Caenorhabditis elegans, a Model Organism for Investigating Immunity

被引:125
作者
Marsh, Elizabeth K. [1 ]
May, Robin C. [1 ]
机构
[1] Univ Birmingham, Sch Biosci, Birmingham, W Midlands, England
基金
英国生物技术与生命科学研究理事会; 英国医学研究理事会;
关键词
PATHOGEN SERRATIA-MARCESCENS; PSEUDOMONAS-AERUGINOSA PAO1; INNATE IMMUNITY; SALMONELLA-TYPHIMURIUM; VIRULENCE FACTORS; C-ELEGANS; CRYPTOCOCCUS-NEOFORMANS; SIGNALING PATHWAY; CANDIDA-ALBICANS; MICROBACTERIUM-NEMATOPHILUM;
D O I
10.1128/AEM.07486-11
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The nematode Caenorhabditis elegans has been a powerful experimental organism for almost half a century. Over the past 10 years, researchers have begun to exploit the power of C. elegans to investigate the biology of a number of human pathogens. This work has uncovered mechanisms of host immunity and pathogen virulence that are analogous to those involved during pathogenesis in humans or other animal hosts, as well as novel immunity mechanisms which appear to be unique to the worm. More recently, these investigations have uncovered details of the natural pathogens of C. elegans, including the description of a novel intracellular microsporidian parasite as well as new nodaviruses, the first identification of viral infections of this nematode. In this review, we consider the application of C. elegans to human infectious disease research, as well as consider the nematode response to these natural pathogens.
引用
收藏
页码:2075 / 2081
页数:7
相关论文
共 83 条
[1]   Salmonella typhimurium proliferates and establishes a persistent infection in the intestine of Caenorhabditis elegans [J].
Aballay, A ;
Yorgey, P ;
Ausubel, FM .
CURRENT BIOLOGY, 2000, 10 (23) :1539-1542
[2]   Programmed cell death mediated by ced-3 and ced-4 protects Caenorhabditis elegans from Salmonella typhimurium-mediated killing [J].
Aballay, A ;
Ausubel, FM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (05) :2735-2739
[3]   Caenorhabditis elegans innate immune response triggered by Salmonella enterica requires intact LPS and is mediated by a MAPK signaling pathway [J].
Aballay, A ;
Drenkard, E ;
Hilbun, LR ;
Ausubel, FM .
CURRENT BIOLOGY, 2003, 13 (01) :47-52
[4]   Resistance to antimicrobial peptides contributes to persistence of Salmonella typhimurium in the C-elegans intestine [J].
Alegado, Rosanna A. ;
Tan, Man-Wah .
CELLULAR MICROBIOLOGY, 2008, 10 (06) :1259-1273
[5]   Identification of innate immunity genes and pathways using a comparative genomics approach [J].
Alper, Scott ;
Laws, Rebecca ;
Lackford, Brad ;
Boyd, Windy A. ;
Dunlap, Paul ;
Freedman, Jonathan H. ;
Schwartz, David A. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (19) :7016-7021
[6]   Specificity and complexity of the Caenorhabditis elegans innate immune response [J].
Alper, Scott ;
McBride, Sandra J. ;
Lackford, Brad ;
Freedman, Jonathan H. ;
Schwartz, David A. .
MOLECULAR AND CELLULAR BIOLOGY, 2007, 27 (15) :5544-5553
[7]  
[Anonymous], 1912, PRIX NOBEL 1911, P51
[8]   Paralysis and killing of Caenorhabditis elegans by enteropathogenic Escherichia coli requires the bacterial tryptophanase gene [J].
Anyanful, A ;
Dolan-Livengood, JM ;
Lewis, T ;
Sheth, S ;
DeZalia, MN ;
Sherman, MA ;
Kalman, LV ;
Benian, GM ;
Kalman, D .
MOLECULAR MICROBIOLOGY, 2005, 57 (04) :988-1007
[9]   Conditioning Protects C. elegans from Lethal Effects of Enteropathogenic E. coli by Activating Genes that Regulate Lifespan and Innate Immunity [J].
Anyanful, Akwasi ;
Easley, Kirk A. ;
Benian, Guy M. ;
Kalman, Daniel .
CELL HOST & MICROBE, 2009, 5 (05) :450-462
[10]   Antifungal chemical compounds identified using a C-elegans pathogenicity assay [J].
Breger, Julia ;
Fuchs, Beth Burgwyn ;
Aperis, George ;
Moy, Terence I. ;
Ausubel, Frederick M. ;
Mylonakis, Eleftherios .
PLOS PATHOGENS, 2007, 3 (02) :168-178