Patent · US5763169A · A · US

Nucleic acid probes for the detection and identification of fungi

(11) Publication number

US5763169A

(21) Application number

US-37312795-A

(22) Filing date

1995-01-13

(30) Priority date

1995-01-13

(43) Publication date

1998-06-09

(45) Date of grant

1998-06-09

(52) CPC

C12N Microorganisms or enzymes; compositions thereof; propagating, preserving, or maintaining microorganisms; mutation or genetic engineering; culture media: 15/1003
C07K Peptides: 14/37
C12Q Measuring or testing processes involving enzymes, nucleic acids or microorganisms; compositions or test papers therefor; processes of preparing such compositions; condition-responsive control in microbiological or enzymological processes: 1/6806, 1/6895
Y10S Technical subjects covered by former uspc cross-reference art collections [xracs] and digests: 435/911, 435/913, 435/921, 435/922, 435/924, 435/929, 435/931, 435/933, 435/939, 435/94, 435/942
Y10T Technical subjects covered by former us classification: 436/143333

(73) Assignee

CHIRON DIAGNOSTICS CORP

(54) Title

Nucleic acid probes for the detection and identification of fungi

(57) Abstract

Nucleic acid probes and primers are described for detecting fungi that cause disease in humans and animals, as well as spoilage of food and beverages. These probes can detect rRNA, rDNA or polymerase chain reaction products from a majority of fungi in clinical, environmental or food samples. Nucleic acid hybridization assay probes specific for Aspergillus fumigatus, Blastomyces dermatitidis, Candida albicans, Coccidioides immitis, Cryptococcus neoformans, Histoplasma capsulatum, Aspergillus flavus, Aspergillus glaucus, Aspergillus niger, Aspergillus terreus, Candida glabrata, Candida guilliermondii, Candida kefyr, Candida krusei, Candida lusitaniae, Candida parapsilosis, Candida tropicalis, Pseudallescheria boydii, and Sporothrix schenckii are also described.

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Claims (29)

A method of determining whether one or more fungal species selected from the group of fungal species consisting of Aspergillus fumigatus, Blastomyces dermatitidis, Candida albicans, Coccidioides immitis, Cryptococcus neoformans, Histoplasma capsulatum, Aspergillus glaucus, Aspergillus niger, Aspergillus terreus, Candida glabrata, Candida guilliermindii, Candida kefyr, Candida krusei, Candida lusitaniae, Candida parapsilosis, Candida tropicalis, Pseudallescheria boydii, Asperillus flavus and Sporothrix schenckii is present in a sample of fungi, said method comprising the following steps: a) extracting nucleic acid material from fungi contained in said sample; b) adding two known oligonucleocide primers, one of said primers being (SEQ ID NO:1) or (SEQ ID NO:2), said primers bracketing a hypervariable region on the 28S rDNA or rRNA present in the fungal species of said group; c) amplifying the sequence between said primers; and d) using one or more labeled probes directed to a portion of the hypervariable region bracketed by said primers, each said labeled probe being specific for one of said fungal species from said group, to determine whether said fungal species identified by each said labeled probe is present in said sample.
The method of claim 1 in which, in said amplifying step, said amplifying procedure is the polymerase chain reaction.
The method of claim 1 in which said one or more probes is selected from the group consisting of (SEQ ID NO:3), (SEQ ID NO:4), (SEQ ID NO:5), (SEQ ID NO:6), (SEQ ID NO:7), (SEQ ID NO:8), (SEQ ID NO:9), (SEQ ID NO:10), (SEQ ID NO:11), (SEQ ID NO:12), (SEQ ID NO:13), (SEQ ID NO:14), (SEQ ID NO:15), (SEQ ID NO:16), (SEQ ID NO:17), (SEQ ID NO:18), (SEQ ID NO:19), (SEQ ID NO:20), (SEQ ID NO:21), (SEQ ID NO:22) and (SEQ ID NO:23).
The method of claim 1 wherein, in step (d), more than one probe is used, each said probe being connected to (a) a different signal moiety or (b) a moiety which allows separation of said probes.
A method of determining whether one or more fungal species selected from the group of fungal species consisting of Aspergillus fumigatus, Blastomyces dermatitidis, Candida albicans, Coccidioides immitis, Cryptococcus neoformans, Histoplasma capsulatum, Aspergillus glaucus, Aspergillus niger, Aspergillus terreus, Candida glabrata, Candida guilliermondii, Candida kefyr, Candida krusei, Candida lusitaniae, Candida parapsilosis, Candida tropicalis, Pseudallescheria boydii, Aspergillus flavus and Sporothrix schenckii is present in a sample of fungi, said method comprising the following steps: a) extracting nucleic acid material from fungi contained in said sample; b) adding a universal fungal probe selected from the group consisting of (SEQ ID NO: 1), (SEQ ID NO:2) and the complements thereof; c) using one or more second probes, each said second probe being specific for one of said fungal species from said group, wherein said one or more second probes each has a nucleotide residue sequence selected from the group consisting of (SEQ ID NO:3), (SEQ ID NO:4), (SEQ ID NO:5), (SEQ ID NO:6), (SEQ ID NO:7), (SEQ ID NO:8), (SEQ ID NO:9), (SEQ ID NO:10), (SEQ ID NO:11), (SEQ ID NO:12), (SEQ ID NO:13), (SEQ ID NO:14), (SEQ ID NO:15), (SEQ ID NO:16), (SEQ ID NO:17), (SEQ ID NO:18), (SEQ ID NO:19), (SEQ ID NO:20), (SEQ ID NO:21), (SEQ ID NO:22), (SEQ ID NO:23) and the complements thereof; and d) determining whether said fungal species identified by each said second probe is present in said sample, wherein at least one of said probes is connected to a signal moiety and at least one of said probes is connected to a moiety that allows separation of said probes.
A method of determining whether one or more fungal species selected from the group of fungal species consisting of Aspergillus fumigatus, Blastomyces dermatitidis, Candida albicans, Coccidioides immitis, Cryptococcus neoformans, Histoplasma capsulatum, Aspergillus glaucus, Aspergillus niger, Aspergillus terreus, Candida glabrata, Candida guilliermondii, Candida kefyr, Candida krudei, Candida lusitaniae, Candida parapsilosis, Candida tropicalis, Pseudallescheria boydii, Aspergillus flavus and Sporothrix schenckii is present in a sample of fungi, said method comprising the following steps: a) extracting nucleic acid material from fungi contained in said sample; and b) using one or more labeled probes, each said labeled probe being specific for one of said fungal species from said group, to determine whether said fungal species identified by each said labeled probe is present in said sample, wherein said one or more labeled probes each has a nucleotide residue sequence selected from the group consisting of (SEQ ID NO:3), (SEQ ID NO:4), (SEQ ID NO:5), (SEQ ID NO:6), (SEQ ID NO:7), (SEQ ID NO:8), (SEQ ID NO:9), (SEQ ID NO:10), (SEQ ID NO:11), (SEQ ID NO:12), (SEQ ID NO:13), (SEQ ID NO:14), (SEQ ID NO:15), (SEQ ID NO:16), (SEQ ID NO:17), (SEQ ID NO:18), (SEQ ID NO:19), (SEQ ID NO:20), (SEQ ID NO:21), (SEQ ID NO:22), (SEQ ID NO:23) and the complements thereof.
An oligonucleotide probe/primer for fungi, said probe/primer having the nucleotide residue sequence of (SEQ ID NO:1) or the complement thereof.
An oligonucleotide probe/primer for fungi, said probe/primer having the nucleotide residue sequence of (SEQ ID NO:2) or the complement thereof.
An oligonucleotide hybridization probe for Aspergillus fumigatus, said probe having the nucleotide residue sequence of (SEQ ID NO:3) or the complement thereof.
An oligonucleotide hybridization probe for Blascomyces dermatitidis, said probe having the nucleotide residue sequence of (SEQ ID NO:4) or the complement thereof.
An oligonucleotide hybridization probe for Candida albicans, said probe having the nucleotide residue sequence of (SEQ ID NO:5) or the complement thereof.
An oligonucleotide hybridization probe for Coccidioides immitis, said probe having the nucleotide residue sequence of (SEQ ID NO:6) or the complement thereof.
An oligonucleocide hybridization probe for Cryptococcus neoformans, said probe having the nucleotide residue sequence of (SEQ ID NO:7) or the complement thereof.
An oligonucleotide hybridization probe for Cryptococcus neoformans, said probe having the nucleotide residue sequence (SEQ ID NO:8) or the complement thereof.
An oligonucleotide hybridization probe for Hictoplasma capsulatum, said probe having the nucleotide residue sequence of (SEQ ID NO:9) or the complement thereof.
An oligonucleotide hybridization probe for Aspergillus glaucus, said probe having the nucleotide residue sequence of (SEQ ID NO:10) or the complement thereof.
An oligonucleotide hybridization probe for Aspergillus niger, said probe having the nucleotide residue sequence of (SEQ ID NO:11) or the complement thereof.
An oligonucleotide hybridization probe for Aspergillus terreus, said probe having the nucleotide residue sequence of (SEQ ID NO:12) or the complement thereof.
An oligonucleotide hybridization probe for Candida glabrata, said probe having the nucleotide residue sequence of (SEQ ID NO:13) or the complement thereof.
An oligonucleotide hybridization probe for Candida guilliermondii, said probe having the nucleotide residue sequence of (SEQ ID NO:14) or the complement thereof.
An oligonucleotide hybridization probe for Candida kefyr, said probe having the nucleotide residue sequence of (SEQ ID NO:15) or the complement thereof.
An oligonucleotide hybridization probe for Candida krusei, said probe having the nucleotide residue sequence (SEQ ID NO:16) or the complement thereof.
An oligonucleotide hybridization probe for Candida lusitaniae, said probe having the nucleotide residual sequence of (SEQ ID NO 17) or the complement thereof.
An oligonucleotide hybridization probe for Candida parapsilosis, said probe having the nucleotide residue sequence of (SEQ ID NO:18) or the complement thereof.
An oligonucleotide hybridization probe for Candida tropicalis, said probe having the nucleotide residue sequence of (SEQ ID NO:19) or the complement thereof.
An oligonucleocide hybridization probe for Pseudallescheria boydii, said probe having the nucleotide residue sequence of (SEQ ID NO:20) or the complement thereof.
An oligonucleotide hybridization probe for Aspergillus flavus, said probe having the nucleotide residue sequence of (SEQ ID NO:21) or the complement thereof.
An oligonucleotide hybridization probe for Sporothrix schenckii, said probe having the nucleotide residue sequence of (SEQ ID NO:22) or the complement thereof.
An oligonucleotide hybridization probe for Sporothrix schenckii, said probe having the nucleotide residue sequence of (SEQ ID NO:23) or the complement thereof.

Citations (10)

EP0272009A2
EP0422872A2
US4851330A
US5292874A
US5324632A
US5352579A
US5501951A
US5580971A
US5593841A
WO8803957A1

Record as JSON

{
  "publication_number": "US5763169A",
  "country": "US",
  "kind": "A",
  "title": "Nucleic acid probes for the detection and identification of fungi",
  "abstract": "Nucleic acid probes and primers are described for detecting fungi that cause disease in humans and animals, as well as spoilage of food and beverages. These probes can detect rRNA, rDNA or polymerase chain reaction products from a majority of fungi in clinical, environmental or food samples. Nucleic acid hybridization assay probes specific for Aspergillus fumigatus, Blastomyces dermatitidis, Candida albicans, Coccidioides immitis, Cryptococcus neoformans, Histoplasma capsulatum, Aspergillus flavus, Aspergillus glaucus, Aspergillus niger, Aspergillus terreus, Candida glabrata, Candida guilliermondii, Candida kefyr, Candida krusei, Candida lusitaniae, Candida parapsilosis, Candida tropicalis, Pseudallescheria boydii, and Sporothrix schenckii are also described.",
  "claims": [
    "1. A method of determining whether one or more fungal species selected from the group of fungal species consisting of Aspergillus fumigatus, Blastomyces dermatitidis, Candida albicans, Coccidioides immitis, Cryptococcus neoformans, Histoplasma capsulatum, Aspergillus glaucus, Aspergillus niger, Aspergillus terreus, Candida glabrata, Candida guilliermindii, Candida kefyr, Candida krusei, Candida lusitaniae, Candida parapsilosis, Candida tropicalis, Pseudallescheria boydii, Asperillus flavus and Sporothrix schenckii is present in a sample of fungi, said method comprising the following steps: a) extracting nucleic acid material from fungi contained in said sample; b) adding two known oligonucleocide primers, one of said primers being (SEQ ID NO:1) or (SEQ ID NO:2), said primers bracketing a hypervariable region on the 28S rDNA or rRNA present in the fungal species of said group; c) amplifying the sequence between said primers; and d) using one or more labeled probes directed to a portion of the hypervariable region bracketed by said primers, each said labeled probe being specific for one of said fungal species from said group, to determine whether said fungal species identified by each said labeled probe is present in said sample.",
    "2. The method of claim 1 in which, in said amplifying step, said amplifying procedure is the polymerase chain reaction.",
    "3. The method of claim 1 in which said one or more probes is selected from the group consisting of (SEQ ID NO:3), (SEQ ID NO:4), (SEQ ID NO:5), (SEQ ID NO:6), (SEQ ID NO:7), (SEQ ID NO:8), (SEQ ID NO:9), (SEQ ID NO:10), (SEQ ID NO:11), (SEQ ID NO:12), (SEQ ID NO:13), (SEQ ID NO:14), (SEQ ID NO:15), (SEQ ID NO:16), (SEQ ID NO:17), (SEQ ID NO:18), (SEQ ID NO:19), (SEQ ID NO:20), (SEQ ID NO:21), (SEQ ID NO:22) and (SEQ ID NO:23).",
    "4. The method of claim 1 wherein, in step (d), more than one probe is used, each said probe being connected to (a) a different signal moiety or (b) a moiety which allows separation of said probes.",
    "5. A method of determining whether one or more fungal species selected from the group of fungal species consisting of Aspergillus fumigatus, Blastomyces dermatitidis, Candida albicans, Coccidioides immitis, Cryptococcus neoformans, Histoplasma capsulatum, Aspergillus glaucus, Aspergillus niger, Aspergillus terreus, Candida glabrata, Candida guilliermondii, Candida kefyr, Candida krusei, Candida lusitaniae, Candida parapsilosis, Candida tropicalis, Pseudallescheria boydii, Aspergillus flavus and Sporothrix schenckii is present in a sample of fungi, said method comprising the following steps: a) extracting nucleic acid material from fungi contained in said sample; b) adding a universal fungal probe selected from the group consisting of (SEQ ID NO: 1), (SEQ ID NO:2) and the complements thereof; c) using one or more second probes, each said second probe being specific for one of said fungal species from said group, wherein said one or more second probes each has a nucleotide residue sequence selected from the group consisting of (SEQ ID NO:3), (SEQ ID NO:4), (SEQ ID NO:5), (SEQ ID NO:6), (SEQ ID NO:7), (SEQ ID NO:8), (SEQ ID NO:9), (SEQ ID NO:10), (SEQ ID NO:11), (SEQ ID NO:12), (SEQ ID NO:13), (SEQ ID NO:14), (SEQ ID NO:15), (SEQ ID NO:16), (SEQ ID NO:17), (SEQ ID NO:18), (SEQ ID NO:19), (SEQ ID NO:20), (SEQ ID NO:21), (SEQ ID NO:22), (SEQ ID NO:23) and the complements thereof; and d) determining whether said fungal species identified by each said second probe is present in said sample, wherein at least one of said probes is connected to a signal moiety and at least one of said probes is connected to a moiety that allows separation of said probes.",
    "6. A method of determining whether one or more fungal species selected from the group of fungal species consisting of Aspergillus fumigatus, Blastomyces dermatitidis, Candida albicans, Coccidioides immitis, Cryptococcus neoformans, Histoplasma capsulatum, Aspergillus glaucus, Aspergillus niger, Aspergillus terreus, Candida glabrata, Candida guilliermondii, Candida kefyr, Candida krudei, Candida lusitaniae, Candida parapsilosis, Candida tropicalis, Pseudallescheria boydii, Aspergillus flavus and Sporothrix schenckii is present in a sample of fungi, said method comprising the following steps: a) extracting nucleic acid material from fungi contained in said sample; and b) using one or more labeled probes, each said labeled probe being specific for one of said fungal species from said group, to determine whether said fungal species identified by each said labeled probe is present in said sample, wherein said one or more labeled probes each has a nucleotide residue sequence selected from the group consisting of (SEQ ID NO:3), (SEQ ID NO:4), (SEQ ID NO:5), (SEQ ID NO:6), (SEQ ID NO:7), (SEQ ID NO:8), (SEQ ID NO:9), (SEQ ID NO:10), (SEQ ID NO:11), (SEQ ID NO:12), (SEQ ID NO:13), (SEQ ID NO:14), (SEQ ID NO:15), (SEQ ID NO:16), (SEQ ID NO:17), (SEQ ID NO:18), (SEQ ID NO:19), (SEQ ID NO:20), (SEQ ID NO:21), (SEQ ID NO:22), (SEQ ID NO:23) and the complements thereof.",
    "7. An oligonucleotide probe/primer for fungi, said probe/primer having the nucleotide residue sequence of (SEQ ID NO:1) or the complement thereof.",
    "8. An oligonucleotide probe/primer for fungi, said probe/primer having the nucleotide residue sequence of (SEQ ID NO:2) or the complement thereof.",
    "9. An oligonucleotide hybridization probe for Aspergillus fumigatus, said probe having the nucleotide residue sequence of (SEQ ID NO:3) or the complement thereof.",
    "10. An oligonucleotide hybridization probe for Blascomyces dermatitidis, said probe having the nucleotide residue sequence of (SEQ ID NO:4) or the complement thereof.",
    "11. An oligonucleotide hybridization probe for Candida albicans, said probe having the nucleotide residue sequence of (SEQ ID NO:5) or the complement thereof.",
    "12. An oligonucleotide hybridization probe for Coccidioides immitis, said probe having the nucleotide residue sequence of (SEQ ID NO:6) or the complement thereof.",
    "13. An oligonucleocide hybridization probe for Cryptococcus neoformans, said probe having the nucleotide residue sequence of (SEQ ID NO:7) or the complement thereof.",
    "14. An oligonucleotide hybridization probe for Cryptococcus neoformans, said probe having the nucleotide residue sequence (SEQ ID NO:8) or the complement thereof.",
    "15. An oligonucleotide hybridization probe for Hictoplasma capsulatum, said probe having the nucleotide residue sequence of (SEQ ID NO:9) or the complement thereof.",
    "16. An oligonucleotide hybridization probe for Aspergillus glaucus, said probe having the nucleotide residue sequence of (SEQ ID NO:10) or the complement thereof.",
    "17. An oligonucleotide hybridization probe for Aspergillus niger, said probe having the nucleotide residue sequence of (SEQ ID NO:11) or the complement thereof.",
    "18. An oligonucleotide hybridization probe for Aspergillus terreus, said probe having the nucleotide residue sequence of (SEQ ID NO:12) or the complement thereof.",
    "19. An oligonucleotide hybridization probe for Candida glabrata, said probe having the nucleotide residue sequence of (SEQ ID NO:13) or the complement thereof.",
    "20. An oligonucleotide hybridization probe for Candida guilliermondii, said probe having the nucleotide residue sequence of (SEQ ID NO:14) or the complement thereof.",
    "21. An oligonucleotide hybridization probe for Candida kefyr, said probe having the nucleotide residue sequence of (SEQ ID NO:15) or the complement thereof.",
    "22. An oligonucleotide hybridization probe for Candida krusei, said probe having the nucleotide residue sequence (SEQ ID NO:16) or the complement thereof.",
    "23. An oligonucleotide hybridization probe for Candida lusitaniae, said probe having the nucleotide residual sequence of (SEQ ID NO 17) or the complement thereof.",
    "24. An oligonucleotide hybridization probe for Candida parapsilosis, said probe having the nucleotide residue sequence of (SEQ ID NO:18) or the complement thereof.",
    "25. An oligonucleotide hybridization probe for Candida tropicalis, said probe having the nucleotide residue sequence of (SEQ ID NO:19) or the complement thereof.",
    "26. An oligonucleocide hybridization probe for Pseudallescheria boydii, said probe having the nucleotide residue sequence of (SEQ ID NO:20) or the complement thereof.",
    "27. An oligonucleotide hybridization probe for Aspergillus flavus, said probe having the nucleotide residue sequence of (SEQ ID NO:21) or the complement thereof.",
    "28. An oligonucleotide hybridization probe for Sporothrix schenckii, said probe having the nucleotide residue sequence of (SEQ ID NO:22) or the complement thereof.",
    "29. An oligonucleotide hybridization probe for Sporothrix schenckii, said probe having the nucleotide residue sequence of (SEQ ID NO:23) or the complement thereof."
  ],
  "cpc": [
    "C12N 15/1003",
    "C07K 14/37",
    "C12Q 1/6806",
    "C12Q 1/6895",
    "Y10S 435/911",
    "Y10S 435/913",
    "Y10S 435/921",
    "Y10S 435/922",
    "Y10S 435/924",
    "Y10S 435/929",
    "Y10S 435/931",
    "Y10S 435/933",
    "Y10S 435/939",
    "Y10S 435/94",
    "Y10S 435/942",
    "Y10T 436/143333"
  ],
  "assignees": [
    "CHIRON DIAGNOSTICS CORP"
  ],
  "filing_date": "1995-01-13",
  "publication_date": "1998-06-09",
  "grant_date": "1998-06-09",
  "priority_date": "1995-01-13",
  "application_number": "US-37312795-A",
  "family_id": "23471085",
  "citations": [
    "EP0272009A2",
    "EP0422872A2",
    "US4851330A",
    "US5292874A",
    "US5324632A",
    "US5352579A",
    "US5501951A",
    "US5580971A",
    "US5593841A",
    "WO8803957A1"
  ]
}

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