Genetic relationship in the 'Bacillus cereus group' by rep-PCR fingerprinting and sequencing of a Bacillus anthracis-specific rep-PCR fragment

被引:61
作者
Cherif, A
Brusetti, L
Borin, S
Rizzi, A
Boudabous, A
Khyami-Horani, H
Daffonchio, D
机构
[1] Univ Milan, Dipartimento Sci & Tecnol Alimentari & Microbiol, I-20133 Milan, Italy
[2] Univ Tunis, Microbiol Lab, Tunis 33110, Tunisia
[3] Univ Jordan, Dept Microbiol, Amman 11181, Jordan
关键词
Bacillus anthracis; Bacillus cereus group; ywfK; BOX-A1R; genetic relationship; rep-PCR;
D O I
10.1046/j.1365-2672.2003.01945.x
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
Aims: To evaluate the genetic relationship in the Bacillus cereus group by rep-PCR fingerprinting. Methods and Results: A collection of 112 strains of the six species of the B. cereus group was analysed by rep-PCR fingerprinting using the BOX-A1R primer. A relative genetic distinctness was found among the species. Cluster analysis of the rep-PCR patterns showed clusters of B. thuringiensis strains quite separate from those of B. cereus strains. The B. anthracis strains represented an independent lineage in a B. cereus cluster. The B. mycoides, B. pseudomycoides and B. weihenstephanensis strains were clustered into three groups at some distance from the other species. Comparison of sequences of AC-390, a typical B. anthracis rep-PCR fragment, from 27 strains of B. anthracis, B. cereus, B. thuringiensis and B. weihenstephanensis, representative of different clusters identified by rep-PCR fingerprinting, confirmed that B. anthracis diverges from its related species. Conclusions: The genetic relationship deduced from the rep-PCR patterns indicates a relatively clear separation of the six species, suggesting that they can indeed be considered as separate units. Significance and Impact of the Study: rep-PCR fingerprinting can make a contribution in the clarification of the genetic relationships between the species of the B. cereus group.
引用
收藏
页码:1108 / 1119
页数:12
相关论文
共 33 条
[1]   Single strand conformation polymorphism analysis of PCR-tDNA fingerprinting to address the identification of Bacillus species [J].
Borin, S ;
Daffonchio, D ;
Sorlini, C .
FEMS MICROBIOLOGY LETTERS, 1997, 157 (01) :87-93
[2]   Use of long-range repetitive element polymorphism-PCR to differentiate Bacillus anthracis strains [J].
Brumlik, MJ ;
Szymajda, U ;
Zakowska, D ;
Liang, XD ;
Redkar, RJ ;
Patra, G ;
Del Vecchio, VG .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2001, 67 (07) :3021-3028
[3]   Bacillus anthracis diverges from related clades of the Bacillus cereus group in 16S-23S ribosomal DNA intergenic transcribed spacers containing tRNA genes [J].
Cherif, A ;
Borin, S ;
Rizzi, A ;
Ouzari, H ;
Boudabous, A ;
Daffonchio, D .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2003, 69 (01) :33-40
[4]   Characterization of a repetitive element polymorphism-polymerase chain reaction chromosomal marker that discriminates Bacillus anthracis from related species [J].
Cherif, A ;
Borin, S ;
Rizzi, A ;
Ouzari, H ;
Boudabous, A ;
Daffonchio, D .
JOURNAL OF APPLIED MICROBIOLOGY, 2002, 93 (03) :456-462
[5]   Thuricin 7:: a novel bacteriocin produced by Bacillus thuringiensis BMG1.7, a new strain isolated from soil [J].
Cherif, A ;
Ouzari, H ;
Daffonchio, D ;
Cherif, H ;
Ben Slama, K ;
Hassen, A ;
Jaoua, S ;
Boudabous, A .
LETTERS IN APPLIED MICROBIOLOGY, 2001, 32 (04) :243-247
[6]  
Daffonchio D, 1999, APPL ENVIRON MICROB, V65, P1298
[7]   16S-23S rRNA internal transcribed spacers as molecular markers for the species of the 16S rRNA group I of the genus Bacillus [J].
Daffonchio, D ;
Borin, S ;
Consolandi, A ;
Mora, D ;
Manachini, PL ;
Sorlini, C .
FEMS MICROBIOLOGY LETTERS, 1998, 163 (02) :229-236
[8]   PCR fingerprinting of whole genomes:: the spacers between the 16S and 23S rRNA genes and of intergenic tRNA gene regions reveal a different intraspecific genomic variability of Bacillus cereus and Bacillus licheniformis [J].
Daffonchio, D ;
Borin, S ;
Frova, G ;
Manachini, PL ;
Sorlini, C .
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1998, 48 :107-116
[9]   Restriction site insertion-PCR (RSI-PCR) for rapid discrimination and typing of closely related microbial strains [J].
Daffonchio, D ;
Borin, S ;
Consolandi, A ;
Sorlini, C .
FEMS MICROBIOLOGY LETTERS, 1999, 180 (01) :77-83
[10]   Homoduplex and heteroduplex polymorphisms of the amplified ribosomal 16S-23S internal transcribed spacers describe genetic relationships in the "Bacillus cereus group" [J].
Daffonchio, D ;
Cherif, A ;
Borin, S .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2000, 66 (12) :5460-5468