A new quantitative PCR assay for the detection of hepatotoxigenic cyanobacteria

被引:46
|
作者
Al-Tebrineh, J. [1 ]
Gehringer, M. M. [1 ]
Akcaalan, R. [2 ]
Neilan, B. A. [1 ]
机构
[1] Univ New S Wales, Sch Biotechnol & Biomol Sci, Sydney, NSW 2052, Australia
[2] Istanbul Univ, Fac Fisheries, Istanbul, Turkey
基金
澳大利亚研究理事会;
关键词
Microcystin; Nodularin; Quantitative PCR; Melt curve analysis; Cyanobacteria; Harmful algal bloom; REAL-TIME PCR; SYNTHETASE GENE; MICROCYSTIN BIOSYNTHESIS; NODULARIA CYANOBACTERIA; PEPTIDE HEPATOTOXINS; ANABAENA; EVOLUTION; STRAINS; IDENTIFICATION; PLANKTOTHRIX;
D O I
10.1016/j.toxicon.2010.12.018
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Toxin-producing cyanobacteria are a worldwide threat to both human and animal health. The hepatotoxins microcystin and nodularin are the most commonly occurring toxins produced by bloom-forming cyanobacteria. They are cyclic peptides that are synthesized nonribosomally by a multienzyme complexes encoded within the microcystin (mcyS) and nodularin (ndaS) synthetase gene clusters. Early detection of potentially toxic blooms would allow for pre-emptive action to reduce consumer exposure to cyanotoxins. We have developed a quantitative PCR (qPCR) assay based on SYBR-green chemistry for the detection of potentially hepatotoxic cyanobacteria spanning all known microcystin and nodularin producing taxa using primers specifically targeting mcyE and ndaF. The qPCR assay was validated against previously analyzed cyanobacterial bloom samples. Whole cell qPCR using cultured M. aeruginosa PCC7806 and non-toxic M. aeruginosa UTEX2386 had a sensitivity of 1000 cells ml(-1). In summary, we have developed a robust and sensitive molecular method for the detection and quantification of hepatotoxigenic cyanobacteria in bloom samples. This technology offers several advantages over traditional and contemporary testing protocols currently used to assess water quality. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:546 / 554
页数:9
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