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1.
Cell Mol Neurobiol ; 44(1): 60, 2024 Sep 17.
Article in English | MEDLINE | ID: mdl-39287687

ABSTRACT

Microglia are macrophage cells residing in the brain, where they exert a key role in neuronal protection. Through the gut-brain axis, metabolites produced by gut commensal microbes can influence brain functions, including microglial activity. The nuclear factor erythroid 2-related factor 2 (NRF2) is a key regulator of the oxidative stress response in microglia, controlling the expression of cytoprotective genes. Lactobacilli-derived cell-free supernatants (CFSs) are postbiotics that have shown antioxidant and immunomodulatory effects in several in vitro and in vivo studies. This study aimed to explore the effects of lactobacilli CFSs on modulating microglial responses against oxidative stress and inflammation. HMC3 microglia were exposed to lipopolysaccaride (LPS), as an inflammatory trigger, before and after administration of CFSs from three human gut probiotic species. The NRF2 nuclear protein activation and the expression of NRF2-controlled antioxidant genes were investigated by immunoassay and quantitative RT-PCR, respectively. Furthermore, the level of pro- and anti-inflammatory cytokines was evaluated by immunoassay. All CFSs induced a significant increase of NRF2 nuclear activity in basal conditions and upon inflammation. The transcription of antioxidant genes, namely heme oxygenase 1, superoxide dismutase (SOD), glutathione-S transferase, glutathione peroxidase, and catalase also increased, especially after inflammatory stimulus. Besides, higher SOD1 activity was detected relative to inflamed microglia. In addition, CFSs pre-treatment of microglia attenuated pro-inflammatory TNF-α levels while increasing anti-inflammatory IL-10 levels. These findings confirmed that gut microorganisms' metabolites can play a relevant role in adjuvating the microglia cellular response against neuroinflammation and oxidative stress, which are known to cause neurodegenerative diseases.


Subject(s)
Inflammation , Lactobacillus , Microglia , NF-E2-Related Factor 2 , Oxidative Stress , Signal Transduction , Superoxide Dismutase-1 , Humans , NF-E2-Related Factor 2/metabolism , Oxidative Stress/drug effects , Oxidative Stress/physiology , Microglia/metabolism , Microglia/drug effects , Inflammation/metabolism , Inflammation/pathology , Signal Transduction/drug effects , Superoxide Dismutase-1/metabolism , Lipopolysaccharides/pharmacology , Cytokines/metabolism , Antioxidants/metabolism , Antioxidants/pharmacology , Cell Line
2.
Biotechnol Lett ; 43(3): 645-654, 2021 Mar.
Article in English | MEDLINE | ID: mdl-33156458

ABSTRACT

OBJECTIVE: We investigated whether the knock out of small heat shock protein (sHSP) genes (hsp1, hsp2 and hsp3) impact on probiotic features of Lactiplantibacillus plantarum WCFS1, aiming to find specific microbial effectors involved in microbe-host interplay. RESULTS: The probiotic properties of L. plantarum WCFS1 wild type, hsp1, hsp2 and hsp3 mutant clones were evaluated and compared through in vitro trials. Oro-gastro-intestinal assays pointed to significantly lower survival for hsp1 and hsp2 mutants under stomach-like conditions, and for hsp3 mutant under intestinal stress. Adhesion to human enterocyte-like cells was similar for all clones, though the hsp2 mutant exhibited higher adhesiveness. L. plantarum cells attenuated the transcriptional induction of pro-inflammatory cytokines on lipopolysaccharide-treated human macrophages, with some exception for the hsp1 mutant. Intriguingly, this clone also induced a higher IL10/IL12 ratio, which is assumed to indicate the anti-inflammatory potential of probiotics. CONCLUSIONS: sHSP genes deletion determined some differences in gut stress resistance, cellular adhesion and immuno-modulation, also implying effects on in vivo interaction with the host. HSP1 might contribute to immunomodulatory mechanisms, though additional experiments are necessary to test this feature.


Subject(s)
Bacterial Proteins/genetics , Gastrointestinal Microbiome , Heat-Shock Proteins, Small/genetics , Lactobacillus plantarum , Probiotics , Bacterial Adhesion/genetics , Bacterial Proteins/metabolism , Caco-2 Cells , Cells, Cultured , Cytokines/metabolism , Enterocytes/metabolism , Gastrointestinal Microbiome/genetics , Gastrointestinal Microbiome/immunology , Gene Knockout Techniques , Heat-Shock Proteins, Small/metabolism , Host Microbial Interactions/genetics , Host Microbial Interactions/immunology , Humans , Lactobacillus plantarum/genetics , Lactobacillus plantarum/immunology , THP-1 Cells
3.
Int J Mol Sci ; 22(21)2021 Nov 08.
Article in English | MEDLINE | ID: mdl-34769500

ABSTRACT

Lactiplantibacillus plantarum (L. plantarum) is a well-studied and versatile species of lactobacilli. It is found in several niches, including human mucosal surfaces, and it is largely employed in the food industry and boasts a millenary tradition of safe use, sharing a long-lasting relationship with humans. L. plantarum is generally recognised as safe and exhibits a strong probiotic character, so that several strains are commercialised as health-promoting supplements and functional food products. For these reasons, L. plantarum represents a valuable model to gain insight into the nature and mechanisms of antimicrobials as key factors underlying the probiotic action of health-promoting microbes. Probiotic antimicrobials can inhibit the growth of pathogens in the gut ensuring the intestinal homeostasis and contributing to the host health. Furthermore, they may be attractive alternatives to conventional antibiotics, holding potential in several biomedical applications. The aim of this review is to investigate the most relevant papers published in the last ten years, bioprospecting the antimicrobial activity of characterised probiotic L. plantarum strains. Specifically, it focuses on the different chemical nature, the action spectra and the mechanisms underlying the bioactivity of their antibacterial and antiviral agents. Emerging trends in postbiotics, some in vivo applications of L. plantarum antimicrobials, including strengths and limitations of their therapeutic potential, are addressed and discussed.


Subject(s)
Anti-Infective Agents/pharmacology , Bioprospecting/methods , Lactobacillaceae/metabolism , Probiotics/pharmacology , Animals , Humans , Lactobacillaceae/chemistry , Lactobacillaceae/isolation & purification , Probiotics/chemistry , Probiotics/metabolism
4.
Crit Rev Food Sci Nutr ; 60(9): 1552-1580, 2020.
Article in English | MEDLINE | ID: mdl-30880406

ABSTRACT

The dietary consumption of probiotics in the form of pharmaceuticals or functional food can improve human health and contribute to disease prevention. However, the biological activity and health potential of food-delivered probiotics can be severely compromised by the stress conditions encountered by the microorganisms throughout the manufacture process, from probiotic preparation to their inclusion into food, subsequent storage and ingestion. Here, we give an account of the stress factors that can have major negative impacts on probiotic viability and functionality, with a focus on food-related environmental adverse conditions. We also describe some of the mechanisms elicited by the microbial cells to counteract these stresses and summarize a few relevant approaches proposed in literature to develop more robust and competitive probiotics by enhancing their stress tolerance, with the aim to improve the efficacy and health value of probiotic functional food.


Subject(s)
Microbial Viability , Probiotics/standards , Functional Food/microbiology , Functional Food/standards , Humans , Stress, Physiological
5.
Appl Microbiol Biotechnol ; 104(13): 5759-5772, 2020 Jul.
Article in English | MEDLINE | ID: mdl-32388761

ABSTRACT

The influence of riboflavin (B2)-overproducing lactobacilli on the antioxidant status, isoflavone conversion, off-flavor reduction, amino acid profile, and viscosity of B2-bio-enriched fermented soymilk was investigated. Results showed that B2 in fermented soymilk was notably increased from 0.2 to 3.8 µg/mL for Lactobacillus fermentum UFG169 and to 1.9 µg/mL for Lactobacillus plantarum UFG10. The apparent viscosity significantly changed with rising acidity and agglutination of protein. The off-flavor volatile substances (hexanal and nonanal) were significantly reduced in fermented soymilk. Furthermore, a large amount of glucoside form isoflavones was deglycosylated into bioactive aglycones after 4 h up to 32 h. B2 content and isoflavones significantly improved the antioxidant status of soymilk. Partial least squares regression analysis correlated the strain activity and fermentation time with the improved nutritional and functional soymilk qualities. This study demonstrated the strategy for strain development for B2-bio-enriched fermentation to extend the health-promoting benefits of soymilk and soy-related foods. KEY POINTS: • B2-enriched fermentation enhanced the nutrition and functional status of soymilk. • Fermentation time significantly affected the apparent viscosity of fermented soymilk. • Off-flavor volatile substances were significantly reduced or even diminished. • Increased B2and bioactive isoflavones contributed to improved antioxidant potential.


Subject(s)
Fermented Foods/microbiology , Functional Food/microbiology , Lactobacillus/metabolism , Riboflavin/metabolism , Soy Milk , Antioxidants/analysis , Antioxidants/metabolism , Biotransformation , Colony Count, Microbial , Fermentation , Fermented Foods/analysis , Food Microbiology , Functional Food/analysis , Hydrogen-Ion Concentration , Isoflavones/analysis , Isoflavones/metabolism , Lactobacillus/classification , Lactobacillus/growth & development , Microbial Viability , Viscosity , Volatile Organic Compounds/analysis , Volatile Organic Compounds/metabolism
6.
Food Microbiol ; 77: 61-68, 2019 Feb.
Article in English | MEDLINE | ID: mdl-30297057

ABSTRACT

Cereal-based functional beverages represent social, economic, and environmental sustainable opportunities to cope with emerging trends in food consumption and global nutrition. Here we report, for the first time, the polyphasic characterization of three cereal-based kefir-like riboflavin-enriched beverages, obtained from oat, maize and barley flours, and their comparison with classical milk-based kefir. The four matrices were successfully fermented with commercial starters: i) milk-kefir and ii) water-kefir, proving the potential of cereal ingredients in the formulation of dairy-like fermented beverages with milk-kefir starter behavior better in these matrices. In the light of their potentiality, seven riboflavin-producing Andean Lactic Acid Bacteria (LAB) were tested for tolerance to food stresses commonly encountered during food fermentation. Moreover, the LAB strains investigated were screened for spontaneous riboflavin overproducing derivatives. Lactobacillus plantarum M5MA1-B2 with outstanding response to stress, was selected to improve riboflavin content in an in situ fortification approach. The combination of L. plantarum M5MA1-B2 riboflavin overproducing strain with milk kefir starter in oat, lead to cover, for one serving of 100 g, 11.4% of Recommended Dietary Allowance (RDA). Besides, addition of L. plantarum M5MA1-B2 improved performance of water kefir in oat and maize matrices. Proton Transfer Reaction Time-of-Flight Mass Spectrometry (PTR-ToF-MS) analysis provided the on-line Volatile Organic Compounds profiles supporting the best combination of starter, LAB and cereal matrix for novel functional foods development.


Subject(s)
Beverages/microbiology , Edible Grain/microbiology , Kefir/microbiology , Lactobacillales/metabolism , Riboflavin/metabolism , Animals , Avena , Cultured Milk Products , Edible Grain/anatomy & histology , Fermentation , Flour , Food Microbiology , Kefir/analysis , Lactobacillus plantarum/metabolism , Leuconostoc mesenteroides/metabolism , Milk/microbiology , Recommended Dietary Allowances , Volatile Organic Compounds/metabolism , Zea mays
7.
Int J Mol Sci ; 20(16)2019 Aug 15.
Article in English | MEDLINE | ID: mdl-31443334

ABSTRACT

This study reports the first application of a next generation sequencing (NGS) analysis. The analysis was designed to monitor the effect of the management of microbial resources associated with alcoholic fermentation on spontaneous malolactic consortium. Together with the analysis of 16S rRNA genes from the metagenome, we monitored the principal parameters linked to MLF (e.g., malic and lactic acid concentration, pH). We encompass seven dissimilar concrete practices to manage microorganisms associated with alcoholic fermentation: Un-inoculated must (UM), pied-de-cuve (PdC), Saccharomyces cerevisiae (SC), S. cerevisiae and Torulaspora delbrueckii co-inoculated and sequentially inoculated, as well as S. cerevisiae and Metschnikowia pulcherrima co-inoculated and sequentially inoculated. Surprisingly, each experimental modes led to different taxonomic composition of the bacterial communities of the malolactic consortia, in terms of prokaryotic phyla and genera. Our findings indicated that, uncontrolled AF (UM, PdC) led to heterogeneous consortia associated with MLF (with a relevant presence of the genera Acetobacter and Gluconobacter), when compared with controlled AF (SC) (showing a clear dominance of the genus Oenococcus). Effectively, the SC trial malic acid was completely degraded in about two weeks after the end of AF, while, on the contrary, malic acid decarboxylation remained uncomplete after 7 weeks in the case of UM and PdC. In addition, for the first time, we demonstrated that both (i) the inoculation of different non-Saccharomyces (T. delbrueckii and M. pulcherrima) and, (ii) the inoculation time of the non-Saccharomyces with respect to S. cerevisiae resources (co-inoculated and sequentially inoculated) influence the composition of the connected MLF consortia, modulating MLF performance. Finally, we demonstrated the first findings of delayed and inhibited MLF when M. pulcherrima, and T. delbrueckii were inoculated, respectively. In addition, as a further control test, we also assessed the effect of the inoculation with Oenococcus oeni and Lactobacillus plantarum at the end of alcoholic fermentation, as MLF starter cultures. Our study suggests the potential interest in the application of NGS analysis, to monitor the effect of alcoholic fermentation on the spontaneous malolactic consortium, in relation to wine.


Subject(s)
Metagenome/genetics , Wine/microbiology , Fermentation/genetics , Fermentation/physiology , Lactobacillales/genetics , Lactobacillales/metabolism , Lactobacillus plantarum/genetics , Lactobacillus plantarum/metabolism , RNA, Ribosomal, 16S , Saccharomyces cerevisiae/genetics , Saccharomyces cerevisiae/metabolism , Torulaspora/genetics , Torulaspora/metabolism
8.
Appl Microbiol Biotechnol ; 102(23): 9949-9958, 2018 Dec.
Article in English | MEDLINE | ID: mdl-30280241

ABSTRACT

Lactic acid bacteria (LAB), a heterogeneous group of bacteria that produce lactic acid as the main product of carbohydrate degradation, play an important role in the production and protection of fermented foods. Moreover, beside the technological use of these microorganisms added to control and steer food fermentations, their beneficial healthy properties are largely overt. Thus, numerous LAB strains have obtained the probiotic status, which entails the ability to maintain and promote a good health of consumers. In particular, increasing consideration is being focused on probiotic microorganisms that can improve the human immune response against dangerous viral and fungal enemies. For such beneficial microbes, the term "immunobiotics" has been coined. Together with an indirect host-mediated adverse effect against undesirable microorganisms, also a direct antagonistic activity of several LAB strains has been largely demonstrated. The purpose of this review is to provide a fullest possible overview of the antiviral and antifungal activities ascribed to probiotic LAB. The interest in this research field is substantiated by a large number of studies exploring the potential application of these beneficial microorganisms both as biopreservatives and immune-enhancers, aiming to reduce and/or eliminate the use of chemical agents to prevent the development of pathogenic, infectious, and/or degrading causes.


Subject(s)
Biological Control Agents/pharmacology , Lactobacillales , Animals , Anti-Infective Agents/pharmacology , Antifungal Agents/pharmacology , Antiviral Agents/pharmacology , Bacteriocins/biosynthesis , Bacteriocins/pharmacology , Fermentation , Humans , Probiotics
9.
Appl Microbiol Biotechnol ; 102(22): 9871, 2018 11.
Article in English | MEDLINE | ID: mdl-30328491

ABSTRACT

There is an error in the original publication of this paper. The incorrect author name was captured as "Djamel Dridier" instead of "Djamel Drider". The original article has been corrected.

10.
Appl Microbiol Biotechnol ; 102(2): 569-576, 2018 Jan.
Article in English | MEDLINE | ID: mdl-29189899

ABSTRACT

Brettanomyces bruxellensis is a common and significant wine spoilage microorganism. B. bruxellensis strains generally detain the molecular basis to produce compounds that are detrimental for the organoleptic quality of the wine, including some classes of volatile phenols that derive from the sequential bioconversion of specific hydroxycinnamic acids such as ferulate and p-coumarate. Although B. bruxellensis can be detected at any stage of the winemaking process, it is typically isolated at the end of the alcoholic fermentation (AF), before the staring of the spontaneous malolactic fermentation (MLF) or during barrel aging. For this reason, the endemic diffusion of B. bruxellensis leads to consistent economic losses in the wine industry. Considering the interest in reducing sulfur dioxide use during winemaking, in recent years, biological alternatives, such as the use of tailored selected yeast and bacterial strains inoculated to promote AF and MLF, are actively sought as biocontrol agents to avoid the "Bretta" character in wines. Here, we review the importance of dedicated characterization and selection of starter cultures for AF and MLF in wine, in order to reduce or prevent both growth of B. bruxellensis and its production of volatile phenols in the matrix.


Subject(s)
Biological Control Agents , Brettanomyces/growth & development , Fermentation , Food Microbiology , Wine/microbiology , Alcohols/metabolism , Coumaric Acids/metabolism , Food Contamination/prevention & control , Lactobacillales/metabolism , Malates/metabolism , Phenols/analysis , Saccharomyces cerevisiae/metabolism , Vitis/microbiology
11.
Int J Mol Sci ; 18(7)2017 Jul 21.
Article in English | MEDLINE | ID: mdl-28754020

ABSTRACT

Bacterial exopolysaccharides produced by lactic acid bacteria are of increasing interest in the food industry, since they might enhance the technological and functional properties of some edible matrices. In this work, Pediococcus parvulus 2.6, which produces an O2-substituted (1,3)-ß-d-glucan exopolysaccharide only synthesised by bacteria, was proposed as a starter culture for the production of three cereal-based fermented foods. The obtained fermented matrices were naturally bio-fortified in microbial ß-glucans, and used to investigate the prebiotic potential of the bacterial exopolysaccharide by analysing the impact on the survival of a probiotic Lactobacillus plantarum strain under starvation and gastrointestinal simulated conditions. All of the assays were performed by using as control of the P. parvulus 2.6's performance, the isogenic ß-glucan non-producing 2.6NR strain. Our results showed a differential capability of P. parvulus to ferment the cereal flours. During the fermentation step, the ß-glucans produced were specifically quantified and their concentration correlated with an increased viscosity of the products. The survival of the model probiotic L. plantarum WCFS1 was improved by the presence of the bacterial ß-glucans in oat and rice fermented foods under starvation conditions. The probiotic bacteria showed a significantly higher viability when submitted to a simulated intestinal stress in the oat matrix fermented by the 2.6 strain. Therefore, the cereal flours were a suitable substrate for in situ bio-fortification with the bacterial ß-glucan, and these matrices could be used as carriers to enhance the beneficial properties of probiotic bacteria.


Subject(s)
Edible Grain/microbiology , Pediococcus/growth & development , beta-Glucans/metabolism , Avena/microbiology , Fermentation , Food Microbiology , Lactobacillus plantarum/drug effects , Oryza/microbiology , Pediococcus/metabolism , Prebiotics/microbiology , Probiotics , beta-Glucans/pharmacology
12.
Food Microbiol ; 57: 187-94, 2016 Aug.
Article in English | MEDLINE | ID: mdl-27052718

ABSTRACT

Malolactic fermentation (MLF) is a secondary fermentation in wine that usually takes place during or at the end of alcoholic fermentation. Lactobacillus plantarum is able to conduct MLF (particularly under high pH conditions and in co-inoculation with yeasts), and some strains are commercially used as MLF starter cultures. Recent evidences suggest a further use of selected L. plantarum strains for the pre-alcoholic acidification of grape must. In this study, we have carried out an integrated (molecular, technological, and biotechnological) characterization of L. plantarum strains isolated from Apulian wines in order to combine the two protechnological features (MLF performances and must acidification aptitudes). Several parameters such as sugar, pH and ethanol tolerance, resistance to lyophilisation and behaviour in grape must were evaluated. Moreover, the expression of stress gene markers was investigated and was linked to the ability of L. plantarum strains to grow and perform MLF. Co-inoculation of Saccharomyces cerevisiae and L. plantarum in grape must improves the bacterial adaptation to harsh conditions of wine and reduced total fermentation time. For the first time, we applied a polyphasic approach for the characterization of L. plantarum in reason of the MLF performances. The proposed procedure can be generalized as a standard method for the selection of bacterial resources for the design of MLF starter cultures tailored for high pH must.


Subject(s)
Industrial Microbiology/methods , Lactobacillus plantarum/metabolism , Vitis/microbiology , Wine/microbiology , Fermentation , Hydrogen-Ion Concentration , Lactobacillus plantarum/chemistry , Lactobacillus plantarum/genetics , Lactobacillus plantarum/isolation & purification , Malates/metabolism , Saccharomyces cerevisiae/metabolism , Vitis/chemistry , Vitis/metabolism , Wine/analysis
13.
Food Microbiol ; 59: 196-204, 2016 Oct.
Article in English | MEDLINE | ID: mdl-27375260

ABSTRACT

The spoilage potential of Brettanomyces bruxellensis in wine is strongly connected with the aptitude of this yeast to enter in a Viable But Non Culturable (VBNC) state when exposed to the harsh wine conditions. In this work, we characterized the VBNC behaviour of seven strains of B. bruxellensis representing a regional intraspecific biodiversity, reporting conclusive evidence for the assessment of VBNC as a strain-dependent character. The VBNC behaviour was monitored by fluorescein diacetate staining/flow cytometry for eleven days after addition of 0.4, 0.6, 0.8, 1 and 1.2 mg/L of molecular SO2 (entrance in the VBNC state) and after SO2 removal (exit from the VBNC state). Furthermore, one representative strain was selected and RNA-seq analysis performed after exposure to 1.2 mg/L SO2 and during the recovery phase. 30 and 1634 genes were identified as differentially expressed following VBNC entrance and 'resuscitation', respectively. The results reported strongly suggested that the entrance in the SO2-induced VBNC state in B. bruxellensis is associated with both, sulfite toxicity and oxidative stress response, confirming the crucial role of genes/proteins involved in redox cell homeostasis. Among the genes induced during recovery, the expression of genes involved in carbohydrate metabolism and encoding heat shock proteins, as well as enriched categories including amino acid transport and transporter activity was observed. The evidences of a general repression of genes involved in DNA replication suggest the occurrence of a true resuscitation of cell rather than a simple regrowth.


Subject(s)
Brettanomyces/genetics , Brettanomyces/physiology , Food Microbiology , Microbial Viability , Wine/microbiology , Brettanomyces/drug effects , Brettanomyces/growth & development , Carbohydrate Metabolism/genetics , Colony Count, Microbial/methods , Culture Media , Gene Expression Profiling , Heat-Shock Proteins/genetics , Homeostasis , Oxidation-Reduction , Oxidative Stress/genetics , Phenols/metabolism , Sulfites , Sulfur Dioxide/pharmacology , Wine/analysis
14.
Appl Microbiol Biotechnol ; 99(8): 3479-90, 2015 Apr.
Article in English | MEDLINE | ID: mdl-25586576

ABSTRACT

A critical feature of probiotic microorganisms is their ability to colonize the intestine of the host. Although the microbial potential to adhere to the human gut lumen has been investigated in in vitro models, there is still much to discover about their in vivo behaviour. Zebrafish is a vertebrate model that is being widely used to investigate various biological processes shared with humans. In this work, we report on the use of the zebrafish model to investigate the in vivo colonization ability of previously characterized probiotic lactic acid bacteria. Lactobacillus plantarum Lp90, L. plantarum B2 and Lactobacillus fermentum PBCC11.5 were fluorescently tagged by transfer of the pRCR12 plasmid, which encodes the mCherry protein and which was constructed in this work. The recombinant bacteria were used to infect germ-free zebrafish larvae. After removal of bacteria, the colonization ability of the strains was monitored until 3 days post-infection by using a fluorescence stereomicroscope. The results indicated differential adhesion capabilities among the strains. Interestingly, a displacement of bacteria from the medium to the posterior intestinal tract was observed as a function of time that suggested a transient colonization by probiotics. Based on fluorescence observation, L. plantarum strains exhibited a more robust adhesion capability. In conclusion, the use of pRCR12 plasmid for labelling Lactobacillus strains provides a powerful and very efficient tool to monitor the in vivo colonization in zebrafish larvae and to investigate the adhesion ability of probiotic microorganisms.


Subject(s)
Gastrointestinal Tract/microbiology , Genes, Reporter , Lactobacillus plantarum/growth & development , Limosilactobacillus fermentum/growth & development , Luminescent Proteins/analysis , Zebrafish/microbiology , Animals , Limosilactobacillus fermentum/genetics , Lactobacillus plantarum/genetics , Luminescent Proteins/genetics , Microscopy, Fluorescence , Molecular Sequence Data , Plasmids , Sequence Analysis, DNA , Staining and Labeling/methods , Time Factors , Red Fluorescent Protein
15.
Appl Microbiol Biotechnol ; 98(17): 7569-81, 2014 Sep.
Article in English | MEDLINE | ID: mdl-24903812

ABSTRACT

The probiotic potential of Lactobacillus plantarum and Lactobacillus fermentum strains, capable of overproducing riboflavin, was investigated. The riboflavin production was quantified in co-cultures of lactobacilli and human intestinal epithelial cells, and the riboflavin overproduction ability was confirmed. When milk and yogurt were used as carrier matrices, L. plantarum and L. fermentum strains displayed a significant ability to survive through simulated gastrointestinal transit. Adhesion was studied on both biotic and abiotic surfaces. Both strains adhered strongly on Caco-2 cells, negatively influenced the adhesion of Escherichia coli O157:H7, and strongly inhibited the growth of three reference pathogenic microbial strains. Resistance to major antibiotics and potential hemolytic activity were assayed. Overall, this study reveals that these Lactobacillus stains are endowed with promising probiotic properties and thus are candidates for the development of novel functional food which would be both enriched in riboflavin and induce additional health benefits, including a potential in situ riboflavin production, once the microorganisms colonize the host intestine.


Subject(s)
Lactobacillus plantarum/metabolism , Limosilactobacillus fermentum/metabolism , Probiotics/administration & dosage , Riboflavin/metabolism , Antibiosis , Bacterial Adhesion , Caco-2 Cells , Epithelial Cells/microbiology , Escherichia coli O157/physiology , Gastrointestinal Tract/microbiology , Humans , Limosilactobacillus fermentum/physiology , Lactobacillus plantarum/physiology , Models, Theoretical
16.
Appl Microbiol Biotechnol ; 98(8): 3691-700, 2014 Apr.
Article in English | MEDLINE | ID: mdl-24413973

ABSTRACT

Lactobacillus fermentum isolated from sourdough was able to produce riboflavin. Spontaneous roseoflavin-resistant mutants were obtained by exposing the wild strain (named L. fermentum PBCC11) to increasing concentrations of roseoflavin. Fifteen spontaneous roseoflavin-resistant mutants were isolated, and the level of vitamin B2 was quantified by HPLC. Seven mutant strains produced concentrations of vitamin B2 higher than 1 mg L⁻¹. Interestingly, three mutants were unable to overproduce riboflavin even though they were able to withstand the selective pressure of roseoflavin. Alignment of the rib leader region of PBCC11 and its derivatives showed only point mutations at two neighboring locations of the RFN element. In particular, the highest riboflavin-producing isolates possess an A to G mutation at position 240, while the lowest riboflavin producer carries a T to A substitution at position 236. No mutations were detected in the derivative strains that did not have an overproducing phenotype. The best riboflavin overproducing strain, named L. fermentum PBCC11.5, and its parental strain were used to fortify bread. The effect of two different periods of fermentation on the riboflavin level was compared. Bread produced using the coinoculum yeast and L. fermentum PBCC11.5 led to an approximately twofold increase of final vitamin B2 content.


Subject(s)
Bread , Limosilactobacillus fermentum/growth & development , Limosilactobacillus fermentum/metabolism , Metabolic Engineering , Riboflavin/isolation & purification , Riboflavin/metabolism , Chromatography, High Pressure Liquid , DNA Mutational Analysis , Drug Tolerance , Food Handling/methods , Limosilactobacillus fermentum/drug effects , Limosilactobacillus fermentum/genetics , Mutation , Riboflavin/analogs & derivatives , Riboflavin/toxicity , Saccharomyces cerevisiae/growth & development , Saccharomyces cerevisiae/metabolism
17.
Int J Mol Sci ; 15(2): 3025-39, 2014 Feb 20.
Article in English | MEDLINE | ID: mdl-24562330

ABSTRACT

Currently, the majority of prebiotics in the market are derived from non-digestible oligosaccharides. Very few studies have focused on non-digestible long chain complex polysaccharides in relation to their potential as novel prebiotics. Cereals ß-glucans have been investigated for immune-modulating properties and beneficial effects on obesity, cardiovascular diseases, diabetes, and cholesterol levels. Moreover, ß-glucans have been reported to be highly fermentable by the intestinal microbiota in the caecum and colon, and can enhance both growth rate and lactic acid production of microbes isolated from the human intestine. In this work, we report the effects of food matrices containing barley ß-glucans on growth and probiotic features of four Lactobacillus strains. Such matrices were able to improve the growth rate of the tested bacteria both in unstressed conditions and, importantly, after exposure to in vitro simulation of the digestive tract. Moreover, the effect of ß-glucans-containing food on bacterial adhesion to enterocyte-like cells was analyzed and a positive influence on probiotic-enterocyte interaction was observed.


Subject(s)
Edible Grain/metabolism , Lactobacillus/growth & development , beta-Glucans/chemistry , Caco-2 Cells , Cell Adhesion/drug effects , Humans , Lactobacillus/drug effects , Probiotics , beta-Glucans/pharmacology
18.
Recenti Prog Med ; 105(4): 159-65, 2014 Apr.
Article in Italian | MEDLINE | ID: mdl-24770542

ABSTRACT

The Italian Law no. 38/2010 requires that the physician reports in the medical record the type and the intensity of pain, analgesic therapies and clinical results. We developed a training model for 256 primary care physicians (GPs). After a period of intensive training on the content of the law no. 38, diagnostic and pharmacological approach of pain, we carried out a clinical audit by a web based clinical record to assess doctor's compliance to Law no. 38 and the use of opioids. 2631 patients were assessed (age 71,5±13,7 years; median 74). The mean of chronic non oncologic pain intesity was 5.41±2.0 (static) and 6.10±2.32 (dynamic). After a systematic measurement of pain, a better control of patients was achieved (2.22±2.12 points lower for static, 2.37±2.34 lower for dynamic pain (p<0.001 vs basal time). An increased use of opioids have been detected. GPs have also used strong opioids in opioid-naïve patients, avoiding the first or the second step if intensity of pain detected was severe. In fact, a greater pain control was achieved with oxycodone compared to tramadol or codeine (all of them with normal release and combined with acetaminophen). Chronic non cancer pain remains one of the major clinical problems in the primary care setting, especially in the elderly. The standard measurement of parameters related to pain and the proper use of opioids depends on the scientific update and how this is delivered. GPs are crucial to implement the Law 38 and to increase the degree of complexity of the patient to be properly admitted to a SPOKE/HUB center.


Subject(s)
Legislation, Drug , Pain Management/methods , Practice Patterns, Physicians'/legislation & jurisprudence , Primary Health Care/methods , Aged , Aged, 80 and over , Analgesics/therapeutic use , Analgesics, Opioid/therapeutic use , Clinical Audit , Education, Medical, Continuing/methods , Female , Humans , Internet , Italy , Male , Middle Aged , Pain/drug therapy , Primary Health Care/legislation & jurisprudence
19.
Int J Food Microbiol ; 416: 110684, 2024 May 02.
Article in English | MEDLINE | ID: mdl-38513545

ABSTRACT

Urease operon is highly conserved within the species Streptococcus thermophilus and urease-negative strains are rare in nature. S. thermophilus MIMO1, isolated from commercial yogurt, was previously characterized as urease-positive Ni-dependent strain. Beside a mutation in ureQ, coding for a nickel ABC transporter permease, the strain MIMO1 showed a mutation in ureE gene which code for a metallochaperone involved in Ni delivery to the urease catalytic site. The single base mutation in ureE determined a substitution of Asp29 with Asn29 in the metallochaperone in a conserved protein region not involved in the catalytic activity. With the aim to investigate the role Asp29vs Asn29 substitution in UreE on the urease activity of S. thermophilus, ureE gene of the reference strain DSM 20617T (ureEDSM20617) was replaced by ureE gene of strain MIMO1 (ureEMIMO1) to obtain the recombinant ES3. In-gel detection of urease activity revealed that the substitution of Asp29 with Asn29 in UreE resulted in a higher stability of the enzyme complexes. Moreover, the recombinant ES3 showed higher level of urease activity compared to the wildtype without any detectable increase in the expression level of ureC gene, thus highlighting the role of UreE not only in Ni assembly but also on the level of urease activity. During the growth in milk, the recombinant ES3 showed an anticipated urease activity compared to the wildtype, and analogous milk fermentation performance. The overall data obtained by comparing urease-positive and urease-negative strains/mutants confirmed that urease activity strongly impacts on the milk fermentation process and specifically on the yield of the homolactic fermentation.


Subject(s)
Streptococcus thermophilus , Urease , Animals , Urease/genetics , Streptococcus thermophilus/metabolism , Metallochaperones/metabolism , Carrier Proteins/genetics , Nickel/metabolism , Hydrolysis , Milk/metabolism , Urea , Fermentation , Bacterial Proteins/genetics
20.
Int J Food Microbiol ; 426: 110908, 2024 Sep 07.
Article in English | MEDLINE | ID: mdl-39270612

ABSTRACT

Riboflavin (vitamin B2) is essential for human beings and it has to be provided by healthy nutrition. The use of fermentation with riboflavin-overproducing lactic acid bacteria (LAB) represents an ideal strategy to generate, by in situ biofortification, functional drinks. These beverages can positively contribute to consumer health and address nutritional deficiencies. In the present work, the functional capabilities of Weissella cibaria BAL3C-5 C120T for riboflavin-overproduction and dextran-production during fermentation of oat-, rice-, soybean- and almond-based drinks have been evaluated. It was confirmed that the strain was capable of producing riboflavin and dextran in the analysed drinks. This property was especially pronounced in the oat-based drink, where after 24 h of fermentation the strain was able to increase riboflavin and dextran levels up to 3.4 mg/L and 3.2 g/L, respectively. Moreover, under optimized conditions the strain was able to enrich the fermented oat-based drinks with the prebiotic oligosaccharide panose (up to 6.6 g/L). In addition, in the oat-based drinks BAL3C-5 C120T showed a good pH-lowering ability (from 7.0 to 3.8) as well as a high 80 % cell viability after one month of storage. Rheological analysis of the resulting fermented oat-based beverages revealed a thixotropic structure related to a gel-like behaviour which was not observed in the non-fermented control drinks. In summary, these results confirmed the unique characteristics of W. cibaria BAL3C-5 C120T strain for the development of biofortified and functional plant-based beverages with improved nutritional and rheological properties. Analysis of the BAL3C-5 C120T strain survival under gastrointestinal conditions and its autoaggregation properties, also indicated its potential use as a probiotic delivered in an oat-based fermented beverage. In this context, this study also promotes the utilization of W. cibaria species in health and food industries where it has not yet been used as a starter or adjunct culture.

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