Methods for providing bacterial bioagent characterizing information

• US 7,217,510 B2
• Filed: 06/26/2001
• Issued: 05/15/2007
• Est. Priority Date: 06/26/2001
• Status: Expired due to Fees

• Current Assignee: Ibis Biosciences Incorporated (Abbott Laboratories)
• Original Assignee: ISIS Pharmaceuticals Incorporated (Ionis Pharmaceuticals, Inc.)
• Inventors: Hofstadler, Steven A., Sampath, Rangarajan, Griffey, Richard H., McNeil, John, Ecker, David J., Crooke, Stanley T.
• Primary Examiner(s): FREDMAN, JEFFREY NORMAN
• Application Number:
  US09/891,793
• Publication Number:
  US 20030082539A1
• Time in Patent Office: 2,149 Days
• Field of Search: 710/3, 702/19, 702/20, 702/27, 435/6, 435/7.1
• US Class Current: 435/6.19
• CPC Class Codes: G16B 15/00 ICT specially adapted for analysing two-dimensional or three-dimensional molecular structures, e.g. structural or functional relations or structure alignment
• CPC Class Codes: G16B 15/10 Nucleic acid folding
• CPC Class Codes: G16B 20/00 ICT specially adapted for functional genomics or proteomics, e.g. genotype-phenotype associations
• CPC Class Codes: G16B 20/20 Allele or variant detection, e.g. single nucleotide polymorphism [SNP] detection
• CPC Class Codes: G16B 40/10 Signal processing, e.g. from mass spectrometry [MS] or from PCR
• CPC Class Codes: G16B 50/00 ICT programming tools or database systems specially adapted for bioinformatics
• CPC Class Codes: G16B 99/00 Subject matter not provided for in other groups of this subclass
• CPC Class Codes: G16H 50/80 for detecting, monitoring or modelling epidemics or pandemics, e.g. flu
• CPC Class Codes: Y02A 90/10 Information and communication technologies [ICT] supporting adaptation to climate change, e.g. for weather forecasting or climate simulation

Abstract

The present invention relates generally to the field of investigational bioinformatics and more particularly to secondary structure defining databases. The present invention further relates to methods for interrogating a database as a source of molecular masses of known bioagents for comparing against the molecular mass of an unknown or selected bioagent to determine either the identity of the selected bioagent, and/or to determine the origin of the selected bioagent. The identification of the bioagent is important for determining a proper course of treatment and/or irradication of the bioagent in such cases as biological warfare. Furthermore, the determination of the geographic origin of a selected bioagent will facilitate the identification of potential criminal identity.

Claims

1. A method for providing bioagent characterizing information comprising:

a) measuring or calculating with a mass spectrometer a plurality of molecular masses corresponding to a plurality of amplification products, wherein the amplification products are 46 to 166 nucleobases in length, and wherein the amplification products are obtained by amplification of at least one target sequence region of a bioagent nucleic acid gene sequence using a primer pair that hybridizes to the at least one target sequence region of at least nineteen bioagents;

said target sequence region comprising two conserved regions that are hybridizable with the primer pair and that flank a variable region that uniquely varies between at least eight bioagents;

b) interrogating a database stored on a computer readable medium with an identification query, wherein the identification query comprises comparison of the measured molecular mass of step a) with the database;

said database comprises molecular mass calculated for the target sequence regions for at least nineteen bioagents and each of the calculated molecular masses is indexed to bioagent characterizing information;

c) delivering from the database a response that comprises the bioagent characterization information generated by the comparison of the measured and calculated molecular mass of step b) thereby identifying the bioagent associated with amplification product of step a).

2. The method of claim 1 wherein the nucleic acid gene sequence encodes ribosomal RNA or a protein involved in translation, replication, recombination, repair, transcription, nucleotide metabolism, amino acid metabolism, lipid metabolism, energy generation, uptake, or secretion.

3. The method of claim 1 wherein the bioagent characterizing information is a genus name.

4. The method of claim 3 wherein the genus name is Acinetobacter, Aeromonas, Bacillus, Bacteroides, Bartonella, Bordetella, Borrelia, Brucella, Burkholderia, Campylobacter, Chlamydia, Chlamydophila, Clostridium, Coxiella, Enterococcus, Escherichia, Francisella, Fusobacterium, Haemophilus, Helicobacter, Klebsiella, Legionella, Leptospira, Listeria, Moraxella, Mycobacterium, Mycoplasma, Neisseria, Proteus, Pseudomonas, Rhodobacter, Rickettsia, Salmonella, Shigella, Staphylococcus, Streptobacillus, Streptomyces, Treponema, Ureaplasma, Vibrio, or Yersinia.

5. The method of claim 1 wherein the bioagent characterizing information is a species name.

6. The method of claim 1 wherein the bioagent characterizing information is a strain name.

7. The method of claim 1 wherein the response is delivered via a network.

8. The method of claim 7 wherein the network is a local area network, a wide area network, or the internet.

9. The method of claim 1 wherein said mass spectrometer is an electrospray Fourier transform ion cyclotron resonance mass spectrometer or an electrospray time-of-flight mass spectrometer.

10. The method of claim 1 wherein the primer pair comprises at least one modified nucleobase.

11. The method of claim 10 wherein the modified nucleobase comprises 2,6-diaminopurine, propyne C, propyne T, phenoxazine, or G-clamp.

12. The method of claim 1 wherein said bioagent is a biological warfare agent.

13. The method of claim 12 wherein the biological warfare agent comprises Bacillus anthracis, Yersinia pestis, Franciscella tularensis, Brucella suis, Brucella abortus, Brucella melitensis, Burkholderia mallei, Burkholderia pseudomalleii, Salmonella typhi, Rickettsia typhii, Rickettsia prowasekii, Coxiella burnetii, Rhodobacter capsulatus, Chlamydia pneumoniae, Escherichia coli, Shigella dysenteriae, Shigella flexneri, Bacillus cereus, Clostridium botulinum, Coxiella burnetti, Pseudomonas aeruginosa, Legionella pneumophila, or Vibrio cholerae.

27. The method of claim 1 wherein said bioagent is a bacterium, virus, fungus or protozoan.

28. The method of claim 27 wherein the bioagent is arenavirus, bunyavirus, mononegavirales, picornavirus, astrovirus, calcivirus, nidovirales, flavivirus or togavirus.

14. A method for providing bioagent characterizing information comprising:

a) measuring or calculating with a mass spectrometer a plurality of molecular masses corresponding to a plurality of amplification products, wherein the amplification products are 46 to 166 nucleobases in length, and wherein the amplification products are obtained by amplification of at least one target sequence of a bioagent nucleic acid gene sequence using a primer pair that hybridizes to the at least one target sequence region of at least nineteen bioagents said target sequence region comprising two conserved regions that are hybridizable with the primer pair and that flank a variable region that uniquely varies between at least eight bioagents;

b) calculating a base composition from said molecular mass measurement, wherein it identifies the number of A residues, C residues, T residues, G residues, U residues, analogues thereof and mass tag residues thereof;

c) interrogating a database stored on a computer readable medium with an identification query, wherein the identification query comprises comparison of the base composition data from step b) with the database;

said database comprises base composition data calculated for the target sequence regions for at least nineteen of the bioagents and each of the calculated base compositions is indexed to bioagent characterizing information; and

d) delivering from the database a response comprising bioagent characterization information generated by the comparison of said measured and calculated base composition of step c) thereby identifying the bioagent associated with an amplification product of step a).

15. The method of claim 14 wherein the nucleic acid gene sequence encodes ribosomal RNA or a protein involved in translation, replication, recombination, repair, transcription, nucleotide metabolism, amino acid metabolism, lipid metabolism, energy generation, uptake, or secretion.

16. The method of claim 14 wherein the bioagent characterizing information is a genus name.

17. The method of claim 16 wherein the genus name is Acinetobacter, Aeromonas, Bacillus, Bacteriodes, Bartonella, Bordetella, Borrelia, Brucella, Burkholderia, Campylobacter, Chlamydia, Chlamydophila, Clostridium, Coxiella, Enterococcus, Escherichia, Francisella, Fusobacterium, Haemophilus, Helicobacter, Klebsiella, Legionella, Leptospira, Listeria, Moraxella, Mycobacterium, Mycoplasma, Neisseria, Proteus, Pseudomonas, Rhodobacter, Rickettsia, Salmonella, Shigella, Staphylococcus, Streptobacillus, Streptomyces, Treponema, Ureaplasma, Vibrio, or Yersinia.

18. The method of claim 14 wherein the bioagent characterizing information is a species name.

19. The method of claim 14 wherein the bioagent characterizing information is a strain name.

20. The method of claim 14 wherein the response is delivered via a network.

21. The method of claim 20 wherein the network is a local area network, a wide area network, or the internet.

22. The method of claim 14 wherein said mass spectrometer is an electrospray Fourier transform ion cyclotron resonance mass spectrometer or an electrospray time-of-flight mass spectrometer.

23. The method of claim 14 wherein the primer pair comprises at least one modified nucleobase.

24. The method of claim 23 wherein the modified nucleobase comprises 2,6-diaminopurine, propyne C, propyne T, phenoxazine, or G-clamp.

25. The method of claim 14 wherein said bioagent is a biological warfare agent.

26. The method of claim 25 wherein the biological warfare agent comprises Bacillus anthracis, Yersinia pestis, Franciscella tularensis, Brucella suis, Brucella abortus, Brucella melitensis, Burkholderia mallei, Burkholderia pseudomalleii, Salmonella typhi, Rickettsia typhii, Rickettsia prowasekii, Coxiella burnetti, Rhodobacter capsulatus, Chlamydia pneumoniae, Escherichia coli, Shigella dysenteriae, Shigella flexneri, Bacillus cereus, Clostridium botulinum, Coxiella burnetti, Pseudomonas aeruginosa, Legionella pneumophila, or Vibrio cholerae.

29. The method of claim 14 wherein said bioagent is a bacterium, virus, fungus or protozoan.

30. The method of claim 29 wherein the bioagent is arenavirus, bunyavirus, mononegavirales, picornavirus, astrovirus, calcivirus, nidovirales, flavivirus or togavirus.