Hatakeyama Shuji, Ohama Yuki, Okazaki Mitsuhiro, Nukui Yoko, Moriya Kyoji
Division of General Internal Medicine, Jichi Medical University Hospital, Yakushiji, Shimotsuke-shi, Tochigi, 329-0498, Japan.
Division of Infectious Diseases, Jichi Medical University Hospital, Yakushiji, Shimotsuke-shi, Tochigi, 329-0498, Japan.
BMC Infect Dis. 2017 Mar 7;17(1):197. doi: 10.1186/s12879-017-2298-8.
Difficult-to-treat infections caused by rapidly growing mycobacteria (RGM) are increasingly observed in clinical settings. However, studies on antimicrobial susceptibilities and effective treatments against RGM in Japan are limited.
We conducted susceptibility testing of potential antimicrobial agents, including tigecycline and tebipenem, against RGM. Clinical RGM isolates were collected from a university hospital in Japan between December 2010 and August 2013. They were identified using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry and the sequencing of 16S rRNA, rpoB, and hsp65 genes. The samples were utilized for susceptibility testing using 16 antimicrobials, with frozen broth microdilution panels.
Forty-two isolates were obtained: 13, Mycobacterium abscessus complex; 12, Mycobacterium chelonae; 9, Mycobacterium fortuitum; and 8, M. fortuitum group species other than M. fortuitum. Different antimicrobial susceptibility patterns were observed between RGM species. Clarithromycin-susceptible strain rates were determined to be 0, 62, and 100% for M. fortuitum, M. abscessus complex, and M. chelonae, respectively. M. abscessus complex (100%) and >80% M. chelonae isolates were non-susceptible, while 100% M. fortuitum group isolates were susceptible to moxifloxacin. Linezolid showed good activity against 77% M. abscessus complex, 89% M. fortuitum, and 100% M. chelonae isolates. Regardless of species, all tested isolates were inhibited by tigecycline at very low minimal inhibitory concentrations (MICs) of ≤0.5 μg/mL. MICs of tebipenem, an oral carbapenem, were ≤4 μg/mL against all M. fortuitum group isolates.
Our study demonstrates the importance of correct identification and antimicrobial susceptibility testing, including the testing of potential new agents, in the management of RGM infections.
临床环境中由快速生长分枝杆菌(RGM)引起的难治性感染日益常见。然而,日本针对RGM的抗菌药物敏感性及有效治疗方法的研究有限。
我们对包括替加环素和替比培南在内的潜在抗菌药物进行了针对RGM的敏感性测试。2010年12月至2013年8月期间,从日本一家大学医院收集临床RGM分离株。使用基质辅助激光解吸/电离飞行时间质谱以及16S rRNA、rpoB和hsp65基因测序对其进行鉴定。样本用于使用16种抗菌药物的敏感性测试,采用冷冻肉汤微量稀释板。
共获得42株分离株:13株脓肿分枝杆菌复合群;12株龟分枝杆菌;9株偶然分枝杆菌;8株除偶然分枝杆菌外的偶然分枝杆菌菌群物种。不同RGM菌种之间观察到不同的抗菌药物敏感性模式。克拉霉素敏感菌株率在偶然分枝杆菌、脓肿分枝杆菌复合群和龟分枝杆菌中分别为0%、62%和100%。脓肿分枝杆菌复合群(100%)和超过80%的龟分枝杆菌分离株不敏感,而100%的偶然分枝杆菌菌群分离株对莫西沙星敏感。利奈唑胺对77%的脓肿分枝杆菌复合群、89%的偶然分枝杆菌和100%的龟分枝杆菌分离株显示出良好活性。无论菌种如何,所有测试分离株在极低的最低抑菌浓度(MIC)≤0.5μg/mL时均被替加环素抑制。口服碳青霉烯类药物替比培南对所有偶然分枝杆菌菌群分离株的MIC≤4μg/mL。
我们的研究表明,在RGM感染的管理中,正确鉴定和抗菌药物敏感性测试(包括对潜在新药物的测试)非常重要。