PHYLOGENY OF THE MYCOBACTERIUM-CHELONAE-LIKE ORGANISM BASED ON PARTIAL SEQUENCING OF THE 16S RIBOSOMAL-RNA GENE AND PROPOSAL OF MYCOBACTERIUM-MUCOGENICUM SP-NOV

被引:100
作者
SPRINGER, B
BOTTGER, EC
KIRSCHNER, P
WALLACE, RJ
机构
[1] UNIV TEXAS,CTR HLTH,DEPT MICROBIOL,TYLER,TX 75710
[2] HANNOVER MED SCH,INST MED MIKROBIOL,D-30623 HANNOVER,GERMANY
来源
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY | 1995年 / 45卷 / 02期
关键词
D O I
10.1099/00207713-45-2-262
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The Mycobacterium chelonae-like organism (MCLO) is a recently described member of the Mycobacterium fortuitum complex which causes posttraumatic skin infections and catheter sepsis. This taxon is a distinct group biochemically and has a unique mycolic acid profile as determined by high-performance liquid chromatography. Its phylogenetic relationships to other mycobacteria, however, have not been studied previously. We sequenced 1,062 bp of the 16S rRNA genes from three MCLO strains obtained from the American Type Culture Collection and compared our results with the sequences of previously described tars of rapidly growing and slowly growing mycobacteria. Two biochemically typical strains (ATCC 49650(T) [T = type strain] and ATCC 49651) had identical sequences, while the sequence of a biochemically atypical strain (ATCC 49649) differed by 4 bp from the sequence of the two typical strains. The Hamming distances between these MCLO strains and related rapidly growing mycobacteria are comparable to the Hamming distances among taxa of rapidly growing mycobacteria established as species by DNA-DNA hybridization. We propose the name Mycobacterium mucogenicum sp. nov. for this new taxon because of the highly mucoid nature of most isolates on solid media.
引用
收藏
页码:262 / 267
页数:6
相关论文
共 27 条
[1]  
BAESS I, 1982, ACTA PATH MICRO IM B, V90, P371
[2]   PERITONITIS DUE TO A MYCOBACTERIUM-CHELONEI-LIKE ORGANISM ASSOCIATED WITH INTERMITTENT CHRONIC PERITONEAL-DIALYSIS [J].
BAND, JD ;
WARD, JI ;
FRASER, DW ;
PETERSON, NJ ;
SILCOX, VA ;
GOOD, RC ;
OSTROY, PR ;
KENNEDY, J .
JOURNAL OF INFECTIOUS DISEASES, 1982, 145 (01) :9-17
[3]   INFECTIONS WITH MYCOBACTERIUM-CHELONEI IN PATIENTS RECEIVING DIALYSIS AND USING PROCESSED HEMODIALYZERS [J].
BOLAN, G ;
REINGOLD, AL ;
CARSON, LA ;
SILCOX, VA ;
WOODLEY, CL ;
HAYES, PS ;
HIGHTOWER, AW ;
MCFARLAND, L ;
BROWN, JW ;
PETERSEN, NJ ;
FAVERO, MS ;
GOOD, RC ;
BROOME, CV .
JOURNAL OF INFECTIOUS DISEASES, 1985, 152 (05) :1013-1019
[4]   ACTIVITIES OF 4 MACROLIDES, INCLUDING CLARITHROMYCIN, AGAINST MYCOBACTERIUM-FORTUITUM, MYCOBACTERIUM-CHELONAE, AND M-CHELONAE-LIKE ORGANISMS [J].
BROWN, BA ;
WALLACE, RJ ;
ONYI, GO ;
DEROSAS, V ;
WALLACE, RJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1992, 36 (01) :180-184
[5]  
Good R. C., 1985, Clinical Microbiology Newsletter, V7, P133, DOI 10.1016/S0196-4399(85)80012-X
[6]   GAS-CHROMATOGRAPHIC ANALYSIS OF MYCOLIC ACID CLEAVAGE PRODUCTS IN MYCOBACTERIA [J].
GUERRANT, GO ;
LAMBERT, MA ;
MOSS, CW .
JOURNAL OF CLINICAL MICROBIOLOGY, 1981, 13 (05) :899-907
[7]   DIRECT SOLID-PHASE SEQUENCING OF GENOMIC AND PLASMID DNA USING MAGNETIC BEADS AS SOLID SUPPORT [J].
HULTMAN, T ;
STAHL, S ;
HORNES, E ;
UHLEN, M .
NUCLEIC ACIDS RESEARCH, 1989, 17 (13) :4937-4946
[8]   MYCOBACTERIUM-MADAGASCARIENSE SP-NOV [J].
KAZDA, J ;
MULLER, HJ ;
STACKEBRANDT, E ;
DAFFE, M ;
MULLER, K ;
PITULLE, C .
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1992, 42 (04) :524-528
[9]   MYCOBACTERIUM-CONFLUENTIS SP-NOV [J].
KIRSCHNER, P ;
TESKE, A ;
SCHRODER, KH ;
KROPPENSTEDT, RM ;
WOLTERS, J ;
BOTTGER, EC .
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1992, 42 (02) :257-262
[10]   GENETIC-HETEROGENEITY WITHIN MYCOBACTERIUM-FORTUITUM COMPLEX SPECIES - GENOTYPIC CRITERIA FOR IDENTIFICATION [J].
KIRSCHNER, P ;
KIEKENBECK, M ;
MEISSNER, D ;
WOLTERS, J ;
BOTTGER, EC .
JOURNAL OF CLINICAL MICROBIOLOGY, 1992, 30 (11) :2772-2775