Evidence map›Paper›PMID 38913753›Full record

ArticlePLoS pathogens2024

Pseudo-pac site sequences used by phage P22 in generalized transduction of Salmonella.

Jessie L Maier, Craig Gin, Benjamin Callahan, Emma K Sheriff, Breck A Duerkop, Manuel Kleiner

Abstract read
In one paragraph

Article in PLoS pathogens, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. A novel temperate phage fromMicrobiology spectrum · 2026
    Article
  4. Article
  5. Article
  6. Phage Therapy forAntibiotics (Basel, Switzerland) · 2025
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Jessie L MaierDepartment of Plant and Microbial Biology, North Carolina State University, Raleigh, North Carolina, United States of America.ORCID 0009-0001-8575-5386
Craig GinDepartment of Population Health and Pathobiology, North Carolina State University, Raleigh, North Carolina, United States of America.
Benjamin CallahanDepartment of Population Health and Pathobiology, North Carolina State University, Raleigh, North Carolina, United States of America.
Emma K SheriffDepartment of Immunology and Microbiology, University of Colorado - Anschutz Medical Campus, School of Medicine, Aurora, Colorado, United States of America.
Breck A DuerkopDepartment of Immunology and Microbiology, University of Colorado - Anschutz Medical Campus, School of Medicine, Aurora, Colorado, United States of America.
Manuel KleinerDepartment of Plant and Microbial Biology, North Carolina State University, Raleigh, North Carolina, United States of America.ORCID 0000-0001-6904-0287

Funding

Mechanistic basis of bacteriophages for the decolonization of vancomycin resistant enterococci in the intestine.R01AI141479 · NIAID · UNIVERSITY OF COLORADO DENVER · PI DUERKOP, BRECK A · 2018 to 2025
$4.4M
Quantitative Metagenomics and the Vaginal Microbiome of Preterm BirthR35GM133745 · NIGMS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI Benjamin John Callahan · 2019 to 2026
$2.3M
Metaproteomics to investigate intestinal microbiota-host and -diet interactionsR35GM138362 · NIGMS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI KLEINER, MANUEL · 2020 to 2024
$1.9M
NIAID NIH HHS R01 AI141479NIGMS NIH HHS R35 GM133745NIGMS NIH HHS R35 GM138362
6 · The paper itself

Abstract

Salmonella enterica Serovar Typhimurium (Salmonella) and its bacteriophage P22 are a model system for the study of horizontal gene transfer by generalized transduction. Typically, the P22 DNA packaging machinery initiates packaging when a short sequence of DNA, known as the pac site, is recognized on the P22 genome. However, sequences similar to the pac site in the host genome, called pseudo-pac sites, lead to erroneous packaging and subsequent generalized transduction of Salmonella DNA. While the general genomic locations of the Salmonella pseudo-pac sites are known, the sequences themselves have not been determined. We used visualization of P22 sequencing reads mapped to host Salmonella genomes to define regions of generalized transduction initiation and the likely locations of pseudo-pac sites. We searched each genome region for the sequence with the highest similarity to the P22 pac site and aligned the resulting sequences. We built a regular expression (sequence match pattern) from the alignment and used it to search the genomes of two P22-susceptible Salmonella strains-LT2 and 14028S-for sequence matches. The final regular expression successfully identified pseudo-pac sites in both LT2 and 14028S that correspond with generalized transduction initiation sites in mapped read coverages. The pseudo-pac site sequences identified in this study can be used to predict locations of generalized transduction in other P22-susceptible hosts or to initiate generalized transduction at specific locations in P22-susceptible hosts with genetic engineering. Furthermore, the bioinformatics approach used to identify the Salmonella pseudo-pac sites in this study could be applied to other phage-host systems.

Indexed as

Bacteriophage P22Salmonella typhimuriumDNA PackagingGene Transfer, HorizontalGenome, BacterialTransduction, Genetic

Identifiers

PMID38913753
PMCPMC11226127

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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.