Evidence map›Paper›PMID 38649301›Full record

ArticleGigaScience2024

Large-scale genomic survey with deep learning-based method reveals strain-level phage specificity determinants.

Yiyan Yang, Keith Dufault-Thompson, Wei Yan, Tian Cai, Lei Xie, Xiaofang Jiang

Open access · goldAbstract read
In one paragraph

Article in GigaScience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
7.8field-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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. A Novel LyticFoods (Basel, Switzerland) · 2025
    Article
  14. Article
  15. Review
  16. Review
  17. microLife · 2025
    Article
  18. Article
  19. Article
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

6 authors at 2 institutions in 1 country.

Yiyan YangNational Library of Medicine, National Institutes of Health, Bethesda, MD 20894, USA.ORCID 0000-0001-9508-7396
Keith Dufault-ThompsonNational Library of Medicine, National Institutes of Health, Bethesda, MD 20894, USA.ORCID 0000-0002-0991-2255
Wei YanNational Library of Medicine, National Institutes of Health, Bethesda, MD 20894, USA.ORCID 0000-0001-5271-1515
Tian CaiPh.D. Program in Computer Science, The Graduate Center, The City University of New York, New York, NY 10016, USA.
Lei XiePh.D. Program in Computer Science, The Graduate Center, The City University of New York, New York, NY 10016, USA.ORCID 0000-0001-9051-2111
Xiaofang JiangNational Library of Medicine, National Institutes of Health, Bethesda, MD 20894, USA.ORCID 0000-0002-0955-8284
National Institutes of Health · USThe Graduate Center, CUNY · US

Funding

Comparative genomic analysis of bacteria speciesZIALM202010 · NLM · NATIONAL LIBRARY OF MEDICINE · PI JIANG, XIAOFANG · 2020 to 2025
$6.9M
Omics data integration and analysis for structure-based multi-target drug designR01GM122845 · NIGMS · NORTHEASTERN UNIVERSITY · PI Lei Xie · 2017 to 2026
$3.0M
NIGMS NIH HHS R01 GM122845NIH HHS
6 · The paper itself

Abstract

backgroundPhage therapy, reemerging as a promising approach to counter antimicrobial-resistant infections, relies on a comprehensive understanding of the specificity of individual phages. Yet the significant diversity within phage populations presents a considerable challenge. Currently, there is a notable lack of tools designed for large-scale characterization of phage receptor-binding proteins, which are crucial in determining the phage host range.

resultsIn this study, we present SpikeHunter, a deep learning method based on the ESM-2 protein language model. With SpikeHunter, we identified 231,965 diverse phage-encoded tailspike proteins, a crucial determinant of phage specificity that targets bacterial polysaccharide receptors, across 787,566 bacterial genomes from 5 virulent, antibiotic-resistant pathogens. Notably, 86.60% (143,200) of these proteins exhibited strong associations with specific bacterial polysaccharides. We discovered that phages with identical tailspike proteins can infect different bacterial species with similar polysaccharide receptors, underscoring the pivotal role of tailspike proteins in determining host range. The specificity is mainly attributed to the protein's C-terminal domain, which strictly correlates with host specificity during domain swapping in tailspike proteins. Importantly, our dataset-driven predictions of phage-host specificity closely match the phage-host pairs observed in real-world phage therapy cases we studied.

conclusionsOur research provides a rich resource, including both the method and a database derived from a large-scale genomics survey. This substantially enhances understanding of phage specificity determinants at the strain level and offers a valuable framework for guiding phage selection in therapeutic applications.

Indexed as

BacteriophagesDeep LearningHost SpecificityBacteriaGenome, BacterialGenome, ViralGenomicsGlycoside HydrolasesViral Tail ProteinsGlycoside Hydrolasestailspike protein, bacteriophageViral Tail Proteinsbacterial polysaccharidephage–host specificityphage receptor-binding proteinphage therapyserotype

Identifiers

PMID38649301
PMCPMC11034027
OpenAlexW4395016549

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.