TY - JOUR
T1 - Hazard characterization of Alternaria toxins to identify data gaps and improve risk assessment for human health
AU - Louro, Henriqueta
AU - Vettorazzi, Ariane
AU - Mertens, Birgit
AU - Sanders, Julie
AU - López de Cerain, Adela
AU - Spyropoulou, Anastasia
AU - Solhaug, Anita
AU - Straumfors, Anne
AU - Behr, Anne-Cathrin
AU - Zegura, Bojana
AU - Kruse Faeste, Christiane
AU - Ndiaye, Dieynaba
AU - Spilioti, Eliana
AU - Varga, Elisabeth
AU - Dubreil, Estelle
AU - Borsos, Eszter
AU - Crudo, Francesco
AU - Sundstøl Eriksen, Gunnar
AU - Snapkow, Igor
AU - Henri, Jérôme
AU - Machera, Kyriaki
AU - Gaté, Laurent
AU - Le Hégarat, Ludovic
AU - Novak, Matjaž
AU - Smith, Nicola M.
AU - Krapf, Solveig
AU - Hager, Sonja
AU - Fessard, Valérie
AU - Kohl, Yvonne
AU - João Silva, Maria
AU - Dirven, Hubert
AU - Dietrich, Jessica
AU - Marko, Doris
N1 - Funding Information:
The European Partnership for the Assessment of Risks from Chemicals has received funding from the European Union\u2019s Horizon Europe research and innovation program under Grant Agreement No 101057014 and has received co-funding of the authors\u2019 institutions. Views and opinions expressed are, however, those of the author(s) only and do not necessarily reflect those of the European Union or the Health and Digital Executive Agency. Neither the European Union nor the granting authority can be held responsible for them.
Publisher Copyright:
© 2023, The Author(s).
PY - 2024/2
Y1 - 2024/2
N2 - Fungi of the genus Alternaria are ubiquitous plant pathogens and saprophytes which are able to grow under varying temperature and moisture conditions as well as on a large range of substrates. A spectrum of structurally diverse secondary metabolites with toxic potential has been identified, but occurrence and relative proportion of the different metabolites in complex mixtures depend on strain, substrate, and growth conditions. This review compiles the available knowledge on hazard identification and characterization of Alternaria toxins. Alternariol (AOH), its monomethylether AME and the perylene quinones altertoxin I (ATX-I), ATX-II, ATX-III, alterperylenol (ALP), and stemphyltoxin III (STTX-III) showed in vitro genotoxic and mutagenic properties. Of all identified Alternaria toxins, the epoxide-bearing analogs ATX-II, ATX-III, and STTX-III show the highest cytotoxic, genotoxic, and mutagenic potential in vitro. Under hormone-sensitive conditions, AOH and AME act as moderate xenoestrogens, but in silico modeling predicts further Alternaria toxins as potential estrogenic factors. Recent studies indicate also an immunosuppressive role of AOH and ATX-II; however, no data are available for the majority of Alternaria toxins. Overall, hazard characterization of Alternaria toxins focused, so far, primarily on the commercially available dibenzo-α-pyrones AOH and AME and tenuazonic acid (TeA). Limited data sets are available for altersetin (ALS), altenuene (ALT), and tentoxin (TEN). The occurrence and toxicological relevance of perylene quinone-based Alternaria toxins still remain to be fully elucidated. We identified data gaps on hazard identification and characterization crucial to improve risk assessment of Alternaria mycotoxins for consumers and occupationally exposed workers.
AB - Fungi of the genus Alternaria are ubiquitous plant pathogens and saprophytes which are able to grow under varying temperature and moisture conditions as well as on a large range of substrates. A spectrum of structurally diverse secondary metabolites with toxic potential has been identified, but occurrence and relative proportion of the different metabolites in complex mixtures depend on strain, substrate, and growth conditions. This review compiles the available knowledge on hazard identification and characterization of Alternaria toxins. Alternariol (AOH), its monomethylether AME and the perylene quinones altertoxin I (ATX-I), ATX-II, ATX-III, alterperylenol (ALP), and stemphyltoxin III (STTX-III) showed in vitro genotoxic and mutagenic properties. Of all identified Alternaria toxins, the epoxide-bearing analogs ATX-II, ATX-III, and STTX-III show the highest cytotoxic, genotoxic, and mutagenic potential in vitro. Under hormone-sensitive conditions, AOH and AME act as moderate xenoestrogens, but in silico modeling predicts further Alternaria toxins as potential estrogenic factors. Recent studies indicate also an immunosuppressive role of AOH and ATX-II; however, no data are available for the majority of Alternaria toxins. Overall, hazard characterization of Alternaria toxins focused, so far, primarily on the commercially available dibenzo-α-pyrones AOH and AME and tenuazonic acid (TeA). Limited data sets are available for altersetin (ALS), altenuene (ALT), and tentoxin (TEN). The occurrence and toxicological relevance of perylene quinone-based Alternaria toxins still remain to be fully elucidated. We identified data gaps on hazard identification and characterization crucial to improve risk assessment of Alternaria mycotoxins for consumers and occupationally exposed workers.
UR - http://www.scopus.com/inward/record.url?scp=85180709884&partnerID=8YFLogxK
U2 - 10.1007/s00204-023-03636-8
DO - 10.1007/s00204-023-03636-8
M3 - Article
C2 - 38147116
SN - 0340-5761
VL - 98
SP - 425
EP - 469
JO - Archives of Toxicology
JF - Archives of Toxicology
IS - 2
ER -