Effect of Inorganic Salts on the Thermotolerance and Probiotic Properties of Lactobacilli Isolated from Curdled Milk Traditionally Produced in Mezam Division, Cameroon — Oak Academic Publishing
Research ArticleOpen AccessGoogle Scholar indexed
Effect of Inorganic Salts on the Thermotolerance and Probiotic Properties of Lactobacilli Isolated from Curdled Milk Traditionally Produced in Mezam Division, Cameroon
Department of Microbiology and Parasitology, Faculty of Science, University of Buea, Cameroon
,
Department of Microbiology and Parasitology, Faculty of Science, University of Buea, Cameroon
,
Department of Food Science and Nutrition, ENSAI, Ngaoundere, Cameroon
1 Department of Microbiology and Parasitology, Faculty of Science, University of Buea, Cameroon
2 Department of Microbiology and Parasitology, Faculty of Science, University of Buea, Cameroon
3 Department of Food Science and Nutrition, ENSAI, Ngaoundere, Cameroon
The industrial production of most food and probiotic products often requires processing involving high temperatures and physiological stress causing loss of viability of probiotic microbial strains. The viability and stability of probiotic strains is a key determinant of their efficacy during administration in human and animal. Thermotolerance is actually a very important feature for probiotic undergoing industrial processing. This paper aimed at assessing the effect of some mineral salts on the thermotolerance and the probiotic properties of lactobacilli isolated from curded milk produced in Mezam Division, Cameroon. Lactobacilli were isolated by pour plate method on de Man Rogosa and Sharpe (MRS) agar. Lactobacilli were selected based on their ability to suppress in-vitro and in-vivo food borne pathogenic bacteria; Salmonella enterica serovar Enteridis and Esherichia coli . Inhibitory activities against these food borne pathogens were performed by disc diffusion method on Mueller Hinton agar. In-vivo inhibition of Salmonella was achieved using oral administration by gavage of (1.0 × 10 9 CFU/ml) of selected probiotic strain suspended in sterile water. Thermotolerance was assessed by measuring the survival rate of the strain after heating at various temperatures in the presence and absence of mineral salts. Resistance to bile was determined by measuring the survival rate of probiotics after incubation in the presence of oxgallbille and mineral salts. Two catalase negatives isolates were selected based on their capacity to exhibit inhibitory activities in-vitro and in-vivo against food borne pathogens. They were identified as strain of Lactobacillus casei (LS3) and Lactobacillus plantarum (LM4). These strains exhibited significant reduction (P < 0.05) in Salmonella count in caeca swabs of infected chick model. The calcium and magnesium salts increased significantly (P < 0.05) the thermo-tolerance and resistance to bile of probiotic strains studied. These results suggested that calcium and magnesium could be used to monitor the viability of probiotic strains in probiotic products.
Foligne, B., Daniel, C. and Pot, B. (2013) Probiotics from Research to Market: The Possibilities, Risks and Challenges. Current Opinion in Microbiology, 16, 284-292.
Surendran Nair, M., Amalaradjou, M.A. and Venkitanarayanan, K. (2017) Antivirulence Properties of Probiotics in Combating Microbial Pathogenesis. Advances in Applied Microbiology, 98, 1-29.
Zhang, Y., Zhang, L., Du, M., Yi, H., Guo, C., Tuo, Y., et al. (2011) Antimicrobial Activity against Shigellasonnei and Probiotic Properties of Wild Lactobacilli from Fermented Food. Microbiological Research, 167, 27-31.
Walsh, M.C., Rostagno, M.H., Gardiner, G.E., Sutton, A.L., Richert, B.T. and Radcliffe, J.S. (2012) Controlling Salmonella Infection in Weanling Pigs through Water Delivery of Direct-Fed Microbials or Organic Acids. Part I, Effects on Growth Performance, Microbial Populations, and Immune Status. Journal of Animal Science, 90, 261-271. https://doi.org/10.2527/jas.2010-3598
Tsai, C.C., Hsih, H.Y., Chiu, H.H., Lai, Y.Y., Liu, J.H., Yu, B., et al. (2005) Antagonistic Activity against Salmonella Infection in Vitro and in Vivo for Two Lactobacillus Strains from Swine and Poultry. International Journal of Food Microbiology, 102, 185-194.
Truusalu, K., Mikelsaar, R.H., Naaber, P., Karki, T., Kullisaar, T., Zilmer, M., et al. (2008) Eradication of Salmonella Typhimurium Infection in a Murine Model of Typhoid Fever with the Combination of Probiotic Lactobacillus fermentum ME-3 and Ofloxacin. BMC Microbiology, 8, 132. https://doi.org/10.1186/1471-2180-8-132
Wagner, R.D., Johnson, S.J. and Kurniasih Rubin, D. (2009) Probiotic Bacteria Are Antagonistic to Salmonella enterica and Campylobacter jejuni and Influence Host Lymphocyte Responses in Human Microbiota-Associated Immunodeficient and Immunocompetent Mice. Molecular Nutrition & Food Research, 53, 377-388. https://doi.org/10.1002/mnfr.200800101
Svetoch, E.A. and Stern, N.J. (2010) Bacteriocins to Control Campylobacter spp. in Poultry—A Review. Poultry Science, 89, 1763-1768. https://doi.org/10.3382/ps.2010-00659
Saint-Cyr, M.J., Haddad, N., Taminiau, B., Poezevara, T., Quesne, S., Amelot, M., et al. (2017) Use of the Potential Probiotic Strain Lactobacillus salivarius SMXD51 to Control Campylobacter jejuni in Broilers. International Journal of Food Microbiology, 247, 9-17.
Sikorska, H. and Smoragiewicz, W. (2013) Role of Probiotics in the Prevention and Treatment of Meticillin-Resistant Staphylococcus aureus Infections. International Journal of Antimicrobial Agents, 42, 475-481.
Reis, N.A., Saraiva, M.A., Duarte, E.A., de Carvalho, E.A., Vieira, B.B. and Evangelista-Barreto, N.S. (2016) Probiotic Properties of Lactic Acid Bacteria Isolated from Human Milk. Journal of Applied Microbiology, 121, 811-820. https://doi.org/10.1111/jam.13173
Razzak, M.S., Al-Charrakh, A.H. and Al-Greitty, B.H. (2011) Relationship between Lactobacilli and Opportunistic Bacterial Pathogens Associated with Vaginitis. North American Journal of Medical Sciences, 3, 185-192. https://doi.org/10.4297/najms.2011.3185
Park, S.Y. and Lim, S.D. (2015) Probiotic Characteristics of Lactobacillus plantarum FH185 Isolated from Human Feces. Korean Journal for Food Science of Animal Resources, 35, 615-621. https://doi.org/10.5851/kosfa.2015.35.5.615
Yasar, B., Abut, E., Kayadibi, H., Toros, B., Sezikli, M., Akkan, Z., et al. (2010) Efficacy of Probiotics in Helicobacter Pylori Eradication Therapy. The Turkish Journal of Gastroenterology, the Official Journal of Turkish Society of Gastroenterology, 21, 212-217. https://doi.org/10.4318/tjg.2010.0090
Vitor, J.M. and Vale, F.F. (2010) Alternative Therapies for Helicobacter pylori, Probiotics and Phytomedicine. FEMS Immunology and Medical Microbiology, 63, 153-164. https://doi.org/10.1111/j.1574-695X.2011.00865.x
Chen, X., Liu, X.M., Tian, F., Zhang, Q., Zhang, H.P., Zhang, H., et al. (2012) Antagonistic Activities of Lactobacilli against Helicobacter pylori Growth and Infection in Human Gastric Epithelial Cells. Journal of Food Science, 77, M9-M14. https://doi.org/10.1111/j.1750-3841.2011.02498.x
Cekin, A.H., Sahinturk, Y., AkbayHarmandar, F., Uyar, S., Yolcular, B.O. and Cekin, Y. (2017) Use of Probiotics as an Adjuvant to Sequential H. Pylori Eradication Therapy, Impact on Eradication Rates, Treatment Resistance, Treatment-Related Side Effects, and Patient Compliance. The Turkish Journal of Gastroenterology, the Official Journal of Turkish Society of Gastroenterology, 28, 3-11. https://doi.org/10.5152/tjg.2016.0278
Ahmad, K., Fatemeh, F., Mehri, N. and Maryam, S. (2013) Probiotics for the Treatment of Pediatric Helicobacter Pylori Infection: A Randomized Double Blind Clinical Trial. Iranian Journal of Pediatrics, 23, 79-84.
Sharma, M. and Devi, M. (2014) Probiotics: A Comprehensive Approach toward Health Foods. Critical Reviews in Food Science and Nutrition, 54, 537-552. https://doi.org/10.1080/10408398.2011.594185
Coeuret, V., Gueguen, M. and Vernoux, J.P. (2004) Numbers and Strains of Lactobacilli in Some Probiotic Products. International Journal of Food Microbiology, 97, 147-156.
Arnold, C. (2013) The Pros and Cons of Probiotics. The Lancet Infectious Diseases, 13, 571-572.
Altieri, C. (2016) Dairy Propionibacteria as Probiotics, Recent Evidences. World Journal of Microbiology & Biotechnology, 32, 172. https://doi.org/10.1007/s11274-016-2118-0
Ramirez-Chavarin, M.L., Wacher, C., Eslava-Campos, C.A. and PerezChabela, M.L. (2013) Probiotic Potential of Thermotolerant Lactic Acid Bacteria Strains Isolated from Cooked Meat Products. International Food Research Journal, 20, 991-1000.
Leelavatcharamas, V., Arbsuwan, N., Apiraksakorn, J., Laopaiboon, P. and Kishida, M. (2011) Thermotolerantbacteriocin-Producing Lactic Acid Bacteria Isolated from Thai Local Fermented Foods and Their Bacteriocin Productivity. Biocontrol Science, 16, 33-40. https://doi.org/10.4265/bio.16.33
Zhang, Y.R., Xiong, H.R. and Guo, X.H. (2014) Enhanced Viability of Lactobacillus reuterifor Probiotics Production in Mixed Solid-State Fermentation in the Presence of Bacillus subtilis. Folia Microbiologica, 59, 31-36. https://doi.org/10.1007/s12223-013-0264-4
Yeung, T.W., Arroyo-Maya, I.J., McClements, D.J. and Sela, D.A. (2016) Microencapsulation of Probiotics in Hydrogel Particles, Enhancing Lactococcuslactis Subsp. cremoris LM0230 Viability Using Calcium Alginate Beads. Food & Function, 7, 1797-1804. https://doi.org/10.1039/C5FO00801H
Tsvetkov, T. and Brankova, R. (1983) Viability of Micrococci and Lactobacilli upon Freezing and Freeze-Drying in the Presence of Different Cryoprotectants. Cryobiology, 20, 318-323.
Saito, V.S., Dos Santos, T.F., Vinderola, C.G., Romano, C., Nicoli, J.R., Araujo, L.S., et al. (2014) Viability and Resistance of Lactobacilli Isolated from Cocoa Fermentation to Simulated Gastrointestinal Digestive Steps in Soy Yogurt. Journal of Food Science, 79, M208-M213. https://doi.org/10.1111/1750-3841.12326
Cabuk, B. and Harsa, S.T. (2015) Improved Viability of Lactobacillus acidophilus NRRL-B 4495 during Freeze-Drying in Whey Protein-Pullulan Microcapsules. Journal of Microencapsulation, 32, 300-307. https://doi.org/10.3109/02652048.2015.1017618
Buriti, F.C., Castro, I.A. and Saad, S.M. (2010) Viability of Lactobacillus acidophilus in Synbiotic Guava Mousses and Its Survival under in Vitro Simulated Gastrointestinal Conditions. International Journal of Food Microbiology, 137, 121-129.
Yang, Y., Huang, S., Wang, J., Jan, G., Jeantet, R. and Chen, X.D. (2017) Mg2+ Improves the Thermotolerance of Probiotic Lactobacillus rhamnosus GG, Lactobacillus casei Zhang and Lactobacillus plantarum P-8. Letters in Applied Microbiology, 64, 283-288. https://doi.org/10.1111/lam.12716
Tatsinkou, F.B., Natalia, B.E., Gordon, T.N., BongsiysiGilake, N., Irene, A.A. and Samuel, W. (2015) Probiotic Properties of Lactic Acid Bacteria Isolated from Fermented Sap of Palm Tree (Elaeisguineensis). Journal of Microbiology and Antimicrobials, 7, 42-52. https://doi.org/10.5897/JMA2014.0353
Baranyi, J. and Roberts, T.A. (1994) A Dynamic Approach to Predicting Bacterial Growth in Food. International Journal of Food Microbiology, 23, 277-294.
Baty, F. and Delignette-Muller, M.L. (2004) Estimating the Bacterial Lag Time, Which Model, Which Precision? International Journal of Food Microbiology, 91, 261-277.
Foschino, R., Invernizzi, A., Barucco, R. and Stradiotto, K. (2002) Microbial Composition, Including the Incidence of Pathogens, of Goat Milk from the Bergamo Region of Italy during a Lactation Year. The Journal of Dairy Research, 69, 213-225. https://doi.org/10.1017/S0022029902005459
La Ragione, R.M., Narbad, A., Gasson, M.J. and Woodward, M.J. (2004) In Vivo Characterization of Lactobacillus johnsonii FI9785 for Use as a Defined Competitive Exclusion Agent against Bacterial Pathogens in Poultry. Letters in Applied Microbiology, 38, 197-205. https://doi.org/10.1111/j.1472-765X.2004.01474.x
Vila, B., Fontgibell, A., Badiola, I., Esteve-Garcia, E., Jimenez, G., Castillo, M., et al. (2009) Reduction of Salmonella enterica var. Enteritidis Colonization and Invasion by Bacillus cereus var. Toyoi Inclusion in Poultry Feeds. Poultry Science, 88, 975-979. https://doi.org/10.3382/ps.2008-00483
Tatsinkou, F.B., Tavea, F., Jiwoua, C. and Ndjouenkeu, R. (2011) Simultaneous Production of Raw Starch Degrading Highly Thermostable α-Amylase and Lactic Acid by Lactobacillus fermentum 04BBA19. African Journal of Biotechnology, 10, 6564-6574.