Environmental factors influencing the efficacy of probiotic bacteria

Current Opinion in Biotechnology

Volumn 24, Issue 2, 2013, Pages 207-213

  Marco, Maria L ^a   Tachon, Sybille ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CELL ACTIVITY; CLINICAL STUDY; DIGESTIVE TRACT; ENVIRONMENTAL FACTORS; LIVING CELL; MOLECULAR MECHANISM; PROBIOTIC BACTERIA; STANDARDIZED PROCEDURE;

CONSUMER PRODUCTS; DIGESTIVE SYSTEM;

BACTERIA;

IMMUNOGLOBULIN ENHANCER BINDING PROTEIN; INTERLEUKIN 10; INTERLEUKIN 12; POLYPHOSPHATE; PROBIOTIC AGENT;

AGE; BACTERIAL GROWTH; BACTERIAL SURVIVAL; BACTERIAL VIABILITY; BIFIDOBACTERIUM BIFIDUM; BIFIDOBACTERIUM LONGUM INFANTIS; CELL COMPOSITION; COLITIS; COLON; DAIRY PRODUCT; DIET; DRUG DELIVERY SYSTEM; DRUG EFFICACY; DRUG FORMULATION; DUODENUM; ENVIRONMENTAL FACTOR; ETHNICITY; FECES MICROFLORA; GENETICS; HEALTH STATUS; HOST PATHOGEN INTERACTION; HUMAN; ILEUM; IMMUNOMODULATION; INTESTINE FLORA; LACTOBACILLUS ACIDOPHILUS; LACTOBACILLUS BREVIS; LACTOBACILLUS CASEI; LACTOBACILLUS JOHNSONII; LACTOBACILLUS PLANTARUM; LACTOBACILLUS REUTERI; LACTOBACILLUS RHAMNOSUS; MICROBIOME; MOLECULAR MECHANICS; NONHUMAN; NUTRITION; PRESERVATION; PRIORITY JOURNAL; REVIEW; TEMPERATURE;

BACTERIA; CLINICAL TRIALS AS TOPIC; DIET; GASTROINTESTINAL TRACT; HUMANS; METAGENOME; PROBIOTICS; SYMBIOSIS;

EID: 84874975956     PISSN: 09581669     EISSN: 18790429     Source Type: Journal    
DOI: 10.1016/j.copbio.2012.10.002     Document Type: Review

References (51)

1. Floch M.H., Walker W.A., Madsen K., Sanders M.E., Macfarlane G.T., Flint H.J., Dieleman L.A., Ringel Y., Guandalini S., Kelly C.P., et al. Recommendations for probiotic use-2011 update. J Clin Gastroenterol 2011, 45(Suppl):S168-S171.
2. Sanders M.E., Marco M.L. Food formats for effective delivery of probiotics. Annu Rev Food Sci Technol 2010, 1:65-85.
3. Ritchie M.L., Romanuk T.N. A meta-analysis of probiotic efficacy for gastrointestinal diseases. PLoS ONE 2012, 7:e34938.
4. Rauch M., Lynch S.V. The potential for probiotic manipulation of the gastrointestinal microbiome. Cur Opin Biotechnol 2012, 23:192-201.
5. Rijkers G.T., de Vos W.M., Brummer R.J., Morelli L., Corthier G., Marteau P. Health benefits and health claims of probiotics: bridging science and marketing. Br J Nutr 2011, 106:1291-1296.
6. Bravo J.A., Forsythe P., Chew M.V., Escaravage E., Savignac H.M., Dinan T.G., Bienenstock J., Cryan J.F. Ingestion of Lactobacillus strain regulates emotional behavior and central GABA receptor expression in a mouse via the vagus nerve. Proc Natl Acad Sci USA 2011, 108:16050-16055.
7. Chen J., Wang R., Li X.F., Wang R.L. Bifidobacterium adolescentis supplementation ameliorates visceral fat accumulation and insulin sensitivity in an experimental model of the metabolic syndrome. Br J Nutr 2012, 107:1429-1434.
8. Lemon K.P., Armitage G.C., Relman D.A., Fischbach M.A. Microbiota-targeted therapies: an ecological perspective. Sci Transl Med 2012, 4:137rv135.
9. Bron P.A., van Baarlen P., Kleerebezem M. Emerging molecular insights into the interaction between probiotics and the host intestinal mucosa. Nature Rev Microbiol 2012, 10:66-78.
10. Lebeer S., Vanderleyden J., De Keersmaecker S.C. Host interactions of probiotic bacterial surface molecules: comparison with commensals and pathogens. Nat Rev Microbiol 2010, 8:171-184.
11. Fanning S., Hall L.J., Cronin M., Zomer A., MacSharry J., Goulding D., Motherway M.O., Shanahan F., Nally K., Dougan G., et al. Bifidobacterial surface-exopolysaccharide facilitates commensal-host interaction through immune modulation and pathogen protection. Proc Natl Acad Sci USA 2012, 109:2108-2113.
12. Li P., Yu Q., Ye X., Wang Z., Yang Q. Lactobacillus S-layer protein inhibition of Salmonella-induced reorganization of the cytoskeleton and activation of MAPK signalling pathways in Caco-2 cells. Microbiology 2011, 157:2639-2646.
13. Mohamadzadeh M., Pfeiler E.A., Brown J.B., Zadeh M., Gramarossa M., Managlia E., Bere P., Sarraj B., Khan M.W., Pakanati K.C., et al. Regulation of induced colonic inflammation by Lactobacillus acidophilus deficient in lipoteichoic acid. Proc Natl Acad Sci USA 2011, 108(Suppl 1):4623-4630.
14. Meijerink M., van Hemert S., Taverne N., Wels M., de Vos P., Bron P.A., Savelkoul H.F., van Bilsen J., Kleerebezem M., Wells J.M. Identification of genetic loci in Lactobacillus plantarum that modulate the immune response of dendritic cells using comparative genome hybridization. PLoS ONE 2010, 5:e10632.
15. van Hemert S., Meijerink M., Molenaar D., Bron P.A., de Vos P., Kleerebezem M., Wells J.M., Marco M.L. Identification of Lactobacillus plantarum genes modulating the cytokine response of human peripheral blood mononuclear cells. BMC Microbiol 2010, 10:293.
16. Fukuda S., Toh H., Hase K., Oshima K., Nakanishi Y., Yoshimura K., Tobe T., Clarke J.M., Topping D.L., Suzuki T., et al. Bifidobacteria can protect from enteropathogenic infection through production of acetate. Nature 2011, 469:543-547.
17. O'Shea E.F., Cotter P.D., Stanton C., Ross R.P., Hill C. Production of bioactive substances by intestinal bacteria as a basis for explaining probiotic mechanisms: bacteriocins and conjugated linoleic acid. Int J Food Microbiol 2012, 152:189-205.
18. Zhong Y., Huang J., Tang W., Chen B., Cai W. Effects of probiotics, probiotic DNA and the CpG oligodeoxynucleotides on ovalbumin-sensitized Brown-Norway rats via TLR9/NF-κB pathway. FEMS Immunol Med Microbiol 2012, 66:71-82.
19. Lebeer S., Claes I., Tytgat H.L.P., Verhoeven T.L.A., Marien E., von Ossowski I., Reunanen J., Palva A., de Vos W.M., De Keersmaecker S.C.J., et al. Functional analysis of Lactobacillus rhamnosus GG pili in relation to adhesion and immunomodulatory interactions with intestinal epithelial cells. Appl Environ Microbiol 2012, 78:185-193.
20. Kankainen M., Paulin L., Tynkkynen S., von Ossowski I., Reunanen J., Partanen P., Satokari R., Vesterlund S., Hendrickx A.P.A., Lebeer S., et al. Comparative genomic analysis of Lactobacillus rhamnosus GG reveals pili containing a human-mucus binding protein. Proc Natl Acad Sci USA 2009, 106:17193-17198.
21. Motherway M.O., Zomer A., Leahy S.C., Reunanen J., Bottacini F., Claesson M.J., O'Brien F., Flynn K., Casey P.G., Munoz J.A.M., et al. Functional genome analysis of Bifidobacterium breve UCC2003 reveals type IVb tight adherence (Tad) pili as an essential and conserved host-colonization factor. Proc Natl Acad Sci USA 2011, 108:11217-11222.
22. Bernardo D., Sánchez B., Al-Hassi H.O., Mann E.R., Urdaci M.C., Knight S.C., Margolles A. Microbiota/host crosstalk biomarkers: regulatory response of human intestinal dendritic cells exposed to Lactobacillus extracellular encrypted peptide. PLoS ONE 2012, 7:e36262.
23. Yan F., Cao H., Cover T.L., Washington M.K., Shi Y., Liu L., Chaturvedi R., Peek R.M., Wilson K.T., Polk D.B. Colon-specific delivery of a probiotic-derived soluble protein ameliorates intestinal inflammation in mice through an EGFR-dependent mechanism. J Clin Invest 2011, 121:2242-2253.
24. von Schillde M.A., Hormannsperger G., Weiher M., Alpert C.A., Hahne H., Bauerl C., van Huynegem K., Steidler L., Hrncir T., Perez-Martinez G., et al. Lactocepin secreted by Lactobacillus exerts anti-inflammatory effects by selectively degrading proinflammatory chemokines. Cell Host Microbe 2012, 11:387-396.
25. Mills S., Stanton C., Fitzgerald G.F., Ross R.P. Enhancing the stress responses of probiotics for a lifestyle from gut to product and back again. Microb Cell Fact 2011, 10(Suppl 1):S19.
26. Bron P.A., Wels M., Bongers R.S., van Bokhorst-van de Veen H., Wiersma A., Overmars L., Marco M.L., Kleerebezem M. Transcriptomes reveal genetic signatures underlying physiological variations imposed by different fermentation conditions in Lactobacillus plantarum. PLoS ONE 2012, 7:e38720.
27. van Bokhorst-van de Veen H., Lee I.C., Marco M.L., Wels M., Bron P.A., Kleerebezem M. Modulation of Lactobacillus plantarum gastrointestinal robustness by fermentation conditions enables identification of bacterial robustness markers. PLoS ONE 2012, 7:e39053.
28. Kuwana R., Yamamoto N. Increases in GroES and GroEL from Lactobacillus acidophilus L-92 in response to a decrease in medium pH, and changes in cytokine release from splenocytes: transcriptome and proteome analyses. J Biosci Bioeng 2012, 114:9-16.
29. Chichlowski M., De Lartigue G., German J.B., Raybould H.E., Mills D.A. Bifidobacteria isolated from infants and cultured on human milk oligosaccharides affect intestinal epithelial function. J Pediatr Gastroenterol Nutr 2012, 55:321-327.
30. Muller J.A., Ross R.P., Sybesma W.F.H., Fitzgerald G.F., Stanton C. Modification of the technical properties of Lactobacillus johnsonii NCC 533 by supplementing the growth medium with unsaturated fatty acids. Appl Environ Microbiol 2011, 77:6889-6898.
31. De Weirdt R., Crabbe A., Roos S., Vollenweider S., Lacroix C., van Pijkeren J.P., Britton R.A., Sarker S., Van de Wiele T., Nickerson C.A. Glycerol supplementation enhances L. reuteri's protective effect against S. Typhimurium colonization in a 3-D model of colonic epithelium. PLoS ONE 2012, 7:e37116.
32. Goh Y.J., Klaenhammer T.R. Functional roles of aggregation-promoting-like factor in stress tolerance and adherence of Lactobacillus acidophilus NCFM. Appl Environ Microbiol 2010, 76:5005-5012.
33. van Baarlen P., Troost F.J., van Hemert S., van der Meer C., de Vos W.M., de Groot P.J., Hooiveld G.J., Brummer R.J., Kleerebezem M. Differential NF-kappaB pathways induction by Lactobacillus plantarum in the duodenum of healthy humans correlating with immune tolerance. Proc Natl Acad Sci USA 2009, 106:2371-2376.
34. Segawa S., Fujiya M., Konishi H., Ueno N., Kobayashi N., Shigyo T., Kohgo Y. Probiotic-derived polyphosphate enhances the epithelial barrier function and maintains intestinal homeostasis through integrin-p38 MAPK pathway. PLoS ONE 2011, 6:e23278.
35. Wang J., Zhong Z., Zhang W., Bao Q., Wei A., Meng H., Zhang H. Comparative analysis of the gene expression profile of probiotic Lactobacillus casei Zhang with and without fermented milk as a vehicle during transit in a simulated gastrointestinal tract. Res Microbiol 2012, 163:357-365.
36. Hernandez-Hernandez O., Muthaiyan A., Moreno F.J., Montilla A., Sanz M.L., Ricke S.C. Effect of prebiotic carbohydrates on the growth and tolerance of Lactobacillus. Food Microbiol 2012, 30:355-361.
37. Saxelin M., Lassig A., Karjalainen H., Tynkkynen S., Surakka A., Vapaatalo H., Jarvenpaa S., Korpela R., Mutanen M., Hatakka K. Persistence of probiotic strains in the gastrointestinal tract when administered as capsules, yoghurt, or cheese. Int J Food Microbiol 2010, 144:293-300.
38. Deepika G., Rastall R.A., Charalampopoulos D. Effect of food models and low-temperature storage on the adhesion of Lactobacillus rhamnosus GG to Caco-2 cells. J Agric Food Chem 2011, 59:8661-8666.
39. Wu G.D., Chen J., Hoffmann C., Bittinger K., Chen Y.Y., Keilbaugh S.A., Bewtra M., Knights D., Walters W.A., Knight R., et al. Linking long-term dietary patterns with gut microbial enterotypes. Science 2011, 334:105-108.
40. Marco M.L., Peters T.H., Bongers R.S., Molenaar D., van Hemert S., Sonnenburg J.L., Gordon J.I., Kleerebezem M. Lifestyle of Lactobacillus plantarum in the mouse caecum. Environ Microbiol 2009, 11:2747-2757.
41. Marco M.L., de Vries M.C., Wels M., Molenaar D., Mangell P., Ahrne S., de Vos W.M., Vaughan E.E., Kleerebezem M. Convergence in probiotic Lactobacillus gut-adaptive responses in humans and mice. ISME J 2010, 4:1481-1484.
42. Thomas M., Wrzosek L., Ben-Yahia L., Noordine M.L., Gitton C., Chevret D., Langella P., Mayeur C., Cherbuy C., Rul F. Carbohydrate metabolism is essential for the colonization of Streptococcus thermophilus in the digestive tract of gnotobiotic rats. PLoS ONE 2011, 6:e28789.
43. Thomas C.M., Hong T., van Pijkeren J.P., Hemarajata P., Trinh D.V., Hu W., Britton R.A., Kalkum M., Versalovic J. Histamine derived from probiotic Lactobacillus reuteri suppresses TNF via modulation of PKA and ERK signaling. PLoS ONE 2012, 7:e31951.
44. Reid G., Gaudier E., Guarner F., Huffnagle G.B., Macklaim J.M., Munoz A.M., Martini M., Ringel-Kulka T., Sartor B., Unal R., et al. Responders and non-responders to probiotic interventions: how can we improve the odds?. Gut Microbes 2010, 1:200-204.
45. The Human Microbiome Project Consortium Structure, function and diversity of the healthy human microbiome. Nature 2012, 486:207-214.
46. Buhnik-Rosenblau K., Danin-Poleg Y., Kashi Y. Predominant effect of host genetics on levels of Lactobacillus johnsonii bacteria in the mouse gut. Appl Environ Microbiol 2011, 77:6531-6538.
47. Yatsunenko T., Rey F.E., Manary M.J., Trehan I., Dominguez-Bello M.G., Contreras M., Magris M., Hidalgo G., Baldassano R.N., Anokhin A.P., et al. Human gut microbiome viewed across age and geography. Nature 2012, 486:222-227.
48. Sanders M.E. Impact of probiotics on colonizing microbiota of the gut. J Clin Gastroenterol 2011, 45(Suppl):S115-S119.
49. Veiga P., Gallini C.A., Beal C., Michaud M., Delaney M.L., DuBois A., Khlebnikov A., van Hylckama Vlieg J.E., Punit S., Glickman J.N., et al. Bifidobacterium animalis subsp. lactis fermented milk product reduces inflammation by altering a niche for colitogenic microbes. Proc Natl Acad Sci USA 2010, 107:18132-18137.
50. McNulty N.P., Yatsunenko T., Hsiao A., Faith J.J., Muegge B.D., Goodman A.L., Henrissat B., Oozeer R., Cools-Portier S., Gobert G., et al. The impact of a consortium of fermented milk strains on the gut microbiome of gnotobiotic mice and monozygotic twins. Sci Transl Med 2011, 3:106ra106.
51. Holmes E., Kinross J., Gibson G.R., Burcelin R., Jia W., Pettersson S., Nicholson J.K. Therapeutic modulation of microbiota-host metabolic interactions. Sci Transl Med 2012, 4:137rv6.