Live imaging of the genetically intractable obligate intracellular bacteria orientia tsutsugamushi using a panel of fluorescent dyes
Our understanding of the molecular mechanisms of bacterial infection and pathogenesis are disproportionally derived from a small number of well-characterised species and strains. One reason for this is the enormous time and resources required to develop a new organism into experimental system that c...
| Main Authors: | , , , |
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| Format: | Journal article |
| Language: | English |
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Elsevier
2016
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| _version_ | 1826275648926121984 |
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| author | Atwal, S Giengkam, S VanNieuwenhze, M Salje, J |
| author_facet | Atwal, S Giengkam, S VanNieuwenhze, M Salje, J |
| author_sort | Atwal, S |
| collection | OXFORD |
| description | Our understanding of the molecular mechanisms of bacterial infection and pathogenesis are disproportionally derived from a small number of well-characterised species and strains. One reason for this is the enormous time and resources required to develop a new organism into experimental system that can be interrogated at the molecular level, in particular with regards to the development of genetic tools. Live cell imaging by fluorescence microscopy is a powerful technique to study biological processes such as bacterial motility, host cell invasion, and bacterial growth and division. In the absence of genetic tools that enable exogenous expression of fluorescent proteins, fluorescent chemical probes can be used to label and track living cells. A large number of fluorescent chemical probes are commercially available, but these have overwhelmingly been applied to the study of eukaryotic cell systems. Here, we present a methodical analysis of four different classes of probes, which can be used to delineate the cytoplasm, nucleic acids, cell membrane or peptidoglycan of living bacterial cells. We have tested these in the context of the important but neglected human pathogen Orientia tsutsugamushi but expect that the methodology would be broadly applicable to other bacterial species. |
| first_indexed | 2024-03-06T23:01:59Z |
| format | Journal article |
| id | oxford-uuid:627257a4-755e-4f0d-820e-c211b1d0a48c |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-03-06T23:01:59Z |
| publishDate | 2016 |
| publisher | Elsevier |
| record_format | dspace |
| spelling | oxford-uuid:627257a4-755e-4f0d-820e-c211b1d0a48c2022-03-26T18:06:23ZLive imaging of the genetically intractable obligate intracellular bacteria orientia tsutsugamushi using a panel of fluorescent dyesJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:627257a4-755e-4f0d-820e-c211b1d0a48cEnglishSymplectic Elements at OxfordElsevier2016Atwal, SGiengkam, SVanNieuwenhze, MSalje, JOur understanding of the molecular mechanisms of bacterial infection and pathogenesis are disproportionally derived from a small number of well-characterised species and strains. One reason for this is the enormous time and resources required to develop a new organism into experimental system that can be interrogated at the molecular level, in particular with regards to the development of genetic tools. Live cell imaging by fluorescence microscopy is a powerful technique to study biological processes such as bacterial motility, host cell invasion, and bacterial growth and division. In the absence of genetic tools that enable exogenous expression of fluorescent proteins, fluorescent chemical probes can be used to label and track living cells. A large number of fluorescent chemical probes are commercially available, but these have overwhelmingly been applied to the study of eukaryotic cell systems. Here, we present a methodical analysis of four different classes of probes, which can be used to delineate the cytoplasm, nucleic acids, cell membrane or peptidoglycan of living bacterial cells. We have tested these in the context of the important but neglected human pathogen Orientia tsutsugamushi but expect that the methodology would be broadly applicable to other bacterial species. |
| spellingShingle | Atwal, S Giengkam, S VanNieuwenhze, M Salje, J Live imaging of the genetically intractable obligate intracellular bacteria orientia tsutsugamushi using a panel of fluorescent dyes |
| title | Live imaging of the genetically intractable obligate intracellular bacteria orientia tsutsugamushi using a panel of fluorescent dyes |
| title_full | Live imaging of the genetically intractable obligate intracellular bacteria orientia tsutsugamushi using a panel of fluorescent dyes |
| title_fullStr | Live imaging of the genetically intractable obligate intracellular bacteria orientia tsutsugamushi using a panel of fluorescent dyes |
| title_full_unstemmed | Live imaging of the genetically intractable obligate intracellular bacteria orientia tsutsugamushi using a panel of fluorescent dyes |
| title_short | Live imaging of the genetically intractable obligate intracellular bacteria orientia tsutsugamushi using a panel of fluorescent dyes |
| title_sort | live imaging of the genetically intractable obligate intracellular bacteria orientia tsutsugamushi using a panel of fluorescent dyes |
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