Evidence map›Paper›PMID 39241059›Full record

ArticlePLoS pathogens2024

The role of bacterial size, shape and surface in macrophage engulfment of uropathogenic E. coli cells.

Elizabeth Peterson, Bill Söderström, Nienke Prins, Giang H B Le, Lauren E Hartley-Tassell, Chris Evenhuis, Rasmus Birkholm Grønnemose, Thomas Emil Andersen, Jakob Møller-Jensen, Gregory Iosifidis and 4 more

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 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. A deformableMaterials today. Bio · 2026
    Article
  5. Article
  6. Article
  7. Loss of Type 1 Pili and Flagella in UropathogenicPathogens (Basel, Switzerland) · 2025
    Article
  8. Article
  9. 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

14 authors.

Elizabeth PetersonAustralian Institute for Microbiology & Infection, University of Technology Sydney, Australia.
Bill SöderströmAustralian Institute for Microbiology & Infection, University of Technology Sydney, Australia.
Nienke PrinsAustralian Institute for Microbiology & Infection, University of Technology Sydney, Australia.
Giang H B LeSchool of Life Sciences, University of Technology Sydney, Sydney, Australia.
Lauren E Hartley-TassellInstitute for Glycomics, Griffith University, Gold Coast, Australia.
Chris EvenhuisAustralian Institute for Microbiology & Infection, University of Technology Sydney, Australia.
Rasmus Birkholm GrønnemoseResearch Unit of Clinical Microbiology, University of Southern Denmark and Odense University Hospital, Odense, Denmark.
Thomas Emil AndersenResearch Unit of Clinical Microbiology, University of Southern Denmark and Odense University Hospital, Odense, Denmark.
Jakob Møller-JensenDepartment of Biochemistry and Molecular Biology, University of Southern Denmark, Odense, Denmark.
Gregory IosifidisAustralian Institute for Microbiology & Infection, University of Technology Sydney, Australia.
Iain G DugginAustralian Institute for Microbiology & Infection, University of Technology Sydney, Australia.
Bernadette SaundersSchool of Life Sciences, University of Technology Sydney, Sydney, Australia.
Elizabeth J HarryAustralian Institute for Microbiology & Infection, University of Technology Sydney, Australia.
Amy L BottomleyAustralian Institute for Microbiology & Infection, University of Technology Sydney, Australia.ORCID 0000-0003-0255-0869

Funding

Australian Government RTPAustralian Research Council DP220101143
6 · The paper itself

Abstract

Uropathogenic Escherichia coli (UPEC) can undergo extensive filamentation in the host during acute urinary tract infections (UTIs). It has been hypothesised that this morphological plasticity allows bacteria to avoid host immune responses such as macrophage engulfment. However, it is still unclear what properties of filaments are important in macrophage-bacteria interactions. The aim of this work was to investigate the contribution of bacterial biophysical parameters, such as cell size and shape, and physiological parameters, such as cell surface and the environment, to macrophage engulfment efficiency. Viable, reversible filaments of known lengths and volumes were produced in the UPEC strain UTI89 using a variety of methods, including exposure to cell-wall targeting antibiotics, genetic manipulation and isolation from an in vitro human bladder cell model. Quantification of the engulfment ability of macrophages using gentamicin-protection assays and fluorescence microscopy demonstrated that the ability of filaments to avoid macrophage engulfment is dependent on a combination of size (length and volume), shape, cell surface and external environmental factors. UTI89 filamentation and macrophage engulfment efficiency were also found to occur independently of the SOS-inducible filamentation genes, sulA and ymfM in both in vivo and in vitro models of infection. Compared to filaments formed via antibiotic inhibition of division, the infection-derived filaments were preferentially targeted by macrophages. With several strains of UPEC now resistant to current antibiotics, our work identifies the importance of bacterial physiological and morphological states during infection.

Indexed as

Escherichia coli InfectionsMacrophagesUrinary Tract InfectionsUropathogenic Escherichia coliAnimalsHumansMicePhagocytosis

Identifiers

PMID39241059
PMCPMC11410268

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.