Azaspiracid poisoning (AZP) toxins in shellfish: Toxicological and health considerations
It has been almost a decade since a previously unknown human toxic syndrome, azaspiracid poisoning (AZP), emerged as the cause of severe gastrointestinal illness in humans after the consumption of mussels ( Mytilus edulis). Structural studies indicated that these toxins, azaspiracids, were of a new...
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description | It has been almost a decade since a previously unknown human toxic syndrome, azaspiracid poisoning (AZP), emerged as the cause of severe gastrointestinal illness in humans after the consumption of mussels (
Mytilus edulis). Structural studies indicated that these toxins, azaspiracids, were of a new unprecedented class containing novel structural features. It is now known that the prevalent azaspiracids in mussels are AZA1, AZA2 and AZA3, which differ from each other in their degree of methylation. Several hydroxylated and carboxylated analogues of the main azaspiracids have also been identified, presumed to be metabolites of the main toxins. Since its first discovery in Irish mussels, the development of facile sensitive and selective LC-MS/MS methods has resulted in the discovery of AZA in other countries and in other species. Mice studies indicate that this toxin class can cause serious tissue injury, especially to the small intestine, and chronic exposure may increase the likelihood of the development of lung tumours. Studies also show that tissue recovery is very slow following exposure. These observations suggest that AZA is more dangerous than the other known classes of shellfish toxins. Consequently, in order to protect human consumers, proper risk assessment and regulatory control of shellfish and other affected species is of the utmost importance. |
doi_str_mv | 10.1016/j.toxicon.2009.09.009 |
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Mytilus edulis). Structural studies indicated that these toxins, azaspiracids, were of a new unprecedented class containing novel structural features. It is now known that the prevalent azaspiracids in mussels are AZA1, AZA2 and AZA3, which differ from each other in their degree of methylation. Several hydroxylated and carboxylated analogues of the main azaspiracids have also been identified, presumed to be metabolites of the main toxins. Since its first discovery in Irish mussels, the development of facile sensitive and selective LC-MS/MS methods has resulted in the discovery of AZA in other countries and in other species. Mice studies indicate that this toxin class can cause serious tissue injury, especially to the small intestine, and chronic exposure may increase the likelihood of the development of lung tumours. Studies also show that tissue recovery is very slow following exposure. These observations suggest that AZA is more dangerous than the other known classes of shellfish toxins. Consequently, in order to protect human consumers, proper risk assessment and regulatory control of shellfish and other affected species is of the utmost importance.</description><identifier>ISSN: 0041-0101</identifier><identifier>EISSN: 1879-3150</identifier><identifier>DOI: 10.1016/j.toxicon.2009.09.009</identifier><identifier>PMID: 20026101</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Animals ; Azaspiracids ; AZP ; Cell Line, Tumor ; Cell Survival - drug effects ; Chromatography, High Pressure Liquid ; Foodborne Diseases ; Human ; Humans ; Intestine, Small - drug effects ; Intestine, Small - ultrastructure ; LC-MS ; Lung Neoplasms - chemically induced ; Lung Neoplasms - pathology ; Marine ; Marine toxins ; Marine Toxins - chemistry ; Marine Toxins - poisoning ; Metabolites ; Methylation ; Mice ; Microscopy, Electron, Scanning ; Molecular Structure ; Mussels ; Mytilus edulis ; Mytilus edulis - chemistry ; Mytilus edulis - metabolism ; Neurons - drug effects ; Neurons - pathology ; Poisoning ; Shellfish ; Shellfish Poisoning - etiology ; Shellfish Poisoning - metabolism ; Spectrometry, Mass, Electrospray Ionization ; Spiro Compounds - chemistry ; Spiro Compounds - poisoning ; Tandem Mass Spectrometry ; Toxicity Tests ; Toxins ; Tumours</subject><ispartof>Toxicon (Oxford), 2010-08, Vol.56 (2), p.173-190</ispartof><rights>2009</rights><rights>Copyright 2009. Published by Elsevier Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c396t-68f72e212bfddb4e6d33e447f41192ec3d56a51905c43c04790b56225b550293</citedby><cites>FETCH-LOGICAL-c396t-68f72e212bfddb4e6d33e447f41192ec3d56a51905c43c04790b56225b550293</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.toxicon.2009.09.009$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20026101$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Furey, Ambrose</creatorcontrib><creatorcontrib>O'Doherty, Sinead</creatorcontrib><creatorcontrib>O'Callaghan, Keith</creatorcontrib><creatorcontrib>Lehane, Mary</creatorcontrib><creatorcontrib>James, Kevin J.</creatorcontrib><title>Azaspiracid poisoning (AZP) toxins in shellfish: Toxicological and health considerations</title><title>Toxicon (Oxford)</title><addtitle>Toxicon</addtitle><description>It has been almost a decade since a previously unknown human toxic syndrome, azaspiracid poisoning (AZP), emerged as the cause of severe gastrointestinal illness in humans after the consumption of mussels (
Mytilus edulis). Structural studies indicated that these toxins, azaspiracids, were of a new unprecedented class containing novel structural features. It is now known that the prevalent azaspiracids in mussels are AZA1, AZA2 and AZA3, which differ from each other in their degree of methylation. Several hydroxylated and carboxylated analogues of the main azaspiracids have also been identified, presumed to be metabolites of the main toxins. Since its first discovery in Irish mussels, the development of facile sensitive and selective LC-MS/MS methods has resulted in the discovery of AZA in other countries and in other species. Mice studies indicate that this toxin class can cause serious tissue injury, especially to the small intestine, and chronic exposure may increase the likelihood of the development of lung tumours. Studies also show that tissue recovery is very slow following exposure. These observations suggest that AZA is more dangerous than the other known classes of shellfish toxins. Consequently, in order to protect human consumers, proper risk assessment and regulatory control of shellfish and other affected species is of the utmost importance.</description><subject>Animals</subject><subject>Azaspiracids</subject><subject>AZP</subject><subject>Cell Line, Tumor</subject><subject>Cell Survival - drug effects</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Foodborne Diseases</subject><subject>Human</subject><subject>Humans</subject><subject>Intestine, Small - drug effects</subject><subject>Intestine, Small - ultrastructure</subject><subject>LC-MS</subject><subject>Lung Neoplasms - chemically induced</subject><subject>Lung Neoplasms - pathology</subject><subject>Marine</subject><subject>Marine toxins</subject><subject>Marine Toxins - chemistry</subject><subject>Marine Toxins - poisoning</subject><subject>Metabolites</subject><subject>Methylation</subject><subject>Mice</subject><subject>Microscopy, Electron, Scanning</subject><subject>Molecular Structure</subject><subject>Mussels</subject><subject>Mytilus edulis</subject><subject>Mytilus edulis - chemistry</subject><subject>Mytilus edulis - metabolism</subject><subject>Neurons - drug effects</subject><subject>Neurons - pathology</subject><subject>Poisoning</subject><subject>Shellfish</subject><subject>Shellfish Poisoning - etiology</subject><subject>Shellfish Poisoning - metabolism</subject><subject>Spectrometry, Mass, Electrospray Ionization</subject><subject>Spiro Compounds - chemistry</subject><subject>Spiro Compounds - poisoning</subject><subject>Tandem Mass Spectrometry</subject><subject>Toxicity Tests</subject><subject>Toxins</subject><subject>Tumours</subject><issn>0041-0101</issn><issn>1879-3150</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1PGzEQhq2qVQm0P6HIt8Jh07F37Y25VBHiS0JqDzkgLpbXniWONutgbyrg19dLAlekkWyNnvEzfgn5wWDKgMlfq-kQnrwN_ZQDqOlYoD6RCZvVqiiZgM9kAlCxAjJ-QA5TWgFAOVPyKznII1zm_oTczV9M2vhorHd0E3wKve8f6Mn8_u8pHQ19or6naYld1_q0PKOLV20XHrw1HTW9o0s03bCkeZfkHUYz-Hz7Rr60pkv4fX8ekcXlxeL8urj9c3VzPr8tbKnkUMhZW3PkjDetc02F0pUlVlXdVowpjrZ0QhrBFAhblRaqWkEjJOeiEQK4Ko_Iz92zmxget5gGvfbJ5mVNj2GbdC2BQ81ZnUmxI20MKUVs9Sb6tYnPmoEeI9UrvY9Uj5HqsWA0HO8N22aN7n3qLcMM_N4BmL_5z2PUyXrsLTof0Q7aBf-B4j9wYopH</recordid><startdate>20100815</startdate><enddate>20100815</enddate><creator>Furey, Ambrose</creator><creator>O'Doherty, Sinead</creator><creator>O'Callaghan, Keith</creator><creator>Lehane, Mary</creator><creator>James, Kevin J.</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FD</scope><scope>FR3</scope><scope>KR7</scope></search><sort><creationdate>20100815</creationdate><title>Azaspiracid poisoning (AZP) toxins in shellfish: Toxicological and health considerations</title><author>Furey, Ambrose ; O'Doherty, Sinead ; O'Callaghan, Keith ; Lehane, Mary ; James, Kevin J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c396t-68f72e212bfddb4e6d33e447f41192ec3d56a51905c43c04790b56225b550293</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Animals</topic><topic>Azaspiracids</topic><topic>AZP</topic><topic>Cell Line, Tumor</topic><topic>Cell Survival - drug effects</topic><topic>Chromatography, High Pressure Liquid</topic><topic>Foodborne Diseases</topic><topic>Human</topic><topic>Humans</topic><topic>Intestine, Small - drug effects</topic><topic>Intestine, Small - ultrastructure</topic><topic>LC-MS</topic><topic>Lung Neoplasms - chemically induced</topic><topic>Lung Neoplasms - pathology</topic><topic>Marine</topic><topic>Marine toxins</topic><topic>Marine Toxins - chemistry</topic><topic>Marine Toxins - poisoning</topic><topic>Metabolites</topic><topic>Methylation</topic><topic>Mice</topic><topic>Microscopy, Electron, Scanning</topic><topic>Molecular Structure</topic><topic>Mussels</topic><topic>Mytilus edulis</topic><topic>Mytilus edulis - chemistry</topic><topic>Mytilus edulis - metabolism</topic><topic>Neurons - drug effects</topic><topic>Neurons - pathology</topic><topic>Poisoning</topic><topic>Shellfish</topic><topic>Shellfish Poisoning - etiology</topic><topic>Shellfish Poisoning - metabolism</topic><topic>Spectrometry, Mass, Electrospray Ionization</topic><topic>Spiro Compounds - chemistry</topic><topic>Spiro Compounds - poisoning</topic><topic>Tandem Mass Spectrometry</topic><topic>Toxicity Tests</topic><topic>Toxins</topic><topic>Tumours</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Furey, Ambrose</creatorcontrib><creatorcontrib>O'Doherty, Sinead</creatorcontrib><creatorcontrib>O'Callaghan, Keith</creatorcontrib><creatorcontrib>Lehane, Mary</creatorcontrib><creatorcontrib>James, Kevin J.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Civil Engineering Abstracts</collection><jtitle>Toxicon (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Furey, Ambrose</au><au>O'Doherty, Sinead</au><au>O'Callaghan, Keith</au><au>Lehane, Mary</au><au>James, Kevin J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Azaspiracid poisoning (AZP) toxins in shellfish: Toxicological and health considerations</atitle><jtitle>Toxicon (Oxford)</jtitle><addtitle>Toxicon</addtitle><date>2010-08-15</date><risdate>2010</risdate><volume>56</volume><issue>2</issue><spage>173</spage><epage>190</epage><pages>173-190</pages><issn>0041-0101</issn><eissn>1879-3150</eissn><abstract>It has been almost a decade since a previously unknown human toxic syndrome, azaspiracid poisoning (AZP), emerged as the cause of severe gastrointestinal illness in humans after the consumption of mussels (
Mytilus edulis). Structural studies indicated that these toxins, azaspiracids, were of a new unprecedented class containing novel structural features. It is now known that the prevalent azaspiracids in mussels are AZA1, AZA2 and AZA3, which differ from each other in their degree of methylation. Several hydroxylated and carboxylated analogues of the main azaspiracids have also been identified, presumed to be metabolites of the main toxins. Since its first discovery in Irish mussels, the development of facile sensitive and selective LC-MS/MS methods has resulted in the discovery of AZA in other countries and in other species. Mice studies indicate that this toxin class can cause serious tissue injury, especially to the small intestine, and chronic exposure may increase the likelihood of the development of lung tumours. Studies also show that tissue recovery is very slow following exposure. These observations suggest that AZA is more dangerous than the other known classes of shellfish toxins. Consequently, in order to protect human consumers, proper risk assessment and regulatory control of shellfish and other affected species is of the utmost importance.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>20026101</pmid><doi>10.1016/j.toxicon.2009.09.009</doi><tpages>18</tpages></addata></record> |
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subjects | Animals Azaspiracids AZP Cell Line, Tumor Cell Survival - drug effects Chromatography, High Pressure Liquid Foodborne Diseases Human Humans Intestine, Small - drug effects Intestine, Small - ultrastructure LC-MS Lung Neoplasms - chemically induced Lung Neoplasms - pathology Marine Marine toxins Marine Toxins - chemistry Marine Toxins - poisoning Metabolites Methylation Mice Microscopy, Electron, Scanning Molecular Structure Mussels Mytilus edulis Mytilus edulis - chemistry Mytilus edulis - metabolism Neurons - drug effects Neurons - pathology Poisoning Shellfish Shellfish Poisoning - etiology Shellfish Poisoning - metabolism Spectrometry, Mass, Electrospray Ionization Spiro Compounds - chemistry Spiro Compounds - poisoning Tandem Mass Spectrometry Toxicity Tests Toxins Tumours |
title | Azaspiracid poisoning (AZP) toxins in shellfish: Toxicological and health considerations |
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