Cyanobacteria saxitoxin gene cluster and detection of cyanotoxic organisms

Patent metadata

Field	Value
Publication number	US-10415097-B2
Application number	US-201514942830-A
Country	US
Kind code	B2
Filing date	Nov 16, 2015
Priority date	Apr 24, 2008
Publication date	Sep 17, 2019
Grant date	Sep 17, 2019

Abstract

The present invention provides methods for the detection of cyanobacteria, and in particular, methods for the detection of cyanotoxic organisms. The invention further relates to methods of screening for compounds that modulate the activity of polynucleotides and/or polypeptides of the saxitoxin biosynthetic pathways.

First claim

We claim:

1. A method for detecting cyanobacteria in a sample, the method comprising: (a) obtaining a sample for use in the method; and (b) detecting in the sample the presence of: (i) a polynucleotide comprising the sequence of SEQ ID NO: 14 and fragments of SEQ ID NO: 14 and variants having at least 90% sequence identity with SEQ ID NO: 14, wherein the fragment comprises a SXT open reading frame or (ii) complementary DNA (cDNA) encoded by the sequence of (i), and (c) amplifying said cDNA and/or polynucleotide of (i) and/or (ii) from the sample and detecting the amplified sequences.

2. A method for detecting cyanotoxic organisms in a sample, the method comprising: (a) obtaining a sample for use in the method; and (b) detecting in the sample the presence of: (i) a polynucleotide comprising the sequence of SEQ ID NO: 14 and fragments of SEQ ID NO: 14 and variants having at least 90% sequence identity with SEQ ID NO: 14, wherein the fragment comprises an open reading frame, or (ii) a cDNA encoded by the sequence according to (i), amplifying said cDNA and/or polynucleotide of (i) and/or (ii) from the sample by polymerase chain and detecting the amplified sequences.

3. The method according to claim 2 , wherein said cyanotoxic organism is a cyanobacteria or a dinoflagellate.

4. The method according to any of claims 1 - 3 , wherein said amplifying utilizes primers comprising a sequence selected from the group consisting of SEQ ID NO: 70 and SEQ ID NO: 71 and fragments thereof wherein the fragments are about 15 nucleotides to about 30 nucleotides in length.

5. The method according to claim any one of claims 1 - 3 or 4 , further comprising detecting the presence of: (i) a polynucleotide comprising SEQ ID NO: 95, and fragments thereof wherein the fragments comprise a CYR open reading frame; or (ii) a ribonucleic acid or cDNA encoded by the sequence according to (i), or (iii) a polypeptide comprising the sequence of: SEQ ID NO: 96 and fragments thereof wherein the fragments are between about 5 amino acids to about 780 amino acids in length; or (iv) a polypeptide comprising the sequence of SEQ ID NO: 15 and fragments thereof wherein the fragments are between about 5 amino acids to about 1000 amino acids in length.

6. The method according to claim 5 , wherein said detecting of the polynucleotides of (i) or the cDNA of (ii) comprises amplification of said polynucleotides or cDNA.

7. The method according to claim 6 , wherein said polymerase chain reaction utilizes one or more primers comprising a sequence selected from the group consisting of SEQ ID NO: 111, SEQ ID NO: 112, and variants that have at least 90% sequence identity with SEQ ID NO: 111, or SEQ ID NO: 112 and fragments thereof wherein the fragments are 15 nucleotides to 22 nucleotides in length.

8. A method for detecting dinoflagellates in a sample, the method comprising: (a) obtaining a sample for use in the method and (b) detecting in the sample the presence of (i) a polynucleotide comprising the sequence of SEQ ID NO: 14 and variants having at least 90% sequence identity with SEQ ID NO: 14 and fragments thereof wherein the fragments comprise a SXT open reading frame, (ii) cDNA encoded by the sequence of part (i), (iii) amplifying the DNA from the sample and detecting the amplified sequences.

9. The method according to any one of claims 1 - 3 or 8 , wherein said sample comprises one or more isolated or cultured organisms.

10. The method according to any one of claims 1 - 3 or 8 wherein said sample is an environmental sample.

11. The method according to claim 10 , wherein said environmental sample is derived from salt water, fresh water or a blue-green algal bloom.

12. The method of claim 1 , wherein the primers may be optionally labelled or the amplified products may be optionally labelled.

13. The method of claim 2 , wherein the primers may be optionally labelled or the amplified products may be optionally labelled.

14. The method of claim 8 , wherein the primers may be optionally labelled or the amplified products may be optionally labelled.

15. The method according to claim 1 , further comprising detecting in the sample the presence of one or more of a polynucleotide comprising a sequence selected from the group consisting of SEQ ID NO: 1, SEQ ID NO: 2, SEQ ID NO: 4, SEQ ID NO: 6, SEQ ID NO: 8, SEQ ID NO: 10, SEQ ID NO: 12, SEQ ID NO: 16, SEQ ID NO: 18, SEQ ID NO: 20, SEQ ID NO: 22, SEQ ID NO: 24, SEQ ID NO: 26, SEQ ID NO: 28, SEQ ID NO: 30, SEQ ID NO: 32, SEQ ID NO: 34, SEQ ID NO: 36, SEQ ID NO: 38, SEQ ID NO: 40, SEQ ID NO: 42, SEQ ID NO: 44, SEQ ID NO: 46, SEQ ID NO: 48, SEQ ID NO: 50, SEQ ID NO: 52, SEQ ID NO: 54, SEQ ID NO: 56, SEQ ID NO: 58, SEQ ID NO: 60, SEQ ID NO: 62, SEQ ID NO: 64, SEQ ID NO: 66, and SEQ ID NO: 68.

16. The method according to claim 2 , further comprising detecting in the sample the presence of one or more of a polynucleotide comprising a sequence selected from the group consisting of: SEQ ID NO: 20, SEQ ID NO: 22, SEQ ID NO: 24 and SEQ ID NO: 36.

17. The method according to claim 4 , wherein said amplifying further utilizes one or more primers comprising a sequence selected from the group consisting of SEQ ID NO: 72, SEQ ID NO: 73, SEQ ID NO: 74, SEQ ID NO: 75, SEQ ID NO: 76, SEQ ID NO: 77, SEQ ID NO: 78, SEQ ID NO: 79, SEQ ID NO: 113, SEQ ID NO: 114, SEQ ID NO: 115, SEQ ID NO: 116, SEQ ID NO: 117, SEQ ID NO: 118, SEQ ID NO: 119, SEQ ID NO: 120, SEQ ID NO: 121, SEQ ID NO: 122, SEQ ID NO: 123, SEQ ID NO: 124, SEQ ID NO: 125, SEQ ID NO: 126, SEQ ID NO: 127, SEQ ID NO: 128, SEQ ID NO: 129, SEQ ID NO: 130, SEQ ID NO: 131, SEQ ID NO: 132, SEQ 11) NO: 133, SEQ ID NO: 134, and fragments thereof wherein the fragments are about 15 nucleotides to about 30 nucleotides in length.

18. The method according to claim 5 , further comprising detecting the presence of one or more of: (i) a polynucleotide comprising a sequence selected from the group consisting of: SEQ ID NO: 80, SEQ ID NO: 81, SEQ ID NO: 83, SEQ ID NO: 85, SEQ ID NO: 87, SEQ ID NO: 89, SEQ ID NO: 91, SEQ ID NO: 93, SEQ ID NO: 97, SEQ ID NO: 99, SEQ ID NO: 101, SEQ ID NO: 103, SEQ ID NO: 105, SEQ ID NO: 107, SEQ ID NO: 109, or (ii) a ribonucleic acid or cDNA encoded by a sequence according to (i), or (iii) a polypeptide comprising a sequence selected from the group consisting of: SEQ ID NO: 82, SEQ ID NO: 84, SEQ ID NO: 86, SEQ ID NO: 88, SEQ ID NO: 90, SEQ ID NO: 92, SEQ ID NO: 94, SEQ ID NO: 98, SEQ ID NO: 100, SEQ ID NO: 102, SEQ ID NO: 104, SEQ ID NO: 106, SEQ ID NO: 108, and SEQ ID NO:110; or (iv) a polypeptide comprising a sequence selected from the group consisting of SEQ ID NO: 3, SEQ ID NO: 5, SEQ ID NO: 7, SEQ ID NO: 9, SEQ ID NO: 11, SEQ ID NO: 13, SEQ ID NO: 15, SEQ ID NO: 17, SEQ ID NO: 19, SEQ ID NO: 21, SEQ ID NO: 23, SEQ ID NO: 25, SEQ ID NO: 27, SEQ ID NO: 29, SEQ ID NO: 31, SEQ ID NO: 33, SEQ ID NO: 35, SEQ ID NO: 37, SEQ ID NO: 39, SEQ ID NO: 41, SEQ ID NO: 43, SEQ ID NO: 45, SEQ ID NO: 47, SEQ ID NO: 49, SEQ ID NO: 51, SEQ ID NO: 53, SEQ ID NO: 55, SEQ ID NO: 57, SEQ ID NO: 59, SEQ ID NO: 61, SEQ ID NO: 63, SEQ ID NO: 65, SEQ ID NO: 67 and SEQ ID NO: 69.

19. The method according to claim 8 , further comprising detecting in the sample the presence of one or more of a polynucleotide comprising a sequence selected from the group consisting of SEQ ID NO: 1, SEQ ID NO: 2, SEQ ID NO: 4, SEQ ID NO: 6, SEQ ID NO: 8, SEQ ID NO: 10, SEQ ID NO: 12, SEQ ID NO: 16, SEQ ID NO: 18, SEQ ID NO: 20, SEQ ID NO: 22, SEQ ID NO: 24, SEQ ID NO: 26, SEQ ID NO: 28, SEQ ID NO: 30, SEQ ID NO: 32, SEQ ID NO: 34, SEQ ID NO: 36, SEQ ID NO: 38,

Assignees

• Newsouth Innovations Pty Ltd

Inventors

• Neilan Brett A
• Mihali Troco Kaan
• Kellmann Ralf
• Jeon Young Jae

Classifications

• C12N9/90

  Isomerases (5.) · CPC title

• C12N9/78

  acting on carbon to nitrogen bonds other than peptide bonds (3.5) · CPC title

• C12N9/20

  Triglyceride splitting, e.g. by means of lipase · CPC title

• C12N9/13

  transferring sulfur containing groups (2.8) · CPC title

• C12N9/1018

  Carboxy- and carbamoyl transferases (2.1.3) · CPC title