Author:
Christensen Louise D.,van Gennip Maria,Rybtke Morten T.,Wu Hong,Chiang Wen-Chi,Alhede Morten,Høiby Niels,Nielsen Thomas E.,Givskov Michael,Tolker-Nielsen Tim
Abstract
ABSTRACTOpportunistic pathogenic bacteria can engage in biofilm-based infections that evade immune responses and develop into chronic conditions. Because conventional antimicrobials cannot efficiently eradicate biofilms, there is an urgent need to develop alternative measures to combat biofilm infections. It has recently been established that the secondary messenger cyclic diguanosine monophosphate (c-di-GMP) functions as a positive regulator of biofilm formation in several different bacteria. In the present study we investigated whether manipulation of the c-di-GMP level in bacteria potentially can be used for biofilm controlin vivo. We constructed aPseudomonas aeruginosastrain in which a reduction in the c-di-GMP level can be achieved via induction of theEscherichia coliYhjH c-di-GMP phosphodiesterase. Initial experiments showed that induction ofyhjHexpression led to dispersal of the majority of the bacteria inin vitro-grownP. aeruginosabiofilms. Subsequently, we demonstrated thatP. aeruginosabiofilms growing on silicone implants, located in the peritoneal cavity of mice, dispersed after induction of the YhjH protein. Bacteria accumulated temporarily in the spleen after induction of biofilm dispersal, but the mice tolerated the dispersed bacteria well. The present work provides proof of the concept that modulation of the c-di-GMP level in bacteria is a viable strategy for biofilm control.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
85 articles.
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