Detection of fungal pathogens

• US 6,080,543 A
• Filed: 12/08/1997
• Issued: 06/27/2000
• Est. Priority Date: 12/08/1997
• Status: Expired due to Fees

• Current Assignee: E & J Gallo Winery
• Original Assignee: E & J Gallo Winery
• Inventors: Engel, Stacia R., Irelan, Nancy A., Descenzo, Richard A.
• Primary Examiner(s): Myers, Carla J.
• Application Number:
  US08/986,727
• Time in Patent Office: 932 Days
• Field of Search: 435/6, 435/91.2, 435/810, 536/24.32, 536/24.33, 536/23.1
• US Class Current: 435/6.12
• CPC Class Codes: C12Q 1/6895 for plants, fungi or algae
• CPC Class Codes: Y10S 435/81 Packaged device or kit

Abstract

Unique DNA sequences are provided which are useful in identifying different pathogenic fungi, such as those which infect grape plants. These unique DNA sequences can be used to provide oligonucleotide primers in PCR based analysis for the identification of fungal pathogens. The DNA sequences of the present invention include the internal transcribed spacer (ITS) of the ribosomal RNA gene regions of particular fungal pathogens, as well as oligonucleotide primers which are derived from these regions which are capable of identifying the particular pathogen.

Claims

1. An isolated double stranded nucleic acid selected from the group consisting of SEQ ID NOS:

6 to 10 and 12 to 15, and their complementary sequences.

2. An isolated nucleic acid which specifically hybridizes with the nucleic acid of claim 1.

3. An oligonucleotide sequence for identification of a fungal pathogen, wherein said sequence is selected from the group consisting of SEQ ID NOS:

16 to 25.

4. An oligonucleotide primer which is a fragment of the sequences according to claim 3, and which specifically hybridizes to the ITS1 or ITS2 of Eutypella vitis, Eutypa lata, Phomopsis viticola, or Diplodia gossypina.

5. An oligonucleotide primer for identification of a fungal pathogen, wherein said primer specifically amplifies at least a portion of the ITS1 region of SEQ ID NOS:

6, 8, 10, 12 or 14 or at least a portion of the ITS2 region of SEQ ID NOS;

7, 9, 11, 13 or 15, or which specifically amplifies at least a portion of the ITS region of a fungal pathogen selected from the group consisting of Eutypella sp. Eutypa sp. Phomopsis sp. and Diplodia sp. wherein said primer is selected from the group consisting of primers which contain at least 10 contiguous nucleotide bases from one of SEQ ID NOS;

26 to 36, primers which contain at least 10 contiguous nucleotide bases from one of SEQ ID NOS;

26 to 36 contiguous with 1 to 15 flanking nucleotide bases in the 5'"'"' and/or 3'"'"' direction of SEQ ID NOS;

16 to 25, and primers of 10 nucleotide bases or longer which contain at least 5 contiguous nucleotide bases from one of SEQ ID NOS;

26 to 36 contiguous with from 1 to 15 flanking nucleotide bases in the 5'"'"' and/or 3'"'"' direction of SEQ ID NOS;

16 to 25.

22. A kit comprising a carrier to receive therein one or more containers, at least one of said containers comprising an oligonucleotide primer according to claim 5.

6. A pair of oligonucleotide primers for use in the amplification-based detection of an internal transcribed spacer sequence of a fungal pathogen, wherein said primers specifically amplify at least a portion of the ITS1 region of SEQ ID NOS:

6, 8, 10, 12 or 14 or at least a portion of the ITS2 region of SEQ ID NOS;

7, 9, 11, 13 or 15, or which specifically amplify at least a portion of the ITS region of a fungal pathogen selected from the group consisting of Eutypella sp. Eutypa sp. Phomopsis sp. and Diplodia sp., wherein the primers are selected from the group consisting of primers which contain at least 10 contiguous nucleotide bases from one of SEQ ID NOS;

26 to 36, primers which contain at least 10 contiguous nucleotide bases from one of SEQ ID NOS;

26 to 36 contiguous with 1 to 15 flanking nucleotide bases in the 5'"'"' and/or 3'"'"' direction of SEQ ID NOS;

16 to 25, and primers of 10 bases or longer which contain at least 5 contiguous nucleotide bases from one of SEQ ID NOS;

26 to 36 contiguous with from 1 to 15 flanking nucleotide bases in the 5'"'"' and/or 3'"'"' direction of SEQ ID NOS;

16 to 25.

7. The pair of oligonucleotide primers according to claim 6 which comprises SEQ ID NO:

26 and SEQ ID NO;

27.

8. The pair of oligonucleotide primers according to claim 6 which comprises SEQ ID NO:

28 and SEQ ID NO;

29.

9. The pair of oligonucleotide primers according to claim 6 which comprises SEQ ID NO:

28 and SEQ ID NO;

30.

10. The pair of oligonucleotide primers according to claim 6 which comprises SEQ ID NO:

31 and SEQ ID NO;

32.

11. The pair of oligonucleotide primers according to claim 6 which comprises SEQ ID NO:

33 and SEQ ID NO;

34.

12. The pair of oligonucleotide primers according to claim 6 which comprises SEQ ID NO:

35 and SEQ ID NO;

36.

13. A method for detection of a fungal pathogen comprising:

(a) obtaining DNA from an organism, or part thereof, infected with a pathogen, or from a fungal culture isolated from a symptomatic or asymptomatic diseased organism;

(b) amplifying a part of the internal transcribed spacer sequence of said fungal pathogen using said DNA as a template in a polymerase chain reaction with a pair of oligonucleotide primers according to claim 6; and

(c) visualizing said amplified part of the internal transcribed spacer sequence to determine whether said fungal pathogen is present.

14. The method according to claim 13, wherein said fungal pathogen is selected from the group consisting of Eutypella vitis, Eutypa lata, Phomopsis viticola and Diplodia gossypina.

15. The method according to claim 13, wherein said organism or diseased organism is a grape plant.

16. The method according to claim 13, wherein the pair of oligonucleotide primers comprises SEQ ID NO:

26 and SEQ ID NO;

27.

17. The method according to claim 13, wherein the pair of oligonucleotide primers comprises SEQ ID NO:

28 and SEQ ID NO;

29.

18. The method according to claim 13, wherein the pair of oligonucleotide primers comprises SEQ ID NO:

28 and SEQ ID NO;

30.

19. The method according to claim 13, wherein the pair of oligonucleotide primers comprises SEQ ID NO:

31 and SEQ ID NO;

32.

20. The method according to claim 13, wherein the pair of oligonucleotide primers comprises SEQ ID NO:

33 and SEQ ID NO;

34.

21. The method according to claim 13, wherein the pair of oligonucleotide primers comprises SEQ ID NO:

35 and SEQ ID NO;

36.

23. A kit comprising a carrier to receive therein one or more containers, at least one of said containers comprising a pair of oligonucleotide primers according to claim 6.