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The role of the microbiota in respiratory virus-bacterial pathobiont relationships in the upper respiratory tract

Kelly, M. S.; Shi, P.; Boiditswe, S. C.; Qin, E.; Steenhoff, A. P.; Mazhani, T.; Patel, M. Z.; Cunningham, C. K.; Rawls, J. F.; Luinstra, K.; Gilchrist, J.; Maciejewski, J.; Hurst, J. H.; Seed, P. C.; Bulir, D.; Smieja, M.

2024-10-23 infectious diseases
10.1101/2024.10.22.24315478 medRxiv
Show abstract

The mechanisms by which respiratory viruses predispose to secondary bacterial infections remain poorly characterized. Using 2,409 nasopharyngeal swabs from 300 infants in Botswana, we performed a detailed analysis of factors that influence the dynamics of bacterial pathobiont colonization during infancy. We quantify the extent to which viruses increase the acquisition of Haemophilus influenzae, Moraxella catarrhalis, and Streptococcus pneumoniae. We provide evidence of cooperative interactions between these pathobionts while identifying host characteristics and environmental exposures that influence the odds of pathobiont colonization during early life. Using 16S rRNA gene sequencing, we demonstrate that respiratory viruses result in losses of putatively beneficial Corynebacterium and Streptococcus species that are associated with a lower odds of pathobiont acquisition. These findings provide novel insights into viral-bacterial relationships in the URT of direct relevance to respiratory infections and suggest that the URT bacterial microbiota is a potentially modifiable mechanism by which viruses promote bacterial respiratory infections.

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