| Literature DB >> 27350432 |
Takahiro Ohnishi1, Bongsoo Lim, Natsumi Nojima, Ogasawara Kunitoshi, Shunichi Inagaki, Koji Makitsuru, Mari Sasaki, Kunihiko Nakane, Hiroaki Tsuchioka, Kazumi Horikawa, Maiko Kawabe, Yasutaka Minegishi, Nobuo Miyazaki, Yoshiko Sugita-Konishi.
Abstract
Kudoa septempunctata is the causative agent of a food-borne disease associated with the ingestion of raw olive flounder. As the current qRT-PCR method for its detection is time-consuming, a rapid and simple method is required. Recently, a new real-time loop-mediated isothermal amplification (LAMP) method and an immunochromatography method, whose sensitivities are intended to be compatible with that designated in the official analytical method (10(5) spores/g olive flounder), have been developed. To validate these new methods, we performed an inter-laboratory study across seven laboratories. Both methods could not detect less than 10(4) spores/g; however, these methods were able to detect more than 10(5) spores/g in olive flounder samples. These results demonstrated that the sensitivities of these methods were compatible with the designated level in the official analytical method. We concluded that these new methods were acceptable as the screening methods for K. septempunctata.Entities:
Mesh:
Year: 2016 PMID: 27350432 DOI: 10.4265/bio.21.135
Source DB: PubMed Journal: Biocontrol Sci ISSN: 1342-4815 Impact factor: 0.982