Influenza A Virus Infection Predisposes Hosts to Secondary Infection with Different Streptococcus pneumoniae Serotypes with Similar Outcome but Serotype-Specific Manifestation

Author:

Sharma-Chawla Niharika12,Sender Vicky3,Kershaw Olivia4,Gruber Achim D.4,Volckmar Julia1,Henriques-Normark Birgitta35,Stegemann-Koniszewski Sabine12,Bruder Dunja12

Affiliation:

1. Immune Regulation Group, Helmholtz Centre for Infection Research, Braunschweig, Germany

2. Infection Immunology Group, Institute of Medical Microbiology, Infection Prevention and Control, Otto-von-Guericke University, Magdeburg, Germany

3. Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, Sweden

4. Department of Veterinary Medicine, Institute of Veterinary Pathology, Free University Berlin, Berlin, Germany

5. Department of Clinical Microbiology, Karolinska University Hospital, Stockholm, Sweden

Abstract

ABSTRACT Influenza A virus (IAV) and Streptococcus pneumoniae are major causes of respiratory tract infections, particularly during coinfection. The synergism between these two pathogens is characterized by a complex network of dysregulated immune responses, some of which last until recovery following IAV infection. Despite the high serotype diversity of S. pneumoniae and the serotype replacement observed since the introduction of conjugate vaccines, little is known about pneumococcal strain dependency in the enhanced susceptibility to severe secondary S. pneumoniae infection following IAV infection. Thus, we studied how preinfection with IAV alters host susceptibility to different S. pneumoniae strains with various degrees of invasiveness using a highly invasive serotype 4 strain, an invasive serotype 7F strain, and a carrier serotype 19F strain. A murine model of pneumococcal coinfection during the acute phase of IAV infection showed a significantly increased degree of pneumonia and mortality for all tested pneumococcal strains at otherwise sublethal doses. The incidence and kinetics of systemic dissemination, however, remained bacterial strain dependent. Furthermore, we observed strain-specific alterations in the pulmonary levels of alveolar macrophages, neutrophils, and inflammatory mediators ultimately affecting immunopathology. During the recovery phase following IAV infection, bacterial growth in the lungs and systemic dissemination were enhanced in a strain-dependent manner. Altogether, this study shows that acute IAV infection predisposes the host to lethal S. pneumoniae infection irrespective of the pneumococcal serotype, while the long-lasting synergism between IAV and S. pneumoniae is bacterial strain dependent. These results hold implications for developing tailored therapeutic treatment regimens for dual infections during future IAV outbreaks.

Funder

Deutsche Forschungsgemeinschaft

Knut och Alice Wallenbergs Stiftelse

Helmholtz-Gemeinschaft

Stockholms Läns Landsting

Swedish Research Council

Swedish Foundation for Strategic Research

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Immunology,Microbiology,Parasitology

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