A new quantitative PCR assay for detection of potentially anatoxin-producing cyanobacteria

被引:0
作者
Jablonska, Masa [1 ,2 ]
Elersek, Tina [1 ]
机构
[1] Natl Inst Biol, Vecna Pot 121, Ljubljana 1000, Slovenia
[2] Univ Ljubljana, Jamnikova 101, Ljubljana 1000, Slovenia
关键词
Cyanotoxins; Water management; Early warning; Risk assessment; qPCR; ana gene cluster; anaC gene; 1ST REPORT; IDENTIFICATION; BIOSYNTHESIS; FRANCE; GENES;
D O I
10.1016/j.hal.2024.102785
中图分类号
Q17 [水生生物学];
学科分类号
071004 ;
摘要
Anatoxins (ATX) are globally occurring toxins produced by some species of cyanobacteria in aquatic habitats. They can cause acute poisoning in animals, leading to muscle paralysis and respiratory failure, and might also pose a long-term health risk to humans. Thanks to advances in molecular methods and genomic knowledge, it is now possible to rapidly detect and quantify the genes associated with cyanotoxin production for most major groups of cyanotoxins except ATX. The aim of this study was to develop and validate a new quantitative PCR (qPCR) assay for general detection of all potential ATX producers in the environment. After specificity testing in silico and in vitro with 16 cyanobacterial strains (endpoint PCR, amplicon sequencing and qPCR), two assays targeting the anaC gene were thoroughly validated for linearity, amplification efficiency, sensitivity, dynamic range, inter-assay and intra-assay variability, and the influence of background DNA. The assays were then applied to 144 environmental samples of plankton and biofilm from lakes and rivers whose ATX content had previously been measured by liquid chromatography with tandem mass spectrometry (LC-MS/MS). Amplification efficiency of the two designed assays was between 94 % and 103 %, and the limits of quantification and detection were up to, but mostly below, 322 and 32 cells/mL, respectively. Both assays showed better or equal specificity in cyanobacterial cultures than currently available PCR assays and were able to predict the presence of ATX detected by LC-MS/MS in most environmental samples (83 % in plankton and 52-62 % in biofilm). A higher number of discrepancies between qPCR and LC-MS/MS results in biofilm than in plankton samples indicates limited knowledge and sparse genomic data on benthic cyanobacteria. These assays are the first published general qPCR assays targeting all ATX producers and could provide water managers with a rapid and costeffective risk assessment to better protect human and animal health.
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页数:12
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