scholarly journals Clonal Interference and Mutation Bias in Small Bacterial Populations in Droplets

Genes ◽  
2021 ◽  
Vol 12 (2) ◽  
pp. 223
Author(s):  
Philip Ruelens ◽  
J. Arjan G. M. de Visser

Experimental evolution studies have provided key insights into the fundamental mechanisms of evolution. One striking observation is that parallel and convergent evolution during laboratory evolution can be surprisingly common. However, these experiments are typically performed with well-mixed cultures and large effective population sizes, while pathogenic microbes typically experience strong bottlenecks during infection or drug treatment. Yet, our knowledge about adaptation in very small populations, where selection strength and mutation supplies are limited, is scant. In this study, wild-type and mutator strains of the bacterium Escherichia coli were evolved for about 100 generations towards increased resistance to the β-lactam antibiotic cefotaxime in millifluidic droplets of 0.5 µL and effective population size of approximately 27,000 cells. The small effective population size limited the adaptive potential of wild-type populations, where adaptation was limited to inactivating mutations, which caused the increased production of outer-membrane vesicles, leading to modest fitness increases. In contrast, mutator clones with an average of ~30-fold higher mutation rate adapted much faster by acquiring both inactivating mutations of an outer-membrane porin and particularly inactivating and gain-of-function mutations, causing the upregulation or activation of a common efflux pump, respectively. Our results demonstrate how in very small populations, clonal interference and mutation bias together affect the choice of adaptive trajectories by mediating the balance between high-rate and large-benefit mutations.

1970 ◽  
Vol 16 (2) ◽  
pp. 145-150 ◽  
Author(s):  
Motoo Kimura ◽  
Tomoko Ohta

SUMMARYIf a polymorphic locus is maintained in finite populations by frequency-dependent selection with selective neutrality at equilibrium, it is generally accompanied by two genetic loads, i.e. the dysmetric and the drift loads. The former arises because the fitness of the population may not be at a maximum at the equilibrium gene frequency and the latter because genetic drift in small populations displaces the gene frequency from its equilibrium value.In some simple models of frequency-dependent selection considered, the drift load is independent of selection coefficients and is approximately equal to (n−1)/(2Ne), where n is the number of alleles and Ne is the effective population size.


Genetics ◽  
2001 ◽  
Vol 157 (2) ◽  
pp. 911-925
Author(s):  
Renaud Vitalis ◽  
Denis Couvet

Abstract Standard methods for inferring demographic parameters from genetic data are based mainly on one-locus theory. However, the association of genes at different loci (e.g., two-locus identity disequilibrium) may also contain some information about demographic parameters of populations. In this article, we define one- and two-locus parameters of population structure as functions of one- and two-locus probabilities for the identity in state of genes. Since these parameters are known functions of demographic parameters in an infinite island model, we develop moment-based estimators of effective population size and immigration rate from one- and two-locus parameters. We evaluate this method through simulation. Although variance and bias may be quite large, increasing the number of loci on which the estimates are derived improves the method. We simulate an infinite allele model and a K allele model of mutation. Bias and variance are smaller with increasing numbers of alleles per locus. This is, to our knowledge, the first attempt of a joint estimation of local effective population size and immigration rate.


1970 ◽  
Vol 15 (2) ◽  
pp. 257-259 ◽  
Author(s):  
Alan Robertson

SUMMARYIn finite populations, loci maintained segregating by hétérozygote superiority will be disturbed from their equilibrium positions by genetic sampling and the mean fitness of individuals will consequently be reduced. A general expression for this reduction is obtained for the segregation of two alleles. If the probability of continued segregation at the locus is high, the reduction tends to 1/4N, irrespective of the strength of selection, where N is the effective population size. This will always be much less than the segregation load. If n alleles are segregating, so that all heterozygotes have the same fitness, the reduction tends to (n−1)/4N.


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