Singer replied. âBear with me a moment longer. Our major obstacle has been getting the X-FLU gene into human DNA. It has to be done, of course, using a virus.â
Carson nodded. He knew that viruses worked by inserting their own DNA into a hostâs DNA. That made viruses the ideal vector to exchange genes between distantly related species. As a result, most genetic engineering used viruses in this way.
âHereâs how it will work,â Singer continued. âWe insert the X-FLU gene into a flu virus itself. Use the virus as a Trojan horse, if you will. Then we infect a person with that virus. As with any flu vaccine, the person will develop a mild case of influenza. Meanwhile, the virus has inserted the bonobo DNA into the personâs DNA. When he recovers, heâs got the X-FLU gene. And heâll never get the flu again.â
âGene therapy,â Carson said.
âAbsolutely,â Singer replied. âItâs one of the hottest things around today. Gene therapies are promising to cure all kinds of genetic diseases. Like Tay-Sachs disease, PKU syndrome, hemophilia, you name it. Someday, anyone born with a genetic defect will be able to get the right gene and live a normal life. Only in this case, the âdefectâ is susceptibility to the flu. And the change is inheritable .â
Singer mopped his brow. âI get pretty excited, talking about this stuff,â he said, grinning. âI never dreamed I could change the world when I was teaching at CalTech. X-FLU made me believe in God again, it really did.â He cleared his throat.
âWeâre very close, Guy. But thereâs one small problem. When we insert the X-FLU gene into the ordinary flu virus, it turns the ordinary virus virulent. Infinitely more virulent. And brutally contagious. Instead of being an innocuous messenger, the protein coat of the virus seems to mimic a hormone that stimulates the overproduction of cerebrospinal fluid. What you saw in the Fever Tank was the virusâs effect on a chimpanzee. We donât quite know what it will do to a human being, but we know it wonât be pleasant.â He stood up and moved to a nearby window.
âYour job is to redesign the viral coat of the X-FLU âmessengerâ virus. To render it harmless. To allow it to infect its human host without killing it, so that it can transport the X-FLU gene into human DNA.â
Carson opened his mouth to speak, then shut it abruptly. He suddenly understood why Scopes had plucked him out of the mass of GeneDyne talent. Until Fred Peck had set him to doing make-work, his specialty had been altering the protein shells that surround a virus. He knew that the protein coat of a virus could be changed or attenuated using heat, various enzymes, radiation, even through the growing of different strains. Heâd done it all himself. There were many ways to neutralize a virus.
âIt sounds like a straightforward problem,â he said.
âIt should be. But it isnât. For some reason, no matter what you do, the virus always mutates back to its deadly form. When Burt was working on it, he must have inoculated an entire colony of chimps with supposedly safe strains of the X-FLU virus. Each time, the virus reverted, and, well, youâve seen the grim result. Sudden cerebral edema. Burt was a brilliant scientist. If it wasnât for him, weâd have never been able to get PurBlood, our artificial blood product, stabilized and out the door. But the X-FLU problem drove himââ Singer paused. âHe couldnât take the pressure.â
âI can see why people avoid the Fever Tank,â Carson said.
âItâs horrible. And I have grave misgivings about using the chimps. But when you consider the benefits to humanityâ¦â Singer fell silent, looking out over the landscape.
âWhy the secrecy?â Carson finally asked.
âTwo reasons. We believe that at least one other