Project name: Streptococcus pneumoniae TIGR4

Description: A large fraction of the genes from sequenced organisms, particularly non-model species, are of unknown function. This severely limits biological insight, and for pathogenic microorganisms, hampers the development of new approaches to battle infections. There is thus a great need for novel strategies that link genotypes to phenotypes for microorganisms. We describe a high throughput strategy based on the method Tn-seq that can be applied to any genetically manipulatable microorganism. By screening 17 in vitro and two in vivo (carriage and infection) conditions for the pathogen Streptococcus pneumoniae, we create a valuable resource consisting of more than 1800 interactions that is rich in new genotype-phenotype relationships. We describe genes that are involved in differential carbon source utilization in the host, as well as genes that are involved both in virulence and in resistance against specific in vitro stresses, thereby revealing selection pressures the pathogen experiences during carriage and infection. We reveal the secondary response to an antibiotic, including identification of a dual role efflux pump that is also involved in resistance to pH stress. Through genome-wide genetic interaction mapping and gene expression analysis we define the mechanism of attenuation and the regulatory relationship between a two-component system and a core biosynthetic pathway that can be targeted to attenuate colonization. Thus, we have generated a resource that provides detailed insight into the biology and virulence of S. pneumoniae, and provide a road map for similar discovery in other microorganisms.

Data type: other

Sample scope: Monoisolate

Relevance: Medical

Last updated: 2012-05-29