To better understand the assembly of the sturgeon egg microbiome, we purified six bacterial isolates from eggs and characterized their ability to form biofilms under the stress of tobramycin, with and without exogenou...To better understand the assembly of the sturgeon egg microbiome, we purified six bacterial isolates from eggs and characterized their ability to form biofilms under the stress of tobramycin, with and without exogenous protein. In experiments with single species biofilms, tobramycin reduced the metabolic activity of all isolates and increased biofilm biomass of three. The addition of exogenous protein to the assay countered the inhibition of biofilm and metabolic activity by tobramycin of <i>Pseudomonas</i> sp., <i>Brevundimonas</i> sp., <i>Flavobacterium columnare</i> and mixed biofilms of <i>Pseudomonas-F. columnare</i> and <i>Brevundimonas-Hydrogenophaga</i>. Two of the isolates (<i>Pseudomonas</i> spp.) that produced antimicrobial activity, were effective at reducing biofilm formation by <i>Brevundimonas</i>, but enhanced biofilm formation in other isolates. Increasing concentrations of Mg<sup>2+</sup> had no effect on biofilm formation but Ca<sup>2+</sup> enhanced biofilm formation of <i>Pseudomonas aeruginosa</i> PA01 (positive control) and <i>Brevundimonas</i>. Biofilm assembly by these two bacteria was inhibited by low concentrations of Ni<sup>2+</sup>. Mixed biofilms of <i>Brevundimonas</i> and <i>Hydrogenophage</i> consistently produced more robust biofilm than the strains in isolation, suggesting synergism. Established <i>Brevundimonas</i> biofilm appeared adept at recruiting pelagic <i>Acidovorax</i> and <i>Hydrogenophaga</i> into biofilm, suggesting that it plays an important role in the selection of species into the microbiome.展开更多
文摘To better understand the assembly of the sturgeon egg microbiome, we purified six bacterial isolates from eggs and characterized their ability to form biofilms under the stress of tobramycin, with and without exogenous protein. In experiments with single species biofilms, tobramycin reduced the metabolic activity of all isolates and increased biofilm biomass of three. The addition of exogenous protein to the assay countered the inhibition of biofilm and metabolic activity by tobramycin of <i>Pseudomonas</i> sp., <i>Brevundimonas</i> sp., <i>Flavobacterium columnare</i> and mixed biofilms of <i>Pseudomonas-F. columnare</i> and <i>Brevundimonas-Hydrogenophaga</i>. Two of the isolates (<i>Pseudomonas</i> spp.) that produced antimicrobial activity, were effective at reducing biofilm formation by <i>Brevundimonas</i>, but enhanced biofilm formation in other isolates. Increasing concentrations of Mg<sup>2+</sup> had no effect on biofilm formation but Ca<sup>2+</sup> enhanced biofilm formation of <i>Pseudomonas aeruginosa</i> PA01 (positive control) and <i>Brevundimonas</i>. Biofilm assembly by these two bacteria was inhibited by low concentrations of Ni<sup>2+</sup>. Mixed biofilms of <i>Brevundimonas</i> and <i>Hydrogenophage</i> consistently produced more robust biofilm than the strains in isolation, suggesting synergism. Established <i>Brevundimonas</i> biofilm appeared adept at recruiting pelagic <i>Acidovorax</i> and <i>Hydrogenophaga</i> into biofilm, suggesting that it plays an important role in the selection of species into the microbiome.