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Investigating the host-pathogen interaction in Tuberculosis by Bioelectrospray 3D cell culture modelling and label-free imaging

Investigating the host-pathogen interaction in Tuberculosis by Bioelectrospray 3D cell culture modelling and label-free imaging
Investigating the host-pathogen interaction in Tuberculosis by Bioelectrospray 3D cell culture modelling and label-free imaging
Tuberculosis is a deadly infectious disease caused by the bacterium Mycobacterium tuberculosis (Mtb). It constitutes a major cause of death worldwide with approximately 1.5 million people dying from TB every year.1-6 Traditional animal models as well as conventional ‘two-dimensional’ cell cultures do not accurately mimic human tuberculosis infection in vivo, such as the formation of caseating granulomas and degradation of extracellular matrix.We study a bioelectrospray-generated 3D cell culture model of tuberculosis, using diverse imaging techniques. In the 3D culture, Mtb-infected PBMCs (strains: H37Rv, 0414B) are mixed with an alginate-collagen gel. We investigated the host-pathogen interaction at high resolution at various stages of infection using Transmission Electron Microscopy (TEM). We used Micro-Computed Tomography (μCT) to show distribution of PBMCs in 3D in comparison to a human tuberculous lung biopsy. This was then correlated to traditional H&E, and matrix staining of the sectioned tuberculous human lung block. Using label-free microscopy [Coherent Anti-Stokes Raman Scattering (CARS), Second Harmonic Generation (SHG), Two-Photon Excitation Fluorescence (TPEF)], PBMC aggregation and collagen fibres were imaged in the microspheres.More lipid bodies were detected by TEM in the Mtb-infected samples than the uninfected controls. TEM and SHG imaging revealed collagen fibres attached to the surface of PBMCs. CARS microscopy showed that infection with Mtb, as well as the presence of collagen in the 3D matrix, influence the number of PBMC aggregates forming within the 3D culture. Preliminary data from μCT indicate that this technique can provide quantitative data on PBMC aggregates in 3D that can be cross-correlated with human biopsies.A correlative imaging approach between traditional and emerging imaging modalities is necessary in order to gain new insight into the host-pathogen interaction in tuberculosis.
University of Southampton
Konstantinopoulou, Eleni
c0b12984-1c89-41f1-826a-65d0655e1f90
Konstantinopoulou, Eleni
c0b12984-1c89-41f1-826a-65d0655e1f90
Elkington, Paul
60828c7c-3d32-47c9-9fcc-6c4c54c35a15
Mahajan, Sumeet
3e8fb3d0-f384-4182-ac26-b3063056a3c6
Tezera, Liku Bekele
c5598dbf-23a8-4934-96a4-7c783bf9e776

Konstantinopoulou, Eleni (2020) Investigating the host-pathogen interaction in Tuberculosis by Bioelectrospray 3D cell culture modelling and label-free imaging. University of Southampton, Doctoral Thesis, 175pp.

Record type: Thesis (Doctoral)

Abstract

Tuberculosis is a deadly infectious disease caused by the bacterium Mycobacterium tuberculosis (Mtb). It constitutes a major cause of death worldwide with approximately 1.5 million people dying from TB every year.1-6 Traditional animal models as well as conventional ‘two-dimensional’ cell cultures do not accurately mimic human tuberculosis infection in vivo, such as the formation of caseating granulomas and degradation of extracellular matrix.We study a bioelectrospray-generated 3D cell culture model of tuberculosis, using diverse imaging techniques. In the 3D culture, Mtb-infected PBMCs (strains: H37Rv, 0414B) are mixed with an alginate-collagen gel. We investigated the host-pathogen interaction at high resolution at various stages of infection using Transmission Electron Microscopy (TEM). We used Micro-Computed Tomography (μCT) to show distribution of PBMCs in 3D in comparison to a human tuberculous lung biopsy. This was then correlated to traditional H&E, and matrix staining of the sectioned tuberculous human lung block. Using label-free microscopy [Coherent Anti-Stokes Raman Scattering (CARS), Second Harmonic Generation (SHG), Two-Photon Excitation Fluorescence (TPEF)], PBMC aggregation and collagen fibres were imaged in the microspheres.More lipid bodies were detected by TEM in the Mtb-infected samples than the uninfected controls. TEM and SHG imaging revealed collagen fibres attached to the surface of PBMCs. CARS microscopy showed that infection with Mtb, as well as the presence of collagen in the 3D matrix, influence the number of PBMC aggregates forming within the 3D culture. Preliminary data from μCT indicate that this technique can provide quantitative data on PBMC aggregates in 3D that can be cross-correlated with human biopsies.A correlative imaging approach between traditional and emerging imaging modalities is necessary in order to gain new insight into the host-pathogen interaction in tuberculosis.

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Investigating the Host-Pathogen Interaction in Tuberculosis by Bioelectrospray 3D Cell Culture Modelling and Label-Free Imaging
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Published date: September 2020

Identifiers

Local EPrints ID: 447110
URI: http://eprints.soton.ac.uk/id/eprint/447110
PURE UUID: 131024d7-b84c-4af0-bfe2-421a2ce822fa
ORCID for Paul Elkington: ORCID iD orcid.org/0000-0003-0390-0613
ORCID for Liku Bekele Tezera: ORCID iD orcid.org/0000-0002-7898-6709

Catalogue record

Date deposited: 03 Mar 2021 17:31
Last modified: 17 Mar 2024 06:17

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Contributors

Author: Eleni Konstantinopoulou
Thesis advisor: Paul Elkington ORCID iD
Thesis advisor: Sumeet Mahajan
Thesis advisor: Liku Bekele Tezera ORCID iD

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