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Survival of Escherichia coli harboring nucleic acid-hydrolyzing 3D8 scFv during RNA virus infection
Previously, Escherichia coli harboring the codon-optimized 3D8scFv gene (E. coli 3D8scFv) was developed as a feed additive for use in preventing norovirus infection. Here, we evaluated whether the 3D8scFv gene affects the colonization of E coli when E. coli 3D8scFv passes through the mouse gastroint...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Published by Elsevier Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7115797/ https://www.ncbi.nlm.nih.gov/pubmed/29486271 http://dx.doi.org/10.1016/j.yrtph.2018.02.012 |
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author | Park, Jung-Ho Lee, Jae-Woo Choi, Hoonsung Jung, Sun Keun Kim, Jeom Sun Kim, Kyung-Woon Oh, Keon Bong Yang, Hyeon Byun, Sung June |
author_facet | Park, Jung-Ho Lee, Jae-Woo Choi, Hoonsung Jung, Sun Keun Kim, Jeom Sun Kim, Kyung-Woon Oh, Keon Bong Yang, Hyeon Byun, Sung June |
author_sort | Park, Jung-Ho |
collection | PubMed |
description | Previously, Escherichia coli harboring the codon-optimized 3D8scFv gene (E. coli 3D8scFv) was developed as a feed additive for use in preventing norovirus infection. Here, we evaluated whether the 3D8scFv gene affects the colonization of E coli when E. coli 3D8scFv passes through the mouse gastrointestinal tract. To determine the colonization ability of E. coli 3D8scFv, E. coli cells with or without the 3D8scFv gene were fed to mice. Total DNA was extracted from the animals’ stools, stomach, small intestine and colon. All samples were amplified using 3D8scFv gene-specific primer sets. E. coli 3D8scFv begins to be excreted 1 h after feeding and that all E. coli 3D8scFv cells were excreted between 12 and 24 h after the last feeding of the cells. The previously measured gastrointestinal transit time of the mice was between 8 h and 22 h. The results of this study therefore show that E. coli 3D8scFv cannot colonize the gastrointestinal tracts of mice. In addition, if the purified 3D8 scFv protein is used as a feed additive, any associated E. coli 3D8scFv bacteria will not colonize the gastrointestinal tracts of the livestock. Thus, this feed additive meets the safety assessment criteria for the commercial use of bacteria. |
format | Online Article Text |
id | pubmed-7115797 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Published by Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71157972020-04-02 Survival of Escherichia coli harboring nucleic acid-hydrolyzing 3D8 scFv during RNA virus infection Park, Jung-Ho Lee, Jae-Woo Choi, Hoonsung Jung, Sun Keun Kim, Jeom Sun Kim, Kyung-Woon Oh, Keon Bong Yang, Hyeon Byun, Sung June Regul Toxicol Pharmacol Article Previously, Escherichia coli harboring the codon-optimized 3D8scFv gene (E. coli 3D8scFv) was developed as a feed additive for use in preventing norovirus infection. Here, we evaluated whether the 3D8scFv gene affects the colonization of E coli when E. coli 3D8scFv passes through the mouse gastrointestinal tract. To determine the colonization ability of E. coli 3D8scFv, E. coli cells with or without the 3D8scFv gene were fed to mice. Total DNA was extracted from the animals’ stools, stomach, small intestine and colon. All samples were amplified using 3D8scFv gene-specific primer sets. E. coli 3D8scFv begins to be excreted 1 h after feeding and that all E. coli 3D8scFv cells were excreted between 12 and 24 h after the last feeding of the cells. The previously measured gastrointestinal transit time of the mice was between 8 h and 22 h. The results of this study therefore show that E. coli 3D8scFv cannot colonize the gastrointestinal tracts of mice. In addition, if the purified 3D8 scFv protein is used as a feed additive, any associated E. coli 3D8scFv bacteria will not colonize the gastrointestinal tracts of the livestock. Thus, this feed additive meets the safety assessment criteria for the commercial use of bacteria. Published by Elsevier Inc. 2018-04 2018-02-24 /pmc/articles/PMC7115797/ /pubmed/29486271 http://dx.doi.org/10.1016/j.yrtph.2018.02.012 Text en © 2018 Published by Elsevier Inc. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Park, Jung-Ho Lee, Jae-Woo Choi, Hoonsung Jung, Sun Keun Kim, Jeom Sun Kim, Kyung-Woon Oh, Keon Bong Yang, Hyeon Byun, Sung June Survival of Escherichia coli harboring nucleic acid-hydrolyzing 3D8 scFv during RNA virus infection |
title | Survival of Escherichia coli harboring nucleic acid-hydrolyzing 3D8 scFv during RNA virus infection |
title_full | Survival of Escherichia coli harboring nucleic acid-hydrolyzing 3D8 scFv during RNA virus infection |
title_fullStr | Survival of Escherichia coli harboring nucleic acid-hydrolyzing 3D8 scFv during RNA virus infection |
title_full_unstemmed | Survival of Escherichia coli harboring nucleic acid-hydrolyzing 3D8 scFv during RNA virus infection |
title_short | Survival of Escherichia coli harboring nucleic acid-hydrolyzing 3D8 scFv during RNA virus infection |
title_sort | survival of escherichia coli harboring nucleic acid-hydrolyzing 3d8 scfv during rna virus infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7115797/ https://www.ncbi.nlm.nih.gov/pubmed/29486271 http://dx.doi.org/10.1016/j.yrtph.2018.02.012 |
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