Davidson Carla J, White Aaron P, Surette Michael G
Department of Biochemistry and Molecular Biology, and Faculty of Medicine, University of Calgary, Calgary, Alberta, Canada.
ISME J. 2008 Mar;2(3):293-307. doi: 10.1038/ismej.2008.4. Epub 2008 Feb 7.
Rapid evolution of microbes under laboratory conditions can lead to domestication of environmental or clinical strains. In this work, we show that domestication due to laboratory passage in rich medium is extremely rapid. Passaging of wild-type Salmonella in rich medium led to diversification of genotypes contributing to the loss of a spatial phenotype, called the rdar morphotype, within days. Gene expression analysis of the rdar regulatory network demonstrated that mutations were primarily within rpoS, indicating that the selection pressure for scavenging during stationary phase had the secondary effect of impairing this highly conserved phenotype. If stationary phase was omitted from the experiment, radiation of genotypes and loss of the rdar morphotype was also demonstrated, but due to mutations within the cellulose biosynthesis pathway and also in an unknown upstream regulator. Thus regardless of the selection pressure, rapid regulatory changes can be observed on laboratory timescales. The speed of accumulation of rpoS mutations during daily passaging could not be explained by measured fitness and mutation rates. A model of mutation accumulation suggests that to generate the observed accumulation of sigma 38 mutations, this locus must experience a mutation rate of approximately 10(-4) mutations/gene/generation. Sequencing and gene expression of population isolates indicated that there were a wide variety of sigma 38 phenotypes within each population. This suggests that the rpoS locus is highly mutable by an unknown pathway, and that these mutations accumulate rapidly under common laboratory conditions.
微生物在实验室条件下的快速进化会导致环境菌株或临床菌株的驯化。在这项研究中,我们发现,在丰富培养基中进行实验室传代导致的驯化极其迅速。野生型沙门氏菌在丰富培养基中传代,数天内就导致了基因型多样化,进而导致一种称为rdar形态型的空间表型丧失。对rdar调控网络的基因表达分析表明,突变主要发生在rpoS基因内,这表明在稳定期进行清除的选择压力具有损害这种高度保守表型的次要作用。如果在实验中省略稳定期,也会出现基因型辐射和rdar形态型丧失的情况,但这是由于纤维素生物合成途径内以及一个未知上游调节因子中的突变所致。因此,无论选择压力如何,在实验室时间尺度上都能观察到快速的调控变化。每日传代过程中rpoS突变积累的速度无法用测得的适应性和突变率来解释。一个突变积累模型表明,要产生观察到的σ38突变积累,该基因座必须经历大约10^(-4)个突变/基因/代的突变率。群体分离株的测序和基因表达表明,每个群体中存在多种σ38表型。这表明rpoS基因座通过一条未知途径具有高度可变性,并且这些突变在常见实验室条件下迅速积累。