サルモネラ菌検出用バイオセンサー技術を開発(WPI Team Develops Sensor Technology to Detect Salmonella)

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20026-05-07 ウースター工科大学(WPI)

Worcester Polytechnic Instituteの研究チームは、有害細菌を迅速かつ高感度に検出できる新型バイオセンサーの開発を進めている。研究では、細菌特有の分子や代謝産物を認識する生体分子と微小電気デバイスを組み合わせ、食品、水質、医療分野でのリアルタイム検出を目指している。従来の培養法では結果取得に数日を要する場合があるが、新技術では短時間で汚染の有無を判定できる可能性がある。特に食中毒菌や病原性細菌の早期検出により、感染拡大防止や食品安全管理の高度化が期待される。また、小型・低コスト化により現場利用や携帯型診断機器への応用も視野に入る。研究チームは、センサー感度や特異性の向上を進めながら、将来的な実用化と産業応用を目指している。研究は、バイオセンシング技術と公衆衛生分野の発展に寄与する成果と位置付けられている。

サルモネラ菌検出用バイオセンサー技術を開発(WPI Team Develops Sensor Technology to Detect Salmonella)
An experimental microfluidic device containing two rectangular polymers coated with phages and covered with a biocompatible plastic tape was used in the research team’s experiments.

<関連情報>

ファージを搭載したマイクロ流体デバイスによる選択的細菌検出:現場での応用における高い可能性 Phage-Loaded Microfluidic Device for Selective Bacterium Detection with a High Potential for in-the-Field Applications

Hamed Ghavami,Christopher R. Lambert,Jessica Drozd,and Yuxiang Liu
ACS Applied Bio Materials  Published: April 14, 2026
DOI:https://doi.org/10.1021/acsabm.5c01652

Abstract

Detection of foodborne bacteria is critical because these pathogens cause foodborne outbreaks, which is a major public health concern worldwide. Conventional microbiological methods include plating and colony counting, molecular techniques such as polymerase chain reaction (PCR), and enzyme-linked immunosorbent assays (ELISA). These methods can be quite sensitive and specific, but they are also slow, require labor work, and often involve complex sample preparation. These limitations drive the development of faster and point-of-use detection techniques. In this study, we present a microfluidic biosensor platform based on P22 bacteriophage-loaded PDMS surfaces for rapid detection of Salmonella enterica. The PDMS surface had microscale topographical roughness, which helps improve immobilized phage concentration and promotes their capabilities to capture target bacteria. The system allows rapid bacteria detection with an experimentally demonstrated limit of detection of 9.15 × 103 cells/mL and a demonstrated specificity for Salmonella enterica over Staphylococcus aureus employed as a non-target control. Such detection was achieved under continuous flow conditions without the need of incubation, which implies its high potential for in-field applications and in resource-limited locations. This work demonstrates a rapid and selective approach for bacterial detection with strong potential for real-world food and water safety applications.

生物化学工学
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