Evidence map›Paper›PMID 38265716›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2024

Microscope Subcellular Localization of Plant-Interacting Bacterial Effectors in Animal Cell Cultures.

Irene Jiménez-Guerrero, Francisco Javier López-Baena, Carlos Medina

Abstract read
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Article in Methods in molecular biology (Clifton, N.J.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Irene Jiménez-GuerreroDepartment of Microbiology, University of Seville, Seville, Spain.
Francisco Javier López-BaenaDepartment of Microbiology, University of Seville, Seville, Spain.
Carlos MedinaDepartment of Microbiology, University of Seville, Seville, Spain. cmedina1@us.es.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Eukaryote-interacting bacteria have developed along the evolution of an arsenal of tools to interact with potential hosts and to evade their defensive responses. Among these tools, the effector proteins are gaining a special importance due to the high diversity of molecular actions that they play in the host cell, with the final aim of taking the control over the cell. Bacteria inject these effectors into the cytosol of the host cells through distinct ways, as the type III secretion system. The study of the effectors' molecular roles inside the host cell is challenging, due in part to the lack of traceability of such proteins once they are delivered by the bacteria. Here, we describe in depth a methodology that combines the increase of the bacterial effector concentration by protein expression systems with the use of heterologous hosts to facilitate the visualization of the subcellular targeting of the effector inside the host cell by fluorescence microscopy.

Indexed as

EukaryotaEukaryotic CellsAnimalsBacteriaCell Culture TechniquesMicroscopy, FluorescenceBacterial effectorBacterial lysisEffectors’ transfectionFluorescence microscopyHeterologous expression systemSalicylateSalmonellaType III-secreted effectorType III secretion system

Identifiers

What OpenQuestion holds

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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.