COCHRAN et al. V. SONDERMEIJER et al. - Page 11





      Interference No. 103,613                                                                           
            nucleic acid sequences derived from Infectious                                               
            Bronchitis Virus (IBV), Mare k's Disease Virus                                               
            MDV , Newcastle Disease Virus (NDV), Infectious Bursal Disease Virus (IBDV),                 
            Chicken Aneamia Agent (CAA), Reo Virus, Avian Retro Virus, Fowl Adeno Virus,                 
            Turkey Rhinotracheitis Virus, Eimeria species, Salmonella species,                           
            Escherichia coli and Mycoplasma gallisepticum are contemplated for                           
            incorporation into the insertion-region of the HVT genome. [page 8]                          
            (underlying added for emphasis).                                                             
                  In view of the foregoing, the conclusion is inescapable that it would have             
      been prima facie obvious, within the ambit of 35 U.S.C. § 103, to insert a selected                
      foreign gene with an appropriate promoter at any convenient site within the US2 gene (ORF-         
      4) of HVT with the expectation of not disrupting essential viral functions of the                  
      recombinant HVT as suggested by the Australian reference (excerpts I and II above). Of             
      course, excerpt III more specifically relates to the recombinant species of Cochran claim          
      4 (HVT-012); whereas excerpt IV relates to the species of                                          
                  Cochran claim 1 (S-HVT-045). This conclusion is additionally supported by the          
      examiner's § 1.609(b) statement (page 3), which constitutes the basis of this                      
      interference, to the effect that:                                                                  
                  The common invention may be considered as an obvious species within the                
            scope of the genus set forth in patent claim 1, since ORF 4 (US2) is located                 
            within the genomic region from the end of ORF-1 through ORF5, and the StuI                   
            sitewithin ORF4 is an obvious convenient site for insertion. (underlying                     
            added for emphasis)                                                                          
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