Denou Emmanuel, Pridmore Raymond David, Berger Bernard, Panoff Jean-Michel, Arigoni Fabrizio, Brüssow Harald
Nestlé Research Centre, CH-1000 Lausanne 26 Vers-chez-les-Blanc, Switzerland.
J Bacteriol. 2008 May;190(9):3161-8. doi: 10.1128/JB.01637-07. Epub 2008 Jan 25.
Lactobacillus johnsonii strains NCC533 and ATCC 33200 (the type strain of this species) differed significantly in gut residence time (12 versus 5 days) after oral feeding to mice. Genes affecting the long gut residence time of the probiotic strain NCC533 were targeted for analysis. We hypothesized that genes specific for this strain, which are expressed during passage of the bacterium through the gut, affect the phenotype. When the DNA of the type strain was hybridized against a microarray of the sequenced NCC533 strain, we identified 233 genes that were specific for the long-gut-persistence isolate. Whole-genome transcription analysis of the NCC533 strain using the microarray format identified 174 genes that were strongly and consistently expressed in the jejunum of mice monocolonized with this strain. Fusion of the two microarray data sets identified three gene loci that were both expressed in vivo and specific to the long-gut-persistence isolate. The identified genes included LJ1027 and LJ1028, two glycosyltransferase genes in the exopolysaccharide synthesis operon; LJ1654 to LJ1656, encoding a sugar phosphotransferase system (PTS) transporter annotated as mannose PTS; and LJ1680, whose product shares 30% amino acid identity with immunoglobulin A proteases from pathogenic bacteria. Knockout mutants were tested in vivo. The experiments revealed that deletion of LJ1654 to LJ1656 and LJ1680 decreased the gut residence time, while a mutant with a deleted exopolysaccharide biosynthesis cluster had a slightly increased residence time.
将约氏乳杆菌菌株NCC533和ATCC 33200(该菌种的模式菌株)经口投喂给小鼠后,它们在肠道中的停留时间存在显著差异(分别为12天和5天)。对影响益生菌菌株NCC533在肠道中长时间停留的基因进行了分析。我们推测,该菌株特有的、在细菌通过肠道过程中表达的基因会影响其表型。当模式菌株的DNA与已测序的NCC533菌株的微阵列杂交时,我们鉴定出233个对长肠道存留分离株具有特异性的基因。使用微阵列形式对NCC533菌株进行全基因组转录分析,确定了174个在单一定植该菌株的小鼠空肠中强烈且持续表达的基因。将两个微阵列数据集合并后,鉴定出三个在体内表达且对长肠道存留分离株具有特异性的基因座。鉴定出的基因包括LJ1027和LJ1028,这是胞外多糖合成操纵子中的两个糖基转移酶基因;LJ1654至LJ1656,编码一种注释为甘露糖磷酸转移酶系统(PTS)的糖磷酸转移酶转运蛋白;以及LJ1680,其产物与病原菌的免疫球蛋白A蛋白酶具有30%的氨基酸同一性。对基因敲除突变体进行了体内测试。实验表明,缺失LJ1654至LJ1656和LJ1680会缩短肠道停留时间,而胞外多糖生物合成簇缺失的突变体的停留时间略有增加。