Delayed lactose utilization among Shiga toxin-producing Escherichia coli of serogroup O121.
Canada
Escherichia coli Proteins
/ genetics
Flour
/ microbiology
Glucuronidase
/ genetics
Lactose
/ metabolism
Membrane Transport Proteins
Monosaccharide Transport Proteins
Serogroup
Shiga-Toxigenic Escherichia coli
/ genetics
Symporters
Triticum
/ microbiology
United States
beta-Galactosidase
/ genetics
Delayed lactose utilization
Lac operon
O121:H19
Shiga toxin-producing E. coli
Journal
Food microbiology
ISSN: 1095-9998
Titre abrégé: Food Microbiol
Pays: England
ID NLM: 8601127
Informations de publication
Date de publication:
Apr 2022
Apr 2022
Historique:
received:
04
06
2021
revised:
31
08
2021
accepted:
09
09
2021
entrez:
23
11
2021
pubmed:
24
11
2021
medline:
15
12
2021
Statut:
ppublish
Résumé
Two outbreaks of Shiga toxin-producing Escherichia coli O121:H19 associated with wheat flour, in the United States of America and Canada, involved strains with an unusual phenotype, delayed lactose utilization (DLU). These strains do not ferment lactose when initially cultured on MacConkey agar (MAC), but lactose fermentation occurs following subculture to a second plate of MAC. The prevalence of DLU was determined by examining the β-galactosidase activity of 49 strains of E. coli O121, and of 37 other strains of E. coli. Twenty four of forty three O121:H19 and one O121:NM displayed DLU. Two strains (O121:NM and O145:H34) did not have detectable β-galactosidase activity. β-glucuronidase activity of O121 strains was also determined. All but six DLU strains had normal β-glucuronidase activity. β-glucuronidase activity was suppressed on MAC for 17 of 23 O121 non-DLU strains. Genomic analysis found that DLU strains possessed an insertion sequence, IS600 (1267 bp), between lacZ (β-galactosidase) and lacY (β-galactoside permease), that was not present in strains exhibiting normal lactose utilization. The insert might reduce the expression of β-galactoside permease, delaying import of lactose, resulting in the DLU phenotype. The high probability of DLU should be considered when using lactose-containing media for the isolation of STEC O121.
Identifiants
pubmed: 34809935
pii: S0740-0020(21)00169-6
doi: 10.1016/j.fm.2021.103903
pii:
doi:
Substances chimiques
Escherichia coli Proteins
0
LacY protein, E coli
0
Membrane Transport Proteins
0
Monosaccharide Transport Proteins
0
Symporters
0
beta-Galactosidase
EC 3.2.1.23
Glucuronidase
EC 3.2.1.31
Lactose
J2B2A4N98G
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
103903Informations de copyright
Crown Copyright © 2021. Published by Elsevier Ltd. All rights reserved.