Gut microbiota (GM) dysbiosis has been linked to obesity and its metabolic complications such as cardiovascular disease (CVD). The risk of developing CVD increases with elevated concentration of serum triacylglycerol (TAG). In a blinded, randomised two-arm parallel human intervention study we have previously found that four weeks of supplementation with Lactobacillus paracasei subsp. paracasei L. casei W8® (L. casei W8) compared to placebo reduced the concentration of TAG in 64 young healthy adults, an effect, likely mediated by a decreased stearoyl- CoA desaturase-1 (SCD1) activity. In the present study we analysed faecal samples obtained during the intervention study to investigate whether this effect was related to the ability of L. casei W8 to colonise the human gut after supplementation of L. casei W8 (1010 cfu daily) as determined by qPCR specific for L. paracasei and L. casei (L. casei group); whether L. casei W8 consumption affected GM composition as determined by 16S rRNA gene targeted 454/FLX amplicon sequencing; and whether these changes were associated with changes in TAG concentration and SCD1 activity. Faecal samples were collected at baseline, after four weeks supplementation and two weeks after the supplementation was ended, and fasting blood samples were collected at baseline and after 4 weeks. Four weeks supplementation with L. casei W8 did not affect the overall composition of the GM; however, an increase in the relative abundance of the L. casei group from 8.48Ã10â6% of the total GM compared to 2.83Ã10â3% at baseline (P<0.001) was observed. Two weeks after supplementation ended, the relative abundance of the L. casei group was still increased 14 times compared to before the intervention (P<0.01). However, neither the increase in the abundance of the L. casei group nor overall GM composition correlated with changes in blood lipids or SCD1 activity.
Purchase
Buy instant access (PDF download and unlimited online access):
Institutional Login
Log in with Open Athens, Shibboleth, or your institutional credentials
Personal login
Log in with your brill.com account
Agellon, L.B., 2008. Metabolism and function of bile acids, 5th edition. In: Vance, D.E. and Vance J.E. (eds.) Biochemistry of lipids, lipoproteins and membranes. Elsevier, Toronto, Canada, pp. 423-440.
Biochemistry of lipids, lipoproteins and membranes , () 423 -440.
Anderson, J.W. and Gilliland, S.E., 1999. Effect of fermented milk (yogurt) containing Lactobacillus acidophilus L1 on serum cholesterol in hypercholesterolemic humans. Journal of the American College of Nutrition 18: 43-50.
'Effect of fermented milk (yogurt) containing Lactobacillus acidophilus L1 on serum cholesterol in hypercholesterolemic humans ' () 18 Journal of the American College of Nutrition : 43 -50.
Bangsgaard Bendtsen, K.M., Krych, L., Sorensen, D.B., Pang, W., Nielsen, D.S., Josefsen, K., Hansen, L.H., Sorensen, S.J. and Hansen, A.K., 2012. Gut microbiota composition is correlated to grid floor induced stress and behavior in the BALB/c mouse. PLoS ONE. 7: e46231.
'Gut microbiota composition is correlated to grid floor induced stress and behavior in the BALB/c mouse ' () 7 PLoS ONE : e46231.
Bjerg, A.T., Kristensen, M., Ritz, C., Stark, K.D., Holst, J.J., Leser, T.D., Wellejus, A. and Astrup, A., 2014. Four weeks supplementation with Lactobacillus paracasei subsp paracasei L. casei W8 shows modest effect on triacylglycerol in young healthy adults. Beneficial Microbes, in press. DOI: http://dx.doi.org/10.3920/BM2014.0058.
Carraro, L., Maifreni, M., Bartolomeoli, I., Martino, M.E., Novelli, E., Frigo, F., Marino, M. and Cardazzo, B., 2011. Comparison of culture-dependent and -independent methods for bacterial community monitoring during Montasio cheese manufacturing. Research in Microbiology 162: 231-239.
'Comparison of culture-dependent and -independent methods for bacterial community monitoring during Montasio cheese manufacturing ' () 162 Research in Microbiology : 231 -239.
Chaffron, S., Rehrauer, H., Pernthaler, J. and Von Mering, C., 2010. A global network of coexisting microbes from environmental and whole-genome sequence data. Genome Research 20: 947-959.
'A global network of coexisting microbes from environmental and whole-genome sequence data ' () 20 Genome Research : 947 -959.
El, A.S., Hooiveld, G., Tremaroli, V., Backhed, F. and Kleerebezem, M., 2013. The gut microbiota and mucosal homeostasis: colonized at birth or at adulthood, does it matter? Gut Microbes 4: 118-124.
'The gut microbiota and mucosal homeostasis: colonized at birth or at adulthood, does it matter? ' () 4 Gut Microbes : 118 -124.
Fava, F., Lovegrove, J.A., Gitau, R., Jackson, K.G. and Tuohy, K.M., 2006. The gut microbiota and lipid metabolism: implications for human health and coronary heart disease. Current Medicinal Chemistry 13: 3005-3021.
'The gut microbiota and lipid metabolism: implications for human health and coronary heart disease ' () 13 Current Medicinal Chemistry : 3005 -3021.
Fuentes, M.C., Lajo, T., Carrion, J.M. and Cune, J., 2013. Cholesterol-lowering efficacy of Lactobacillus plantarum CECT 7527, 7528 and 7529 in hypercholesterolaemic adults. British Journal of Nutrition 109: 1866-1872.
'Cholesterol-lowering efficacy of Lactobacillus plantarum CECT 7527, 7528 and 7529 in hypercholesterolaemic adults ' () 109 British Journal of Nutrition : 1866 -1872.
Guo, Z., Liu, X.M., Zhang, Q.X., Shen, Z., Tian, F.W., Zhang, H., Sun, Z.H., Zhang, H.P. and Chen, W., 2011. Influence of consumption of probiotics on the plasma lipid profile: a meta-analysis of randomised controlled trials. Nutrition Metabolism Cardiovascular Diseases 21: 844-850.
'Influence of consumption of probiotics on the plasma lipid profile: a meta-analysis of randomised controlled trials ' () 21 Nutrition Metabolism Cardiovascular Diseases : 844 -850.
Hansen, C.H., Krych, L., Nielsen, D.S., Vogensen, F.K., Hansen, L.H., Sorensen, S.J., Buschard, K. and Hansen, A.K., 2012. Early life treatment with vancomycin propagates Akkermansia muciniphila and reduces diabetes incidence in the NOD mouse. Diabetologia 55: 2285-2294.
'Early life treatment with vancomycin propagates Akkermansia muciniphila and reduces diabetes incidence in the NOD mouse ' () 55 Diabetologia : 2285 -2294.
Huang, Y. and Zheng, Y., 2010. The probiotic Lactobacillus acidophilus reduces cholesterol absorption through the down-regulation of Niemann-Pick C1-like 1 in Caco-2 cells. British Journal of Nutrition 103: 473-478.
'The probiotic Lactobacillus acidophilus reduces cholesterol absorption through the down-regulation of Niemann-Pick C1-like 1 in Caco-2 cells ' () 103 British Journal of Nutrition : 473 -478.
Jensen, G.M., Kristensen, M. and Astrup, A., 2012. Effect of alginate supplementation on weight loss in obese subjects completing a 12-wk energy-restricted diet: a randomized controlled trial. American Journal of Clinical Nutrition 96: 5-13.
'Effect of alginate supplementation on weight loss in obese subjects completing a 12-wk energy-restricted diet: a randomized controlled trial ' () 96 American Journal of Clinical Nutrition : 5 -13.
Kakiyama, G., Pandak, W.M., Gillevet, P.M., Hylemon, P.B., Heuman, D.M., Daita, K., Takei, H., Muto, A., Nittono, H., Ridlon, R.M., White, M.B., Noble, N.A., Monteith, P., Fuchs, M., Thacker, L.R., Sikaroodi, M. and Bajaj, J.S., 2013. Modulation of the fecal bile acid profile by gut microbiota in cirrhosis. Journal of Hepatology 58:949-955.
'Modulation of the fecal bile acid profile by gut microbiota in cirrhosis ' () 58 Journal of Hepatology : 949 -955.
Kirjavainen, P., Ouwehand, A., Isolauri, E. and Salminen, S., 1998. The ability of probiotic bacteria to bind to human intestinal mucus. FEMS Microbiology Letters 167: 185-189.
'The ability of probiotic bacteria to bind to human intestinal mucus ' () 167 FEMS Microbiology Letters : 185 -189.
Krych, L., Hansen, C.H., Hansen, A.K., Van den Berg, F.W. and Nielsen, D.S., 2013. Quantitatively different, yet qualitatively alike: a meta-analysis of the mouse core gut microbiome with a view towards the human gut microbiome. PLoS One. 8: e62578.
'Quantitatively different, yet qualitatively alike: a meta-analysis of the mouse core gut microbiome with a view towards the human gut microbiome ' () 8 PLoS One : e62578.
Lahtinen, S.J., Forssten, S., Aakko, J., Granlund, L., Rautonen, N. and Salminen, S., 2012. Probiotic cheese containing Lactobacillus rhamnosus HN001 and Lactobacillus acidophilus NCFMA (R) modifies subpopulations of fecal lactobacilli and Clostridium difficile in the elderly. Age 34: 133-143.
'Probiotic cheese containing Lactobacillus rhamnosus HN001 and Lactobacillus acidophilus NCFMA (R) modifies subpopulations of fecal lactobacilli and Clostridium difficile in the elderly ' () 34 Age : 133 -143.
Larsen, N., Vogensen, F.K., Gobel, R., Michaelsen, K.F., Abu Al- Soud, W. and Sorensen, S.J., 2011. Predominant genera of fecal microbiota in children with atopic dermatitis are not altered by intake of probiotic bacteria Lactobacillus acidophilus NCFM and Bifidobacterium animalis subsp lactis Bi-07. FEMS Microbiology Ecology 75: 482-496.
'Predominant genera of fecal microbiota in children with atopic dermatitis are not altered by intake of probiotic bacteria Lactobacillus acidophilus NCFM and Bifidobacterium animalis subsp lactis Bi-07 ' () 75 FEMS Microbiology Ecology : 482 -496.
Le Chatelier, E., Nielsen, T., Qin, J., Prifti, E., Hildebrand, F., Falony, G., Almeida, M., Arumugam, M., Batto, J.M., Kennedy, S., Leonard, P., Li, J., Burgdorf, K., Grarup, N., Jorgensen, T., Brandslund, I., Nielsen, H.B., Juncker, A.S., Bertalan, M., Levenez, F., Pons, N., Rasmussen, S., Sunagawa, S., Tap, J., Tims, S., Zoetendal, E.G., Brunak, S., Clement, K., Dore, J., Kleerebezem, M., Kristiansen, K., Renault, P., Sicheritz-Ponten, T., De Vos, W.M., ZuckeSr, J.D., Raes, J., Hansen, T., Bork, P., Wang, J., Ehrlich, S.D., Pedersen, O., Guedon, E., Delorme, C., Layec, S., Khaci, G., Van de Guchte, M., Vandemeulebrouck, G., Jamet, A., Dervyn, R., Sanchez, N., Maguin, E., Haimet, F., Winogradski, Y., Cultrone, A., Leclerc, M., Juste, C., Blottiere, H., Pelletier, E., LePaslier, D., Artiguenave, F., Bruls, T., Weissenbach, J., Turner, K., Parkhill, J., Antolin, M., Manichanh, C., Casellas, F., Boruel, N., Varela, E., Torrejon, A., Guarner, F., Denariaz, G., Derrien, M., Van Hylckama Vlieg, J.E., Veiga, P., Oozeer, R., Knol, J., Rescigno, M., Brechot, C., MâRini, C., Merieux, A. and Yamada, T., 2013. Richness of human gut microbiome correlates with metabolic markers. Nature 500: 541-546.
'Richness of human gut microbiome correlates with metabolic markers ' () 500 Nature : 541 -546.
Lozupone, C.A., Stombaugh, J.I., Gordon, J.I., Jansson, J.K. and Knight, R., 2012. Diversity, stability and resilience of the human gut microbiota. Nature 489: 220-230.
'Diversity, stability and resilience of the human gut microbiota ' () 489 Nature : 220 -230.
O'Hara, A.M. and Shanahan, F., 2006. The gut flora as a forgotten organ. European Molecular Biology Organization (EMBO) Reports 7: 688-693.
'The gut flora as a forgotten organ ' () 7 European Molecular Biology Organization (EMBO) Reports : 688 -693.
Pavlovic, N., Stankov, K. and Mikov, M., 2012. Probiotics--interactions with bile acids and impact on cholesterol metabolism. Applied Biochemistry and Biotechnology 168: 1880-1895.
'Probiotics--interactions with bile acids and impact on cholesterol metabolism ' () 168 Applied Biochemistry and Biotechnology : 1880 -1895.
Ridlon, J., Kang, D. and Hylemon, P., 2006. Bile salt biotransformations by human intestinal bacteria. Journal of Lipid Research 47: 241-259.
'Bile salt biotransformations by human intestinal bacteria ' () 47 Journal of Lipid Research : 241 -259.
Rinttilä, T., Kassinen, A., Malinen, E., Krogius, L. and Palva, A., 2004. Development of an extensive set of 16S rDNA-targeted primers for quantification of pathogenic and indigenous bacteria in faecal samples by real-time PCR. Journal of Applied Microbiology 97: 1166-1177.
'Development of an extensive set of 16S rDNA-targeted primers for quantification of pathogenic and indigenous bacteria in faecal samples by real-time PCR ' () 97 Journal of Applied Microbiology : 1166 -1177.
Santacruz, A., Marcos, A., Warnberg, J., Marti, A., Martin-Matillas, M., Campoy, C., Moreno, L.A., Veiga, O., Redondo-Figuero, C., Garagorri, J.M., Azcona, C., Delgado, M., Garcia-Fuentes, M., Collado, M.C. and Sanz, Y., 2009. Interplay between weight loss and gut microbiota composition in overweight adolescents. Obesity 17: 1906-1915.
'Interplay between weight loss and gut microbiota composition in overweight adolescents ' () 17 Obesity : 1906 -1915.
Stecher, B., Chaffron, S., Kappeli, R., Hapfelmeier, S., Freedrich, S., Weber, T.C., Kirundi, J., Suar, M., McCoy, K.D., Von, M.C., Macpherson, A.J. and Hardt, W.D., 2010. Like will to like: abundances of closely related species can predict susceptibility to intestinal colonization by pathogenic and commensal bacteria. PLoS Pathogens 6: e1000711.
'Like will to like: abundances of closely related species can predict susceptibility to intestinal colonization by pathogenic and commensal bacteria ' () 6 PLoS Pathogens : e1000711.
Tamura, M., Hori, S. and Nakagawa, H., 2009. Lactobacillus collinoides JCM1123(T): effects on mouse plasma cholesterol and isoflavonoids in the caecum. Antonie Van Leeuwenhoek International 96: 621-626.
'Lactobacillus collinoides JCM1123(T): effects on mouse plasma cholesterol and isoflavonoids in the caecum ' () 96 Antonie Van Leeuwenhoek International : 621 -626.
Tremaroli, V. and Backhed, F., 2012. Functional interactions between the gut microbiota and host metabolism. Nature 489: 242-249.
'Functional interactions between the gut microbiota and host metabolism ' () 489 Nature : 242 -249.
Xie, N., Cui, Y., Yin, Y., Zhao, X., Yang, J. and Wang, Z., 2011. Effects of two Lactobacillus strains on lipid metabolism and intestinal microflora in rats fed a high-cholesterol diet. BMC Complementary and Alternative Medicine 11: 53.
'Effects of two Lactobacillus strains on lipid metabolism and intestinal microflora in rats fed a high-cholesterol diet ' () 11 BMC Complementary and Alternative Medicine : 53.
Yin, X., Peng, J., Zhao, L., Yu, Y., Zhang, X., Liu, P., Feng, Q., Hu, Y. and Pang, X., 2013. Structural changes of gut microbiota in a rat non-alcoholic fatty liver disease model treated with a Chinese herbal formula. Systematic and Applied Microbiology 36: 188-196.
'Structural changes of gut microbiota in a rat non-alcoholic fatty liver disease model treated with a Chinese herbal formula ' () 36 Systematic and Applied Microbiology : 188 -196.
| All Time | Past 365 days | Past 30 Days | |
|---|---|---|---|
| Abstract Views | 662 | 257 | 25 |
| Full Text Views | 40 | 12 | 2 |
| PDF Views & Downloads | 55 | 20 | 4 |
Gut microbiota (GM) dysbiosis has been linked to obesity and its metabolic complications such as cardiovascular disease (CVD). The risk of developing CVD increases with elevated concentration of serum triacylglycerol (TAG). In a blinded, randomised two-arm parallel human intervention study we have previously found that four weeks of supplementation with Lactobacillus paracasei subsp. paracasei L. casei W8® (L. casei W8) compared to placebo reduced the concentration of TAG in 64 young healthy adults, an effect, likely mediated by a decreased stearoyl- CoA desaturase-1 (SCD1) activity. In the present study we analysed faecal samples obtained during the intervention study to investigate whether this effect was related to the ability of L. casei W8 to colonise the human gut after supplementation of L. casei W8 (1010 cfu daily) as determined by qPCR specific for L. paracasei and L. casei (L. casei group); whether L. casei W8 consumption affected GM composition as determined by 16S rRNA gene targeted 454/FLX amplicon sequencing; and whether these changes were associated with changes in TAG concentration and SCD1 activity. Faecal samples were collected at baseline, after four weeks supplementation and two weeks after the supplementation was ended, and fasting blood samples were collected at baseline and after 4 weeks. Four weeks supplementation with L. casei W8 did not affect the overall composition of the GM; however, an increase in the relative abundance of the L. casei group from 8.48Ã10â6% of the total GM compared to 2.83Ã10â3% at baseline (P<0.001) was observed. Two weeks after supplementation ended, the relative abundance of the L. casei group was still increased 14 times compared to before the intervention (P<0.01). However, neither the increase in the abundance of the L. casei group nor overall GM composition correlated with changes in blood lipids or SCD1 activity.
| All Time | Past 365 days | Past 30 Days | |
|---|---|---|---|
| Abstract Views | 662 | 257 | 25 |
| Full Text Views | 40 | 12 | 2 |
| PDF Views & Downloads | 55 | 20 | 4 |