Rios-Covian David, Cuesta Isabel, Alvarez-Buylla Jorge R, Ruas-Madiedo Patricia, Gueimonde Miguel, de Los Reyes-Gavilán Clara G
Probiotics and Prebiotics Group, Department of Microbiology and Biochemistry of Dairy Products, Instituto de Productos Lácteos de Asturias, Consejo Superior de Investigaciones Científicas (IPLA-CSIC), Villaviciosa, Asturias, Spain.
Scientific and Technical Facilities, Instituto de Productos Lácteos de Asturias, Consejo Superior de Investigaciones Científicas (IPLA-CSIC), Villaviciosa, Asturias, Spain.
BMC Microbiol. 2016 Jul 15;16(1):150. doi: 10.1186/s12866-016-0773-9.
Bacteroides fragilis is the most frequent species at the human intestinal mucosal surface, it contributes to the maturation of the immune system although is also considered as an opportunistic pathogen. Some Bifidobacterium strains produce exopolysaccharides (EPS), complex carbohydrate polymers that promote changes in the metabolism of B. fragilis when this microorganism grows in their presence. To demonstrate that B. fragilis can use EPS from bifidobacteria as fermentable substrates, purified EPS fractions from two strains, Bifidobacterium longum E44 and Bifidobacterium animalis subsp. lactis R1, were added as the sole carbon source in cultures of B. fragilis DSMZ 2151 in a minimal medium. Bacterial counts were determined during incubation and the evolution of organic acids, short chain fatty acids (SCFA) and evolution of EPS fractions was analysed by chromatography.
Growth of B. fragilis at early stages of incubation was slower in EPS than with glucose, microbial levels remaining higher in EPS at prolonged incubation times. A shift in metabolite production by B. fragilis occurred from early to late stages of growth, leading to the increase in the production of propionate and acetate whereas decrease lactate formation. The amount of the two peaks with different molar mass of the EPS E44 clearly decreased along incubation whereas a consumption of the polymer R1 was not so evident.
This report demonstrates that B. fragilis can consume some EPS from bifidobacteria, with a concomitant release of SCFA and organic acids, suggesting a role for these biopolymers in bacteria-bacteria cross-talk within the intestine.
脆弱拟杆菌是人类肠道黏膜表面最常见的菌种,它有助于免疫系统的成熟,尽管也被视为一种机会致病菌。一些双歧杆菌菌株会产生胞外多糖(EPS),即复杂的碳水化合物聚合物,当脆弱拟杆菌在其存在的情况下生长时,这些聚合物会促进脆弱拟杆菌代谢的变化。为了证明脆弱拟杆菌能够将双歧杆菌的EPS用作可发酵底物,将来自两株菌,即长双歧杆菌E44和动物双歧杆菌乳亚种R1的纯化EPS组分,作为唯一碳源添加到脆弱拟杆菌DSMZ 2151在基本培养基中的培养物中。在培养过程中测定细菌数量,并通过色谱法分析有机酸、短链脂肪酸(SCFA)的变化以及EPS组分的变化。
在培养早期,脆弱拟杆菌在EPS中的生长比在葡萄糖中慢,在延长培养时间后,EPS中的微生物水平仍然较高。脆弱拟杆菌代谢产物的产生在生长早期到晚期发生了变化,导致丙酸和乙酸的产生增加,而乳酸形成减少。随着培养进行,EPS E44具有不同摩尔质量的两个峰的量明显减少,而聚合物R1的消耗则不那么明显。
本报告表明,脆弱拟杆菌可以消耗一些来自双歧杆菌的EPS,同时释放SCFA和有机酸,这表明这些生物聚合物在肠道内细菌与细菌的相互作用中发挥作用。