenic, immunotoxic, nephrotoxic, hepatotoxic, and neurotoxic (Cimbalo et al., 2020). This substance is linked to renal tumors, testicular cancer, and acute renal failure when inhaled for at least 8 hours in a closed storage grain (Awuchi et al., 2021). Studies indicate that pigs exhibit a highly sensitive reaction to nephropathy, as they experience kidney failure when exposed to OTA (Reddy and Bhoola, 2010). Again, chick, quail, rabbit, hamster, rat, and mouse studies showed teratogenicity, where the newborn babies had cranial facial abnormalities and reduced birth weight (Heussner and Bingle, 2015).

Pre-Harvest Interventions

Mycotoxins affect crops from growth to harvesting, with vulnerability varying between major crop varieties and subsequent contamination. Maize and rice are the major crops with high and low vulnerability to mycotoxigenic fungi contamination, respectively (Latham et al., 2023). Fungal contamination is elevated due to plant stress, which is accelerated by water scarcity, intense nutrient competition, high temperatures, plant diseases, and insect infestations (Damianidis et al., 2018; Krnjaja et al., 2019). Good handling of crop practices and timely harvesting might be the profound reason for mitigating AFs contamination (Sultan et al., 2024). Damaged seeds during sowing should be removed, and the choice of resistant varieties can be a means of reducing the risk of contamination (Oppong et al., 2022). Resistance to mycotoxins in pre-harvest crops can be significantly mitigated using resistant hybrid varieties, good agricultural practices, and biological control measures (Dövényi-Nagy et al., 2020). Fig. 3 presents the summary of recent research trends in mycotoxins in crop production.

https://cdn.apub.kr/journalsite/sites/kspa/2025-007-03/N0570070303/images/kspa_2025_073_200_F3.jpg
Fig. 3.

Summary of recent research trends related to mycotoxins in agriculture.

Resistant varieties

Given their significance in mitigating the effects of mycotoxigenic contamination, breeding programs for disease-resistant seed varieties, whether private or public, are urgently needed (Mesterházy et al., 2012). The development of resistant inbred lines and hybrids is a promising method to reduce mycotoxin contamination and diseases caused by A. flavus and F. verticillioides (Stagnati et al., 2020). Institutions like CIMMYT, IITA, and SERAT are producing inbred lines and hybrids resistant to mycotoxigenic fungi, including A. flavus and AF contamination, to suppress contamination (Warburton et al., 2022). Evaluation which has been done by Stagnati et al. (2020) on maize breeds originated from Italian, US, and Canadian breeding, 17 out of 46 performed well in resisting AER and FER, also Brown et al. (2016), their evaluation exhibited the possibility of reducing mycotoxin contamination using resistant inbred lines and hybrids. Mahuku et al. (2019) study found that both local and hybrid maize seeds in Kenya contain mycotoxins, indicating increased consumption of aflatoxin beyond the accepted standard (Table 2).

Table 2.

Prevalence and descriptive statistics of aflatoxin B1 (AFB1) in maize collected from farmer’s fields in Eastern and Southwestern regions of Kenya and proportions of maize samples with AFB1 levels (Mahuku et al., 2019).

Region Year N Positive samples Aflatoxins concentration
range of positive
samples (µg/kg)
Median
(µg/kg)
Proportion of positive samples
exceeding EAC regulatory limit (≥5 µg/kg)
N % N %
Eastern 2009 40 13 32.5 2.0-9091.8 45.7 11 84.6
2010 193 127 65.8 0.1-1454.8 7.4 76 59.8
2011 183 134 72.5 1.0-581.5 4.9 66 49.3
Total 416 274 65.9 0.01-9091.8 6.2 153 55.8
South-western 2010 233 157 67.4 1.0-722.2 6.9 93 59.2
2011 140 76 54.4 0.9-63.1 2.2 9 11.8
Total 373 233 62.5 0.98-722.2 4.01 102 43.8
Overall 789 507 64.3 0.01-9091.8 5.2 255 50.3

N: number of samples

Biocontrol

Biocontrol intervention is a cost-effective and environmentally friendly method for suppressing AFs contamination, competing with fungi AFs producers (Agbetiameh et al., 2019). Identifying vulnerable crop stages to AFs attacks and applying non-aflatoxigenic genotypes to suppress contamination is crucial for efficient endemic non-aflatoxigenic biocontrol before the flowering stage (Jung et al., 2024). Additionally, selecting the biocontrol agent should consider the strains that cannot produce other mycotoxins (Kagot et al., 2019).

The competitive exclusion of non-aflatoxigenic strains led to a decrease in the A. flavus population and a minimized level of AFs due to competition for nutrients (Hruska et al., 2014). According to Atehnkeng et al. (2014) in Nigeria and Argentina, native endemic strains of A. flavus successfully lower the population of A. flavus and the concentrations of AFs in treated grains, leading to a 65–95% decrease in field and stored grains. Zanon et al. (2022) and (Agbetiameh et al., 2019) demonstrated endemic atoxigenic A. flavus strains mitigated AFs concentrations on maize and ground nuts. Research shows endemic atoxigenic A. flavus strains are superior in colonizing toxigenic A. flavus, making them ideal for mitigating AFs concentrations in high-risk contaminated areas (Agbetiameh et al., 2019).

The mitigation of AFs concentration is not only achieved through the selection of endemic atoxigenic strains but also depends on weather conditions, farm field hygiene, and seed inoculation rate (Torres et al., 2014). Furthermore, biocontrol must be employed along by appropriate agricultural practices paired with post-harvest treatments such sorting and adequate storage (Kagot et al., 2019). Lavkor et al. (2019) study in Turkey found that non-toxigenic afla-guard bio-pesticide significantly reduced Afs contamination in peanuts, compared to control plots (Table 3).

Table 3.

Effect of biological control treatments on aflatoxin contamination of peanuts in harvest, drying, and pre-storage periods in 2015 and 2016 (Lavkor et al., 2019).

Treatment Harvest Drying Pre-storage Harvest Drying Pre-storage
% Effect (Abbott)
2015 2016
Soil1 99.82 99.41 99.82 90.29 90.10 91.64
Multiple2 99.68 99.04 99.24 91.38 90.66 92.39
Foliar3 98.44 97.38 98.93 90.02 89.07 91.29

1Afla-guard applied to soil during sowing (907 g/da)

2Afla-guard applied to soil during sowing (455 g/da) and 40 days after planting (455 g/da)

3Afla-guard applied to foliar at 60 days after planting (907 g/da)

The efficient reduction of cyclopiazonic acid and AFs by organic volatile chemicals and extrolites of non-aflatoxigenic strains can be a potential method for AFs mitigation (Moore et al., 2019). Aspergillus species produce various extrolites compounds, including asperfuran, aspergillic acid, aspirochlorin, citreoisocoumarin, cyclopiazonic acids, ditryptophenaline, flavimin, kojic acid, miyakamides, paspaline, and paspalinine, to suppress AF concentrations. (Frisvad et al., 2019). Since excessive extrolites secretion might result in health problems including diarrhea and stomach upset, it is essential to choose biocontrol strains that do not cause these problems (Peles et al., 2021).

The profound strategies to be considered for desired results in controlling and minimizing the AFs concentrations are formulation and application of respective biocontrol strains (Prajapati et al., 2020). Three bioformulations based on A. flavus and A. parasiticus, including solid-state fermented rice, Pesta, and pregelatinized corn flour granules, were found to effectively reduce AFs in peanuts (Unnevehr and Grace, 2013), these forms were inoculated with spores of atoxigenic strains of A. flavus and/or A. parasiticus and found to be efficient and long term viable in suppressing AFs concentrations (Peles et al., 2021), similarly in Argentina the single and mixed inoculated three bioformulations based on A. flavus AFCHG2 and ARG5/30 strains were applied on maize (Zanon et al., 2022).

For biocontrol isolation, bioplastic is used to coat seeds with non-toxic fungal spores, which take the place of cereals like sorghum, barley, and wheat. The starch-based bioplastic granules effectively reduced AFs concentrations in corn kernels by entrapping nontoxigenic A. flavus spores in the soil. Research investigates the use of bioplastic-coated seeds combined with endemic atoxigenic strains and traditional biopesticides to lower AFs concentrations before planting (Accinelli et al., 2018). Insecticides or fungicides are added to the film coating, and seeds are coated with bioplastic based on starch and biopesticides to lower AF concentrations without compromising crop yields. also, studied the bioplastic starch-based covering reduced AFs concentrations without affecting the viability and growth of maize seeds and seedlings when applied to maize kernels (Moral et al., 2020).

Good agricultural practices (GAP)

No way of hindering mycotoxin formation at any stage of crop production from the growth up to the processing stage, as the fungal spores are readily available to the plant debris. Properly managing debris and residue through burying can create humus in the soil, increasing nutrients and potentially eliminating waste from the farm field. Most of the time, the soil-borne diseases are incorporated into the soil by cultivating a single crop for an extended period. High humidity and water activity affect mycotoxin production, attracting insects, microorganisms, and diseases. Early harvesting crops with a high risk of mycotoxin can lessen vulnerability, while delaying can increase crop contamination and fungal infections in high-risk. Maintaining ideal temperature and air circulation, along with plant spacing, reduces crop losses, prevents fungal spores and AFs, and promotes better quality and high yields.

Good agricultural practices, including crop rotation and resistant varieties, and post-harvest measures like proper drying, storage, and monitoring, help minimize mycotoxin contamination in stored crops (Phokane et al., 2019). GAP enhances crop quality and quantity by reducing insect infestations and losses (Ngum et al., 2022), while pre-harvest strategies like crop rotation, intercropping, and fertilizer use minimize mycotoxin formation risk (Daou et al., 2021). By disrupting the infectious cycle of insects, crop rotation and intercropping significantly limit the production of mycotoxins while enhancing soil fertility and supplying nutrients (Mir et al., 2022). Legumes give more nitrogen than maize; therefore, cultivating them together reduces the availability of maize AFs, whereas growing them alone raises the danger of mycotoxicosis (Baijukya et al., 2016).

Analytical approach to mycotoxins

Mycotoxin analytical detection has advanced significantly, and several techniques have been developed to guarantee precise and effective screening. The two primary categories of this analytical approach, screening procedures and confirmatory methods, each have specific functions in mycotoxin analysis (Jesna et al., 2024). Screening methods, such as enzyme-linked immunosorbent assays (ELISA) and lateral flow immunoassays (LFAs), are designed for rapid and preliminary detection of mycotoxins (Sharma et al., 2023). These techniques are especially helpful in field situations where prompt outcomes are required. For example, Wu et al. (2020) The study showcased the effectiveness of immunoassays in on-site testing by developing a calibration curve-implanted ELISA for quantitatively assessing multiple mycotoxins in cereal samples. Nji and Mwanza, (2024) showed the value of rapid screening techniques by analyzing South African maize for three years using liquid chromatography and tandem mass spectrometry (LC-MS/MS). Furthermore, Zhang et al. (2017) study, used amorphous carbon nanoparticles to successfully detect three Fusarium mycotoxins in maize, demonstrated the promise of multiplex LFA development.

Conversely, confirmatory techniques are necessary for precise mycotoxin identification and quantification. Because of their great sensitivity and specificity, methods like (LC-MS/MS) are regarded as the gold standard (Płaza-Altamer et al., 2024). In mycotoxin detection techniques, the combination of stable isotope dilution with LC-MS/MS improves accessibility, efficiency, and quantification while permitting remote extraction (Malachová et al., 2018). Additionally, Pantano et al. (2021) demonstrated the adaptability of this strategy by highlighting the use of the QuEChERS method in combination with LC-MS/MS for detecting mycotoxins in cereal goods and spices. Another noteworthy development is the incorporation of high-resolution mass spectrometry (HRMS), which enables the simultaneous identification of many mycotoxins, including newly discovered pollutants (Lapris et al., 2024).

Although immunoassays yield data quickly, they might not be specific enough to meet regulatory requirements, thus confirming techniques must be used (Csenki et al., 2023). A thorough mycotoxin analysis approach requires the use of both screening and confirmatory procedures as they enable quick evaluation and thorough characterization of contamination levels (Tittlemier et al., 2023).

Conclusion

The hygiene of the farm field plays a significant role in determining the occurrence of mycotoxins; for instance, the crop residues may contain fungal spores of toxigenic strains when they are left on the field. Good agricultural practices, resistant cultivars, and the use of biocontrol of non-toxigenic strains of counterpart toxigenic strains showed a promising sign of mitigating mycotoxin concentration. Furthermore, the use of starch-based bioplastic formulation to coat the kernel seeds containing the non-toxigenic fungal spore and biopesticide has become more efficient in suppressing mycotoxin contamination and still maintaining environmental friendliness. For better results, these methods should be employed altogether to ensure the safety of the food from the field to the plate.

We recommend prioritizing integrated pre-harvest packages that combine atoxigenic biocontrol with resistant cultivars, optimized planting dates and irrigation where feasible, and residue and rotation management, tailored to local agroecological risk profiles to maximize and stabilize reductions in mycotoxin contamination. Measurement and reporting should be standardized by using validated analytical methods (preferably LC-MS/MS or HPLC-FLD with QA/QC), presenting effect sizes with confidence intervals, clearly stating sample sizes, seasons and locations, and reporting the proportion of samples below regulatory thresholds to enable cross-study comparisons and policy relevance. Region-specific decision-support should be embedded into practice by leveraging forecasting of heat, drought, and insect pressure to guide planting windows, irrigation scheduling, and the timing of biocontrol or fungicide applications. Adoption pathways must be strengthened by pairing interventions with farmer training, reliable input supply chains for biocontrol products, and cost-sharing mechanisms, while documenting cost-effectiveness and scalability across smallholder and commercial systems. Finally, compliance and transparency gaps should be closed by including PRISMA-style review methods, data availability statements with accessible evidence tables, and standardized declarations for funding, conflicts of interest, and permissions.

A short research agenda emerges from these priorities. Multi-year, multi-location trials are needed to quantify the performance and stability of integrated packages under climate extremes and varying pest pressures, explicitly reporting heterogeneity and moderators. Comparative effectiveness and economic evaluations should test leading strategies head-to-head, integrating full cost, yield, and risk metrics alongside adoption studies. Delivery innovations warrant investigation, including improved formulations and seed or soil delivery systems for biocontrol, with rigorous assessments of persistence, ecological safety, and resistance risks. Data standards should be advanced by building open repositories of harmonized field-trial datasets to enable robust meta-analyses and calibration of risk models. Finally, climate-informed risk models that integrate remote sensing and seasonal forecasts should be prospectively validated to optimize intervention timing and inform policy and extension at regional scales.

Acknowledgements

The research was supported by the Institute of International Research and Development through the Korea International Cooperation Agency (KOICA) Scholarship Program of Kyungpook National University, Republic of Korea. Also, this work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korea government(Ministry of Science and ICT) (RS-2024-00338052).

Conflict of Interest

The corresponding author, Tusan Park, is the editor-in-chief of Precision Agriculture Science and Technology but was not involved in the peer-review process or the decisions made during the publishing process.

References

1

Abdullah, R., Kamarozaman, N.S., Ab Dullah, S.S., Aziz, M.Y., Aziza, H.B.A. 2025. Health risks evaluation of mycotoxins in plant-based supplements marketed in Malaysia. Scientific Reports 15(1): 1244. https://doi.org/10.1038/s41598-025-85280-z

10.1038/s41598-025-85280-z39774309PMC11707365
2

Accinelli, C., Abbas, H.K., Shier, W.T. 2018. A bioplastic-based seed coating improves seedling growth and reduces production of coated seed dust. Journal of Crop Improvement 32(3): 318-330. https://doi.org/10.1080/15427528.2018.1425792

10.1080/15427528.2018.1425792
3

Adetunji, M., Atanda, O., Ezekiel, C.N., Sulyok, M., Warth, B., Beltrán, E., Krska, R., Obadina, O., Bakare, A., Chilaka, C.A. 2014. Fungal and bacterial metabolites of stored maize (Zea mays L.) from five agro-ecological zones of Nigeria. Mycotoxin Research 30(2): 89-102. https://doi.org/10.1007/s12550-014-0194-2

10.1007/s12550-014-0194-2
4

Agbetiameh, D., Ortega-Beltran, A., Awuah, R.T., Atehnkeng, J., Islam, M.S., Callicott, K.A., Cotty, P.J., Bandyopadhyay, R. 2019. Potential of atoxigenic aspergillus flavus vegetative compatibility groups associated with maize and groundnut in Ghana as biocontrol agents for aflatoxin management. Frontiers in Microbiology 10: 2069. https://doi.org/10.3389/fmicb.2019.02069

10.3389/fmicb.2019.0206931555251PMC6743268
5

Agriopoulou, S., Stamatelopoulou, E., Varzakas, T. 2020. Advances in occurrence, importance, and mycotoxin control strategies: Prevention and detoxification in foods. Foods 9(2): 137. https://doi.org/10.3390/foods9020137

10.3390/foods902013732012820PMC7074356
6

Al-Falih, A. M. 2024. Overview on mycotoxins health hazard to humans and animals. Environmental Analysis & Ecology Studies 12(4): 1504-1514. https://doi.org/10.31031/EAES.2024.12.000794

10.31031/EAES.2024.12.000794
7

Alp, D., Bulantekin, Ö. 2021. The microbiological quality of various foods dried by applying different drying methods: a review. European Food Research and Technology 247: 1333-1343. https://doi.org/10.1007/s00217-021-03731-z

10.1007/s00217-021-03731-z33824622PMC8017434
8

Alshannaq, A., Yu, J.-H. 2017. Occurrence, toxicity, and analysis of major mycotoxins in food. International Journal of Environmental Research and Public Health 14(6): 632. https://doi.org/10.3390/ijerph14060632

10.3390/ijerph1406063228608841PMC5486318
9

Andriani, L., Kusrini, N., Maswadi. 2024. Losses in each stage of rice harvest and postharvest. Jurnal Ilmu Pertanian Indonesia 30(1): 85-98. https://doi.org/10.18343/jipi.30.1.85

10.18343/jipi.30.1.85
10

Anumudu, C.K., Ekwueme, C.T., Uhegwu, C.C., Ejileugha, C., Augustine, J., Okolo, C.A., Onyeaka, H. 2025. A review of the mycotoxin family of fumonisins, their biosynthesis, metabolism, methods of detection and effects on humans and animals. International Journal of Molecular Sciences 26(1): 184. https://doi.org/10.3390/ijms26010184

10.3390/ijms2601018439796041PMC11719890
11

Atehnkeng, J., Ojiambo, P.S., Cotty, P.J., Bandyopadhyay, R. 2014. Field efficacy of a mixture of atoxigenic Aspergillus flavus Link: FR vegetative compatibility groups in preventing aflatoxin contamination in maize (Zea mays L.). Biological Control 72: 62-70. https://doi.org/10.1016/j.biocontrol.2014.02.009

10.1016/j.biocontrol.2014.02.009
12

Awuchi, C.G., Ondari, E.N., Ogbonna, C.U., Upadhyay, A.K., Baran, K., Okpala, C.O.R., Korzeniowska, M., Guiné, R.P.F. 2021. Mycotoxins affecting animals, foods, humans and plants: Types, occurrence, toxicities, action mechanisms, prevention and detoxification strategies- A revisit. Foods 10(6): 1279. https://doi.org/10.3390/foods10061279

10.3390/foods1006127934205122PMC8228748
13

Baijukya, F., Wairegi, L., Giller, K., Zingore, S., Chikowo, R., Mapfumo, P. 2016. Maize-legume cropping guide. Africa Soil Health Consortium.

14

Bisrat, A. 2024. Effect of aflatoxin exposure in livestock and public health: review. Research in: Agricultural & Veterinary Sciences 8(3): 101-120. https://doi.org/10.62476/ravs83101

10.62476/ravs83101
15

Brown, R.L., Williams, W.P., Windham, G.L., Menkir, A., Chen, Z.-Y. 2016. Evaluation of African-bred maize germplasm lines for resistance to aflatoxin accumulation. Agronomy 6(2): 24. https://doi.org/10.3390/agronomy6020024

10.3390/agronomy6020024
16

Bryden, W.L. 2012. Mycotoxin contamination of the feed supply chain: Implications for animal productivity and feed security. Animal Feed Science and Technology 173(1-2): 134-158. https://doi.org/10.1016/j.anifeedsci.2011.12.014

10.1016/j.anifeedsci.2011.12.014
17

Cai, Y.T., McLaughlin, M., Zhang, K. 2020. Advancing the FDA/office of regulatory affairs mycotoxin program: New analytical method approaches to addressing needs and challenges. Journal of AOAC International 103(3): 705-709. https://doi.org/10.1093/jaocint/qsz007

10.1093/jaocint/qsz007
18

Chilaka, C.A., De Boevre, M., Atanda, O.O., De Saeger, S. 2017. The status of fusarium mycotoxins in sub-Saharan Africa: A review of emerging trends and post-harvest mitigation strategies towards food control. Toxins 9(1): 19. https://doi.org/10.3390/toxins9010019

10.3390/toxins901001928067768PMC5308251
19

Cimbalo, A., Alonso-Garrido, M., Font, G., Manyes, L. 2020. Toxicity of mycotoxins in vivo on vertebrate organisms: A review. Food and Chemical Toxicology 137: 111161. https://doi.org/10.1016/j.fct.2020.111161

10.1016/j.fct.2020.111161
20

Csenki, E., Mikulás, V., Freitag, S., Fomina, P., Hlavatsch, M., Femenias, A., Bosman, A.J., Ruggeri, F.S., Smirnova, M., Salentijn, G., Mizaikoff, B., Krska, R., Scholderer, J., Kohler, A., Kasza, G. 2023. Stakeholder assessment for mycotoxin analysis: exploring the demand along the European food supply chain. World Mycotoxin Journal 16(4): 287-299. https://doi.org/10.1163/18750796-20232883

10.1163/18750796-20232883
21

Damianidis, D., Ortiz, B.V., Bowen, K.L., Windham, G.L., Hoogenboom, G., Hagan, A., Knappenberger, T., Abbas, H.K., Scully, B.T., Mourtzinis, S. 2018. Minimum temperature, rainfall, and agronomic management impacts on corn grain aflatoxin contamination. Agronomy Journal 110(5): 1697-1708. https://doi.org/10.2134/agronj2017.11.0628

10.2134/agronj2017.11.0628
22

Daou, R., Joubrane, K., Maroun, R. G., Khabbaz, L. R., Ismail, A., El Khoury, A. 2021. Mycotoxins: Factors influencing production and control strategies. AIMS Agriculture and Food 6(1): 416-447. https://doi.org/10.3934/agrfood.2021025

10.3934/agrfood.2021025
23

Dövényi-Nagy, T., Rácz, C., Molnár, K., Bakó, K., Szláma, Z., Jóźwiak, Á., Farkas, Z., Pócsi, I., Dobos, A.C. 2020. Pre-harvest modelling and mitigation of aflatoxins in maize in a changing climatic environment—A review. Toxins 12(12): 768. https://doi.org/10.3390/toxins12120768

10.3390/toxins1212076833291729PMC7761929
24

El-Sayed, R.A., Jebur, A.B., Kang, W., El-Demerdash, F.M. 2022. An overview on the major mycotoxins in food products: characteristics, toxicity, and analysis. Journal of Future Foods 2(2): 91-102. https://doi.org/10.1016/j.jfutfo.2022.03.002

10.1016/j.jfutfo.2022.03.002
25

Eskola, M., Kos, G., Elliott, C.T., Hajšlová, J., Mayar, S., Krska, R. 2020. Worldwide contamination of food-crops with mycotoxins: Validity of the widely cited ‘FAO estimate’ of 25%. Critical Reviews in Food Science and Nutrition 60(16): 2773-2789. https://doi.org/10.1080/10408398.2019.1658570

10.1080/10408398.2019.1658570
26

Ezekiel, C.N., Ayeni, K.I., Akinyemi, M.O., Sulyok, M., Oyedele, O.A., Babalola, D.A., Ogara, I.M., Krska, R. 2021. Dietary risk assessment and consumer awareness of mycotoxins among household consumers of cereals, nuts and legumes in north-central nigeria. Toxins 13(9): 635. https://doi.org/10.3390/toxins13090635

10.3390/toxins1309063534564639PMC8472633
27

Frisvad, J.C., Hubka, V., Ezekiel, C.N., Hong, S.-B., Nováková, A., Chen, A.J., Arzanlou, M., Larsen, T.O., Sklenář F., Mahakarnchanakul, W., Samson, R.A., Houbraken, J. 2019. Taxonomy of Aspergillus section Flavi and their production of aflatoxins, ochratoxins and other mycotoxins. Studies in Mycology 93(1): 1-63. https://doi.org/10.1016/j.simyco.2018.06.001

10.1016/j.simyco.2018.06.00130108412PMC6080641
28

Haque, M.A., Wang, Y., Shen, Z., Li, X., Saleemi, M.K., He, C. 2020. Mycotoxin contamination and control strategy in human, domestic animal and poultry: A review. Microbial Pathogenesis 142: 104095. https://doi.org/10.1016/j.micpath.2020.104095

10.1016/j.micpath.2020.104095
29

Heussner, A.H., Bingle, L.E.H. 2015. Comparative ochratoxin toxicity: A review of the available data. Toxins 7(10): 4253-4282. https://doi.org/10.3390/toxins7104253

10.3390/toxins710425326506387PMC4626733
30

Hruska, Z., Rajasekaran, K., Yao, H., Kincaid, R., Darlington, D., Brown, R. L., Bhatnagar, D., Cleveland, T. E. 2014. Co-inoculation of aflatoxigenic and non-aflatoxigenic strains of Aspergillus flavus to study fungal invasion, colonization, and competition in maize kernels. Frontiers in Microbiology 5: 122. https://doi.org/10.3389/fmicb.2014.00122

10.3389/fmicb.2014.0012224734028PMC3973917
31

Imade, F., Ankwasa, E.M., Geng, H., Ullah, S., Ahmad, T., Wang, G., Zhang, C., Dada, O., Xing, F., Zheng, Y., Liu, Y. 2021. Updates on food and feed mycotoxin contamination and safety in Africa with special reference to Nigeria. Mycology 12(4): 245-260. https://doi.org/10.1080/21501203.2021.1941371

10.1080/21501203.2021.194137134900380PMC8654414
32

Ismaiel, A.A., Papenbrock, J. 2015. Mycotoxins: Producing fungi and mechanisms of phytotoxicity. Agriculture 5(3): 493-537. https://doi.org/10.3390/agriculture5030492

10.3390/agriculture5030492
33

Jesna, N.B., Thara, S.S., Nair, C.B. 2024. Recent advances in mycotoxin detection: A review. Journal of Advances in Biology & Biotechnology 27(11): 564-578. https://doi.org/10.9734/jabb/2024/v27i111641

10.9734/jabb/2024/v27i111641
34

Jung, K.S., Kim, H.M., Lee, J., Ganbat, D., Lee, S.E. 2024. Biocontrol of aflatoxin-producing aspergillus flavus ATCC 22546 by a non-aflatoxigenic aspergillus flavus ATCC 9643. Applied Sciences 14(14): 6142. https://doi.org/10.3390/app14146142

10.3390/app14146142
35

Kagot, V., Okoth, S., De Boevre, M., De Saeger, S. 2019. Biocontrol of Aspergillus and Fusarium mycotoxins in Africa: benefits and limitations. Toxins 11(2): 109. https://doi.org/10.3390/toxins11020109

10.3390/toxins1102010930781776PMC6409615
36

Karanth, S., Feng, S., Patra, D., Pradhan, A.K. 2023. Linking microbial contamination to food spoilage and food waste: the role of smart packaging, spoilage risk assessments, and date labeling. Frontiers in Microbiology 14: 1198124. https://doi.org/10.3389/fmicb.2023.1198124

10.3389/fmicb.2023.119812437426008PMC10325786
37

Kępińska-Pacelik, J., Biel, W. 2021. Alimentary risk of mycotoxins for humans and animals. Toxins 13(11): 822. https://doi.org/10.3390/toxins13110822

10.3390/toxins1311082234822606PMC8622594
38

Khan, R., Anwar, F., Ghazali, F.M. 2024. A comprehensive review of mycotoxins: Toxicology, detection, and effective mitigation approaches. Heliyon 10(8): e28361. https://doi.org/10.1016/j.heliyon.2024.e28361

10.1016/j.heliyon.2024.e2836138628751PMC11019184
39

Khan, Z., Humera, A., Ayesha, Q.B., Ahmed, K.F. 2024. Environmental variations and mycotoxin dynamics: Impacts on structure toxicity and health risks. International Journal for Multidisciplinary Research 6(6): 1-17. https://doi.org/10.36948/ijfmr.2024.v06i06.31176

10.36948/ijfmr.2024.v06i06.31176
40

Kibugu, J., Mburu, D., Munga, L., Lusweti, F., Grace, D., Lindahl, J. 2022. Mycotoxin hazards in the Kenyan food and feed market - A retrospective study. African Journal of Food, Agriculture, Nutrition and Development 22(1): 19306-19325. https://doi.org/10.18697/ajfand.106.20995

10.18697/ajfand.106.20995
41

Kim, H.S., Lohmar, J.M., Busman, M., Brown, D.W., Naumann, T.A., Divon, H.H., Uhlig, S., Proctor, R.H. 2020. Identification and distribution of gene clusters required for synthesis of sphingolipid metabolism inhibitors in diverse species of the filamentous fungus Fusarium. BMC Genomics 21: 510. https://doi.org/10.1186/s12864-020-06896-1

10.1186/s12864-020-06896-132703172PMC7376913
42

Kościelecka, K., Kuć, A., Kubik-Machura, D., Męcik-Kronenberg, T., Włodarek, J., Radko, L. 2023. Endocrine effect of some mycotoxins on humans: A clinical review of the ways to mitigate the action of mycotoxins. Toxins 15(9): 515. https://doi.org/10.3390/toxins15090515

10.3390/toxins1509051537755941PMC10535190
43

Krnjaja, V., Mandić, V., Stanković, S., Obradović, A., Vasić, T., Lukić, M., Bijelić, Z. 2019. Influence of plant density on toxigenic fungal and mycotoxin contamination of maize grains. Crop Protection 116: 126-131. https://doi.org/10.1016/j.cropro.2018.10.021

10.1016/j.cropro.2018.10.021
44

Kyei, N.N.A., Cramer, B., Humpf, H.U., Degen, G.H., Ali, N., Gabrysch, S. 2022. Assessment of multiple mycotoxin exposure and its association with food consumption: a human biomonitoring study in a pregnant cohort in rural Bangladesh. Archives of Toxicology 96(7): 2123-2138. https://doi.org/10.1007/s00204-022-03288-0

10.1007/s00204-022-03288-035441239PMC9151532
45

Lapris, M., Errico, M., Rocchetti, G., Gallo, A. 2024. The potential of multi-screening methods and omics technologies to detect both regulated and emerging mycotoxins in different matrices. Foods 13(11): 1746. https://doi.org/10.3390/foods13111746

10.3390/foods1311174638890974PMC11171533
46

Latham, R.L., Boyle, J.T., Barbano, A., Loveman, W.G., Brown, N.A. 2023. Diverse mycotoxin threats to safe food and feed cereals. Essays in Biochemistry 67(5): 797-809. https://doi.org/10.1042/EBC20220221

10.1042/EBC2022022137313591PMC10500202
47

Lavkor, İ., Arioglu, H., Var, İ., Oztemiz, S. 2019. Biological control of aflatoxigenic fungi on peanut: For the pre-harvest approach. Turkish Journal of Field Crops 24(1): 21-27. https://doi.org/10.17557/tjfc.562634

10.17557/tjfc.562634
48

Leggieri, M.C., Giorni, P., Pietri, A., Battilani, P. 2019. Aspergillus flavus and Fusarium verticillioides interaction: Modeling the impact on mycotoxin production. Frontiers in Microbiology 10: 2653. https://doi.org/10.3389/fmicb.2019.02653

10.3389/fmicb.2019.0265331781087PMC6861442
49

Li, H., Li, S., Yang, H., Wang, Y., Wang, J., Zheng, N. 2019. L-proline alleviates kidney injury caused by AFB1 and AFM1 through regulating excessive apoptosis of kidney cells. Toxins 11(4): 226. https://doi.org/10.3390/toxins11040226

10.3390/toxins1104022630995739PMC6521284
50

Liew, W.P.P., Mohd-Redzwan, S. 2018. Mycotoxin: Its impact on gut health and microbiota. Frontiers in Cellular and Infection Microbiology 8: 60. https://doi.org/10.3389/fcimb.2018.00060

10.3389/fcimb.2018.0006029535978PMC5834427
51

Loi, M., Logrieco, A.F., Pusztahelyi, T., Leiter, É., Hornok, L., Pócsi, I. 2023. Advanced mycotoxin control and decontamination techniques in view of an increased aflatoxin risk in Europe due to climate change. Frontiers in Microbiology 13: 1085891. https://doi.org/10.3389/fmicb.2022.1085891

10.3389/fmicb.2022.108589136762096PMC9907446
52

Mader, A., Riede, O., Pabel, U., Dietrich, J., Sommerkorn, K., Pieper, R. 2023. The one health approach in the context of global commodity chains, crises, and food and feed safety. Bundesgesundheitsblatt - Gesundheitsforschung - Gesundheitsschutz 66(6): 644-651. https://doi.org/10.1007/s00103-023-03714-3

10.1007/s00103-023-03714-337256408PMC10230465
53

Mafe, A.N., Büsselberg, D. 2024. Mycotoxins in food: Cancer Risks and strategies for control. Foods 13(21): 3502. https://doi.org/10.3390/foods13213502

10.3390/foods1321350239517285PMC11545588
54

Mahuku, G., Nzioki, H.S., Mutegi, C., Kanampiu, F., Narrod, C., Makumbi, D. 2019. Pre-harvest management is a critical practice for minimizing aflatoxin contamination of maize. Food Control 96: 219-226. https://doi.org/10.1016/j.foodcont.2018.08.032

10.1016/j.foodcont.2018.08.03230713368PMC6251936
55

Malachová, A., Stránská, M., Václavíková, M., Elliott, C. T., Black, C., Meneely, J., Hajšlová, J., Ezekiel, C. N., Schuhmacher, R., Krska, R. 2018. Advanced LC-MS-based methods to study the co-occurrence and metabolization of multiple mycotoxins in cereals and cereal-based food. Analytical and Bioanalytical Chemistry 410(3): 801-825. https://doi.org/10.1007/s00216-017-0750-7

10.1007/s00216-017-0750-729273904PMC5775372
56

Mamo, F.T., Abate, B.A., Tesfaye, K., Nie, C., Wang, G., Liu, Y. 2020. Mycotoxins in Ethiopia: A review on prevalence, economic and health impacts. Toxins 12(10): 648. https://doi.org/10.3390/toxins12100648

10.3390/toxins1210064833049980PMC7601512
57

Marin, S., Ramos, A.J., Cano-Sancho, G., Sanchis, V. 2013. Mycotoxins: Occurrence, toxicology, and exposure assessment. Food and Chemical Toxicology 60: 218-237. https://doi.org/10.1016/j.fct.2013.07.047

10.1016/j.fct.2013.07.047
58

Mesterházy, Á., Lemmens, M., Reid, L. M. 2012. Breeding for resistance to ear rots caused by Fusarium spp. in maize - A review. Plant Breeding 131(1): 1-19. https://doi.org/10.1111/j.1439-0523.2011.01936.x

10.1111/j.1439-0523.2011.01936.x
59

Milićević, D.R., Skrinjar, M., Baltić, T. 2010. Real and perceived risks for mycotoxin contamination in foods and feeds: challenges for food safety control. Toxins 2(4): 572-592. https://doi.org/10.3390/toxins2040572

10.3390/toxins204057222069600PMC3153222
60

Mir, M.S., Saxena, A., Kanth, R.H., Raja, W., Dar, K.A., Mahdi, S.S., Bhat, T.A., Naikoo, N. B., Nazir, A., Amin, Z., Mansoor, T., Myint, M.Z., Khan, M.R., Mohammad, I., Mir, S.A. 2022. Role of intercropping in sustainable insect-pest management: A review. International Journal of Environment and Climate Change 12(11): 3390-3404. https://doi.org/10.9734/ijecc/2022/v12i111390

10.9734/ijecc/2022/v12i111390
61

Moore, G.G., Lebar, M.D., Carter‐Wientjes, C.H. 2019. The role of extrolites secreted by nonaflatoxigenic Aspergillus flavus in biocontrol efficacy. Journal of applied microbiology 126(4): 1257-1264.https://doi.org/10.1111/jam.14175

10.1111/jam.14175
62

Moral, J., Garcia-Lopez, M. T., Camiletti, B. X., Jaime, R., Michailides, T. J., Bandyopadhyay, R., Ortega-Beltran, A. 2020. Present status and perspective on the future use of aflatoxin biocontrol products. Agronomy 10(4): 491. https://doi.org/10.3390/agronomy10040491

10.3390/agronomy10040491
63

Moretti, A., Logrieco, A.F., Susca, A. 2017. Mycotoxins: An underhand food problem. Methods in Molecular Biology. In Mycotoxigenic Fungi. Edited by Moretti, A. and Susca, A. pp.3-12. Humana Press. NY. USA.

10.1007/978-1-4939-6707-0_1
64

Muthomi, J.W., Ndung’u, J.K., Gathumbi, J.K., Mutitu, E.W., Wagacha, J.M. 2008. The occurrence of Fusarium species and mycotoxins in Kenyan wheat. Crop Protection 27(8): 1215-1219. https://doi.org/10.1016/j.cropro.2008.03.001

10.1016/j.cropro.2008.03.001
65

Ngum, N.Q., Babalola, O.O., Ekwomadu, T.I., Nleya, N., Mulunda, M. 2022. Six main contributing factors to high levels of mycotoxin contamination in African foods. Toxins 14(5): 318. https://doi.org/10.3390/toxins14050318

10.3390/toxins1405031835622564PMC9146326
66

Nji, Q.N., Mwanza, M. 2024. Three-year multi-mycotoxin analysis of South African commercial maize from three provinces. Frontiers of Fungal Biology 5: 1426782. https://doi.org/10.3389/ffunb.2024.1426782

10.3389/ffunb.2024.142678239687344PMC11647527
67

Oluwakayode, A., Greer, B., He, Q., Sulyok, M., Meneely, J., Krska, R., Medina, A. 2024. The influence of different abiotic conditions on the concentrations of free and conjugated deoxynivalenol and zearalenone in stored wheat. Mycotoxin Research. 40: 591-603. https://doi.org/10.1007/s12550-024-00541-6

10.1007/s12550-024-00541-639028531PMC11480129
68

Omotayo, O.P., Omotayo, A.O., Mwanza, M., Babalola, O.O. 2019. Prevalence of mycotoxins and their consequences on human health. Toxicological Research 35: 1-7. https://doi.org/10.5487/TR.2019.35.1.001

10.5487/TR.2019.35.1.00130766652PMC6354945
69

Oppong, A., Appiah Jnr, K., Appiah-Kubi, Z., Adu-Amoah, R., Adu-Dapaah, H. 2022. Mitigating aflatoxin contamination in maize: Breeding for stable resistant cultivars. Frontiers in Horticulture 1: 1029804. https://doi.org/10.3389/fhort.2022.1029804

10.3389/fhort.2022.1029804
70

Ortega-Beltran, A., Bandyopadhyay, R. 2021. Contributions of integrated aflatoxin management strategies to achieve the sustainable development goals in various African countries. Global Food Security 30: 100559. https://doi.org/10.1016/j.gfs.2021.100559

10.1016/j.gfs.2021.100559
71

Ortiz, C.S., Richards, C., Terry, A., Parra, J., Shim, W.B. 2015. Genetic variability and geographical distribution of mycotoxigenic Fusarium verticillioides strains isolated from maize fields in Texas. Plant Pathology Journal 31(3): 203-211. https://doi.org/10.5423/PPJ.OA.02.2015.0020

10.5423/PPJ.OA.02.2015.002026361468PMC4564145
72

Pandey, A.K., Samota, M.K., Kumar, A., Silva, A.S., Dubey, N.K. 2023. Fungal mycotoxins in food commodities: present status and future concerns. Frontiers in Sustainable Food Systems 7: 1162595. https://doi.org/10.3389/fsufs.2023.1162595

10.3389/fsufs.2023.1162595
73

Pantano, L., La Scala, L., Olibrio, F., Galluzzo, F. G., Bongiorno, C., Buscemi, M.D., Macaluso, A., Vella, A. 2021. QuEChERS LC-MS/MS screening method for mycotoxin detection in cereal products and spices. International Journal of Environmental Research and Public Health 18(7): 3774. https://doi.org/10.3390/ijerph18073774

10.3390/ijerph1807377433916634PMC8038554
74

Peles, F., Sipos, P., Kovács, S., Győri, Z., Pócsi, I., Pusztahelyi, T. 2021. Biological control and mitigation of aflatoxin contamination in commodities. Toxins 13(2): 104. https://doi.org/10.3390/toxins13020104

10.3390/toxins1302010433535580PMC7912779
75

Petrović, E., Ćosić, J., Vrandečić, K., Godena, S. 2023. Occurrence of mycotoxins in food and beverages. Journal of Central European Agriculture 24(1): 137-150. https://doi.org/10.5513/JCEA01/24.1.3704

10.5513/JCEA01/24.1.3704
76

Phokane, S., Flett, B.C., Ncube, E., Rheeder, J.P., Rose, L.J. 2019. Agricultural practices and their potential role in mycotoxin contamination of maize and groundnut subsistence farming. South African Journal of Science 115(9-10): 6221. https://doi.org/10.17159/sajs.2019/6221

10.17159/sajs.2019/6221
77

Płaza-Altamer, A., Nizioł, J., Ruman, T. 2024. Analysis of mycotoxins using laser desorption/ionization mass spectrometry with infrared pulsed fiber laser-produced silver-109-nanoparticles. Chemical Technology & Biotechnology, 109-114. https://doi.org/10.7862/rc.2024.7

10.7862/rc.2024.7
78

Prajapati, S., Kumar, N., Kumar, S., Iakharan, L., Maurya, S. 2020. Biological control a sustainable approach for plant diseases management: A review. Journal of Pharmacognosy and Phytochemistry 9(2): 1514-1523.

79

Pustjens, A.M., Castenmiller, J.J.M., te Biesebeek, J.D., de Rijk, T.C., van Dam, R.C.J., Boon, P.E. 2022. Dietary exposure to mycotoxins of 1- and 2-year-old children from a Dutch Total Diet Study. World Mycotoxin Journal 15(1): 85-97. https://doi.org/10.3920/WMJ2020.2676

10.3920/WMJ2020.2676
80

Reddy, L., Bhoola, K. 2010. Ochratoxins-food contaminants: Impact on human health. Toxins 2(4): 771-779. https://doi.org/10.3390/toxins2040771

10.3390/toxins204077122069609PMC3153213
81

Rodrigues, I., Naehrer, K. 2012. A three-year survey on the worldwide occurrence of mycotoxins in feedstuffs and feed. Toxins 4(9): 663-675. https://doi.org/10.3390/toxins4090663

10.3390/toxins409066323105974PMC3475222
82

Roucou, A., Bergez, C., Méléard, B., Orlando, B. 2021. A fumonisin prevention tool for targeting and ranking agroclimatic conditions favoring exposure in French maize-growing areas. Toxins 13(3): 214. https://doi.org/10.3390/toxins13030214

10.3390/toxins1303021433809408PMC8001851
83

Sharma, R., Saini, P., Kanwar, A., Saharan, M., Nitin, J. M. 2023. A review of various methods for the detection of foodborne pathogens and toxins. International Journal of Veterinary Sciences and Animal Husbandry 8(6): 77-81. https://doi.org/10.22271/veterinary.2023.v8.i6b.814

10.22271/veterinary.2023.v8.i6b.814
84

Stagnati, L., Martino, M., Battilani, P., Busconi, M., Lanubile, A., Marocco, A. 2020. Development of early maturity maize hybrids for resistance to fusarium and aspergillus ear rots and their associated mycotoxins. World Mycotoxin Journal 13(4): 459-471. https://doi.org/10.3920/WMJ2019.2554

10.3920/WMJ2019.2554
85

Sultan, H.M., Nosheen, S., Qurat-Ul-Ain, Hafeez, F., Ahmed, U., Zubair, M., Bibi, A., Irfan, F. 2024. A comprehensive review on Aflatoxin contamination, its impact on human health and management strategies. Journal of Health and Rehabilitation Research 4(2): 1212-1220. https://doi.org/10.61919/jhrr.v4i2.1087

10.61919/jhrr.v4i2.1087
86

Syafinatunnajah, G., Rizkia, A., Widyantari, D.D., Putri, N.P.W.P.N., Budyono, C. 2023. Hepatocellular carcinoma: Risk factors and diagnosis. Jurnal Biologi Tropis 23(1): 236-244. https://doi.org/10.29303/jbt.v23i1.5750

10.29303/jbt.v23i1.5750
87

Tittlemier, S.A., Cramer, B., DeRosa, M.C., Lattanzio, V.M.T., Malone, R., Maragos, C., Stranska, M., Sumarah, M.W. 2023. Developments in mycotoxin analysis: an update for 2021-22. World Mycotoxin Journal 16(1): 3-24. https://doi.org/10.3920/WMJ2022.2822

10.3920/WMJ2022.2822
88

Torres, A.M., Barros, G.G., Palacios, S.A., Chulze, S.N., Battilani, P. 2014. Review on pre-and post-harvest management of peanuts to minimize aflatoxin contamination. Food Research International 62: 11-19. https://doi.org/10.1016/j.foodres.2014.02.023

10.1016/j.foodres.2014.02.023
89

Unnevehr, L.J., Grace, D. 2013. Aflatoxins - finding solutions for improved food safety. International Food Policy Research Institute. https://doi.org/10.2499/9780896296763

10.2499/9780896296763
90

Warburton, M.L., Jeffers, D., Smith, J.S., Scapim, C., Uhdre, R., Thrash, A., Williams, W.P. 2022. Comparative analysis of multiple GWAS results identifies metabolic pathways associated with resistance to A. flavus infection and aflatoxin accumulation in maize. Toxins 14(11): 738. https://doi.org/10.3390/toxins14110738

10.3390/toxins1411073836355988PMC9695789
91

Wen, J., Kong, W., Hu, Y., Wang, J., Yang, M. 2014. Multi-mycotoxins analysis in ginger and related products by UHPLC-FLR detection and LC-MS/MS confirmation. Food Control 43: 82-87. https://doi.org/10.1016/j.foodcont.2014.02.038

10.1016/j.foodcont.2014.02.038
92

Wu, Y., Yu, J., Li, F., Li, J., Shen, Z. 2020. A calibration curve implanted enzyme-linked immunosorbent assay for simultaneously quantitative determination of multiplex mycotoxins in cereal samples, soybean and peanut. Toxins 12(11): 718. https://doi.org/10.3390/toxins12110718

10.3390/toxins1211071833202953PMC7696722
93

Zanon, M.S.A., Bossa, M., Chiotta, M.L., Oddino, C., Giovanini, D., Cardoso, M.L., Bartosik, R.E., Chulze, S.N. 2022. Pre-harvest strategy for reducing aflatoxin accumulation during storage of maize in Argentina. International Journal of Food Microbiology 380: 109887. https://doi.org/10.1016/j.ijfoodmicro.2022.109887

10.1016/j.ijfoodmicro.2022.109887
94

Zhang, X., Yu, X., Wen, K., Li, C., Mujtaba Mari, G., Jiang, H., Shi, W., Shen, J., Wang, Z. 2017. Multiplex lateral flow immunoassays based on amorphous carbon nanoparticles for detecting three Fusantium mycotoxins in maize. Journal of Agricultural and Food Chemistry 65(36): 8063-8071. https://doi.org/10.1021/acs.jafc.7b02827

10.1021/acs.jafc.7b02827
95

Zingales, V., Taroncher, M., Martino, P.A., Ruiz, M.J., Caloni, F. 2022. Climate change and effects on molds and mycotoxins. Toxins 14(7): 445. https://doi.org/10.3390/toxins14070445

10.3390/toxins1407044535878185PMC9319892
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