Affiliation:
1. Department of Civil and Environmental Engineering, University of Hawaii at Manoa, Honolulu, Hawaii, USA
Abstract
ABSTRACT
Presently, the understanding of bacterial enteric diseases in the community and their virulence factors relies almost exclusively on clinical disease reporting and examination of clinical pathogen isolates. This study aimed to investigate the feasibility of an alternative approach that monitors potential enteropathogenic
Escherichia coli
(EPEC) and enterohemorrhagic
E. coli
(EHEC) prevalence and intimin gene (
eae
) diversity in a community by directly quantifying and characterizing target virulence genes in the sanitary sewage. The quantitative PCR (qPCR) quantification of the
eae
,
stx
1
, and
stx
2
genes in sanitary sewage samples collected over a 13-month period detected
eae
in all 13 monthly sewage samples at significantly higher abundance (93 to 7,240 calibrator cell equivalents [CCE]/100 ml) than
stx
1
and
stx
2
, which were detected sporadically. The prevalence level of potential EPEC in the sanitary sewage was estimated by calculating the ratio of
eae
to
uidA
, which averaged 1.0% (σ = 0.4%) over the 13-month period. Cloning and sequencing of the
eae
gene directly from the sewage samples covered the majority of the
eae
diversity in the sewage and detected 17 unique
eae
alleles belonging to 14 subtypes. Among them,
eae
-β2 was identified to be the most prevalent subtype in the sewage, with the highest detection frequency in the clone libraries (41.2%) and within the different sampling months (85.7%). Additionally, sewage and environmental
E. coli
isolates were also obtained and used to determine the detection frequencies of the virulence genes as well as
eae
genetic diversity for comparison.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
Cited by
25 articles.
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