Methods and compositions for detecting candida species
AssigneeGen-Probe Incorporated
InventorsAngela S. HUDSON, Damon K. GETMAN, Alice JIANG, Barbara EATON
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Abstract
Disclosed are methods utilizing specific amplification of Candida sp. target nucleic acid for detecting the presence or absence of Candida sp. in a sample. Also disclosed are corresponding oligomers, including amplification oligomers, capture probes and detection probes, and combinations thereof, as well as corresponding reaction mixtures and kits.
Claims93
A method for determining the presence or absence of Candida sp. In a sample, the method comprising:
- (1) contacting a sample, said sample suspected of containing Candida sp., with at least one of a first amplification oligomer combination and a second amplification oligomer combination, wherein
- (a) the first amplification oligomer combination comprises first and second Candida-specific amplification oligomers for amplifying a first Candida sp. Target nucleic acid region or a second Candida sp. Target nucleic acid region, wherein said first target region corresponds to a region of SEQ ID NO:129 from about nucleotide position 133 or 161 to about nucleotide position 259 and said second region corresponds to a region of SEQ ID NO:130 from about nucleotide position 202 to about nucleotide position 308, and wherein the first and second Candida-specific amplification oligomers respectively comprise first and second Candida-specific target-hybridizing sequences;
- and
- (b) the second amplification oligomer combination comprises first and second C. glabrata-specific amplification oligomers for amplifying a third Candida sp. Target nucleic acid region, wherein said third target region corresponds to a region of SEQ ID NO:131 from about nucleotide position 355 to about nucleotide position 554, and wherein the first and second C. glabrata-specific amplification oligomers respectively comprise first and second C. glabrata-specific target-hybridizing sequences;
- (2) performing an in vitro nucleic acid amplification reaction, wherein any Candida sp. Target nucleic acid, if present in the sample, is used as a template for generating one or more amplification products corresponding to at least one of the first, second, and third target regions;
- and
- (3) detecting the presence or absence of the one or more amplification products, thereby determining the presence or absence of Candida sp. In the sample.
An oligomer combination for determining the presence or absence of Candida sp. In a sample, the oligomer combination comprising:
- at least one of a first amplification oligomer combination and a second amplification oligomer combination, wherein
- (a) the first amplification oligomer combination comprises first and second Candida-specific amplification oligomers for amplifying a first Candida sp. Target nucleic acid region or a second Candida sp. Target nucleic acid region, wherein said first target region corresponds to a region of SEQ ID NO:129 from about nucleotide position 133 or 161 to about nucleotide position 259 and said second region corresponds to a region of SEQ ID NO:130 from about nucleotide position 202 to about nucleotide position 308, and wherein the first and second Candida-specific amplification oligomers respectively comprise first and second Candida-specific target-hybridizing sequences;
- and
- (b) the second amplification oligomer combination comprises first and second C. glabrata-specific amplification oligomers for amplifying a third Candida sp. Target nucleic acid region, wherein said third target region corresponds to a region of SEQ ID NO:131 from about nucleotide position 355 to about nucleotide position 554, and wherein the first and second C. glabrata-specific amplification oligomers respectively comprise first and second C. glabrata-specific target-hybridizing sequences.
A detection probe for detecting a Candida sp. Target nucleic acid, wherein said detection probe is
- a Candida-specific detection probe comprising a Candida-specific detection probe target-hybridizing sequence selected from the group consisting of
- (A1) a sequence of from 18 to 22 contiguous nucleotides contained in the sequence of SEQ ID NO:145 and that includes at least the sequence of SEQ ID NO:146,
- (B1) the DNA equivalent or an RNA/DNA chimeric of (A1), and
- (C1) the full complement of (A1) or (B1), or
- a C. glabrata-specific detection probe comprising a C. glabrata-specific detection probe target-hybridizing sequence selected from the group consisting of
- (A2) a sequence of from 17 to 23 contiguous nucleotides contained in the sequence of SEQ ID NO:147 and that includes at least the sequence of SEQ ID NO:148,
- (B2) a sequence that substantially corresponds to the sequence of residues 1-17 of SEQ ID NO:18,
- (C2) a sequence that substantially corresponds to the sequence of residues 1-20 of SEQ ID NO:21,
- (D2) the DNA equivalent or an RNA/DNA chimeric of any of (A2)-(C2), and
- (E2) the full complement of any one of (A2)-(D2).
Dependencies are inferred from the claim text.