Exploring the parallel development of microbial systems in neonates with cystic fibrosis
- PMID: 23131830
- PMCID: PMC3509432
- DOI: 10.1128/mBio.00408-12
Exploring the parallel development of microbial systems in neonates with cystic fibrosis
Abstract
Recent studies have greatly extended our understanding of the microbiota present in and on the human body. Here, advanced sequencing strategies have provided unprecedented analytical power. The important implications that the emerging data have for human health emphasize the need to intensify research in this area (D. A. Relman, Nature 486:194-195, 2012). It is already clear from these studies that the microbiotas characterized in different body locations of healthy individuals are both complex and diverse (The Human Microbiome Project Consortium, Nature 486:215-221). These studies also provide a point of contrast for investigations that aim to characterize the microbiota present in disease conditions. In this regard, Madan et al. (mBio 3(4):e00251-12, 2012) monitored the development over time of microbiota in the oropharynges and feces of neonates with cystic fibrosis and explored the potential for interactions between these complex microbial systems.
Comment on
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Serial analysis of the gut and respiratory microbiome in cystic fibrosis in infancy: interaction between intestinal and respiratory tracts and impact of nutritional exposures.mBio. 2012 Aug 21;3(4):e00251-12. doi: 10.1128/mBio.00251-12. Print 2012. mBio. 2012. PMID: 22911969 Free PMC article.
References
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- Stressmann FA, et al. 2012. Long-term cultivation-independent microbial diversity analysis demonstrates that bacterial communities infecting the adult cystic fibrosis lung show stability and resilience. Thorax 67:867–873 - PubMed
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