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Marquiegui-Alvaro, A.

Publications and source records attributed to Marquiegui-Alvaro, A..

2 recordsLinked to original sources

Cohabiting microbes can impact one another's mutation rates creating a mutational eco-evo feedback loop

Eco-evolutionary feedbacks are typically thought to require an ecological change driving Darwinian selection. However, ecology can drive other evolutionary mechanisms too. In many microbial species mutation rates are elevated at low population density, mediated by nutrient availability and reactive oxygen species (ROS). These findings from monoculture populations led us to hypothesise that the presence and density of a cohabiting species will also affect mutation rates. Using Escherichia coli as a focal species we explore the mutational effects on both parties of co-culture with either Enterococcus faecalis or Pseudomonas aeruginosa. These species co-occur in multiple clinical settings and have different abilities to degrade ROS. In both co-culture systems we find evidence that the presence of a stronger ROS degrader reduces mutation rates in the weaker ROS degrading species. At the same time increasing population density of the weaker ROS degrader increases mutation rates in the stronger ROS degrading species. Simultaneous mutation rate estimation in co-cultured species raises multiple experimental challenges addressed here. Despite these challenges, we find evidence for a novel form of eco-evo feedback in which the environment shapes the supply of mutational variation to the population. This in turn feeds back to alter the chance of evolutionary rescue for one species or another during a subsequent environmental change. Such effects potentially matter not only for our fundamental understanding of the interplay between ecology and evolution, but for the treatment of polymicrobial infections in which rates of resistance evolution may be altered by the cross-species mutational effects of cohabiting species.

evolutionary biology↗

Using auxotrophic donor strains to explore pQBR57 plasmid host range among environmental soil bacterial isolates

Plasmid host range (PHR) plays a key role in the spread of ecologically important genes, alongside applications in microbiome engineering, and environmental biotechnology. PHR is a complex trait arising from the combination of plasmid, donor and recipient properties. Most studies of PHR use a single donor strain, leaving the role of the donor unexplored, and often require genetically tagged recipient strains for counter selection, which limits use of non-genetically tractable strains. Here we developed a PHR screening method using auxotrophic donors that bypasses the need to genetically tag recipients, thus allowing the screening of culturable environmental bacterial strains. Specifically, we used two auxotrophic donors (P. fluorescens and P. putida), and the plasmid pQBR57-tphKAB, an environmental plasmid engineered for terephthalic acid bioremediation. We screened a library of 101 soil isolates, as potential recipients, including common soil genera of soil bacteria, Pseudomonas, Bacillus and Xanthomonas. We only observed conjugation into other Pseudomonas, but donor identity affected PHR, with P. fluorescens conjugating the plasmid into more recipient strains than P. putida. Phylogenomic analysis revealed that transconjugants clustered with P. citronellosis and P. putida lineages. In strains that were close relatives of transconjugants but who were unable to acquire the plasmid, we observed 5 defence systems not present in transconjugants that may act as barriers to plasmid acquisition. Our method provides a rapid, tag-free framework for screening PHR in environmental isolates and for investigating the influence of donor identity on plasmid conjugation.

microbiology↗