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A PiggyBac mediated approach for lactoferricin gene transfer in bovine mammary epithelial stem cells for management of bovine mastitis
The antibacterial and anti-inflammatory properties of lactoferricin have been ascribed to its ability to sequester essential iron. The objective of the study was to clone bovine lactoferricin (LFcinB) gene into PiggyBac Transposon vector, expression study in the bovine mammary epithelial stem cells...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5732805/ https://www.ncbi.nlm.nih.gov/pubmed/29262639 http://dx.doi.org/10.18632/oncotarget.22210 |
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author | Sharma, Neelesh Huynh, Do Luong Kim, Sung Woo Ghosh, Mrinmoy Sodhi, Simrinder Singh Singh, Amit Kumar Kim, Nam Eun Lee, Sung Jin Hussain, Kafil Oh, Sung Jong Jeong, Dong Kee |
author_facet | Sharma, Neelesh Huynh, Do Luong Kim, Sung Woo Ghosh, Mrinmoy Sodhi, Simrinder Singh Singh, Amit Kumar Kim, Nam Eun Lee, Sung Jin Hussain, Kafil Oh, Sung Jong Jeong, Dong Kee |
author_sort | Sharma, Neelesh |
collection | PubMed |
description | The antibacterial and anti-inflammatory properties of lactoferricin have been ascribed to its ability to sequester essential iron. The objective of the study was to clone bovine lactoferricin (LFcinB) gene into PiggyBac Transposon vector, expression study in the bovine mammary epithelial stem cells (bMESCs) and also to determine the antimicrobial property of recombinant LFcinB against bovine mastitis-causing organisms. The PiggyBac-LFcinB was transfected into bMESCs by electroporation and a three fold of LFcinB secretion was observed in the transfected bMESCs medium by ELISA assay. Furthermore, the assessment of antimicrobial activity against mastitis causing pathogens Staphylococcus aureus and Escherichia coli demonstrated convincing evidence to prove strong antibacterial activity of LFcinB with 14.0±1.0 mm and 18.0±1.5 mm zone of inhibition against both organisms, respectively. The present study provides the convincing evidence to suggest the potential of PiggyBac transposon system to transfer antibacterial peptide into bMESCs or cow mammary gland and also pave the way to use bovine mammary gland as the bioreactors. Simultaneously, it also suggest toward commercial utilization of LFcinB bioreactor system in pharmaceutical industry. |
format | Online Article Text |
id | pubmed-5732805 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-57328052017-12-19 A PiggyBac mediated approach for lactoferricin gene transfer in bovine mammary epithelial stem cells for management of bovine mastitis Sharma, Neelesh Huynh, Do Luong Kim, Sung Woo Ghosh, Mrinmoy Sodhi, Simrinder Singh Singh, Amit Kumar Kim, Nam Eun Lee, Sung Jin Hussain, Kafil Oh, Sung Jong Jeong, Dong Kee Oncotarget Research Paper The antibacterial and anti-inflammatory properties of lactoferricin have been ascribed to its ability to sequester essential iron. The objective of the study was to clone bovine lactoferricin (LFcinB) gene into PiggyBac Transposon vector, expression study in the bovine mammary epithelial stem cells (bMESCs) and also to determine the antimicrobial property of recombinant LFcinB against bovine mastitis-causing organisms. The PiggyBac-LFcinB was transfected into bMESCs by electroporation and a three fold of LFcinB secretion was observed in the transfected bMESCs medium by ELISA assay. Furthermore, the assessment of antimicrobial activity against mastitis causing pathogens Staphylococcus aureus and Escherichia coli demonstrated convincing evidence to prove strong antibacterial activity of LFcinB with 14.0±1.0 mm and 18.0±1.5 mm zone of inhibition against both organisms, respectively. The present study provides the convincing evidence to suggest the potential of PiggyBac transposon system to transfer antibacterial peptide into bMESCs or cow mammary gland and also pave the way to use bovine mammary gland as the bioreactors. Simultaneously, it also suggest toward commercial utilization of LFcinB bioreactor system in pharmaceutical industry. Impact Journals LLC 2017-10-31 /pmc/articles/PMC5732805/ /pubmed/29262639 http://dx.doi.org/10.18632/oncotarget.22210 Text en Copyright: © 2017 Sharma et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Sharma, Neelesh Huynh, Do Luong Kim, Sung Woo Ghosh, Mrinmoy Sodhi, Simrinder Singh Singh, Amit Kumar Kim, Nam Eun Lee, Sung Jin Hussain, Kafil Oh, Sung Jong Jeong, Dong Kee A PiggyBac mediated approach for lactoferricin gene transfer in bovine mammary epithelial stem cells for management of bovine mastitis |
title | A PiggyBac mediated approach for lactoferricin gene transfer in bovine mammary epithelial stem cells for management of bovine mastitis |
title_full | A PiggyBac mediated approach for lactoferricin gene transfer in bovine mammary epithelial stem cells for management of bovine mastitis |
title_fullStr | A PiggyBac mediated approach for lactoferricin gene transfer in bovine mammary epithelial stem cells for management of bovine mastitis |
title_full_unstemmed | A PiggyBac mediated approach for lactoferricin gene transfer in bovine mammary epithelial stem cells for management of bovine mastitis |
title_short | A PiggyBac mediated approach for lactoferricin gene transfer in bovine mammary epithelial stem cells for management of bovine mastitis |
title_sort | piggybac mediated approach for lactoferricin gene transfer in bovine mammary epithelial stem cells for management of bovine mastitis |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5732805/ https://www.ncbi.nlm.nih.gov/pubmed/29262639 http://dx.doi.org/10.18632/oncotarget.22210 |
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