Comparative sequence analysis of the internal transcribed spacer 1 of Ochrobactrum species

被引:23
作者
Lebuhn, Michael [1 ]
Bathe, Stephan
Achouak, Wafa
Hartmann, Anton
Heulin, Thierry
Schloter, Michael
机构
[1] Tech Univ Munich, Inst Water Qual Control & Waste Management, D-85748 Garching, Germany
[2] GSF, Natl Ctr Environm & Hlth, Inst Soil Ecol, D-85764 Neuherberg, Germany
[3] Univ Mediterranee, CEA Cadarache,Lab Ecol Microbienne Rhizosphere, CNRS,DEVM, UMR 6191,DSV, F-13108 St Paul Les Durance, France
关键词
ochrobactrion; internal transcribed spacer 1; 16S rDNA; DNA-DNA hybridization; microdiversity; phylogeny;
D O I
10.1016/j.syapm.2005.11.003
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The internal 16S/23S rDNA (rrs/rrl) internal spacer region I (ITS1) of 54 Ochrobactrum strains and close relatives was analysed. Separation of ITS1 containing PCR products by gel-electrophoresis, DGGE, cloning and sequencing revealed ITS1 length and sequence heterogeneity. We found up to 5 different allelic ITS1 stretches within a single strain (Ochrobactrum intermedium LMG 3301(T)), and 2-3 different ITS1 alleles in O. tritici. Within ITS1, ITS1c, being part of the conserved double-stranded rrn processing stem dsPS1, produced the most reliable segment tree. The overall ITS1, ITS1c and rrs phylogenetic tree topologies were generally consistent, but there was evidence for horizontal rrn (segment) transfer in O. tritici LMG 2134 (formerly O. anthropi). Good correlations were found between ITS1, ITS1c and rrs sequence similarity and DNA-DNA hybridization values indicating that phylogenetic analysis of ITS1 and ITS1c both can be used to preliminarily deduce the phylogenetic affiliation if HGT was excluded. Strains sharing > 96.19% ITS1c (> 95.11% ITS1) similarity fell within a species, and <= 68.42% ITS1c (,<= 70.33% ITS1) similarity outside a genus. Both ITS I and ITS I c analysis resolved microdiversity more profoundly than rrs analysis and revealed clades (genomovars) within O. anthropi that were also produced in rep cluster analysis. There was no evidence for habitat-specific ITS1 genomovars within Ochrobactrum species. Diversity of Ochrobactrum was higher in soil than at the rhizoplane below and at the species level. Isolates from soil contained only I rrn type whereas isolates from human clinical. animal and rhizoplane specimens could contain more. (c) 2005 Elsevier GmbH. All rights reserved.
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页码:265 / 275
页数:11
相关论文
共 34 条
[1]   Isolation and characterization of bacteria capable of degrading phenol and reducing nitrate under low-oxygen conditions [J].
Baek, SH ;
Kim, KH ;
Yin, CR ;
Jeon, CO ;
Im, WT ;
Kim, KK ;
Lee, ST .
CURRENT MICROBIOLOGY, 2003, 47 (06) :462-466
[2]  
Bathe S, 2004, FEMS MICROBIOL LETT, V235, P215, DOI 10.1111/j.1574-6968.2004.tb09591.x
[3]  
BATHE S, 2005, IN PRESS FEMS MICORO
[4]  
ENGEL M, 1999, THESIS LEHRSTUHL MIK
[5]   Diversity of activated sludge bacteria receiving the 3-chloroaniline-degradative plasmid pC1gfp [J].
Goris, J ;
Boon, N ;
Lebbe, L ;
Verstraete, W ;
De Vos, P .
FEMS MICROBIOLOGY ECOLOGY, 2003, 46 (02) :221-230
[6]   New approaches to typing and identification of bacteria using the 16S-23S rDNA spacer region [J].
Gurtler, V ;
Stanisich, VA .
MICROBIOLOGY-SGM, 1996, 142 :3-16
[7]   The role of recombination and mutation in 16S-23S rDNA spacer rearrangements [J].
Gürtler, V .
GENE, 1999, 238 (01) :241-252
[8]   Rates and consequences of recombination between rRNA operons [J].
Hashimoto, JQ ;
Stevenson, BS ;
Schmidt, TM .
JOURNAL OF BACTERIOLOGY, 2003, 185 (03) :966-972
[9]   OCHROBACTRUM-ANTHROPI GEN-NOV, SP-NOV FROM HUMAN CLINICAL SPECIMENS AND PREVIOUSLY KNOWN AS GROUP VD [J].
HOLMES, B ;
POPOFF, M ;
KIREDJIAN, M ;
KERSTERS, K .
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1988, 38 (04) :406-416
[10]   Ochrobactrum anthropi bacteremia [J].
Jelveh, N ;
Cunha, BA .
HEART & LUNG, 1999, 28 (02) :145-146