| Literature DB >> 27243947 |
Tomomi Yamasaki1, Shiro Miyake1,2, Satoshi Nakano3, Hiroyuki Morimura2, Yuki Hirakawa1, Miki Nagao3, Yoshio Iijima4, Hiroshi Narita5, Satoshi Ichiyama3.
Abstract
A surface plasmon resonance-based immunosensor (SPR-immunosensor) was developed for the detection of Shiga toxin-producing Escherichia coli (STEC) belonging to the O-antigen groups O26, O91, O103, O111, O115, O121, O128, O145, O157, and O159. The polyclonal antibodies (PoAbs) generated against each of the STEC O-antigen types in rabbits were purified and were immobilized on the sensor chip at 0.5 mg/mL. The limit of detection for STEC O157 by the SPR-immunosensor was found to be 6.3 × 10(4) cells for 75 s. Each of the examined 10 O-antigens on the STECs was detected by the corresponding PoAb with almost no reaction to the other PoAbs. The detected STECs were sufficiently removed from the PoAbs using gelatin or agarose gel without deactivation of the PoAbs, enabling repeatable use of the sensor chip. The developed SPR-immunosensor can be applied for the detection of multiple STEC O-antigens. Furthermore, the new antigen removal technique using the gel displacement approach can be utilized with various immunosensors to improve the detection of pathogens in clinical and public health settings.Entities:
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Year: 2016 PMID: 27243947 DOI: 10.1021/acs.analchem.6b00797
Source DB: PubMed Journal: Anal Chem ISSN: 0003-2700 Impact factor: 6.986