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A combination of PhP typing and β-D-glucuronidase gene sequence variation analysis for differentiation of Escherichia coli from humans and animals
Journal article   Peer reviewed

A combination of PhP typing and β-D-glucuronidase gene sequence variation analysis for differentiation of Escherichia coli from humans and animals

Nicole Masters, Melodie Christie, Mohammad Katouli and Helen Stratton
Canadian Journal of Microbiology, Vol.61(6), pp.409-416
2015
url
https://doi.org/10.1139/cjm-2015-0048View
Published Version

Abstract

E. coli β-d-glucuronidase gene numerical analysis PhP typing
We investigated the usefulness of the β-D-glucuronidase gene variance in E. coli as a MST tool using a novel algorithm for comparison of sequences from a pre-screened set of host specific isolates using a high resolution PhP typing method. A total of 65 common biochemical phenotypes belonging to 318 E. coli strains isolated from humans, domestic and wild animals were analysed for nucleotide variations at 10 loci along a 518bp fragment of the 1812bp β-D-glucuronidase gene. Neighbour-Joining analysis of loci variations revealed 86 (76.8%) human isolates and 91.2% of animal isolates were correctly identified. Pair-wise hierarchical clustering improved assignment; where 92 (82.1%) human and 204 (99%) animal strains were assigned to their respective cluster. Our data shows initial typing of isolates and selection of common types from different hosts prior to analysis of the β-D-glucuronidase gene sequence improves source identification. We also concluded that numerical profiling of the nucleotide variations can be used as a valuable approach to differentiate human from animal E. coli. This study signifies the usefulness of the β-D-glucuronidase gene as a marker for differentiating human faecal pollution from animal sources.

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Domestic collaboration
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Biochemistry & Molecular Biology
Biotechnology & Applied Microbiology
Immunology
Microbiology

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