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Highly sensitive SERS platform for pathogen analysis by cyclic DNA nanostructure@AuNP tags and cascade primer exchange reaction.


ABSTRACT: The capacity to identify small amounts of pathogens in real samples is extremely useful. Herein, we proposed a sensitive platform for detecting pathogens using cyclic DNA nanostructure@AuNP tags (CDNA) and a cascade primer exchange reaction (cPER). This platform employs wheat germ agglutinin-modified Fe3O4@Au magnetic nanoparticles (WMRs) to bind the E. coli O157:H7, and then triggers the cPER to generate branched DNA products for CDNA tag hybridization with high stability and amplified SERS signals. It can identify target pathogens as low as 1.91 CFU/mL and discriminate E. coli O157:H7 in complex samples such as water, milk, and serum, demonstrating comparable or greater sensitivity and accuracy than traditional qPCR. Moreover, the developed platform can detect low levels of E. coli O157:H7 in mouse serum, allowing the discrimination of mice with early-stage infection. Thus, this platform holds promise for food analysis and early infection diagnosis.

SUBMITTER: Xiao Y 

PROVIDER: S-EPMC10895721 | biostudies-literature | 2024 Feb

REPOSITORIES: biostudies-literature

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Highly sensitive SERS platform for pathogen analysis by cyclic DNA nanostructure@AuNP tags and cascade primer exchange reaction.

Xiao Yunju Y   Luo Shihua S   Qiu Jiuxiang J   Zhang Ye Y   Liu Weijiang W   Zhao Yunhu Y   Zhu YiTong Y   Deng Yangxi Y   Lu Mengdi M   Liu Suling S   Lin Yong Y   Huang Aiwei A   Wang Wen W   Hu Xuejiao X   Gu Bing B  

Journal of nanobiotechnology 20240226 1


The capacity to identify small amounts of pathogens in real samples is extremely useful. Herein, we proposed a sensitive platform for detecting pathogens using cyclic DNA nanostructure@AuNP tags (CDNA) and a cascade primer exchange reaction (cPER). This platform employs wheat germ agglutinin-modified Fe<sub>3</sub>O<sub>4</sub>@Au magnetic nanoparticles (WMRs) to bind the E. coli O157:H7, and then triggers the cPER to generate branched DNA products for CDNA tag hybridization with high stability  ...[more]

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