Cargando…

Comparative genetics of Enterococcus faecalis intestinal tissue isolates before and after surgery in a rat model of colon anastomosis

We have recently demonstrated that collagenolytic Enterococcus faecalis plays a key and causative role in the pathogenesis of anastomotic leak, an uncommon but potentially lethal complication characterized by disruption of the intestinal wound following segmental removal of the colon (resection) and...

Descripción completa

Detalles Bibliográficos
Autores principales: Christley, Scott, Shogan, Benjamin, Levine, Zoe, Koo, Hyun, Guyton, Kristina, Owens, Sarah, Gilbert, Jack, Zaborina, Olga, Alverdy, John C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7188289/
https://www.ncbi.nlm.nih.gov/pubmed/32343730
http://dx.doi.org/10.1371/journal.pone.0232165
_version_ 1783527288597381120
author Christley, Scott
Shogan, Benjamin
Levine, Zoe
Koo, Hyun
Guyton, Kristina
Owens, Sarah
Gilbert, Jack
Zaborina, Olga
Alverdy, John C.
author_facet Christley, Scott
Shogan, Benjamin
Levine, Zoe
Koo, Hyun
Guyton, Kristina
Owens, Sarah
Gilbert, Jack
Zaborina, Olga
Alverdy, John C.
author_sort Christley, Scott
collection PubMed
description We have recently demonstrated that collagenolytic Enterococcus faecalis plays a key and causative role in the pathogenesis of anastomotic leak, an uncommon but potentially lethal complication characterized by disruption of the intestinal wound following segmental removal of the colon (resection) and its reconnection (anastomosis). Here we hypothesized that comparative genetic analysis of E. faecalis isolates present at the anastomotic wound site before and after surgery would shed insight into the mechanisms by which collagenolytic strains are selected for and predominate at sites of anastomotic disruption. Whole genome optical mapping of four pairs of isolates from rat colonic tissue obtained following surgical resection (herein named “pre-op” isolates) and then 6 days later from the anastomotic site (herein named “post-op” isolates) demonstrated that the isolates with higher collagenolytic activity formed a distinct cluster. In order to perform analysis at a deeper level, a single pair of E. faecalis isolates (16A pre-op and 16A post-op) was selected for whole genome sequencing and assembled using a hybrid assembly algorithm. Comparative genomics demonstrated absence of multiple gene clusters, notably a pathogenicity island in the post-op isolate. No differences were found in the fsr-gelE-sprE genes (EF1817-1822) responsible for regulation and production of collagenolytic activity. Analysis of unique genes among the 16A pre-op and post-op isolates revealed the predominance of transporter systems-related genes in the pre-op isolate and phage-related and hydrolytic enzyme-encoding genes in the post-op isolate. Despite genetic differences observed between pre-op and post-op isolates, the precise genetic determinants responsible for their differential expression of collagenolytic activity remains unknown.
format Online
Article
Text
id pubmed-7188289
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-71882892020-05-06 Comparative genetics of Enterococcus faecalis intestinal tissue isolates before and after surgery in a rat model of colon anastomosis Christley, Scott Shogan, Benjamin Levine, Zoe Koo, Hyun Guyton, Kristina Owens, Sarah Gilbert, Jack Zaborina, Olga Alverdy, John C. PLoS One Research Article We have recently demonstrated that collagenolytic Enterococcus faecalis plays a key and causative role in the pathogenesis of anastomotic leak, an uncommon but potentially lethal complication characterized by disruption of the intestinal wound following segmental removal of the colon (resection) and its reconnection (anastomosis). Here we hypothesized that comparative genetic analysis of E. faecalis isolates present at the anastomotic wound site before and after surgery would shed insight into the mechanisms by which collagenolytic strains are selected for and predominate at sites of anastomotic disruption. Whole genome optical mapping of four pairs of isolates from rat colonic tissue obtained following surgical resection (herein named “pre-op” isolates) and then 6 days later from the anastomotic site (herein named “post-op” isolates) demonstrated that the isolates with higher collagenolytic activity formed a distinct cluster. In order to perform analysis at a deeper level, a single pair of E. faecalis isolates (16A pre-op and 16A post-op) was selected for whole genome sequencing and assembled using a hybrid assembly algorithm. Comparative genomics demonstrated absence of multiple gene clusters, notably a pathogenicity island in the post-op isolate. No differences were found in the fsr-gelE-sprE genes (EF1817-1822) responsible for regulation and production of collagenolytic activity. Analysis of unique genes among the 16A pre-op and post-op isolates revealed the predominance of transporter systems-related genes in the pre-op isolate and phage-related and hydrolytic enzyme-encoding genes in the post-op isolate. Despite genetic differences observed between pre-op and post-op isolates, the precise genetic determinants responsible for their differential expression of collagenolytic activity remains unknown. Public Library of Science 2020-04-28 /pmc/articles/PMC7188289/ /pubmed/32343730 http://dx.doi.org/10.1371/journal.pone.0232165 Text en © 2020 Christley et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Christley, Scott
Shogan, Benjamin
Levine, Zoe
Koo, Hyun
Guyton, Kristina
Owens, Sarah
Gilbert, Jack
Zaborina, Olga
Alverdy, John C.
Comparative genetics of Enterococcus faecalis intestinal tissue isolates before and after surgery in a rat model of colon anastomosis
title Comparative genetics of Enterococcus faecalis intestinal tissue isolates before and after surgery in a rat model of colon anastomosis
title_full Comparative genetics of Enterococcus faecalis intestinal tissue isolates before and after surgery in a rat model of colon anastomosis
title_fullStr Comparative genetics of Enterococcus faecalis intestinal tissue isolates before and after surgery in a rat model of colon anastomosis
title_full_unstemmed Comparative genetics of Enterococcus faecalis intestinal tissue isolates before and after surgery in a rat model of colon anastomosis
title_short Comparative genetics of Enterococcus faecalis intestinal tissue isolates before and after surgery in a rat model of colon anastomosis
title_sort comparative genetics of enterococcus faecalis intestinal tissue isolates before and after surgery in a rat model of colon anastomosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7188289/
https://www.ncbi.nlm.nih.gov/pubmed/32343730
http://dx.doi.org/10.1371/journal.pone.0232165
work_keys_str_mv AT christleyscott comparativegeneticsofenterococcusfaecalisintestinaltissueisolatesbeforeandaftersurgeryinaratmodelofcolonanastomosis
AT shoganbenjamin comparativegeneticsofenterococcusfaecalisintestinaltissueisolatesbeforeandaftersurgeryinaratmodelofcolonanastomosis
AT levinezoe comparativegeneticsofenterococcusfaecalisintestinaltissueisolatesbeforeandaftersurgeryinaratmodelofcolonanastomosis
AT koohyun comparativegeneticsofenterococcusfaecalisintestinaltissueisolatesbeforeandaftersurgeryinaratmodelofcolonanastomosis
AT guytonkristina comparativegeneticsofenterococcusfaecalisintestinaltissueisolatesbeforeandaftersurgeryinaratmodelofcolonanastomosis
AT owenssarah comparativegeneticsofenterococcusfaecalisintestinaltissueisolatesbeforeandaftersurgeryinaratmodelofcolonanastomosis
AT gilbertjack comparativegeneticsofenterococcusfaecalisintestinaltissueisolatesbeforeandaftersurgeryinaratmodelofcolonanastomosis
AT zaborinaolga comparativegeneticsofenterococcusfaecalisintestinaltissueisolatesbeforeandaftersurgeryinaratmodelofcolonanastomosis
AT alverdyjohnc comparativegeneticsofenterococcusfaecalisintestinaltissueisolatesbeforeandaftersurgeryinaratmodelofcolonanastomosis