Evidence map›Paper›PMID 40678166›Full record

ArticleFrontiers in tuberculosis2025

Predicting fitness in

Ethan Bustad, Edson Petry, Oliver Gu, Braden T Griebel, Tige R Rustad, David R Sherman, Jason H Yang, Shuyi Ma

Abstract read
In one paragraph

Article in Frontiers in tuberculosis, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Ethan BustadCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA, United States.
Edson PetryCenter for Emerging and Re-Emerging Pathogens, Rutgers New Jersey Medical School, Newark, NJ, United States.
Oliver GuCenter for Emerging and Re-Emerging Pathogens, Rutgers New Jersey Medical School, Newark, NJ, United States.
Braden T GriebelCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA, United States.
Tige R RustadCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA, United States.
David R ShermanDepartment of Microbiology, University of Washington, Seattle, WA, United States.
Jason H YangCenter for Emerging and Re-Emerging Pathogens, Rutgers New Jersey Medical School, Newark, NJ, United States.
Shuyi MaCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA, United States.

Funding

Technology CoreU19AI135976 · NIAID · SEATTLE CHILDREN'S HOSPITAL · PI BALIGA, NITIN S · 2018 to 2022
$17.0M
Systems Biology CoreU19AI162598 · NIAID · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI ALLAND, DAVID, ELLNER, JERROLD J. · 2021 to 2025
$13.9M
Genetic, Metabolic and Regulatory Control of MIC and Relapse in M. tuberculosisR01AI146194 · NIAID · UNIVERSITY OF WASHINGTON · PI ALLAND, DAVID, SHERMAN, DAVID R · 2020 to 2024
$4.1M
A multifactorial pipeline to dissect combinatorial drug efficacy in TuberculosisR01AI150826 · NIAID · UNIVERSITY OF WASHINGTON · PI SHERMAN, DAVID R · 2021 to 2024
$2.9M
Network Dissection of Host-Pathogen Interactions in Mycobacterium tuberculosis InfectionDP2AI164249 · NIAID · SEATTLE CHILDREN'S HOSPITAL · PI MA, SHUYI · 2021 to 2025
$2.8M
Effects of Host Metabolic Variation on Antibiotic SusceptibilityR00GM118907 · NIGMS · RBHS-NEW JERSEY MEDICAL SCHOOL · PI YANG, JASON HUNG-YING · 2020 to 2022
$747k
NIAID NIH HHS DP2 AI164249NIAID NIH HHS R01 AI146194NIAID NIH HHS R01 AI150826NIAID NIH HHS U19 AI135976NIAID NIH HHS U19 AI162598NIGMS NIH HHS R00 GM118907
6 · The paper itself

Abstract

Introduction: Methods: We assembled a large Mtb RNA expression compendium and applied this to infer a comprehensive Mtb transcriptional regulatory network and compute condition-specific transcription factor activity (TFA) profiles. Using transcriptomic and functional genomics data, we trained an interpretable machine learning model that predicts Mtb fitness from TFA profiles. Results: We demonstrated that a TFA-based model can predict Mtb growth arrest and growth resumption under hypoxia and reaeration using gene expression data alone. This model also directly elucidates the transcriptional programs driving these growth phenotypes. Discussion: These integrative network modeling and machine learning analyses enable the prediction of mycobacterial fitness across different environmental and genetic contexts with mechanistic detail. We envision these models can inform the future design of prognostic assays and therapeutic interventions that can cripple Mtb growth and survival to cure tuberculosis disease.

Indexed as

growth regulationhypoxiainterpretable machine learningMycobacterium tuberculosisnetwork inferencenetwork modelingstress adaptationtranscriptional regulation

Identifiers

PMID40678166
PMCPMC12269550

What OpenQuestion holds

Textmetadata
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.