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Genomic Subtraction To Identify and Characterize Sequences of Shiga Toxin-Producing Escherichia coli O91:H21
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ABSTRACT
To identify Shiga toxin-producing
Escherichia coli
genes associated with severe human disease, a genomic subtraction technique was used with hemolytic-uremic syndrome-associated O91:H21 strain CH014 and O6:H10 bovine strains. The method was adapted to the Shiga toxin-producing
E. coli
genome: three rounds of subtraction were used to isolate DNA fragments specific to strain CH014. The fragments were characterized by genetic support analysis, sequencing, and hybridization to the genome of a collection of Shiga toxin-producing
E. coli
strains. A total of 42 fragments were found, 19 of which correspond to previously identified unique DNA sequences in the enterohemorrhagic
E. coli
EDL933 reference strain, including 7 fragments corresponding to prophage sequences and others encoding candidate virulence factors, such a SepA homolog protein and a fimbrial usher protein. In addition, the subtraction procedure yielded plasmid-related sequences from
Shigella flexneri
and enteropathogenic and Shiga toxin-producing
E. coli
virulence plasmids. We found that lateral gene transfer is extensive in strain CH014, and we discuss the role of genomic mobile elements, especially bacteriophages, in the evolution and possible transfer of virulence determinants.
American Society for Microbiology
Title: Genomic Subtraction To Identify and Characterize Sequences of Shiga Toxin-Producing
Escherichia coli
O91:H21
Description:
ABSTRACT
To identify Shiga toxin-producing
Escherichia coli
genes associated with severe human disease, a genomic subtraction technique was used with hemolytic-uremic syndrome-associated O91:H21 strain CH014 and O6:H10 bovine strains.
The method was adapted to the Shiga toxin-producing
E.
coli
genome: three rounds of subtraction were used to isolate DNA fragments specific to strain CH014.
The fragments were characterized by genetic support analysis, sequencing, and hybridization to the genome of a collection of Shiga toxin-producing
E.
coli
strains.
A total of 42 fragments were found, 19 of which correspond to previously identified unique DNA sequences in the enterohemorrhagic
E.
coli
EDL933 reference strain, including 7 fragments corresponding to prophage sequences and others encoding candidate virulence factors, such a SepA homolog protein and a fimbrial usher protein.
In addition, the subtraction procedure yielded plasmid-related sequences from
Shigella flexneri
and enteropathogenic and Shiga toxin-producing
E.
coli
virulence plasmids.
We found that lateral gene transfer is extensive in strain CH014, and we discuss the role of genomic mobile elements, especially bacteriophages, in the evolution and possible transfer of virulence determinants.
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