• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to project page

2020 Fiscal Year Final Research Report

Development of effective pre-treatment method for the detection of Mycobacteria

Research Project

  • PDF
Project/Area Number 18K12125
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Review Section Basic Section 90130:Medical systems-related
Research Institution公益財団法人結核予防会 結核研究所

Principal Investigator

Mitarai Satoshi  公益財団法人結核予防会 結核研究所, 抗酸菌部, 部長 (30501671)

Project Period (FY) 2018-04-01 – 2021-03-31
Keywords結核菌 / 検体処理 / 抗酸菌濃縮 / 誘電泳動 / 核酸増幅法
Outline of Final Research Achievements

An effective concentration method is required to detect Mycobacterium tuberculosis (MTB) in paucibacillary specimens. Dielectrophoresis (DEP), a phenomenon in which a force is exerted on a dielectric particle subjected to a non-uniform electric field, is useful for concentrating bacteria. To investigate whether the DEP method increases nucleic acid amplification test (NAAT) sensitivity. First, the capture rates were examined for multiple electrode settings by calculating the bacterial load before and after DEP with real-time PCR. Second, LAMP was performed using samples with 10 consecutive negative results by conventional LAMP and DEP treated samples.
The capture rate was the highest with 100 kHz frequency (73.2-84.9%). LAMP with DEP was performed using conventional LAMP-negative specimens, and eight of ten tests (80%) were positive. The sensitivity was higher than that of the conventional LAMP method (p = 0.0007). The DEP method has the potential to increase NAAT sensitivity for MTB.

Free Research Field

臨床細菌学

Academic Significance and Societal Importance of the Research Achievements

誘電泳動法によって抗酸菌(結核菌)の効率的濃縮条件を決定した。またその技術により結核菌の核酸増幅法による検出感度を上昇させることが可能であることを実証した。これは現状の結核菌核酸増幅法検査の弱点である検体濃縮過程に寄与する技術であり、学術的には抗酸菌の誘電泳動濃縮が可能であることを証明し、社会的にはこの技術の応用で結核菌検査の高感度化・迅速診断に寄与しうる。

URL: 

Published: 2022-01-27  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi