Quick method for detecting enzymes and microorganisms
The present invention concerns an in vitro method for detecting an enzyme or a microorganism in a biological sample, comprising the steps of: a1) concentrating the microorganisms present in the biological sample, optionally after a a0) culture step of the microorganisms; b1) placing in suspension the microorganisms concentrated at step a1) in a solution containing at least one chromogenic or fluorogenic substrate capable of releasing a chromophore or fluorophore after hydrolysis by the enzyme to be detected; c1) detecting potential release of the chromophore or fluorophore obtained at step b1); the release of the chromophore or fluorophore detected at step c1) indicating the presence of the enzyme to be detected.
1. An in vitro method for detecting an enzyme of a microorganism from a biological sample, comprising the steps of:
a1) concentrating the microorganisms present in the biological sample, optionally after a a0) culture step of the microorganisms;
b1) placing in suspension the microorganisms concentrated at a1) in a solution comprising at least one chromogenic or fluorogenic substrate capable of releasing a chromophore or a fluorophore after hydrolysis by the enzyme to be detected;
c1) detecting potential release of the chromophore or fluorophore obtained at step b1);
the release of the chromophore or fluorophore detected at step c1) indicating the presence of the enzyme to be detected.
2. The method according to claim 1 wherein the biological sample is a blood sample or urine sample.
3. The method according to claim 1 wherein the culture step a0) is a blood culture step.
4. The method according to claim 1 further comprising, if the biological sample is a sample containing blood or red blood cells, a step to lyse the red blood cells present in the biological sample before step b1) for placing in suspension.
5. The method according to claim 1 further comprising, if the biological sample is a sample containing blood or red blood cells, a step to lyse the red blood cells present in the biological sample before the concentration step a1).
6. The method according to claim 1 wherein the enzyme to be detected is chosen from the group formed by extended spectrum β-lactamases, cephalosporinases, carbapenemases, glycosidases and esterases.
7. The method according to claim 1 wherein the microorganism is resistant to 3 rd generation cephalosporins, and the enzyme to be detected is chosen from the group formed by extended spectrum β-lactamases, cephalosporinases and carbapenemases.
8. The method according to claim 7 wherein at step b1) the chromogenic or fluorogenic substrate is placed in the presence of at least one β-lactamase inhibitor.
9. The method according to claim 7 , wherein the chromogenic substrate is the compound HMRZ-86 ((7R)-7-[2-(aminothiazol-4-yl)-(z)-2-(1-carboxy-1-methylethoxyimino)acetamido]-3-(2,4-dinitrostyryl)-3-cephem-4-carboxylic acid thrifluoroacetate, E-isomer) or a salt thereof.
10. The method according to claim 1 wherein the concentration step a1) comprises the centrifugation of the biological sample followed by removal of the supernatant obtained.
11. The method according to claim 1 wherein, if the biological sample is a sample containing blood or red blood cells, the microorganism concentration step a1) is preceded by a step a′) to prepare the biological sample, comprising:
(i) agglutination of the red blood cells, and
(ii) separation of the agglutinated red blood cells from the microorganisms present in the sample.
12. An in vitro method for detecting an enzyme of a microorganism from a biological sample, comprising the steps of:
a1) concentrating the microorganisms present in the biological sample, optionally after a a0) culture step of the microorganisms;
b1) placing in suspension the microorganisms concentrated at a1) in a solution comprising at least one chromogenic or fluorogenic substrate capable of releasing a chromophore or a fluorophore after hydrolysis by the enzyme to be detected;
c1) detecting potential release of the chromophore or fluorophore obtained at step b1);
the release of the chromophore or fluorophore detected at step c1) indicating the presence of the enzyme to be detected, and
wherein the chromogenic substrate is the compound HMRZ-86 ((7R)-7-[2-(aminothiazol-4-yl)-(z)-2-(1-carboxy-1-methylethoxyimino)acetamido]-3-(2,4-dinitrostyryl)-3-cephem-4-carboxylic acid thrifluoroacetate, E-isomer) or a salt thereof.