• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

基于注射器的生物传感器,利用工程噬菌体快速检测饮用水中的低浓度大肠杆菌(ECOR13)。

A Syringe-Based Biosensor to Rapidly Detect Low Levels of Escherichia Coli (ECOR13) in Drinking Water Using Engineered Bacteriophages.

机构信息

Department of Food Science, Cornell University, Ithaca, NY 14853, USA.

Intellectual Ventures Laboratory/Global Good, Bellevue, WA 98007, USA.

出版信息

Sensors (Basel). 2020 Mar 31;20(7):1953. doi: 10.3390/s20071953.

DOI:10.3390/s20071953
PMID:32244369
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7181147/
Abstract

A sanitized drinking water supply is an unconditional requirement for public health and the overall prosperity of humanity. Potential microbial and chemical contaminants of drinking water have been identified by a joint effort between the World Health Organization (WHO) and the United Nations Children's Fund (UNICEF), who together establish guidelines that define, in part, that the presence of () in drinking water is an indication of inadequate sanitation and a significant health risk. As is a nearly ubiquitous resident of mammalian gastrointestinal tracts, no detectable counts in 100 mL of drinking water is the standard used worldwide as an indicator of sanitation. The currently accepted EPA method relies on filtration, followed by growth on selective media, and requires 24-48 h from sample to results. In response, we developed a rapid bacteriophage-based detection assay with detection limit capabilities comparable to traditional methods in less than a quarter of the time. We coupled membrane filtration with selective enrichment using genetically engineered bacteriophages to identify less than 20 colony forming units (CFU) in 100 mL drinking water within 5 h. The combination of membrane filtration with phage infection produced a novel assay that demonstrated a rapid, selective, and sensitive detection of an indicator organism in large volumes of drinking water as recommended by the leading world regulatory authorities.

摘要

提供清洁饮用水是公共卫生和全人类繁荣的必要条件。世界卫生组织(WHO)和联合国儿童基金会(UNICEF)共同努力,确定了饮用水中可能存在的微生物和化学污染物。这两个组织共同制定了指导方针,部分规定了饮用水中()的存在表明卫生条件不足,存在重大健康风险。由于()几乎普遍存在于哺乳动物的胃肠道中,因此,100 毫升饮用水中未检测到()的计数被全世界用作卫生指标。目前,美国环保署(EPA)认可的方法依赖于过滤,然后在选择性培养基上生长,从采样到得出结果需要 24-48 小时。有鉴于此,我们开发了一种快速基于噬菌体的检测方法,其检测限能力与传统方法相当,但所需时间不到其四分之一。我们将膜过滤与使用基因工程噬菌体进行选择性富集相结合,在 5 小时内从 100 毫升饮用水中鉴定出不到 20 个菌落形成单位(CFU)。膜过滤与噬菌体感染的结合产生了一种新的检测方法,该方法可快速、选择性和灵敏地检测大量饮用水中的指示生物,符合世界主要监管机构的建议。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b474/7181147/62ea7050e8b0/sensors-20-01953-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b474/7181147/39a89affa842/sensors-20-01953-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b474/7181147/fbc693bcc4fb/sensors-20-01953-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b474/7181147/84faaf69a344/sensors-20-01953-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b474/7181147/d959d8c7ee5a/sensors-20-01953-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b474/7181147/6c5e1c121022/sensors-20-01953-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b474/7181147/62ea7050e8b0/sensors-20-01953-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b474/7181147/39a89affa842/sensors-20-01953-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b474/7181147/fbc693bcc4fb/sensors-20-01953-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b474/7181147/84faaf69a344/sensors-20-01953-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b474/7181147/d959d8c7ee5a/sensors-20-01953-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b474/7181147/6c5e1c121022/sensors-20-01953-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b474/7181147/62ea7050e8b0/sensors-20-01953-g006.jpg

相似文献

1
A Syringe-Based Biosensor to Rapidly Detect Low Levels of Escherichia Coli (ECOR13) in Drinking Water Using Engineered Bacteriophages.基于注射器的生物传感器,利用工程噬菌体快速检测饮用水中的低浓度大肠杆菌(ECOR13)。
Sensors (Basel). 2020 Mar 31;20(7):1953. doi: 10.3390/s20071953.
2
Filter-based assay for Escherichia coli in aqueous samples using bacteriophage-based amplification.基于噬菌体扩增的水样中大肠杆菌的滤膜法检测。
Anal Chem. 2013 Aug 6;85(15):7213-20. doi: 10.1021/ac400961b. Epub 2013 Jul 12.
3
A phage-based assay for the rapid, quantitative, and single CFU visualization of E. coli (ECOR #13) in drinking water.基于噬菌体的检测方法,可快速、定量、单 CFU 可视化检测饮用水中的大肠杆菌 (ECOR #13)。
Sci Rep. 2018 Oct 2;8(1):14630. doi: 10.1038/s41598-018-33097-4.
4
Reporter bacteriophage T7 utilizes a novel NanoLuc::CBM fusion for the ultrasensitive detection of Escherichia coli in water.报告噬菌体 T7 利用一种新颖的 NanoLuc::CBM 融合蛋白对水中的大肠杆菌进行超灵敏检测。
Analyst. 2018 Aug 20;143(17):4074-4082. doi: 10.1039/c8an00781k.
5
Phage based electrochemical detection of Escherichia coli in drinking water using affinity reporter probes.基于噬菌体的电化学检测饮用水中的大肠杆菌使用亲和报告探针。
Analyst. 2019 Feb 11;144(4):1345-1352. doi: 10.1039/c8an01850b.
6
Development of a biosensor protein bullet as a fluorescent method for fast detection of Escherichia coli in drinking water.开发一种生物传感器蛋白子弹作为快速检测饮用水中大肠杆菌的荧光方法。
PLoS One. 2018 Jan 5;13(1):e0184277. doi: 10.1371/journal.pone.0184277. eCollection 2018.
7
A microfluidic device and instrument prototypes for the detection of in water samples using a phage-based bioluminescence assay.基于噬菌体生物发光检测法的水中检测的微流控装置和仪器原型。
Lab Chip. 2022 May 31;22(11):2155-2164. doi: 10.1039/d1lc00888a.
8
Bacterial contamination of drinking water sources in rural villages of Mohale Basin, Lesotho: exposures through neighbourhood sanitation and hygiene practices.莱索托莫哈利流域农村村庄饮用水源的细菌污染:通过邻里环境卫生和卫生习惯的暴露。
Environ Health Prev Med. 2019 May 15;24(1):33. doi: 10.1186/s12199-019-0790-z.
9
Qualitative detection of E. coli in distributed drinking water using real-time reverse transcription PCR targeting 16S rRNA: Validation and practical experiences.采用实时荧光 RT-PCR 检测 16S rRNA 对分散式饮用水中大肠杆菌的定性检测:验证和实际经验。
Water Res. 2024 Aug 1;259:121843. doi: 10.1016/j.watres.2024.121843. Epub 2024 May 28.
10
A biosensor platform for rapid detection of E. coli in drinking water.一种用于快速检测饮用水中大肠杆菌的生物传感器平台。
Enzyme Microb Technol. 2016 Feb;83:22-8. doi: 10.1016/j.enzmictec.2015.11.007. Epub 2015 Nov 26.

引用本文的文献

1
Biosensor: An Emerging Technological Tool for Microorganisms and Its Disease Diagnosis.生物传感器:一种用于微生物及其疾病诊断的新兴技术工具。
Indian J Microbiol. 2023 Dec;63(4):395-397. doi: 10.1007/s12088-023-01142-0. Epub 2023 Nov 17.
2
Bacteriophage-Based Biosensors: A Platform for Detection of Foodborne Bacterial Pathogens from Food and Environment.基于噬菌体的生物传感器:从食物和环境中检测食源性病原体细菌的平台。
Biosensors (Basel). 2022 Oct 21;12(10):905. doi: 10.3390/bios12100905.
3
Comparative Analysis of NanoLuc Luciferase and Alkaline Phosphatase Luminescence Reporter Systems for Phage-Based Detection of Bacteria.

本文引用的文献

1
A phage-based assay for the rapid, quantitative, and single CFU visualization of E. coli (ECOR #13) in drinking water.基于噬菌体的检测方法,可快速、定量、单 CFU 可视化检测饮用水中的大肠杆菌 (ECOR #13)。
Sci Rep. 2018 Oct 2;8(1):14630. doi: 10.1038/s41598-018-33097-4.
2
Reporter bacteriophage T7 utilizes a novel NanoLuc::CBM fusion for the ultrasensitive detection of Escherichia coli in water.报告噬菌体 T7 利用一种新颖的 NanoLuc::CBM 融合蛋白对水中的大肠杆菌进行超灵敏检测。
Analyst. 2018 Aug 20;143(17):4074-4082. doi: 10.1039/c8an00781k.
3
Efficacy of microbial sampling recommendations and practices in sub-Saharan Africa.
用于基于噬菌体的细菌检测的纳米荧光素酶和碱性磷酸酶发光报告系统的比较分析
Bioengineering (Basel). 2022 Sep 16;9(9):479. doi: 10.3390/bioengineering9090479.
4
The Use of Bacteriophages in Biotechnology and Recent Insights into Proteomics.噬菌体在生物技术中的应用及蛋白质组学的最新见解。
Antibiotics (Basel). 2022 May 13;11(5):653. doi: 10.3390/antibiotics11050653.
5
Luminescent Phage-Based Detection of : From Engineering to Diagnostics.基于发光噬菌体的检测:从工程到诊断
Pharmaceuticals (Basel). 2021 Apr 9;14(4):347. doi: 10.3390/ph14040347.
6
Application of Bacteriophages in Nanotechnology.噬菌体在纳米技术中的应用。
Nanomaterials (Basel). 2020 Sep 29;10(10):1944. doi: 10.3390/nano10101944.
7
Reporter Phage-Based Detection of Bacterial Pathogens: Design Guidelines and Recent Developments.基于噬菌体的细菌病原体检测:设计准则和最新进展。
Viruses. 2020 Aug 26;12(9):944. doi: 10.3390/v12090944.
8
Recent Progress in the Detection of Bacteria Using Bacteriophages: A Review.利用噬菌体检测细菌的最新进展:综述。
Viruses. 2020 Aug 3;12(8):845. doi: 10.3390/v12080845.
撒哈拉以南非洲微生物采样建议和实践的效果。
Water Res. 2018 May 1;134:115-125. doi: 10.1016/j.watres.2018.01.054. Epub 2018 Feb 3.
4
Recombinant Peptidomimetic-Nano Luciferase Tracers for Sensitive Single-Step Immunodetection of Small Molecules.用于小分子灵敏单步免疫检测的重组肽模拟物-纳米荧光素酶示踪剂。
Anal Chem. 2018 Feb 6;90(3):2230-2237. doi: 10.1021/acs.analchem.7b04601. Epub 2018 Jan 16.
5
Recent advances in bacteriophage-based methods for bacteria detection.基于噬菌体的细菌检测方法的最新进展。
Drug Discov Today. 2018 Feb;23(2):448-455. doi: 10.1016/j.drudis.2017.11.007. Epub 2017 Nov 20.
6
Correlation between E. coli levels and the presence of foodborne pathogens in surface irrigation water: Establishment of a sampling program.大肠杆菌水平与地表灌溉水中食源性致病菌存在的相关性:采样方案的建立。
Water Res. 2018 Jan 1;128:226-233. doi: 10.1016/j.watres.2017.10.041. Epub 2017 Oct 23.
7
Current Technical Approaches for the Early Detection of Foodborne Pathogens: Challenges and Opportunities.当前用于食源性病原体早期检测的技术方法:挑战与机遇。
Int J Mol Sci. 2017 Sep 30;18(10):2078. doi: 10.3390/ijms18102078.
8
Detection of Bacillus anthracis spores from environmental water using bioluminescent reporter phage.利用生物发光报告噬菌体从环境水样中检测炭疽芽孢杆菌孢子。
J Appl Microbiol. 2017 Nov;123(5):1184-1193. doi: 10.1111/jam.13569. Epub 2017 Sep 21.
9
Sensitive detection of viable Escherichia coli O157:H7 from foods using a luciferase-reporter phage phiV10lux.利用荧光素酶报告噬菌体 phiV10lux 对食品中具有活力的大肠杆菌 O157:H7 进行灵敏检测。
Int J Food Microbiol. 2017 Aug 2;254:11-17. doi: 10.1016/j.ijfoodmicro.2017.05.002. Epub 2017 May 5.
10
Screening for Novel Small-Molecule Inhibitors Targeting the Assembly of Influenza Virus Polymerase Complex by a Bimolecular Luminescence Complementation-Based Reporter System.利用基于双分子发光互补的报告系统筛选靶向流感病毒聚合酶复合物组装的新型小分子抑制剂。
J Virol. 2017 Feb 14;91(5). doi: 10.1128/JVI.02282-16. Print 2017 Mar 1.