Evidence map›Paper›PMID 37620325›Full record

ArticleNature communications2023

Next-generation proteomics for quantitative Jumbophage-bacteria interaction mapping.

Andrea Fossati, Deepto Mozumdar, Claire Kokontis, Melissa Mèndez-Moran, Eliza Nieweglowska, Adrian Pelin, Yuping Li, Baron Guo, Nevan J Krogan, David A Agard and 2 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
7.9field-weighted citation impact, top 2% of its field
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

25 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. The biology of jumbo phages.Nature communications · 2026
    Review
  5. Article
  6. Bacteriophage genome-wide transposon mutagenesis.bioRxiv : the preprint server for biology · 2025
    Article
  7. Review
  8. The Biology of Nucleus-Forming Jumbo Phages.Annual review of genetics · 2025
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 1 country.

Andrea Fossati *J. David Gladstone Institutes, San Francisco, 94158, CA, USA.ORCID http://orcid.org/0000-0001-5170-4903
Deepto Mozumdar *Department of Immunology and Microbiology, University of California San Francisco, San Francisco, 94158, CA, USA.
Claire KokontisDepartment of Immunology and Microbiology, University of California San Francisco, San Francisco, 94158, CA, USA.
Melissa Mèndez-MoranDepartment of Biochemistry, University of California San Francisco, San Francisco, 94143, CA, USA.ORCID http://orcid.org/0000-0003-0817-7292
Eliza NieweglowskaDepartment of Biochemistry, University of California San Francisco, San Francisco, 94143, CA, USA.ORCID http://orcid.org/0000-0002-9204-3002
Adrian PelinJ. David Gladstone Institutes, San Francisco, 94158, CA, USA.
Yuping LiDepartment of Immunology and Microbiology, University of California San Francisco, San Francisco, 94158, CA, USA.ORCID http://orcid.org/0000-0003-2057-3271
Baron GuoDepartment of Immunology and Microbiology, University of California San Francisco, San Francisco, 94158, CA, USA.
Nevan J KroganJ. David Gladstone Institutes, San Francisco, 94158, CA, USA.ORCID http://orcid.org/0000-0003-4902-337X
David A AgardDepartment of Biochemistry, University of California San Francisco, San Francisco, 94143, CA, USA.ORCID http://orcid.org/0000-0003-3512-695X
Joseph Bondy-DenomyDepartment of Immunology and Microbiology, University of California San Francisco, San Francisco, 94158, CA, USA. Joseph.Bondy-Denomy@ucsf.edu.ORCID http://orcid.org/0000-0002-4909-9481
Danielle L SwaneyJ. David Gladstone Institutes, San Francisco, 94158, CA, USA. danielle.swaney@ucsf.edu.ORCID http://orcid.org/0000-0001-6119-6084
University of California, San Francisco · USGladstone Institutes · USQB3 · US

Funding

Tetrad: Genetics, Cell Biology, Biochemistry and Molecular Biology Training GrantT32GM139786 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Natalia Jura, David Paul Toczyski · 2021 to 2026
$6.5M
Microbial Pathogenesis and Host DefenseT32AI060537 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Joanne N. Engel · 2004 to 2026
$6.5M
ChimeraX -- Next Generation Visualization and Analysis Software for Multiscale ModelingR01GM129325 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI FERRIN, THOMAS E · 2018 to 2025
$5.2M
Genetic and Proteomic Approaches to Reveal Bacterial Vulnerabilities to Phage PredationR01AI167412 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Joseph Bondy-Denomy · 2022 to 2026
$3.5M
Investigating the mechanisms that make jumbophages impervious to bacterial immune systemsR01AI171041 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Joseph Bondy-Denomy · 2022 to 2026
$2.1M
Elucidation of the mechanisms of jumbophage genome protection during infectionF32GM149125 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MOZUMDAR, DEEPTO · 2023 to 2024
$143k
NIAID NIH HHS R01 AI167412NIAID NIH HHS R01 AI171041NIAID NIH HHS T32 AI060537NIGMS NIH HHS F32 GM149125NIGMS NIH HHS R01 GM129325NIGMS NIH HHS T32 GM139786
6 · The paper itself

Abstract

Host-pathogen interactions are pivotal in regulating establishment, progression, and outcome of an infection. While affinity-purification mass spectrometry has become instrumental in characterizing such interactions, it suffers from limitations in scalability and biological authenticity. Here we present the use of co-fractionation mass spectrometry for high throughput analysis of host-pathogen interactions from native viral infections of two jumbophages (ϕKZ and ϕPA3) in Pseudomonas aeruginosa. This approach enabled the detection of > 6000 unique host-pathogen interactions for each phage, encompassing > 50% of their respective proteomes. This deep coverage provided evidence for interactions between KZ-like phage proteins and the host ribosome, and revealed protein complexes for previously undescribed phage ORFs, including a ϕPA3 complex showing strong structural and sequence similarity to ϕKZ non-virion RNA polymerase. Interactome-wide comparison across phages showed similar perturbed protein interactions suggesting fundamentally conserved mechanisms of phage predation within the KZ-like phage family. To enable accessibility to this data, we developed PhageMAP, an online resource for network query, visualization, and interaction prediction ( https://phagemap.ucsf.edu/ ). We anticipate this study will lay the foundation for the application of co-fractionation mass spectrometry for the scalable profiling of host-pathogen interactomes and protein complex dynamics upon infection.

Indexed as

BacteriophagesProteomicsBacteriaChemical FractionationChromatography, Affinity

Identifiers

PMID37620325
PMCPMC10449902
OpenAlexW4386142019

What Socratic 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 Socratic graph.