Functional assays in marine biotoxin detection

被引:43
作者
Rossini, GP [1 ]
机构
[1] Univ Modena, Dipartimento Sci Biomed, I-41100 Modena, Italy
关键词
harmful algal blooms; in vitro assay; receptor; signal transduction; effector;
D O I
10.1016/j.tox.2004.10.012
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The contamination of seafood by algal toxins regularly affects animals living in several areas of the world, and the number of toxic phycotoxins which are being characterized is steadily increasing. The extreme dynamics characterizing the field of algal toxins has stimulated the development of tools to be implemented in the monitoring of contamination of seafood by individual toxin classes. Under these circumstances, functional assays which can encompass the analytical potential of chemical methods and the predictive features of biological tests are sought. A variety of functional assays for the detection of phycotoxins has been developed in the last 20 years, and the analysis of their features reveals that their specificity is related to the hierarchical level of the biological response to the toxin that has been exploited for its detection. Ideally, analytical methods which could allow accurate estimates of the overall toxicity of multiple classes of toxins in a single procedure would provide the best means for the highest standards in consumer protection and the most rational and economical tools in the management of risks posed by phycotoxins in a wider scale. The achievement of a "systemic functional assay for marine biotoxins" does not appear to be at hand, but its inclusion among the foreseeable events is fully justified by the new research tools and approaches which have become available for the high throughput analysis of entire molecular domains at the cellular level. (C) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:451 / 462
页数:12
相关论文
共 57 条
[21]   A TISSUE-CULTURE ASSAY FOR DIRECT DETECTION OF SODIUM-CHANNEL BLOCKING TOXINS IN BACTERIAL CULTURE SUPERNATES [J].
GALLACHER, S ;
BIRKBECK, TH .
FEMS MICROBIOLOGY LETTERS, 1992, 92 (01) :101-108
[22]  
Hallegraeff G.M., 2004, Manual on Harmful Marine Microalgae
[23]  
Hallegraeff GM, 2004, MANUAL HARMFUL MARIN
[24]   LIQUID CHROMATOGRAPHY-LINKED PROTEIN PHOSPHATASE BIOASSAY - A HIGHLY SENSITIVE MARINE BIOSCREEN FOR OKADAIC ACID AND RELATED DIARRHETIC SHELLFISH TOXINS [J].
HOLMES, CFB .
TOXICON, 1991, 29 (4-5) :469-477
[25]  
*JAP MIN HLTH WELF, 1981, FOOD SANITATION RES, V7, P60
[26]   PARALYTIC SHELLFISH POISON (SAXITOXIN FAMILY) BIOASSAYS - AUTOMATED END-POINT DETERMINATION AND STANDARDIZATION OF THE INVITRO TISSUE-CULTURE BIOASSAY, AND COMPARISON WITH THE STANDARD MOUSE BIOASSAY [J].
JELLETT, JF ;
MARKS, LJ ;
STEWART, JE ;
DOREY, ML ;
WATSONWRIGHT, W ;
LAWRENCE, JF .
TOXICON, 1992, 30 (10) :1143-1156
[27]   A TISSUE-CULTURE ASSAY FOR TETRODOTOXIN, SAXITOXIN AND RELATED TOXINS [J].
KOGURE, K ;
TAMPLIN, ML ;
SIMIDU, U ;
COLWELL, RR .
TOXICON, 1988, 26 (02) :191-197
[28]   Development of a F actin-based live-cell fluorimetric microplate assay for diarrhetic shellfish toxins [J].
Leira, F ;
Alvarez, C ;
Cabado, AG ;
Vieites, JM ;
Vieytes, MR ;
Botana, LM .
ANALYTICAL BIOCHEMISTRY, 2003, 317 (02) :129-135
[29]   Characterization of F-actin depolymerization as a major toxic event induced by pectenotoxin-6 in neuroblastoma cells [J].
Leira, F ;
Cabado, AG ;
Vieytes, MR ;
Roman, Y ;
Alfonso, A ;
Botana, LM ;
Yasumoto, T ;
Malaguti, C ;
Rossini, GP .
BIOCHEMICAL PHARMACOLOGY, 2002, 63 (11) :1979-1988
[30]   Detection of sodium channel activators by a rapid fluorimetric microplate assay [J].
Louzao, MC ;
Vieytes, MR ;
Yasumoto, T ;
Botana, LM .
CHEMICAL RESEARCH IN TOXICOLOGY, 2004, 17 (04) :572-578