| Literature DB >> 31126758 |
Hannah M Rowe1, Erik Karlsson1, Haley Echlin1, Ti-Cheng Chang2, Lei Wang3, Tim van Opijnen4, Stanley B Pounds3, Stacey Schultz-Cherry1, Jason W Rosch5.
Abstract
The capacity of Streptococcus pneumoniae to successfully transmit and colonize new human hosts is a critical aspect of pneumococcal population biology and a prerequisite for invasive disease. However, the bacterial mechanisms underlying this process remain largely unknown. To identify bacterial factors required for transmission, we conducted a high-throughput genetic screen with a transposon sequencing (Tn-seq) library of a pneumococcal strain in a ferret transmission model. Key players in both metabolism and transcriptional regulation were identified as required for efficient bacterial transmission. Targeted deletion of the putative C3-degrading protease CppA, iron transporter PiaA, or competence regulatory histidine kinase ComD significantly decreased transmissibility in a mouse model, further validating the screen. Maternal vaccination with recombinant surface-exposed PiaA and CppA alone or in combination blocked transmission in offspring and were more effective than capsule-based vaccines. These data underscore the possibility of targeting pneumococcal transmission as a means of eliminating invasive disease in the population.Entities:
Keywords: Streptococcus pneumoniae; ferret; influenza; transmission
Mesh:
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Year: 2019 PMID: 31126758 PMCID: PMC6598203 DOI: 10.1016/j.chom.2019.04.012
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 21.023