Evidence map›Paper›PMID 41619738›Full record

ArticleCell host & microbe2026

Chemical inhibition of a bacterial immune system.

Zhiyu Zang, Olivia K Duncan, Dziugas Sabonis, Iana Fedorova, Yun Shi, Gause Miraj, Shuai Le, Jun Deng, Yuhao Zhu, Yanyao Cai and 11 more

Abstract read
In one paragraph

Article in Cell host & microbe, 2026. 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. Article
  2. Article
  3. Balancing of immune activation and suppression during phage infection.bioRxiv : the preprint server for biology · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors.

Zhiyu ZangDepartment of Chemistry, Indiana University Bloomington, Bloomington, IN 47405, USA.
Olivia K DuncanDepartment of Chemistry, Indiana University Bloomington, Bloomington, IN 47405, USA.
Dziugas SabonisInstitute of Biotechnology, Life Sciences Center, Vilnius University, Vilnius 10257, Lithuania.
Iana FedorovaDepartment of Microbiology and Immunology, University of California, San Francisco, San Francisco, CA 94158, USA.
Yun ShiInstitute for Biomedicine and Glycomics, Griffith University, Gold Coast, QLD 4215, Australia.
Gause MirajInstitute for Biomedicine and Glycomics, Griffith University, Gold Coast, QLD 4215, Australia.
Shuai LeDepartment of Microbiology, College of Basic Medical Sciences, Key Laboratory of Microbial Engineering Committee in Chongqing, Army Medical University, Chongqing 400038, China.
Jun DengDepartment of Microbiology, College of Basic Medical Sciences, Key Laboratory of Microbial Engineering Committee in Chongqing, Army Medical University, Chongqing 400038, China.
Yuhao ZhuDepartment of Microbiology, College of Basic Medical Sciences, Key Laboratory of Microbial Engineering Committee in Chongqing, Army Medical University, Chongqing 400038, China.
Yanyao CaiDepartment of Chemistry, Indiana University Bloomington, Bloomington, IN 47405, USA.
Chengqian ZhangDepartment of Chemistry, Indiana University Bloomington, Bloomington, IN 47405, USA.
Garima AryaDepartment of Immunology and Microbiology, University of Colorado Anschutz Medical Campus, School of Medicine, Aurora, CO 80045, USA.
Shelley A H DixonDepartment of Pediatrics, Herman B. Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Steven P AngusDepartment of Pediatrics, Herman B. Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Breck A DuerkopDepartment of Immunology and Microbiology, University of Colorado Anschutz Medical Campus, School of Medicine, Aurora, CO 80045, USA.
Haihua LiangCollege of Medicine, Southern University of Science and Technology, Shenzhen 518055, Guangdong, China.
Robert H PepinDepartment of Chemistry, Indiana University Bloomington, Bloomington, IN 47405, USA.
Thomas VeInstitute for Biomedicine and Glycomics, Griffith University, Gold Coast, QLD 4215, Australia.
Joseph Bondy-DenomyDepartment of Microbiology and Immunology, University of California, San Francisco, San Francisco, CA 94158, USA.
Giedre TamulaitieneInstitute of Biotechnology, Life Sciences Center, Vilnius University, Vilnius 10257, Lithuania.
Joseph P GerdtDepartment of Chemistry, Indiana University Bloomington, Bloomington, IN 47405, USA. Electronic address: jpgerdt@iu.edu.

Funding

Mechanistic basis of bacteriophages for the decolonization of vancomycin resistant enterococci in the intestine.R01AI141479 · NIAID · UNIVERSITY OF COLORADO DENVER · PI DUERKOP, BRECK A · 2018 to 2025
$4.4M
Elucidation of the first interspecies chemical signaling mechanisms in Capsaspora owczarzaki--the predator of a human pathogen and a model for the evolution of animal multicellularityR35GM138376 · NIGMS · TRUSTEES OF INDIANA UNIVERSITY · PI Joseph P. Gerdt · 2020 to 2026
$3.0M
NRSA Training CoreTL1TR002531 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI FOTI, DANIEL JUSTIN, HURLEY, THOMAS D. · 2018 to 2022
$2.5M
NCATS NIH HHS TL1 TR002531NIAID NIH HHS R01 AI141479NIGMS NIH HHS R35 GM138376
6 · The paper itself

Abstract

The rise of antibiotic resistance motivates a revived interest in phage therapy. However, bacteria possess dozens of anti-phage immune systems that confer resistance to therapeutic phages. Chemical inhibitors of these anti-phage immune systems could be employed as adjuvants to overcome resistance in phage-based therapies. Here, we report a class of chemical inhibitors that selectively inhibit type II Thoeris anti-phage immune systems from diverse bacteria-including antibiotic-resistant pathogens, thereby sensitizing phage-resistant bacteria to phages. These inhibitors block the biosynthesis of a histidine-ADPR intracellular "alarm" signal by ThsB, thereby preventing ThsA from arresting phage replication. Chemical inhibition of the Thoeris defense improves the efficacy of a model phage therapy against a phage-resistant clinical isolate of P. aeruginosa in a mouse infection, suggesting a therapeutic potential. These findings demonstrate that the selective inhibition of anti-phage defense systems can improve the efficacy of therapeutic phages, suggesting a strategy to circumvent phage-therapy resistance.

Indexed as

BacteriaBacteriophagesPseudomonas aeruginosaAnimalsAnti-Bacterial AgentsBacterial ProteinsMicePhage TherapyPseudomonas InfectionsAnti-Bacterial AgentsBacterial Proteinsantibacterial adjuvantantibiotic resistanceanti-phage defense systembacterial immunitybacteriophagechemical inhibitorphage therapyPseudomonas aeruginosaThoeris system

Identifiers

PMID41619738
PMCPMC12866962

What OpenQuestion holds

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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.