Department of Animal Sciences, Marine Animal Ecology Group, Wageningen University, Wageningen, The Netherlands.
Wetsus, European Centre of Excellence for Sustainable Water Technology, Leeuwarden, The Netherlands.
Environ Toxicol Chem. 2023 Jan;42(1):130-142. doi: 10.1002/etc.5505. Epub 2022 Dec 1.
Gene expression profiling in Caenorhabditis elegans has been demonstrated to be a potential bioanalytical tool to detect the toxic potency of environmental contaminants. The RNA transcripts of genes responding to toxic exposure can be used as biomarkers for detecting these toxins. For routine application in environmental quality monitoring, an easy-to-use multiplex assay is required to reliably quantify expression levels of these biomarkers. In the present study, a bead-based assay was developed to fingerprint gene expression in C. elegans by quantitating messenger RNAs (mRNAs) of multiple target genes directly from crude nematode lysates, circumventing RNA extraction and purification steps. The assay uses signal amplification rather than target amplification for direct measurement of toxin-induced RNA transcripts. Using a 50-gene panel, the expression changes of four candidate reference genes and 46 target mRNAs for various contaminants and wastewaters were successfully measured, and the expression profiles indicated the type of toxin present. Moreover, the multiplex assay response was in line with previous results obtained with more time-consuming reverse-transcription quantitative polymerase chain reaction and microarray analyses. In addition, the transcriptomic profiles of nematodes exposed to wastewater samples and extracts prepared from tissues of swimming crabs were evaluated. The profiles indicated the presence of organic pollutants. The present study illustrates the successful development of a multiplex fluorescent bead-based approach using nematode C. elegans crude lysates for gene expression profiling of target RNAs. This method can be used to routinely fingerprint the presence of toxic contaminants in environmental samples and to identify the most biologically active fraction of the contaminant mixture in a toxicity identification and evaluation approach. Environ Toxicol Chem 2023;42:130-142. © 2022 The Authors. Environmental Toxicology and Chemistry published by Wiley Periodicals LLC on behalf of SETAC.
在秀丽隐杆线虫中进行基因表达谱分析已被证明是一种潜在的生物分析工具,可用于检测环境污染物的毒性。对有毒暴露有反应的基因的 RNA 转录本可用作检测这些毒素的生物标志物。为了在环境质量监测中进行常规应用,需要一种易于使用的多重分析来可靠地定量这些生物标志物的表达水平。在本研究中,开发了一种基于珠子的测定法,通过直接从粗线虫裂解物中定量测定多个靶基因的信使 RNA(mRNA),从而在秀丽隐杆线虫中进行基因表达谱分析,绕过了 RNA 提取和纯化步骤。该测定法使用信号放大而不是靶标放大来直接测量毒素诱导的 RNA 转录物。使用 50 个基因组,成功测量了各种污染物和废水的四个候选参考基因和 46 个靶标 mRNA 的表达变化,并且表达谱表明存在的毒素类型。此外,多重分析的反应与使用更耗时的逆转录定量聚合酶链反应和微阵列分析获得的先前结果一致。此外,还评估了暴露于废水样品和用游泳蟹组织制备的提取物的线虫的转录组谱。这些图谱表明存在有机污染物。本研究说明了使用秀丽隐杆线虫粗裂解物成功开发用于靶标 RNA 基因表达谱分析的多重荧光珠基方法。该方法可用于常规鉴定环境样品中有毒污染物的存在,并在毒性鉴定和评估方法中识别污染物混合物中最具生物活性的部分。Environ Toxicol Chem 2023;42:130-142. © 2022 作者。环境毒理学和化学由 Wiley 期刊出版公司代表 SETAC 出版。