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Published online ahead of print on 21 April 2009 as doi:10.1099/mic.0.026559-0
Microbiology 2009;155:1940.

Microbiology (2009), DOI 10.1099/mic.0.026559-0
© 2009 Society for General Microbiology

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Microbiology 0 (2009), mic.0.026559; DOI  10.1099/mic.0.026559-0
© 2009 Society for General Microbiology


Meningococcal biofilm growth on an abiotic surface - a model for epithelial colonisation?

Cliona A O' Dwyer1, Ming-Shi Li1, Paul R Langford1 and J. Simon Kroll2,3

1 Imperial College London;
2 Imperial College, London

ABSTRACT

Neisseria meningitidis colonises the human nasopharynx asymptomatically, often for prolonged periods, but occasionally invades from this site to cause life-threatening infection. In the nasopharynx aggregated organisms are closely attached to the epithelial surface, in a state in which the expression of components of the bacterial envelope differs significantly from that found in organisms multiplying exponentially in liquid phase culture or in the blood. We and others have hypothesised that here they are in the biofilm state, and to explore this we have investigated biofilm formation by the serogroup B strain MC58 on an abiotic surface, in a sorbarod system. Transcriptional changes were analysed, focussing on alteration in gene expression relevant to polysaccharide capsulation, lipooligosaccharide and outer membrane protein synthesis – all phenotypes of importance in epithelial colonisation. We report down-regulation of genes controlling capsulation and the production of core oligosaccharide, and up-regulation of genes encoding a range of outer membrane components, reflecting phenotypic changes that have been established to occur in the colonising state. A limited comparison with organisms recovered from an extended period of co-cultivation with epithelial cells suggests that this model system may better mirror natural colonisation than do short-term meningococcal/epithelial cell co-cultivation systems. Modelling prolonged meningococcal colonisation with a sorbarod system offers insight into gene expression during this important, but experimentally relatively inaccessible, phase of human infection.

3 E-mail: s.kroll{at}imperial.ac.uk







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