Gleaning Insights from Fecal Microbiota Transplantation and Probiotic Studies for the Rational Design of Combination Microbial Therapies

被引:57
作者
Hudson, Lauren E. [1 ]
Anderson, Sarah E. [2 ,3 ]
Corbett, Anita H. [4 ]
Lamb, Tracey J. [1 ]
机构
[1] Emory Univ, Sch Med, Dept Pediat Infect Dis, Atlanta, GA 30322 USA
[2] Emory Univ, Sch Med, Dept Microbiol & Immunol, Atlanta, GA 30322 USA
[3] Emory Univ, Emory Antibiot Resistance Ctr, Atlanta, GA 30322 USA
[4] Emory Univ, Dept Biol, Atlanta, GA 30322 USA
基金
美国国家卫生研究院;
关键词
Clostridium difficile; fecal microbiota transplantation; microbiota; probiotics; ulcerative colitis; CLOSTRIDIUM-DIFFICILE INFECTION; INFLAMMATORY-BOWEL-DISEASE; ANTIBIOTIC-ASSOCIATED DIARRHEA; ACTIVE ULCERATIVE-COLITIS; HUMAN DENDRITIC CELLS; SACCHAROMYCES-BOULARDII INTERFERES; LACTOBACILLUS-ACIDOPHILUS CL1285; EPITHELIAL BARRIER DISRUPTION; BIFIDOBACTERIA-FERMENTED MILK; INTRAVENOUS IMMUNE GLOBULIN;
D O I
10.1128/CMR.00049-16
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Beneficial microorganisms hold promise for the treatment of numerous gastrointestinal diseases. The transfer of whole microbiota via fecal transplantation has already been shown to ameliorate the severity of diseases such as Clostridium difficile infection, inflammatory bowel disease, and others. However, the exact mechanisms of fecal microbiota transplant efficacy and the particular strains conferring this benefit are still unclear. Rationally designed combinations of microbial preparations may enable more efficient and effective treatment approaches tailored to particular diseases. Here we use an infectious disease, C. difficile infection, and an inflammatory disorder, the inflammatory bowel disease ulcerative colitis, as examples to facilitate the discussion of how microbial therapy might be rationally designed for specific gastrointestinal diseases. Fecal microbiota transplantation has already shown some efficacy in the treatment of both these disorders; detailed comparisons of studies evaluating commensal and probiotic organisms in the context of these disparate gastrointestinal diseases may shed light on potential protective mechanisms and elucidate how future microbial therapies can be tailored to particular diseases.
引用
收藏
页码:191 / 231
页数:41
相关论文
共 385 条
[1]   FECAL ELASTASE REFLECTS DISEASE-ACTIVITY IN ACTIVE ULCERATIVE-COLITIS [J].
ADEYEMI, EO ;
HODGSON, HJF .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1992, 27 (02) :139-142
[2]   In vitro characterization of the digestive stress response and immunomodulatory properties of microorganisms isolated from smear-ripened cheese [J].
Adouard, Nadege ;
Foligne, Benoit ;
Dewulf, Joelle ;
Bouix, Marielle ;
Picque, Daniel ;
Bonnarme, Pascal .
INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 2015, 197 :98-107
[3]   Mechanism of cytokine modulation of epithelial tight junction barrier [J].
Al-Sadi, Rana ;
Boivin, Michel ;
Ma, Thomas .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2009, 14 :2765-2778
[4]   Weight Gain After Fecal Microbiota Transplantation [J].
Alang, Neha ;
Kelly, Colleen R. .
OPEN FORUM INFECTIOUS DISEASES, 2015, 2 (01)
[5]   Mucosal Barrier Depletion and Loss of Bacterial Diversity are Primary Abnormalities in Paediatric Ulcerative Colitis [J].
Alipour, Misagh ;
Zaidi, Deenaz ;
Valcheva, Rosica ;
Jovel, Juan ;
Martinez, Ines ;
Sergi, Consolato ;
Walter, Jens ;
Mason, Andrew L. ;
Wong, Gane Ka-Shu ;
Dieleman, Levinus A. ;
Carroll, Matthew W. ;
Huynh, Hien Q. ;
Wine, Eytan .
JOURNAL OF CROHNS & COLITIS, 2016, 10 (04) :462-471
[6]   Recurrent Clostridium difficile infection associates with distinct bile acid and microbiome profiles [J].
Allegretti, J. R. ;
Kearney, S. ;
Li, N. ;
Bogart, E. ;
Bullock, K. ;
Gerber, G. K. ;
Bry, L. ;
Clish, C. B. ;
Alm, E. ;
Korzenik, J. R. .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2016, 43 (11) :1142-1153
[7]   Lactobacilli and bifidobacteria in the prevention of antibiotic-associated diarrhoea and Clostridium difficile diarrhoea in older inpatients (PLACIDE): a randomised, double-blind, placebo-controlled, multicentre trial [J].
Allen, Stephen J. ;
Wareham, Kathie ;
Wang, Duolao ;
Bradley, Caroline ;
Hutchings, Hayley ;
Harris, Wyn ;
Dhar, Anjan ;
Brown, Helga ;
Foden, Alwyn ;
Gravenor, Michael B. ;
Mack, Dietrich .
LANCET, 2013, 382 (9900) :1249-1257
[8]   Banking on stool despite an uncertain future [J].
Amirtha, Tina .
SCIENCE, 2016, 352 (6291) :1261-1262
[9]   Clostridium difficile infection: epidemiology, risk factors and management [J].
Ananthakrishnan, Ashwin N. .
NATURE REVIEWS GASTROENTEROLOGY & HEPATOLOGY, 2011, 8 (01) :17-26
[10]   Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47 [J].
Anderson, Carl A. ;
Boucher, Gabrielle ;
Lees, Charlie W. ;
Franke, Andre ;
D'Amato, Mauro ;
Taylor, Kent D. ;
Lee, James C. ;
Goyette, Philippe ;
Imielinski, Marcin ;
Latiano, Anna ;
Lagace, Caroline ;
Scott, Regan ;
Amininejad, Leila ;
Bumpstead, Suzannah ;
Baidoo, Leonard ;
Baldassano, Robert N. ;
Barclay, Murray ;
Bayless, Theodore M. ;
Brand, Stephan ;
Buening, Carsten ;
Colombel, Jean-Frederic ;
Denson, Lee A. ;
De Vos, Martine ;
Dubinsky, Marla ;
Edwards, Cathryn ;
Ellinghaus, David ;
Fehrmann, Rudolf S. N. ;
Floyd, James A. B. ;
Florin, Timothy ;
Franchimont, Denis ;
Franke, Lude ;
Georges, Michel ;
Glas, Juergen ;
Glazer, Nicole L. ;
Guthery, Stephen L. ;
Haritunians, Talin ;
Hayward, Nicholas K. ;
Hugot, Jean-Pierre ;
Jobin, Gilles ;
Laukens, Debby ;
Lawrance, Ian ;
Lemann, Marc ;
Levine, Arie ;
Libioulle, Cecile ;
Louis, Edouard ;
McGovern, Dermot P. ;
Milla, Monica ;
Montgomery, Grant W. ;
Morley, Katherine I. ;
Mowat, Craig .
NATURE GENETICS, 2011, 43 (03) :246-U94