Macrolide Treatment for Mycobacterium abscessus and Mycobacterium massillense Infection and Inducible Resistance

被引:146
作者
Choi, Go-Eun [2 ,3 ]
Shin, Sung Jae [4 ,5 ]
Won, Choul-Jae [4 ,5 ]
Min, Ki-Nam [2 ,3 ]
Oh, Taegwon [4 ,5 ]
Hahn, Mi-Young [6 ,7 ]
Lee, Keehoon [4 ,5 ]
Lee, Soo Hyun [8 ]
Daley, Charles L. [9 ]
Kim, Seonwoo [10 ]
Jeong, Byeong-Ho [1 ]
Jeon, Kyeongman [1 ]
Koh, Won-Jung [1 ]
机构
[1] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Div Pulm & Crit Care Med,Dept Med, Seoul 135710, South Korea
[2] Chungnam Natl Univ, Coll Med, Res Inst Med Sci, Taejon, South Korea
[3] Chungnam Natl Univ, Coll Med, Dept Microbiol, Taejon, South Korea
[4] Yonsei Univ, Coll Med, Dept Microbiol, Seoul, South Korea
[5] Yonsei Univ, Coll Med, Inst Immunol & Immunol Dis, Seoul, South Korea
[6] Yonsei Univ, Dept Syst Biol, Seoul 120749, South Korea
[7] Yonsei Univ, Inst Life Sci & Biotechnol, Seoul 120749, South Korea
[8] Korea Inst Sci & Technol, Biomol Funct Res Ctr, Seoul, South Korea
[9] Natl Jewish Hlth, Dept Med, Div Mycobacterial & Resp Infect, Denver, CO USA
[10] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Biostat Team,Samsung Biomed Res Inst, Seoul 135710, South Korea
关键词
Mycobacterium abscessus; Mycobacterium massiliense; clarithromycin; azithromycin; inducible resistance; FDA-APPROVED DRUGS; PULMONARY-DISEASE; ANTIMICROBIAL ACTIVITY; DOUBLE-BLIND; SP-NOV; CLARITHROMYCIN; GENE; AZITHROMYCIN; MASSILIENSE; THERAPY;
D O I
10.1164/rccm.201111-2005OC
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Rationale: Macrolides, such as clarithromycin (CLR) and azithromycin (AZM), are frequently the only oral antibiotics that are active against Mycobacterium abscessus and M. massiliense infections. Objectives: To compare the activity of CLR and AZM in experimental models. Methods: We compared the treatment efficacies of CLR and AZM and determined the correlation between efficacy and induced erythromycin ribosome methyltransferase gene (erm)(41) expression in experimental models of M. abscessus and M. massiliense infections. Measurements and Main Results: In all tested M. abscessus isolates, a high level of inducible CLR resistance developed (minimal inhibitory concentration [MIC] on Day 3 versus Day 14; P < 0.001). Whereas the AZM MIC increased on Day 14 (P < 0.01 versus Day 3), the level was significantly lower than the CLR MIC on Day 14 (P < 0.001). However, the MICs of CLR and AZM for the M. massiliense isolates did not change. Compared with CLR, AZM presented greater antibiotic activity against M. abscessus in vitro, ex vivo, and in vivo (P < 0.05), whereas both macrolides were comparably effective against M. massiliense. In M. abscessus infection, the level of erm(41) expression was higher after exposure to CLR than after exposure to AZM (P < 0.001). Experiments using an erm(41)-knockout M. abscessus mutant and an M. massiliense transformant expressing M. abscessus erm(41) confirmed that erm(41) was responsible for inducible CLR resistance. Conclusions: CLR induces greater erm(41) expression and thus higher macrolide resistance than AZM in M. abscessus infection. AZM may be more effective against M. abscessus, whereas both macrolides appear to be equally effective against M. massiliense.
引用
收藏
页码:917 / 925
页数:9
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