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Infection and Immunity, April 2003, p. 2087-2094, Vol. 71, No. 4
0019-9567/03/$08.00+0     DOI: 10.1128/IAI.71.4.2087-2094.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.

Pneumolysin-Dependent and -Independent Gene Expression Identified by cDNA Microarray Analysis of THP-1 Human Mononuclear Cells Stimulated by Streptococcus pneumoniae

P. David Rogers,1 Justin Thornton,2 Katherine S. Barker,1 D. Olga McDaniel,3 Gordon S. Sacks,4 Edwin Swiatlo,2,5 and Larry S. McDaniel2,3,5*

Departments of Clinical Pharmacy and Pharmaceutical Sciences, University of Tennessee Health Science Center, Memphis, Tennessee,1 Departments of Microbiology,2 Surgery,3 Division of Infectious Diseases, Department of Medicine, University of Mississippi Medical Center, Jackson, Mississippi,5 Pharmacy Practice Division, University of Wisconsin, Madison, Wisconsin4

Received 12 August 2002/ Returned for modification 24 September 2002/ Accepted 18 December 2002

Pneumolysin is an important virulence factor of Streptococcus pneumoniae, interacting with the membranes of host cells to elicit a multitude of inflammatory responses. We used cDNA microarrays to identify genes which are responsive to S. pneumoniae in a pneumolysin-dependent and -independent fashion. The THP-1 human monocytic cell line was coincubated for 3 h with medium alone, with the virulent type 2 S. pneumoniae strain D39, or with the isogenic strain PLN, which does not express pneumolysin. RNA was isolated from the monocytes and hybridized on cDNA microarrays. Of 4,133 genes evaluated, 142 were found to be responsive in a pneumolysin-dependent fashion, whereas 40 were found to be responsive independent of pneumolysin. Genes that were up-regulated in cells exposed to D39 relative to those exposed to PLN included genes encoding proteins such as mannose binding lectin 1, lysozyme, {alpha}-1 catenin, cadherin 17, caspases 4 and 6, macrophage inflammatory protein 1ß (MIP-1ß), interleukin 8 (IL-8), monocyte chemotactic protein 3 (MCP-3), IL-2 receptor ß (IL-2Rß), IL-15 receptor {alpha} (IL-15R{alpha}), interferon receptor 2, and prostaglandin E synthase. Down-regulated genes included those encoding complement component receptor 2/CD21, platelet-activating factor acetylhydrolase, and oxidized low-density lipoprotein receptor 1 (OLR1). Pneumolysin-independent responses included down-regulation of the genes encoding CD68, CD53, CD24, transforming growth factor ß2, and signal transducers and activators of transcription 1. These results demonstrate the striking effects of pneumolysin on the host cell upon exposure to S. pneumoniae.

* Corresponding author. Mailing address: Department of Surgery, University of Mississippi Medical Center, 2500 N. State St., Jackson, MS 39216. Phone: (601) 984-6880. Fax: (601) 984-1708. E-mail: lmcdaniel{at}microbio.umsmed.edu.

Editor: J. N. Weiser

Infection and Immunity, April 2003, p. 2087-2094, Vol. 71, No. 4
0019-9567/03/$08.00+0     DOI: 10.1128/IAI.71.4.2087-2094.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.



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