De novo peptide databases enable protein-based stable isotope probing of microbial communities with up to species-level resolution
preprint · bioRxiv · 2024
| Date | 2024-11-26 |
| Type | preprint |
| Venue | bioRxiv |
| Publisher | openRxiv |
| Contribution | downstream-application |
| DOI | 10.1101/2024.11.25.625156 |
| Citations (OpenAlex) | 0 |
Peer-reviewed version: De novo peptide databases enable protein-based stable isotope probing of microbial communities with up to species-level resolution (2025-08-26, Environmental Microbiome)
Abstract
BackgroundProtein-based stable isotope probing (Protein-SIP) is a powerful approach that can directly link individual taxa to activity and substrate assimilation, elucidating metabolic pathways and trophic relationships within microbial communities. In Protein-SIP, peptides and corresponding taxa are identified by database matching, making database quality crucial for accurate analyses. For samples with unknown community composition, Protein-SIP typically employs either unrestricted reference databases or metagenome-derived databases. While (meta)genome-derived databases represent the gold standard, they may be incomplete and are typically resource-intensive to generate. In contrast, unrestricted reference databases can inflate the search space and require complex post-processing. ResultsHere, we explore the feasibility of using de novo peptide sequencing to construct peptide databases directly from mass spectrometry raw data. We then use the mass spectrometric data from labeled cultures to quantify isotope incorporation into specific peptides. We benchmark our approach against the canonical approach in which a sample-matching (meta)genome-derived protein sequence database is used on three different datasets: 1) a proteome analysis from a defined microbial community containing 13C-labeled E. coli cells, 2) time-course data of an anammox-dominated continuous reactor after feeding with 13C-labeled bicarbonate, and 3) a model of the human distal gut simulating a high-protein and high-fiber diet cultivated in either 2H2O or H218O. Our results show that de novo peptide databases are applicable to different isotopes, detecting similar amounts of labeled peptides compared to sample-matching (meta)genome-derived databases, and also identify labeled peptides missed by this canonical approach. Furthermore, we show that peptide-centric Protein-SIP allows up to species-specific resolution and enables the assessment of activity related to individual biological processes. Finally, we provide access to our modular Python pipeline to assist the construction of de novo peptide databases and subsequent peptide-centric Protein-SIP data analysis (https://git.ufz.de/meb/denovo-sip). ConclusionsDe novo peptide databases enable Protein-SIP of microbial communities without prior knowledge of the composition and can be used complementarily to (meta)genome-derived databases or as a standalone alternative in exploratory or resource-limited settings.
Methods and tools
- De novo peptide databases for Protein-SIP: Builds peptide databases from de novo sequencing of the raw data and uses them for protein-based stable isotope probing of microbial communities, reaching species-level resolution.
Data deposited
- De novo assembled databases allow species-specific protein-based stable isotope probing of microbiomes without prior knowledge of the community composition (as deposited) · PXD057215
Data used
- Quantification of mock microbial communities with metagenomes, 16S rRNA gene amplicons and metaproteomics (as deposited) · PXD006118
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