# Combination of Whole Genome Sequencing and Metagenomics for Microbiological Diagnostics

**Authors:** Srinithi Purushothaman, Marco Meola, Adrian Egli

PMC · DOI: 10.3390/ijms23179834 · International Journal of Molecular Sciences · 2022-08-30

## TL;DR

This paper reviews how combining whole genome sequencing and metagenomics can improve microbiological diagnostics and patient care.

## Contribution

The paper introduces a framework for integrating WGS and metagenomics data to enhance diagnostic accuracy and clinical outcomes.

## Key findings

- Combining WGS and metagenomics can provide synergistic insights for microbiological diagnostics.
- Customized bioinformatics pipelines and databases are essential for integrating these technologies.
- Such integration can improve infection control and pathogen surveillance.

## Abstract

Whole genome sequencing (WGS) provides the highest resolution for genome-based species identification and can provide insight into the antimicrobial resistance and virulence potential of a single microbiological isolate during the diagnostic process. In contrast, metagenomic sequencing allows the analysis of DNA segments from multiple microorganisms within a community, either using an amplicon- or shotgun-based approach. However, WGS and shotgun metagenomic data are rarely combined, although such an approach may generate additive or synergistic information, critical for, e.g., patient management, infection control, and pathogen surveillance. To produce a combined workflow with actionable outputs, we need to understand the pre-to-post analytical process of both technologies. This will require specific databases storing interlinked sequencing and metadata, and also involves customized bioinformatic analytical pipelines. This review article will provide an overview of the critical steps and potential clinical application of combining WGS and metagenomics together for microbiological diagnosis.

## Full-text entities

- **Genes:** beta-lactamase [NCBI Gene 4290808]
- **Diseases:** COVID-19 (MESH:D000086382), pneumonia (MESH:D011014), TB (MESH:D014390), sepsis (MESH:D018805), abscesses (MESH:D000038), cancer (MESH:D009369), encephalitis (MESH:D004660), meningitis (MESH:D008580), infection (MESH:D007239), Influenza (MESH:D007251), urinary tract infection (MESH:D014552)
- **Chemicals:** carbapenem (MESH:D015780), daptomycin (MESH:D017576), agar (MESH:D000362)
- **Species:** Enterococcus faecium (species) [taxon 1352], Chlamydia trachomatis (species) [taxon 813], Mycobacterium tuberculosis (species) [taxon 1773], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Homo sapiens (human, species) [taxon 9606], Enterococcus faecalis (species) [taxon 1351], Pseudomonas aeruginosa (species) [taxon 287], Enterobacter hormaechei (CDC Enteric Group 75, species) [taxon 158836], Escherichia coli (E. coli, species) [taxon 562], Acinetobacter baumannii (species) [taxon 470], Staphylococcus aureus (species) [taxon 1280], metagenome (species) [taxon 256318]

## Full text

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## Figures

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## References

176 references — full list in the complete paper: https://tomesphere.com/paper/PMC9456280/full.md

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Source: https://tomesphere.com/paper/PMC9456280