Phenotypic assays for Mycobacterium tuberculosis infection

被引:13
作者
Song, Ok-Ryul [1 ]
Deboosere, Nathalie [1 ]
Delorme, Vincent [1 ,2 ]
Queval, Christophe J. [1 ]
Deloison, Gaspard [1 ]
Werkmeister, Elisabeth [1 ]
Lafont, Frank [1 ]
Baulard, Alain [1 ]
Iantomasi, Raffaella [1 ]
Brodin, Priscille [1 ]
机构
[1] Univ Lille, CNRS, INSERM, CHU Lille,Inst Pasteur Lille,U1019,UMR 8204 CIIL, F-59000 Lille, France
[2] Inst Pasteur Korea, TB Res Lab, Seongnam Si 13488, Gyeonggi Do, South Korea
基金
新加坡国家研究基金会;
关键词
mycobacterium tuberculosis; cell-based assay; confocal imaging; automated image-analysis; drug discovery; genetic screening; FOAMY MACROPHAGES; ACIDIFICATION; GRANULOMAS; ATPASE; CELLS;
D O I
10.1002/cyto.a.23129
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Tuberculosis (TB) is still a major global threat, killing more than one million persons each year. With the constant increase of Mycobacterium tuberculosis strains resistant to first- and second-line drugs, there is an urgent need for the development of new drugs to control the propagation of TB. Although screenings of small molecules on axenic M. tuberculosis cultures were successful for the identification of novel putative anti-TB drugs, new drugs in the development pipeline remains scarce. Host-directed therapy may represent an alternative for drug development against TB. Indeed, M. tuberculosis has multiple specific interactions within host phagocytes, which may be targeted by small molecules. In order to enable drug discovery strategies against microbes residing within host macrophages, we developed multiple fluorescence-based HT/CS phenotypic assays monitoring the intracellular replication of M. tuberculosis as well as its intracellular trafficking. What we propose here is a population-based, multi-parametric analysis pipeline that can be used to monitor the intracellular fate of M. tuberculosis and the dynamics of cellular events such as phagosomal maturation (acidification and permeabilization), zinc poisoning system or lipid body accumulation. Such analysis allows the quantification of biological events considering the host-pathogen interplay and may thus be derived to other intracellular pathogens. (c) 2017 International Society for Advancement of Cytometry
引用
收藏
页码:983 / 994
页数:12
相关论文
共 41 条
[1]   Drug Tolerance in Replicating Mycobacteria Mediated by a Macrophage-Induced Efflux Mechanism [J].
Adams, Kristin N. ;
Takaki, Kevin ;
Connolly, Lynn E. ;
Wiedenhoft, Heather ;
Winglee, Kathryn ;
Humbert, Olivier ;
Edelstein, Paul H. ;
Cosma, Christine L. ;
Ramakrishnan, Lalita .
CELL, 2011, 145 (01) :39-53
[2]   RESPONSE OF CULTURED MACROPHAGES TO MYCOBACTERIUM-TUBERCULOSIS, WITH OBSERVATIONS ON FUSION OF LYSOSOMES WITH PHAGOSOMES [J].
ARMSTRONG, JA ;
HART, PD .
JOURNAL OF EXPERIMENTAL MEDICINE, 1971, 134 (03) :713-+
[3]   Blood Monocytes: Development, Heterogeneity, and Relationship with Dendritic Cells [J].
Auffray, Cedric ;
Sieweke, Michael H. ;
Geissmann, Frederic .
ANNUAL REVIEW OF IMMUNOLOGY, 2009, 27 :669-692
[4]   Metallobiology of host-pathogen interactions: an intoxicating new insight [J].
Botella, Helene ;
Stadthagen, Gustavo ;
Lugo-Villarino, Geanncarlo ;
de Chastellier, Chantal ;
Neyrolles, Olivier .
TRENDS IN MICROBIOLOGY, 2012, 20 (03) :106-112
[5]   High Content Phenotypic Cell-Based Visual Screen Identifies Mycobacterium tuberculosis Acyltrehalose-Containing Glycolipids Involved in Phagosome Remodeling [J].
Brodin, Priscille ;
Poquet, Yannick ;
Levillain, Florence ;
Peguillet, Isabelle ;
Larrouy-Maumus, Gerald ;
Gilleron, Martine ;
Ewann, Fanny ;
Christophe, Thierry ;
Fenistein, Denis ;
Jang, Jichan ;
Jang, Mi-Seon ;
Park, Sei-Jin ;
Rauzier, Jean ;
Carralot, Jean-Philippe ;
Shrimpton, Rachel ;
Genovesio, Auguste ;
Gonzalo-Asensio, Jesus A. ;
Puzo, Germain ;
Martin, Carlos ;
Brosch, Roland ;
Stewart, Graham R. ;
Gicquel, Brigitte ;
Neyrolles, Olivier .
PLOS PATHOGENS, 2010, 6 (09)
[6]   Reversible Lipid Accumulation and Associated Division Arrest of Mycobacterium aviuum in Lipoprotein-Induced Foamy Macrophages May Resemble Key Events during Latency and Reactivation of Tuberculosis [J].
Caire-Braendli, Irene ;
Papadopoulos, Alexia ;
Malaga, Wladimir ;
Marais, David ;
Canaan, Stephane ;
Thilo, Lutz ;
de Chastellier, Chantal .
INFECTION AND IMMUNITY, 2014, 82 (02) :476-490
[7]   Host Evasion and Exploitation Schemes of Mycobacterium tuberculosis [J].
Cambier, C. J. ;
Falkow, Stanley ;
Ramakrishnan, Lalita .
CELL, 2014, 159 (07) :1497-1509
[8]  
Christophe T, 2010, FUTURE MED CHEM, V2, P1283, DOI [10.4155/fmc.10.223, 10.4155/FMC.10.223]
[9]   Micropilot: automation of fluorescence microscopy-based imaging for systems biology [J].
Conrad, Christian ;
Wuensche, Annelie ;
Tan, Tze Heng ;
Bulkescher, Jutta ;
Sieckmann, Frank ;
Verissimo, Fatima ;
Edelstein, Arthur ;
Walter, Thomas ;
Liebel, Urban ;
Pepperkok, Rainer ;
Ellenberg, Jan .
NATURE METHODS, 2011, 8 (03) :246-+
[10]   Mycobacterial ESX-1 secretion system mediates host cell lysis through bacterium contact-dependent gross membrane disruptions [J].
Conrad, William H. ;
Osman, Morwan M. ;
Shanahan, Jonathan K. ;
Chu, Frances ;
Takaki, Kevin K. ;
Cameron, James ;
Hopkinson-Woolley, Digby ;
Brosch, Roland ;
Ramakrishnan, Lalita .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2017, 114 (06) :1371-1376