Abstract

BackgroundStrains of extraintestinal pathogenic Escherichia coli (ExPEC) can invade and colonize extraintestinal sites and cause a wide range of infections. Genomic analysis of ExPEC has mainly focused on isolates of human and avian origins, with porcine ExPEC isolates yet to be sequenced. To better understand the genomic attributes underlying the pathogenicity of porcine ExPEC, we isolated two E. coli strains PCN033 and PCN061 from pigs, assessed their in vivo virulence, and completed and compared their genomes.ResultsAnimal experiments demonstrated that strain PCN033, but not PCN061, was pathogenic in a pig model. The chromosome of PCN033 was 384 kb larger than that of PCN061. Among the PCN033-specific sequences, genes encoding adhesins, unique lipopolysaccharide, unique capsular polysaccharide, iron acquisition and transport systems, and metabolism were identified. Additionally, a large plasmid PCN033p3 harboring many typical ExPEC virulence factors was identified in PCN033. Based on the genetic variation between PCN033 and PCN061, corresponding phenotypic differences in flagellum-dependent swarming motility and metabolism were verified. Furthermore, the comparative genomic analyses showed that the PCN033 genome shared many similarities with genomic sequences of human ExPEC strains. Additionally, comparison of PCN033 genome with other nine characteristic E. coli genomes revealed 425 PCN033-special coding sequences. Genes of this subset included those encoding type I restriction-modification (R-M) system, type VI secretion system (T6SS) and membrane-associated proteins.ConclusionsThe genetic and phenotypic differences between PCN033 and PCN061 could partially explain their differences in virulence, and also provide insight towards the molecular mechanisms of porcine ExPEC infections. Additionally, the similarities between the genomes of PCN033 and human ExPEC strains suggest that some connections between porcine and human ExPEC strains exist. The first completed genomic sequence for porcine ExPEC and the genomic differences identified by comparative analyses provide a baseline understanding of porcine ExPEC genetics and lay the foundation for their further study.Electronic supplementary materialThe online version of this article (doi:10.1186/s12864-015-1890-9) contains supplementary material, which is available to authorized users.

Highlights

  • Strains of extraintestinal pathogenic Escherichia coli (ExPEC) can invade and colonize extraintestinal sites and cause a wide range of infections

  • Previous research has shown that Hcp2 of E. coli RS218 contributes to its interaction with human brain microvascular endothelial cells (HBMECs) [70]. Outside of this Type VI secretion system (T6SS) gene cluster, we identified a third hemolysin coregulated protein (Hcp) that shared 32.2 % identity with Hcp1 and another valine-glycine repeat protein G (VgrG); this Hcp protein exhibited 99 % identity with VgrG1

  • The first full genomic analysis of porcine ExPEC strain demonstrates that porcine ExPEC strain PCN033 shared many similarities with human ExPEC strains

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Summary

Introduction

Strains of extraintestinal pathogenic Escherichia coli (ExPEC) can invade and colonize extraintestinal sites and cause a wide range of infections. Characteristic ExPEC VFs include various adhesins (P and type I fimbriae), structural components of the bacterial outer membrane (capsule, lipopolysaccharide), iron acquisition and utilization systems (aerobactin and salmochelin siderophores), toxins (hemolysin, cytotoxic necrosis factor) and secretion systems [4, 5]. These VFs are frequently encoded on mobile genetic elements in unique organization [1]. Possession of ColV plasmids are a defining trait of APEC and these plasmids are key players in APEC pathogenesis [6]

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