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Characterisation of the immune compounds in koala milk using a combined transcriptomic and proteomic approach

Production of milk is a key characteristic of mammals, but the features of lactation vary greatly between monotreme, marsupial and eutherian mammals. Marsupials have a short gestation followed by a long lactation period, and milk constituents vary greatly across lactation. Marsupials are born immuno...

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Autores principales: Morris, Katrina M., O’Meally, Denis, Zaw, Thiri, Song, Xiaomin, Gillett, Amber, Molloy, Mark P., Polkinghorne, Adam, Belov, Katherine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5054531/
https://www.ncbi.nlm.nih.gov/pubmed/27713568
http://dx.doi.org/10.1038/srep35011
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author Morris, Katrina M.
O’Meally, Denis
Zaw, Thiri
Song, Xiaomin
Gillett, Amber
Molloy, Mark P.
Polkinghorne, Adam
Belov, Katherine
author_facet Morris, Katrina M.
O’Meally, Denis
Zaw, Thiri
Song, Xiaomin
Gillett, Amber
Molloy, Mark P.
Polkinghorne, Adam
Belov, Katherine
author_sort Morris, Katrina M.
collection PubMed
description Production of milk is a key characteristic of mammals, but the features of lactation vary greatly between monotreme, marsupial and eutherian mammals. Marsupials have a short gestation followed by a long lactation period, and milk constituents vary greatly across lactation. Marsupials are born immunologically naïve and rely on their mother’s milk for immunological protection. Koalas (Phascolarctos cinereus) are an iconic Australian species that are increasingly threatened by disease. Here we use a mammary transcriptome, two milk proteomes and the koala genome to comprehensively characterise the protein components of koala milk across lactation, with a focus on immune constituents. The most abundant proteins were well-characterised milk proteins, including β-lactoglobulin and lactotransferrin. In the mammary transcriptome, 851 immune transcripts were expressed, including immunoglobulins and complement components. We identified many abundant antimicrobial peptides, as well as novel proteins with potential antimicrobial roles. We discovered that marsupial VELP is an ortholog of eutherian Glycam1, and likely has an antimicrobial function in milk. We also identified highly-abundant koala endogenous-retrovirus sequences, identifying a potential transmission route from mother to young. Characterising the immune components of milk is key to understanding protection of marsupial young, and the novel immune compounds identified may have applications in clinical research.
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spelling pubmed-50545312016-10-19 Characterisation of the immune compounds in koala milk using a combined transcriptomic and proteomic approach Morris, Katrina M. O’Meally, Denis Zaw, Thiri Song, Xiaomin Gillett, Amber Molloy, Mark P. Polkinghorne, Adam Belov, Katherine Sci Rep Article Production of milk is a key characteristic of mammals, but the features of lactation vary greatly between monotreme, marsupial and eutherian mammals. Marsupials have a short gestation followed by a long lactation period, and milk constituents vary greatly across lactation. Marsupials are born immunologically naïve and rely on their mother’s milk for immunological protection. Koalas (Phascolarctos cinereus) are an iconic Australian species that are increasingly threatened by disease. Here we use a mammary transcriptome, two milk proteomes and the koala genome to comprehensively characterise the protein components of koala milk across lactation, with a focus on immune constituents. The most abundant proteins were well-characterised milk proteins, including β-lactoglobulin and lactotransferrin. In the mammary transcriptome, 851 immune transcripts were expressed, including immunoglobulins and complement components. We identified many abundant antimicrobial peptides, as well as novel proteins with potential antimicrobial roles. We discovered that marsupial VELP is an ortholog of eutherian Glycam1, and likely has an antimicrobial function in milk. We also identified highly-abundant koala endogenous-retrovirus sequences, identifying a potential transmission route from mother to young. Characterising the immune components of milk is key to understanding protection of marsupial young, and the novel immune compounds identified may have applications in clinical research. Nature Publishing Group 2016-10-07 /pmc/articles/PMC5054531/ /pubmed/27713568 http://dx.doi.org/10.1038/srep35011 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Morris, Katrina M.
O’Meally, Denis
Zaw, Thiri
Song, Xiaomin
Gillett, Amber
Molloy, Mark P.
Polkinghorne, Adam
Belov, Katherine
Characterisation of the immune compounds in koala milk using a combined transcriptomic and proteomic approach
title Characterisation of the immune compounds in koala milk using a combined transcriptomic and proteomic approach
title_full Characterisation of the immune compounds in koala milk using a combined transcriptomic and proteomic approach
title_fullStr Characterisation of the immune compounds in koala milk using a combined transcriptomic and proteomic approach
title_full_unstemmed Characterisation of the immune compounds in koala milk using a combined transcriptomic and proteomic approach
title_short Characterisation of the immune compounds in koala milk using a combined transcriptomic and proteomic approach
title_sort characterisation of the immune compounds in koala milk using a combined transcriptomic and proteomic approach
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5054531/
https://www.ncbi.nlm.nih.gov/pubmed/27713568
http://dx.doi.org/10.1038/srep35011
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