Literature DB >> 24874674

Draft Genome Sequence of Bacillus cereus Strain BcFL2013, a Clinical Isolate Similar to G9241.

Jay E Gee1, Chung K Marston2, Scott A Sammons3, Mark A Burroughs3, Alex R Hoffmaster2.   

Abstract

Bacillus cereus strains, such as G9241, causing anthrax-like illnesses have recently been discovered. We report the genome sequence of a clinical strain, B. cereus BcFL2013, which is similar to G9241, recovered from a patient in Florida.
Copyright © 2014 Gee et al.

Entities:  

Year:  2014        PMID: 24874674      PMCID: PMC4038879          DOI: 10.1128/genomeA.00469-14

Source DB:  PubMed          Journal:  Genome Announc


GENOME ANNOUNCEMENT

Bacillus cereus is generally a harmless bacterium and is common in the environment. Strains of this species that cause disease are typically associated with food-borne emesis and diarrhea. More rarely is it associated with serious illness. B. cereus strains with similarities to Bacillus anthracis, the cause of anthrax, have been identified recently, which are linked to serious cases of pneumonia (1–3). The first B. cereus strain characterized, G9241, was isolated from a case of pneumonia in a welder in Louisiana in 1994 (2). In 2003, three more strains from Texas were isolated, including two clinical isolates, B. cereus 03BB87 and 03BB102, associated with two fatal cases of pneumonia (1). The features of interest in G9241 associated with virulence are the presence of two plasmids, pBCXO1 and pBC210. pBCXO1, homologous to plasmid pXO1 of B. anthracis, contains the genes encoding anthrax toxins (pagA, cya, and lef), as well as hasACB, which encodes hyaluronic acid capsule formation. pBC210 contains bpsXABCDEFGH, which encodes an exopolysaccharide (4). In 2013, we investigated a case of human cutaneous infection in Florida, which was similar in appearance to an anthrax eschar. The investigation yielded isolate B. cereus BcFL2013, which has features similar to those of G9241. Here, we report the draft genome sequence of strain BcFL2013. A 101 × 101 paired-end run was performed on an Illumina GAIIx using TruSeq chemistry and yielded 10,182,400 reads. A de novo assembly was performed using CLC Genomics Workbench 6.0.4 (CLC Inc., Aarhus, Denmark) and yielded 84 contigs consisting of 5.46 Mb, with an N50 of 139,961 bp. We analyzed the genome of BcFL2013 in silico by multilocus sequence typing (MLST) which uses the sequences of seven housekeeping genes to assign sequence types (ST) (5). We found that BcFL2013 belongs to ST78, matching G9241 and 03BB87. We determined that it has one of the operons associated with capsule production in G9241, hasACB, also associated with pBCXO1, which consists of the hyaluronan synthase (hasA), UTP-glucose-1-phosphate uridylyltransferase (hasC), and UDP-glucose 6-dehydrogenase (hasB) genes, with each gene having 100% identity with the corresponding gene from G9241. We did not detect the other G9241 capsule operon, bpsXABCDEFGH. We mapped the genome of BcFL2013 to that of plasmid pBCXO1 of G9241, which indicated that a homolog of this plasmid is present with >99.98% identity, but it included a 2.5-kb deletion. We determined that the anthrax toxin genes pagA, cya, and lef were also present and that the sequences have 100% identity to those found in G9241. Mapping the genome of BcFL2013 to plasmid pBC210 of G9241 indicated a homolog of the plasmid was present but had only approximately half the sequence of the 209,385 bp noted for pBC210. The study of the genome sequences of these B. cereus strains with characteristics more often associated with B. anthracis will provide insights into their potential for virulence.

Nucleotide sequence accession numbers.

This whole-genome shotgun project has been deposited at DDBJ/EMBL/GenBank under the accession no. JHQN00000000. The version described in this paper is version JHQN01000000.
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