Cell detection device and cell detection method
A cell detector and detecting method enhance detection sensitivity for microbes according to the ATP method and reduce the detection period. The cell detector includes a sealing container having a culture portion for containing a culture medium containing the specimen, a sealable specimen introducing portion, and a luminescent reagent portion that emits light upon contact with the culture medium, a contact mechanism for controlling the contact between the culture medium and the luminescent reagent portion, a photodetector for detecting a luminescence resulting from the contact between the culture medium and the luminescent reagent portion, and a calculation unit for calculating a luminescent quantity from detection signals of the photodetector to determine cell proliferation on the basis of change in the luminescent quantity over time. The culture portion and the luminescent reagent portion are separately positioned, and the contact mechanism intermittently brings the culture medium and the luminescent reagent into contact.
1 . A cell detector for detecting cells in a specimen, the cell detector comprising:
a sealing container that is configured to receive the specimen, wherein the sealing container includes:
a culture medium that is configured to be moveable within the sealing container between a first position and a second position within the sealing container,
a sealable specimen introducing portion, wherein the specimen is introduced to the culture medium via the sealable specimen introducing portion, and
a luminescent reagent that contains a luciferase,
a photodetector that detects a luminescence generated when the luciferase catalyzes a reaction between adenosine triphosphate (ATP) derived from the cells of the specimen and luciferin;
one or more controllers;
a contact mechanism for intermittently controlling a contact between the culture medium and the luminescent reagent; and
a processor that is communicatively coupled to the photodetector, the contact mechanism, and the one or more controllers, wherein the processor and the one or more controllers are collectively configured to:
control the contact mechanism to control contact between the culture medium and the luminescent reagent through a cycle after the specimen is received into the sealing container, wherein during the cycle, the contact mechanism intermittently moves the culture medium or the luminescent reagent from the first position where a portion of the culture medium does not contact the luminescent reagent to the second position where the portion contacts the luminescent reagent,
receive signals from the photodetector,
calculate a luminescent quantity based on the signals received from the photodetector,
repeat the cycle at least two times, and
determine cell proliferation based on changes in the calculated luminescent quantity during the cycles.
2 . The cell detector according to claim 1 , wherein the processor and the one or more controllers are further collectively configured to:
calculate a determination result based on the cell proliferation, and
display the determination result.
3 . The cell detector according to claim 1 , wherein the processor and the one or more controllers are further collectively configured to:
adjust composition of a gas outside of the sealing container, wherein the sealing container is configured to seal the cells but to be permeable by the gas.
4 . The cell detector according to claim 1 , wherein the processor and the one or more controllers are further collectively configured to:
regulate a temperature of the sealing container.
5 . The cell detector according to claim 1 , further comprising:
a gas sensor in the sealing container, wherein
the gas sensor includes a fluorescent dye that emits fluorescence having a different color tone depending on a volatile metabolite produced by microbes in the specimen and the gas sensor is configured to identify a microbial species according to the color tone.
6 . The cell detector according to claim 1 , wherein the cycle moves the culture medium from the first position to the second position and back to the first position after a predetermined period of time has elapsed.
7 . The cell detector according to claim 1 , wherein the sealing container is further configured to receive the luciferin.
8 . The cell detector according to claim 1 , wherein the luciferin is included in the luminescent reagent.
9 . The cell detector according to claim 1 , wherein the contact mechanism includes a plunger and a plunger controller.
10 . The cell detector according to claim 1 , wherein the contact mechanism includes a sealing container driving unit.
11 . The cell detector according to claim 1 , wherein the contact mechanism includes an optical fiber and an optical fiber driving unit.
12 . The cell detector according to claim 1 , wherein the contact mechanism includes a magnet and a magnet driving unit.
13 . The cell detector according to claim 1 , wherein during the cycle, the contact mechanism further moves the culture medium back to the first position from the second position.
14 . The cell detector according to claim 12 , wherein
the luminescent reagent is fixed to a surface of magnetic beads that are controlled by the magnetic drive unit.
15 . The cell detector according to claim 11 , wherein
the luminescent reagent is fixed to one end of the optical fiber, and
the optical fiber is configured such that the other end is connected to the photodetector, the one end is inserted from the sealable specimen introducing portion into the sealing container, and the one end can be put in and out of the culture medium.