Process for typing of HCV isolates
First Claim
1. Use of at least one probe, with said probe being (i) capable of hybridizing to a genotype specific target region, present in an analyte strand, in the domain extending from the nucleotides at positions −
- 291 to −
66 of the 5′
untranslated region of one of the HCV isolates, or with said probe being (ii) complementary to any of the above-defined probes, for genotyping HCV isolates present in a biological sample.
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Abstract
The invention relates to a process for genotyping any HCV isolate present in a biological sample, previously identified as being HCV positive, and for classifying said isolate according to the percentage of homology with other HCV isolates, comprising the steps of:
contacting said sample in which the ribonucleotides or deoxyribonucleotides have been made accessible, if need be, under suitable denaturation, with at least one probe from about 10 to about 40 nucleotides, with said probe being liable to hybridize to a region being in the domain extending from nucleotide at position −291 to nucleotide at position −66 of the 5′ untranslated region of one of the HCV isolates represented by their cDNA sequences, with said numbering of position beginning with the first ATG codon of the open reading frame encoding the HCV polyprotein, or with said probe being complementary to the above-defined probes,
detecting the complexes possibly formed between said probe and the nucleotide sequence of the HCV isolate to be identified.
17 Citations
23 Claims
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1. Use of at least one probe, with said probe being (i) capable of hybridizing to a genotype specific target region, present in an analyte strand, in the domain extending from the nucleotides at positions −
- 291 to −
66 of the 5′
untranslated region of one of the HCV isolates, or with said probe being (ii) complementary to any of the above-defined probes, for genotyping HCV isolates present in a biological sample. - View Dependent Claims (18, 20)
- 291 to −
-
2. Process for genotyping HCV isolates present in a biological sample;
- comprising the steps of;
contacting said sample in which the ribonucleotides or deoxyribonucleotides have been made accessible, if need be, under suitable denaturation, with at least one probe, with said probe being (i) capable of hybridizing to a region in the domain extending from nucleotides at positions −
291 to −
66 of the 5′
untranslated region of one of the HCV isolates, or with said probe being (ii) complementary to any of the above-defined probes, and,detecting the complexes possibly formed between said probe and the nucleotide sequence of the HCV isolate to be identified. - View Dependent Claims (3, 4, 5, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 19, 21, 22, 23)
- comprising the steps of;
-
6. Probe having a sequence such that it targets at least one of the following sequences:
Specification