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Lytic Bacteriophage EFA1 Modulates HCT116 Colon Cancer Cell Growth and Upregulates ROS Production in an Enterococcus faecalis Co-culture System
Enterococcus faecalis is an opportunistic pathogen in the gut microbiota that’s associated with a range of difficult to treat nosocomial infections. It is also known to be associated with some colorectal cancers. Its resistance to a range of antibiotics and capacity to form biofilms increase its vir...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8044584/ https://www.ncbi.nlm.nih.gov/pubmed/33868210 http://dx.doi.org/10.3389/fmicb.2021.650849 |
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author | Kabwe, Mwila Meehan-Andrews, Terri Ku, Heng Petrovski, Steve Batinovic, Steven Chan, Hiu Tat Tucci, Joseph |
author_facet | Kabwe, Mwila Meehan-Andrews, Terri Ku, Heng Petrovski, Steve Batinovic, Steven Chan, Hiu Tat Tucci, Joseph |
author_sort | Kabwe, Mwila |
collection | PubMed |
description | Enterococcus faecalis is an opportunistic pathogen in the gut microbiota that’s associated with a range of difficult to treat nosocomial infections. It is also known to be associated with some colorectal cancers. Its resistance to a range of antibiotics and capacity to form biofilms increase its virulence. Unlike antibiotics, bacteriophages are capable of disrupting biofilms which are key in the pathogenesis of diseases such as UTIs and some cancers. In this study, bacteriophage EFA1, lytic against E. faecalis, was isolated and its genome fully sequenced and analyzed in silico. Electron microscopy images revealed EFA1 to be a Siphovirus. The bacteriophage was functionally assessed and shown to disrupt E. faecalis biofilms as well as modulate the growth stimulatory effects of E. faecalis in a HCT116 colon cancer cell co-culture system, possibly via the effects of ROS. The potential exists for further testing of bacteriophage EFA1 in these systems as well as in vivo models. |
format | Online Article Text |
id | pubmed-8044584 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80445842021-04-15 Lytic Bacteriophage EFA1 Modulates HCT116 Colon Cancer Cell Growth and Upregulates ROS Production in an Enterococcus faecalis Co-culture System Kabwe, Mwila Meehan-Andrews, Terri Ku, Heng Petrovski, Steve Batinovic, Steven Chan, Hiu Tat Tucci, Joseph Front Microbiol Microbiology Enterococcus faecalis is an opportunistic pathogen in the gut microbiota that’s associated with a range of difficult to treat nosocomial infections. It is also known to be associated with some colorectal cancers. Its resistance to a range of antibiotics and capacity to form biofilms increase its virulence. Unlike antibiotics, bacteriophages are capable of disrupting biofilms which are key in the pathogenesis of diseases such as UTIs and some cancers. In this study, bacteriophage EFA1, lytic against E. faecalis, was isolated and its genome fully sequenced and analyzed in silico. Electron microscopy images revealed EFA1 to be a Siphovirus. The bacteriophage was functionally assessed and shown to disrupt E. faecalis biofilms as well as modulate the growth stimulatory effects of E. faecalis in a HCT116 colon cancer cell co-culture system, possibly via the effects of ROS. The potential exists for further testing of bacteriophage EFA1 in these systems as well as in vivo models. Frontiers Media S.A. 2021-03-31 /pmc/articles/PMC8044584/ /pubmed/33868210 http://dx.doi.org/10.3389/fmicb.2021.650849 Text en Copyright © 2021 Kabwe, Meehan-Andrews, Ku, Petrovski, Batinovic, Chan and Tucci. https://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) and the copyright owner(s) 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 Kabwe, Mwila Meehan-Andrews, Terri Ku, Heng Petrovski, Steve Batinovic, Steven Chan, Hiu Tat Tucci, Joseph Lytic Bacteriophage EFA1 Modulates HCT116 Colon Cancer Cell Growth and Upregulates ROS Production in an Enterococcus faecalis Co-culture System |
title | Lytic Bacteriophage EFA1 Modulates HCT116 Colon Cancer Cell Growth and Upregulates ROS Production in an Enterococcus faecalis Co-culture System |
title_full | Lytic Bacteriophage EFA1 Modulates HCT116 Colon Cancer Cell Growth and Upregulates ROS Production in an Enterococcus faecalis Co-culture System |
title_fullStr | Lytic Bacteriophage EFA1 Modulates HCT116 Colon Cancer Cell Growth and Upregulates ROS Production in an Enterococcus faecalis Co-culture System |
title_full_unstemmed | Lytic Bacteriophage EFA1 Modulates HCT116 Colon Cancer Cell Growth and Upregulates ROS Production in an Enterococcus faecalis Co-culture System |
title_short | Lytic Bacteriophage EFA1 Modulates HCT116 Colon Cancer Cell Growth and Upregulates ROS Production in an Enterococcus faecalis Co-culture System |
title_sort | lytic bacteriophage efa1 modulates hct116 colon cancer cell growth and upregulates ros production in an enterococcus faecalis co-culture system |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8044584/ https://www.ncbi.nlm.nih.gov/pubmed/33868210 http://dx.doi.org/10.3389/fmicb.2021.650849 |
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