Functional genomics study of Pseudomonas putida to determine traits associated with avoidance of a myxobacterial predator
Predation contributes to the structure and diversity of microbial communities. Predatory myxobacteria are ubiquitous to a variety of microbial habitats and capably consume a broad diversity of microbial prey. Predator–prey experiments utilizing myxobacteria have provided details into predatory mecha...
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Veröffentlicht in: | Scientific reports 2021-08, Vol.11 (1), p.16445-16445, Article 16445 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Predation contributes to the structure and diversity of microbial communities. Predatory myxobacteria are ubiquitous to a variety of microbial habitats and capably consume a broad diversity of microbial prey. Predator–prey experiments utilizing myxobacteria have provided details into predatory mechanisms and features that facilitate consumption of prey. However, prey resistance to myxobacterial predation remains underexplored, and prey resistances have been observed exclusively from predator–prey experiments that included the model myxobacterium
Myxococcus xanthus
. Utilizing a predator–prey pairing that instead included the myxobacterium,
Cystobacter ferrugineus,
with
Pseudomonas putida
as prey, we observed surviving phenotypes capable of eluding predation. Comparative transcriptomics between
P. putida
unexposed to
C. ferrugineus
and the survivor phenotype suggested that increased expression of efflux pumps, genes associated with mucoid conversion, and various membrane features contribute to predator avoidance. Unique features observed from the survivor phenotype when compared to the parent
P. putida
include small colony variation, efflux-mediated antibiotic resistance, phenazine-1-carboxylic acid production, and increased mucoid conversion. These results demonstrate the utility of myxobacterial predator–prey models and provide insight into prey resistances in response to predatory stress that might contribute to the phenotypic diversity and structure of bacterial communities. |
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ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/s41598-021-96046-8 |