bioRxiv Science⌕ Search

Biology subjects

Then, P.

Publications and source records attributed to Then, P..

3 recordsLinked to original sources

The enemy of my enemy: A bacterial antagonist rescues Chlamydomonas by inactivating a toxin from a rival

Microbial interactions are shaped by multiple community members, yet the underlying mechanisms remain poorly understood. Here, we investigated a tripartite interaction between the microalga Chlamydomonas reinhardtii and two Pseudomonas bacteria that coexist in the same soil habitat. In pairwise cultures, all three interactions are amensalistic (-like): Pseudomonas protegens Pf-5 antagonizes both C. reinhardtii and Pseudomonas fluorescens HKI0770 without benefit, while P. fluorescens inhibits C. reinhardtii without profiting from the alga. However, in a tripartite culture, P. fluorescens protects C. reinhardtii from P. protegens and promotes algal recovery. This protection is not stopped when the used carbon source, acetate, is supplemented. The P. fluorescens rescue effect is associated with reduced levels of the polyyne toxin protegencin produced by P. protegens. Protegencin levels, detected by Raman microspectroscopy, are decreased by application of spent medium or protein extracts from P. fluorescens, while heat- and protease-treatment abolish this activity. A heat-sensitive, proteinaceous factor, likely an enzyme(s), appears to contribute to protegencin inactivation. Our results show that P. fluorescens rescues C. reinhardtii by inactivating protegencin, despite being inhibited by P. protegens. These findings demonstrate the importance of investigating higher-order effects, since additional community members can transform pairwise antagonistic interactions into conditional protection through toxin inactivation.

microbiology↗

Tripartite synergy - Metabolic crosstalk between two bacterial mutualists and a marine microalga promotes algal fitness

Marine microalgae form major parts of phytoplankton and are highly relevant for global CO2 fixation. Although microalgae have lived together with bacteria in the oceans for billions of years, these ecosystem-relevant interactions remain largely uncharacterized. Here, we have studied biotic interactions between two marine bacteria and a marine microalga. We show that an N2-fixing Vibrio provides ammonium for Chlamydomonas sp. and a Marinobacterium. Both microorganisms cannot survive in an ammonium-free environment. In exchange, the microalga promotes the growth of both bacteria, via secretion of heat-resistant metabolites in case of Marinobacterium. Reciprocally, the Marinobacterium releases heat-resistant metabolites that stimulate algal growth and increase its photosynthetic pigments, Photosystem II quantum yield, and starch accumulation. Electron microscopy reveals a strengthened starch sheath around the algal pyrenoid and indicates a modified periplasmic space for metabolic exchange. Our data highlight a tight synergy of a marine microbial trio promoting each others growth and algal fitness.

microbiology↗

Nanoscopy on the Chea(i)p

Super-resolution microscopy allows for stunning images with a resolution well beyond the optical diffraction limit, but the imaging techniques are demanding in terms of instrumentation and software. Using scientific-grade cameras, solid-state lasers and top-shelf microscopy objective lenses drives the price and complexity of the system, limiting its use to well-funded institutions. However, by harnessing recent developments in CMOS image sensor technology and low-cost illumination strategies, super-resolution microscopy can be made available to the mass-markets for a fraction of the price. Here, we present a 3D printed, self-contained super-resolution microscope with a price tag below 1000 $ including the objective and a cellphone. The system relies on a cellphone to both acquire and process images as well as control the hardware, and a photonic-chip enabled illumination. The system exhibits 100nm optical resolution using single-molecule localization microscopy and can provide live super-resolution imaging using light intensity fluctuation methods. Furthermore, due to its compactness, we demonstrate its potential use inside bench-top incubators and high biological safety level environments imaging SARS-CoV-2 viroids. By the development of low-cost instrumentation and by sharing the designs and manuals, the stage for democratizing super-resolution imaging is set.

microbiology↗