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Dispersed cells represent a distinct stage in the transition from bacterial biofilm to planktonic lifestyles

Bacteria assume distinct lifestyles during the planktonic and biofilm modes of growth. Increased levels of the intracellular messenger c-di-GMP determine the transition from planktonic to biofilm growth, while a reduction causes biofilm dispersal. It is generally assumed that cells dispersed from bi...

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Bibliographic Details
Published in:Nature communications 2014-07, Vol.5 (1), p.4462-4462, Article 4462
Main Authors: Chua, Song Lin, Liu, Yang, Yam, Joey Kuok Hoong, Chen, Yicai, Vejborg, Rebecca Munk, Tan, Bryan Giin Chyuan, Kjelleberg, Staffan, Tolker-Nielsen, Tim, Givskov, Michael, Yang, Liang
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Language:English
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Summary:Bacteria assume distinct lifestyles during the planktonic and biofilm modes of growth. Increased levels of the intracellular messenger c-di-GMP determine the transition from planktonic to biofilm growth, while a reduction causes biofilm dispersal. It is generally assumed that cells dispersed from biofilms immediately go into the planktonic growth phase. Here we use single-nucleotide resolution transcriptomic analysis to show that the physiology of dispersed cells from Pseudomonas aeruginosa biofilms is highly different from those of planktonic and biofilm cells. In dispersed cells, the expression of the small regulatory RNAs RsmY and RsmZ is downregulated, whereas secretion genes are induced. Dispersed cells are highly virulent against macrophages and Caenorhabditis elegans compared with planktonic cells. In addition, they are highly sensitive towards iron stress, and the combination of a biofilm-dispersing agent, an iron chelator and tobramycin efficiently reduces the survival of the dispersed cells. Bacteria can grow as free living planktonic cells or as part of surface-associated biofilms. Here the authors show, for the opportunistic pathogen Pseudomonas aeruginosa , that cells recently dispersed from biofilms are physiologically different from, and more virulent than, planktonic and biofilm cells.
ISSN:2041-1723
2041-1723
DOI:10.1038/ncomms5462