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Meningococcal biofilm growth on an abiotic surface – a model for epithelial colonization?

Molecular Infectious Diseases Group, Department of Paediatrics, Faculty of Medicine, Imperial College London, Wright–Fleming Institute, St Mary's Hospital Campus, Norfolk Place, London W2 1PG, UK

Neisseria meningitidis colonizes 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 hypothesized 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, focusing on alteration in gene expression relevant to polysaccharide capsulation, lipooligosaccharide and outer-membrane protein synthesis – all phenotypes of importance in epithelial colonization. We report downregulation of genes controlling capsulation and the production of core oligosaccharide, and upregulation of genes encoding a range of outer-membrane components, reflecting phenotypic changes that have been established to occur in the colonizing 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 colonization than do short-term meningococcal/epithelial cell co-cultivation systems. Modelling prolonged meningococcal colonization with a sorbarod system offers insight into gene expression during this important, but experimentally relatively inaccessible, phase of human infection.

Correspondence
J. Simon Kroll
s.kroll{at}imperial.ac.uk

The array design and fully annotated microarray data for this study are available in µG@Sbase (accession no. E-BUGS-75; http://bugs.sgul.ac.uk/E-BUGS-75) and ArrayExpress (accession no. E-BUGS-75).

Two supplementary tables, listing the genes up- and downregulated in N. meningitidis MC58 wild-type and its capsule-negative mutant, are available with the online version of this paper.