RegR, a Global LacI/GalR Family Regulator, Modulates Virulence and Competence in Streptococcus pneumoniae

Author:

Chapuy-Regaud Sabine1,Ogunniyi A. David2,Diallo Nicole3,Huet Yvette3,Desnottes Jean-François3,Paton James C.2,Escaich Sonia4,Trombe Marie-Claude1

Affiliation:

1. Laboratoire “Interactions et Signalisation Cellulaire: Relation Hôte Pathogène,” Institut Louis Bugnard, Centre Hospitalo-Universitaire de Rangueil, Université Paul Sabatier, 31403 Toulouse Cedex

2. Department of Molecular Biosciences, Adelaide University, Adelaide, South Australia 5005, Australia

3. Aventis Pharma, 94403 Vitry sur Seine

4. Mutabilis SA, Faculté de Médecine Necker, 75730 Paris Cedex 15, France

Abstract

ABSTRACT The homolactic and catalase-deficient pathogen Streptococcus pneumoniae is not only tolerant to oxygen but requires the activity of its NADH oxidase, Nox, to develop optimal virulence and competence for genetic transformation. In this work, we show that the global regulator RegR is also involved in these traits. Genetic dissection revealed that RegR regulates competence and the expression of virulence factors, including hyaluronidase. In bacteria grown in vitro, RegR represses hyaluronidase. At neutral pH, it increases adherence to A549 epithelial cells, and at alkaline pH, it acts upstream of the CiaRH two-component signaling system to activate competence. These phenotypes are not associated with changes in antibiotic resistance, central metabolism, and carbohydrate utilization. Although the RegR 0 (where 0 indicates the loss of the protein) mutation is sufficient to attenuate experimental virulence of strain 23477 in mice, the introduction of an additional hyl 0 (where 0 indicates the loss of function) mutation in the RegR 0 strain 23302 dramatically reduces its virulence. This indicates that residual virulence of the RegR 0 Hyl + derivative is due to hyaluronidase and supports the dual role of RegR in virulence. This LacI/GalR regulator, not essential for in vitro growth in rich media, is indeed involved in the adaptive response of the pneumococcus via its control of competence, adherence, and virulence.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Immunology,Microbiology,Parasitology

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