SUSCEPTIBILITY OF PSEUDOMONAS SPECIES TO THE NOVEL ANTIBIOTICS MUREIDOMYCINS

被引:19
作者
ISONO, F
KODAMA, K
INUKAI, M
机构
[1] SANKYO CO LTD,FERMENTAT RES LABS,1-2-58 HIROMACHI,SHINAGAWA KU,TOKYO 140,JAPAN
[2] SANKYO CO LTD,TSUKUBA RES CTR,TSUKUBA,IBARAKI,JAPAN
关键词
D O I
10.1128/AAC.36.5.1024
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Strains of Pseudomonas aeruginosa, including imipenem- or ofloxacin-resistant clinical isolates, and some other species in the genus Pseudomonas were inhibited by novel antibiotics of the mureidomycin (MRD) group. On the other hand, almost all other gram-positive and gram-negative bacteria were resistant to MRDs, though the antibiotics potently inhibited the in vitro peptidoglycan synthesis of Escherichia coli and P. aeruginosa. All of the strains in the genus Pseudomonas that were inhibited by less-than-or-equal-to 200-mu-g of MRDs per ml were classified into the rRNA groups I and III, and none of the tested strains of rRNA group I were resistant to MRDs, suggesting that these two groups are closely related to each other evolutionarily. Among group I strains, P. aeruginosa, P. mendocina, P. stutzeri, and P. alcaligenes were more susceptible than the others, suggesting a closer relationship among these species.
引用
收藏
页码:1024 / 1027
页数:4
相关论文
共 14 条
[1]   NUMERICAL TAXONOMY OF PSEUDOMONAS-ALCALIGENES, PSEUDOMONAS-PSEUDOALCALIGENES, PSEUDOMONAS-MENDOCINA, PSEUDOMONAS-STUTZERI, AND RELATED BACTERIA [J].
GAVINI, F ;
HOLMES, B ;
IZARD, D ;
BEJI, A ;
BERNIGAUD, A ;
JAKUBCZAK, E .
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1989, 39 (02) :135-144
[2]  
GIAMARELLOU H, 1987, AM J MED, V82, P346
[3]   MUREIDOMYCINS-A-D, NOVEL PEPTIDYLNUCLEOSIDE ANTIBIOTICS WITH SPHEROPLAST FORMING ACTIVITY .1. TAXONOMY, FERMENTATION, ISOLATION AND PHYSICOCHEMICAL PROPERTIES [J].
INUKAI, M ;
ISONO, F ;
TAKAHASHI, S ;
ENOKITA, R ;
SAKAIDA, Y ;
HANEISHI, T .
JOURNAL OF ANTIBIOTICS, 1989, 42 (05) :662-666
[4]   MUREIDOMYCINS-A-D, NOVEL PEPTIDYLNUCLEOSIDE ANTIBIOTICS WITH SPHEROPLAST FORMING ACTIVITY .3. BIOLOGICAL PROPERTIES [J].
ISONO, F ;
KATAYAMA, T ;
INUKAI, M ;
HANEISHI, T .
JOURNAL OF ANTIBIOTICS, 1989, 42 (05) :674-679
[5]   MUREIDOMYCINS-A-D, NOVEL PEPTIDYLNUCLEOSIDE ANTIBIOTICS WITH SPHEROPLAST FORMING ACTIVITY .2. STRUCTURAL ELUCIDATION [J].
ISONO, F ;
INUKAI, M ;
TAKAHASHI, S ;
HANEISHI, T ;
KINOSHITA, T ;
KUWANO, H .
JOURNAL OF ANTIBIOTICS, 1989, 42 (05) :667-673
[6]  
ISOO F, 1991, ANTIMICROB AGENTS CH, V35, P234
[7]   DEOXYRIBONUCLEIC-ACID SIMILARITIES AMONG PSEUDOMONAS SPECIES [J].
JOHNSON, JL ;
PALLERONI, NJ .
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1989, 39 (03) :230-235
[8]   EMERGENCE OF RESISTANCE TO IMIPENEM IN PSEUDOMONAS-AERUGINOSA [J].
LYNCH, MJ ;
DRUSANO, GL ;
MOBLEY, HLT .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1987, 31 (12) :1892-1896
[9]   OUTER-MEMBRANE BARRIER AS A MECHANISM OF ANTIMICROBIAL RESISTANCE [J].
NIKAIDO, H .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1989, 33 (11) :1831-1836
[10]   GROUPING OF PSEUDOMONAS SPECIES ON THE BASIS OF CELLULAR FATTY-ACID COMPOSITION AND THE QUINONE SYSTEM WITH SPECIAL REFERENCE TO THE EXISTENCE OF 3-HYDROXY FATTY-ACIDS [J].
OYAIZU, H ;
KOMAGATA, K .
JOURNAL OF GENERAL AND APPLIED MICROBIOLOGY, 1983, 29 (01) :17-+