Fast and Highly Sensitive Detection of Pathogens Wreathed with Magnetic Nanoparticles Using Dark-Field Microscopy

被引:22
作者
Chen, Fenglei [1 ]
Tang, Fang [2 ]
Yang, Chih-Tsung [3 ,4 ]
Zhao, Xinyao [5 ]
Wang, Jun [5 ]
Thierry, Benjamin [3 ,4 ]
Bansal, Vipul [6 ]
Dai, Jianjun [2 ]
Zhou, Xin [1 ]
机构
[1] Yangzhou Univ, Jiangsu Coinnovat Ctr Prevent & Control Important, Joint Int Res Lab Agr & Agri Prod Safety, Coll Vet Med,Minist Educ China, Yangzhou 225009, Jiangsu, Peoples R China
[2] Nanjing Agr Univ, Coll Vet Med, Key Lab Anim Bacteriol, Minist Agr, Nanjing 210095, Jiangsu, Peoples R China
[3] Univ South Australia, Future Ind Inst, Mawson Lakes Campus, Mawson Lakes, SA 5095, Australia
[4] Univ South Australia, ARC Ctr Excellence Convergent Bio & Nano Sci & Te, Mawson Lakes Campus, Mawson Lakes, SA 5095, Australia
[5] Southeast Univ, Sch Biol Sci & Med Engn, Nanjing 210009, Jiangsu, Peoples R China
[6] RMIT Univ, Sch Sci, NanoBiotechnol Res Lab, Ian Potter NanoBioSensing Facil, Melbourne, Vic 3001, Australia
基金
澳大利亚研究理事会; 中国国家自然科学基金;
关键词
pathogens detection; dark-field microscope; magnetic nanoparticles; Cryptosporidium parvum; garland-like structure; REAL-TIME PCR; ENHANCED LIGHT-SCATTERING; CRYPTOSPORIDIUM-PARVUM; IMMUNOMAGNETIC SEPARATION; RAPID DETECTION; SPP; OOCYSTS; GIARDIA; ASSAY; TRANSMISSION; PARASITES;
D O I
10.1021/acssensors.8b00785
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Cryptosporidium parvum (C. parvum) is a highly potent zoonotic pathogen, which can do significant harm to both human beings and livestock. However, existing technologies or methods are deficient for rapid on-site detection of water contaminated with C. parvum. Better detection approaches are needed to allow water management agencies to stop major breakouts of the pathogen. Herein, we present a novel detection method for cryptosporidium in a tiny drop of sample using a magnetic nanoparticle (MNP) probe combined with dark-field microscopy in 30 min. The designed MNP probes bind with high affinity to C. parvum, resulting in the formation of a golden garland-like structure under dark-field microscopy. This MNP-based dark-field counting strategy yields an amazing PCR-like sensitivity of 8 attomolar (aM) (5 pathogens in 1 mu L). Importantly, the assay is very rapid (similar to 30 min) and is very simple to perform as it involves only one step of mixing and magnetic separation, followed by dropping on a slide for counting under dark-field microscope. By combining the advantages of the specific light-scattering characteristic of MNP probe under dark field and the selective magnetic separation ability of functionalized MNP, the proposed MNP-based dark-field enumeration method offers low cost and significant translational potential.
引用
收藏
页码:2175 / 2181
页数:13
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