Evidence map›Paper›PMID 41574341›Full record

ArticleFrontiers in microbiology2025

Comparison between metatranscriptomics and viral metagenomics, 16S, and host transcriptomics for comprehensive profiling of the respiratory microbiome and host response.

Gregory Destras, Marina Sabatier, Antonin Bal, Bruno Simon, Quentin Semanas, Hadrien Regue, Theophile Boyer, Dominique Ploin, Yves Gillet, Bruno Lina and 2 more

Abstract read
In one paragraph

Article in Frontiers in microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Oral and plasma microbiome in the context of acute febrile illness.medRxiv : the preprint server for health sciences · 2026
    Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Gregory DestrasLaboratoire de Virologie, Centre National de Référence France-Sud des Virus des Infections Respiratoires, Plateforme de séquençage Genepii, Hospices Civils de Lyon, Groupement Hospitalier Nord, Lyon, France.
Marina SabatierLaboratoire de Virologie, Centre National de Référence France-Sud des Virus des Infections Respiratoires, Plateforme de séquençage Genepii, Hospices Civils de Lyon, Groupement Hospitalier Nord, Lyon, France.
Antonin BalLaboratoire de Virologie, Centre National de Référence France-Sud des Virus des Infections Respiratoires, Plateforme de séquençage Genepii, Hospices Civils de Lyon, Groupement Hospitalier Nord, Lyon, France.
Bruno SimonLaboratoire de Virologie, Centre National de Référence France-Sud des Virus des Infections Respiratoires, Plateforme de séquençage Genepii, Hospices Civils de Lyon, Groupement Hospitalier Nord, Lyon, France.
Quentin SemanasLaboratoire de Virologie, Centre National de Référence France-Sud des Virus des Infections Respiratoires, Plateforme de séquençage Genepii, Hospices Civils de Lyon, Groupement Hospitalier Nord, Lyon, France.
Hadrien RegueLaboratoire de Virologie, Centre National de Référence France-Sud des Virus des Infections Respiratoires, Plateforme de séquençage Genepii, Hospices Civils de Lyon, Groupement Hospitalier Nord, Lyon, France.
Theophile BoyerLaboratoire de Virologie, Centre National de Référence France-Sud des Virus des Infections Respiratoires, Plateforme de séquençage Genepii, Hospices Civils de Lyon, Groupement Hospitalier Nord, Lyon, France.
Dominique PloinHospices Civils de Lyon, Hôpital Femme Mère Enfant, Service de Réanimation Pédiatrique et d'Accueil des Urgences, Bron, France.
Yves GilletHospices Civils de Lyon, Hôpital Femme Mère Enfant, Service de Réanimation Pédiatrique et d'Accueil des Urgences, Bron, France.
Bruno LinaLaboratoire de Virologie, Centre National de Référence France-Sud des Virus des Infections Respiratoires, Plateforme de séquençage Genepii, Hospices Civils de Lyon, Groupement Hospitalier Nord, Lyon, France.
Hussein AnaniLaboratoire de Virologie, Centre National de Référence France-Sud des Virus des Infections Respiratoires, Plateforme de séquençage Genepii, Hospices Civils de Lyon, Groupement Hospitalier Nord, Lyon, France.
Laurence JossetLaboratoire de Virologie, Centre National de Référence France-Sud des Virus des Infections Respiratoires, Plateforme de séquençage Genepii, Hospices Civils de Lyon, Groupement Hospitalier Nord, Lyon, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Omics-based studies focusing on a single kingdom, such as bacterial 16S gene sequencing, viral metagenomics, and human mRNA sequencing, are commonly used to explore the microbiome and its association with host responses. But combining these approaches is often expensive and time-consuming. Metatranscriptomics provides a snapshot of the entire active microbiome through bulk RNA sequencing in a single test, yet its performance relative to kingdom-specific methods has not been systematically assessed. Methods: We compared metatranscriptomics with three kingdom-specific sequencing approaches in 20 nasopharyngeal aspirates from infants 7 months of age hospitalized for bronchiolitis at the Hospices Civils de Lyon. Results: Applying specific sequencing depth thresholds (≥1,000 bacterial reads, ≥100,000 human reads, and detection of an internal RNA control), metatranscriptomics showed high detection concordance and correlated abundance for RNA viruses and human coding genes. Metatranscriptomics also detected RNA from both eukaryotic and prokaryotic DNA viruses, suggesting potential for identifying transcriptional activity. For the bacteriome, 82% of genera exceeding 0.5% relative abundance were captured, revealing distinct transcriptional profiles at the species level. Metatranscriptomics reproduced multi-omics-derived host-microbiome endotypes and revealed stronger key microbial associations, particularly for transcriptionally active microorganisms. Discussion: These findings indicate that a single metatranscriptomics run can complement or replace kingdom-specific approaches for profiling RNA viruses and the host transcriptome, while also identifying transcriptionally active bacteria and DNA viruses. Low-abundance or latent microorganisms may still require targeted assays. Metatranscriptomics thus provides a cost- and time-efficient strategy for integrated microbiome research and holds promise for clinical applications in acute infections and cases of diagnostic uncertainty.

Indexed as

16S gene sequencingcomparisonhuman transcriptomicsmetatranscripomicsmicrobiomemulti-omicsviral metagenomics

Identifiers

PMID41574341
PMCPMC12819617

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.