Literature DB >> 17435283

Differentiation between Bacillus thuringiensis strains by gyrB PCR-Sau3AI fingerprinting.

Mireille Kallassy Awad1, Imène Saadaoui, Souad Rouis, Slim Tounsi, Samir Jaoua.   

Abstract

gyrB DNA fragments of seven Bacillus thuringiensis local collection family representatives were amplified by PCR and sequenced. Several differences in their corresponding sequences were evidenced. Both in silico and in vitro restriction maps of gyrB sequences and fragments respectively confirmed that EcoRI and Sau3AI could be used to differentiate between B. thuringiensis strains. However, the phylogeny analysis showed that only the gyrB PCR-Sau3AI allows a strains classification that correlates very well with that obtained on the basis of the sequences analysis. Thus, these finds show that gyrB PCR- Sau3AI digestion could be considered as an efficient, rapid, and easy method to make a distinction, not only between strains belonging to the Bacillus cereus group, but also between those belonging to B. thuringiensis.

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Year:  2007        PMID: 17435283     DOI: 10.1007/bf02686112

Source DB:  PubMed          Journal:  Mol Biotechnol        ISSN: 1073-6085            Impact factor:   2.695


  16 in total

1.  How close is close: 16S rRNA sequence identity may not be sufficient to guarantee species identity.

Authors:  G E Fox; J D Wisotzkey; P Jurtshuk
Journal:  Int J Syst Bacteriol       Date:  1992-01

2.  Genotypic Diversity among Bacillus cereus and Bacillus thuringiensis Strains.

Authors:  C R Carlson; D A Caugant; A B Kolstø
Journal:  Appl Environ Microbiol       Date:  1994-06       Impact factor: 4.792

3.  Selective Process for Efficient Isolation of Soil Bacillus spp.

Authors:  R S Travers; P A Martin; C F Reichelderfer
Journal:  Appl Environ Microbiol       Date:  1987-06       Impact factor: 4.792

4.  Comparative analysis of the individual protoxin components in P1 crystals of Bacillus thuringiensis subsp. kurstaki isolates NRD-12 and HD-1.

Authors:  L Masson; G Préfontaine; L Péloquin; P C Lau; R Brousseau
Journal:  Biochem J       Date:  1990-07-15       Impact factor: 3.857

5.  Studies on DNA replication in the bacteriophage T4 in vitro system.

Authors:  B M Alberts; J Barry; P Bedinger; T Formosa; C V Jongeneel; K N Kreuzer
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1983

6.  Construction and characterization of a recombinant Bacillus thuringiensis subsp. israelensis strain that produces Cry11B.

Authors:  H W Park; A Delécluse; B A Federici
Journal:  J Invertebr Pathol       Date:  2001-07       Impact factor: 2.841

7.  Discrimination of Bacillus cereus and Bacillus thuringiensis with 16S rRNA and gyrB gene based PCR primers and sequencing of their annealing sites.

Authors:  M L Chen; H Y Tsen
Journal:  J Appl Microbiol       Date:  2002       Impact factor: 3.772

8.  Arbitrary primer polymerase chain reaction, a powerful method to identify Bacillus thuringiensis serovars and strains.

Authors:  R Brousseau; A Saint-Onge; G Préfontaine; L Masson; J Cabana
Journal:  Appl Environ Microbiol       Date:  1993-01       Impact factor: 4.792

9.  Bacillus anthracis diverges from related clades of the Bacillus cereus group in 16S-23S ribosomal DNA intergenic transcribed spacers containing tRNA genes.

Authors:  Ameur Cherif; Sara Borin; Aurora Rizzi; Hadda Ouzari; Abdellatif Boudabous; Daniele Daffonchio
Journal:  Appl Environ Microbiol       Date:  2003-01       Impact factor: 4.792

10.  Use of 16S rRNA, 23S rRNA, and gyrB gene sequence analysis to determine phylogenetic relationships of Bacillus cereus group microorganisms.

Authors:  Sergei G Bavykin; Yuri P Lysov; Vladimir Zakhariev; John J Kelly; Joany Jackman; David A Stahl; Alexey Cherni
Journal:  J Clin Microbiol       Date:  2004-08       Impact factor: 5.948

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