Population structure and evolution of the Bacillus cereus group - PubMed (original) (raw)
Population structure and evolution of the Bacillus cereus group
Fergus G Priest et al. J Bacteriol. 2004 Dec.
Abstract
Representative strains of the Bacillus cereus group of bacteria, including Bacillus anthracis (11 isolates), B. cereus (38 isolates), Bacillus mycoides (1 isolate), Bacillus thuringiensis (53 isolates from 17 serovars), and Bacillus weihenstephanensis (2 isolates) were assigned to 59 sequence types (STs) derived from the nucleotide sequences of seven alleles, glpF, gmk, ilvD, pta, pur, pycA, and tpi. Comparisons of the maximum likelihood (ML) tree of the concatenated sequences with individual gene trees showed more congruence than expected by chance, indicating a generally clonal structure to the population. The STs followed two major lines of descent. Clade 1 comprised B. anthracis strains, numerous B. cereus strains, and rare B. thuringiensis strains, while clade 2 included the majority of the B. thuringiensis strains together with some B. cereus strains. Other species were allocated to a third, heterogeneous clade. The ML trees and split decomposition analysis were used to assign STs to eight lineages within clades 1 and 2. These lineages were defined by bootstrap analysis and by a preponderance of fixed differences over shared polymorphisms among the STs. Lineages were named with reference to existing designations: Anthracis, Cereus I, Cereus II, Cereus III, Kurstaki, Sotto, Thuringiensis, and Tolworthi. Strains from some B. thuringiensis serovars were wholly or largely assigned to a single ST, for example, serovar aizawai isolates were assigned to ST-15, serovar kenyae isolates were assigned to ST-13, and serovar tolworthi isolates were assigned to ST-23, while other serovars, such as serovar canadensis, were genetically heterogeneous. We suggest a revision of the nomenclature in which the lineage and clone are recognized through name and ST designations in accordance with the clonal structure of the population.
Figures
FIG. 1.
ML phylogenetic tree for the concatenated gene sequences for the 59 STs included in the study. Strain identifications: , B. anthracis; ○, B. cereus; ▵, B. thuringiensis; ▪, B. mycoides; □, B. weihenstephanensis. All horizontal branch lengths were drawn to a scale of substitutions per site, and the tree was rooted at the midpoint for the purpose of clarity only. All bootstrap support values of >80% are shown next to the appropriate nodes. The 85% bootstrap value associated with clade 2 excludes the highly divergent ST-9 type.
FIG. 2.
Maximum likelihood phylogenetic trees obtained for the concatenated sequence and the seven loci. ST designations are given in Table 1. All horizontal branch lengths were drawn to scale.
FIG. 2.
Maximum likelihood phylogenetic trees obtained for the concatenated sequence and the seven loci. ST designations are given in Table 1. All horizontal branch lengths were drawn to scale.
FIG. 3.
Maximum likelihood analysis of phylogenetic congruence in the B. cereus group. An ML tree that was reconstructed from the data for the concatenated loci and each of the seven loci was compared to each of the eight ML trees, with the branch lengths optimized for each analysis. The differences in likelihood (Δ−ln L) are shown for each tree (open symbols) and for 200 random trees (closed symbols).
Similar articles
- Bacillus weihenstephanensis characteristics are present in Bacillus cereus and Bacillus mycoides strains.
Soufiane B, Côté JC. Soufiane B, et al. FEMS Microbiol Lett. 2013 Apr;341(2):127-37. doi: 10.1111/1574-6968.12106. Epub 2013 Mar 12. FEMS Microbiol Lett. 2013. PMID: 23413955 - Fluorescent amplified fragment length polymorphism analysis of Bacillus anthracis, Bacillus cereus, and Bacillus thuringiensis isolates.
Hill KK, Ticknor LO, Okinaka RT, Asay M, Blair H, Bliss KA, Laker M, Pardington PE, Richardson AP, Tonks M, Beecher DJ, Kemp JD, Kolstø AB, Wong AC, Keim P, Jackson PJ. Hill KK, et al. Appl Environ Microbiol. 2004 Feb;70(2):1068-80. doi: 10.1128/AEM.70.2.1068-1080.2004. Appl Environ Microbiol. 2004. PMID: 14766590 Free PMC article. - Multilocus sequence analysis of Bacillus thuringiensis serovars navarrensis, bolivia and vazensis and Bacillus weihenstephanensis reveals a common phylogeny.
Soufiane B, Baizet M, Côté JC. Soufiane B, et al. Antonie Van Leeuwenhoek. 2013 Jan;103(1):195-205. doi: 10.1007/s10482-012-9800-5. Epub 2012 Oct 17. Antonie Van Leeuwenhoek. 2013. PMID: 23073664 - Sequence diversity of the Bacillus thuringiensis and B. cereus sensu lato flagellin (H antigen) protein: comparison with H serotype diversity.
Xu D, Côté JC. Xu D, et al. Appl Environ Microbiol. 2006 Jul;72(7):4653-62. doi: 10.1128/AEM.00328-06. Appl Environ Microbiol. 2006. PMID: 16820457 Free PMC article. - Biology and taxonomy of Bacillus cereus, Bacillus anthracis, and Bacillus thuringiensis.
Vilas-Bôas GT, Peruca AP, Arantes OM. Vilas-Bôas GT, et al. Can J Microbiol. 2007 Jun;53(6):673-87. doi: 10.1139/W07-029. Can J Microbiol. 2007. PMID: 17668027 Review.
Cited by
- Evaluating the Safety of Bacillus cereus GW-01 Obtained from Sheep Rumen Chyme.
Xu B, Huang X, Qin H, Lei Y, Zhao S, Liu S, Liu G, Zhao J. Xu B, et al. Microorganisms. 2024 Jul 18;12(7):1457. doi: 10.3390/microorganisms12071457. Microorganisms. 2024. PMID: 39065225 Free PMC article. - Bacillus cereus Biovar Anthracis Causing Anthrax in Sub-Saharan Africa-Chromosomal Monophyly and Broad Geographic Distribution.
Antonation KS, Grützmacher K, Dupke S, Mabon P, Zimmermann F, Lankester F, Peller T, Feistner A, Todd A, Herbinger I, de Nys HM, Muyembe-Tamfun JJ, Karhemere S, Wittig RM, Couacy-Hymann E, Grunow R, Calvignac-Spencer S, Corbett CR, Klee SR, Leendertz FH. Antonation KS, et al. PLoS Negl Trop Dis. 2016 Sep 8;10(9):e0004923. doi: 10.1371/journal.pntd.0004923. eCollection 2016 Sep. PLoS Negl Trop Dis. 2016. PMID: 27607836 Free PMC article. - Strategy for identification of Bacillus cereus and Bacillus thuringiensis strains closely related to Bacillus anthracis.
Daffonchio D, Raddadi N, Merabishvili M, Cherif A, Carmagnola L, Brusetti L, Rizzi A, Chanishvili N, Visca P, Sharp R, Borin S. Daffonchio D, et al. Appl Environ Microbiol. 2006 Feb;72(2):1295-301. doi: 10.1128/AEM.72.2.1295-1301.2006. Appl Environ Microbiol. 2006. PMID: 16461679 Free PMC article. - Complete Genome Sequence of Bacillus cereus CC-1, A Novel Marine Selenate/Selenite Reducing Bacterium Producing Metallic Selenides Nanomaterials.
Che L, Xu W, Zhan J, Zhang L, Liu L, Zhou H. Che L, et al. Curr Microbiol. 2019 Jan;76(1):78-85. doi: 10.1007/s00284-018-1587-9. Epub 2018 Oct 20. Curr Microbiol. 2019. PMID: 30343326 - Toxigenic Genes, Pathogenic Potential and Antimicrobial Resistance of Bacillus cereus Group Isolated from Ice Cream and Characterized by Whole Genome Sequencing.
Fraccalvieri R, Bianco A, Difato LM, Capozzi L, Del Sambro L, Simone D, Catanzariti R, Caruso M, Galante D, Normanno G, Palazzo L, Tempesta M, Parisi A. Fraccalvieri R, et al. Foods. 2022 Aug 17;11(16):2480. doi: 10.3390/foods11162480. Foods. 2022. PMID: 36010481 Free PMC article.
References
- Ankarloo, J., D. A. Caugant, B. M. Hansen, A. Berg, A.-B. Kolstø, and A. Lovgren. 2000. Genome stability of Bacillus thuringiensis subsp. israelensis isolates. Curr. Microbiol. 40:51-56. - PubMed
- Ash, C., and M. D. Collins. 1992. Comparative analysis of 23S ribosomal RNA gene sequences of Bacillus anthracis and emetic Bacillus cereus determined by PCR-direct sequencing. FEMS Microbiol. Lett. 73:75-80. - PubMed
- Ash, C., J. A. Farrow, M. Dorsch, E. Stackebrandt, and M. D. Collins. 1991. Comparative analysis of Bacillus anthracis, Bacillus cereus, and related species on the basis of reverse transcriptase sequencing of 16S rRNA. Int. J. Syst. Bacteriol. 41:343-346. - PubMed
- Carlson, C. R., T. Johansen, and A.-B. Kolstø. 1996. The chromosome map of Bacillus thuringiensis subsp. canadensis HD224 is highly similar to that of Bacillus cereus type strain ATCC 14579. FEMS Microbiol. Lett. 141:163-167. - PubMed
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous