Xác định và đặc trưng hóa Lactiplantibacillus plantarum BI-59.1 probiotic phân lập từ tejuino và khả năng sản xuất biofilm của nó

Romero-Luna HE, Hernández-Sánchez H, Dávila-Ortiz G (2017) Traditional fermented beverages from Mexico as a potential probiotic source. Ann Microbiol 67:577–586. https://doi.org/10.1007/s13213-017-1290-2 Massieu G, Cravioto RO, Guzman J, Olivera H (1959) Contribucion adicional al estudio de la composicion de alimentos Mexicanos. Ciencia, México 19:53–56 Rubio-Castillo ÁE, Santiago-López L, Vallejo-Cordoba B et al (2021) Traditional non-distilled fermented beverages from Mexico to based on maize: an approach to Tejuino beverage. Int J Gastron Food Sci 23:100283. https://doi.org/10.1016/j.ijgfs.2020.100283 Silva MS, Ramos CL, González-Avila M et al (2017) Probiotic properties of Weissella cibaria and Leuconostoc citreum isolated from tejuino: a typical Mexican beverage. LWT - Food Sci Technol 86:227–232. https://doi.org/10.1016/j.lwt.2017.08.009 Reid G (2016) Probiotics: definition, scope and mechanisms of action. Best Pract Res Clin Gastroenterol 30:17–25. https://doi.org/10.1016/j.bpg.2015.12.001 Pérez-Armendáriz B, Cardoso-Ugarte GA (2020) Traditional fermented beverages in Mexico: Biotechnological, nutritional, and functional approaches. Food Res Int 136:109307. https://doi.org/10.1016/j.foodres.2020.109307 Prasad J, Gill H, Smart J, Gopal PK (1998) Selection and characterisation of Lactobacillus and Bifidobacterium strains for use as probiotics. Int Dairy J 8:993–1002. https://doi.org/10.1016/S0958-6946(99)00024-2 Surendran Nair M, Amalaradjou MA, Venkitanarayanan K (2017) Antivirulence properties of probiotics in combating microbial pathogenesis. Adv Appl Microbiol 98:1–29. https://doi.org/10.1016/bs.aambs.2016.12.001 Sanders ME, Akkermans LMA, Haller D et al (2010) Gut Microbes Safety assessment of probiotics for human use Introduction and Scope. Rev Gut Microbes 1:164–185. https://doi.org/10.4161/gmic.1.3.12127 Hardy H, Harris J, Lyon E et al (2013) Probiotics, prebiotics and immunomodulation of gut mucosal defences: homeostasis and immunopathology. Nutrients 5:1869–1912. https://doi.org/10.3390/nu5061869 Laparra JM, Sanz Y (2010) Interactions of gut microbiota with functional food components and nutraceuticals. Pharmacol Res 61:219–225. https://doi.org/10.1016/j.phrs.2009.11.001 Donlan RM (2002) Biofilms: microbial life on surfaces. Emerg Infect Dis 8:881–890. https://doi.org/10.3201/eid0809.020063 Baggi G, Cavalca L, Francia P, Zangrossi M (2004) Chlorophenol removal from soil suspensions: effects of a specialised microbial inoculum and a degradable analogue. Biodegradation 15:153–160. https://doi.org/10.1023/B:BIOD.0000026479.12672.d0 Esteve-Zarzoso B, Belloch C, Uruburu F, Querol A (1999) Identification of yeasts by RFLP analysis of the 5.8S rRNA gene and the two ribosomal internal transcribed spacers. Int J Syst Bacteriol 49:329–337. https://doi.org/10.1099/00207713-49-1-329 García A, Navarro K, Sanhueza E et al (2017) Characterization of Lactobacillus fermentum UCO-979C, a probiotic strain with a potent anti-Helicobacter pylori activity. Electron J Biotechnol 25:75–83. https://doi.org/10.1016/j.ejbt.2016.11.008 Tang H, Yuan J, Chong X, Wei H (2007) Antibiotic susceptibility of strains in Chinese medical probiotic products. J Med Coll PLA 22:149–152. https://doi.org/10.1016/S1000-1948(07)60032-X Georgieva RN, Iliev IN, Chipeva VA et al (2008) Identification and in vitro characterisation of Lactobacillus plantarum strains from artisanal Bulgarian white brined cheeses. J Basic Microbiol 48:234–244. https://doi.org/10.1002/jobm.200700355 Peres CM, Alves M, Hernandez-Mendoza A et al (2014) Novel isolates of lactobacilli from fermented Portuguese olive as potential probiotics. LWT - Food Sci Technol 59:234–246. https://doi.org/10.1016/j.lwt.2014.03.003 Davies FL (1983) Methods in food and dairy microbiology. Trends Biotechnol 1:65–66. https://doi.org/10.1016/0167-7799(83)90074-4 Felten A, Barreau C, Bizet C et al (1999) Lactobacillus species identification, H2O2 production, and antibiotic resistance and correlation with human clinical status. J Clin Microbiol 37:729–733. https://doi.org/10.1128/jcm.37.3.729-733.1999 Singh AK, Ramesh A (2008) Succession of dominant and antagonistic lactic acid bacteria in fermented cucumber: insights from a PCR-based approach. Food Microbiol 25:278–287. https://doi.org/10.1016/j.fm.2007.10.010 Baccigalupi L, Di Donato A, Parlato M et al (2005) Small surface-associated factors mediate adhesion of a food-isolated strain of Lactobacillus fermentum to Caco-2 cells. Res Microbiol 156:830–836. https://doi.org/10.1016/j.resmic.2005.05.001 Salas-Jara MJ, Sanhueza EA, Retamal-Díaz A et al (2016) Probiotic Lactobacillus fermentum UCO-979C biofilm formation on AGS and Caco-2 cells and Helicobacter pylori inhibition. Biofouling 32:1245–1257. https://doi.org/10.1080/08927014.2016.1249367 Begley M, Hill C, Gahan CGM (2006) Bile salt hydrolase activity in probiotics. Appl Environ Microbiol 72:1729–1738 Verna EC, Lucak S (2010) Use of probiotics in gastrointestinal disorders: what to recommend? Ther Adv Gastroenterol 3:307–319. https://doi.org/10.1177/1756283X10373814 Yadav R, Puniya AK, Shukla P (2016) Probiotic properties of Lactobacillus plantarum RYPR1 from an indigenous fermented beverage raabadi. Front Microbiol 7:1683. https://doi.org/10.3389/fmicb.2016.01683 Mathara JM, Schillinger U, Kutima PM et al (2008) Functional properties of Lactobacillus plantarum strains isolated from Maasai traditional fermented milk products in Kenya. Curr Microbiol 56:315–321. https://doi.org/10.1007/s00284-007-9084-6 Scott KP (2002) The role of conjugative transposons in spreading antibiotic resistance between bacteria that inhabit the gastrointestinal tract. Cell Mol Life Sci 59:2071–2082. https://doi.org/10.1007/s000180200007 Imperial ICVJ, Ibana JA (2016) Addressing the antibiotic resistance problem with probiotics: reducing the risk of its double-edged sword effect. Front Microbiol 07:1983. https://doi.org/10.3389/fmicb.2016.01983 Shao Y, Zhang W, Guo H et al (2015) Comparative studies on antibiotic resistance in Lactobacillus casei and Lactobacillus plantarum. Food Control 50:250–258. https://doi.org/10.1016/j.foodcont.2014.09.003 Klarin B, Larsson A, Molin G, Jeppsson B (2019) Susceptibility to antibiotics in isolates of Lactobacillus plantarum RAPD -type Lp299v, harvested from antibiotic treated, critically ill patients after administration of probiotics. Microbiologyopen 8:e00642. https://doi.org/10.1002/mbo3.642 Cheng KW, Tseng CH, Tzeng CC et al (2019) Pharmacological inhibition of bacterial β-glucuronidase prevents irinotecan-induced diarrhea without impairing its antitumor efficacy in vivo. Pharmacol Res 139:41–49. https://doi.org/10.1016/j.phrs.2018.10.029 Son SH, Jeon HL, Jeon EB et al (2017) Potential probiotic Lactobacillus plantarum Ln4 from kimchi: evaluation of β-galactosidase and antioxidant activities. LWT - Food Sci Technol 85:181–186. https://doi.org/10.1016/j.lwt.2017.07.018 Abdulhussain Kareem R, Razavi SH (2020) Plantaricin bacteriocins: as safe alternative antimicrobial peptides in food preservation—A review. J Food Saf 40:e12735. https://doi.org/10.1111/jfs.12735 Diep DB, Straume D, Kjos M et al (2009) An overview of the mosaic bacteriocin pln loci from Lactobacillus plantarum. Peptides 30:1562–1574 da Silva SS, Vitolo M, González JMD, de Oliveira RPS (2014) Overview of Lactobacillus plantarum as a promising bacteriocin producer among lactic acid bacteria. Food Res Int 64:527–536. https://doi.org/10.1016/j.foodres.2014.07.041 Calasso M, Di CR, De AM et al (2013) Effects of the peptide pheromone plantaricin a and cocultivation with Lactobacillus sanfranciscensis DPPMA174 on the exoproteome and the adhesion capacity of Lactobacillus plantarum DC400. Appl Environ Microbiol 79:2657–2669. https://doi.org/10.1128/AEM.03625-12 Kubota H, Senda S, Nomura N et al (2008) Biofilm formation by lactic acid bacteria and resistance to environmental stress. J Biosci Bioeng 106:381–386. https://doi.org/10.1263/jbb.106.381 Kubota H, Senda S, Tokuda H et al (2009) Stress resistance of biofilm and planktonic Lactobacillus plantarum subsp. plantarum JCM 1149. Food Microbiol 26:592–597. https://doi.org/10.1016/j.fm.2009.04.001 Fernández Ramírez MD, Smid EJ, Abee T, Nierop Groot MN (2015) Characterisation of biofilms formed by Lactobacillus plantarum WCFS1 and food spoilage isolates. Int J Food Microbiol 207:23–29. https://doi.org/10.1016/j.ijfoodmicro.2015.04.030 Aoudia N, Rieu A, Briandet R et al (2016) Biofilms of Lactobacillus plantarum and Lactobacillus fermentum: Effect on stress responses, antagonistic effects on pathogen growth and immunomodulatory properties. Food Microbiol 53:51–59. https://doi.org/10.1016/j.fm.2015.04.009 Monteagudo-Mera A, Rastall RA, Gibson GR et al (2019) Adhesion mechanisms mediated by probiotics and prebiotics and their potential impact on human health. Appl Microbiol Biotechnol 103:6463–6472 Collado MC, Gueimonde M, Salminen S (2010) Probiotics in adhesion of pathogens. Bioactive foods in promoting health. Elsevier, Amsterdam, pp 353–370 Zhang K, Riba A, Nietschke M et al (2018) Minimal SPI1-T3SS effector requirement for Salmonella enterocyte invasion and intracellular proliferation in vivo. PLoS Pathog 14:e1006925. https://doi.org/10.1371/journal.ppat.1006925 Buntin N, de Vos WM, Hongpattarakere T (2017) Variation of mucin adhesion, cell surface characteristics, and molecular mechanisms among Lactobacillus plantarum isolated from different habitats. Appl Microbiol Biotechnol 101:7663–7674. https://doi.org/10.1007/s00253-017-8482-3 Segers ME, Lebeer S (2014) Towards a better understanding of Lactobacillus rhamnosus GG - host interactions. Microb Cell Fact 13:S7. https://doi.org/10.1186/1475-2859-13-S1-S7 Bueno SM, Riquelme S, Riedel CA, Kalergis AM (2012) Mechanisms used by virulent Salmonella to impair dendritic cell function and evade adaptive immunity. Immunology 137:28–36. https://doi.org/10.1111/j.1365-2567.2012.03614.x Bermudez-Brito M, Muñoz-Quezada S, Gómez-Llorente C et al (2015) Lactobacillus paracasei CNCM I-4034 and its culture supernatant modulate Salmonella-induced inflammation in a novel transwell co-culture of human intestinal-like dendritic and Caco-2 cells. BMC Microbiol 15:1–15. https://doi.org/10.1186/s12866-015-0408-6 Wan MLY, Chen Z, Shah NP, El-Nezami H (2018) Effects of Lactobacillus rhamnosus GG and Escherichia coli Nissle 1917 cell-free supernatants on modulation of mucin and cytokine secretion on human intestinal epithelial HT29-MTX cells. J Food Sci 83:1999–2007. https://doi.org/10.1111/1750-3841.14168 Mukai T, Asasaka T, Sato E et al (2002) Inhibition of binding of Helicobacter pylori to the glycolipid receptors by probiotic Lactobacillus reuteri. FEMS Immunol Med Microbiol 32:105–110. https://doi.org/10.1111/j.1574-695x.2002.tb00541.x