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Role of Plasmid Plasticity and Mobile Genetic Elements in the Entomopathogen Bacillus Thuringiensis Serovar Israelensis

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Specialty Microbiology
Date 2018 Sep 12
PMID 30203090
Citations 22
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Abstract

Bacillus thuringiensis is a well-known biopesticide that has been used for more than 80 years. This spore-forming bacterium belongs to the group of Bacillus cereus that also includes, among others, emetic and diarrheic pathotypes of B. cereus, the animal pathogen Bacillus anthracis and the psychrotolerant Bacillus weihenstephanensis. Bacillus thuringiensis is rather unique since it has adapted its lifestyle as an efficient pathogen of specific insect larvae. One of the peculiarities of B. thuringiensis strains is the extent of their extrachromosomal pool, with strains harbouring more than 10 distinct plasmid molecules. Among the numerous serovars of B. thuringiensis, 'israelensis' is certainly emblematic since its host spectrum is apparently restricted to dipteran insects like mosquitoes and black flies, vectors of human and animal diseases such as malaria, yellow fever, or river blindness. In this review, the putative role of the mobile gene pool of B. thuringiensis serovar israelensis in its pathogenicity and dedicated lifestyle is reviewed, with specific emphasis on the nature, diversity, and potential mobility of its constituents. Variations among the few related strains of B. thuringiensis serovar israelensis will also be reported and discussed in the scope of this specialised insect pathogen, whose lifestyle in the environment remains largely unknown.

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References
1.
Gonzalez Jr J, Carlton B . Patterns of plasmid DNA in crystalliferous and acrystalliferous strains of Bacillus thuringiensis. Plasmid. 1980; 3(1):92-8. DOI: 10.1016/s0147-619x(80)90038-4. View

2.
Verheust C, Fornelos N, Mahillon J . The Bacillus thuringiensis phage GIL01 encodes two enzymes with peptidoglycan hydrolase activity. FEMS Microbiol Lett. 2004; 237(2):289-95. DOI: 10.1016/j.femsle.2004.06.045. View

3.
Bazinet A . Pan-genome and phylogeny of Bacillus cereus sensu lato. BMC Evol Biol. 2017; 17(1):176. PMC: 5541404. DOI: 10.1186/s12862-017-1020-1. View

4.
Daugelavicius R, Gaidelyte A, Cvirkaite-Krupovic V, Bamford D . On-line monitoring of changes in host cell physiology during the one-step growth cycle of Bacillus phage Bam35. J Microbiol Methods. 2007; 69(1):174-9. DOI: 10.1016/j.mimet.2006.12.023. View

5.
Varani A, Siguier P, Gourbeyre E, Charneau V, Chandler M . ISsaga is an ensemble of web-based methods for high throughput identification and semi-automatic annotation of insertion sequences in prokaryotic genomes. Genome Biol. 2011; 12(3):R30. PMC: 3129680. DOI: 10.1186/gb-2011-12-3-r30. View