Congener-independent immunoassay for microcystins and nodularins

被引:216
作者
Fischer, WJ
Garthwaite, I
Miles, CO
Ross, KM
Aggen, JB
Chamberlin, AR
Towers, NR
Dietrich, DR [1 ]
机构
[1] Univ Konstanz, D-78457 Constance, Germany
[2] AgRes Ruakura, Toxinol & Food Safety Res, Hamilton, New Zealand
[3] Univ Calif Irvine, Dept Chem, Irvine, CA 92697 USA
[4] Nestec Ltd, Nestle Res Ctr, CH-1000 Lausanne 26, Switzerland
关键词
D O I
10.1021/es011182f
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Cyanobacteria (blue-green algae) (e.g., Microcystis and Nodularia spp.) capable of producing toxic peptides are found in fresh and brackish water worldwide. These toxins include the microcystin (MC) heptapeptides (> 60 congeners) and the nodularin pentapeptides (ca. 5 congeners). Cyanobacterial cyclic peptide toxins are harmful to man, other mammals, birds, and fish. Acute exposure to high concentrations of these toxins causes liver damage, while subchronic or chronic exposure may promote liver tumor formation. The detection of cyclic peptide cyanobacterial toxins in surface and drinking waters has been hampered by the low limits of detection required and that the present routine detection is restricted to a few of the congeners, The unusual beta -amino acid ADDA (4E,6E-3-amino-9-mothoxy-2,6,8-trimethyl-1-10-phenyldeca-4,6-dienoic acid) is present in most (> 80%) of the known toxic penta- and heptapeptide toxin congeners. Here, we report the synthesis of two ADDA-haptens, the raising of antibodies to ADDA, and the development of a competitive indirect ELISA for the detection of microcystins and nodularins utilizing these antibodies. The assay has a limit of quantitation of 0.02-0.07 ng/mL (depending on which congeners are present), lower than the WHO-proposed guideline (1 ng/mL) for drinking water, irrespective of the sample matrix (raw water, drinking water, or pure toxin in PBS). This new ELISA is robust, can be performed without sample preconcentration, detects toxins in freshwater samples at lower concentrations than does the protein phosphatase inhibition assay, and shows very good cross-reactivity with all cyanobacterial cyclic peptide toxin congeners tested to date (MC-LR, -RR, -YR, -LW, -LF, 3-desmethyl-MC-LR, 3-desmethyl-MIC-RR, and nodularin).
引用
收藏
页码:4849 / 4856
页数:8
相关论文
共 38 条
[1]   USE OF A COLORIMETRIC PROTEIN PHOSPHATASE INHIBITION ASSAY AND ENZYME-LINKED-IMMUNOSORBENT-ASSAY FOR THE STUDY OF MICROCYSTINS AND NODULARINS [J].
AN, JS ;
CARMICHAEL, WW .
TOXICON, 1994, 32 (12) :1495-1507
[2]  
[Anonymous], 1998, HLTH CRIT OTH SUPP I
[3]   Enzymatic pathway for the bacterial degradation of the cyanobacterial cyclic peptide toxin microcystin LR [J].
Bourne, DG ;
Jones, GJ ;
Blakeley, RL ;
Jones, A ;
Negri, AP ;
Riddles, P .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1996, 62 (11) :4086-4094
[4]   CYANOBACTERIA SECONDARY METABOLITES - THE CYANOTOXINS [J].
CARMICHAEL, WW .
JOURNAL OF APPLIED BACTERIOLOGY, 1992, 72 (06) :445-459
[5]  
Carmichael WW, 1997, ADV BOT RES, V27, P211
[6]   PRODUCTION AND CHARACTERIZATION OF ANTIBODIES AGAINST MICROCYSTINS [J].
CHU, FS ;
HUANG, X ;
WEI, RD ;
CARMICHAEL, WW .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1989, 55 (08) :1928-1933
[7]  
CHU FS, 1990, J ASSOC OFF ANA CHEM, V73, P451
[8]   MOTUPORIN, A POTENT PROTEIN PHOSPHATASE INHIBITOR ISOLATED FROM THE PAPUA-NEW-GUINEA SPONGE THEONELLA-SWINHOEI GRAY [J].
DESILVA, ED ;
WILLIAMS, DE ;
ANDERSEN, RJ ;
KLIX, H ;
HOLMES, CFB ;
ALLEN, TM .
TETRAHEDRON LETTERS, 1992, 33 (12) :1561-1564
[9]   ISOLATION AND CHARACTERIZATION OF THE MINOR COMPONENTS ASSOCIATED WITH MICROCYSTINS LR AND RR IN THE CYANOBACTERIUM (BLUE-GREEN-ALGAE) [J].
HARADA, K ;
MATSUURA, K ;
SUZUKI, M ;
WATANABE, MF ;
OISHI, S ;
DAHLEM, AM ;
BEASLEY, VR ;
CARMICHAEL, WW .
TOXICON, 1990, 28 (01) :55-64
[10]  
Harada K., 1996, TOXIC MICROCYSTIS, P103