Trott D J, Stanton T B, Jensen N S, Duhamel G E, Johnson J L, Hampson D J
School of Veterinary Studies, Murdoch University, Western Australia, Australia.
Int J Syst Bacteriol. 1996 Jan;46(1):206-15. doi: 10.1099/00207713-46-1-206.
Phenotypic and genetic traits of porcine intestinal spirochete strain P43/6/78T (= ATCC 51139T) (T = type strain), which is pathogenic and weakly beta-hemolytic, were determined in order to confirm the taxonomic position of this organism and its relationships to previously described species of intestinal spirochetes. In BHIS broth, P43/6/78T cells had a doubling time of 1 to 2 h and grew to a maximum cell density of 2 x 10(9) cells per ml at 37 to 42 degrees C. They hydrolyzed hippurate, utilized D-glucose, D-fructose, sucrose, D-trehalose, D-galactose, D-mannose, maltose, N-acetyl-D-glucosamine, D-glucosamine, pyruvate, L-fucose, D-cellobiose, and D-ribose as growth substrates, and produced acetate, butyrate, ethanol, H2, and CO2 as metabolic products. They consumed substrate amounts of oxygen and had a G+C content (24.6 mol%) similar to that of Serpulina hyodysenteriae B78T (25.9 mol%). Phenotypic traits that could be used to distinguish strain P43/6/78T from S. hyodysenteriae and Serpulina innocens included its ultrastructural appearance (each strain P43/6/78T cell had 8 or 10 periplasmic flagella, with 4 or 5 flagella inserted at each end, and the cells were thinner and shorter and had more pointed ends than S. hyodysenteriae and S. innocens cells), its faster growth rate in liquid media, its hydrolysis of hippurate, its lack of beta-glucosidase activity, and its metabolism of D-ribose. DNA-DNA relative reassociation experiments in which the S1 nuclease method was used revealed that P43/6/78T was related to, but was genetically distinct from, both S. hyodysenteriae B78T (level of sequence homology, 25 to 32%) and S. innocens B256T (level of sequence homology, 24 to 25%). These and previous results indicate that intestinal spirochete strain P43/6/78T represents a distinct Serpulina species. Therefore, we propose that strain P43/6/78 should be designated as the type strain of a new species, Serpulina pilosicoli.
猪肠道螺旋体菌株P43/6/78T(= ATCC 51139T)(T = 模式菌株)具有致病性且β-溶血能力较弱,为确定该微生物的分类地位及其与先前描述的肠道螺旋体物种的关系,对其表型和遗传特征进行了测定。在BHIS肉汤中,P43/6/78T细胞的倍增时间为1至2小时,在37至42摄氏度下生长至最大细胞密度为每毫升2×10⁹个细胞。它们能水解马尿酸盐,利用D-葡萄糖、D-果糖、蔗糖、D-海藻糖、D-半乳糖、D-甘露糖、麦芽糖、N-乙酰-D-葡萄糖胺、D-葡萄糖胺、丙酮酸、L-岩藻糖、D-纤维二糖和D-核糖作为生长底物,并产生乙酸盐、丁酸盐、乙醇、H₂和CO₂作为代谢产物。它们消耗底物量的氧气,其G+C含量(24.6摩尔%)与猪痢疾短螺旋体B78T(25.9摩尔%)相似。可用于区分P43/6/78T菌株与猪痢疾短螺旋体和无害短螺旋体的表型特征包括其超微结构外观(每个P43/6/78T菌株细胞有8或10根周质鞭毛,两端各插入4或5根鞭毛,且细胞比猪痢疾短螺旋体和无害短螺旋体细胞更细、更短且末端更尖)、其在液体培养基中更快的生长速度、其对马尿酸盐的水解、其缺乏β-葡萄糖苷酶活性以及其对D-核糖的代谢。使用S1核酸酶法进行的DNA-DNA相对重结合实验表明,P43/6/78T与猪痢疾短螺旋体B78T(序列同源性水平为25%至32%)和无害短螺旋体B256T(序列同源性水平为24%至25%)均相关,但在遗传上不同。这些结果以及先前的结果表明,肠道螺旋体菌株P43/6/78T代表一个独特的短螺旋体物种。因此,我们建议将菌株P43/6/78指定为一个新物种——鬃毛短螺旋体(Serpulina pilosicoli)的模式菌株。