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DOI10.1002/etc.3885
Tools to minimize interlaboratory variability in vitellogenin gene expression monitoring programs
Jastrow, Aaron1; Gordon, Denise A.2; Auger, Kasie M.3; Punska, Elizabeth C.3; Arcaro, Kathleen F.3; Keteles, Kristen4; Winkelman, Dana5; Lattier, David2; Biales, Adam2; Lazorchak, James M.2
发表日期2017-11-01
ISSN0730-7268
卷号36期号:11页码:3102-3107
英文摘要

The egg yolk precursor protein vitellogenin is widely used as a biomarker of estrogen exposure in male fish. However, standardized methodology is lacking and little is known regarding the reproducibility of results among laboratories using different equipment, reagents, protocols, and data analysis programs. To address this data gap we tested the reproducibility across laboratories to evaluate vitellogenin gene (vtg) expression and assessed the value of using a freely available software data analysis program. Samples collected from studies of male fathead minnows (Pimephales promelas) exposed to 17-ethinylestradiol (EE2) and minnows exposed to processed wastewater effluent were evaluated for vtg expression in 4 laboratories. Our results indicate reasonable consistency among laboratories if the free software for expression analysis LinRegPCR is used, with 3 of 4 laboratories detecting vtg in fish exposed to 5ng/L EE2 (n=5). All 4 laboratories detected significantly increased vtg levels in 15 male fish exposed to wastewater effluent compared with 15 male fish held in a control stream. Finally, we were able to determine that the source of high interlaboratory variability from complementary deoxyribonucleic acid (cDNA) to quantitative polymerase chain reaction (qPCR) analyses was the expression analysis software unique to each real-time qPCR machine. We successfully eliminated the interlaboratory variability by reanalyzing raw fluorescence data with independent freeware, which yielded cycle thresholds and polymerase chain reaction (PCR) efficiencies that calculated results independently of proprietary software. Our results suggest that laboratories engaged in monitoring programs should validate their PCR protocols and analyze their gene expression data following the guidelines established in the present study for all gene expression biomarkers. Environ Toxicol Chem 2017;36:3102-3107. Published 2017 Wiley Periodicals Inc. on behalf of SETAC. This article is a US government work and, as such, is in the public domain in the United States of America.


英文关键词Real-time polymerase chain reaction;Fathead minnow;Bioassay;Estrogen;Wastewater;Interlaboratory variability
语种英语
WOS记录号WOS:000413923500028
来源期刊ENVIRONMENTAL TOXICOLOGY AND CHEMISTRY
来源机构美国环保署
文献类型期刊论文
条目标识符http://gcip.llas.ac.cn/handle/2XKMVOVA/60485
作者单位1.US EPA, Reg Lab 5, Chicago, IL USA;
2.US EPA, Natl Exposure Res Lab, Off Res & Dev, Cincinnati, OH 45268 USA;
3.Univ Massachusetts, Dept Vet & Anim Sci, Amherst, MA 01003 USA;
4.US EPA, Natl Enforcement Invest Ctr, Denver, CO USA;
5.Colorado State Univ, US Geol Survey, Colorado Cooperat Fish & Wildlife Res Unit, Ft Collins, CO 80523 USA
推荐引用方式
GB/T 7714
Jastrow, Aaron,Gordon, Denise A.,Auger, Kasie M.,et al. Tools to minimize interlaboratory variability in vitellogenin gene expression monitoring programs[J]. 美国环保署,2017,36(11):3102-3107.
APA Jastrow, Aaron.,Gordon, Denise A..,Auger, Kasie M..,Punska, Elizabeth C..,Arcaro, Kathleen F..,...&Lazorchak, James M..(2017).Tools to minimize interlaboratory variability in vitellogenin gene expression monitoring programs.ENVIRONMENTAL TOXICOLOGY AND CHEMISTRY,36(11),3102-3107.
MLA Jastrow, Aaron,et al."Tools to minimize interlaboratory variability in vitellogenin gene expression monitoring programs".ENVIRONMENTAL TOXICOLOGY AND CHEMISTRY 36.11(2017):3102-3107.
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