The Bacillus cereus group:: novel aspects of population structure and genome dynamics

被引:108
作者
Tourasse, N. J. [1 ]
Helgason, E. [1 ]
Okstad, O. A. [1 ]
Hegna, I. K. [1 ]
Kolsto, A. -B. [1 ]
机构
[1] Univ Oslo, Sch Pharm, Dept Pharmaceut Biosci Microbiol, N-0316 Oslo, Norway
关键词
Bacillus cereus group; clonal complex; genome dynamics; intron; IStron; MLST; repeated sequences;
D O I
10.1111/j.1365-2672.2006.03087.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 provide new insights into the population and genomic structure of the Bacillus cereus group of bacteria. Methods and Results: The genetic relatedness among B. cereus group strains was assessed by multilocus sequence typing (MLST) using an optimized scheme based on seven chromosomal housekeeping genes. A set of 48 strains from different clinical sources was included, and six clonal complexes containing several genetically similar isolates from unrelated patients were identified. Interestingly, several clonal groups contained strains that were isolated from similar human sources. Furthermore, comparative whole genome sequence analysis of 16 strains led to the discovery of novel ubiquitous genome features of the B. cereus group, such as atypical group II introns, IStrons, and hitherto uncharacterized repeated elements. Conclusions: The B. cereus group constitutes a coherent population unified by the presence of ubiquitous and specific genetic elements which do not show any pattern, either in their sequences or genomic locations, which allows to differentiate between the member species of the group. Nevertheless, the population is very dynamic, as particular lineages of clinical origin can evolve to form clonal complexes. At the genome level, the dynamic behaviour is indicated by the presence of numerous mobile and repeated elements. Significance and Impact of the Study: The B. cereus group of bacteria comprises species that are of medical and economic importance. The MLST data, along with the primers and protocols used, will be available in a public, web-accessible database (http://mlstoslo.uio.no).
引用
收藏
页码:579 / 593
页数:15
相关论文
共 80 条
[21]  
Galtier N, 1996, COMPUT APPL BIOSCI, V12, P543
[22]   GENETIC-VARIABILITY OF BACILLUS-ANTHRACIS AND RELATED SPECIES [J].
HARRELL, LJ ;
ANDERSEN, GL ;
WILSON, KH .
JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (07) :1847-1850
[23]   The IStron CdISt1 of Clostridium difficile:: molecular symbiosis of a group I intron and an insertion element [J].
Hasselmayer, O ;
Nitsche, C ;
Braun, V ;
von Eichel-Streiber, C .
ANAEROBE, 2004, 10 (02) :85-92
[24]   Clostridium difficile IStron CdISt1:: Discovery of a variant encoding two complete transposase-like proteins [J].
Hasselmayer, O ;
Braun, V ;
Nitsche, C ;
Moos, M ;
Rupnik, M ;
von Eichel-Streiber, C .
JOURNAL OF BACTERIOLOGY, 2004, 186 (08) :2508-2510
[25]   The natural history of group I introns [J].
Haugen, P ;
Simon, DM ;
Bhattacharya, D .
TRENDS IN GENETICS, 2005, 21 (02) :111-119
[26]   Genetic structure of population of Bacillus cereus and B-thuringiensis isolates associated with periodontitis and other human infections [J].
Helgason, E ;
Caugant, DA ;
Olsen, I ;
Kolsto, AB .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (04) :1615-1622
[27]   Bacillus anthracis, Bacillus cereus, and Bacillus thuringiensis -: One species on the basis of genetic evidence [J].
Helgason, E ;
Okstad, OA ;
Caugant, DA ;
Johansen, HA ;
Fouet, A ;
Mock, M ;
Hegna, I ;
Kolsto, AB .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2000, 66 (06) :2627-2630
[28]   Multilocus sequence typing scheme for bacteria of the Bacillus cereus group [J].
Helgason, E ;
Tourasse, NJ ;
Meisal, R ;
Caugant, DA ;
Kolsto, AB .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2004, 70 (01) :191-201
[29]   Genetic diversity of Bacillus cereus/B. thuringiensis isolates from natural sources [J].
Helgason E. ;
Caugant D.A. ;
Lecadet M.-M. ;
Chen Y. ;
Mahillon J. ;
Lövgren A. ;
Hegna I. ;
Kvaløy K. ;
Kolstø A.-B. .
Current Microbiology, 1998, 37 (2) :80-87
[30]   Correlation between serovars of Bacillus thuringiensis and type I β-exotoxin production [J].
Hernández, CS ;
Martínez, C ;
Porcar, M ;
Caballero, P ;
Ferré, J .
JOURNAL OF INVERTEBRATE PATHOLOGY, 2003, 82 (01) :57-62