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Benyei, E. B.

Publications and source records attributed to Benyei, E. B..

2 recordsLinked to original sources

Pseudomonas aeruginosa lasR is a keystone gene in polymicrobial cultures

The airways of people with cystic fibrosis (CF) are often co-infected by Pseudmonas aeruginosa and a variety of other co-habiting microbes; the infections are polymicrobial. P. aeruginosa isolates from the CF airways are also known to commonly acquire mutations in the quorum sensing regulator, lasR. The appearance of these lasR mutants is associated with a worsening clinical prognosis. In this work, we show that loss of lasR function has a significant impact on the stability of inter-species interactions in a polymicrobial ecosystem, and in particular on the dynamics of a common CF-associated fungus, Candida albicans. Titres of C. albicans were stable in the presence of wild type P. aeruginosa and Staphylococcus aureus. However, when wild type P. aeruginosa was replaced by a {Delta}lasR mutant, C. albicans titres progressively declined over time. This instability could be reversed by ectopic expression of a Type VI Secretion System effector cluster (tsi) in the {Delta}lasR mutant. We also noted that challenge of the polymicrobial cultures with a clinically-relevant combination of antibiotics (colistin and ciprofloxacin) led to a hyphal bloom of the fungus. This bloom was abolished in the {Delta}lasR mutant, but again, was restored by ectopic expression of the tsi cluster. Finally, we show that whereas wild type P. aeruginosa is relatively agnostic to the presence of other microbes, the {Delta}lasR mutant is not and undergoes substantial transcriptional reprogramming. Our data indicate that lasR has a large and previously unrecognised impact on inter-species interactions. We therefore propose that lasR is an ecological keystone gene.

microbiology↗

Hyphal growth determines spatial organization and coexistence in a pathogenic polymicrobial community within alveoli-like geometries

The bodies of macroorganisms host microbes living in multi-species communities. Sequencing approaches have revealed that different organs host different microbiota and tend to be infected by different pathogens, drawing correlations between environmental parameters at the organ level and microbial composition. However, less is known about the microscale dimension of microbial ecology, particularly during infection. In this study, we focus on the role of microscale spatial structure, studying its influence on the ecology of a polymicrobial infection of P. aeruginosa, S. aureus and C. albicans. Although these pathogens are commonly found together in the lungs of chronically ill patients, it is unclear whether they coexist or compete and segregate in different niches. We find that, while P. aeruginosa quickly outcompetes C. albicans and S. aureus on large surfaces, robust spatial organization and coexistence emerges in microfluidic microchambers that mimic the spatial characteristics of alveoli. In these microenvironments, slowly growing C. albicans is able to leverage fast eccentric hyphal growth to conquer boundary spaces, where it establishes itself excluding the other pathogens. We show that the emerging spatial patterning is robust to changes in the virulence of the community, enabling coexistence and potentially determining infection severity and outcomes. Our findings reveal a previously unrecognized role of mechanical forces in shaping infection dynamics, suggesting that microenvironmental structure is a critical determinant of pathogen coexistence, virulence, and treatment outcomes. Because adaptations, such as changes in morphology, are widespread among microbes, these results are generalizable to other ecologies and environments.

microbiology↗