Evidence map›Paper›PMID 23724076›Full record

ArticlePloS one2013

The phage lytic proteins from the Staphylococcus aureus bacteriophage vB_SauS-phiIPLA88 display multiple active catalytic domains and do not trigger staphylococcal resistance.

Lorena Rodríguez-Rubio, Beatriz Martínez, Ana Rodríguez, David M Donovan, Friedrich Götz, Pilar García

Abstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing 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

31 citing papers in PubMed.

  1. Review
  2. Article
  3. Recent Advances in Endolysin Engineering.Antibiotics (Basel, Switzerland) · 2025
    Review
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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

6 authors.

Lorena Rodríguez-RubioDairySafe Group, Department of Technology and Biotechnology of Dairy Products, Instituto de Productos Lácteos de Asturias-Consejo Superior de Investigaciones Científicas, Villaviciosa, Asturias, Spain.
Beatriz Martínez
Ana Rodríguez
David M Donovan
Friedrich Götz
Pilar García

Funding

Triple action chimera: eradication of nasal S. aureus by cell wall hydrolasesR01AI075077 · NIAID · U.S. AGRICULTURAL RESEARCH CENTER · PI DONOVAN, DAVID MATTHEW · 2008 to 2010
$697k
NIAID NIH HHS 1R01AI075077-01A1NIAID NIH HHS R01 AI075077
6 · The paper itself

Abstract

The increase in antibiotic resistance world-wide revitalized the interest in the use of phage lysins to combat pathogenic bacteria. In this work, we analyzed the specific cleavage sites on the staphylococcal peptidoglycan produced by three phage lytic proteins. The investigated cell wall lytic enzymes were the endolysin LysH5 derived from the S. aureus bacteriophage vB_SauS-phi-IPLA88 (phi-IPLA88) and two fusion proteins between lysostaphin and the virion-associated peptidoglycan hydrolase HydH5 (HydH5SH3b and HydH5Lyso). We determined that all catalytic domains present in these proteins were active. Additionally, we tested for the emergence of resistant Staphylococcus aureus to any of the three phage lytic proteins constructs. Resistant S. aureus could not be identified after 10 cycles of bacterial exposure to phage lytic proteins either in liquid or plate cultures. However, a quick increase in lysostaphin resistance (up to 1000-fold in liquid culture) was observed. The lack of resistant development supports the use of phage lytic proteins as future therapeutics to treat staphylococcal infections.

Indexed as

Catalytic DomainDrug Resistance, BacterialAmino Acid SequenceEndopeptidasesLysostaphinMass SpectrometryMolecular Sequence DataN-Acetylmuramoyl-L-alanine AmidasePeptidoglycanStaphylococcus aureusStaphylococcus PhagesendolysinEndopeptidasesLysostaphinN-Acetylmuramoyl-L-alanine AmidasePeptidoglycan

Identifiers

PMID23724076
PMCPMC3665550

What OpenQuestion holds

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LicenceCC0
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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.