Paniz-Mondolfi Alberto Enrique, Greninger Alexander L, Ladutko Lynn, Brown-Elliott Barbara A, Vasireddy Ravikiran, Jakubiec Wesley, Vasireddy Sruthi, Wallace Richard J, Simmon Keith E, Dunn Bruce E, Jackoway Gary, Vora Surabhi B, Quinn Kevin K, Qin Xuan, Campbell Sheldon
Department of Laboratory Medicine, Yale School of Medicine/Yale-New Haven Hospital, New Haven, CT, USA.
Department of Laboratory Medicine, University of Washington, Seattle, WA, USA.
Int J Syst Evol Microbiol. 2017 Nov;67(11):4345-4351. doi: 10.1099/ijsem.0.002216. Epub 2017 Oct 6.
A previously undescribed, rapidly growing, scotochromogenic species of the genus Mycobacterium (represented by strains PB739 and GK) was isolated from two clinical sources - the sputum of a 76-year-old patient with severe chronic obstructive pulmonary disease, history of tuberculosis exposure and Mycobacterium avium complex isolated years prior; and the blood of a 15-year-old male with B-cell acute lymphoblastic leukaemia status post bone marrow transplant. The isolates grew as dark orange colonies at 25-37 °C after 5 days, sharing features in common with other closely related species. Analysis of the complete 16S rRNA gene sequence (1492 bp) of strain PB739 demonstrated that the isolate shared 98.8 % relatedness with Mycobacterium wolinskyi. Partial 429 bp hsp65 and 744 bp rpoB region V sequence analyses revealed that the sequences of the novel isolate shared 94.8 and 92.1 % similarity with those of Mycobacterium neoaurum and Mycobacterium aurum, respectively. Biochemical profiling, antimicrobial susceptibility testing, HPLC/gas-liquid chromatography analyses and multilocus sequence typing support the taxonomic status of these isolates (PB739 and GK) as representatives of a novel species. Both isolates were susceptible to the Clinical and Laboratory Standards Institute recommended antimicrobials for susceptibility testing of rapidly growing mycobacteria including amikacin, ciprofloxacin, moxifloxacin, doxycycline/minocycline, imipenem, linezolid, clarithromycin and trimethropin/sulfamethoxazole. Both isolates PB739 and GK showed intermediate susceptibility to cefoxitin. We propose the name Mycobacterium grossiae sp. nov. for this novel species and have deposited the type strain in the DSMZ and CIP culture collections. The type strain is PB739 (=DSM 104744=CIP 111318).
从两个临床样本中分离出一种此前未被描述的、快速生长的产暗色素分枝杆菌属菌种(由PB739和GK菌株代表)。一个样本来自一名76岁患有严重慢性阻塞性肺疾病、有结核接触史且数年前分离出鸟分枝杆菌复合群的患者的痰液;另一个样本来自一名15岁接受骨髓移植后处于B细胞急性淋巴细胞白血病状态的男性的血液。这些分离株在25 - 37°C培养5天后生长为深橙色菌落,与其他密切相关菌种有共同特征。对PB739菌株完整的16S rRNA基因序列(1492 bp)分析表明,该分离株与沃林斯基分枝杆菌的亲缘关系为98.8%。对429 bp的hsp65和744 bp的rpoB区域V序列进行部分分析显示,该新分离株的序列与新金色分枝杆菌和金色分枝杆菌的序列相似性分别为94.8%和92.1%。生化分析、抗菌药物敏感性测试、高效液相色谱/气相色谱分析以及多位点序列分型支持将这些分离株(PB739和GK)作为一个新菌种的分类地位。这两个分离株对临床和实验室标准协会推荐的用于快速生长分枝杆菌药敏试验的抗菌药物敏感,包括阿米卡星、环丙沙星、莫西沙星、多西环素/米诺环素、亚胺培南、利奈唑胺、克拉霉素和甲氧苄啶/磺胺甲恶唑。PB739和GK这两个分离株对头孢西丁表现出中度敏感性。我们提议将这个新菌种命名为格罗斯分枝杆菌(Mycobacterium grossiae sp. nov.),并已将模式菌株保藏于德国微生物和细胞培养物保藏中心(DSMZ)和法国国家微生物保藏中心(CIP)。模式菌株为PB739(=DSM 104744 =CIP 111318)。