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Detection of non-reference porcine endogenous retrovirus loci in the Vietnamese native pig genome

The Vietnamese native pig (VnP)—a porcine breed with a small body—has proven suitable as a biomedical animal model. Here, we demonstrate that, compared to other breeds, VnPs have fewer copies of porcine endogenous retroviruses (PERVs), which pose a risk for xenotransplantation of pig organs to human...

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Autores principales: Ishihara, Shinya, Kumagai, Masahiko, Arakawa, Aisaku, Taniguchi, Masaaki, Cuc, Ngo Thi Kim, Pham, Lan Doan, Mikawa, Satoshi, Kikuchi, Kazuhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9213404/
https://www.ncbi.nlm.nih.gov/pubmed/35729348
http://dx.doi.org/10.1038/s41598-022-14654-4
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author Ishihara, Shinya
Kumagai, Masahiko
Arakawa, Aisaku
Taniguchi, Masaaki
Cuc, Ngo Thi Kim
Pham, Lan Doan
Mikawa, Satoshi
Kikuchi, Kazuhiro
author_facet Ishihara, Shinya
Kumagai, Masahiko
Arakawa, Aisaku
Taniguchi, Masaaki
Cuc, Ngo Thi Kim
Pham, Lan Doan
Mikawa, Satoshi
Kikuchi, Kazuhiro
author_sort Ishihara, Shinya
collection PubMed
description The Vietnamese native pig (VnP)—a porcine breed with a small body—has proven suitable as a biomedical animal model. Here, we demonstrate that, compared to other breeds, VnPs have fewer copies of porcine endogenous retroviruses (PERVs), which pose a risk for xenotransplantation of pig organs to humans. More specifically, we sought to characterize non-reference PERVs (nrPERVs) that were previously unidentified in the reference genome. To this end, we used whole-genome sequencing data to identify nrPERV loci with long terminal repeat (LTR) sequences in VnPs. RetroSeq was used to estimate nrPERV loci based on the most current porcine reference genome (Sscrofa11.1). LTRs were detected using de novo sequencing read assembly near the loci containing the target site duplication sequences in the inferred regions. A total of 21 non-reference LTR loci were identified and separated into two subtypes based on phylogenetic analysis. Moreover, PERVs within the detected LTR loci were identified, the presence of which was confirmed using conventional PCR and Sanger sequencing. These novel loci represent previously unknown PERVs as they have not been identified in the porcine reference genome. Thus, our RetroSeq method accurately detects novel PERV loci, and can be applied for development of a useful biomedical model.
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spelling pubmed-92134042022-06-23 Detection of non-reference porcine endogenous retrovirus loci in the Vietnamese native pig genome Ishihara, Shinya Kumagai, Masahiko Arakawa, Aisaku Taniguchi, Masaaki Cuc, Ngo Thi Kim Pham, Lan Doan Mikawa, Satoshi Kikuchi, Kazuhiro Sci Rep Article The Vietnamese native pig (VnP)—a porcine breed with a small body—has proven suitable as a biomedical animal model. Here, we demonstrate that, compared to other breeds, VnPs have fewer copies of porcine endogenous retroviruses (PERVs), which pose a risk for xenotransplantation of pig organs to humans. More specifically, we sought to characterize non-reference PERVs (nrPERVs) that were previously unidentified in the reference genome. To this end, we used whole-genome sequencing data to identify nrPERV loci with long terminal repeat (LTR) sequences in VnPs. RetroSeq was used to estimate nrPERV loci based on the most current porcine reference genome (Sscrofa11.1). LTRs were detected using de novo sequencing read assembly near the loci containing the target site duplication sequences in the inferred regions. A total of 21 non-reference LTR loci were identified and separated into two subtypes based on phylogenetic analysis. Moreover, PERVs within the detected LTR loci were identified, the presence of which was confirmed using conventional PCR and Sanger sequencing. These novel loci represent previously unknown PERVs as they have not been identified in the porcine reference genome. Thus, our RetroSeq method accurately detects novel PERV loci, and can be applied for development of a useful biomedical model. Nature Publishing Group UK 2022-06-21 /pmc/articles/PMC9213404/ /pubmed/35729348 http://dx.doi.org/10.1038/s41598-022-14654-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Ishihara, Shinya
Kumagai, Masahiko
Arakawa, Aisaku
Taniguchi, Masaaki
Cuc, Ngo Thi Kim
Pham, Lan Doan
Mikawa, Satoshi
Kikuchi, Kazuhiro
Detection of non-reference porcine endogenous retrovirus loci in the Vietnamese native pig genome
title Detection of non-reference porcine endogenous retrovirus loci in the Vietnamese native pig genome
title_full Detection of non-reference porcine endogenous retrovirus loci in the Vietnamese native pig genome
title_fullStr Detection of non-reference porcine endogenous retrovirus loci in the Vietnamese native pig genome
title_full_unstemmed Detection of non-reference porcine endogenous retrovirus loci in the Vietnamese native pig genome
title_short Detection of non-reference porcine endogenous retrovirus loci in the Vietnamese native pig genome
title_sort detection of non-reference porcine endogenous retrovirus loci in the vietnamese native pig genome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9213404/
https://www.ncbi.nlm.nih.gov/pubmed/35729348
http://dx.doi.org/10.1038/s41598-022-14654-4
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