Evidence map›Paper›PMID 33788901›Full record

ArticlePLoS pathogens2021

Staphylococcus aureus cell wall structure and dynamics during host-pathogen interaction.

Joshua A F Sutton, Oliver T Carnell, Lucia Lafage, Joe Gray, Jacob Biboy, Josie F Gibson, Eric J G Pollitt, Simone C Tazoll, William Turnbull, Natalia H Hajdamowicz and 6 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
3.8field-weighted citation impact, top 5% 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

52 citing papers in PubMed, 85 citations in OpenAlex.

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  19. Bisphosphonate-Conjugated Sitafloxacin for Treatment ofPharmaceuticals (Basel, Switzerland) · 2025
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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

16 authors at 2 institutions in 1 country.

Joshua A F SuttonDepartment of Molecular Biology and Biotechnology, University of Sheffield, Western Bank, Sheffield, United Kingdom.ORCID 0000-0002-0440-610X
Oliver T CarnellDepartment of Molecular Biology and Biotechnology, University of Sheffield, Western Bank, Sheffield, United Kingdom.ORCID 0000-0001-8847-5489
Lucia LafageDepartment of Molecular Biology and Biotechnology, University of Sheffield, Western Bank, Sheffield, United Kingdom.ORCID 0000-0002-8105-5083
Joe GrayBiosciences Institute, Newcastle University, Newcastle upon Tyne, United Kingdom.ORCID 0000-0003-2338-0301
Jacob BiboyCentre for Bacterial Cell Biology, Biosciences Institute, Newcastle University, Newcastle upon Tyne, United Kingdom.
Josie F GibsonDepartment of Molecular Biology and Biotechnology, University of Sheffield, Western Bank, Sheffield, United Kingdom.ORCID 0000-0002-4299-2488
Eric J G PollittDepartment of Biomedical Science, University of Sheffield, Firth Court, Western Bank, Sheffield, United Kingdom.ORCID 0000-0003-2406-2241
Simone C TazollDepartment of Molecular Biology and Biotechnology, University of Sheffield, Western Bank, Sheffield, United Kingdom.
William TurnbullDepartment of Molecular Biology and Biotechnology, University of Sheffield, Western Bank, Sheffield, United Kingdom.ORCID 0000-0001-9217-4961
Natalia H HajdamowiczThe Florey Institute for Host-Pathogen Interactions, University of Sheffield, Sheffield, United Kingdom.
Bartłomiej SalamagaDepartment of Molecular Biology and Biotechnology, University of Sheffield, Western Bank, Sheffield, United Kingdom.ORCID 0000-0001-9157-5800
Grace R PidwillDepartment of Molecular Biology and Biotechnology, University of Sheffield, Western Bank, Sheffield, United Kingdom.ORCID 0000-0002-5193-3631
Alison M CondliffeThe Florey Institute for Host-Pathogen Interactions, University of Sheffield, Sheffield, United Kingdom.ORCID 0000-0002-6697-8648
Stephen A RenshawThe Florey Institute for Host-Pathogen Interactions, University of Sheffield, Sheffield, United Kingdom.ORCID 0000-0003-1790-1641
Waldemar VollmerCentre for Bacterial Cell Biology, Biosciences Institute, Newcastle University, Newcastle upon Tyne, United Kingdom.
Simon J FosterDepartment of Molecular Biology and Biotechnology, University of Sheffield, Western Bank, Sheffield, United Kingdom.ORCID 0000-0001-7432-7805
University of Sheffield · GBNewcastle University · GB

Funding

Biotechnology and Biological Sciences Research Council BB/L006162/1Medical Research Council MR/N002679/1Medical Research Council MR/N013840/1Medical Research Council MR/R001111/1Medical Research Council MR/S014934/1Wellcome Trust 212197/Z/19/Z
6 · The paper itself

Abstract

Peptidoglycan is the major structural component of the Staphylococcus aureus cell wall, in which it maintains cellular integrity, is the interface with the host, and its synthesis is targeted by some of the most crucial antibiotics developed. Despite this importance, and the wealth of data from in vitro studies, we do not understand the structure and dynamics of peptidoglycan during infection. In this study we have developed methods to harvest bacteria from an active infection in order to purify cell walls for biochemical analysis ex vivo. Isolated ex vivo bacterial cells are smaller than those actively growing in vitro, with thickened cell walls and reduced peptidoglycan crosslinking, similar to that of stationary phase cells. These features suggested a role for specific peptidoglycan homeostatic mechanisms in disease. As S. aureus missing penicillin binding protein 4 (PBP4) has reduced peptidoglycan crosslinking in vitro its role during infection was established. Loss of PBP4 resulted in an increased recovery of S. aureus from the livers of infected mice, which coincided with enhanced fitness within murine and human macrophages. Thicker cell walls correlate with reduced activity of peptidoglycan hydrolases. S. aureus has a family of 4 putative glucosaminidases, that are collectively crucial for growth. Loss of the major enzyme SagB, led to attenuation during murine infection and reduced survival in human macrophages. However, loss of the other three enzymes Atl, SagA and ScaH resulted in clustering dependent attenuation, in a zebrafish embryo, but not a murine, model of infection. A combination of pbp4 and sagB deficiencies resulted in a restoration of parental virulence. Our results, demonstrate the importance of appropriate cell wall structure and dynamics during pathogenesis, providing new insight to the mechanisms of disease.

Indexed as

AnimalsCell WallHost-Pathogen InteractionsMicePeptidoglycanStaphylococcal InfectionsStaphylococcus aureusVirulenceZebrafishPeptidoglycan

Identifiers

PMID33788901
PMCPMC8041196
OpenAlexW3140810348

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.