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Comparable stx 2a expression and phage production levels between Shiga toxin-producing Escherichia coli strains from human and bovine origin.

Authors :
Burgán J
Krüger A
Lucchesi PMA
Source :
Zoonoses and public health [Zoonoses Public Health] 2020 Feb; Vol. 67 (1), pp. 44-53. Date of Electronic Publication: 2019 Dec 23.
Publication Year :
2020

Abstract

Shiga toxin-producing Escherichia coli (STEC) can cause diarrhoea and severe diseases in humans, such as haemolytic uraemic syndrome. STEC virulence is considered to correlate with the amount of Shiga toxins (Stx) produced, especially Stx2, whose subtype Stx2a is most frequently associated with high virulence. Stx are encoded in prophages, which play an important role in STEC pathogenesis. The aim of this study was to evaluate stx <subscript>2a</subscript> expression levels and Stx2a phage production using qPCR and the double-agar-layer method in 29 STEC strains, corresponding to serotypes O26:H11 (6), O91:H21 (1), O145:H- (11) and O157:H7 (11), isolated from cattle and humans. Results were then tested for possible associations with serotype, origin or some genetic features. We observed heterogeneous levels of stx <subscript>2a</subscript> expression and Stx2a phage production. However, statistical comparisons identified a higher stx <subscript>2a</subscript> expression in response to mitomycin C in strains isolated from cattle than in those from humans. At the same time, compared to stx <subscript>2a</subscript> /stx <subscript>2c</subscript> strains, stx <subscript>2a</subscript> strains showed a higher increase in phage production under induced conditions. Notably, most of the strains studied, regardless of serotype and origin, carried inducible Stx2a phages and evidenced expression of stx <subscript>2a</subscript> that increased along with phage production levels under induced conditions.<br /> (© 2019 Blackwell Verlag GmbH.)

Details

Language :
English
ISSN :
1863-2378
Volume :
67
Issue :
1
Database :
MEDLINE
Journal :
Zoonoses and public health
Publication Type :
Academic Journal
Accession number :
31868306
Full Text :
https://doi.org/10.1111/zph.12653