PLoS ONE (Jan 2012)

Comparative analysis of genome sequences covering the seven cronobacter species.

  • Susan Joseph,
  • Prerak Desai,
  • Yongmei Ji,
  • Craig A Cummings,
  • Rita Shih,
  • Lovorka Degoricija,
  • Alain Rico,
  • Pius Brzoska,
  • Stephen E Hamby,
  • Naqash Masood,
  • Sumyya Hariri,
  • Hana Sonbol,
  • Nadia Chuzhanova,
  • Michael McClelland,
  • Manohar R Furtado,
  • Stephen J Forsythe

DOI
https://doi.org/10.1371/journal.pone.0049455
Journal volume & issue
Vol. 7, no. 11
p. e49455

Abstract

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Species of Cronobacter are widespread in the environment and are occasional food-borne pathogens associated with serious neonatal diseases, including bacteraemia, meningitis, and necrotising enterocolitis. The genus is composed of seven species: C. sakazakii, C. malonaticus, C. turicensis, C. dublinensis, C. muytjensii, C. universalis, and C. condimenti. Clinical cases are associated with three species, C. malonaticus, C. turicensis and, in particular, with C. sakazakii multilocus sequence type 4. Thus, it is plausible that virulence determinants have evolved in certain lineages.We generated high quality sequence drafts for eleven Cronobacter genomes representing the seven Cronobacter species, including an ST4 strain of C. sakazakii. Comparative analysis of these genomes together with the two publicly available genomes revealed Cronobacter has over 6,000 genes in one or more strains and over 2,000 genes shared by all Cronobacter. Considerable variation in the presence of traits such as type six secretion systems, metal resistance (tellurite, copper and silver), and adhesins were found. C. sakazakii is unique in the Cronobacter genus in encoding genes enabling the utilization of exogenous sialic acid which may have clinical significance. The C. sakazakii ST4 strain 701 contained additional genes as compared to other C. sakazakii but none of them were known specific virulence-related genes.Genome comparison revealed that pair-wise DNA sequence identity varies between 89 and 97% in the seven Cronobacter species, and also suggested various degrees of divergence. Sets of universal core genes and accessory genes unique to each strain were identified. These gene sequences can be used for designing genus/species specific detection assays. Genes encoding adhesins, T6SS, and metal resistance genes as well as prophages are found in only subsets of genomes and have contributed considerably to the variation of genomic content. Differences in gene content likely contribute to differences in the clinical and environmental distribution of species and sequence types.