Primer and probe for detection of
View Patent ↗The object of the present invention is to provide a novel primer for use in the detection of Mycobacterium avium ( M. avium ), and a method for detection of M. avium conveniently, rapidly and with high precision by using the primer. More specifically, disclosed are an oligonucleotide which comprises a part or an entire of the nucleotide sequence selected from SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:37, SEQ ID NO:38, SEQ ID NO:39, SEQ ID NO:40, SEQ ID NO:41, SEQ ID NO:42, SEQ ID NO:130, SEQ ID NO:131, SEQ ID NO:132, SEQ ID NO:133, SEQ ID NO:134, SEQ ID NO:135 and SEQ ID NO:136, or a part or an entire of the sequence complementary to the nucleotide sequence, and which is capable of hybridizing with the nucleotide sequence for a Mycobacterium avium gene; a primer and a probe for use in the detection of M. avium , which comprises the oligonucleotide; and a method for detection of M. avium using the primer and/or probe.
1. A primer pair for detecting Mycobacterium avium consisting of a first primer and a second primer
wherein the first primer is not more than about 50 nucleotides in length and comprises an oligonucleotide that comprises the nucleotide sequence of SEQ ID NO: 179;
wherein at least one of the first primer or the second primer is labeled with a labeling substance, which is bound via a covalent bond or a linker; and
wherein the first primer and the second primer are together capable of amplifying a genomic DNA fragment of Mycobacterium avium genome.
2. The primer pair according to claim 1 , wherein the labeling substance is selected from a radioisotope, an enzyme, a fluorescent substance, a luminescent substance, and biotin.
3. The primer pair according to claim 1 , wherein the second primer of said primer pair is not more than about 50 nucleotides in length and comprises the nucleotide sequence of SEQ ID NO: 180.
4. The primer pair according to claim 3 , wherein the first primer and the second primer are each no more than about 25 nucleotides in length.
5. The primer pair according to claim 3 , wherein the oligonucleotide of the first primer consists of the nucleotide sequence of SEQ ID NO: 179 and an oligonucleotide of the second primer consists of the nucleotide sequence of SEQ ID NO: 180.
6. A reagent kit comprising:
(i) a primer set for detecting Mycobacterium avium consisting of
(a) a first primer consisting of a primer that is not more than about 50 nucleotides in length and comprises an oligonucleotide that comprises the nucleotide sequence of SEQ ID NO: 179, is labeled with a labeling substance, which is bound via a covalent bond or a linker, and is capable of hybridizing with a genomic DNA fragment of Mycobacterium avium genome; and
(b) optionally, an additional primer, wherein the additional primer is not more than about 50 nucleotides in length and comprises a contiguous portion of at least 15 nucleotides of the complementary sequence of SEQ ID NO:136, and is capable of hybridizing with the genomic DNA fragment of Mycobacterium avium genome;
(ii) (1) a nucleic acid synthetase and/or (2) a substrate for a nucleic acid synthetase and/or (3) a double strand intercalator and/or (4) a signal detection substance; and
(iii) wherein all primers for detecting Mycobacterium avium in the reagent kit are capable of specifically hybridizing to the Mycobacterium avium genome under highly stringent conditions.
7. The reagent kit according to claim 6 , further comprising:
a probe, wherein the probe comprises (a) an oligonucleotide that comprises a nucleotide sequence selected from:
SEQ ID NO: 136, or the full nucleotide sequence complementary thereto; wherein the probe is no longer than about 1100 nucleotides; or
SEQ ID NO: 179 or 180, or the full nucleotide sequence complementary thereto; wherein the probe is no longer than about 50 nucleotides; or
SEQ ID NO: 204, or the full nucleotide sequence complementary thereto; or
20-50 consecutive nucleotides of SEQ ID NO: 204, or the full nucleotide sequence complementary thereto; and
optionally (b) a labeling substance, which is bound to the oligonucleotide via a covalent bond or a linker; and wherein the probe is capable of hybridizing with a genomic DNA fragment of Mycobacterium avium genome.
8. A reagent kit comprising:
(i) a primer pair for detecting Mycobacterium avium consisting of a first primer and a second primer, wherein (a) the first primer is not more than about 50 nucleotides in length and comprises an oligonucleotide that comprises the nucleotide sequence of SEQ ID NO: 179; (b) at least one of the first primer or the second primer is labeled with a labeling substance, which is bound via a covalent bond or a linker; and (c) the first primer and the second primer are capable of hybridizing with a genomic DNA fragment of Mycobacterium avium genome; and
(ii) (1) a nucleic acid synthetase and/or (2) a substrate for a nucleic acid synthetase and/or (3) a double strand intercalator and/or (4) a signal detection substance; and
(iii) wherein all primers for detecting Mycobacterium avium in the reagent kit are capable of specifically hybridizing to the Mycobacterium avium genome under highly stringent conditions.
9. The reagent kit according to claim 8 , further comprising:
a probe, wherein the probe comprises (a) an oligonucleotide that comprises a nucleotide sequence selected from:
SEQ ID NO: 136, or the full nucleotide sequence complementary thereto; wherein the probe is no longer than about 1100 nucleotides; or
SEQ ID NO: 179 or 180, or the full nucleotide sequence complementary thereto; wherein the probe is no longer than about 50 nucleotides; or
SEQ ID NO: 204, or the full nucleotide sequence complementary thereto; or
20-50 consecutive nucleotides of SEQ ID NO: 204, or the full nucleotide sequence complementary thereto; and
optionally (b) a labeling substance, which is bound to the oligonucleotide via a covalent bond or a linker; and wherein the probe is capable of hybridizing with a genomic DNA fragment of Mycobacterium avium genome.
10. The reagent kit according to claim 8 , wherein the second primer of said primer pair comprises SEQ ID NO: 180.
11. The reagent kit according to claim 8 , wherein the labeling substance is selected from a radioisotope, an enzyme, a fluorescent substance, a luminescent substance, and biotin.
12. The reagent kit according to claim 8 , wherein the second primer of said primer pair is not more than about 50 nucleotides in length and comprises the nucleotide sequence of SEQ ID NO: 180.
13. The reagent kit according to claim 12 , wherein the first primer and the second primer are each no more than about 25 nucleotides in length.
14. A reagent kit comprising:
(i) a probe consisting of
(a) an oligonucleotide that comprises a nucleotide sequence selected from:
SEQ ID NO: 136, or the full length sequence complementary thereto; wherein the probe is no longer than about 1100 nucleotides; or
SEQ ID NO: 179 or 180, or the full nucleotide sequence complementary thereto; wherein the probe is no longer than about 50 nucleotides; or
SEQ ID NO: 204, or the full nucleotide sequence complementary thereto; or
20-50 consecutive nucleotides of SEQ ID NO: 204, or the full nucleotide sequence complementary thereto; and
(b) a labeling substance bound to the oligonucleotide via a covalent bond or a linker; wherein the labeling substance comprises a reporter fluorescent dye and a quencher dye; and wherein the probe is capable of hybridizing with a genomic DNA fragment of Mycobacterium avium genome; and
(ii) a primer composition for detecting Mycobacterium avium consisting essentially of a first primer or a primer pair;
wherein (a) the first primer is not more than about 50 nucleotides in length and comprises an oligonucleotide that comprises the nucleotide sequence of SEQ ID NO: 179; and optionally (b) a labeling substance which is bound to the oligonucleotide via a covalent bond or a linker; wherein the first primer is capable of hybridizing with a genomic DNA fragment of Mycobacterium avium genome; and
wherein the primer pair consists of the first primer and a second primer, and the first primer and the second primer are capable of amplifying a genomic DNA fragment of Mycobacterium avium genome; and
(iii) (1) a nucleic acid synthetase and/or (2) a substrate for a nucleic acid synthetase and/or (3) a double strand intercalator and/or (4) a signal detection substance.
15. The reagent kit according to claim 14 , wherein the reporter fluorescent dye is covalently bound to the 5′-terminal of the oligonucleotide and the quencher dye is covalently bound to the 3′-terminal of the oligonucleotide.