Intracellular doppler spectroscopy of live tissue sentinels for a fast in-vitro bacterial infection assay

Abstract Living organisms are frequently used as sentinels to monitor changes in the environment, and organoids can serve a similar function as in vitro sentinels detecting microbiological processes. One such process of great interest is pathogenic infection, which causes alterations in the cellular...

Full description

Saved in:
Bibliographic Details
Main Authors: Dawith Lim, Zhen Hua, Fernanda da Cunha, John Turek, Michael Ladisch, David Nolte
Format: Article
Language:English
Published: Nature Portfolio 2025-07-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-025-08523-z
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1849335140981932032
author Dawith Lim
Zhen Hua
Fernanda da Cunha
John Turek
Michael Ladisch
David Nolte
author_facet Dawith Lim
Zhen Hua
Fernanda da Cunha
John Turek
Michael Ladisch
David Nolte
author_sort Dawith Lim
collection DOAJ
description Abstract Living organisms are frequently used as sentinels to monitor changes in the environment, and organoids can serve a similar function as in vitro sentinels detecting microbiological processes. One such process of great interest is pathogenic infection, which causes alterations in the cellular dynamics of the sentinels. Doppler light scattering is well suited to measure such changes, as it is sensitive to the intracellular dynamics of the organoids even when the microbe density is too dilute to detect directly. In this paper, we present measurements of the endogenous changes of intracellular dynamics of DLD organoids (microclusters) in response to bacterial infection, detected using a long-coherence form of biodynamic imaging (BDI), a dynamic-contrast digital holography technique that captures the Doppler shifts encoded in the dynamic speckles. With a stable common-path digital holography system and using small in-vitro tissue microclusters, clinically relevant inoculum doses as low as 100 cfu/mL cause detectable changes in intracellular Doppler spectra within hours of infection and several hours before the proliferating bacteria population causes direct light scattering. Because it can measure effects for small bacterial populations, the method shows promise as a fast diagnostic tool to detect the presence of bacteria in patient fluid samples faster than traditional methods.
format Article
id doaj-art-46b566ffe0b74f1aba4c30ff62fdabfd
institution Kabale University
issn 2045-2322
language English
publishDate 2025-07-01
publisher Nature Portfolio
record_format Article
series Scientific Reports
spelling doaj-art-46b566ffe0b74f1aba4c30ff62fdabfd2025-08-20T03:45:23ZengNature PortfolioScientific Reports2045-23222025-07-0115111310.1038/s41598-025-08523-zIntracellular doppler spectroscopy of live tissue sentinels for a fast in-vitro bacterial infection assayDawith Lim0Zhen Hua1Fernanda da Cunha2John Turek3Michael Ladisch4David Nolte5Department of Physics, Purdue UniversityNational Eye Institute, National Institutes of HealthDepartment of Agricultural & Biological Engineering, Purdue UniversityDepartment of Basic Medical Sciences, Purdue UniversityDepartment of Agricultural & Biological Engineering, Purdue UniversityDepartment of Physics, Purdue UniversityAbstract Living organisms are frequently used as sentinels to monitor changes in the environment, and organoids can serve a similar function as in vitro sentinels detecting microbiological processes. One such process of great interest is pathogenic infection, which causes alterations in the cellular dynamics of the sentinels. Doppler light scattering is well suited to measure such changes, as it is sensitive to the intracellular dynamics of the organoids even when the microbe density is too dilute to detect directly. In this paper, we present measurements of the endogenous changes of intracellular dynamics of DLD organoids (microclusters) in response to bacterial infection, detected using a long-coherence form of biodynamic imaging (BDI), a dynamic-contrast digital holography technique that captures the Doppler shifts encoded in the dynamic speckles. With a stable common-path digital holography system and using small in-vitro tissue microclusters, clinically relevant inoculum doses as low as 100 cfu/mL cause detectable changes in intracellular Doppler spectra within hours of infection and several hours before the proliferating bacteria population causes direct light scattering. Because it can measure effects for small bacterial populations, the method shows promise as a fast diagnostic tool to detect the presence of bacteria in patient fluid samples faster than traditional methods.https://doi.org/10.1038/s41598-025-08523-z
spellingShingle Dawith Lim
Zhen Hua
Fernanda da Cunha
John Turek
Michael Ladisch
David Nolte
Intracellular doppler spectroscopy of live tissue sentinels for a fast in-vitro bacterial infection assay
Scientific Reports
title Intracellular doppler spectroscopy of live tissue sentinels for a fast in-vitro bacterial infection assay
title_full Intracellular doppler spectroscopy of live tissue sentinels for a fast in-vitro bacterial infection assay
title_fullStr Intracellular doppler spectroscopy of live tissue sentinels for a fast in-vitro bacterial infection assay
title_full_unstemmed Intracellular doppler spectroscopy of live tissue sentinels for a fast in-vitro bacterial infection assay
title_short Intracellular doppler spectroscopy of live tissue sentinels for a fast in-vitro bacterial infection assay
title_sort intracellular doppler spectroscopy of live tissue sentinels for a fast in vitro bacterial infection assay
url https://doi.org/10.1038/s41598-025-08523-z
work_keys_str_mv AT dawithlim intracellulardopplerspectroscopyoflivetissuesentinelsforafastinvitrobacterialinfectionassay
AT zhenhua intracellulardopplerspectroscopyoflivetissuesentinelsforafastinvitrobacterialinfectionassay
AT fernandadacunha intracellulardopplerspectroscopyoflivetissuesentinelsforafastinvitrobacterialinfectionassay
AT johnturek intracellulardopplerspectroscopyoflivetissuesentinelsforafastinvitrobacterialinfectionassay
AT michaelladisch intracellulardopplerspectroscopyoflivetissuesentinelsforafastinvitrobacterialinfectionassay
AT davidnolte intracellulardopplerspectroscopyoflivetissuesentinelsforafastinvitrobacterialinfectionassay