Evidence map›Paper›PMID 40767516›Full record

ArticlemSystems2025

Impact of study design, contamination, and data characteristics on results and interpretation of microbiome studies.

Jose Agudelo, Aaron W Miller

Abstract read
In one paragraph

Article in mSystems, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Comparative Evaluation of Enrichment and Selective Culture Strategies for DetectingVector borne and zoonotic diseases (Larchmont, N.Y.) · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Microbial dysbiosis in cholangiocarcinoma.Frontiers in microbiology · 2026
    Review
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

2 authors.

Jose AgudeloDepartment of Cardiovascular and Metabolic Sciences, Cleveland Clinic, Cleveland, Ohio, USA.
Aaron W MillerDepartment of Cardiovascular and Metabolic Sciences, Cleveland Clinic, Cleveland, Ohio, USA.ORCID 0000-0001-8342-1449

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Advances in high-throughput molecular techniques have enabled microbiome studies in low-biomass environments, which pose unique challenges due to contamination risks. While best-practice guidelines can reduce contamination by over 90%, the impact of residual contamination and data set variability on statistical outcomes remains understudied. Here, we quantitatively assessed how study design factors influence microbiome analyses using simulated and real-world data sets. Alpha diversity was affected by sample number and community dissimilarity, but not by the number of unique taxa. Beta diversity was influenced primarily by unique taxa and group dissimilarity, with a marginal effect of sample number. The number of differentially abundant taxa depended on the number of unique taxa but was also influenced by sample number, depending on thealgorithm. Notably, contamination had a marginal impact on weighted beta diversity but altered the number of differentially abundant taxa when at least 10 contaminants were present, with a greater effect as contamination increased. Findings closely mirrored results from seven real-world low-biomass data sets. Overall, group dissimilarity and the number of unique taxa were the primary drivers of statistical outcomes. The DESeq2 algorithm outperformed ANCOM-BC when exposed to stochastically distributed contamination, but algorithms were equivocal under contamination weighted toward one group. In all cases, the rate of false positives in differential abundance analyses was <15%. Importantly, in both simulated and real-world data, contamination rarely impacts whether microbiome differences were detected but did affect the number of differentially abundant taxa. Thus, when validated protocols with internal negative controls are used, residual contamination minimally impacts statistical outcomes. Alpha diversity was affected by sample number and community dissimilarity, but not by the number of unique taxa. Beta diversity was influenced primarily by unique taxa and group dissimilarity, with a marginal effect of sample number. The number of differentially abundant taxa depended on the number of unique taxa but was also influenced by sample number, depending on the algorithm. Notably, contamination had a marginal impact on weighted beta diversity but altered the number of differentially abundant taxa when at least 10 contaminants were present, with a greater effect as contamination increased. Findings closely mirrored results from seven real-world low-biomass data sets. Overall, group dissimilarity and the number of unique taxa were the primary drivers of statistical outcomes. The DESeq2 algorithm outperformed ANCOM-BC when exposed to stochastically distributed contamination, but algorithms were equivocal under contamination weighted toward one group. In all cases, the rate of false positives in differential abundance analyses was <15%. Importantly, in both simulated and real-world data, contamination rarely whether microbiome differences were detected but did affect the number of differentially abundant taxa. Thus, when validated protocols with internal negative controls are used, residual contamination minimally impacts statistical outcomes.IMPORTANCEMicrobiome studies in low-biomass environments face challenges due to contamination. However, even after implementing strict contamination prevention, control, and analysis measures, the impact of residual contamination on the validity of statistical outcomes in such studies remains a topic of ongoing discussion. Our analyses reveal that key drivers of microbiome study outcomes are group dissimilarity and the number of unique taxa, while contamination has minimal impact on statistical outcomes, primarily limited to the number of differentially abundant taxa detected. A common approach to contamination control involves removing taxa based on published contaminant lists. However, our analysis shows that these lists are highly inconsistent across studies, limiting reliability. Instead, our results support the use of internal negative controls as the most robust means of identifying and mitigating contamination. Collectively, data show that low-biomass microbiome studies have reduced power to detect differences between groups. However, when differences are observed, they are unlikely to be contamination-driven. By prioritizing validated protocols that prevent, assess, and eliminate contaminants through the use of internal negative controls, researchers can minimize the impact of contamination and improve the reliability of results.

Indexed as

MicrobiotaResearch DesignAlgorithmsHumanscontaminationlow microbial biomassmicrobiomereal-world datasimulated datastudy design

Identifiers

PMID40767516
PMCPMC12456016

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.