Method and kit for evaluation of HIV mutations

Chemistry: molecular biology and microbiology – Measuring or testing process involving enzymes or... – Involving virus or bacteriophage

Reexamination Certificate

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C435S091100, C435S091200, C536S024320, C536S024330

Reexamination Certificate

active

06265152

ABSTRACT:

BACKGROUND OF THE INVENTION
Genetic testing to determine the presence of or a susceptibility to a disease condition offers incredible opportunities for improved medical care, and the potential for such testing increases almost daily as ever increasing numbers of disease-associated genes and/or mutations are identified. A major hurdle which must be overcome to realize this potential, however, is the high cost of testing. This is particularly true in the case of highly polymorphic genes where the need to test for a large number of variations may make the test procedure appear to be so expensive that routine testing can never be achieved.
Testing for changes in DNA sequence can proceed via complete sequencing of a target nucleic acid molecule, although many persons in the art believe that such testing is too expensive to ever be routine. Changes in DNA sequence can also be detected by a technique called ‘single-stranded conformational polymorphism” (“SSCP”) described by Orita et al.,
Genomics
5:874-879 (1989), or by a modification thereof referred to a dideoxy-fingerprinting (“ddF”) described by Sarkar et al.,
Genomics
13:4410443 (1992). SSCP and ddF both evaluate the pattern of bands created when DNA fragments are electrophoretically separated on a non-denaturing electrophoresis gel. This pattern depends on a combination of the size of the fragments and of the three-dimensional conformation of the undenatured fragments. Thus, the pattern cannot be used for sequencing, because the theoretical spacing of the fragment bands is not equal.
This application relates to a particular test which can be useful as part of a testing protocol for the detection and characterization of human immunodeficiency virus (HIV).
SUMMARY OF THE INVENTION
The method of the invention provides a method for obtaining information about the allelic type of a sample of genetic material derived from an HIV-infected sample. A test is performed in which the sequence is determined in the 3′-direction for all four bases. This test will identify substantially all of the samples in which the sequence of the sample is determined in both the 3′ and 5′-direction for all four bases.
To perform the method of the invention, reagents suitable for the tests are suitably packaged as a kit. The kit contains reagents for performing a four-base sequence determination on one or both strands of the target DNA. One-stranded sequence determination could be performed all in the 3′-direction, all in the 5′-direction, or as a combination of the two strands.


REFERENCES:
patent: 4358535 (1982-11-01), Falkow et al.
patent: 4563417 (1986-01-01), Albarella et al.
patent: 4683195 (1987-07-01), Mullis et al.
patent: 4683202 (1987-07-01), Mullis
patent: 4942124 (1990-07-01), Church
patent: 4962020 (1990-10-01), Tabor et al.
patent: 5008182 (1991-04-01), Sninsky et al.
patent: 5124247 (1992-06-01), Ansorge
patent: 5171534 (1992-12-01), Smith et al.
patent: 5176995 (1993-01-01), Sninsky et al.
patent: 5219727 (1993-06-01), Wang et al.
patent: 5283171 (1994-02-01), Manos et al.
patent: 5403707 (1995-04-01), Atwood et al.
patent: 5409810 (1995-04-01), Larder
patent: 5427911 (1995-06-01), Ruano et al.
patent: 5451512 (1995-09-01), Apple et al.
patent: 5453355 (1995-09-01), Birkenmeyer et al.
patent: 5545527 (1996-08-01), Stevens
patent: 5629153 (1997-05-01), Urdea
patent: 5795722 (1998-08-01), Lacroix
patent: 5834189 (1998-11-01), Stevens
patent: 5837464 (1998-11-01), Capon et al.
patent: 5856088 (1999-01-01), McDonough et al.
patent: 5888736 (1999-03-01), Lacroix et al.
patent: 5977086 (1999-11-01), Lisziewicz et al.
patent: 6087093 (2000-07-01), Lieven et al.
patent: 403 333 (1992-10-01), None
patent: 9215711 (1992-09-01), None
patent: 92/16180 (1992-10-01), None
patent: 9219771 (1992-11-01), None
patent: WO93 13223 (1993-07-01), None
patent: WO97 23650 (1997-07-01), None
patent: 9723650 (1997-07-01), None
patent: WO97 24974 (1997-07-01), None
Demeter, et al., The Journal of Infectious Diseases (1995); 172:1480-1485; The University of Chicago.
Sarkar et al., “Dideoxy Fingerprinting (ddF) : A Rapod and Efficient Screen for the Presence of Mutations”Genomics13: 441-443 (1992).
Lin et al., “Characterization of Genetic Defects of Hemophilia A in Patients of Chinese Origin”Genomics18: 496-504 (1993) .
Langemeir et al, “Application of Cycle Dideoxy Fingerprinting to Screening Heterogenouse Populations of the Equine Infectious Anemia Virus”,BioTechniques17: 484-490 (1994).
Krishnamani et al., “Detection of a NovelArginine VasopressinDefect by Dideoxy Fingerprinting”J. Clin. Endocrinol. &Metabol. 77: 596-598 (1993).
Nelson et al., “Sequencing two DNA templates in five channels by digital compression”,Proc. Nat'l Acad/ Sci.(USA) 90: 1647-1651 (1993).
Ansorge et al., “One Label, one tube, Sanger DNA sequencing in one and two lanes on a gel”,Nucl. Acids Res. 18: 3419-3420 (1990).
Negri et al., “A Single-Reaction Method for DNA Sequence Determinaitin”Anal. Biochem197: 389-395 (1991).
Schinazi et al., “Mutation in retroviral genes associated with drug resistance”,Int'l Antiviral news5: 129-142 (1997).
Chamberlain et al., “Detection of Gene Deletions Using Multiplex Polymerase Chain Reactions”,Meth. Molec. Biol. 9: 299-312 (1991).
Ellison et al., “Detection of Mutations and Polymorphisms Using Fluorescence-Based Dideoxy Fingerprinting (F-ddF)”,Biotechniques 17: 742-753 (1994).
Eisenstein, B.I., “The Polymerase Chain reaction”,New Engl. J. Med. 322: 178-183 (1990).
Murakawa et al., “Direct Detection of HIV-1 RNA from AIDS and ARC Patient Samples”,DNA7: 287-295 (1988) .
Ruano et al., “Coupled Amplification and Sequencing of Genomic DNA”,Proc. Nat'l Acad Sci(USA) 88: 2815-2819 (1991).
Frenkel, L.M., et al., “Specific, Sensitive, and Rapid Assay for Human Immunodeficiency Virus Type 1 pl Mutations Associated with Resistance to Zidovudine and Didanosine”, Journal of Clinical Microbiology, vol. 33, No. 2, pp. 342-347, Feb. 1995.
Sanger, F., et al., “DNA Sequencing with Chain-Terminating Inhibitors”, Proc. Natl. Acad. Sci. USA, vol. 74, No. 12, pp. 5463-5467, Dec. 1977.
Kretz, K., et al., “Cycle Sequencing”, PCR Methods and Applications, vol. 3, No. 5, pp. S107-S112, Apr. 1994.
Wiemann, S. et al., “Simultaneous On-Line DNA Sequencing on Both Strands with Two Fluorescent Dyes”, Analytical Diochemistry, vol. 224, No. 1, pp. 117-121, Jan. 1995.
Haas, J., “Detection, Differentiation and Typing of Human Immunodeficiency Virus by Polymerase Chain Reaction”, Springer, Berlin, Germany, 1995, pp. 13-18.
Wahlberg, J., et al., “Automated Magnetic Preparation of DNA Templates for Solid Phase Sequencing”, Electrophoresis, vol. 13, pp. 547-551, 1992.
Larder, et al., Nature 365, 671-673, 1993.

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