Genome stability of Bacillus thuringiensis subsp israelensis isolates

被引:21
作者
Ankarloo, J
Caugant, DA
Ankarloo, J
Caugant, DA
Hansen, BM
Berg, A
Kolsto, AB
Lövgren, A
机构
[1] Univ Stockholm, Dept Microbiol, S-10691 Stockholm, Sweden
[2] Natl Inst Publ Hlth, Dept Bacteriol, N-0403 Oslo, Norway
[3] Natl Environm Res Inst, Dept Marine Ecol & Microbiol, DK-4000 Roskilde, Denmark
[4] Univ Oslo, Ctr Biotechnol, Dept Microbiol, N-0316 Oslo, Norway
关键词
D O I
10.1007/s002849910010
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Swedish soil isolates biochemically classified as Bacillus thuringiensis subsp. israelensis were further examined for genetic diversity by multilocus enzyme electrophoresis (MLEE), random amplified polymorphic DNA analysis (RAPD), pulse field gel electrophoresis (PFGE), and Southern blotting, and were compared with reference strains. All the tested strains belonging to the Br. israelensis serotype H14 were found to be identical, as judged from the RAPD analysis. MLEE analysis gave a similar result; only one H14 strain was found to differ from the remaining H14 strains by one null allele. PFGE analysis confirmed a very close relationship between the H14 strains but revealed an SfiI restriction fragment of variable size. Southern blot analyses were carried out with probes for the chromosomally encoded flagellin gene(s) and the plasmid-encoded mosquitocidal toxins. All probes gave similar hybridization patterns in the H14 strains. The mosquito toxin probes hybridized only to the H14 strains, except for one probe hybridizing to strain 6:3, which was originally isolated from the same soil sample as strains 6:11 and 6:12. Because the RAPD, MLEE, and PFGE analyses showed that strain 6:3 appears to be unrelated to strains 6:11 and 6.12, the presence of a mosquito toxin sequence in strain 6:3 may suggest that gene transfer has occurred.
引用
收藏
页码:51 / 56
页数:6
相关论文
共 36 条
[21]  
KRIEG A, 1986, BACILLUS THURINGIENS
[22]   DISTRIBUTION OF BACILLUS-THURINGIENSIS STRAINS IN SOUTHERN SWEDEN [J].
LANDEN, R ;
BRYNE, M ;
ABDELHAMEED, A .
WORLD JOURNAL OF MICROBIOLOGY & BIOTECHNOLOGY, 1994, 10 (01) :45-50
[23]   Highly plastic chromosomal organization in Salmonella typhi [J].
Liu, SL ;
Sanderson, KE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (19) :10303-10308
[24]   Localization of putative virulence genes on a physical map of the Bacillus thuringiensis subsp. gelechiae chromosome [J].
Lövgren, A ;
Carlson, CR ;
Eskils, K ;
Kolsto, AB .
CURRENT MICROBIOLOGY, 1998, 37 (04) :245-250
[25]   MOLECULAR CHARACTERIZATION OF IMMUNE INHIBITOR-A, A SECRETED VIRULENCE PROTEASE FROM BACILLUS-THURINGIENSIS [J].
LOVGREN, A ;
ZHANG, M ;
ENGSTROM, A ;
DALHAMMAR, G ;
LANDEN, R .
MOLECULAR MICROBIOLOGY, 1990, 4 (12) :2137-2146
[26]   IDENTIFICATION OF 2 EXPRESSED FLAGELLIN GENES IN THE INSECT PATHOGEN BACILLUS-THURINGIENSIS SUBSP ALESTI [J].
LOVGREN, A ;
ZHANG, MY ;
ENGSTROM, A ;
LANDEN, R .
JOURNAL OF GENERAL MICROBIOLOGY, 1993, 139 :21-30
[27]  
Maniatis T., 1982, MOL CLONING A LAB MA
[28]   ANALYSIS OF COMMON ANTIGEN OF FLAGELLA IN BACILLUS-CEREUS AND BACILLUS-THURINGIENSIS [J].
MURAKAMI, T ;
HIRAOKA, K ;
MIKAMI, T ;
MATSUMOTO, T ;
KATAGIRI, S ;
SHINAGAWA, K ;
SUZUKI, M .
FEMS MICROBIOLOGY LETTERS, 1993, 107 (2-3) :179-183
[29]   DNA RELATEDNESS AMONG BACILLUS-THURINGIENSIS SEROVARS [J].
NAKAMURA, LK .
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1994, 44 (01) :125-129
[30]  
NARAHARA A, 1992, GENE, V122, P181