4.4 Article

Anatomical Site-Specific Carbohydrate Availability Impacts Streptococcus pneumoniae Virulence and Fitness during Colonization and Disease

期刊

INFECTION AND IMMUNITY
卷 90, 期 1, 页码 -

出版社

AMER SOC MICROBIOLOGY
DOI: 10.1128/IAI.00451-21

关键词

carbohydrate availability; Streptococcus pneumoniae; carbon metabolism; host-pathogen interactions

资金

  1. NIH National Institute of Allergy and Infectious Diseases (NIAID) [AI148368, AI114800, AI156898, AI146149]
  2. NIH [T32 HL129948, S10RR026478]
  3. comprehensive cancer center (NCI grant) [P30 CA013148]

向作者/读者索取更多资源

Streptococcus pneumoniae shows different physiological and virulence responses to different carbohydrate availabilities. Differences in carbohydrate availability between the nasopharynx and invasive disease sites directly influence the metabolic activity, growth rate, and physiological state of S. pneumoniae. This anatomical site-specific carbohydrate availability directly affects the virulence traits of S. pneumoniae and promotes relative fitness.
Streptococcus pneumoniae colonizes the nasopharynx asymptomatically but can also cause severe life-threatening disease. Importantly, stark differences in carbohydrate availability exist between the nasopharynx and invasive disease sites, such as the bloodstream, which most likely impact S. pneumoniae's behavior. Herein, using chemically defined medium (CDM) supplemented with physiological levels of carbohydrates, we examined how anatomical site-specific carbohydrate availability impacted S. pneumoniae physiology and virulence. S. pneumoniae cells grown in CDM modeling the nasopharynx (CDM-N) had reduced metabolic activity and a lower growth rate, demonstrated mixed acid fermentation with marked H2O2, production, and were in a carbon-catabolite repression (CCR)-derepressed state versus S. pneumoniae cells grown in CDM modeling blood (CDM-B). Using transcriptome sequencing (RNA-seq), we determined the transcriptome for the S. pneumoniae wild-type (WT) strain and its isogenic CCR-deficient mutant in CDM-N and CDM-B. Genes with altered expression as a result of changes in carbohydrate availability or catabolite control protein deficiency, respectively, were primarily involved in carbohydrate metabolism, but also encoded established virulence determinants, such as polysaccharide capsule and surface adhesins. We confirmed that anatomical site-specific carbohydrate availability directly influenced established S. pneumoniae virulence traits. S. pneumoniae cells grown in CDM-B formed shorter chains, produced more capsule, were less adhesive, and were more resistant to macrophage killing in an opsonophagocytosis assay. Moreover, growth of S. pneumoniae in CDM-N or CDM-B prior to the challenge of mice impacted relative fitness in a colonization model and invasive disease model, respectively. Thus, anatomical site-specific carbohydrate availability alters S. pneumoniae physiology and virulence, in turn promoting anatomical site-specific fitness.

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