Evidence map›Paper›PMID 42749893›Full record

ArticleNature microbiology2026

Prophage-encoding engineered bacteria enable prophylactic lytic phage therapy for enteric infection in mice.

Rogerio A Bataglioli, Hiba Baaziz, Hallie F Avalos, Lindsay Smith, Zachary R Baker, Rita J Makhlouf, David da Silva Barreira, Harsimran Kaur, Teresa Southard, Bryan B Hsu

Abstract read
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Article in Nature microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Rogerio A BataglioliDepartment of Biological Sciences, Fralin Life Sciences Institute, and the Center for Emerging, Zoonotic and Arthropod-borne Pathogens, Virginia Tech, Blacksburg, VA, USA.ORCID http://orcid.org/0000-0003-4987-1168
Hiba BaazizDepartment of Biological Sciences, Fralin Life Sciences Institute, and the Center for Emerging, Zoonotic and Arthropod-borne Pathogens, Virginia Tech, Blacksburg, VA, USA.
Hallie F AvalosDepartment of Biological Sciences, Fralin Life Sciences Institute, and the Center for Emerging, Zoonotic and Arthropod-borne Pathogens, Virginia Tech, Blacksburg, VA, USA.
Lindsay SmithDepartment of Biological Sciences, Fralin Life Sciences Institute, and the Center for Emerging, Zoonotic and Arthropod-borne Pathogens, Virginia Tech, Blacksburg, VA, USA.
Zachary R BakerDepartment of Biological Sciences, Fralin Life Sciences Institute, and the Center for Emerging, Zoonotic and Arthropod-borne Pathogens, Virginia Tech, Blacksburg, VA, USA.
Rita J MakhloufDepartment of Biological Sciences, Fralin Life Sciences Institute, and the Center for Emerging, Zoonotic and Arthropod-borne Pathogens, Virginia Tech, Blacksburg, VA, USA.
David da Silva BarreiraDepartment of Biological Sciences, Fralin Life Sciences Institute, and the Center for Emerging, Zoonotic and Arthropod-borne Pathogens, Virginia Tech, Blacksburg, VA, USA.ORCID http://orcid.org/0000-0003-1958-8409
Harsimran KaurDepartment of Biological Sciences, Fralin Life Sciences Institute, and the Center for Emerging, Zoonotic and Arthropod-borne Pathogens, Virginia Tech, Blacksburg, VA, USA.
Teresa SouthardDepartment of Biomedical Sciences and Pathobiology, VA-MD College of Veterinary Medicine, Virginia Tech, Blacksburg, VA, USA.
Bryan B HsuDepartment of Biological Sciences, Fralin Life Sciences Institute, and the Center for Emerging, Zoonotic and Arthropod-borne Pathogens, Virginia Tech, Blacksburg, VA, USA. bhsu@vt.edu.ORCID http://orcid.org/0000-0002-8219-1124

Funding

Investigating the role of phage in the gut microbiomeR35GM147484 · NIGMS · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI Bryan Boen Hsu · 2022 to 2026
$1.9M
Pharmaceutical Research and Manufacturers of America Foundation (PhRMA Foundation) PFDL23 1003168U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R35GM147484
6 · The paper itself

Abstract

Phage therapy is a promising antibacterial approach but it has limited efficacy against enteric bacterial infections, such as Salmonella enterica Typhimurium (STm). Here we hypothesized that establishing high concentrations of a pathogen-targeting phage in the gut before infection would prophylactically protect against future infection. To this end, we engineered non-pathogenic Escherichia coli to encode a prophage that produces obligately lytic phage progeny targeting STm while overcoming its host defence systems, including restriction-modification systems. We show that prophylactic gut colonization with this lytic phage-producing lysogen of E. coli produces high levels of lytic phage before infection, inhibits the establishment of STm after infection and improves survival in mouse models of STm-induced colitis. Using a mutant STm strain limited to intestinal colonization, we show that phage-producing E. coli consistently colonized, produced high phage levels and eliminated STm from the intestinal tract. Our findings present a proof-of-concept that prophylactic prophage therapy can protect against an enteric infection.

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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.