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用于产柱孢藻毒素蓝藻的实时荧光定量PCR检测方法的开发与现场测试。

Development and field testing of a real-time PCR assay for cylindrospermopsin-producing cyanobacteria.

作者信息

Rasmussen J P, Giglio S, Monis P T, Campbell R J, Saint C P

机构信息

Cooperative Centre for Water Quality and Treatment, Australian Water Quality Centre, SA Water Corporation, Salisbury, South Australia, Australia.

出版信息

J Appl Microbiol. 2008 May;104(5):1503-15. doi: 10.1111/j.1365-2672.2007.03676.x. Epub 2007 Dec 20.

Abstract

AIMS

To develop and test a real-time PCR assay to detect and quantify genes specific to Cylindrospermopsis sp. and cylindrospermopsin-producing cyanobacteria.

METHOD AND RESULTS

A duplex real-time PCR assay was developed that targets a cylindrospermopsin-specific and Cylindrospermopsis raciborskii-specific DNA sequence. The C. raciborskii-specific sequence was based on the rpoC1 DNA-dependent RNA polymerase gene, whilst the cylindrospermopsin-specific sequence was selected by surveying an extensive number of potential cylindrospermopsin-producing cyanobacterial strains for genes implicated in toxin production, aoaA, aoaB and aoaC. In toxic strains, sequences of each of these three genes were always present; whilst in nontoxic strains the distribution of these sequences was patchy, resulting in what are likely to be natural deletion mutants. The real-time assay was optimized on a fixed and portable device, with results indicating that the reliable limit of detection for the assay was 100 copies per reaction or 1000 cells ml(-1) for both target sequences on both devices. In routine environmental samples enumerated by microscopy, the assay results were positive for all samples where C. raciborskii cells were observed at >1000 cells ml(-1) and negative in 15 samples where no C. raciborskii cells were observed. In field samples, the number of copies of the rpoC1 sequence more closely approximated the number of cells enumerated by microscopy, the number of copies of the pks sequence and detection of the toxin-specific sequence matched the results of toxin testing.

CONCLUSIONS

The duplex real-time PCR assay was a sensitive and rapid method for detecting potential cylindrospermopsin-producing cyanobacteria in the laboratory or in the field. The observation of probable natural deletion mutants provides further evidence that the aoaA, aoaB and aoaC genes are involved in toxin production.

SIGNIFICANCE AND IMPACT OF THE STUDY

This assay provides a new monitoring capability for tracking cylindrospermopsin-producing cyanobacteria that are an emerging threat to water quality.

摘要

目的

开发并测试一种实时荧光定量聚合酶链反应(PCR)检测方法,用于检测和定量圆柱鞘丝藻属特定基因以及产柱孢藻毒素的蓝藻细菌。

方法与结果

开发了一种双链实时荧光定量PCR检测方法,该方法针对柱孢藻毒素特异性和拉氏圆柱鞘丝藻特异性DNA序列。拉氏圆柱鞘丝藻特异性序列基于rpoC1 DNA依赖性RNA聚合酶基因,而柱孢藻毒素特异性序列是通过对大量潜在产柱孢藻毒素的蓝藻细菌菌株进行调查,筛选出与毒素产生相关的基因aoaA、aoaB和aoaC后选定的。在有毒菌株中,这三个基因的序列总是存在;而在无毒菌株中,这些序列的分布是不连续的,这可能导致了自然缺失突变体的产生。该实时检测方法在固定便携式设备上进行了优化,结果表明该检测方法在两种设备上对两个靶序列的可靠检测限均为每个反应100个拷贝或每毫升1000个细胞。在通过显微镜计数的常规环境样本中,对于所有观察到拉氏圆柱鞘丝藻细胞浓度大于每毫升1000个细胞的样本,检测结果均为阳性;而在15个未观察到拉氏圆柱鞘丝藻细胞的样本中,检测结果均为阴性。在野外样本中,rpoC1序列的拷贝数更接近显微镜计数的细胞数,pks序列的拷贝数以及毒素特异性序列的检测结果与毒素检测结果相符。

结论

双链实时荧光定量PCR检测方法是一种在实验室或野外检测潜在产柱孢藻毒素蓝藻细菌的灵敏且快速的方法。对可能的自然缺失突变体的观察提供了进一步证据,证明aoaA、aoaB和aoaC基因与毒素产生有关。

研究的意义和影响

该检测方法为追踪对水质构成新威胁的产柱孢藻毒素蓝藻细菌提供了一种新的监测能力。

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