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ULTIMATE COMPUTING - Quantum Consciousness Studies

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188 Viruses/Ambiguous Life Forms<br />

animate to inanimate material, and that viruses are somewhere in the middle.<br />

Some vital characteristics of living things include locomotion, nutrition, growth,<br />

respiration, excretion, sensitivity and reproduction. By these criteria viruses are<br />

not alive, however “inanimate” materials like crystals do manifest life-like<br />

growth, nutrition, reproduction, and locomotion. Defining life by the apparent<br />

ability to defy the second law of thermodynamics (creating order from disorder)<br />

by assembling complex organized biological structure from the disordered<br />

nonliving world ignores the fact that the thermodynamic law remains inviolate<br />

overall. Molecular level cytoskeletal protein subunits or viral particles assemble<br />

into more highly ordered structures, however the hydrophobic exclusion of water<br />

from protein subunits counteracts the change in entropy and the net effect remains<br />

order proceeding to disorder.<br />

There are three general theories as to the origin of viruses (Scott, 1985). The<br />

first is that viruses originated very early in evolution before the advent of<br />

eukaryotic cells. According to this view, modern viruses are direct descendants of<br />

primitive early molecules floating in the primordial soup or mud (Chapter 3). The<br />

second idea is that they are derived from parasites which invaded other cells and<br />

gradually became simpler, de-evolving to be totally concerned only with survival<br />

and multiplication. The third notion, which dominates current beliefs, is that<br />

viruses evolved from genetic material of cellular life: the “escaped gene”<br />

hypothesis.<br />

9.5 Domesticated Viruses<br />

The capabilities of viruses may be harnessed (Scott, 1985). Two hundred<br />

years ago Edward Jenner began to develop safe and effective anti-viral vaccines, a<br />

technique which amplifies the body’s immune system. Slopek and co-workers<br />

(1983) have treated patients afflicted with drug resistant bacterial infection by<br />

using viral bacteriophages selected for their effectiveness against the resistant<br />

organism. British scientists (Williams, Smith and Huggins, 1983) have used<br />

bacteriophages to treat intestinal infections in animals and direct use of viruses to<br />

combat bacterial infections in humans have also been attempted. Bacteriophages<br />

have potential advantages over modern drugs: they are highly specific, can leave<br />

the host cells unharmed with minimal side effects, and could be produced<br />

inexpensively. However, bacteria could develop resistances to bacteriophages as<br />

they do to some drugs.<br />

Other researchers have used exploited viruses to mass produce natural<br />

proteins in “genetic engineering.” For example, the “Epstein-Barr” virus has been<br />

used to transform selected immune cells which then multiply and produce large<br />

quantities of specific antibodies useful in medicine and industry. In some cases<br />

viruses are changed into novel forms for use as live vaccines. Genes for influenza<br />

and hepatitis B organisms can be combined in a vaccine virus genome to protect<br />

us against diseases such as hepatitis B and the flu. Genes encoding proteins of<br />

parasites such as the protozoan that causes malaria are being added to suitable<br />

viral genomes (Smith, 1984). Viruses can transfer foreign genes into bacterial<br />

cells. Gene coding for any wanted protein can be linked up to the genetic material<br />

of a virus and, when the virus infects suitable bacterial cells, the foreign gene is<br />

carried in with it. Once inside, the transferred gene may then begin to direct the<br />

manufacture of plentiful supplies of the protein it codes for. Viruses are thus<br />

being turned into versatile ferrymen which can carry a whole range of proteins<br />

into humans and livestock.<br />

Other exciting possibilities include transferring new genes into human cells.<br />

Many research groups including Richard Mulligan and cohorts at MIT (Kolata, et<br />

al., 1984) are trying to construct viruses that will carry new genes to human cells

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