FACTORS DETERMING THE ADHESIVE CAPACITY OF LACTOBACILLUS BACTERIA

Publications

Share / Export Citation / Email / Print / Text size:

Postępy Mikrobiologii - Advancements of Microbiology

Polish Society of Microbiologists

Subject: Microbiology

GET ALERTS

ISSN: 0079-4252
eISSN: 2545-3149

DESCRIPTION

3
Reader(s)
19
Visit(s)
0
Comment(s)
0
Share(s)

SEARCH WITHIN CONTENT

FIND ARTICLE

Volume / Issue / page

Related articles

VOLUME 56 , ISSUE 2 (April 2017) > List of articles

FACTORS DETERMING THE ADHESIVE CAPACITY OF LACTOBACILLUS BACTERIA

Anna Paliwoda * / Adriana Nowak

Keywords : adhezja, bakterie mlekowe, Lactobacillus,   adhesion, lactic acid bacteria, Lactobacillus

Citation Information : Postępy Mikrobiologii - Advancements of Microbiology. Volume 56, Issue 2, Pages 196-204, DOI: https://doi.org/10.21307/PM-2017.56.2.196

License : (CC BY-NC-ND 4.0)

Published Online: 21-May-2019

ARTICLE

ABSTRACT

The ability of Lactobacillus to adhere to the intestinal epithelium is one of the most important criterion in the selection of probiotic strains. Adherence allows microorganisms to survive and temporarily colonize the digestive system, which is necessary to induce beneficial effects on the host. Adhesion is a very complex, multistep process and, although there are many proposed theories, the exact mechanism is still not fully understood. A crucial role in the formation of the adhesive interactions plays the bacterial cell wall and its components, such as exopolisaccharydes, lipoteichoic acids and various proteins e.g. S-layer proteins.

Content not available PDF Share

FIGURES & TABLES

REFERENCES

1. Aleksandrzak-Piekarczyk T., Koryszewska-Bagińska A., Grynberg M., Nowak A., Cukrowska B., Kozakova H., Bardowski J.: Genomic and functional characterization of the unusual pLOCK 0919 plasmid harboring the spaCBA pili cluster in Lactobacillus casei LOCK 0919. Genome Biol. Evol. 8, 202–217 (2015)

2. Åvall-Jääskeläinen S., Palva A.: Lactobacillus surface layers and their applications. FEMS Microbiol. Rev. 29, 511–529 (2005)

3. Beaussart A., El-Kirat-Chatel S., Herman P., Alsteens D., Mahillon J., Hols P., Dufrene Y.F.: Single-cell force spectroscopy of probiotic bacteria. Biophys. J. 14, 1886–1892 (2013)

4. Boekhorst J., Helmer Q., Kleerebezem M., Siezen R.J.: Comparative analysis of proteins with a mucusbinding domain found exclusively in lactic acid bacteria. Microbiology, 152, 273–280 (2006)

5. Buck B.L., Altermann E., Svingerud T., Klaenhammer T.R.: Functional analysis of putative adhesion factors in Lactobacillus acidophilus NCFM. A. Environ. Microbiol. 12, 8344–8351 (2005)

6. Buda B., Dylus E., Górska-Frączek S., Brzozowska E., Gamian A.: Właściwości biologiczne białek powierzchniowych bakterii
z rodzaju Lactobacillus. Post. Hig. Med. Dosw. 67, 229–237 (2013)

7. Call E.K., Klaenhammer T.R.: Relevance and application of sortase and sortase-dependent proteins in lactic acid bacteria. Front. Microbiol. 4, 1–10 (2013)

8. Collado M.C., Surono I., Meriluoto J., Salminen S.: Indigenous dadih lactic acid bacteria: cell-surface properties and interactions with pathogens. Food Microbiology and Safety, 3, 89–93 (2007)

9. Collado M.C., Isolauri E., Salminen S., Sanz Y.: The impact of probiotic on gut health. Curr. Drug. Metab. 10, 68–78 (2009)

10. Czaczyk K., Olejnik A., Miężał P., Grajek W.: Poszukiwanie prostych modeli do badania adhezji bakterii probiotycznych. Żywn. Nauk. Technol. Ja. 1, 84–96 (2005)

11. Deepika G., Karunakaran E., Hurley C. R., Biggs C.A., Charalampopoulos D.: Influence of fermentation conditions on the surface properties and adhesion of Lactobacillus rhamnosus GG. Microb. Cell Fact. 11, 1–12 (2012)

12. Dertli E., Mayer M.J., Narbad A.: Impact of the exopolysaccharide layer on biofilms, adhesion and resistance to stress in Lactobacillus johnsonii FI9785. BMC Microbiology, 15, 1–9 (2015)

13. Derrien M., Van Passel M.W.J., Van de Bovenkamp J.H.B, Schipper R., De Vos W., Dekker J.: Mucin-bacterial interactions in the human oral cavity and digestive tract. Gut Microbes, 1, 254–268 (2010)

14. Duary R.K., Rajput Y.S., Batish V.K., Grover S.: Assessing the adhesion of putative indigenous probiotic lactobacilli to human colonic epithelial cells. Indian J. Med. Res. 134, 664–671 (2011)

15. Etzold S., Kober O.I., Mackenzie D.A., Tailford L.E., Gunning A.P., Walshaw J., Hemmings A.M., Juge N.: Structural basis for adaptation of lactobacilli to gastrointestinal mucus. Environ. Microbiol. 16, 888–903 (2014)

16. Fernandes M.S., Cruz A.G., Arroyo D.M., Faria J.F., Cristianini M., Sant’Ana A.S.: On the behavior of Listeria innocua and Lactobacillus acidophilus co-inoculated in a dairy dessert and the potential impacts on food safety and product’s functionality. Food Control, 34, 331–335 (2013)

17. Flemming H.C., Wingender J.: The biofilm matrix. Nat. Rev. Microbiol. 8, 623–633 (2010)

18. Goh Y.J., Klaenhammer T.R.: Functional roles of aggregation-promoting-like factor in stress tolerance and adherence of Lactobacillus acidophilus NCFM. Appl. Environ. Microb. 15, 5005–5012 (2010)

19. Golowczyc M.A., Mobili P., Garrote G.L., de Los Angeles Serradel M. Abraham A.G., De Antoni G.L.: Interaction between Lactobacillus kefir and Saccharomyces lipolytica isolated from kefir grains: evidence for lectin-like activity of bacterial surface proteins. J. Dairy Res. 76, 111–116 (2009)

20. Hendrickx A.P.A., Budzik J.M., Oh S.Y., Schneewind O.: Architects at the bacterial surface-sortases and the assembly of pili with isopeptide bonds. Nat. Rev. Microbiol. 9, 166–176 (2011)

21. Hori K., Matsumoto S.: Bacterial adhesion: From mechanism to control. Biochem. Eng. J. 48, 424–434 (2010)

22. Hynönen U., Palva A.: Lactobacillus surface layer proteins: structure, function and applications. Appl. Microbiol. Biot. 97, 5225–5243 (2013)

23. Juge N.: Microbial adhesins to gastrointestinal mucus. Trends Microbiol. 1, 30–39 (2012)

24. Kadlec R., Jakubec M.: The effect of prebiotics on adherence of probiotics. J. Dairy Sci. 97, 1983–1990 (2014)

25. Kankainen M., de Vos W.M. i wsp.: Comparative genomic analysis of Lactobacillus rhamnosus GG reveals pili contain-
ing a humanmucus binding protein. Proc. Natl. Acad. Sci. 40, 17193–17198 (2009)

26. Kleerebezem M., Hols P., Bernard E., Rolain T., Zhou M., Siezen R.J., Bron P.A.: The extracellular biology of the Lactobacilli. FEMS Microbiol. Rev. 34, 199–230 (2010)

27. Kołwzan B.: Analiza zjawiska biofilmu – warunki jego powstawania i funkcjonowania. Ochrona środowiska, 4, 3–14 (2011)

28. Kos B., Šuškowić J., Vukowić S., Šimpraga M., Frece J., Matošic S.: Adhesion and aggregation ability of probiotic strain Lactobacillus acidophilus M92. J. Appl. Microbiol. 94, 981–987 (2003)

29. Laparra J.M., Sanz Y.: Comparison of in vitro models to study bacterial adhesion to the intestinal epithelium. Lett. Appl. Microbiol. 49, 695–701 (2009)

30. Lebeer S., Vanderleyden J., De Keersmaecker S.C.J.: Genes and molecules of lactobacilli supporting probiotic action. Microbiol. Mol. Biol. R. 4, 728–764 (2008)

31. Li G.: Intestinal Probiotics: Interactions with bile salts and reduction of cholesterol. Procedia Environmental Sciences, 12, 1180–1186 (2012)

32. Lim S.M., Ahn D.H.: Factors affecting adhesion of lactic acid bacteria to Caco-2 cells and inhibitory effect on infection of Salmonella Typhimurium. J. Microbiol. Biotechn. 22, 1731–1739 (2012)

33. Linden S.K., Sutton P., Karlsson N.G., Korolik V., McGuckin: Mucins in the mucosal barrier to infection. Mucosal Immunol. 3, 183–197 (2008)

34. Lorca G., Torino M.I., Fond D.V., Ljungh A.A.: Lactobacilli express cell surface proteins which mediate binding of immobilized collagen and fibronectin. FEMS Microbiol. Lett. 206, 31–37 (2002)

35. Lukić J., Strahinić I., Jovčić B., Filipić B., Topisirović L., Kojić M., Begović J.: Different roles for Lactococcal aggregation factor and mucin binding protein in adhesion to gastrointestinal mucosa. Appl. Environ. Microb. 22, 7993–8000 (2012)

36. Muñoz-Provencio D., Llopis M., Antolin M., de Torres I., Guarner F., Pérez-Martínez G., Monedero V.: Adhesion properties of Lactobacillus casei strains to resected intestinal fragments and components of the extracellular matrix. Arch. Microbiol. 191, 153–161 (2009)

37. Nikolic M., Jovcic B., Kojic M., Topisirovic L.: Surface properties of Lactobacillus and Leuconostoc isolates from homemade cheeses showing auto-aggregation ability. Eur. Food Res.Technol. 231, 925–931 (2010)

38. Nishiyama K, M. Sugiyama, T. Mukai. Adhesion properties of lactic acid bacteria on intestinal mucin. Microorganisms, 4, 34 (2016)

39. O’Flaherty S., Goh Y.J., Klaenhammer T.R.: Genomic of probiotic bacteria (w) Prebiotics and Probiotics Science and Technology, red. D. Charalampopoulos, R.A. Rastall, Springer, New York, 2009 s. 681–727

40. Ouwehand A.C., Salminen S. :In vitro adhesion assays for probiotics and their in vivo relevance: a review. Microb. Ecol. Health D. 15, 175–184 (2003)

41. Percival S.L., Malic S., Cruz H., Williams D.W.: Introduction to biofilms. Biofilms and Veterinary Medicine, 6, 41–68 (2011)

42. Polak-Berecka M., Waśko A., Paduch R., Skrzypek T., Sroka-Bartnicka A.: The effect of cell surface components on adhesion ability of Lactobacillus rhamnosus. Antonie van Leeuwenhoek, 106, 751–762 (2014)

43. Pretzer G., Snel J., Molenaar D., Wiersma A., Bron P.A., Lambert J., de Vos W.M., van der Meer R., Smits M.A., Kleerebezem M.: Biodiversity-based identification and functional characterization of the mannose-specific adhesin of Lactobacillus plantarum. J. Bacteriol. 17, 6128–6136 (2005)

44. Ramiah K., van Reenen C.A., Dicks L.M.T.: Surface-bound proteins of Lactobacillus plantarum 423 that contribute to adhesion of Caco-2 cells and their role in competitive exclusion and displacement of Clostridium sporogenes and Enterococcus faecalis. Res.Microbiol. 159, 470–475 (2008)

45. Roos S., Jonsson H.: A high-molecular mass cell-surface protein from Lactobacillus reuteri 1063 adheres to mucus components. Microbiology, 148, 433–442 (2002)

46. Ruas-Madiego P., Gueimonde M., Margolles A., Reyes-Gavilán C.G., Salminen S.: Exopolysaccharides produced by probiotic strains modify the adhesion of probiotics and enteropathogens to human intestinal mucus. J. Food Protect. 8, 2011–2015 (2006)

47. Sánchez B., Bressollier P., Urdaci M.C.: Exported proteins in probiotic bacteria: adhesion to intestinal surfaces, host immunomodulation and molecular cross-talking with the host. FEMS Immunol. Med. Mic. 54, 1–17 (2008)

48. Saran S., Bisht M.S., Singh K., Teotia U.V.S.: Comparing adhesion attributes of two isolates of Lactobacillus acidophilus of assessment of prebiotics, honey and inulin. Int. J. Scientific and Research Publications, 2, 1–7 (2012)

49. Schaär-Zamaretti P., Ubbink J.: The cell wall of lactic acid bacteria: surface constituents and macromolecular conformations. Biophys. J. 85, 4076–4092 (2003)

50. Schachtsiek M., Hammes W.P. Hertel Ch.: Characterization of Lactobacillus coryniformis DSM 20001T Surface Protein Cpf Mediating Coaggregation with and Aggregation among Pathogens. App. Environ. Microbiol. 12, 7078–7085 (2004)

51. Sengupta R., Altermann E., Anderson R.C., McNabb W.C., Moughan P.J., Roy N.C.: The role of cell surface architecture of Lactobacilli in host-microbe interactions in the gastrointestinal tract. Mediat. Infamm. DOI: 10.1155/2013/237921 (2013)

52. Siegel S.D., Liu J., Ton-That H.: Biogenesis of the Gram-positive bacterial cell envelope, Curr. Opin. Microbiol. 34, 31–37 (2016)
53. Sullan R.M.A., Beaussart A., Tripathi P., Derclaye S., El-Kirat-Chatel S., Li J.K., Schneider Y., Vanderleyden J., Lebeer S., Dufrene Y.F.: Single-cell force spectroscopy of pili-mediated adhesion, Nanoscale, 6, 1134–1143 (2014)

54. Sun Z., Kong J., Hu S., Kong W., Lu W., Liu W.: Characterization of a S-layer protein from Lactobacillus crispatus K313 and the domains responsible for binding to cell wall and adherence to collagen. App. Microbiol. Biotechn. 97, 1941–1952 (2013)

55. Tallant T., Deb A., Kar N., Lupica J., De Veer M.J., Di Donato J.A.: Flagellin acting via TLR5 is the major activator of key signaling pathways leading to NF-κB and proinflammatory gene program activation in intestinal epithelial cells. BMC Microbiol. 4, 33, (2004)

56. Thi T.T., Prigent-Combaret C., Dorel C., Lejeune P.: First stages of biofilm formation: Characterization and quantification of bacterial functions involved in colonization process. Methods Enzymol. 336, 152–159 (2001)

57. Tuo Y., Yu H., Ai L., Wu Z., Guo B., Chen W.: Aggregation and adhesion properties of 22 Lactobacillus strains. J. Dairy Scien. 96, 4252–4257 (2013)

58. Tuomola E.M., Salminen S.J.: Adhesion of some probiotic and dairy Lactobacillus strains to Caco-2 cell cultures. Int. J. Food Microbiol. 41, 45–51 (1998)

59. Van Pijkeren J.P., O’Toole P.W. i wsp.: Comparative and functional analysis of sortase-dependent proteins in the predicted secretome of Lactobacillus salivarius UCC118. Appl. Environ. Microbiol. 72, 4143–4153 (1998)

60. Van Tassel M.L., Miller M.J.: Lactobacillus adhesion to mucus. Nutrients, 3, 613–636 (2011)

61. Vélez M.P., De Keersmaecker S.C.J., Vanderleyden J.: Adherence factors of Lactobacillus in the human gastrointestinal tract. FEMS Microbiol. Lett. 276, 140–148 (2007)

62. Von Ossowski I., Satokari R., Reunanen J., Lebeer S., De Keersmaecker S.C.J., Vanderleyden J., de Vos W.M., Palva A.: Functional characterization of a mucus-specific LPXTG surface adhesin from probiotic Lactobacillus rhamnosus GG. Appl. Environ. Microbiol. 77, 4465–4472 (2011)

EXTRA FILES

COMMENTS