Skip to main content

The Probiotic Message

  • Chapter
  • First Online:
  • 1319 Accesses

Part of the book series: SpringerBriefs in Food, Health, and Nutrition ((BRIEFSFOOD))

Abstract

This chapter focuses on the most relevant evidence relating to the bacterial quorum-sensing mechanisms that occur at gastrointestinal level between probiotic bacteria or intestinal inhabitants, and between probiotics and host. Some insights into the language-like exchange at interkingdom level are also given.

This is a preview of subscription content, log in via an institution.

Buying options

Chapter
USD   29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD   39.99
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD   54.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Learn about institutional subscriptions

References

  1. FAO/WHO (2001) Evaluation of health and nutritional properties of powder milk and live lactic acid bacteria. Food and Agriculture Organization of the United Nations and World Health Organization expert consultation report, FAO, Rome

    Google Scholar 

  2. Boirivant M, Strober W (2007) The mechanism of action of probiotics. Curr Opin Gastroenterol 23:679–692

    Article  Google Scholar 

  3. Fedorak RN, Madsen JL (2004) Probiotics and the management of inflammatory bowel disease. Inflamm Bowel Dis 10:286–299

    Article  Google Scholar 

  4. Marco ML, Pavan S, Kleerebezem M (2006) Towards understanding molecular modes of probiotic action. Curr Opin Biotechnol 17:204–210

    Article  CAS  Google Scholar 

  5. Diggle SP, Matthijs S, Wright VJ, Fletcher MP, Chabra SR, Lamont IL, Kong X, Hider RC, Cornelis P, Cámara M, Williams P (2007) The Pseudomonas aeruginosa 4-quinolone signal molecules HHQ and PQS play multifunctional roles in quorum sensing and iron entrapment. Chem Biol 14:87–96

    Article  CAS  Google Scholar 

  6. Van Pijkeren JP, Canchaya C, Ryan KA, Li Y, Claesson MJ, Sheil B, Steidler L, O’Mahony L, Fitzgerald GF, van Sinderen D, O’Toole PW (2006) Comparative and functional analysis of sortase-dependent proteins in the predicted secretome of Lactobacillus salivarius UCC118. Appl Environ Microbiol 72:4143–4153

    Article  Google Scholar 

  7. Lebeer S, Vanderleyden J, De Keersmaecker SCJ (2008) Genes and molecules of lactobacilli supporting probiotic action. Microbiol Mol Biol Rev 72:728–764

    Article  CAS  Google Scholar 

  8. De Keersmaecker SCJ, Vanderleyden J (2003) Constraints on detection of autoinducer-2 (AI-2) signalling molecules using Vibrio harvey as a reporter. Microbiology 149:1953–1956

    Article  Google Scholar 

  9. Higgins DA, Pomianek ME, Kraml CM, Taylor RK, Semmelhack MF, Bassler BL (2007) The major Vibrio cholarae autoinducer and its role in virulence factor production. Nature 450:883–886

    Article  CAS  Google Scholar 

  10. Tannock GW, Ghazally S, Walter J, Loach D, Brooks H, Cook G, Surette M, Simmers C, Bremer P, Dal Bello F, Hertel C (2005) Ecological behaviour of Lactobacillus reuteri 100–23 is affected by mutation of the luxS gene. Appl Environ Microbiol 71:8419–8425

    Article  CAS  Google Scholar 

  11. Wilson CM, Aggio RBM, O’Toole PW, Villas-Boas S, Tannock GW (2012) Transcriptional and metabolomic consequences of luxS inactivation reveal a metabolic rather than quorum sensing role for LuxS in Lactobacillus reuteri 100–23. J Bacteriol 194:1743–1746

    Article  Google Scholar 

  12. Laughton JM, Devillard E, Heinrichs DE, Reid G, McCormick JK (2006) Inhibition of expression of a staphylococcal superantigen-like protein by a soluble factor from Lactobacillus reuteri. Microbiology 152:1155–1167

    Article  CAS  Google Scholar 

  13. Lebeer S, Claes IJJ, Verhoeven TLA, Shen C, Lambrichts I, Ceuppens JL, Vanderleyden J, De Keersmaecker SCJ (2008) Impact of luxS and suppressor mutations on the gastrointestinal transit of Lactobacillus rhamnosus GG. Appl Environ Microbiol 74:4711–4718

    Article  CAS  Google Scholar 

  14. Lebeer S, De Keersmaecker SCJ, Verhoeven TLA, Fadda AA, Marchal K, Vanderleyden J (2007) Functional analysis of luxS in the probiotic strain Lactobacillus rhamnosus GG reveals a central metabolic role important for growth and biofilm formation. J Bacteriol 189:860–871

    Article  CAS  Google Scholar 

  15. Leahy SC, Higgins DG, Fitzgerald GF, van Sinderen D (2005) Getting better with bifidobacteria. J Appl Microbiol 98:1303–1315

    Article  CAS  Google Scholar 

  16. Yuan J, Wang B, Sun Z, Bo X, Yuan X, He X, Zhao H, Du X, Wang F, Jiang Z, Zhang L, Jia L, Wang Y, Wei KH, Wang J, Zhang X, Sun Y, Huang L, Zeng M (2008) Analysis of host-inducing proteome changes in Bifidobacterium longum NCC2705 grown in vivo. J Prot Res 7:375–385

    Article  CAS  Google Scholar 

  17. Ruiz L, Sánchez B, de los Reyes-Gávilan CG, Gueimond M, Margolles A (2009) Coculture of Bifidobacterium longum and Bifidobacterium breve alters their protein expression profiles and anzymatic activities. Int J Food Microbiol 133:148–153

    Article  CAS  Google Scholar 

  18. Gueimonde M, Noriega L, Margolles A, de los Reyes-Gavilán CG (2007) Induction of alpha-L-arabinofuranosidase activity by monomeric carbohydrates in Bifidobacterium longum and ubiquity of encoding genes. Arch Microbiol 187:145–153

    Article  CAS  Google Scholar 

  19. Chen H, Teplitski M, Robinson JB, Rolfe BG, Bauer WD (2003) Proteomic analysis of wild-type Sinorhizobium meliloti responses to N-acyl homoserine lactone quorum sensing signal and the transition to stationary phase. J Bacteriol 185:5029–5036

    Article  CAS  Google Scholar 

  20. De Dea Lindner J, Canchaya C, Zhang Z, Neviani E, Fitzgerald GF, van Sinderen D, Ventura M (2007) Exploting Bifidobacterium genomes: the molecular basis of stress response. Int J Food Microbiol 120:13–24

    Article  Google Scholar 

  21. Ventura M, Fitzgerald GF, van Sinderen D (2005) Genetic and transcriptional organization of the clpC locus in Bifidobacterium breve UCC 2003. Appl Environ Microbiol 71:6282–6291

    Article  CAS  Google Scholar 

  22. Mohammadi T, Karczmarek A, Crouvoisier M, Bouhss A, Mengin-Lecreulx D, den Blaauwen T (2007) The essential peptidoglycan glycosyltransferase MurG forms a complex with proteins involved in lateral envelop growth as well as with proteins involved in cell division in Escherichia coli. Mol Microbiol 65:1106–1121

    Article  CAS  Google Scholar 

  23. Sánchez B, Champomier-Vergès MC, Anglede P, Baraige F, de los Reyes-Gavilàn CG, Margolles A, Zagorec M (2008) A preliminary analysis of Bifidobacterium longum exported proteins by two-dimensional electrophoresis. J Mol Microbiol Biotechnol 14:74–79

    Article  Google Scholar 

  24. Tabasco R, Paarup T, Janer C, Pelaez C, Requena T (2007) Selective enumeration and identification of mixed cultures of Streptococcus thermophilus, Lactobacillus delbrueckii subsp. bulgaricus, L. acidophilus, L. paracasei subsp. paracasei and Bifidobacterium lactis in fermented milk. Int Dairy J 17:1107–1114

    Article  CAS  Google Scholar 

  25. Hooper LV, Gordon JI (2001) Commensal host–bacterial relationships in the gut. Science 292:1115–1118

    Article  CAS  Google Scholar 

  26. Hughes DT, Sperandio V (2008) Inter-kingdom signalling: communication between bacteria and their hosts. Nat Rev Microbiol 6:111–120

    Article  CAS  Google Scholar 

  27. Freestone PP, Haigh RD, Williams PH, Lyte M (2003) Involvement of enterobactin in norepinephrine mediated iron supply from transferrin to enterohaemorrhagic Escherichia coli. FEMS Microbiol Lett 222:39–43

    Article  CAS  Google Scholar 

  28. Freestone PP, Lyte M, Neal CP, Maggs AF, Haigh RD, Williams PH (2000) The mammalian neuroendocrine hormone norepinephrine supplies iron for bacterial growth in the presence of transferrin or lactoferrin. J Bacteriol 182:6091–6098

    Article  CAS  Google Scholar 

  29. Burton CL, Chhabra SR, Swift S, Baldwin TJ, Withers H, Hill SJ, Williams P (2002) The growth response of Escherichia coli to neurotransmitters and related catecholamine drugs requires a functional enterobactin biosynthesis and uptake system. Infect Immun 70:5913–5923

    Article  CAS  Google Scholar 

  30. Sperandio V, Torres AG, Jarvis B, Nataro JP, Kaper JB (2003) Bacteria–host communication: the language of hormones. Proc Natl Acad Sci USA 100:8951–8956

    Article  CAS  Google Scholar 

  31. Fujiya M, Musch MW, Nakagawa Y, Hu S, Alverdy J, Kohgo Y, Schneewind O, Jabri B, Chang EB (2007) The Bacillus subtilis quorum sensing molecule CSF contributes to intestinal homeostasis via OCTN2, a host cell membrane transporter. Cell Host Microbe 1:299–308

    Article  CAS  Google Scholar 

  32. Diep DB, Mathiesen G, Eijsink VG, Nes IF (2009) Use of lactobacilli and their pheromone-based regulatory mechanism in gene expression and drug delivery. Curr Pharm Biotechnol 10:62–73

    Article  CAS  Google Scholar 

  33. Di Cagno R, De Angelis M, Calasso M, Vincentini O, Vernocchi P, Ndagijimana M, De Vincenzi M, Dessi MR, Guerzoni ME, Gobbetti M (2010) Quorum sensing in sourdough Lactobacillus plantarum DC400: induction of plantaricin A (PlnA) under co-cultivation with other lactic acid bacteria and effect of PlnA on bacterial and Caco-2 cells. Proteomics 10:2175–2190

    Article  Google Scholar 

  34. Yan F, Cao H, Cover TL, Whitehead R, Washington MK, Polk DB (2007) Soluble proteins produced by probiotic bacteria regulate intestinal epithelial cell survival and growth. Gastroenterology 132:562–575

    Article  CAS  Google Scholar 

  35. Marzani B, Pinto D, Minervini F, Calasso M, Di Cagno R, Giuliani G, Gobbetti M, De Angelis M (2012) The antimicrobial peptide pheromone Plantaricin A increases antioxidant defenses of human keratinocytes and modulates the expression of filaggrin, involucrin, β-defensin 2 and tumor necrosis factor-α genes. Exp Dermatol. doi:10.1111/j.1600-0625.2012.01538.x

  36. Morini F, Dusatti F, Bonina FP, Saija A, Ferro M (2000) Iron induced lipid peroxidation in human skin-derived cell lines: protection by a red orange extract. ATLA Altern Lab Anim 28:427–433

    Google Scholar 

  37. Calcabrini C, De Bellis R, Mancini U, Cucchiarini L, Potenza L, De Sanctis R, Patrone V, Scesa C, Dachà M (2010) Rhodiola rosea ability to enrich cellular antioxidant defences of cultured human keratinocytes. Arch Dermatol Res 302:191–200

    Article  Google Scholar 

  38. Pinto D, Marzani B, Minervini F, Calasso M, Giuliani GM, Gobbetti M, De Angelis M, Plantaricin A (2011) synthesized by Lactobacillus plantarum induces in vitro proliferation and migration of human keratinocytes and increases the expression of TGF-β1, FGF7, VEGF-A and IL-8 genes. Peptides 32:1815–1824

    Article  CAS  Google Scholar 

  39. Sarmadi BH, Ismail A (2010) Antioxidative peptides from food proteins: a review. Peptides 31:1949–1956

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

Copyright information

© 2012 Marco Gobbetti and Rafaella Di Cagno

About this chapter

Cite this chapter

Gobbetti, M., Di Cagno, R. (2012). The Probiotic Message. In: Bacterial Communication in Foods. SpringerBriefs in Food, Health, and Nutrition. Springer, Boston, MA. https://doi.org/10.1007/978-1-4614-5656-8_4

Download citation

Publish with us

Policies and ethics