Evidence map›Paper›PMID 38940509›Full record

ArticlemSphere2024

The F plasmid conjutome: the repertoire of

Abu Amar M Al Mamun, Kimberley Kissoon, Yang Grace Li, Erin Hancock, Peter J Christie

Abstract read
In one paragraph

Article in mSphere, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Experimental Approaches to Visualize Effector Protein Translocation During Host-Pathogen Interactions.BioEssays : news and reviews in molecular, cellular and developmental biology · 2025
    Review
  5. Review
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

5 authors.

Abu Amar M Al MamunDepartment of Microbiology and Molecular Genetics, McGovern Medical School at UTHealth, Houston, Texas, USA.
Kimberley KissoonDepartment of Microbiology and Molecular Genetics, McGovern Medical School at UTHealth, Houston, Texas, USA.
Yang Grace LiDepartment of Microbiology and Molecular Genetics, McGovern Medical School at UTHealth, Houston, Texas, USA.
Erin HancockDepartment of Microbiology and Molecular Genetics, McGovern Medical School at UTHealth, Houston, Texas, USA.
Peter J ChristieDepartment of Microbiology and Molecular Genetics, McGovern Medical School at UTHealth, Houston, Texas, USA.ORCID 0000-0002-9799-7067

Funding

TRANSLOCATION OF DNA ACROSS THE AGROBACTERIUM ENVELOPER01GM048746 · NIGMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI CHRISTIE, PETER J. · 1998 to 2018
$6.9M
Biological And Structural Diversity Of Bacterial Type IV Secretion SystemsR35GM131892 · NIGMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI PETER j. CHRISTIE · 2019 to 2026
$3.8M
Mitigation of Stress Responses By Protein Transfer Through Conjugation MachinesR21AI159970 · NIAID · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI CHRISTIE, PETER J. · 2021 to 2022
$429k
NIAID NIH HHS R21 AI159970NIGMS NIH HHS R01 GM048746NIGMS NIH HHS R35 GM131892
6 · The paper itself

Abstract

Bacterial conjugation systems pose a major threat to human health through their widespread dissemination of mobile genetic elements (MGEs) carrying cargoes of antibiotic resistance genes. Using the Cre Recombinase Assay for Translocation (CRAfT), we recently reported that the IncFV pED208 conjugation system also translocates at least 16 plasmid-encoded proteins to recipient bacteria. Here, we deployed a high-throughput CRAfT screen to identify the repertoire of chromosomally encoded protein substrates of the pED208 system. We identified 32 substrates encoded by the IMPORTANCE: Conjugation systems comprise a major subfamily of the type IV secretion systems (T4SSs) and are the progenitors of a second large T4SS subfamily dedicated to translocation of protein effectors. This study examined the capacity of conjugation machines to function as protein translocators. Using a high-throughput reporter screen, we determined that 32 chromosomally encoded proteins are delivered through an F plasmid conjugation system. The translocated proteins potentially enhance the establishment of the co-transferred F plasmid or mitigate mating-induced stresses. Translocation signals located C-terminally or internally conferred substrate recognition by the F system and, remarkably, many substrates also were translocated through heterologous conjugation systems. Our findings highlight the plasticity of conjugation systems in their capacities to co-translocate DNA and many protein substrates.

Indexed as

Conjugation, GeneticEscherichia coliEscherichia coli ProteinsType IV Secretion SystemsF FactorProtein TransportEscherichia coli ProteinsType IV Secretion Systemsconjugationeffector translocatorF plasmidhorizontal DNA transferprotein translocationtype IV secretion

Identifiers

PMID38940509
PMCPMC11288057

What OpenQuestion holds

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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.