Data di Pubblicazione:
2015
Citazione:
EXPLORING LACTOBACILLUS PARACASEI PROBIOSIS AND METABOLIC POTENTIAL / S. Balzaretti ; tutor: S. Guglielmetti ; co-tutor: S. Iametti ; coordinator: M.G. Fortina. DIPARTIMENTO DI SCIENZE PER GLI ALIMENTI, LA NUTRIZIONE E L'AMBIENTE, 2015 Dec 10. 28. ciclo, Anno Accademico 2015. [10.13130/s-balzaretti_phd2015-12-10].
Abstract:
Probiotics have been used so far for the prevention and treatment of various medical conditions and to support general wellness: for this reason, they are currently the subject of significant microbiological and clinical research. In fact, a body of literature suggests that including probiotics in the diet can be a strategy to reduce host-related immune diseases and, in general, modulate the intestinal microbiota composition. Although the mechanisms of action of probiotics are still largely unknown, particularly at molecular level, it is well understood that they can act in different ways, through interaction with the other bacteria residing the same niche, as well as the host, at both local and systemic levels. The genus Lactobacillus, which has important industrial applications as fermented food starter and probiotic adjunct, is a taxonomically broad and heterogeneous group and includes the species Lactobacillus paracasei, which is generally associated with habitats rich in nutrients, such as dairy food and human ecosystems, like gut and vagina.
The main purpose of my PhD activity, concerned the study of two L. paracasei strains, named DG and LPC-S01, isolated from two different ecological niches (human gut and vagina, respectively). They are already available on the market, included in two products as food supplements, but their characterization is still incomplete, particularly for LPC-S01. In order to deepen the knowledge about these strains, the first part of the work focused on exploring L. paracasei DG and LPC-S01 essential characteristics to define potential probiotics, by using L. paracasei Shirota as reference strain. The comparative genomic analyses evidenced that strain LPC-S01, a bacterium isolated from human vagina, but plausibly having its origin in the gut, resulted having the genetic features of a niche-generalist member of its species. Similarly, strain DG exhibited the potential ability to adapt to a wide range of environmental conditions if compared with other strains of dairy origin. In vitro tests conventionally used to evidence probiotic properties revealed that strains LPC-S01 and DG possessed comparable ability to resist to gastro-intestinal transit, as evidenced by tolerance to bile, and to decrease NF-κB activation in Caco-2 cells, with respect to strain Shirota. Moreover, LPC-S01 displayed higher tolerance to gastric juice and higher capacity to adhere to Caco-2 epithelial cells (whereas Shirota showed inability to adhere on Caco-2-cells). The in vitro observations were confirmed by setting up a pilot intervention trial on healthy adult volunteers, that demonstrated that LPC-S01 and DG can transiently colonize the gastrointestinal tract of the host, persisting for at least 5 days after the end of a 7-days oral consumption (corresponding to an average of 7 evacuations).
Thanks to the comparative genomic analysis on L. paracasei strains DG and LPC-S01, we identified two gene clusters putatively coding for exopolysaccharides biosynthesis related enzymes. Exopolysaccharides (EPSs), apart from their industrial applications, are found to be associated with many physiological functions, although their mechanism of action has not been fully clarified yet. In collaboration with Prof. Andy Laws, University of Huddersfield (United Kingdom), the second part of the work focused on the identification of the potential EPSs matrix from both strains DG and LPC-S01, and their structural characterization. Nonetheless, in the experimental conditions tested so far, only DG resulted able to synthetize EPSs. After performing its purification, we characterized DG derived EPS repeating unit by NMR spectroscopy based approaches. DG EPS structure resulted peculiar and unique compared to those identified in other la
The main purpose of my PhD activity, concerned the study of two L. paracasei strains, named DG and LPC-S01, isolated from two different ecological niches (human gut and vagina, respectively). They are already available on the market, included in two products as food supplements, but their characterization is still incomplete, particularly for LPC-S01. In order to deepen the knowledge about these strains, the first part of the work focused on exploring L. paracasei DG and LPC-S01 essential characteristics to define potential probiotics, by using L. paracasei Shirota as reference strain. The comparative genomic analyses evidenced that strain LPC-S01, a bacterium isolated from human vagina, but plausibly having its origin in the gut, resulted having the genetic features of a niche-generalist member of its species. Similarly, strain DG exhibited the potential ability to adapt to a wide range of environmental conditions if compared with other strains of dairy origin. In vitro tests conventionally used to evidence probiotic properties revealed that strains LPC-S01 and DG possessed comparable ability to resist to gastro-intestinal transit, as evidenced by tolerance to bile, and to decrease NF-κB activation in Caco-2 cells, with respect to strain Shirota. Moreover, LPC-S01 displayed higher tolerance to gastric juice and higher capacity to adhere to Caco-2 epithelial cells (whereas Shirota showed inability to adhere on Caco-2-cells). The in vitro observations were confirmed by setting up a pilot intervention trial on healthy adult volunteers, that demonstrated that LPC-S01 and DG can transiently colonize the gastrointestinal tract of the host, persisting for at least 5 days after the end of a 7-days oral consumption (corresponding to an average of 7 evacuations).
Thanks to the comparative genomic analysis on L. paracasei strains DG and LPC-S01, we identified two gene clusters putatively coding for exopolysaccharides biosynthesis related enzymes. Exopolysaccharides (EPSs), apart from their industrial applications, are found to be associated with many physiological functions, although their mechanism of action has not been fully clarified yet. In collaboration with Prof. Andy Laws, University of Huddersfield (United Kingdom), the second part of the work focused on the identification of the potential EPSs matrix from both strains DG and LPC-S01, and their structural characterization. Nonetheless, in the experimental conditions tested so far, only DG resulted able to synthetize EPSs. After performing its purification, we characterized DG derived EPS repeating unit by NMR spectroscopy based approaches. DG EPS structure resulted peculiar and unique compared to those identified in other la
Tipologia IRIS:
Tesi di dottorato
Elenco autori:
S. Balzaretti
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