Genome wide expression profiling reveals suppression of host defence responses during colonisation by Neisseria meningitidis but not N. lactamica
Author(s)
Wong, EEH
Li, M-S
Kroll, JS
Hibberd, ML
Langford, PR
Type
Journal Article
Abstract
Both Neisseria meningitidis and the closely related bacterium Neisseria lactamica colonise human nasopharyngeal mucosal surface, but only N. meningitidis invades the bloodstream to cause potentially life-threatening meningitis and septicaemia. We have hypothesised that the two neisserial species differentially modulate host respiratory epithelial cell gene expression reflecting their disease potential. Confluent monolayers of 16HBE14 human bronchial epithelial cells were exposed to live and/or dead N. meningitidis (including capsule and pili mutants) and N. lactamica, and their transcriptomes were compared using whole genome microarrays. Changes in expression of selected genes were subsequently validated using Q-RT-PCR and ELISAs. Live N. meningitidis and N. lactamica induced genes involved in host energy production processes suggesting that both bacterial species utilise host resources. N. meningitidis infection was associated with down-regulation of host defence genes. N. lactamica, relative to N. meningitidis, initiates up-regulation of proinflammatory genes. Bacterial secreted proteins alone induced some of the changes observed. The results suggest N. meningitidis and N. lactamica differentially regulate host respiratory epithelial cell gene expression through colonisation and/or protein secretion, and that this may contribute to subsequent clinical outcomes associated with these bacteria.
Editor(s)
Borrow, R
Date Issued
2011-10-20
Date Acceptance
2011-09-20
Citation
PLOS One, 2011, 6 (10), pp.e26130-e26130
ISSN
1932-6203
Publisher
Public Library of Science
Start Page
e26130
End Page
e26130
Journal / Book Title
PLOS One
Volume
6
Issue
10
Copyright Statement
© 2011 Wong et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
License URL
Identifier
http://www.ncbi.nlm.nih.gov/pubmed/22028815
Publication Status
Published
Coverage Spatial
USA
Article Number
e26130