Abstract

The Clermont scheme has been used for subtyping of Escherichia coli since it was initially described in early 2000. Since then, researchers have used the scheme to type and sub-type commensal E. coli and pathogenic E. coli, such as extraintestinal pathogenic E. coli (ExPEC), and compare their phylogenetic assignment by pathogenicity, serogroup, distribution among ExPEC of different host species and complement of virulence and resistance traits. Here, we compare assignments of human and avian ExPEC and commensal E. coli using the old and revised Clermont schemes to determine if the new scheme provides a refined snapshot of isolate classification. 1,996 E. coli from human hosts and poultry, including 84 human neonatal meningitis E. coli isolates, 88 human vaginal E. coli, 696 human uropathogenic E. coli, 197 healthy human fecal E. coli, 452 avian pathogenic E. coli (APEC), 200 retail poultry E. coli, 80 crop and gizzard E. coli from healthy poultry at slaughter and 199 fecal E. coli from healthy birds at slaughter. All isolates were subject to phylogenetic analysis using the Clermont et al. (2000, 2013) schemes and compared to determine the effect of the new classification on strain designation. Most of the isolates’ strain designation remained where they were originally assigned. Greatest designation change occurred in APEC where 53.8% of isolates were reclassified; while classification rates among human strains ranged from 8 to 14%. However, some significant changes were observed for UPEC associated strains with significant (P < 0.05) designation changes observed from A to C and D to E or F phylogenetic types; a similar designation change was noted among NMEC for D to F designation change. Among the APEC significant designation changes were observed from A to C and D to E and F. These studies suggest that the new scheme provides a tighter and more meaningful definition of some ExPEC; while the new typing scheme has a significant impact on APEC classification. A comparison of phylogenetic group assignment by content of virulence, resistance, replicon and pathogenicity island genes in APEC suggests that insertion of pathogenicity islands into the genome appears to correlate closely with revised phylogenetic assignment.

Highlights

  • Escherichia coli are common inhabitants of the intestinal tracts of mammals and one of the most extensively studied bacteria worldwide

  • A total of 1996 strains of E. coli were included in this study consisting of 84 strains associated with neonatal meningitis, these have been described elsewhere but consist of strains isolated from neonatal meningitis cases in the US and Netherlands (Johnson et al, 2002; Logue et al, 2012)

  • Most uropathogenic E. coli (UPEC) strains were typed as B2 and D by the older scheme and these two types still dominated in the revised scheme but not all classified by the two typing methods with a considerable number of A and D strains reclassifying to the newer types B2, C, E, and F with significant redistribution (P < 0.05) noted for A to C and D to E and F classification

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Summary

Introduction

Escherichia coli are common inhabitants of the intestinal tracts of mammals and one of the most extensively studied bacteria worldwide They may inhabit a host as harmless symbionts, or depending on their panoply of virulence traits and/or certain predisposing conditions, they may be responsible for both intestinal and extra-intestinal disease. Pathogenic E. coli may be subdivided into Intestinal Pathogenic E. coli (InPEC) or Extraintestinal Pathogenic E. coli (ExPEC) pathotypes depending on their host target tissue and disease syndrome they cause. The ExPEC causing meningitis in human newborns tends be of certain serogroups, in particular O18 (Logue et al, 2012; Nicholson et al, 2016a,b) They tend to possess large virulence plasmids and K1 capsular antigen (Rodriguez-Siek et al, 2005a). Avian Pathogenic E. coli (APEC), the ExPEC causing colibacillosis in birds, are typified by possession of large virulence plasmids (Rodriguez-Siek et al, 2005b; Barnes et al, 2008; Johnson et al, 2008a), and there is great diversity in the serogroups of APEC, the more common ones reported are O1, O2, and O78 (Rodriguez-Siek et al, 2005b; Nolan et al, 2013)

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