Literature DB >> 33938877

Analysis of the Lipid Composition of Mycobacteria by Thin Layer Chromatography.

Sandra Guallar-Garrido1, Marina Luquin1, Esther Julián2.   

Abstract

Mycobacteria species can differ from one another in the rate of growth, presence of pigmentation, the colony morphology displayed on solid media, as well as other phenotypic characteristics. However, they all have in common the most relevant character of mycobacteria: its unique and highly hydrophobic cell wall. Mycobacteria species contain a membrane-covalent linked complex that includes arabinogalactan, peptidoglycan, and long-chains of mycolic acids with types that differ between mycobacteria species. Additionally, mycobacteria can also produce lipids that are located, non-covalently linked, on their cell surfaces, such as phthiocerol dimycocerosates (PDIM), phenolic glycolipids (PGL), glycopeptidolipids (GPL), acyltrehaloses (AT), or phosphatidil-inositol mannosides (PIM), among others. Some of them are considered virulence factors in pathogenic mycobacteria, or critical antigenic lipids in host-mycobacteria interaction. For these reasons, there is a significant interest in the study of mycobacterial lipids due to their application in several fields, from understanding their role in the pathogenicity of mycobacteria infections, to a possible implication as immunomodulatory agents for the treatment of infectious diseases and other pathologies such as cancer. Here, a simple approach to extract and analyze the total lipid content and the mycolic acid composition of mycobacteria cells grown in a solid medium using mixtures of organic solvents is presented. Once the lipid extracts are obtained, thin-layer chromatography (TLC) is performed to monitor the extracted compounds. The example experiment is performed with four different mycobacteria: the environmental fast-growing Mycolicibacterium brumae and Mycolicibacterium fortuitum, the attenuated slow-growing Mycobacterium bovis bacillus Calmette-Guérin (BCG), and the opportunistic pathogen fast-growing Mycobacterium abscessus, demonstrating that methods shown in the present protocol can be used to a wide range of mycobacteria.

Entities:  

Year:  2021        PMID: 33938877     DOI: 10.3791/62368

Source DB:  PubMed          Journal:  J Vis Exp        ISSN: 1940-087X            Impact factor:   1.355


  3 in total

1.  Mycobacterial surface characters remodeled by growth conditions drive different tumor-infiltrating cells and systemic IFN-γ/IL-17 release in bladder cancer treatment.

Authors:  Sandra Guallar-Garrido; Víctor Campo-Pérez; Míriam Pérez-Trujillo; Cecilia Cabrera; Jordi Senserrich; Alejandro Sánchez-Chardi; Rosa Maria Rabanal; Elisabet Gómez-Mora; Estela Noguera-Ortega; Marina Luquin; Esther Julián
Journal:  Oncoimmunology       Date:  2022-03-23       Impact factor: 8.110

2.  Iron deprivation enhances transcriptional responses to in vitro growth arrest of Mycobacterium tuberculosis.

Authors:  Sogol Alebouyeh; Jorge A Cárdenas-Pestana; Lucia Vazquez; Rafael Prados-Rosales; Patricia Del Portillo; Joaquín Sanz; Maria Carmen Menéndez; Maria J García
Journal:  Front Microbiol       Date:  2022-10-04       Impact factor: 6.064

3.  BCG Substrains Change Their Outermost Surface as a Function of Growth Media.

Authors:  Sandra Guallar-Garrido; Farners Almiñana-Rapún; Víctor Campo-Pérez; Eduard Torrents; Marina Luquin; Esther Julián
Journal:  Vaccines (Basel)       Date:  2021-12-29
  3 in total

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