US2013171620A1PendingUtilityA1

Viral variants and methods for detecting same

Individually held — no corporate assignee on recordPriority: Nov 8, 1996Filed: Jul 12, 2012Published: Jul 4, 2013
Est. expiryNov 8, 2016(expired)· nominal 20-yr term from priority
C12N 2730/10122C12N 9/1276C07K 14/005C12N 7/00
54
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Claims

Abstract

The present invention relates generally to viral variants exhibiting reduced interactivity with immunological reagents. More particularly, the present invention is directed to hepatitis B variants exhibiting complete or partial resistance to nucleoside analogs and/or reduced interactivity with antibodies to viral surface components. The present invention further contemplates assays for detecting such viral variants which assays are useful in monitoring anti-viral therapeutic agents.

Claims

exact text as granted — not AI-modified
We claim: 
     
         1 . An isolated HBV mutant, comprising one or more mutations in the gene encoding the HBV polymerase resulting in decreased sensitivity to a nucleoside analogue compared to a wild-type HBV, wherein said mutation(s) result(s) in at least one amino acid addition, substitution and/or deletion in the A domain corresponding to amino acid residues 421-436 of a wild-type HBV polymerase and/or in the D domain corresponding to amino acid residues 576-588 of a wild-type HBV polymerase and/or in the E domain corresponding to amino acid residues 592-600 of a wild-type HBV polymerase, or in a region proximal thereto. 
     
     
         2 . An isolated HBV mutant according to  claim 1 , comprising one or more mutations in the gene encoding the HBV polymerase resulting in decreased sensitivity to a nucleoside analogue compared to a wild-type HBV, wherein said mutation(s) result(s) in at least one amino acid addition, substitution and/or deletion in the A domain corresponding to amino acid residues 421-436 of a wild-type HBV polymerase. 
     
     
         3 . An isolated HBV mutant according to  claim 1 , comprising one or more mutations in the gene encoding the HBV polymerase resulting in decreased sensitivity to a nucleoside analogue compared to a wild-type HBV, wherein said mutation(s) result(s) in at least one amino acid addition, substitution and/or deletion in the D domain corresponding to amino acid residues 576-588 of a wild-type HBV polymerase. 
     
     
         4 . An isolated HBV mutant according to  claim 1 , comprising one or more mutations in the gene encoding the HBV polymerase resulting in decreased sensitivity to a nucleoside analogue compared to a wild-type HBV, wherein said mutation(s) result(s) in at least one amino acid addition, substitution and/or deletion in the E domain corresponding to amino acid residues 592-600 of a wild-type HBV polymerase. 
     
     
         5 . A method for determining the potential for an HBV to exhibit reduced sensitivity to a nucleoside analogue, said method comprising isolating DNA or corresponding mRNA from said HBV and screening for one or more mutation(s) in the nucleotide sequence encoding HBV DNA polymerase resulting in at least one amino acid substitution, deletion and/or addition in the D domain or E domain or a region proximal thereto of said DNA polymerase wherein the presence of such a mutation is an indication of the likelihood of resistance to said nucleoside analogue. 
     
     
         6 . A method for determining whether an HBV isolate encodes a variant DNA polymerase, said method comprising determining the amino acid sequence of its DNA polymerase directly or via a nucleotide sequence and comparing same to the amino acid sequence below (SEQ ID NO:29): 
       
         
           
                 
               
                                 DOMAIN A 
                 
                   421       430         440        450 
                 
                     S N   D LSWLSLD VSAAFYH   I   P PL HPAAMPHLL I   V  GSSGL S   D RYVA 
                 
                     
                 
                   460         470            480          490 
                 
                   RLSS T   N S R   N N I *N  N Y H Q H   Y   G   R *** D   N LH  D   N   S   Y CSR N   Q LYVS L L   M LLY K   Q T Y   F G R   W   
                 
                     
                 
                                DOMAIN B 
                 
                   500         510        520         530 
                 
                   KLHL Y L   S   A HPI I   V  LGFRK I   L PMG V   G  GLSPFLLAQF  TSAI C   L   A   S   V   M   V   T   R   C R 
                 
                     
                 
                                DOMAIN C 
                 
                   540         550             560 
                 
                   AF F   P HC L     V   A   V F S   A Y MDD V L M VLGA   K   R   S   T   V   G   Q   E H L S R E S   F L F   Y   T   A   A   S   
                 
                     
                 
                                DOMAIN D      DOMAIN E 
                 
                   570            580        590         600  
                 
                     V   I   T   C   N   S   F   V LL S     D   L   V GI HLNP N   Q KTKR W GY SLNFMGY V   I I G   
                 
             
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
               
            
           
         
         where the presence of a different amino acid from the consensus sequence in the D or E domain indicates a putative HBV mutant. 
       
     
     
         7 . The method according to one of  claim 5  or  claim 6 , wherein the screening for a mutation or determining the amino acid sequence comprises sequencing said isolated HBV DNA or corresponding DNA. 
     
     
         8 . The method according to one of  claim 5  or  claim 6 , wherein the screening for a mutation or determining the amino acid sequence comprises a PCR method or PCR-based method. 
     
     
         9 . The method according to one of  claim 5  or  claim 6 , wherein the screening for a mutation or determining the amino acid sequence comprises a hybridization method. 
     
     
         10 . A method for determining whether an HBV isolate encodes a variant DNA polymerase said method comprising determining the amino acid sequence of the A domain (corresponding to amino acid residues 421-436) or a region proximal thereto (corresponding to amino acid residues 437-456) directly or via a nucleotide sequence and comparing same to the A domain or the region proximal thereto of the following amino acid sequence (SEQ ID NO:29): 
       
         
           
                 
               
                                 DOMAIN A 
                 
                   421       430         440        450 
                 
                     S N   D LSWLSLD VSAAFYH   I   P PL HPAAMPHLL I   V  GSSGL S   D RYVA 
                 
                     
                 
                   460         470            480          490 
                 
                   RLSS T   N S R   N N I *N  N Y H Q H   Y   G   R *** D   N LH  D   N   S   Y CSR N   Q LYVS L L   M LLY K   Q T Y   F G R   W   
                 
                     
                 
                                DOMAIN B 
                 
                   500         510        520         530 
                 
                   KLHL Y L   S   A HPI I   V  LGFRK I   L PMG V   G  GLSPFLLAQF  TSAI C   L   A   S   V   M   V   T   R   C R 
                 
                     
                 
                                DOMAIN C 
                 
                   540         550             560 
                 
                   AF F   P HC L     V   A   V F S   A Y MDD V L M VLGA   K   R   S   T   V   G   Q   E H L S R E S   F L F   Y   T   A   A   S   
                 
                     
                 
                               DOMAIN D       DOMAIN E 
                 
                   570          580          590         600  
                 
                     V   I   T   C   N   S   F   V LL S     D   L   V GI HLNP N   Q KTKR W GY SLNFMGY V   I I G   
                 
             
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
               
            
           
         
       
     
     
         11 . A method for determining whether an HBV isolate encodes a variant DNA polymerase according to  claim 10  said method comprising determining the amino acid sequence of the D domain (corresponding to amino acid residues 576-588) or a region proximal thereto directly or via a nucleotide sequence and comparing same to the D domain or the region proximal thereto of the following amino acid sequence (SEQ ID NO:29): 
       
         
           
                 
               
                                  DOMAIN A 
                 
                   421       430         440        450 
                 
                     S N   D LSWLSLD VSAAFYH   I   P PL HPAAMPHLL I   V  GSSGL S   D RYVA 
                 
                     
                 
                   460         470            480          490 
                 
                   RLSS T   N S R   N N I *N  N Y H Q H   Y   G   R *** D   N LH  D   N   S   Y CSR N   Q LYVS L L   M LLY K   Q T Y   F G R   W   
                 
                     
                 
                                DOMAIN B 
                 
                   500         510        520         530 
                 
                   KLHL Y L   S   A HPI I   V  LGFRK I   L PMG V   G  GLSPFLLAQF  TSAI C   L   A   S   V   M   V   T   R   C R 
                 
                     
                 
                                DOMAIN C 
                 
                   540         550             560 
                 
                   AF F   P HC L     V   A   V F S   A Y MDD V L M VLGA   K   R   S   T   V   G   Q   E H L S R E S   F L F   Y   T   A   A   S   
                 
                     
                 
                               DOMAIN D       DOMAIN E 
                 
                   570          580          590         600  
                 
                     V   I   T   C   N   S   F   V LL S     D   L   V GI HLNP N   Q KTKR W GY SLNFMGY V   I I G   
                 
             
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
               
            
           
         
       
     
     
         12 . A method for determining whether an HBV isolate encodes a variant DNA polymerase according to  claim 10  said method comprising determining the amino acid sequence of the E domain (corresponding to amino acid residues 592-600) or a region proximal thereto directly or via a nucleotide sequence and comparing same to the E domain or the region proximal thereto of the following amino acid sequence (SEQ ID NO:29) 
       
         
           
                 
               
                                 DOMAIN A 
                 
                   421       430         440        450 
                 
                     S N   D LSWLSLD VSAAFYH   I   P PL HPAAMPHLL I   V  GSSGL S   D RYVA 
                 
                     
                 
                   460         470            480          490 
                 
                   RLSS T   N S R   N N I *N  N Y H Q H   Y   G   R *** D   N LH  D   N   S   Y CSR N   Q LYVS L L   M LLY K   Q T Y   F G R   W   
                 
                     
                 
                                DOMAIN B 
                 
                   500         510        520         530 
                 
                   KLHL Y L   S   A HPI I   V  LGFRK I   L PMG V   G  GLSPFLLAQF  TSAI C   L   A   S   V   M   V   T   R   C R 
                 
                     
                 
                                DOMAIN C 
                 
                   540         550             560 
                 
                   AF F   P HC L     V   A   V F S   A Y MDD V L M VLGA   K   R   S   T   V   G   Q   E H L S R E S   F L F   Y   T   A   A   S   
                 
                     
                 
                               DOMAIN D       DOMAIN E 
                 
                   570          580          590         600  
                 
                     V   I   T   C   N   S   F   V LL S     D   L   V GI HLNP N   Q KTKR W GY SLNFMGY V   I I G   
                 
             
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
               
            
           
         
       
     
     
         13 . The method according to  claim 10 , wherein the determining comprises screening for a mutation comprises sequencing said isolated HBV DNA or corresponding DNA. 
     
     
         14 . The method according to  claim 10 , wherein the determining comprises screening for a mutation comprises a PCR method or PCR-based method. 
     
     
         15 . The method according to  claim 10 , wherein the determining comprises screening for a mutation comprises a hybridization method. 
     
     
         16 . HBV isolate encoding a variant DNA polymerase as detected by the method of any one of the  claims 10 - 12 . 
     
     
         17 . A kit for assays for detecting a HBV isolate according to  claim 16  comprising one or more reagents chosen from the group consisting of nucleic acid hybridisation technology as PCR and reagents for immunologically based detection techniques.

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