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Probiotics, prebiotics, and the host microbiome: the science of translation

  1. Probiotics, Prebiotics, and the Host Microbiome: The Science of Translation http://www.nyas.org/events/Detail.aspx?cid=c60ea8d5-44f0-4aaa-a8ff-3e5f008186f6
  2. Trueman Paul, Hurry Manjusha, Bending Matthew, Hutton John, The feasibility of harmonizing health technology assessments across jurisdictions: A case study of drug eluting stents, 10.1017/s0266462309990389
  3. Whitehead S J, Lee L, Fang Z, Sisson G, Hutton J, Logan R P H, OC-087 Can faecal calprotectin reduce the demand for colonoscopy in patients with irritable bowel syndrome?: Abstract OC-087, 10.1136/gut.2009.208991i
  4. Qin Junjie, Li Ruiqiang, Raes Jeroen, Arumugam Manimozhiyan, Burgdorf Kristoffer Solvsten, Manichanh Chaysavanh, Nielsen Trine, Pons Nicolas, Levenez Florence, Yamada Takuji, Mende Daniel R., Li Junhua, Xu Junming, Li Shaochuan, Li Dongfang, Cao Jianjun, Wang Bo, Liang Huiqing, Zheng Huisong, Xie Yinlong, Tap Julien, Lepage Patricia, Bertalan Marcelo, Batto Jean-Michel, Hansen Torben, Le Paslier Denis, Linneberg Allan, Nielsen H. Bjørn, Pelletier Eric, Renault Pierre, Sicheritz-Ponten Thomas, Turner Keith, Zhu Hongmei, Yu Chang, Li Shengting, Jian Min, Zhou Yan, Li Yingrui, Zhang Xiuqing, Li Songgang, Qin Nan, Yang Huanming, Wang Jian, Brunak Søren, Doré Joel, Guarner Francisco, Kristiansen Karsten, Pedersen Oluf, Parkhill Julian, Weissenbach Jean, Antolin Maria, Artiguenave François, Blottiere Hervé, Borruel Natalia, Bruls Thomas, Casellas Francesc, Chervaux Christian, Cultrone Antonella, Delorme Christine, Denariaz Gérard, Dervyn Rozenn, Forte Miguel, Friss Carsten, van de Guchte Maarten, Guedon Eric, Haimet Florence, Jamet Alexandre, Juste Catherine, Kaci Ghalia, Kleerebezem Michiel, Knol Jan, Kristensen Michel, Layec Severine, Le Roux Karine, Leclerc Marion, Maguin Emmanuelle, Melo Minardi Raquel, Oozeer Raish, Rescigno Maria, Sanchez Nicolas, Tims Sebastian, Torrejon Toni, Varela Encarna, de Vos Willem, Winogradsky Yohanan, Zoetendal Erwin, Bork Peer, Ehrlich S. Dusko, Wang Jun, A human gut microbial gene catalogue established by metagenomic sequencing, 10.1038/nature08821
  5. Palmer Chana, Bik Elisabeth M, DiGiulio Daniel B, Relman David A, Brown Patrick O, Development of the Human Infant Intestinal Microbiota, 10.1371/journal.pbio.0050177
  6. Dominguez-Bello M. G., Costello E. K., Contreras M., Magris M., Hidalgo G., Fierer N., Knight R., Delivery mode shapes the acquisition and structure of the initial microbiota across multiple body habitats in newborns, 10.1073/pnas.1002601107
  7. Morowitz M. J., Denef V. J., Costello E. K., Thomas B. C., Poroyko V., Relman D. A., Banfield J. F., Strain-resolved community genomic analysis of gut microbial colonization in a premature infant, 10.1073/pnas.1010992108
  8. Yatsunenko, Nature, 486, 222 (2012)
  9. Cho Ilseung, Yamanishi Shingo, Cox Laura, Methé Barbara A., Zavadil Jiri, Li Kelvin, Gao Zhan, Mahana Douglas, Raju Kartik, Teitler Isabel, Li Huilin, Alekseyenko Alexander V., Blaser Martin J., Antibiotics in early life alter the murine colonic microbiome and adiposity, 10.1038/nature11400
  10. Trasande L, Blustein J, Liu M, Corwin E, Cox L M, Blaser M J, Infant antibiotic exposures and early-life body mass, 10.1038/ijo.2012.132
  11. Cani P. D., Amar J., Iglesias M. A., Poggi M., Knauf C., Bastelica D., Neyrinck A. M., Fava F., Tuohy K. M., Chabo C., Waget A., Delmee E., Cousin B., Sulpice T., Chamontin B., Ferrieres J., Tanti J.-F., Gibson G. R., Casteilla L., Delzenne N. M., Alessi M. C., Burcelin R., Metabolic Endotoxemia Initiates Obesity and Insulin Resistance, 10.2337/db06-1491
  12. Cani P. D., Bibiloni R., Knauf C., Waget A., Neyrinck A. M., Delzenne N. M., Burcelin R., Changes in Gut Microbiota Control Metabolic Endotoxemia-Induced Inflammation in High-Fat Diet-Induced Obesity and Diabetes in Mice, 10.2337/db07-1403
  13. Rabot S., Membrez M., Bruneau A., Gerard P., Harach T., Moser M., Raymond F., Mansourian R., Chou C. J., Germ-free C57BL/6J mice are resistant to high-fat-diet-induced insulin resistance and have altered cholesterol metabolism, 10.1096/fj.10-164921
  14. Bäckhed Fredrik, Manchester Jill K., Semenkovich Clay F., Gordon Jeffrey I., Mechanisms underlying the resistance to diet-induced obesity in germ-free mice, 10.1073/pnas.0605374104
  15. Turnbaugh Peter J., Bäckhed Fredrik, Fulton Lucinda, Gordon Jeffrey I., Diet-Induced Obesity Is Linked to Marked but Reversible Alterations in the Mouse Distal Gut Microbiome, 10.1016/j.chom.2008.02.015
  16. Carvalho B. M., Guadagnini D., Tsukumo D. M. L., Schenka A. A., Latuf-Filho P., Vassallo J., Dias J. C., Kubota L. T., Carvalheira J. B. C., Saad M. J. A., Modulation of gut microbiota by antibiotics improves insulin signalling in high-fat fed mice, 10.1007/s00125-012-2648-4
  17. Daubioul, J. Nutr., 132, 967 (2002)
  18. Muccioli Giulio G, Naslain Damien, Bäckhed Fredrik, Reigstad Christopher S, Lambert Didier M, Delzenne Nathalie M, Cani Patrice D, The endocannabinoid system links gut microbiota to adipogenesis, 10.1038/msb.2010.46
  19. Cani P. D., Possemiers S., Van de Wiele T., Guiot Y., Everard A., Rottier O., Geurts L., Naslain D., Neyrinck A., Lambert D. M., Muccioli G. G., Delzenne N. M., Changes in gut microbiota control inflammation in obese mice through a mechanism involving GLP-2-driven improvement of gut permeability, 10.1136/gut.2008.165886
  20. Everard A., Belzer C., Geurts L., Ouwerkerk J. P., Druart C., Bindels L. B., Guiot Y., Derrien M., Muccioli G. G., Delzenne N. M., de Vos W. M., Cani P. D., Cross-talk between Akkermansia muciniphila and intestinal epithelium controls diet-induced obesity, 10.1073/pnas.1219451110
  21. van Nood Els, Vrieze Anne, Nieuwdorp Max, Fuentes Susana, Zoetendal Erwin G., de Vos Willem M., Visser Caroline E., Kuijper Ed J., Bartelsman Joep F.W.M., Tijssen Jan G.P., Speelman Peter, Dijkgraaf Marcel G.W., Keller Josbert J., Duodenal Infusion of Donor Feces for Recurrent Clostridium difficile, 10.1056/nejmoa1205037
  22. Vrieze Anne, Van Nood Els, Holleman Frits, Salojärvi Jarkko, Kootte Ruud S., Bartelsman Joep F.W.M., Dallinga–Thie Geesje M., Ackermans Mariette T., Serlie Mireille J., Oozeer Raish, Derrien Muriel, Druesne Anne, Van Hylckama Vlieg Johan E.T., Bloks Vincent W., Groen Albert K., Heilig Hans G.H.J., Zoetendal Erwin G., Stroes Erik S., de Vos Willem M., Hoekstra Joost B.L., Nieuwdorp Max, Transfer of Intestinal Microbiota From Lean Donors Increases Insulin Sensitivity in Individuals With Metabolic Syndrome, 10.1053/j.gastro.2012.06.031
  23. Karlsson Fredrik H., Tremaroli Valentina, Nookaew Intawat, Bergström Göran, Behre Carl Johan, Fagerberg Björn, Nielsen Jens, Bäckhed Fredrik, Gut metagenome in European women with normal, impaired and diabetic glucose control, 10.1038/nature12198
  24. de Vos Willem M., Nieuwdorp Max, Genomics: A gut prediction, 10.1038/nature12251
  25. Early Years Collaborative, The Scottish Government http://www.scotland.gov.uk/Topics/People/Young-People/Early-Years-and-Family/early-years-collaborative
  26. Deshpande Girish, Rao Shripad, Patole Sanjay, Progress in the field of probiotics: year 2011 : , 10.1097/mog.0b013e328341373e
  27. Bernardo Wanderley Marques, Aires Felipe Toyama, Carneiro Renata Mota, Sá Fernando Pereira de, Rullo Vera Esteves Vagnozzi, Burns Dennis Alexander, Effectiveness of Probiotics in the Prophylaxis of Necrotizing Enterocolitis in Preterm Neonates: A Systematic Review and Meta-analysis, 10.1016/j.jped.2013.02.004
  28. Goldenberg, Cochrane Database Syst. Rev., 5, CD006095 (2013)
  29. Macklaim Jean M., Cohen Craig R., Donders Gilbert, Gloor Gregory B., Hill Janet E., Parham Groesbeck P., Ravel Jacques, Spear Gregory, van de Wijgert Janneke, Reid Gregor, Exploring a Road Map to Counter Misconceptions About the Cervicovaginal Microbiome and Disease, 10.1177/1933719112446075
  30. Hao, Cochrane Database Syst. Rev., CD006895 (2011)
  31. Isolauri Erika, Rautava Samuli, Salminen Seppo, Probiotics in the Development and Treatment of Allergic Disease, 10.1016/j.gtc.2012.08.007
  32. Gut Microbiota for Health http://www.gutmicrobiota forhealth.com/
  33. Sudo Nobuyuki, Chida Yoichi, Aiba Yuji, Sonoda Junko, Oyama Naomi, Yu Xiao-Nian, Kubo Chiharu, Koga Yasuhiro, Postnatal microbial colonization programs the hypothalamic-pituitary-adrenal system for stress response in mice : Commensal microbiota and stress response, 10.1113/jphysiol.2004.063388
  34. Neufeld K. M., Kang N., Bienenstock J., Foster J. A., Reduced anxiety-like behavior and central neurochemical change in germ-free mice : Behavior in germ-free mice, 10.1111/j.1365-2982.2010.01620.x
  35. Neufeld Karen-Anne M., Kang Nancy, Bienenstock John, Foster Jane A., Effects of intestinal microbiota on anxiety-like behavior, 10.4161/cib.15702
  36. Tazoe, J. Physiol. Pharmacol., 59, 251 (2008)
  37. de La Serre C. B., Ellis C. L., Lee J., Hartman A. L., Rutledge J. C., Raybould H. E., Propensity to high-fat diet-induced obesity in rats is associated with changes in the gut microbiota and gut inflammation, 10.1152/ajpgi.00098.2010
  38. Lee S., Belitsky B. R., Brinker J. P., Kerstein K. O., Brown D. W., Clements J. D., Keusch G. T., Tzipori S., Sonenshein A. L., Herrmann J. E., Development of a Bacillus subtilis-Based Rotavirus Vaccine, 10.1128/cvi.00135-10
  39. Lee Sangun, Belitsky Boris R., Brown David W., Brinker James P., Kerstein Kathryn O., Herrmann John E., Keusch Gerald T., Sonenshein Abraham L., Tzipori Saul, Efficacy, heat stability and safety of intranasally administered Bacillus subtilis spore or vegetative cell vaccines expressing tetanus toxin fragment C, 10.1016/j.vaccine.2010.08.016
  40. Sokol H., Seksik P., Furet J. P., Firmesse O., Nion-Larmurier I., Beaugerie L., Cosnes J., Corthier G., Marteau P., Doré J., Low counts of Faecalibacterium prausnitzii in colitis microbiota : , 10.1002/ibd.20903
  41. Sokol H., Pigneur B., Watterlot L., Lakhdari O., Bermudez-Humaran L. G., Gratadoux J.-J., Blugeon S., Bridonneau C., Furet J.-P., Corthier G., Grangette C., Vasquez N., Pochart P., Trugnan G., Thomas G., Blottiere H. M., Dore J., Marteau P., Seksik P., Langella P., Faecalibacterium prausnitzii is an anti-inflammatory commensal bacterium identified by gut microbiota analysis of Crohn disease patients, 10.1073/pnas.0804812105
  42. Kalliomaki, Am. J. Clin. Nutr., 87, 534 (2008)
  43. Furet J.-P., Kong L.-C., Tap J., Poitou C., Basdevant A., Bouillot J.-L., Mariat D., Corthier G., Dore J., Henegar C., Rizkalla S., Clement K., Differential Adaptation of Human Gut Microbiota to Bariatric Surgery-Induced Weight Loss: Links With Metabolic and Low-Grade Inflammation Markers, 10.2337/db10-0253
  44. Rajilić–Stojanović Mirjana, Biagi Elena, Heilig Hans G.H.J., Kajander Kajsa, Kekkonen Riina A., Tims Sebastian, de Vos Willem M., Global and Deep Molecular Analysis of Microbiota Signatures in Fecal Samples From Patients With Irritable Bowel Syndrome, 10.1053/j.gastro.2011.07.043
  45. Guidance for Industry: Investigational New Drug Applications (INDs) http://www.fda.gov/downloads/Drugs/Guidances/UCM229175.pdf
  46. Guidance for Industry: Early Clinical Trials with Live Biotherapeutic Products http://www.fda.gov/downloads/BiologicsBloodVaccines/GuidanceComplianceRegulatory-Information/Guidances/General/UCM292704.pdf
  47. Backhed F., Host-Bacterial Mutualism in the Human Intestine, 10.1126/science.1104816
  48. Cebra, Am. J. Clin. Nutr., 69, 1046S (1999)
  49. Schippa Serena, Iebba Valerio, Santangelo Floriana, Gagliardi Antonella, De Biase Riccardo Valerio, Stamato Antonella, Bertasi Serenella, Lucarelli Marco, Conte Maria Pia, Quattrucci Serena, Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Allelic Variants Relate to Shifts in Faecal Microbiota of Cystic Fibrosis Patients, 10.1371/journal.pone.0061176
  50. Reid Gregor, Younes Jessica A., Van der Mei Henny C., Gloor Gregory B., Knight Rob, Busscher Henk J., Microbiota restoration: natural and supplemented recovery of human microbial communities, 10.1038/nrmicro2473
  51. Bravo Javier A, Julio-Pieper Marcela, Forsythe Paul, Kunze Wolfgang, Dinan Timothy G, Bienenstock John, Cryan John F, Communication between gastrointestinal bacteria and the nervous system, 10.1016/j.coph.2012.09.010
  52. Hooper Lora V., Midtvedt Tore, Gordon Jeffrey I., HOWHOST-MICROBIALINTERACTIONSSHAPE THENUTRIENTENVIRONMENT OF THEMAMMALIANINTESTINE, 10.1146/annurev.nutr.22.011602.092259
  53. Velagapudi Vidya R., Hezaveh Rahil, Reigstad Christopher S., Gopalacharyulu Peddinti, Yetukuri Laxman, Islam Sama, Felin Jenny, Perkins Rosie, Borén Jan, Orešič Matej, Bäckhed Fredrik, The gut microbiota modulates host energy and lipid metabolism in mice, 10.1194/jlr.m002774
  54. Koenig J. E., Spor A., Scalfone N., Fricker A. D., Stombaugh J., Knight R., Angenent L. T., Ley R. E., Succession of microbial consortia in the developing infant gut microbiome, 10.1073/pnas.1000081107
  55. Hicks Lauri A., Taylor Thomas H., Hunkler Robert J., U.S. Outpatient Antibiotic Prescribing, 2010, 10.1056/nejmc1212055
  56. Delzenne Nathalie M., Neyrinck Audrey M., Bäckhed Fredrik, Cani Patrice D., Targeting gut microbiota in obesity: effects of prebiotics and probiotics, 10.1038/nrendo.2011.126
  57. Cryan John F., Dinan Timothy G., Mind-altering microorganisms: the impact of the gut microbiota on brain and behaviour, 10.1038/nrn3346
Bibliographic reference Petschow, Bryon ; Doré, Joël ; Hibberd, Patricia ; Dinan, Timothy ; Reid, Gregor ; et. al. Probiotics, prebiotics, and the host microbiome: the science of translation. In: Annals / New York Academy of Sciences, Vol. 1306, no.Annals Reports, p. 1-17 (2013)
Permanent URL http://hdl.handle.net/2078.1/146421