Apte S P, Apte P P
Chemologic LLC, NA, 2313 welch place, Mansfield, TX 76063, USA.
Med Hypotheses. 2006;67(2):359-61. doi: 10.1016/j.mehy.2006.01.043. Epub 2006 Mar 20.
Conventional antimicrobial drugs that target microbial life processes impose a selection pressure on pathogens and attenuate pathogen imposed selection pressure on human hosts. The simultaneous increase and decrease that result in pathogen and human host evolvability/adaptability, respectively, distorts the natural Darwinian evolutionary process. Such drugs may create an aberrant Darwinian genotype in human hosts that is ill prepared to resist emerging virulent pathogenic strains in the event of a decrease in host ontogenic potential. In contrast, antimicrobial drugs that target host human genes exert a selective pressure both on the human genome (without population decimation) as well as on pathogenic microbes. Such drugs maintain the evolvability/adaptability of the host in tandem with that of the pathogens in the context of Darwinian evolution. Such drugs retain the capacity of the human host to evolve genotypes that may confer resistance to future pathogenic microbial strains, to assimilate prokaryotic endosymbionts and to increase the probability of survival in the event of a decrease in host ontogenic potential.
针对微生物生命过程的传统抗菌药物会对病原体施加选择压力,并减轻病原体对人类宿主施加的选择压力。分别导致病原体和人类宿主进化能力/适应性同时增加和降低的情况,扭曲了自然的达尔文进化过程。这类药物可能在人类宿主中产生一种异常的达尔文基因型,一旦宿主个体发育潜力下降,这种基因型就难以抵抗新出现的致病菌株。相比之下,针对人类宿主基因的抗菌药物会对人类基因组(不会导致种群灭绝)以及致病微生物施加选择压力。在达尔文进化的背景下,这类药物能使宿主与病原体的进化能力/适应性保持同步。这类药物能使人类宿主保留进化出可能对未来致病微生物菌株产生抗性的基因型的能力,同化原核内共生体,并在宿主个体发育潜力下降时提高生存概率。