Abstract

Pneumococcal infections have increasingly high mortality rates despite the availability of vaccines and antibiotics. Therefore, the identification of new virulence determinants and the understanding of the molecular mechanisms behind pathogenesis have become of paramount importance in the search of new targets for drug development. The exoribonuclease RNase R has been involved in virulence in a growing number of pathogens. In this work, we used Galleria mellonella as an infection model to demonstrate that the presence of RNase R increases the pneumococcus virulence. Larvae infected with the RNase R mutant show an increased expression level of antimicrobial peptides. Furthermore, they have a lower bacterial load in the hemolymph in the later stages of infection, leading to a higher survival rate of the larvae. Interestingly, pneumococci expressing RNase R show a sudden drop in bacterial numbers immediately after infection, resembling the eclipse phase observed after intravenous inoculation in mice. Concomitantly, we observed a lower number of mutant bacteria inside larval hemocytes and a higher susceptibility to oxidative stress when compared to the wild type. Together, our results indicate that RNase R is involved in the ability of pneumococci to evade the host immune response, probably by interfering with internalization and/or replication inside the larval hemocytes.

Highlights

  • Streptococcus pneumoniae is an opportunistic pathogen that can be usually found as a harmless commensal of the human upper respiratory tract

  • We show that RNase R has an important role in the pathogenicity of S. pneumonia and present evidence indicating that this enzyme might have a role in host–microbe interaction

  • Our results suggest that RNase R might promote the pneumococcus ability to evade the immune response of the host, probably by interfering with the proliferation of pneumococci inside the larvae hemocytes

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Summary

Introduction

Streptococcus pneumoniae is an opportunistic pathogen that can be usually found as a harmless commensal of the human upper respiratory tract. This bacterium can colonize the nasopharynx of healthy individuals in an asymptomatic manner, propagation of pneumococcal cells beyond its niche along the nasal epithelium can lead to invasive diseases (reviewed in [1]). In 2017, S. pneumoniae was included by the World Health Organization (WHO) as one of the 12 priority pathogens. The switch that makes this bacterium change from colonizer to pathogen is triggered by the opportunity to invade the bloodstream, tissues, or organs of the host [2]. Translocation from the nasopharynx to deeper tissues exposes

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