Process of directly detecting and identifying a microorganism in a biological sample diluted in an enrichment broth
A process of detecting at least one microorganism present in a sample placed in a closed container. The process includes: a) placing said sample in contact in the container with a culture medium, a revealing system capable of allowing the detection, and a support capable of capturing the microorganism(s) to be detected, the support comprising magnetic particles, b) closing the container, c) placing the container under conditions capable of allowing growth of the microorganism(s), d) applying a magnetic field to the magnetic particles for bringing together the magnetic particles, and e) detecting in real-time inside the closed container, using a detection means, the presence of the microorganism(s) fixed onto the capture support.
1 . A process of detecting at least one microorganism present in a sample placed in a closed container, the process comprising:
a) placing the sample in the container in contact with:
a culture medium,
a revealing system capable of allowing the detection, and
a support capable of capturing the microorganism(s) to be detected, the support comprising magnetic particles,
b) closing the container,
c) placing the container under conditions capable of allowing growth of the microorganism(s),
c′) transferring all or part of a mixture comprising sample, the culture medium, and the support capable of capturing the microorganism(s) to be detected and potentially the revealing system, from the container to at least one second container,
d) applying a magnetic field to the magnetic particles for bringing together the magnetic particles, and
e) detecting in real-time inside the closed container, using a detection means, the presence of the microorganism(s) fixed onto the capture support.
2 . The process according to claim 1 , wherein at least one specific or non-specific binding partner of the microorganism(s) is fixed onto the magnetic particles.
3 . The process according to claim 2 , wherein the specific binding partner is selected from the group consisting of antibodies, Fab fragments, Fab′ fragments, recombinant or non-recombinant phage proteins, and phages.
4 . The process according to claim 1 , further comprising confirming the detection of the microorganism(s) in a step f).
5 . The process according to claim 4 , wherein the confirming in step f) is accomplished using a detection means that is identical to or different from the detection means used for the detection in step e).
6 . The process according to claim 1 , wherein the detection means is selected from the group consisting of: an electrical detection means, an electrochemical detection means, an optical detection means, an acoustic detection means, a thermal detection means, a mechanical detection means, and a magnetic detection means.
7 . The process according to claim 1 , wherein the detection means is an electrical detection means, an electrochemical detection means, or an optical detection means.
8 . The process according to claim 1 , wherein the detection means is a Raman spectrometer.
9 . The process according to claim 1 , wherein the support for capturing the microorganism(s) also constitutes the detection means.
10 . The process according to claim 1 , wherein the application of the magnetic field is repeated.
11 . The process according to claim 1 , wherein the container is a homogenisation bag, a flask, a bottle, or a pillbox.
12 . The process according to claim 1 , wherein the detection means is connected to a data analysis system.
13 . The process according to claim 12 , wherein the connection between the capture support or the detection means and the data analysis device system is a wired connection or a wireless connection.
14 . The process according to claim 1 , wherein the sample is a food sample, a biological sample, or an environmental sample.
15 . The process according to claim 1 , wherein the detection in step e) is demonstrated by an appearance of real-time agglutination of the magnetic particles.