Antagonistics against pathogenic Bacillus cereus in milk fermentation by Lactobacillus plantarum ZDY2013 and its anti-adhesion effect on Caco-2 cells against pathogens

Journal of Dairy Science

Volumn 99, Issue 4, 2016, Pages 2666-2674

  Zhang, Zhihong ^a   Tao, Xueying ^a   Shah, Nagendra P ^b   Wei, Hua ^a  

^a NANCHANG UNIVERSITY   (China)

^b UNIVERSITY OF HONG KONG   (Hong Kong)

Author keywords

Antiadhesion; Bacillus cereus; Cytotoxic effect; Lactobacillus plantarum ZDY2013; Milk fermentation

Indexed keywords

PROBIOTIC AGENT;

ANIMAL; ANTIBIOSIS; BACILLUS CEREUS; BACTERIUM ADHERENCE; CACO-2 CELL LINE; FERMENTATION; HUMAN; INTESTINE; LACTOBACILLUS PLANTARUM; METABOLISM; MICROBIOLOGY; MILK; PHYSIOLOGY;

ANIMALS; ANTIBIOSIS; BACILLUS CEREUS; BACTERIAL ADHESION; CACO-2 CELLS; FERMENTATION; HUMANS; INTESTINES; LACTOBACILLUS PLANTARUM; MILK; PROBIOTICS;

EID: 84955610576     PISSN: 00220302     EISSN: 15253198     Source Type: Journal    
DOI: 10.3168/jds.2015-10587     Document Type: Article

References (36)

1. Abedi D., Feizizadeh S., Akbari V., Jafarian-Dehkordi A. In vitro anti-bacterial and anti-adherence effects of Lactobacillus delbrueckii subsp bulgaricus on Escherichia coli. Res. Pharm. Sci 2013, 8:260-268.
2. Adams M.R., Nicolaides L. Review of the sensitivity of different foodborne pathogens to fermentation. Food Contr 1997, 8:227-239.
3. Ahmed A.A., Moustafa M.K., Marth E.H. Incidence of Bacillus cereus in milk and some milk products. J. Food Prot 1983, 46:126-128.
4. Bravo-Ferrada B.M., Gonçalves S., Semorile L., Santos N., Tymczyszyn E., Hollmann A. Study of surface damage on cell envelope assessed by AFM and flow cytometry of Lactobacillus plantarum exposed to ethanol and dehydration. J. Appl. Microbiol 2015, 118:1409-1417.
5. Chouraqui J.-P., Van Egroo L.-D., Fichot M.-C. Acidified milk formula supplemented with Bifidobacterium lactis: Impact on infant diarrhea in residential care settings. J. Pediatr. Gastroenterol. Nutr 2004, 38:288-292.
6. Collado M.C., Meriluoto J., Salminen S. Role of commercial probiotic strains against human pathogen adhesion to intestinal mucus. Lett. Appl. Microbiol 2007, 45:454-460.
7. Collado M.C., Jalonen L., Meriluoto J., Salminen S. Protection mechanism of probiotic combination against human pathogens: in vitro adhesion to human intestinal mucus. Asia Pac. J. Clin. Nutr 2006, 15:570-575.
8. Crowley S., Mahony J., van Sinderen D. Broad-spectrum antifungal-producing lactic acid bacteria and their application in fruit models. Folia Microbiol. (Praha) 2013, 58:291-299.
9. da Silva Sabo S., Vitolo M., González J.M.D., de Souza Oliveira R.P. Overview of Lactobacillus plantarum as a promising bacteriocin producer among lactic acid bacteria. Food Res. Int 2014, 64:527-536.
10. Dennis D., Kaplan N.O. D-and L-lactic acid dehydrogenases in Lactobacillus plantarum. J. Biol. Chem 1960, 235:810-818.
11. Derrien M., van Hylckama Vlieg J.E. Fate, activity, and impact of ingested bacteria within the human gut microbiota. Trends Microbiol 2015, 23:354-366.
12. Feng Y., Gong J., Yu H., Jin Y., Zhu J., Han Y. Identification of changes in the composition of ileal bacterial microbiota of broiler chickens infected with Clostridium perfringens. Vet. Microbiol 2010, 140:116-121.
13. García-Ruiz A., de Llano D.G., Esteban-Fernández A., Requena T., Bartolomé B., Moreno-Arribas M.V. Assessment of probiotic properties in lactic acid bacteria isolated from wine. Food Microbiol 2014, 44:220-225.
14. Górska S., Schwarzer M., Jachymek W., Srutkova D., Brzozowska E., Kozakova H., Gamian A. Distinct immunomodulation of bone marrow-derived dendritic cell responses to Lactobacillus plantarum WCFS1 by two different polysaccharides Isolated from Lactobacillus rhamnosus LOCK 0900. Appl. Environ. Microbiol 2014, 80:6506-6516.
15. Huang R., Pan M., Wan C., Shah N.P., Tao X., Wei H. Physiological and transcriptional response as well as cross protection of Lactobacillus plantarum ZDY2013 under acid stress. J. Dairy Sci 2016, http://dx.doi.org/10.3168/jds.2015-9993.
16. Huang R., Tao X., Wan C., Li S., Xu H., Xu F., Shah N.P., Wei H. In vitro probiotic characteristics of Lactobacillus plantarum ZDY 2013 and its modulatory effect on gut microbiota of mice. J. Dairy Sci 2015, 98:5850-5861.
17. Hwang J.Y., Park J. Characteristics of enterotoxin distribution, hemolysis, lecithinase, and starch hydrolysis of Bacillus cereus isolated from infant formulas and ready-to-eat foods. J. Dairy Sci 2015, 98:1652-1660.
18. Kuda T., Nemoto M., Kawahara M., Oshio S., Takahashi H., Kimura B. Induction of the superoxide anion radical scavenging capacity of dried 'funori' Gloiopeltis furcata by Lactobacillus plantarum S-SU1 fermentation. Food Funct 2015, 6:2535-2541.
19. Leahy S.C., Higgins D., Fitzgerald G., Sinderen D.v. Getting better with bifidobacteria. J. Appl. Microbiol 2005, 98:1303-1315.
20. Leite A.M., Miguel M., Peixoto R., Ruas-Madiedo P., Paschoalin V., Mayo B., Delgado S. Probiotic potential of selected lactic acid bacteria strains isolated from Brazilian kefir grains. J. Dairy Sci 2015, 98:3622-3632.
21. Li S., Zhao Y., Zhang L., Zhang X., Huang L., Li D., Niu C., Yang Z., Wang Q. Antioxidant activity of Lactobacillus plantarum strains isolated from traditional Chinese fermented foods. Food Chem 2012, 135:1914-1919.
22. Marco M.L., Tachon S. Environmental factors influencing the efficacy of probiotic bacteria. Curr. Opin. Biotechnol 2013, 24:207-213.
23. Minnaard J., Lievin-Le Moal V., Coconnier M.-H., Servin A.L., Pérez P.F. Disassembly of F-actin cytoskeleton after interaction of Bacillus cereus with fully differentiated human intestinal Caco-2 cells. Infect. Immun 2004, 72:3106-3112.
24. Ngamwongsatit P., Buasri W., Pianariyanon P., Pulsrikarn C., Ohba M., Assavanig A., Panbangred W. Broad distribution of enterotoxin genes (hblCDA, nheABC, cytK, and entFM) among Bacillus thuringiensis and Bacillus cereus as shown by novel primers. Int. J. Food Microbiol 2008, 121:352-356.
25. Ramarao N., Lereclus D. Adhesion and cytotoxicity of Bacillus cereus and Bacillus thuringiensis to epithelial cells are FlhA and PlcR dependent, respectively. Microbes Infect 2006, 8:1483-1491.
26. Røssland E., Langsrud T., Sørhaug T. Influence of controlled lactic fermentation on growth and sporulation of Bacillus cereus in milk. Int. J. Food Microbiol 2005, 103:69-77.
27. Ruas-Madiedo P., Medrano M., Salazar N., Los Reyes-Gavilán D., Pérez P., Abraham A. Exopolysaccharides produced by Lactobacillus and Bifidobacterium strains abrogate in vitro the cytotoxic effect of bacterial toxins on eukaryotic cells. J. Appl. Microbiol 2010, 109:2079-2086.
28. Rukure G., Bester B.H. Survival and growth of Bacillus cereus during Gouda cheese manufacturing. Food Contr 2001, 12:31-36.
29. Siciliano R.A., Mazzeo M.F. Molecular mechanisms of probiotic action: a proteomic perspective. Curr. Opin. Microbiol 2012, 15:390-396.
30. Stenfors Arnesen L.P., Fagerlund A., Granum P.E. From soil to gut: Bacillus cereus and its food poisoning toxins. FEMS Microbiol. Rev 2008, 32:579-606.
31. Šušković J., Kos B., Beganović J., Leboš Pavunc A., Habjanič K., Matošić S. Antimicrobial activity-the most important property of probiotic and starter lactic acid bacteria. Food Technol. Biotechnol 2010, 48:296-307.
32. Yang Y., Tao W.-Y., Liu Y.-J., Zhu F. Inhibition of Bacillus cereus by lactic acid bacteria starter cultures in rice fermentation. Food Contr 2008, 19:159-161.
33. Zago M., Fornasari M.E., Carminati D., Burns P., Suàrez V., Vinderola G., Reinheimer J., Giraffa G. Characterization and probiotic potential of Lactobacillus plantarum strains isolated from cheeses. Food Microbiol 2011, 28:1033-1040.
34. Zhang Y., Vadlani P.V. Lactic acid production from biomass-derived sugars via co-fermentation of Lactobacillus brevis and Lactobacillus plantarum. J. Biosci. Bioeng 2015, 119:694-699.
35. Zhang Z., Feng L., Xu H., Liu C., Shah N.P., Wei H. Detection of viable enterotoxin-producing Bacillus cereus and analysis of toxigenicity from ready-to-eat foods and infant formula milk powder by multiplex PCR. J. Dairy Sci 2016, http://dx.doi.org/10.3168/jds.2015-10147.
36. Zhang Z., Liu W., Xu H., Aguilar Z.P., Shah N.P., Wei H. Propidium monoazide combined with real-time PCR for selective detection of viable Staphylococcus aureus in milk powder and meat products. J. Dairy Sci 2015, 98:1625-1633.