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首页> 外文期刊>DNA and Cell Biology >A Mesocosm of Lactobacillus johnsonii, Bifidobacterium longum, and Escherichia coli in the Mouse Gut
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A Mesocosm of Lactobacillus johnsonii, Bifidobacterium longum, and Escherichia coli in the Mouse Gut

机译:小鼠肠道中的约翰逊乳杆菌,长双歧杆菌和大肠杆菌的介观

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The relative contribution of competition and cooperation at the microbe-microbe level is not well understood for the bacteria constituting the gut microbiota. The high number and variability of human gut commensals have hampered the analysis. To get some insight into the question how so many different bacterial species can coexist in the mammalian gut, we studied the interaction between three human gut commensals (Escherichia coli K-12, Lactobacillus johnsonii NCC533, and Bifidobacterium longum NCC2705) in the intestine of gnotobiotic mice. The bacterial titers and their anatomical distribution were studied in the colonized mice. L. johnsonii achieved the highest cell counts in the stomach, while B. longum dominated the colon. The colon was also the intestinal location in which B. longum displayed the highest number of expressed genes, followed by the cecum and the small intestine. Addition of further bacterial strains led to strikingly different results. A Lactobacillus paracasei strain coexisted, while a second B. longum strain was excluded from the system. Notably, this strain lacked an operon involved in the degradation, import, and metabolism of mannosylated glycans. Subsequent introduction of the E. coli Nissle strain resulted in the elimination of L. johnsonii NCC533 and E. coli K-12, while B. longum NCC2705 showed a transient decrease in population size, demonstrating the dynamic nature of microbe-microbe interactions. The study of such simple interacting bacterial systems might help to derive some basic rules governing microbial ecology within the mammalian gut.
机译:对于构成肠道菌群的细菌,人们还不太清楚竞争与合作在微生物-微生物水平上的相对贡献。人类肠道菌膜数量众多且变化多端,妨碍了分析。为了深入了解哺乳动物肠道中可以共存多种细菌的问题,我们研究了三种人类肠道菌(大肠杆菌K-12,约翰逊乳杆菌NCC533和长双歧杆菌NCC2705)之间的相互作用。老鼠。在定植的小鼠中研究了细菌滴度及其解剖分布。约翰逊氏菌在胃中获得了最高的细胞计数,而长双歧杆菌则占据了结肠。结肠也是长双歧杆菌显示最多表达基因的肠道位置,其次是盲肠和小肠。添加更多细菌菌株导致了截然不同的结果。副干酪乳杆菌菌株共存,而第二个长双歧杆菌被排除在系统外。值得注意的是,该菌株缺乏涉及甘露糖基聚糖的降解,输入和代谢的操纵子。随后引入大肠杆菌Nissle菌株导致消除了约翰逊氏菌NCC533和大肠杆菌K-12,而长双歧杆菌NCC2705则显示种群数量的短暂减少,表明了微生物与微生物相互作用的动态特性。对这种简单相互作用的细菌系统的研究可能有助于得出控制哺乳动物肠道内微生物生态学的一些基本规则。

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