bioRxiv Science⌕ Search

Biology subjects

Birzu, G.

Publications and source records attributed to Birzu, G..

7 recordsLinked to original sources

Extensive recombination, selection, and asexual blooms shapethe diversity of the dominant clade of Prochlorococcus

The tiny and enormously abundant marine cyanobacterium Prochlorococcus marinus contains many levels of population structure, with sequenced isolates spanning four orders of magnitude of diversity. It is divided into several major clades which exhibit the classic structure of distinct species, with little gene exchange across clade boundaries. The diversity within the dominant clade, High Light II (HLII), exceeds that of many bacterial species but exhibits little global population structure beyond some small tight genomic clusters. Few ecological distinctions within HLII have been found. What causes and sustains for millions of years the extensive diversity of this globally mixed population? In this work, hundreds of single cell genomes are analyzed and used to elucidate patterns of core and flexible gene flow, delineate subtle geographical correlations, and quantitatively test several scenarios for the evolutionary history of HLII. We find that recombination connects the entire HLII clade and that genes more than a few kb apart along the genome evolve largely independently. On shorter timescales, primarily-asexual blooms occur, but the clonal backbones of the resulting closely-related cell clusters are steadily eroded by recombination with the rest of HLII. Although a small number of genes have ocean-specific alleles, there is no evidence for genetically-stable ecotypes within the clade. We conjecture that spatiotemporally variable selection drives conditionally-beneficial variants of genomic segments to rise to high abundance while horizontally-transferring throughout the population.

evolutionary biology↗

Hybridization breaks species barriers in long-term coevolution of a cyanobacterial population

Bacterial species often undergo rampant recombination yet maintain cohesive genomic identity. Ecological differences can generate recombination barriers between species and sustain genomic clusters in the short term. But can these forces prevent genomic mixing during long-term coevolution? Cyanobacteria in Yellowstone hot springs comprise several diverse species that have coevolved for hundreds of thousands of years, providing a rare natural experiment. By analyzing more than 300 single-cell genomes, we show that despite each species forming a distinct genomic cluster, much of the diversity within species is the result of hybridization driven by selection, which has mixed their ancestral genotypes. This widespread mixing is contrary to the prevailing view that ecological barriers can maintain cohesive bacterial species and highlights the importance of hybridization as a source of genomic diversity.

microbiology↗

A resource for the comparison and integration of heterogeneous microbiome networks

Naturally occurring microbial communities often comprise thousands of taxa involved in complex networks of interactions. These interactions can be mediated by several mechanisms, including the competition for resources, the exchange of signals and nutrients, cell-cell contact and antibiotic warfare. In addition to direct measurements and computational predictions of interactions, abundant data on microbial co-occurrence associations can be inferred from correlations of taxa across samples, which can be estimated from metagenomic, and amplicon datasets. The analysis and interpretation of interaction and correlation networks are limited by the challenge of comparing across different datasets, due to heterogeneity of the data itself and to the lack of a platform to facilitate such comparisons. Here, we introduce the Microbial Interaction Network Database (MIND) - a web-based platform for the integrative analysis of different types of microbial networks, freely available at http://microbialnet.org/. In addition to containing a growing body of curated data, including amplicon-based co-occurrence networks, genome-scale model-derived networks, metabolic influence networks and horizontal gene transfer networks, MIND allows users to upload and analyze newly generated networks using a JSON format and standard NCBI taxonomy. The platform provides convenient functions to compare and query multiple networks simultaneously, and to visualize and export networks and datasets. Through some illustrative examples, we demonstrate how the platform might facilitate discoveries and help generate new hypotheses on host-associated and environmentally important microbial ecosystems through the power of knowledge integration.

systems biology↗

Genealogical structure changes as range expansions transition from pushed to pulled

Range expansions accelerate evolution through multiple mechanisms including gene surfing and genetic drift. The inference and control of these evolutionary processes ultimately relies on the information contained in genealogical trees. Currently, there are two opposing views on how range expansions shape genealogies. In invasion biology, expansions are typically approximated by a series of population bottlenecks producing genealogies with only pairwise mergers between lineages--a process known as the Kingman coalescent. Conversely, traveling-wave models predict a coalescent with multiple mergers, known as the Bolthausen-Sznitman coalescent. Here, we unify these two approaches and show that expansions can generate an entire spectrum of coalescent topologies. Specifically, we show that tree topology is controlled by growth dynamics at the front and exhibits large differences between pulled and pushed expansions. These differences are explained by the fluctuations in the total number of descendants left by the early founders. High growth cooperativity leads to a narrow distribution of reproductive values and the Kingman coalescent. Conversely, low growth cooperativity results in a broad distribution, whose exponent controls the merger sizes in the genealogies. These broad distribution and non-Kingman tree topologies emerge due to the fluctuations in the front shape and position and do not occur in quasi-deterministic simulations. Overall, our results show that range expansions provide a robust mechanism for generating different types of multiple mergers, which could be similar those observed in populations with strong selection or high fecundity. Thus, caution should be exercised in making inferences about the origin of non-Kingman genealogies. Significance statementSpatial dynamics are important for understanding genetic diversity in many contexts, such as cancer and infectious diseases. Coalescent theory offers a powerful framework for interpreting and predicting patters of genetic diversity in populations, but incorporating spatial structure into the theory has proven difficult. Here, we address this long-standing problem by studying the coalescent in a spatially expanding population. We find the topology of the coalescent changes depending on the growth dynamics at the front. Using analytical arguments, we show that the transition between coalescent topologies is universal and is controlled by a parameter related to the expansion velocity. Our theory makes precise predictions about the effects of population dynamics on genetic diversity at the expansion front, which we confirm in simulations.

evolutionary biology↗

Inferring microbial co-occurrence networks from amplicon data: a systematic evaluation

Microbes tend to organize into communities consisting of hundreds of species involved in complex interactions with each other. 16S ribosomal RNA (16S rRNA) amplicon profiling provides snapshots that reveal the phylogenies and abundance profiles of these microbial communities. These snapshots, when collected from multiple samples, have the potential to reveal which microbes co-occur, providing a glimpse into the network of associations in these communities. The inference of networks from 16S data is prone to statistical artifacts. There are many tools for performing each step of the 16S analysis workflow, but the extent to which these steps affect the final network is still unclear. In this study, we perform a meticulous analysis of each step of a pipeline that can convert 16S sequencing data into a network of microbial associations. Through this process, we map how different choices of algorithms and parameters affect the co-occurrence network and estimate steps that contribute most significantly to the variance. We further determine the tools and parameters that generate the most accurate and robust co-occurrence networks based on comparison with mock and synthetic datasets. Ultimately, we develop a standardized pipeline (available at https://github.com/segrelab/MiCoNE) that follows these default tools and parameters, but that can also help explore the outcome of any other combination of choices. We envisage that this pipeline could be used for integrating multiple data-sets, and for generating comparative analyses and consensus networks that can help understand and control microbial community assembly in different biomes. ImportanceTo understand and control the mechanisms that determine the structure and function of microbial communities, it is important to map the interrelationships between its constituent microbial species. The surge in the high-throughput sequencing of microbial communities has led to the creation of thousands of datasets containing information about microbial abundances. These abundances can be transformed into networks of co-occurrences across multiple samples, providing a glimpse into the structure of microbiomes. However, processing these datasets to obtain co-occurrence information relies on several complex steps, each of which involves multiple choices of tools and corresponding parameters. These multiple options pose questions about the accuracy and uniqueness of the inferred networks. In this study, we address this workflow and provide a systematic analysis of how these choices of tools and parameters affect the final network, and on how to select those that are most appropriate for a particular dataset.

microbiology↗

Genetic drift in range expansions is very sensitive to density feedback in dispersal and growth

Theory predicts rapid genetic drift in expanding populations due to the serial founder effect at the expansion front. Yet, many natural populations maintain high genetic diversity in the newly colonized regions. Here, we investigate whether density-dependent dispersal could provide a resolution of this paradox. We find that genetic drift is dramatically suppressed when dispersal rates increase with the population density because many more migrants from the diverse, high-density regions arrive at the expansion edge. When density-dependence is weak or negative, the effective population size of the front scales only logarithmically with the carrying capacity. The dependence, however, switches to a sublinear power law and then to a linear increase as the density-dependence becomes strongly positive. To understand these results, we introduce a unified framework that predicts how the strength of genetic drift depends on the density-dependence in both dispersal and growth. This theory reveals that the transitions between different regimes of diversity loss are controlled by a single, universal parameter: the ratio of the expansion velocity to the geometric mean of dispersal and growth rates at expansion edge. Importantly, our results suggest that positive density-dependence could dramatically alter evolution in expanding populations even when its contributions to the expansion velocity is small.

evolutionary biology↗

Neither pulled nor pushed: Genetic drift and front wandering uncover a new class of reaction-diffusion waves

Short AbstractTraveling waves describe diverse natural phenomena from crystal growth in physics to range expansions in biology. Two classes of waves exist with very different properties: pulled and pushed. Pulled waves are driven by high growth rates at the expansion edge, where the number of organisms is small and fluctuations are large. In contrast, fluctuations are suppressed in pushed waves because the region of maximal growth is shifted towards the population bulk. Although it is commonly believed that expansions are either pulled or pushed, we found an intermediate class of waves with bulk-driven growth, but exceedingly large fluctuations. These waves are unusual because their properties are controlled by both the leading edge and the bulk of the front.\n\nLong AbstractEpidemics, flame propagation, and cardiac rhythms are classic examples of reaction-diffusion waves that describe a switch from one alternative state to another. Only two types of waves are known: pulled, driven by the leading edge, and pushed, driven by the bulk of the wave. Here, we report a distinct class of semi-pushed waves for which both the bulk and the leading edge contribute to the dynamics. These hybrid waves have the kinetics of pushed waves, but exhibit giant fluctuations similar to pulled waves. The transitions between pulled, semi-pushed, and fully-pushed waves occur at universal ratios of the wave velocity to the Fisher velocity. We derive these results in the context of a species invading a new habitat by examining front diffusion, rate of diversity loss, and fluctuation-induced corrections to the expansion velocity. All three quantities decrease as a power law of the population density with the same exponent. We analytically calculate this exponent taking into account the fluctuations in the shape of the wave front. For fully-pushed waves, the exponent is -1 consistent with the central limit theorem. In semi-pushed waves, however, the fluctuations average out much more slowly, and the exponent approaches 0 towards the transition to pulled waves. As a result, a rapid loss of genetic diversity and large fluctuations in the position of the front occur even for populations with cooperative growth and other forms of an Allee effect. The evolutionary outcome of spatial spreading in such populations could therefore be less predictable than previously thought.

ecology↗