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Wagner-Döbler, I.

Publications and source records attributed to Wagner-Döbler, I..

2 recordsLinked to original sources

A neutral process of genome reduction in marine bacterioplankton

Marine bacterioplankton communities are dominated by cells equipped with small genomes. Streamlining selection has been accepted as the main force driving their genome reduction. Here, we report that a neutral evolutionary mechanism governs genome reduction in the Roseobacter group that represents 5-20% of the bacterioplankton cells in coastal waters. Using representative strains that fall into three genome size groups (2-3, 3-4, and 4-5 Mbp), we measured their genomic mutation rates () through long-term mutation accumulation experiments followed by genome sequencing the resulting 437 mutant lines. We further calculated their effective population sizes (Ne) based on and the neutral genetic diversity of the studied species, the latter estimated based on multiple genome sequences of natural isolates collected from global oceans with their population structure considered. A surprising finding is that Ne scales positively with genome size, which is the opposite of the expectation from the streamlining selection theory. As the strength of random genetic drift is the inverse of Ne, this result instead suggests drift as the primary driver of genome reduction. Additionally, we report a negative scaling between and genome size, which is the first experimental evidence for the long-lasting hypothesis that mutation rate increases play a part in marine bacterial genome reduction. As scales inversely with Ne, genetic drift appears to be the ultimate cause of genome reduction in these Roseobacters. Our finding discounts, but is insufficient to reject, the streamlining theory because streamlining process is expected to be more effective in oligotrophic open ocean waters.

microbiology↗

Role of XerCD in release of over-replicated DNA through Outer Membrane Vesicles in Escherichia coli

Outer membrane vesicles (OMVs) are universally produced by prokaryotes and play important roles in symbiotic and pathogenic interactions. Here we show that the Gammaproteobacterium Escherichia coli produces OMVs that contain DNA enriched for the region around the terminus of replication ter, and specifically for the recognition sequence dif of the two site-specific recombinases XerCD, similar to OMVs from the Alphaproteobacterium Dinoroseobacter shibae. In deletion mutants of xerC or xerD, the enriched region around ter becomes broader while the peak directly at the dif sequence itself is reduced. ImportanceImprecise termination of replication can lead to over-replicated parts of bacterial chromosomes that have to be excised and removed from the dividing cell. The underlying mechanism is so far poorly understood. Our data suggest a conserved mechanism for repair and removal of over-replicated DNA through outer membrane vesicles and an active role of the site-specific XerCD recombinase complex therein.

microbiology↗