The global dissemination of plasmids encoding antibiotic resistance represents an urgent issue for human health and society. While the fitness costs for host cells associated with plasmid acquisition are expected to limit plasmid dissemination in the absence of positive selection of plasmid traits, compensatory evolution can reduce this burden. Experimental data suggest that compensatory mutations can be located on either the chromosome or the plasmid, and these are likely to have contrasting effects on plasmid dynamics. Whereas chromosomal mutations are inherited vertically through bacterial fission, plasmid mutations can be inherited both vertically and horizontally and potentially reduce the initial cost of the plasmid in new host cells. Here we show using mathematical models and simulations that the dynamics of plasmids depends critically on the genomic location of the compensatory mutation. We demonstrate that plasmid-located compensatory evolution is better at enhancing plasmid persistence, even when its effects are smaller than those provided by chromosomal compensation. Moreover, either type of compensatory evolution facilitates the survival of resistance plasmids at low drug concentrations. These insights contribute to an improved understanding of the conditions and mechanisms driving the spread and the evolution of antibiotic resistance plasmids.IMPORTANCEUnderstanding the evolutionary forces that maintain antibiotic resistance genes in a population, especially when antibiotics are not used, is an important problem for human health and society. The most common platform for the dissemination of antibiotic resistance genes is conjugative plasmids. Experimental studies showed that mutations located on the plasmid or the bacterial chromosome can reduce the costs plasmids impose on their hosts, resulting in antibiotic resistance plasmids being maintained even in the absence of antibiotics. While chromosomal mutations are only vertically inherited by the daughter cells, plasmid mutations are also provided to bacteria that acquire the plasmid through conjugation. Here we demonstrate how the mode of inheritance of a compensatory mutation crucially influences the ability of plasmids to spread and persist in a bacterial population.
Estimating carbon stocks in wooded systems is crucial to quantify national greenhouse gas balance estimates. However, inaccurate estimates are likely due to the divergent architecture of many species. The monkey puzzle tree Araucaria araucana, with its umbrella-like architecture is a vivid example. This species, often found in monodominant stands at high elevations, is the greatest carbon reservoir in the landscape, hence estimating its carbon storage is crucial. To provide the necessary basis for these estimations, we documented the variation in basic density and moisture content along the stem profile, identified the most suitable biomass estimation models, and quantified biomass allocation for three age ranges. We measured, felled, weighed, and separated trees into three categories: stem wood, stem bark, and foliage (branches + scaly leaves). The log-linear form of the simple allometric equation Y = aX b , based on diameter at breast height as the explanatory variable, covered a large part of the variation and showed good cross-validation performance (>0.96). Models using more covariates achieved lower absolute errors, but the estimation of the additional model parameters was associated with greater uncertainty. A multi-objective model comparison revealed that the best additional covariate to further improve biomass estimation was total tree height. The mean absolute percentage error was 9.8% for the total aboveground biomass, 8% for stem wood, 12% for stem bark and 24% for foliage. Changes in biomass distribution among tree components were related to age. For older trees, there was a relative increase in stem wood, a decreased proportion of foliage, but no change in stem bark. The proportion of stem bark biomass is similar to that of Araucaria angustifolia, but higher than in other conifers and most trees in general. Our results provide key properties for A. araucana and general guidance for the selection of easily-measurable variables allowing for excellent predictive power for local biomass estimation.
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