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Transfer of Viral Communities between Human Individuals during Fecal Microbiota Transplantation

Fecal microbiota transplantation (FMT) is a highly effective treatment for refractory Clostridium difficile infections. However, concerns persist about unwanted cotransfer of pathogenic microbes such as viruses. Here we studed FMT from a single healthy human donor to three pediatric ulcerative colit...

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Autores principales: Chehoud, Christel, Dryga, Anatoly, Hwang, Young, Nagy-Szakal, Dorottya, Hollister, Emily B., Luna, Ruth Ann, Versalovic, James, Kellermayer, Richard, Bushman, Frederic D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Microbiology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4817255/
https://www.ncbi.nlm.nih.gov/pubmed/27025251
http://dx.doi.org/10.1128/mBio.00322-16
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author Chehoud, Christel
Dryga, Anatoly
Hwang, Young
Nagy-Szakal, Dorottya
Hollister, Emily B.
Luna, Ruth Ann
Versalovic, James
Kellermayer, Richard
Bushman, Frederic D.
author_facet Chehoud, Christel
Dryga, Anatoly
Hwang, Young
Nagy-Szakal, Dorottya
Hollister, Emily B.
Luna, Ruth Ann
Versalovic, James
Kellermayer, Richard
Bushman, Frederic D.
author_sort Chehoud, Christel
collection PubMed
description Fecal microbiota transplantation (FMT) is a highly effective treatment for refractory Clostridium difficile infections. However, concerns persist about unwanted cotransfer of pathogenic microbes such as viruses. Here we studed FMT from a single healthy human donor to three pediatric ulcerative colitis patients, each of whom received a course of 22 to 30 FMT treatments. Viral particles were purified from donor and recipient stool samples and sequenced; the reads were then assembled into contigs corresponding to viral genomes or partial genomes. Transfer of selected viruses was confirmed by quantitative PCR. Viral contigs present in the donor could be readily detected in recipients, with up to 32 different donor viral contigs appearing in a recipient sample. Reassuringly, none of these were viruses are known to replicate on human cells. Instead, viral contigs either scored as bacteriophage or could not be attributed taxonomically, suggestive of unstudied phage. The two most frequently transferred gene types were associated with temperate-phage replication. In addition, members of Siphoviridae, the group of typically temperate phages that includes phage lambda, were found to be transferred with significantly greater efficiency than other groups. On the basis of these findings, we propose that the temperate-phage replication style may promote efficient phage transfer between human individuals. In summary, we documented transfer of multiple viral lineages between human individuals through FMT, but in this case series, none were from viral groups known to infect human cells.
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spelling pubmed-48172552016-04-04 Transfer of Viral Communities between Human Individuals during Fecal Microbiota Transplantation Chehoud, Christel Dryga, Anatoly Hwang, Young Nagy-Szakal, Dorottya Hollister, Emily B. Luna, Ruth Ann Versalovic, James Kellermayer, Richard Bushman, Frederic D. mBio Research Article Fecal microbiota transplantation (FMT) is a highly effective treatment for refractory Clostridium difficile infections. However, concerns persist about unwanted cotransfer of pathogenic microbes such as viruses. Here we studed FMT from a single healthy human donor to three pediatric ulcerative colitis patients, each of whom received a course of 22 to 30 FMT treatments. Viral particles were purified from donor and recipient stool samples and sequenced; the reads were then assembled into contigs corresponding to viral genomes or partial genomes. Transfer of selected viruses was confirmed by quantitative PCR. Viral contigs present in the donor could be readily detected in recipients, with up to 32 different donor viral contigs appearing in a recipient sample. Reassuringly, none of these were viruses are known to replicate on human cells. Instead, viral contigs either scored as bacteriophage or could not be attributed taxonomically, suggestive of unstudied phage. The two most frequently transferred gene types were associated with temperate-phage replication. In addition, members of Siphoviridae, the group of typically temperate phages that includes phage lambda, were found to be transferred with significantly greater efficiency than other groups. On the basis of these findings, we propose that the temperate-phage replication style may promote efficient phage transfer between human individuals. In summary, we documented transfer of multiple viral lineages between human individuals through FMT, but in this case series, none were from viral groups known to infect human cells. American Society of Microbiology 2016-03-29 /pmc/articles/PMC4817255/ /pubmed/27025251 http://dx.doi.org/10.1128/mBio.00322-16 Text en Copyright © 2016 Chehoud et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Chehoud, Christel
Dryga, Anatoly
Hwang, Young
Nagy-Szakal, Dorottya
Hollister, Emily B.
Luna, Ruth Ann
Versalovic, James
Kellermayer, Richard
Bushman, Frederic D.
Transfer of Viral Communities between Human Individuals during Fecal Microbiota Transplantation
title Transfer of Viral Communities between Human Individuals during Fecal Microbiota Transplantation
title_full Transfer of Viral Communities between Human Individuals during Fecal Microbiota Transplantation
title_fullStr Transfer of Viral Communities between Human Individuals during Fecal Microbiota Transplantation
title_full_unstemmed Transfer of Viral Communities between Human Individuals during Fecal Microbiota Transplantation
title_short Transfer of Viral Communities between Human Individuals during Fecal Microbiota Transplantation
title_sort transfer of viral communities between human individuals during fecal microbiota transplantation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4817255/
https://www.ncbi.nlm.nih.gov/pubmed/27025251
http://dx.doi.org/10.1128/mBio.00322-16
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