Cargando…

Tumor Grafting Induces Changes of Gut Microbiota in Athymic Nude Mice in the Presence and Absence of Medicinal Gynostemma Saponins

Recent findings have revealed that gut microbiota plays a substantial role in modulating diseases such as autism, rheumatoid arthritis, allergies, and cancer that occur at sites distant to the gut. Athymic nude mice have been employed for tumorigenic research for decades; however, the relationships...

Descripción completa

Detalles Bibliográficos
Autores principales: Chen, Lei, Tai, William C. S., Brar, Manreetpal S., Leung, Frederick C. C., Hsiao, W. L. Wendy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4439139/
https://www.ncbi.nlm.nih.gov/pubmed/25992551
http://dx.doi.org/10.1371/journal.pone.0126807
_version_ 1782372461208141824
author Chen, Lei
Tai, William C. S.
Brar, Manreetpal S.
Leung, Frederick C. C.
Hsiao, W. L. Wendy
author_facet Chen, Lei
Tai, William C. S.
Brar, Manreetpal S.
Leung, Frederick C. C.
Hsiao, W. L. Wendy
author_sort Chen, Lei
collection PubMed
description Recent findings have revealed that gut microbiota plays a substantial role in modulating diseases such as autism, rheumatoid arthritis, allergies, and cancer that occur at sites distant to the gut. Athymic nude mice have been employed for tumorigenic research for decades; however, the relationships between the gut microbiome and host’s response in drug treatment to the grafted tumors have not been explored. In this study, we analyzed the fecal microbiome of nonxenograft and xenograft nude mice treated with phytosaponins from a popular medicinal plant, Gynostemma pentaphyllum (Gp). Analysis of enterobacterial repetitive intergenic consensus (ERIC)-PCR data showed that the microbiota profile of xenograft mice departed from that of the nonxenograft mice. After ten days of treatment with Gp saponins (GpS), the microbiota of the treated mice was closer to the microbiota at Day 0 before the implantation of the tumor. Data obtained from 16S pyrosequencing of fecal samples reiterates the differences in microbiome between the nonxenograft and xenograft mice. GpS markedly increased the relative abundance of Clostridium cocleatum and Bacteroides acidifaciens, for which the beneficial effects on the host have been well documented. This study, for the first time, characterizes the properties of gut microbiome in nude mice responding to tumor implant and drug treatment. We also demonstrate that dietary saponins such as GpS can potentially regulate the gut microbial ecosystem by increasing the number of symbionts. Interestingly, this regulation of the gut ecosystem might, at least in part, be responsible for or contribute to the anticancer effect of GpS.
format Online
Article
Text
id pubmed-4439139
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-44391392015-05-29 Tumor Grafting Induces Changes of Gut Microbiota in Athymic Nude Mice in the Presence and Absence of Medicinal Gynostemma Saponins Chen, Lei Tai, William C. S. Brar, Manreetpal S. Leung, Frederick C. C. Hsiao, W. L. Wendy PLoS One Research Article Recent findings have revealed that gut microbiota plays a substantial role in modulating diseases such as autism, rheumatoid arthritis, allergies, and cancer that occur at sites distant to the gut. Athymic nude mice have been employed for tumorigenic research for decades; however, the relationships between the gut microbiome and host’s response in drug treatment to the grafted tumors have not been explored. In this study, we analyzed the fecal microbiome of nonxenograft and xenograft nude mice treated with phytosaponins from a popular medicinal plant, Gynostemma pentaphyllum (Gp). Analysis of enterobacterial repetitive intergenic consensus (ERIC)-PCR data showed that the microbiota profile of xenograft mice departed from that of the nonxenograft mice. After ten days of treatment with Gp saponins (GpS), the microbiota of the treated mice was closer to the microbiota at Day 0 before the implantation of the tumor. Data obtained from 16S pyrosequencing of fecal samples reiterates the differences in microbiome between the nonxenograft and xenograft mice. GpS markedly increased the relative abundance of Clostridium cocleatum and Bacteroides acidifaciens, for which the beneficial effects on the host have been well documented. This study, for the first time, characterizes the properties of gut microbiome in nude mice responding to tumor implant and drug treatment. We also demonstrate that dietary saponins such as GpS can potentially regulate the gut microbial ecosystem by increasing the number of symbionts. Interestingly, this regulation of the gut ecosystem might, at least in part, be responsible for or contribute to the anticancer effect of GpS. Public Library of Science 2015-05-20 /pmc/articles/PMC4439139/ /pubmed/25992551 http://dx.doi.org/10.1371/journal.pone.0126807 Text en © 2015 Chen 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Chen, Lei
Tai, William C. S.
Brar, Manreetpal S.
Leung, Frederick C. C.
Hsiao, W. L. Wendy
Tumor Grafting Induces Changes of Gut Microbiota in Athymic Nude Mice in the Presence and Absence of Medicinal Gynostemma Saponins
title Tumor Grafting Induces Changes of Gut Microbiota in Athymic Nude Mice in the Presence and Absence of Medicinal Gynostemma Saponins
title_full Tumor Grafting Induces Changes of Gut Microbiota in Athymic Nude Mice in the Presence and Absence of Medicinal Gynostemma Saponins
title_fullStr Tumor Grafting Induces Changes of Gut Microbiota in Athymic Nude Mice in the Presence and Absence of Medicinal Gynostemma Saponins
title_full_unstemmed Tumor Grafting Induces Changes of Gut Microbiota in Athymic Nude Mice in the Presence and Absence of Medicinal Gynostemma Saponins
title_short Tumor Grafting Induces Changes of Gut Microbiota in Athymic Nude Mice in the Presence and Absence of Medicinal Gynostemma Saponins
title_sort tumor grafting induces changes of gut microbiota in athymic nude mice in the presence and absence of medicinal gynostemma saponins
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4439139/
https://www.ncbi.nlm.nih.gov/pubmed/25992551
http://dx.doi.org/10.1371/journal.pone.0126807
work_keys_str_mv AT chenlei tumorgraftinginduceschangesofgutmicrobiotainathymicnudemiceinthepresenceandabsenceofmedicinalgynostemmasaponins
AT taiwilliamcs tumorgraftinginduceschangesofgutmicrobiotainathymicnudemiceinthepresenceandabsenceofmedicinalgynostemmasaponins
AT brarmanreetpals tumorgraftinginduceschangesofgutmicrobiotainathymicnudemiceinthepresenceandabsenceofmedicinalgynostemmasaponins
AT leungfrederickcc tumorgraftinginduceschangesofgutmicrobiotainathymicnudemiceinthepresenceandabsenceofmedicinalgynostemmasaponins
AT hsiaowlwendy tumorgraftinginduceschangesofgutmicrobiotainathymicnudemiceinthepresenceandabsenceofmedicinalgynostemmasaponins