Abstract
Coexisting microbial cells of the same species often exhibit genetic variation that can affect phenotypes ranging from nutrient preference to pathogenicity. Here we present inStrain, a program that uses metagenomic paired reads to profile intra-population genetic diversity (microdiversity) across whole genomes and compares microbial populations in a microdiversity-aware manner, greatly increasing the accuracy of genomic comparisons when benchmarked against existing methods. We use inStrain to profile >1,000 fecal metagenomes from newborn premature infants and find that siblings share significantly more strains than unrelated infants, although identical twins share no more strains than fraternal siblings. Infants born by cesarean section harbor Klebsiella with significantly higher nucleotide diversity than infants delivered vaginally, potentially reflecting acquisition from hospital rather than maternal microbiomes. Genomic loci that show diversity in individual infants include variants found between other infants, possibly reflecting inoculation from diverse hospital-associated sources. inStrain can be applied to any metagenomic dataset for microdiversity analysis and rigorous strain comparison.
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Data availability
The data supporting the findings of this study are available within the paper and its supplementary information files. Reads from infant samples are available under BioProject PRJNA294605 (SRA studies SRP052967, SRP114966 and SRP012558; and SRA accessions SRR5405607 to SRR5406014), reads from Zymo samples are available under BioProject PRJNA648136 and de novo assembled genomes are available at https://doi.org/10.6084/m9.figshare.c.4740080.v1.
Code availability
inStrain is available as an open-source Python program on GitHub (https://github.com/MrOlm/inStrain) and documentation is online at https://instrain.readthedocs.io/en/latest/.
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Acknowledgements
This research was supported by the National Institutes of Health (NIH) under award no. RAI092531A to J.F.B. and M.J.M., the Alfred P. Sloan Foundation under grant no. APSF-2012-10-05 to J.F.B., a National Science Foundation Graduate Research Fellowship to M.R.O. under grant no. DGE 1106400 and Chan Zuckerberg Biohub. The study was approved by the University of Pittsburgh Institutional Review Board (protocol no. PRO10090089).
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Contributions
M.R.O., M.J.M. and J.F.B. designed the study. M.R.O. performed metagenomic analyses. M.R.O., A.C.-C. and K.B.-G. contributed to software development and population genomic analyses. B.A.F. performed all DNA extractions. M.R.O. and J.F.B. wrote the manuscript and all authors contributed to manuscript revisions.
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J.F.B. is a founder of Metagenomi.
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Supplementary information
Supplementary Information
Supplementary Figs. 1–7.
Supplementary Table 1.
Information related to inStrain benchmarking.
Supplementary Table 2.
Ability of inStrain, MIDAS and MetaPhlAn2 to detect genomes present in the Zymo samples using public reference genomes.
Supplementary Table 3.
Raw data related to comparison of SNV detection by metagenomic inStrain analysis compared with isolate sequencing.
Supplementary Table 4.
Strain-level comparisons within infant samples, between infant coReads and strain identities.
Supplementary Table 5.
Abundance of subspecies in all infants, individual samples and controls, and information about subspecies genomes and representatives.
Supplementary Table 6.
Detailed SNS and SNV information for Enterococcus faecalis bacteriophage subspecies 482_10.ph.
Supplementary Software Manual 1.
inStrain program documentation.
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Olm, M.R., Crits-Christoph, A., Bouma-Gregson, K. et al. inStrain profiles population microdiversity from metagenomic data and sensitively detects shared microbial strains. Nat Biotechnol 39, 727–736 (2021). https://doi.org/10.1038/s41587-020-00797-0
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DOI: https://doi.org/10.1038/s41587-020-00797-0
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