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identifier PRJEB33762
type bioproject
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title Genome analysis of Clostridium perfringens BEC-positive, toxinotype D and E strains isolated from healthy children
description Clostridium perfringens toxinotype D, toxinotype E, and gastroenteritis-linked BEC/CPILE-positive strains have never been reported in healthy children. We isolated, whole-genome sequenced and bioinformatically characterised three C. perfringens isolates—type D (IQ1), type E (IQ2) and BEC/CPILE-positive (IQ3), recovered from the stools of three healthy two-year-olds, which were further compared to 128 C. perfringens genomes available from NCBI. The analysis uncovered a previously under-described putative toxin gene alv (alveolysin) encoded by isolates IQ2 and IQ3, which appeared to be a clade-specific trait associated with strains from domestic animals. A plasmid analysis indicated that the iota-toxin was encoded on a near-intact previously described plasmid pCPPB-1 in type E strain IQ2. The BEC genes becA and becB were carried on a near-identical pCPOS-1 plasmid previously associated with Japanese gastroenteritis outbreaks. Furthermore, a close phylogenetic relatedness was inferred between the French C. perfringens type E isolates cp515.17 and newly sequenced IQ2, suggesting geographical links. This study describes novel C. perfringens isolates from healthy individuals which encode important toxin genes, indicating the potential spread of these veterinary and clinically important strains and mobile genetic elements, and highlights areas for future research.
data type Genome sequencing and assembly
organization
publication
Genomic Analysis of Clostridium perfringens BEC/CPILE-Positive, Toxinotype D and E Strains Isolated from Healthy Children.
properties 
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dbXrefs
sra-run  ERR3457852ERR3457853ERR3457854
sra-submission  ERA2054972
biosample  SAMEA5818796SAMEA5818795SAMEA5818797
sra-study  ERP116580
sra-sample  ERS3607388ERS3607389ERS3607390
sra-experiment  ERX3479647ERX3479648ERX3479649
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status public
visibility unrestricted-access
dateCreated 2019-09-21T00:00:00Z
dateModified 2019-09-21T00:00:00Z
datePublished