Compositions and methods for detecting cryptococcus neoformans
Disclosed are oligonucleotides useful in methods for determining whether a sample contains Cryptococcus neoformans , a causative agent for human cryptococcosis. These oligonucleotides, which have nucleotide sequences derived from a coding segment of the gene encoding the fungal specific transcription factor gene in Cryptococcus neoformans , are useful as forward and reverse primers for a polymerase chain reaction using nucleic acids from a biological sample as templates, and as probes for detecting any resultant amplicon. Detection of an amplicon indicates the sample contains Cryptococcus neoformans . Real-time PCR and detection using florescence resonance energy transfer is disclosed.
1. A method of detecting presence of Cryptococcus neoformans in a biological sample, comprising:
(a) mixing
(i) DNA extracted from said biological sample,
(ii) a primer pair comprising a forward primer and a reverse primer that target a fungal specific transcription factor gene of Cryptococcus neoformans , and
(iii) a hybridization probe, in a PCR vessel, wherein said hybridization probe comprises a fluorescent moiety;
(b) amplifying, in a real-time PCR reaction, under conditions to allow production of an amplicon; and
(c) detecting a presence or absence of Cryptococcus neoformans , by detecting a presence or absence of a fluorescent signal resulting from the formation of said amplicon, wherein the presence of a fluorescent signal is indicative of the presence of Cryptococcus neoformans.
2. The method of claim 1 , wherein said forward primer consists essentially of nucleotide sequence 1121-1144 set forth in SEQ ID NO: 1, nucleotide sequence 1480-1499, or nucleotide sequence 2105-2124 set forth in SEQ ID NO: 1, said reverse primer consists essentially of nucleotide sequence 1512-1533 set forth in SEQ ID NO: 2, nucleotide sequence 1165-1184, or nucleotide sequence 508-527 set forth in SEQ ID NO: 2, and said hybridization probe consists essentially of nucleotide sequence 1150-1178 of SEQ ID NO: 1 or nucleotide sequence 1583-1611 of SEQ ID NO: 2.
3. The method of claim 2 , wherein said forward primer has at least 99% identity to a nucleotide sequence 1121-1144 set forth in SEQ ID NO: 1, nucleotide sequence 1480-1499 set forth in SEQ ID NO: 1, or nucleotide sequence 2105-2124 set forth in SEQ ID NO: 1, said reverse primer has at least 99% identity to a nucleotide sequence 1512-1533 set forth in SEQ ID NO: 2, nucleotide sequence 1165-1184 set forth in SEQ ID NO: 2, or nucleotide sequence 508-527 set forth in SEQ ID NO: 2, and said hybridization probe has at least 99% identity to a nucleotide sequence 1150-1178 of SEQ ID NO: 1 or nucleotide sequence 1583-1611 of SEQ ID NO: 2.
4. The method of claim 2 , wherein said forward primer has at least 95% identity to a nucleotide sequence 1121-1144 set forth in SEQ ID NO: 1, nucleotide sequence 1480-1499 set forth in SEQ ID NO: 1, or nucleotide sequence 2105-2124 set forth in SEQ ID NO: 1, said reverse primer has at least 95% identity to a nucleotide sequence 1512-1533 set forth in SEQ ID NO: 2, nucleotide sequence 1165-1184 set forth in SEQ ID NO: 2, or nucleotide sequence 508-527 set forth in SEQ ID NO: 2, and said hybridization probe has at least 95% identity to a nucleotide sequence 1150-1178 of SEQ ID NO: 1 or nucleotide sequence 1583-1611 of SEQ ID NO: 2.
5. The method of claim 2 , wherein said forward primer has at least 90% identity to a nucleotide sequence 1121-1144 set forth in SEQ ID NO: 1, nucleotide sequence 1480-1499 set forth in SEQ ID NO: 1, or nucleotide sequence 2105-2124 set forth in SEQ ID NO: 1, said reverse primer has at least 90% identity to a nucleotide sequence 1512-1533 set forth in SEQ ID NO: 2, nucleotide sequence 1165-1184 set forth in SEQ ID NO: 2, or nucleotide sequence 508-527 set forth in SEQ ID NO: 2, and said hybridization probe has at least 90% identity to a nucleotide sequence 1150-1178 of SEQ ID NO: 1 or nucleotide sequence 1583-1611 of SEQ ID NO: 2.
6. The method of claim 1 , wherein said forward primer has a nucleotide sequence selected from the group consisting of SEQ ID NO: 3, SEQ ID NO: 6, SEQ ID NO: 8, and said reverse primer has a nucleotide sequence selected from the group consisting of SEQ ID NO: 4, SEQ ID NO: 7, and SEQ ID NO: 9.
7. The method of claim 1 , wherein said fluorescein moiety is 6-carboxy-fluorescein.
8. A method of detecting presence of Cryptococcus neoformans in a biological sample, comprising:
(a) mixing
(i) DNA extracted from said biological sample, and
(ii) a primer pair comprising a forward primer and a reverse primer that target a fungal specific transcription factor gene of Cryptococcus neoformans;
(b) amplifying, in a PCR reaction, under conditions to allow production of an amplicon; and
(c) detecting a presence or absence of Cryptococcus neoformans in said sample.