Evidence map›Paper›PMID 34931815›Full record

ArticleAnalytical chemistry2022

Bacteria Detection at a Single-Cell Level through a Cyanotype-Based Photochemical Reaction.

Jiri Dietvorst, Amparo Ferrer-Vilanova, Sharath Narayana Iyengar, Aman Russom, Núria Vigués, Jordi Mas, Lluïsa Vilaplana, Maria-Pilar Marco, Gonzalo Guirado, Xavier Muñoz-Berbel

Abstract read
In one paragraph

Article in Analytical chemistry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Paper-based sensors for bacteria detection.Nature reviews bioengineering · 2023
    Review
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

10 authors.

Jiri DietvorstInstituto de Microelectrónica de Barcelona (IMB-CNM, CSIC), Bellaterra (Barcelona) 08193, Spain.
Amparo Ferrer-VilanovaInstituto de Microelectrónica de Barcelona (IMB-CNM, CSIC), Bellaterra (Barcelona) 08193, Spain.ORCID 0000-0002-4223-8442
Sharath Narayana IyengarDivision of Nanobiotechnology, Department of Protein Science, Science for life laboratory, KTH Royal Institute of Technology, Stockholm 17165, Sweden.ORCID 0000-0001-5348-3526
Aman RussomDivision of Nanobiotechnology, Department of Protein Science, Science for life laboratory, KTH Royal Institute of Technology, Stockholm 17165, Sweden.
Núria ViguésDepartament of Genetics and Microbiology, Universitat Autònoma de Barcelona, Bellaterra (Barcelona) 08193, Spain.
Jordi MasDepartament of Genetics and Microbiology, Universitat Autònoma de Barcelona, Bellaterra (Barcelona) 08193, Spain.
Lluïsa VilaplanaNanobiotechnology for diagnostics (Nb4D), Department of Chemical and Biomolecular Nanotechnology, Institute for Advanced Chemistry of Catalonia (IQAC, CSIC), Barcelona 08034, Spain.
Maria-Pilar MarcoNanobiotechnology for diagnostics (Nb4D), Department of Chemical and Biomolecular Nanotechnology, Institute for Advanced Chemistry of Catalonia (IQAC, CSIC), Barcelona 08034, Spain.ORCID 0000-0002-4064-1668
Gonzalo GuiradoDepartament de Química, Universitat Autònoma de Barcelona, Bellaterra (Barcelona) 08193, Spain.ORCID 0000-0003-2128-7007
Xavier Muñoz-BerbelInstituto de Microelectrónica de Barcelona (IMB-CNM, CSIC), Bellaterra (Barcelona) 08193, Spain.ORCID 0000-0002-6447-5756

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The detection of living organisms at very low concentrations is necessary for the early diagnosis of bacterial infections, but it is still challenging as there is a need for signal amplification. Cell culture, nucleic acid amplification, or nanostructure-based signal enhancement are the most common amplification methods, relying on long, tedious, complex, or expensive procedures. Here, we present a cyanotype-based photochemical amplification reaction enabling the detection of low bacterial concentrations up to a single-cell level. Photocatalysis is induced with visible light and requires bacterial metabolism of iron-based compounds to produce Prussian Blue. Bacterial activity is thus detected through the formation of an observable blue precipitate within 3 h of the reaction, which corresponds to the concentration of living organisms. The short time-to-result and simplicity of the reaction are expected to strongly impact the clinical diagnosis of infectious diseases.

Indexed as

BacteriaCommunicable DiseasesHumansNucleic Acid Amplification Techniques

Identifiers

PMID34931815
PMCPMC8771638

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.