4.8 Article

Non-diphtheriae Corynebacterium species are associated with decreased risk of pneumococcal colonization during infancy

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ISME JOURNAL
卷 16, 期 3, 页码 655-665

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SPRINGERNATURE
DOI: 10.1038/s41396-021-01108-4

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资金

  1. Burroughs Wellcome Fund/American Society of Tropical Medicine and Hygiene Postdoctoral Fellowship in Tropical Infectious Diseases
  2. Children's Hospital of Philadelphia
  3. Pincus Family Foundation
  4. Penn Center for AIDS Research, a National Institutes of Health (NIH) [P30-AI045008]
  5. NIH through the Duke Center for AIDS Research [P30AI064518]
  6. NIH Career Development Award [K23-AI135090]
  7. Society for Pediatric Research
  8. NIH [7R01-GM108494]
  9. VECD Global Health Fellowship - Office of AIDS Research
  10. Fogarty International Center of the NIH [D43-TW009337]
  11. NIH through the Penn Center for AIDS Research [P30-AI045008]

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This study conducted in sub-Saharan Africa examined the nasopharyngeal microbiome of 179 mother-infant dyads to investigate the relationship between Corynebacterium abundance and Streptococcus pneumoniae colonization in infants. Results showed a negative correlation between Corynebacterium abundance and S. pneumoniae colonization, with in vitro experiments demonstrating growth inhibition of S. pneumoniae by secreted factors from Corynebacterium strains isolated from infants. Additionally, antibiotic exposure and seasonal variations were associated with changes in Corynebacterium abundance, suggesting potential implications for preventing pneumococcal infections.
Streptococcus pneumoniae (pneumococcus) is a leading cause of severe infections among children and adults. Interactions between commensal microbes in the upper respiratory tract and S. pneumoniae are poorly described. In this study, we sought to identify interspecies interactions that modify the risk of S. pneumoniae colonization during infancy and to describe development of the upper respiratory microbiome during infancy in a sub-Saharan African setting. We collected nasopharyngeal swabs monthly (0-6 months of age) or bimonthly (6-12 months of age) from 179 mother-infant dyads in Botswana. We used 16S ribosomal RNA gene sequencing to characterize the nasopharyngeal microbiome and identified S. pneumoniae colonization using a species-specific PCR assay. We detect S. pneumoniae colonization in 144 (80%) infants at a median age of 71 days and identify a strong negative association between the relative abundance of the bacterial genera Corynebacterium within the infant nasopharyngeal microbiome and the risk of S. pneumoniae colonization. Using in vitro cultivation experiments, we demonstrate growth inhibition of S. pneumoniae by secreted factors from strains of several Corynebacterium species isolated from these infants. Finally, we demonstrate that antibiotic exposures and the winter season are associated with a decline in the relative abundance of Corynebacterium within the nasopharyngeal microbiome, while breastfeeding is associated with an increase in the Corynebacterium relative abundance. Our findings provide novel insights into the interspecies interactions that contribute to colonization resistance to S. pneumoniae and suggest that the nasopharyngeal microbiome may be a previously unrecognized mechanism by which environmental factors influence the risk of pneumococcal infections during childhood. Moreover, this work lays the foundation for future studies seeking to use targeted manipulation of the nasopharyngeal microbiome to prevent infections caused by S. pneumoniae.

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