IP Library Granted Patent US 7,494,778
Granted Patent B2
US 7,494,778 · App. 11/644,669 · Granted Feb 24, 2009

Nucleotide sequences specific to

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Quick Facts
Patent No.
US 7,494,778
App. No.
11/644,669
Granted
Feb 24, 2009
Kind
B2
Abstract

Described herein is the identification of nucleotide sequences specific to Francisella tularensis that serves as a marker or signature for identification of this bacterium. In addition, forward and reverse primers and hybridization probes derived from these nucleotide sequences that are used in nucleotide detection methods to detect the presence of the bacterium are disclosed.

Claims (16)

1. A set of polynucleotides comprising a first isolated polynucleotide and a second isolated polynucleotide, wherein the first isolated polynucleotide consists of SEQ ID NO: 4 or the complement thereof and the second polynucleotide consists of SEQ ID NO: 8 or the complement thereof.

2. The set of polynucleotides of claim 1 , comprising at least one further isolated polynucleotide consisting of a nucleic acid sequence selected from the group consisting of SEQ ID NOS: 12, 16, 20, 24, 28 and 32 or the complement thereof.

3. The set of polynucleotides of claim 2 , comprising eight isolated polynucleotides each consisting of one of SEQ ID NOS: 4, 8, 12, 16, 20, 24, 28 and 32 or the complements thereof.

4. The set of polynucleotides of claim 1 , further comprising a set of oligonucleotides wherein each oligonucleotide consists of one of SEQ ID NOS: 1, 2, 3, 5, 6, or 7.

5. The set of polynucleotides of claim 3 , further comprising a set of oligonucleotides, wherein each oligonucleotide consists of one of SEQ ID NOS: 1, 2, 3, 5, 6, 7, 9, 10, 11, 13, 14, 15, 17, 18, 19, 21, 22, 23, 25, 26, 27, 29, 30, or 31.

6. A method for detection of Francisella tularensis in a sample comprising: (i) providing a sample; and (ii) performing a PCR assay to detect the set of polynucleotides of claim 1 in the sample, wherein detection of the first isolated polynucleotide and the second isolated polynucleotide in the sample indicates the presence of Francisella tularensis in the sample, wherein the first isolated polynucleotide consists of SEQ ID NO: 4 or the complement thereof and the second polynucleotide consists of SEQ ID NO: 8 or the complement thereof.

7. The method of claim 6 , wherein said assay is a fluorogenic 5′ nuclease PCR assay.

8. A method for detection of Francisella tularensis in a sample comprising: (i) providing a sample; and (ii) performing a PCR assay to detect the set of polynucleotides of claim 3 in the sample, wherein detection of the set of polynucleotides of claim 3 in the sample indicates the presence of Francisella tularensis in the sample, wherein the first isolated polynucleotide consists of SEQ ID NO: 4 or the complement thereof, the second polynucleotide consists of SEQ ID NO: 8 or the complement thereof, the third polynucleotide consists of SEQ ID NO: 12 or the complement thereof, the forth polynucleotide consists of SEQ ID NO: 16 or the complement thereof, the fifth polynucleotide consists of SEQ ID NO: 20 or the complement thereof, the sixth polynucleotide consists of SEQ ID NO: 24 or the complement thereof, the seventh polynucleotide consists of SEQ ID NO: 28 or the complement thereof, and the eighth polynucleotide consists of SEQ ID NO: 32 or the complement thereof.

9. The method of claim 6 , wherein said PCR comprises standard PCR.

10. The method of claim 6 , wherein

said assay is performed using a first forward primer consisting of SEQ ID NO:1, a first reverse primer consisting of SEQ ID NO:2, and a first hybridization probe consisting of SEQ ID NO:3 for detection of SEQ ID NO:4 and using a second forward primer consisting of SEQ ID NO:5, a second reverse primer consisting of SEQ ID NO:6, and a second hybridization probe consisting of SEQ ID NO:7 for detection of SEQ ID NO:8; and

detecting the presence of SEQ ID NO:4 and SEQ ID NO:8 by fluorogenic 5′ nuclease PCR assay, wherein the presence of SEQ ID NO:4 and SEQ ID NO:8 indicates the presence of Francisella tularensis in the sample.

11. The method of claim 6 , wherein each Amplicon is detected in a separate reaction tube.

12. The method of claim 8 , wherein each Amplicon is detected in a separate reaction tube.

13. The method of claim 6 , wherein the sample is from an air monitor.

14. The method of claim 8 , wherein the sample is from an air monitor.

Assignments (3)
CONFIRMATORY LICENSE Recorded Jun 18, 2012
From: LAWRENCE LIVERMORE NATIONAL SECURITY, LLC
To: U.S. DEPARTMENT OF ENERGY
Reel/Frame 028391/0960 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 18, 2009
From: MCCREADY, PAULA M.; RADNEDGE, LYNDSAY; ANDERSON, GARY L.; OTT, LINDA L.; SLEZAK, THOMAS R.; KUCZMARSKI, THOMAS A.; VITALIS, ELIZABETH A.
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 022699/0069 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 4, 2007
From: REGENTS OF THE UNIVERSITY OF CALIFORNIA, THE
To: LAWRENCE LIVERMORE NATIONAL SECURITY, LLC
Reel/Frame 020012/0032 →