Adaptation and response of Bifidobacterium animalis subsp lactis to bile:: a proteomic and physiological approach

被引:97
作者
Sanchez, Borja
Champomier-Verges, Marie-Christine [1 ]
Stuer-Lauridsen, Birgitte
Ruas-Madiedo, Patricia
Anglade, Patricia
Baraige, Fabienne
de los Reyes-Gavilan, Clara G.
Johansen, Eric
Zagorec, Monique
Margolles, Abelardo
机构
[1] INRA, Unite Flore Lact & Environm Carne UR309, F-78350 Jouy En Josas, France
[2] CSIC, Inst Prod Lacteos Asturias, E-33300 Villaviciosa, Asturias, Spain
[3] Chr Hansen AS, DK-2970 Horsholm, Denmark
关键词
D O I
10.1128/AEM.00637-07
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Bile salts are natural detergents that facilitate the digestion and absorption of the hydrophobic components of the diet. However, their amphiphilic nature makes them very inhibitory for bacteria and strongly influences bacterial survival in the gastrointestinal tract. Adaptation to and tolerance of bile stress is therefore crucial for the persistence of bacteria in the human colonic niche. Bifidobacterium animalis subsp. lactis, a probiotic bacterium with documented health benefits, is applied largely in fermented dairy products. In this study, the effect of bile salts on proteomes of B. animalis subsp. lactis IPLA 4549 and its bile-resistant derivative B. animalis subsp. lactis 4549dOx was analyzed, leading to the identification of proteins which may represent the targets of bile salt response and adaptation in B. animalis subsp. lactis. The comparison of the wild-type and the bile-resistant strain responses allowed us to hypothesize about the resistance mechanisms acquired by the derivative resistant strain and about the bile salt response in B. animalis subsp. lactis. In addition, significant differences in the levels of metabolic end products of the bifid shunt and in the redox status of the cells were also detected, which correlate with some differences observed between the proteomes. These results indicate that adaptation and response to bile in B. animalis subsp. lactis involve several physiological mechanisms that are jointly dedicated to reduce the deleterious impact of bile on the cell's physiology.
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页码:6757 / 6767
页数:11
相关论文
共 58 条
[1]   A NOVEL DNA-BINDING PROTEIN WITH REGULATORY AND PROTECTIVE ROLES IN STARVED ESCHERICHIA-COLI [J].
ALMIRON, M ;
LINK, AJ ;
FURLONG, D ;
KOLTER, R .
GENES & DEVELOPMENT, 1992, 6 (12B) :2646-2654
[2]   Identification by fluorescence spectroscopy of lactic acid bacteria isolated from a small-scale facility producing traditional dry sausages [J].
Ammor, S ;
Yaakoubi, K ;
Chevallier, I ;
Dufour, E .
JOURNAL OF MICROBIOLOGICAL METHODS, 2004, 59 (02) :271-281
[3]  
Araya M., 2002, GUIDELINES EVALUATIO
[4]   Bile salt hydrolase activity in probiotics [J].
Begley, M ;
Hill, C ;
Gahan, CGM .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2006, 72 (03) :1729-1738
[5]   The interaction between bacteria and bile [J].
Begley, M ;
Gahan, CGM ;
Hill, C .
FEMS MICROBIOLOGY REVIEWS, 2005, 29 (04) :625-651
[6]   Activation of the promoters of genes associated with DNA damage, oxidative stress, ER stress and protein malfolding by the bile salt, deoxycholate [J].
Bernstein, H ;
Payne, CM ;
Bernstein, C ;
Schneider, J ;
Beard, SE ;
Crowley, CL .
TOXICOLOGY LETTERS, 1999, 108 (01) :37-46
[7]   DNA micro-array-based identification of bile-responsive genes in Lactobacillus plantarum [J].
Bron, PA ;
Molenaar, D ;
Vos, WM ;
Kleerebezem, M .
JOURNAL OF APPLIED MICROBIOLOGY, 2006, 100 (04) :728-738
[8]   Genetic characterization of the bile salt response in Lactobacillus plantarum and analysis of responsive promoters in vitro and in situ in the gastrointestinal tract [J].
Bron, PA ;
Marco, M ;
Hoffer, SM ;
Van Mullekom, E ;
de Vos, WM ;
Kleerebezem, M .
JOURNAL OF BACTERIOLOGY, 2004, 186 (23) :7829-7835
[9]   The bacterial enhancer-dependent σ54 (σN) transcription factor [J].
Buck, M ;
Gallegos, MT ;
Studholme, DJ ;
Guo, YL ;
Gralla, JD .
JOURNAL OF BACTERIOLOGY, 2000, 182 (15) :4129-4136
[10]   Immune response to orally consumed antigens and probiotic bacteria [J].
Chin, J ;
Turner, B ;
Barchia, I ;
Mullbacher, A .
IMMUNOLOGY AND CELL BIOLOGY, 2000, 78 (01) :55-66