Evidence map›Paper›PMID 41839722›Full record

ArticleACS applied materials & interfaces2026

Spatially Organized DNA-Templated Silver Nanoclusters as Potent Antimicrobial Agents for ESKAPE Infections.

Elizabeth Skelly, Krishna Majithia, Laura P Rebolledo, Camila Fonseca Rizek, Silvia Figueiredo Costa, Alora R Dunnavant, Cheyenne Vasquez, Alexander J Lushnikov, Alexey V Krasnoslobodtsev, Taejin Kim and 5 more

Abstract read
In one paragraph

Article in ACS applied materials & interfaces, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Elizabeth SkellyChemistry and Nanoscale Science Program, Department of Chemistry, University of North Carolina at Charlotte, Charlotte, North Carolina 28223, United States.ORCID 0000-0003-1157-0845
Krishna MajithiaDepartment of Biology, University of North Carolina at Charlotte, Charlotte, North Carolina 28223, United States.
Laura P RebolledoChemistry and Nanoscale Science Program, Department of Chemistry, University of North Carolina at Charlotte, Charlotte, North Carolina 28223, United States.
Camila Fonseca RizekLaboratório de Investigação Médica 49, Departamento de Infectologia e Medicina Tropical da Faculdade de Medicina da Universidade de São Paulo, Av. Dr. Eneas de Carvalho Aguiar, 470, São Paulo 05403-000, Brazil.
Silvia Figueiredo CostaLaboratório de Investigação Médica 49, Departamento de Infectologia e Medicina Tropical da Faculdade de Medicina da Universidade de São Paulo, Av. Dr. Eneas de Carvalho Aguiar, 470, São Paulo 05403-000, Brazil.
Alora R DunnavantChemistry and Nanoscale Science Program, Department of Chemistry, University of North Carolina at Charlotte, Charlotte, North Carolina 28223, United States.ORCID 0009-0005-3369-6600
Cheyenne VasquezChemistry and Nanoscale Science Program, Department of Chemistry, University of North Carolina at Charlotte, Charlotte, North Carolina 28223, United States.
Alexander J LushnikovDepartment of Physics, University of Nebraska Omaha, Omaha, Nebraska 68182, United States.
Alexey V KrasnoslobodtsevDepartment of Physics, University of Nebraska Omaha, Omaha, Nebraska 68182, United States.
Taejin KimDepartment of Physical Sciences, West Virginia University Institute of Technology, Beckley, West Virginia 25801, United States.
Morgan R ChandlerMIMETAS US, Inc, Gaithersburg, Maryland 20878, United States.ORCID 0000-0003-3078-6000
Renata de Freitas SaitoCentro de Investigação Translacional em Oncologia (LIM24), Departamento de Radiologia e Oncologia, Faculdade de Medicina da Universidade de São Paulo and Instituto do Câncer do Estado de São Paulo, São Paulo, São Paulo 01246-000, Brazil.
Roger ChammasCentro de Investigação Translacional em Oncologia (LIM24), Departamento de Radiologia e Oncologia, Faculdade de Medicina da Universidade de São Paulo and Instituto do Câncer do Estado de São Paulo, São Paulo, São Paulo 01246-000, Brazil.
M Brittany JohnsonDepartment of Biology, University of North Carolina at Charlotte, Charlotte, North Carolina 28223, United States.
Kirill A AfoninChemistry and Nanoscale Science Program, Department of Chemistry, University of North Carolina at Charlotte, Charlotte, North Carolina 28223, United States.ORCID 0000-0002-6917-3183

Funding

SMART NANPs: new molecular platform for communication with human immune system and modulation of therapeutic responsesR35GM139587 · NIGMS · UNIVERSITY OF NORTH CAROLINA CHARLOTTE · PI AFONIN, KIRILL A · 2021 to 2025
$1.8M
Augmenting host innate immune responses against Staphylococcal osteomyelitis with antimicrobial nucleic acid structuresR21AI190691 · NIAID · UNIVERSITY OF NORTH CAROLINA CHARLOTTE · PI AFONIN, KIRILL A, JOHNSON, MORGAN BRITTANY · 2025 to 2025
$402k
NIAID NIH HHS R21 AI190691NIGMS NIH HHS R35 GM139587
6 · The paper itself

Abstract

Antibiotic-resistant bacteria cause more than one million deaths annually worldwide. The rapid evolution and horizontal gene transfer among pathogens frequently render newly developed antibiotics ineffective shortly after their introduction, underscoring the urgent need for alternative therapeutic strategies. Nanoscale silver is well known for its innate antimicrobial activity but typically requires high concentrations for efficacy that causes toxicities and limits broader clinical applications. To overcome these limitations, we introduce programmable, self-assembling DNA scaffolds that template, stabilize, and spatially organize multiple copies of monodisperse silver nanoclusters (DNA-AgNCs). These nanoscale assemblies enhance the antimicrobial potency of formulations while exhibiting intrinsic fluorescence, providing a dual functionality for therapeutic and fluorescence probing applications. Comprehensive characterization revealed DNA-AgNCs with superior stability and potent activity against clinically relevant antibiotic-resistant ESKAPE pathogens. Also, DNA-AgNCs significantly reduced the intracellular bacterial burden in primary murine bone cells infected with

Indexed as

Anti-Bacterial AgentsDNAMetal NanoparticlesSilverStaphylococcus aureusAnimalsDNA NanostructuresMiceMicrobial Sensitivity TestsReactive Oxygen SpeciesAnti-Bacterial AgentsDNAReactive Oxygen SpeciesSilverbone infectionESKAPE pathogensresistant bacteriasilver nanoclustersstaphylococcus aureus

Identifiers

PMID41839722
PMCPMC13049360

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.