Abstract
Streptococcus pneumoniae is the main bacterial pathogen involved in pneumonia. Pneumococcal acquisition and colonization density is probably affected by viral co-infections, the local microbiome composition and mucosal immunity. Here, we report the interactions between live-attenuated influenza vaccine (LAIV), successive pneumococcal challenge, and the healthy adult nasal microbiota and mucosal immunity using an experimental human challenge model. Nasal microbiota profiles at baseline are associated with consecutive pneumococcal carriage outcome (non-carrier, low-dense and high-dense pneumococcal carriage), independent of LAIV co-administration. Corynebacterium/Dolosigranulum-dominated profiles are associated with low-density colonization. Lowest rates of natural viral co-infection at baseline and post-LAIV influenza replication are detected in the low-density carriers. Also, we detected the fewest microbiota perturbations and mucosal cytokine responses in the low-density carriers compared to non-carriers or high-density carriers. These results indicate that the complete respiratory ecosystem affects pneumococcal behaviour following challenge, with low-density carriage representing the most stable ecological state.
Highlights
Streptococcus pneumoniae is the main bacterial pathogen involved in pneumonia
For the primary study[15,16], we found that antecedent live-attenuated influenza vaccine (LAIV) vaccination, that is, LAIV administration followed by pneumococcal colonization, did not impact overall pneumococcal acquisition, yet did drive time to acquisition, and transiently increased pneumococcal carriage rate and density compared to controls
All volunteers were screened for pneumococcal carriage at baseline (Fig. 1); individuals positive for natural pneumococcal carriage were excluded from further analysis (n = 4; 3%)
Summary
Streptococcus pneumoniae is the main bacterial pathogen involved in pneumonia. Pneumococcal acquisition and colonization density is probably affected by viral co-infections, the local microbiome composition and mucosal immunity. We first assessed the associations between baseline nasal microbiota composition, natural viral co-infection (i.e. before pneumococcal inoculation and vaccination) and pneumococcal carriage outcome.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.