Evidence map›Paper›PMID 32571216›Full record

ArticleBMC microbiology2020

Size-dependent activity of silver nanoparticles on the morphological switch and biofilm formation of opportunistic pathogenic yeasts.

Bettina Szerencsés, Nóra Igaz, Ákos Tóbiás, Zsombor Prucsi, Andrea Rónavári, Péter Bélteky, Dániel Madarász, Csaba Papp, Ildikó Makra, Csaba Vágvölgyi and 3 more

Open access · goldAbstract read
In one paragraph

Article in BMC microbiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

24 citing papers in PubMed, 45 citations in OpenAlex.

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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

13 authors at 1 institution in 1 country.

Bettina SzerencsésDepartment of Microbiology, University of Szeged, Szeged, Hungary.
Nóra IgazDepartment of Biochemistry and Molecular Biology, Faculty of Science and Informatics, University of Szeged, Közép fasor 52, Szeged, H-6726, Hungary.
Ákos TóbiásDepartment of Biochemistry and Molecular Biology, Faculty of Science and Informatics, University of Szeged, Közép fasor 52, Szeged, H-6726, Hungary.
Zsombor PrucsiDepartment of Biochemistry and Molecular Biology, Faculty of Science and Informatics, University of Szeged, Közép fasor 52, Szeged, H-6726, Hungary.
Andrea RónaváriDepartment of Applied and Environmental Chemistry, University of Szeged, Szeged, Hungary.
Péter BéltekyDepartment of Applied and Environmental Chemistry, University of Szeged, Szeged, Hungary.
Dániel MadarászDepartment of Applied and Environmental Chemistry, University of Szeged, Szeged, Hungary.
Csaba PappDepartment of Microbiology, University of Szeged, Szeged, Hungary.
Ildikó MakraDepartment of Biochemistry and Molecular Biology, Faculty of Science and Informatics, University of Szeged, Közép fasor 52, Szeged, H-6726, Hungary.
Csaba VágvölgyiDepartment of Microbiology, University of Szeged, Szeged, Hungary.
Zoltán KónyaDepartment of Applied and Environmental Chemistry, University of Szeged, Szeged, Hungary.
Ilona PfeifferDepartment of Microbiology, University of Szeged, Szeged, Hungary.
Mónika KiricsiDepartment of Biochemistry and Molecular Biology, Faculty of Science and Informatics, University of Szeged, Közép fasor 52, Szeged, H-6726, Hungary. kiricsim@gmail.com.ORCID 0000-0002-8416-2052
University of Szeged · HU

Funding

Hungarian Goverment and European Union GINOP-2.3.2-15-2016-00038Hungarian Government and European Union GINOP-2.3.2-15-2016-00035Hungarian Ministry of Technology and Innovation UNKP-18-3-I-SZTE-42
6 · The paper itself

Abstract

backgroundDimorphism and biofilm formation are important virulence factors of some opportunistic human pathogenic yeasts. Such species commensally colonize skin or mucosal surfaces generally in yeast form, but under particular circumstances, convert into virulent hyphae and disseminate internal organs or cause mucocutaneous infections. The yeast-to-hypha shape-conversion promotes the development of a biofilm, a thick extracellular matrix with sessile cells within. The biofilm is capable to prevent the penetration of antifungal drugs, rendering the surviving biofilm-resident cells intrinsic sources of recurrent infections. The aim of this study was to evaluate the ability of silver nanoparticles (AgNPs) to attenuate the morphological switch and biofilm formation of several opportunistic pathogenic yeasts and to determine whether this feature depends on the nanoparticle size.

resultsAgNPs in three different sizes were prepared by chemical reduction approach and characterized by transmission electron microscopy, ultraviolet-visible spectroscopy and dynamic light scattering. The antifungal activity was evaluated by the microdilution method, the inhibitory capacity on biofilm formation and the biofilm degradation ability of differently sized AgNPs was assessed by viability assay. The morphological state of opportunistic pathogenic yeast cells in monoculture and in co-culture with human keratinocytes in the presence of AgNPs was examined by flow cytometry and scanning electron microscopy. All the three AgNPs inhibited the growth of the examined opportunistic pathogenic yeasts, nevertheless, AgNPs with the smallest diameter exhibited the most prominent toxic activities. AgNPs attenuated the biofilm formation in a nanoparticle size-dependent manner; however, their biofilm destruction capacity was negligible. AgNPs with the smallest size exerted the most significant effect on suppressing the morphological change of pathogens in monoculture as well as in a co-culture with keratinocytes.

conclusionsOur results confirm that AgNPs are capable to hinder yeast-to-hypha morphological conversion and biofilm formation of opportunistic pathogens and this biological effect of AgNPs is size-dependent.

Indexed as

Antifungal AgentsBiofilmsCell LineDynamic Light ScatteringFungiHumansHyphaeKeratinocytesMetal NanoparticlesMicrobial Sensitivity TestsMicroscopy, Electron, ScanningMicroscopy, Electron, TransmissionParticle SizeSilverAntifungal AgentsSilverBiofilm formationHuman keratinocytesMorphological switchPathogenic yeastsSilver nanoparticlesToxicity

Identifiers

PMID32571216
PMCPMC7309973
OpenAlexW3036696096

What OpenQuestion holds

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LicenceCC BY
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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.