4.7 Article

Transcriptome studies on Streptococcus pneumoniae, illustration of early response genes to THP-1 human macrophages

Journal

GENOMICS
Volume 93, Issue 1, Pages 72-82

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ygeno.2008.09.008

Keywords

Streptococcus pneumoniae; Microarray; Macrophage; Pathogen-host interaction; Early response genes; PIcR regulator

Funding

  1. Saskatchewan Health Research Foundation (SHRF)
  2. Delfari Bridging Fund of the University of Saskatchewan
  3. Pathogen Functional Genomics Resource Center (PFGRC)

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Pathogen-host interaction plays an essential role in pathogenicity. In this study, we investigated transcriptomes of one Streptococcus pneumoniae TIGR4-derived unencapsulated strain upon exposure to THP-1 human macrophage-like cells for 0.5 h, 1 h and 3 h, respectively. Expression of most genes was up-regulated and the changes of selected genes were validated by qRT-PCR. To characterize the functions of the identified genes, one locus of genes (SP1057-SP1063) was deleted in TIGR4 by insertion replacement mutagenesis. Compared to the wild-type strain, the constructed mutant exhibited lower binding and internalization activities to the THP-1 macrophages at early incubation time periods (0.5 h and/or 1 h) but not at 3 h. However, no change was observed in the intracellular survival assays. These data indicate that the SP1057-SP1063 locus is involved in the early stage of interaction with host macrophages. Further sequence and PCR analyses suggest that the SP1057-SP1063 locus was acquired by lateral transfer. (C) 2008 Elsevier Inc. All rights reserved

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