One-tube nested PCR for detecting
The present invention relates to a kit and method for detecting M. tuberculosis of suspected patient. The present invention also relates to primers and probe used to detect M. tuberculosis by performing one tube nested PCR.
1. A kit for detecting the presence or absence of Mycobacterium tuberculosis in a sample using a nested polymerase chain reaction, comprising
(I) an outer pair of oligonucleotide primers selected from the group consisting of (a) SEQ ID NOS: 2 and 4, and (b) SEQ ID NOS: 3 and 5, and
(ii) an inner pair of oligonucleotide primers selected from the group consisting of (c) SEQ ID NOS: 6 and 8, and (d) SEQ ID NOS: 7 and 9.
2. The kit of claim 1 , wherein the outer pair of oligonucleotide primers is SEQ ID NOS: 2 and 4, and the inner pair of oligonucleotide primers is SEQ ID NOS: 6 and 8.
3. The kit of claim 1 , wherein the inner pair of oligonucleotide primers is labeled by a detectable group selected from the group consisting of fluorescent molecules, radioactive molecules, chromogenic substrates, biotin, acridinium ester and acridinium-9-carboxamide.
4. The kit of claim 1 , which further comprises a probe wherein the sequence of the probe is SEQ ID NO. 10.
5. A method for detecting the presence or absence of Mycobacterium tuberculosis in a sample using a nested polymerase chain reaction, comprising
(I) adding into one tube with DNA from the sample, buffer, dNTP, Taq polymerase, probe having SEQ ID NO: 10, an outer pair of oligonucleotide primers selected from the group consisting of (a) SEQ ID NOS: 2 and 4, and (b) SEQ ID NOS: 3 and 5, and an inner pair of oligonucleotide primers selected from the group consisting of (c) SEQ ID NOS: 6 and 8, and (d) SEQ ID NOS: 7 and 9 to form a mixture, wherein the concentration of the outer pair of oligonucleotide primers to the concentration of the inner pair of oligonucleotide primers is 1:5 o 1:100;
(ii) performing first 20-50 cycles of amplification for PCR products from the outer primers in the first-stage polymerase chain reaction;
(iii) performing following 10-30 cycles of amplification PCR products from for the inner primers in the second-stage polymerase chain reaction; and
(iv) identifying M. tuberculosis by the probe.
6. The method of claim 5 , wherein the temperature of annealing and the temperature of extension in the first-stage polymerase chain reaction is at 72° C.
7. The method of claim 5 , which further comprises treating the mixture of step (I) over 5 minutes at 94° C.
8. The method of claim 5 , wherein the outer pair of oligonucleotide primers is SEQ ID NOS: 2 and 4, and the inner pair of oligonucleotide primers is SEQ ID NOS: 6 and 8.
9. The method of claim 5 , wherein the concentration of the outer pair of oligonucleotide primers to inner pair of oligonucleotide primers is 1:10 to 1:50.
10. The method of claim 9 , wherein the concentration of the outer pair of oligonucleotide primers to inner pair of oligonucleotide primers is 1:20.
11. The method of claim 5 , wherein the cycle of amplification for PCR products from the outer primers is 25-45.
12. The method of claim 11 , wherein the cycle of amplification for PCR products from the outer primers in the first polymerase chain reaction is 35.
13. The method of claim 5 , wherein the cycle of amplification for PCR products from the inner primers is 10-30.
14. The method of claim 13 , wherein the cycle of amplification for PCR products from the inner primers is 20.
15. The method of claim 5 , wherein the inner pair of oligonucleotide primers is labeled by a detectable group selected from the group consisting of fluorescent molecules, radioactive molecules, chromogenic substrates, biotin, acridinium ester and acridinium-9-carboxamide.
16. The method of claim 5 , wherein the probe is SEQ ID No. 10.
17. The method of claim 5 , wherein the nested PCR reaction is performed in one tube.