Antimicrobial effectors in the nematode Caenorhabditis elegans: an outgroup to the Arthropoda

被引:59
作者
Dierking, Katja [1 ]
Yang, Wentao [1 ]
Schulenburg, Hinrich [1 ]
机构
[1] Univ Kiel, Dept Evolutionary Ecol & Genet, D-24098 Kiel, Germany
关键词
Caenorhabditis elegans; antimicrobial peptides; lysozymes; caenopores; caenacins; reactive oxygen species; SALMONELLA-TYPHIMURIUM INFECTION; SAPOSIN-LIKE PROTEIN; C; ELEGANS; INNATE IMMUNITY; HOST-DEFENSE; DUAL OXIDASE; LIFE-SPAN; PEPTIDES; BACTERIA; GENES;
D O I
10.1098/rstb.2015.0299
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Nematodes and arthropods likely form the taxon Ecdysozoa. Information on antimicrobial effectors from the model nematode Caenorhabditis elegans may thus shed light on the evolutionary origin of these defences in arthropods. This nematode species possesses an extensive armory of putative antimicrobial effector proteins, such as lysozymes, caenopores (or saposin-like proteins), defensin-like peptides, caenacins and neuropeptide-like proteins, in addition to the production of reactive oxygen species and autophagy. As C. elegans is a bacterivore that lives in microbe-rich environments, some of its effector peptides and proteins likely function in both digestion of bacterial food and pathogen elimination. In this review, we provide an overview of C. elegans immune effector proteins and mechanisms. We summarize the experimental evidence of their antimicrobial function and involvement in the response to pathogen infection. We further evaluate the microbe-induced expression of effector genes using WormExp, a recently established database for C. elegans gene expression analysis. We emphasize the need for further analysis at the protein level to demonstrate an antimicrobial activity of these molecules both in vitro and in vivo. This article is part of the themed issue 'Evolutionary ecology of arthropod antimicrobial peptides'.
引用
收藏
页数:12
相关论文
共 103 条
[91]   Ingestion of bacterially expressed dsRNAs can produce specific and potent genetic interference in Caenorhabditis elegans [J].
Timmons, L ;
Court, DL ;
Fire, A .
GENE, 2001, 263 (1-2) :103-112
[92]   Overexpression of an antimicrobial peptide derived from C. elegans using an aggregation-prone protein coexpression system [J].
Tomisawa, Satoshi ;
Hojo, Eri ;
Umetsu, Yoshitaka ;
Ohki, Shinya ;
Kato, Yusuke ;
Miyazawa, Mitsuhiro ;
Mizuguchi, Mineyuki ;
Kamiya, Masakatsu ;
Kumaki, Yasuhiro ;
Kikukawa, Takashi ;
Kawano, Keiichi ;
Demura, Makoto ;
Aizawa, Tomoyasu .
AMB EXPRESS, 2013, 3 :1-8
[93]   p38 MAPK regulates expression of immune response genes and contributes to longevity in C. elegans [J].
Troemel, Emily R. ;
Chu, Stephanie W. ;
Reinke, Valerie ;
Lee, Siu Sylvia ;
Ausubel, Frederick M. ;
Kim, Dennis H. .
PLOS GENETICS, 2006, 2 (11) :1725-1739
[94]   Microsporidia Are Natural Intracellular Parasites of the Nematode Caenorhabditis elegans [J].
Troemel, Emily R. ;
Felix, Marie-Anne ;
Whiteman, Noah K. ;
Barriere, Antoine ;
Ausubel, Frederick M. .
PLOS BIOLOGY, 2008, 6 (12) :2736-2752
[95]   Ce-Duox1/BLI-3 Generated Reactive Oxygen Species Trigger Protective SKN-1 Activity via p38 MAPK Signaling during Infection in C. elegans [J].
van der Hoeven, Ransome ;
McCallum, Katie C. ;
Cruz, Melissa R. ;
Garsin, Danielle A. .
PLOS PATHOGENS, 2011, 7 (12)
[96]   Innate Host Defense Requires TFEB-Mediated Transcription of Cytoprotective and Antimicrobial Genes [J].
Visvikis, Orane ;
Ihuegbu, Nnamdi ;
Labed, Sid A. ;
Luhachack, Lyly G. ;
Alves, Anna-Maria F. ;
Wollenberg, Amanda C. ;
Stuart, Lynda M. ;
Stormo, Gary D. ;
Irazoqui, Javier E. .
IMMUNITY, 2014, 40 (06) :896-909
[97]   C. elegans Epidermal Wounding Induces a Mitochondrial ROS Burst that Promotes Wound Repair [J].
Xu, Suhong ;
Chisholm, Andrew D. .
DEVELOPMENTAL CELL, 2014, 31 (01) :48-60
[98]   Synergistic interactions between mammalian antimicrobial defense peptides [J].
Yan, H ;
Hancock, REW .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2001, 45 (05) :1558-1560
[99]   WormExp: a web-based application for a Caenorhabditis elegans-specific gene expression enrichment analysis [J].
Yang, Wentao ;
Dierking, Katja ;
Schulenburg, Hinrich .
BIOINFORMATICS, 2016, 32 (06) :943-945
[100]   Antimicrobial peptides of multicellular organisms [J].
Zasloff, M .
NATURE, 2002, 415 (6870) :389-395