Evidence map›Paper›PMID 26283379›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2015

Structural remodeling of bacteriophage T4 and host membranes during infection initiation.

Bo Hu, William Margolin, Ian J Molineux, Jun Liu

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 136 papers.

0numbers the graph read from it
0cells of the map it votes in
136citing 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

136 citing papers in PubMed.

  1. Article
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  17. Article
  18. The spike tip protein of bacteriophage T4.bioRxiv : the preprint server for biology · 2025
    Article
  19. Article
  20. A dinoflagellate-infecting giant virus with a micron-length tail.bioRxiv : the preprint server for biology · 2025
    Article

76 more citing papers are in PubMed but not listed here.

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

4 authors.

Bo HuDepartment of Pathology and Laboratory Medicine, The University of Texas Medical School at Houston, Houston, TX 77030;
William MargolinDepartment of Microbiology & Molecular Genetics, The University of Texas Medical School at Houston, Houston, TX 77030;
Ian J MolineuxCenter for Infectious Disease, Department of Molecular Biosciences, Institute for Cell and Molecular Biology, The University of Texas at Austin, Austin, TX 78712 molineux@austin.utexas.edu Jun.Liu.1@uth.tmc.edu.
Jun LiuDepartment of Pathology and Laboratory Medicine, The University of Texas Medical School at Houston, Houston, TX 77030; molineux@austin.utexas.edu Jun.Liu.1@uth.tmc.edu.

Funding

Targeting and assembly of E. coli division proteinsR01GM061074 · NIGMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MARGOLIN, WILLIAM · 2000 to 2018
$5.7M
Structural basis of phage infection and DNA ejectionR01GM110243 · NIGMS · YALE UNIVERSITY · PI LIU, JUN, MOLINEUX, IAN J · 2014 to 2024
$3.1M
Direct Detector for a 300kV Cryoelectron MicroscopeS10OD016279 · OD · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI WAXHAM, M. NEAL · 2013 to 2013
$599k
NIGMS NIH HHS GM110243NIGMS NIH HHS GM61074NIGMS NIH HHS R01 GM061074NIGMS NIH HHS R01 GM110243NIH HHS S10 OD016279NIH HHS S10OD016279
6 · The paper itself

Abstract

The first stages of productive bacteriophage infections of bacterial host cells require efficient adsorption to the cell surface followed by ejection of phage DNA into the host cytoplasm. To achieve this goal, a phage virion must undergo significant structural remodeling. For phage T4, the most obvious change is the contraction of its tail. Here, we use skinny E. coli minicells as a host, along with cryo-electron tomography and mutant phage virions, to visualize key structural intermediates during initiation of T4 infection. We show for the first time that most long tail fibers are folded back against the tail sheath until irreversible adsorption, a feature compatible with the virion randomly walking across the cell surface to find an optimal site for infection. Our data confirm that tail contraction is triggered by structural changes in the baseplate, as intermediates were found with remodeled baseplates and extended tails. After contraction, the tail tube penetrates the host cell periplasm, pausing while it degrades the peptidoglycan layer. Penetration into the host cytoplasm is accompanied by a dramatic local outward curvature of the cytoplasmic membrane as it fuses with the phage tail tip. The baseplate hub protein gp27 and/or the ejected tape measure protein gp29 likely form the transmembrane channel for viral DNA passage into the cell cytoplasm. Building on the wealth of prior biochemical and structural information, this work provides new molecular insights into the mechanistic pathway of T4 phage infection.

Indexed as

Host-Pathogen InteractionsBacteriophage T4Cell MembraneCryoelectron MicroscopyGenes, ViralViral Tail ProteinsVirionViral Tail Proteinscryo-ETinfected cellmembrane curvaturephage T4structure

Identifiers

PMID26283379
PMCPMC4568249

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.