Applications of bioluminescence imaging to the study of infectious diseases

被引:168
作者
Hutchens, Martha
Luker, Gary D. [1 ]
机构
[1] Univ Michigan, Sch Med, Program Immunol, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Sch Med, Dept Radiol, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Sch Med, Dept Microbiol & Immunol, Ann Arbor, MI 48109 USA
关键词
SIMPLEX-VIRUS TYPE-1; LIVING MICE; IN-VIVO; FIREFLY LUCIFERASE; TOXOPLASMA-GONDII; CANDIDA-ALBICANS; HIGH-THROUGHPUT; REPLICATION; EXPRESSION; REVEALS;
D O I
10.1111/j.1462-5822.2007.00995.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Bioluminescence imaging (BLI) has emerged as a powerful new method to analyse infectious diseases in animal models. BLI offers real-time monitoring of spatial and temporal progression of infection in the same animal, as opposed to euthanizing a cohort of animals and quantifying colony or plaque forming units at multiple time points. Pathogens or mice are engineered to express genetically encoded luciferase enzymes from bacteria, insects, or the sea pansy. The seminal study showing the feasibility of detecting microbially generated luminescence within a living mouse was published by Contag and colleagues in 1995, using Salmonella typhimurium transformed with the lux operon from Photorhabdus luminescens. Following this, they and others performed many studies of infection by bioluminescent Gram-negative and Gram-positive bacteria. Viruses can also be engineered to encode luciferase. Our laboratory has used bioluminescent reporter viruses to follow HSV and vaccinia pathogenesis; others have used an alphavirus or novirhabdovirus. Recently, even eukaryotic parasites Plasmodium, Leishmania and Toxoplasma have been transformed with luciferase and yielded unique insights into their in vivo behaviour. We expect that both the range of organisms and the molecular events able to be studied by BLI will continue to expand, yielding important insights into mechanisms of pathogenesis.
引用
收藏
页码:2315 / 2322
页数:8
相关论文
共 29 条
[1]   Optical imaging of Renilla luciferase reporter gene expression in living mice [J].
Bhaumik, S ;
Gambhir, SS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (01) :377-382
[2]   Non-invasive bioluminescence imaging for monitoring herpes simplex virus type 1 hematogenous infection [J].
Burgos, Javier S. ;
Guzman-Sanchez, Fernando ;
Sastre, Isabel ;
Fillat, Cristina ;
Valdivieso, Fernando .
MICROBES AND INFECTION, 2006, 8 (05) :1330-1338
[3]   Photonic detection of bacterial pathogens in living hosts [J].
Contag, CH ;
Contag, PR ;
Mullins, JI ;
Spilman, SD ;
Stevenson, DK ;
Benaron, DA .
MOLECULAR MICROBIOLOGY, 1995, 18 (04) :593-603
[4]   Luciferase Imaging of neurotropic viral infection in intact animals [J].
Cook, SH ;
Griffin, DE .
JOURNAL OF VIROLOGY, 2003, 77 (09) :5333-5338
[5]  
CORBISIER P, 1993, FEMS MICROBIOL LETT, V110, P231, DOI 10.1016/0378-1097(93)90471-D
[6]   Expression of firefly luciferase in Candida albicans and its use in the selection of stable transformants [J].
Doyle, TC ;
Nawotka, KA ;
Purchio, AF ;
Akin, AR ;
Francis, KP ;
Contag, PR .
MICROBIAL PATHOGENESIS, 2006, 40 (02) :69-81
[7]   Visualizing fungal infections in living mice using bioluminescent pathogenic Candida albicans strains transformed with the firefly luciferase gene [J].
Doyle, TC ;
Nawotka, KA ;
Kawahara, CB ;
Francis, KP ;
Contag, PR .
MICROBIAL PATHOGENESIS, 2006, 40 (02) :82-90
[8]   Monitoring bioluminescent Staphylococcus aureus infections in living mice using a novel luxABCDE construct [J].
Francis, KP ;
Joh, D ;
Bellinger-Kawahara, C ;
Hawkinson, MJ ;
Purchio, TF ;
Contag, PR .
INFECTION AND IMMUNITY, 2000, 68 (06) :3594-3600
[9]   Visualizing pneumococcal infections in the lungs of live mice using bioluminescent Streptococcus pneumoniae transformed with a novel gram-positive lux transposon [J].
Francis, KP ;
Yu, J ;
Bellinger-Kawahara, C ;
Joh, D ;
Hawkinson, MJ ;
Xiao, G ;
Purchio, TF ;
Caparon, MG ;
Lipsitch, M ;
Contag, PR .
INFECTION AND IMMUNITY, 2001, 69 (05) :3350-3358
[10]   Murine malaria parasite sequestration:: CD36 is the major receptor, but cerebral pathology is unlinked to sequestration [J].
Franke-Fayard, B ;
Janse, CJ ;
Cunha-Rodrigues, M ;
Ramesar, J ;
Büscher, P ;
Que, I ;
Löwik, C ;
Voshol, PJ ;
den Boer, MAM ;
van Duinen, SG ;
Febbraio, M ;
Mota, MM ;
Waters, AP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (32) :11468-11473