Evidence map›Paper›PMID 41429878›Full record

ArticleScientific reports2025

Rapid and gentle volumetric imaging of host-pathogen interactions in salmon skin cells using projective oblique plane microscopy.

Jon-Richard Sommernes, Dhivya Borra Thiyagarajan, Florian Ströhl

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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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.

Jon-Richard SommernesDepartment of Physics and Technology, UiT The Arctic University of Norway, Tromsø, Norway.
Dhivya Borra ThiyagarajanThe Norwegian College of Fishery Science, UiT The Arctic University of Norway, Tromsø, Norway.
Florian StröhlDepartment of Physics and Technology, UiT The Arctic University of Norway, Tromsø, Norway. florian.strohl@uit.no.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High-speed, low-phototoxicity volumetric imaging is essential to quantify host–pathogen interactions in marine animal cell models, such as internalization of bacteria by Atlantic salmon skin keratocytes (SKCs). We developed an oblique plane microscopy (OPM) platform with an integrated projective OPM (pOPM) mode that preserves standard sample mounting and supports ultra-fast, optically sectioned projections. Leveraging the sparsity of bacterial signal, two pOPM projections at distinct viewing angles allow 3D localization by triangulation, reducing acquisition time and light dose by up to approximately 150-fold relative to full volumetric stacks. The hybrid workflow combines pOPM for rapid, gentle detection with OPM for volumetric context. We characterized system performance using 120 nm fluorescent beads and achieved near-diffraction-limited resolution across a 20 μm depth. In live, two-colour imaging of infected primary SKCs, we acquired 238 × 158 × 18 µm3 volumes in 5.3 s and performed 3 h time-lapse recordings at 10 min intervals at 4 h, 28 h, and 52 h post-infection. Automated analysis segmented cells, detected bacterial clusters, and classified their spatial relationship to cells, revealing internalization fractions of approximately 18%, 54%, and 52% at 4 h, 28 h, and 52 h post-infection, respectively. These results demonstrate that OPM and pOPM can quantify SKC–bacteria interactions with subcellular resolution over extended fields and timescales, providing a platform to investigate mechanisms of bacterial internalization and clearance relevant to aquaculture health.

Indexed as

Host-Pathogen InteractionsKeratinocytesMicroscopySalmo salarSkinAnimalsImaging, Three-Dimensional

Identifiers

PMID41429878
PMCPMC12748573

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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.