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Commensal E. coli Stx2 lysogens produce high levels of phages after spontaneous prophage induction

Enterohemorrhagic E. coli (EHEC) is a food-borne pathogen that causes disease ranging from uncomplicated diarrhea to life-threatening hemolytic uremic syndrome (HUS) and nervous system complications. Shiga toxin 2 (Stx2) is the major virulence factor of EHEC and is critical for development of HUS. T...

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Autores principales: Iversen, Hildegunn, L' Abée-Lund, Trine M., Aspholm, Marina, Arnesen, Lotte P. S., Lindbäck, Toril
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4315091/
https://www.ncbi.nlm.nih.gov/pubmed/25692100
http://dx.doi.org/10.3389/fcimb.2015.00005
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author Iversen, Hildegunn
L' Abée-Lund, Trine M.
Aspholm, Marina
Arnesen, Lotte P. S.
Lindbäck, Toril
author_facet Iversen, Hildegunn
L' Abée-Lund, Trine M.
Aspholm, Marina
Arnesen, Lotte P. S.
Lindbäck, Toril
author_sort Iversen, Hildegunn
collection PubMed
description Enterohemorrhagic E. coli (EHEC) is a food-borne pathogen that causes disease ranging from uncomplicated diarrhea to life-threatening hemolytic uremic syndrome (HUS) and nervous system complications. Shiga toxin 2 (Stx2) is the major virulence factor of EHEC and is critical for development of HUS. The genes encoding Stx2 are carried by lambdoid bacteriophages and the toxin production is tightly linked to the production of phages during lytic cycle. It has previously been suggested that commensal E. coli could amplify the production of Stx2-phages and contribute to the severity of disease. In this study we examined the susceptibility of commensal E. coli strains to the Stx2-converting phage ϕ734, isolated from a highly virulent EHEC O103:H25 (NIPH-11060424). Among 38 commensal E. coli strains from healthy children below 5 years, 15 were lysogenized by the ϕ734 phage, whereas lytic infection was not observed. Three of the commensal E. coli ϕ734 lysogens were tested for stability, and appeared stable and retained the phage for at least 10 cultural passages. When induced to enter lytic cycle by H(2)O(2) treatment, 8 out of 13 commensal lysogens produced more ϕ734 phages than NIPH-11060424. Strikingly, five of them even spontaneously (non-induced) produced higher levels of phage than the H(2)O(2) induced NIPH-11060424. An especially high frequency of HUS (60%) was seen among children infected by NIPH-11060424 during the outbreak in 2006. Based on our findings, a high Stx2 production by commensal E. coli lysogens cannot be ruled out as a contributor to the high frequency of HUS during this outbreak.
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spelling pubmed-43150912015-02-17 Commensal E. coli Stx2 lysogens produce high levels of phages after spontaneous prophage induction Iversen, Hildegunn L' Abée-Lund, Trine M. Aspholm, Marina Arnesen, Lotte P. S. Lindbäck, Toril Front Cell Infect Microbiol Microbiology Enterohemorrhagic E. coli (EHEC) is a food-borne pathogen that causes disease ranging from uncomplicated diarrhea to life-threatening hemolytic uremic syndrome (HUS) and nervous system complications. Shiga toxin 2 (Stx2) is the major virulence factor of EHEC and is critical for development of HUS. The genes encoding Stx2 are carried by lambdoid bacteriophages and the toxin production is tightly linked to the production of phages during lytic cycle. It has previously been suggested that commensal E. coli could amplify the production of Stx2-phages and contribute to the severity of disease. In this study we examined the susceptibility of commensal E. coli strains to the Stx2-converting phage ϕ734, isolated from a highly virulent EHEC O103:H25 (NIPH-11060424). Among 38 commensal E. coli strains from healthy children below 5 years, 15 were lysogenized by the ϕ734 phage, whereas lytic infection was not observed. Three of the commensal E. coli ϕ734 lysogens were tested for stability, and appeared stable and retained the phage for at least 10 cultural passages. When induced to enter lytic cycle by H(2)O(2) treatment, 8 out of 13 commensal lysogens produced more ϕ734 phages than NIPH-11060424. Strikingly, five of them even spontaneously (non-induced) produced higher levels of phage than the H(2)O(2) induced NIPH-11060424. An especially high frequency of HUS (60%) was seen among children infected by NIPH-11060424 during the outbreak in 2006. Based on our findings, a high Stx2 production by commensal E. coli lysogens cannot be ruled out as a contributor to the high frequency of HUS during this outbreak. Frontiers Media S.A. 2015-02-03 /pmc/articles/PMC4315091/ /pubmed/25692100 http://dx.doi.org/10.3389/fcimb.2015.00005 Text en Copyright © 2015 Iversen, L' Abée-Lund, Aspholm, Arnesen and Lindbäck. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Iversen, Hildegunn
L' Abée-Lund, Trine M.
Aspholm, Marina
Arnesen, Lotte P. S.
Lindbäck, Toril
Commensal E. coli Stx2 lysogens produce high levels of phages after spontaneous prophage induction
title Commensal E. coli Stx2 lysogens produce high levels of phages after spontaneous prophage induction
title_full Commensal E. coli Stx2 lysogens produce high levels of phages after spontaneous prophage induction
title_fullStr Commensal E. coli Stx2 lysogens produce high levels of phages after spontaneous prophage induction
title_full_unstemmed Commensal E. coli Stx2 lysogens produce high levels of phages after spontaneous prophage induction
title_short Commensal E. coli Stx2 lysogens produce high levels of phages after spontaneous prophage induction
title_sort commensal e. coli stx2 lysogens produce high levels of phages after spontaneous prophage induction
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4315091/
https://www.ncbi.nlm.nih.gov/pubmed/25692100
http://dx.doi.org/10.3389/fcimb.2015.00005
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