共 68 条
Inter-individual differences in the gene content of human gut bacterial species
被引:147
作者:

Zhu, Ana
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机构:
European Mol Biol Lab, D-69117 Heidelberg, Germany European Mol Biol Lab, D-69117 Heidelberg, Germany

Sunagawa, Shinichi
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机构:
European Mol Biol Lab, D-69117 Heidelberg, Germany European Mol Biol Lab, D-69117 Heidelberg, Germany

Mende, Daniel R.
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机构:
European Mol Biol Lab, D-69117 Heidelberg, Germany
Univ Hawaii, Daniel K Inouye Ctr Microbial Oceanog Res & Educ, Honolulu, HI 96822 USA European Mol Biol Lab, D-69117 Heidelberg, Germany

Bork, Peer
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机构:
European Mol Biol Lab, D-69117 Heidelberg, Germany European Mol Biol Lab, D-69117 Heidelberg, Germany
机构:
[1] European Mol Biol Lab, D-69117 Heidelberg, Germany
[2] Univ Hawaii, Daniel K Inouye Ctr Microbial Oceanog Res & Educ, Honolulu, HI 96822 USA
来源:
基金:
欧洲研究理事会;
芬兰科学院;
关键词:
PAN-GENOME;
BACTEROIDES-THETAIOTAOMICRON;
SYMBIOTIC BACTERIA;
ORTHOLOGOUS GROUPS;
IN-VIVO;
DATABASE;
MICROBIOTA;
EVOLUTION;
DYNAMICS;
ENZYMES;
D O I:
10.1186/s13059-015-0646-9
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
Background: Gene content differences in human gut microbes can lead to inter-individual phenotypic variations such as digestive capacity. It is unclear whether gene content variation is caused by differences in microbial species composition or by the presence of different strains of the same species; the extent of gene content variation in the latter is unknown. Unlike pan-genome studies of cultivable strains, the use of metagenomic data can provide an unbiased view of structural variation of gut bacterial strains by measuring them in their natural habitats, the gut of each individual in this case, representing native boundaries between gut bacterial populations. We analyzed publicly available metagenomic data from fecal samples to characterize inter-individual variation in gut bacterial species. Results: A comparison of 11 abundant gut bacterial species showed that the gene content of strains from the same species differed, on average, by 13% between individuals. This number is based on gene deletions only and represents a lower limit, yet the variation is already in a similar range as observed between completely sequenced strains of cultivable species. We show that accessory genes that differ considerably between individuals can encode important functions, such as polysaccharide utilization and capsular polysaccharide synthesis loci. Conclusion: Metagenomics can yield insights into gene content variation of strains in complex communities, which cannot be predicted by phylogenetic marker genes alone. The large degree of inter-individual variability in gene content implies that strain resolution must be considered in order to fully assess the functional potential of an individual's human gut microbiome.
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