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...
Saved in:
| Main Authors: | , , , , , |
|---|---|
| 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 |