| Literature DB >> 34235675 |
Nathalie Deboosere1, Imène Belhaouane2, Arnaud Machelart2, Eik Hoffmann2, Alexandre Vandeputte2, Priscille Brodin3.
Abstract
Mycobacterium tuberculosis is able to colonize, persist, and massively replicate in host cells, such as phagocytes and epithelial cells. The intracellular stage of the bacteria is critical to the development of tuberculosis pathogenesis. The detailed mechanisms of intracellular trafficking of the bacillus are not fully understood and require further investigations. Therefore, increasing the knowledge of this process will help to develop therapeutic tools that will lower the burden of tuberculosis. M. tuberculosis is genetically tractable and tolerates the expression of heterologous fluorescent proteins. Thus, the intracellular distribution of the bacteria expressing fluorescent tracers can be easily defined using confocal microscopy. Advances in imaging techniques and images-based analysis allow the rapid quantification of biological objects in complex environments. In this chapter, we detailed high-content / high-throughput imaging methods to track the bacillus within host cell settings.Entities:
Keywords: Automated confocal microscopy; Drug discovery; High-content/high-throughput screening; Image-based analysis; Mycobacterium tuberculosis; Phenotypic assays; siRNA library
Year: 2021 PMID: 34235675 DOI: 10.1007/978-1-0716-1460-0_29
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745