Compositions for use in identification of influenza viruses

• US 20100248219A1
• Filed: 10/17/2006
• Published: 09/30/2010
• Est. Priority Date: 10/17/2005
• Status: Abandoned Application

• Current Assignee: Ibis Biosciences Incorporated (Abbott Laboratories)
• Original Assignee: Ibis Biosciences Incorporated (Abbott Laboratories)
• Inventors: Sampath, Rangarajan, Li, Feng, Hall, Thomas A., Eshoo, Mark W.
• Application Number:
  US11/582,873
• Publication Number:
  US 20100248219A1
• Time in Patent Office: Days
• US Class Current: 435/6
• CPC Class Codes: C12Q 1/701 Specific hybridization probes

Abstract

The present invention provides oligonucleotide primers, compositions, and kits containing the same for rapid identification of viruses which are members of the influenza virus family by amplification of a segment of viral nucleic acid followed by molecular mass analysis.

Claims

1. A composition comprising a purified oligonucleotide primer pair wherein each member of said primer pair is 20 to 35 nucleobases in length and wherein the forward primer comprises at least 70% sequence identity with SEQ ID NO:

55 and the reverse primer comprises at least 70% sequence identity with SEQ ID NO;

56.

2. The composition of claim 1 wherein at least one of said forward primer or said reverse primer comprises at least one modified nucleobase.

3. The composition of claim 2 wherein said modified nucleobase is a mass modified nucleobase.

4. The composition of claim 3 wherein said the mass modified nucleobase is 5-Iodo-C.

5. The composition of claim 2 wherein said the modified nucleobase is a universal nucleobase.

6. The composition of claim 5 wherein said universal nucleobase is inosine.

7. The composition of claim 1 wherein at least one of said forward primer or said reverse primer lacks a non-templated T residue at its 5′

-end.

8. The composition of claim 2 wherein said modified nucleobase comprises a molecular mass modifying tag.

60. The composition of claim 1 wherein said forward primer comprises at least 80% sequence identity with SEQ ID NO:

55.

61. The composition of claim 1 wherein said forward primer comprises 100% sequence identity with SEQ ID NO:

55.

62. The composition of claim 1 wherein said reverse primer comprises at least 80% sequence identity with SEQ ID NO:

56.

63. The composition of claim 1 wherein said reverse primer comprises 100% sequence identity with SEQ ID NO:

56.

9. A kit comprising an oligonucleotide primer pair wherein each primer of said primer pair is 20 to 35 nucleobases in length and wherein the forward primer comprises at least 70% sequence identity with SEQ ID NO:

55 and the reverse primer comprises at least 70% sequence identity with SEQ ID NO;

56.

10. -59. (canceled)

64. A method for identifying an influenza virus comprising:

a) obtaining a sample suspected of comprising at least one bioagent;

b) amplifying one or more nucleic acids from said sample using a primer pair configured to generate amplicons from two or more members of the orthomyxovirdae family by hybridizing a forward primer and a reverse primer to conserved regions of a PA encoding gene, said conserved regions flanking a region that varies between said two or more members of said orthomyxovirdae family wherein said amplifying of said one or more nucleic acids results in at least one amplicon and wherein said at least one amplicon is between 45 consecutive nucleobases in length and 200 consecutive nucleobases in length; and

c) determining a molecular mass of said at least one amplicon using a mass spectrometer.

65. The method of claim 64 further comprising the step of calculating a base composition from said determined molecular mass.

66. The method of claim 64 further comprising the step of comparing said determined molecular mass to a plurality of molecular masses indexed to said primer pair of step b) and indexed to a known member of the orthomyxovirdae family, wherein a match between said determined molecular mass and a member of said plurality of molecular masses identifies said at least one bioagent as one or more of a genus, a species, a sub-species, a serotype or a genotype of the orthomyxovirdae family.

67. The method of claim 65 further comprising the step of comparing said calculated base composition to a plurality of base compositions indexed to said primer pair of step b) and indexed to a known member of the orthomyxovirdae family, wherein a match between said calculated base composition and a member of said plurality of base compositions identifies said at least one bioagent as one or more of a genus, a species, a sub-species, a serotype or a genotype of an the othhomyxovirdae family.

68. The method of claim 64 wherein said sample comprises at least one nucleic acid belonging to a member of the orthopoxyirdae family, said member selected from the group consisting of influenzavirus A genus, influenzavirus B genus, influenzavirus C genus, influenza A virus species, influenza B virus species and combinations thereof.

69. The method of claim 64 wherein said PA encoding gene is from an orthomyxovirus family member selected from the group consisting of influenzavirus A genus, influenzavirus B genus and influenzavirus C genus.

70. The method of claim 69 wherein said PA encoding gene is from influenzavirus A genus.

71. The method of claim 64 wherein said forward primer comprises at least 70% sequence identity to SEQ ID NO:

55.

72. The method of claim 64 wherein said forward primer comprises at least 80% sequence identity to SEQ ID NO:

55.

73. The method of claim 64 wherein said forward primer comprises at least 90% sequence identity to SEQ ID NO:

55.

74. The method of claim 64 wherein said forward primer comprises 100% sequence identity to SEQ ID NO:

55.

75. The method of claim 64 wherein said reverse primer comprises at least 70% sequence identity to SEQ ID NO:

56.

76. The method of claim 64 wherein said reverse primer comprises at least 80% sequence identity to SEQ ID NO:

56.

77. The method of claim 64 wherein said reverse primer comprises at least 90% sequence identity to SEQ ID NO:

56.

78. The method of claim 64 wherein said reverse primer comprises 100% sequence identity to SEQ ID NO:

56.

79. The method of claim 64 wherein at least one of said forward primer or said reverse primer comprises at least one modified nucleobase.

80. The method of claim 79 wherein said modified nucleobase is a mass modified nucleobase.

81. The method of claim 80 wherein said mass modified nucleobase is 5-Iodo-C.

82. The method of claim 79 wherein said modified nucleobase is a universal nucleobase.

83. The method of claim 82 wherein said universal nucleobase is inosine.

84. The method of claim 64 wherein at least one of said forward primer or said reverse primer comprises a non-templated T residue at its 5′

-end.

85. The method of claim 79 wherein said modified nucleobase comprises a molecular mass modifying tag.

86. The method of claim 64 wherein said amplifying step comprises use of at least one additional primer pair configured to hybridize with conserved regions of a gene selected from the group consisting of PB1, NUC, M1, PA, NS1, NS2, PB2 and a combination thereof.

87. The method of claim 64 wherein said at least one bioagent in said sample is identified by one or more of its genus, species, sub-species, serotype, genotype, or combination thereof.

88. The method of claim 64 wherein said region that varies between two or more members of said orthomyxoviridae family comprises base composition variability between the two or more members of said orthomyxoviridae family.

89. A composition comprising a primer pair configured to generate amplicons from two or more members of the orthomyxovirdae family by hybridizing a forward primer and a reverse primer to conserved regions of a PA encoding gene in two or more members of said orthomyxovirdae family, said primer pair comprising a forward primer of at least 15 oligonucleotides and reverse primer of at least 15 oligonucleotides, said conserved regions flanking a region that varies between said two or more members of said orthomyxovirdae family wherein upon amplification of a nucleic acid from a member of said orthomyxovirdae family said primer pair generates an amplicon between 45 consecutive nucleobases in length and 200 consecutive nucleobases in length.