Trichothecene: Difference between revisions
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{{short description|A group of mycotoxins produced by various fungi}} | |||
{{Use dmy dates|date=October 2023}} | |||
'''Trichothecenes''' are a group of [[mycotoxins]] produced by various species of [[fungi]], particularly those belonging to the genera ''[[Fusarium]]'', ''[[Myrothecium]]'', ''[[Trichoderma]]'', and ''[[Stachybotrys]]''. These compounds are known for their potent [[toxicity]] and have been implicated in a variety of [[animal]] and [[human]] health issues. | |||
==Structure and Classification== | |||
Trichothecenes are [[sesquiterpenes]] characterized by a [[tricyclic]] 12,13-epoxytrichothec-9-ene skeleton. They are divided into four main types based on their chemical structure: Type A, Type B, Type C, and Type D. Each type has distinct functional groups that influence their [[biological activity]] and [[toxicity]]. | |||
[[File:Trichothecenes.png|thumb|right|Chemical structure of trichothecenes.]] | |||
===Type A=== | |||
Type A trichothecenes, such as [[T-2 toxin]] and [[HT-2 toxin]], lack a ketone group at the C-8 position. They are among the most toxic trichothecenes and are known to inhibit [[protein synthesis]]. | |||
===Type B=== | |||
Type B trichothecenes, including [[deoxynivalenol]] (DON) and [[nivalenol]], possess a ketone group at the C-8 position. These compounds are commonly found in [[contaminated]] [[cereal]] grains. | |||
===Type C=== | |||
Type C trichothecenes have an additional epoxide group, which increases their [[reactivity]] and potential [[toxicity]]. | |||
== | ===Type D=== | ||
Type D trichothecenes are characterized by a macrocyclic ring, which is formed by esterification of the hydroxyl groups. This structure is found in compounds like [[satratoxin]] and [[verrucarin]]. | |||
[[File:Tricothecene_Classifications.jpg|thumb|right|Classification of trichothecenes.]] | |||
==Mechanism of Action== | |||
Trichothecenes exert their toxic effects primarily by inhibiting [[protein synthesis]] in [[eukaryotic cells]]. They bind to the 60S ribosomal subunit, preventing the elongation of the [[polypeptide]] chain. This inhibition leads to [[cell death]] and [[apoptosis]]. | |||
[[File:Control_Of_The_Apoptosis_Mecanisms.pdf|thumb|right|Mechanisms of apoptosis control by trichothecenes.]] | |||
==Health Effects== | |||
Exposure to trichothecenes can cause a range of health effects, including [[gastrointestinal]] distress, [[immunosuppression]], and [[dermatitis]]. In severe cases, exposure can lead to [[hemorrhagic]] [[syndrome]]s and [[neurotoxicity]]. | |||
== | ===Alimentary Toxic Aleukia=== | ||
One of the most notorious outbreaks associated with trichothecenes is [[alimentary toxic aleukia]] (ATA), which occurred in the [[Soviet Union]] during the 1940s. This condition was caused by the consumption of [[moldy]] [[grain]] contaminated with trichothecenes. | |||
[[File:Alimentary_Toxic_Aleukia.png|thumb|right|Symptoms of alimentary toxic aleukia.]] | |||
== | ==Decontamination and Control== | ||
Decontamination of trichothecene-contaminated materials is challenging due to their [[chemical stability]]. Methods such as [[deepoxydation]] and [[thermal]] [[degradation]] have been explored to reduce their [[toxicity]]. | |||
[[File:Deepoxydation.jpg|thumb|right|Deepoxydation process for trichothecene decontamination.]] | |||
[[ | ==Related Pages== | ||
[[ | * [[Mycotoxin]] | ||
[[ | * [[Fusarium]] | ||
* [[Deoxynivalenol]] | |||
* [[Stachybotrys]] | |||
{{ | ==References== | ||
{{Reflist}} | |||
[[Category:Mycotoxins]] | |||
[[Category:Sesquiterpenes]] | |||
[[Category:Fungal toxins]] | |||
Latest revision as of 23:52, 9 February 2025
A group of mycotoxins produced by various fungi
Trichothecenes are a group of mycotoxins produced by various species of fungi, particularly those belonging to the genera Fusarium, Myrothecium, Trichoderma, and Stachybotrys. These compounds are known for their potent toxicity and have been implicated in a variety of animal and human health issues.
Structure and Classification[edit]
Trichothecenes are sesquiterpenes characterized by a tricyclic 12,13-epoxytrichothec-9-ene skeleton. They are divided into four main types based on their chemical structure: Type A, Type B, Type C, and Type D. Each type has distinct functional groups that influence their biological activity and toxicity.

Type A[edit]
Type A trichothecenes, such as T-2 toxin and HT-2 toxin, lack a ketone group at the C-8 position. They are among the most toxic trichothecenes and are known to inhibit protein synthesis.
Type B[edit]
Type B trichothecenes, including deoxynivalenol (DON) and nivalenol, possess a ketone group at the C-8 position. These compounds are commonly found in contaminated cereal grains.
Type C[edit]
Type C trichothecenes have an additional epoxide group, which increases their reactivity and potential toxicity.
Type D[edit]
Type D trichothecenes are characterized by a macrocyclic ring, which is formed by esterification of the hydroxyl groups. This structure is found in compounds like satratoxin and verrucarin.

Mechanism of Action[edit]
Trichothecenes exert their toxic effects primarily by inhibiting protein synthesis in eukaryotic cells. They bind to the 60S ribosomal subunit, preventing the elongation of the polypeptide chain. This inhibition leads to cell death and apoptosis.
File:Control Of The Apoptosis Mecanisms.pdf
Health Effects[edit]
Exposure to trichothecenes can cause a range of health effects, including gastrointestinal distress, immunosuppression, and dermatitis. In severe cases, exposure can lead to hemorrhagic syndromes and neurotoxicity.
Alimentary Toxic Aleukia[edit]
One of the most notorious outbreaks associated with trichothecenes is alimentary toxic aleukia (ATA), which occurred in the Soviet Union during the 1940s. This condition was caused by the consumption of moldy grain contaminated with trichothecenes.

Decontamination and Control[edit]
Decontamination of trichothecene-contaminated materials is challenging due to their chemical stability. Methods such as deepoxydation and thermal degradation have been explored to reduce their toxicity.

Related Pages[edit]
References[edit]
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