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Infection and Immunity, October 2004, p. 6068-6075, Vol. 72, No. 10
0019-9567/04/$08.00+0     DOI: 10.1128/IAI.72.10.6068-6075.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

The Streptococcus pyogenes Capsule Is Required for Adhesion of Bacteria to Virus-Infected Alveolar Epithelial Cells and Lethal Bacterial-Viral Superinfection

Shigefumi Okamoto,1 Shigetada Kawabata,1,2* Yutaka Terao,1 Hideaki Fujitaka,1 Yoshinobu Okuno,3 and Shigeyuki Hamada1

Department of Oral and Molecular Microbiology, Osaka University Graduate School of Dentistry, Suita-Osaka,1 PRESTO, Japan Science and Technology Agency, Kawaguchi-Saitama,2 Department of Infectious Diseases, Osaka Prefectural Institute of Public Health, Osaka, Japan3

Received 21 October 2003/ Returned for modification 10 June 2004/ Accepted 14 July 2004

An apparent worldwide resurgence of invasive group A Streptococcus (GAS) infections remains unexplained. However, we recently demonstrated in mice that when an otherwise nonlethal intranasal GAS infection is preceded by a nonlethal influenza A virus (IAV) infection, induction of lethal invasive GAS infections is often the result. In the present study, we established several isogenic mutants from a GAS isolate and evaluated several virulence factors as candidates responsible for the induction of invasive GAS infections. Disruption of the synthesis of the capsule, Mga, streptolysin O, streptolysin S, or streptococcal pyrogenic exotoxin B of GAS significantly reduced mortality among mice superinfected with IAV and a mutant. In addition, the number of GAS organisms adhering to IAV-infected alveolar epithelial cells was markedly reduced with the capsule-depleted mutant, although this was not the case with the other mutants. Wild-type GAS was found to bind directly to IAV particles, whereas the nonencapsulated mutant showed much less ability to bind. These results suggest that the capsule plays a key role in the invasion of host tissues by GAS following superinfection with IAV and GAS.

* Corresponding author. Mailing address: Department of Oral and Molecular Microbiology, Osaka University Graduate School of Dentistry, 1-8 Yamadaoka, Suita, Osaka 565-0871, Japan. Phone: 81-6-6879-2898. Fax: 81-6-6878-4755. E-mail: kawabata{at}dent.osaka-u.ac.jp.

Editor: V. J. DiRita

Infection and Immunity, October 2004, p. 6068-6075, Vol. 72, No. 10
0019-9567/04/$08.00+0     DOI: 10.1128/IAI.72.10.6068-6075.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.



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