Fukano Hanako, Wada Shinpei, Kurata Osamu, Katayama Kinya, Fujiwara Nagatoshi, Hoshino Yoshihiko
Laboratory of Aquatic Medicine, Nippon Veterinary and Life Science University, 1-7-1 Kyonancho, Musashino, Tokyo, 180-8602, Japan.
Department of Mycobacteriology, Leprosy Research Center, National Institute of Infectious Diseases, 4-2-1 Aoba, Higashi-Murayama, Tokyo, 189-0002, Japan.
Int J Syst Evol Microbiol. 2017 Aug;67(8):2811-2817. doi: 10.1099/ijsem.0.002028.
A previously undescribed rapidly growing, non-pigmented mycobacterium was identified based on biochemical and nucleic acid analyses, as well as growth characteristics. Seven isolates were cultured from samples collected from five thread-sail filefish (Stephanolepis cirrhifer) and two farmed black scraper (Thamnaconus modestus). Bacterial growth occurred at 15-35 °C on Middlebrook 7H11 agar. The bacteria were positive for catalase activity at 68 °C and urease activity, intermediate for iron uptake, and negative for Tween 80 hydrolysis, nitrate reduction, semi-quantitative catalase activity and arylsulfatase activity at day 3. No growth was observed on Middlebrook 7H11 agar supplemented with picric acid, and very little growth was observed in the presence of 5 % NaCl. α- and α'-mycolates were identified in the cell walls, and a unique profile of the fatty acid methyl esters and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) profiles of the protein and cell-wall lipids were acquired. Sequence analysis revealed that the seven isolates shared identical sequences for the 16S rRNA, rpoB, hsp65, recA and sodA genes. Phylogenetic analysis of the five gene sequences confirmed that the isolates were unique, but closely related to Mycobacterium chelonae. Antibiotic susceptibility testing revealed the minimum inhibitory concentration (MIC) of clarithromycin against this novel species was <0.25 µg ml, which was lower than that for Mycobacterium salmoniphilum. The hsp65 PCR restriction enzyme analysis pattern differed from those of M. chelonae and M. salmoniphilum. Based on these findings, the name Mycobacterium stephanolepidis sp. nov. is proposed for this novel species, with the type strain being NJB0901 (=JCM 31611=KCTC 39843).
基于生化分析、核酸分析以及生长特性,鉴定出一种此前未被描述的快速生长的非色素产生型分枝杆菌。从五条细纹狮子鱼(Stephanolepis cirrhifer)和两条养殖黑鲳(Thamnaconus modestus)采集的样本中培养出七株菌株。细菌在Middlebrook 7H11琼脂上于15 - 35°C生长。这些细菌在68°C时过氧化氢酶活性呈阳性,脲酶活性呈阳性,铁摄取呈中间型,在第3天吐温80水解、硝酸盐还原、半定量过氧化氢酶活性和芳基硫酸酯酶活性呈阴性。在添加苦味酸的Middlebrook 7H11琼脂上未观察到生长,在5% NaCl存在的情况下观察到极少生长。在细胞壁中鉴定出α - 和α'- 霉菌酸,并获得了脂肪酸甲酯以及蛋白质和细胞壁脂质的基质辅助激光解吸/电离飞行时间质谱(MALDI - TOF MS)图谱的独特谱型。序列分析表明,这七株菌株的16S rRNA、rpoB、hsp65、recA和sodA基因具有相同序列。对这五个基因序列的系统发育分析证实,这些菌株是独特的,但与龟分枝杆菌密切相关。抗生素敏感性测试显示,克拉霉素对该新物种的最低抑菌浓度(MIC)<0.25 μg/ml,低于嗜鱼分枝杆菌。hsp65 PCR限制性酶切分析图谱与龟分枝杆菌和嗜鱼分枝杆菌不同。基于这些发现,提议将该新物种命名为斯蒂芬诺鳞分枝杆菌(Mycobacterium stephanolepidis sp. nov.),模式菌株为NJB0901(=JCM 31611 = KCTC 39843)。