Dietary trehalose enhances virulence of epidemic Clostridium difficile

被引:270
作者
Collins, J. [1 ]
Robinson, C. [2 ]
Danhof, H. [1 ]
Knetsch, C. W. [3 ]
van Leeuwen, H. C. [3 ]
Lawley, T. D. [4 ]
Auchtung, J. M. [1 ]
Britton, R. A. [1 ]
机构
[1] Baylor Coll Med, Dept Mol Virol & Microbiol, One Baylor Plaza, Houston, TX 77030 USA
[2] Univ Oregon, Inst Mol Biol, 1318 Franklin Blvd, Eugene, OR 97403 USA
[3] Leiden Univ, Med Ctr, Dept Med Microbiol, Albinusdreef 2, NL-2333 ZA Leiden, Netherlands
[4] Wellcome Trust Sanger Inst, Wellcome Trust Genome Campus, Hinxton CB10 1SA, Cambs, England
基金
美国国家卫生研究院;
关键词
EMERGENCE; INFECTION; STRAIN; SPREAD; MALABSORPTION; RESISTANCE; MORTALITY; DISEASE;
D O I
10.1038/nature25178
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Clostridium difficile disease has recently increased to become a dominant nosocomial pathogen in North America and Europe, although little is known about what has driven this emergence. Here we show that two epidemic ribotypes (RT027 and RT078) have acquired unique mechanisms to metabolize low concentrations of the disaccharide trehalose. RT027 strains contain a single point mutation in the trehalose repressor that increases the sensitivity of this ribotype to trehalose by more than 500-fold. Furthermore, dietary trehalose increases the virulence of a RT027 strain in a mouse model of infection. RT078 strains acquired a cluster of four genes involved in trehalose metabolism, including a PTS permease that is both necessary and sufficient for growth on low concentrations of trehalose. We propose that the implementation of trehalose as a food additive into the human diet, shortly before the emergence of these two epidemic lineages, helped select for their emergence and contributed to hypervirulence.
引用
收藏
页码:291 / +
页数:18
相关论文
共 37 条
[1]  
Auchtung JM, 2016, METHODS MOL BIOL, V1476, P235, DOI 10.1007/978-1-4939-6361-4_18
[2]  
BERGOZ R, 1971, GASTROENTEROLOGY, V60, P909
[3]  
BERGOZ R, 1973, SCAND J GASTROENTERO, V8, P657
[4]   Proline-Dependent Regulation of Clostridium difficile Stickland Metabolism [J].
Bouillaut, Laurent ;
Self, William T. ;
Sonenshein, Abraham L. .
JOURNAL OF BACTERIOLOGY, 2013, 195 (04) :844-854
[5]   Humanized microbiota mice as a model of recurrent Clostridium difficile disease [J].
Collins, James ;
Auchtung, Jennifer M. ;
Schaefer, Laura ;
Eaton, Kathryn A. ;
Britton, Robert A. .
MICROBIOME, 2015, 3 :35
[6]   Rapid and Reliable DNA Assembly via Ligase Cycling Reaction [J].
de Kok, Stefan ;
Stanton, Leslie H. ;
Slaby, Todd ;
Durot, Maxime ;
Holmes, Victor F. ;
Patel, Kedar G. ;
Platt, Darren ;
Shapland, Elaine B. ;
Serber, Zach ;
Dean, Jed ;
Newman, Jack D. ;
Chandran, Sunil S. .
ACS SYNTHETIC BIOLOGY, 2014, 3 (02) :97-106
[7]   Mutagenic Analysis of the Clostridium difficile Flagellar Proteins, FliC and FliD, and Their Contribution to Virulence in Hamsters [J].
Dingle, Tanis C. ;
Mulvey, George L. ;
Armstrong, Glen D. .
INFECTION AND IMMUNITY, 2011, 79 (10) :4061-4067
[8]   Emergence and spread of predominantly community-onset Clostridium difficile PCR ribotype 244 infection in Australia, 2010 to 2012 [J].
Eyre, D. W. ;
Tracey, L. ;
Elliott, B. ;
Slimings, C. ;
Huntington, P. G. ;
Stuart, R. L. ;
Korman, T. M. ;
Kotsiou, G. ;
McCann, R. ;
Griffiths, D. ;
Fawley, W. N. ;
Armstrong, P. ;
Dingle, K. E. ;
Walker, A. S. ;
Peto, T. E. ;
Crook, D. W. ;
Wilcox, M. H. ;
Riley, T. V. .
EUROSURVEILLANCE, 2015, 20 (10)
[9]   Clostridium difficile Has Two Parallel and Essential Sec Secretion Systems [J].
Fagan, Robert P. ;
Fairweather, Neil F. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (31) :27483-27493
[10]   Emergence of Clostridium difficile infection due to a new hypervirulent strain, polymerase chain reaction ribotype 078 [J].
Goorhuis, Abraham ;
Bakker, Dennis ;
Corver, Jeroen ;
Debast, Sylvia B. ;
Harmanus, Celine ;
Notermans, Daan W. ;
Bergwerff, Aldert A. ;
Dekker, Frido W. ;
Kuijper, Ed J. .
CLINICAL INFECTIOUS DISEASES, 2008, 47 (09) :1162-1170