Metagenomic Sequencing and Quantitative Real-Time PCR for Fecal Pollution Assessment in an Urban Watershed

被引:21
作者
Brumfield, Kyle D. [1 ,2 ]
Cotruvo, Joseph A. [3 ]
Shanks, Orin C. [4 ]
Sivaganesan, Mano [4 ]
Hey, Jessica [4 ]
Hasan, Nur A. [2 ]
Huq, Anwar [1 ]
Colwell, Rita R. [1 ,2 ,5 ]
Leddy, Menu B. [6 ]
机构
[1] Univ Maryland, Maryland Pathogen Res Inst, College Pk, MD 20742 USA
[2] Univ Maryland, Inst Adv Comp Studies, College Pk, MD 20742 USA
[3] Joseph Cotruvo & Associates LLC, Washington, DC USA
[4] US EPA, Off Res & Dev, Cincinnati, OH 45268 USA
[5] CosmosID Inc, Rockville, MD 20850 USA
[6] Essential Environm & Engn Syst, Huntington Beach, CA 92649 USA
来源
FRONTIERS IN WATER | 2021年 / 3卷
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
whole metagenome sequence; fecal indicator bacteria; microbial source tracking; quantitative real-time PCR; metagenomic analysis; culture; rainfall-runoff; WATERBORNE DISEASE OUTBREAKS; ANTIBIOTIC-RESISTANCE GENES; RIBOSOMAL-RNA; AEROMONAS-HYDROPHILA; BACTERIAL COMMUNITY; UNITED-STATES; CONTAMINATION; MARKERS; IDENTIFICATION; ASSAYS;
D O I
10.3389/frwa.2021.626849
中图分类号
TV21 [水资源调查与水利规划];
学科分类号
081501 ;
摘要
Microbial contamination of recreation waters is a major concern globally, with pollutants originating from many sources, including human and other animal wastes often introduced during storm events. Fecal contamination is traditionally monitored by employing culture methods targeting fecal indicator bacteria (FIB), namely E. coli and enterococci, which provides only limited information of a few microbial taxa and no information on their sources. Host-associated qPCR and metagenomic DNA sequencing are complementary methods for FIB monitoring that can provide enhanced understanding of microbial communities and sources of fecal pollution. Whole metagenome sequencing (WMS), quantitative real-time PCR (qPCR), and culture-based FIB tests were performed in an urban watershed before and after a rainfall event to determine the feasibility and application of employing a multi-assay approach for examining microbial content of ambient source waters. Cultivated E. coli and enterococci enumeration confirmed presence of fecal contamination in all samples exceeding local single sample recreational water quality thresholds (E. coli, 410 MPN/100 mL; enterococci, 107 MPN/100 mL) following a rainfall. Test results obtained with qPCR showed concentrations of E. coli, enterococci, and human-associated genetic markers increased after rainfall by 1.52-, 1.26-, and 1.11-fold log(10) copies per 100 mL, respectively. Taxonomic analysis of the surface water microbiome and detection of antibiotic resistance genes, general FIB, and human-associated microorganisms were also employed. Results showed that fecal contamination from multiple sources (human, avian, dog, and ruminant), as well as FIB, enteric microorganisms, and antibiotic resistance genes increased demonstrably after a storm event. In summary, the addition of qPCR and WMS to traditional surrogate techniques may provide enhanced characterization and improved understanding of microbial pollution sources in ambient waters.
引用
收藏
页数:17
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