Abstract
Kodo millet, a staple food in North India, is frequently consumed, but its consumption can lead to intoxication and poisoning. Kodo millet is a rich source of nutrition, with anti-oxidant and medicinal properties, and is typically cultivated in dry and semi-arid regions. It is often infected by fungal species rather than bacterial and virus pathogens, causing economic crop loss and adversely affecting grain and fodder yield. Ergot, a parasitic fungal endophyte found in Kodo millet ear heads, can cause poisoning when consumed. Moreover, Kodo millet grains are frequently infested with Aspergillus tamarii Kita, which produces a significant amount of the mycotoxin cyclopiazonic acid (CPA). Cyclopiazonic acid (CPA) is a neurotoxin produced by certain A. flavus and Aspergillus oryzae strains, which produce aflatoxins. Mycotoxicosis outbreaks in humans are not well characterized, and the direct correlation between mycotoxin consumption and toxic effects In Vivo is not well established. CPA, a specific inhibitor of sarcoplasmic reticulum Ca2+-ATPase, can adversely affect broiler chicken health, as demonstrated by toxicological evaluation of aflatoxins and CPA alone or in combination. Most toxins have reported acute and chronic effects in prokaryotic and eukaryotic systems, including humans, despite thefact that their specific modes of action are unclear. This review explores fungal pathogens, the toxicity of CPA to animals and humans, both by itself and in combination with other mycotoxins, as well as biocontrol strategies and storage methods for better utilization of Kodo grains post harvest.
Funding
This research received no external funding.
Institutional Review Board Statement
Not applicable.
Informed Consent Statement
Not applicable.
Data Availability Statement
No new data were created.
Conflicts of Interest
The author declares no conflicts of interest.
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