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Identification and characterization of differentially expressed exosomal microRNAs in bovine milk infected with Staphylococcus aureus

BACKGROUND: MicroRNAs (miRNAs) in milk-derived exosomes may reflect pathophysiological changes caused by mastitis. This study profiled miRNAs in exosomes from both normal milk and mastitic milk infected by Staphylococcus aureus (S. aureus). The potential targets for differentially expressed (DE) miR...

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Autores principales: Ma, Shaoyang, Tong, Chao, Ibeagha-Awemu, Eveline M., Zhao, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6896338/
https://www.ncbi.nlm.nih.gov/pubmed/31805863
http://dx.doi.org/10.1186/s12864-019-6338-1
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author Ma, Shaoyang
Tong, Chao
Ibeagha-Awemu, Eveline M.
Zhao, Xin
author_facet Ma, Shaoyang
Tong, Chao
Ibeagha-Awemu, Eveline M.
Zhao, Xin
author_sort Ma, Shaoyang
collection PubMed
description BACKGROUND: MicroRNAs (miRNAs) in milk-derived exosomes may reflect pathophysiological changes caused by mastitis. This study profiled miRNAs in exosomes from both normal milk and mastitic milk infected by Staphylococcus aureus (S. aureus). The potential targets for differentially expressed (DE) miRNAs were predicted and the target genes for bta-miR-378 and bta-miR-185 were also validated. RESULTS: Total RNA from milk exosomes was collected from healthy cows (n = 3, the control group) and S. aureus infected cows (n = 6, the SA group). Two hundred ninety miRNAs (221 known and 69 novel ones) were identified. Among them, 22 known and 15 novel miRNAs were differentially expressed. Target genes of DE miRNAs were significantly enriched in intracellular protein transport, endoplasmic reticulum and identical protein binding. The expression of two miRNAs (bta-miR-378 and bta-miR-185) with high read counts and log(2) fold changes (> 3.5) was significantly higher in mastitic milk infected with S. aureus. One target gene (VAT1L) of bta-miR-378 and five target genes (DYRK1B, MLLT3, HP1BP3, NPR2 and PGM1) of bta-miR-185 were validated. CONCLUSION: DE miRNAs in exosomes from normal and S. aureus infected milk were identified. The predicted targets for two DE miRNAs (bta-miR-378 and bta-miR-185) were further validated. The linkage between the validated target genes and diseases suggested that we should pay particular attention to exosome miRNAs from mastitic milk in terms of milk safety.
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spelling pubmed-68963382019-12-11 Identification and characterization of differentially expressed exosomal microRNAs in bovine milk infected with Staphylococcus aureus Ma, Shaoyang Tong, Chao Ibeagha-Awemu, Eveline M. Zhao, Xin BMC Genomics Research Article BACKGROUND: MicroRNAs (miRNAs) in milk-derived exosomes may reflect pathophysiological changes caused by mastitis. This study profiled miRNAs in exosomes from both normal milk and mastitic milk infected by Staphylococcus aureus (S. aureus). The potential targets for differentially expressed (DE) miRNAs were predicted and the target genes for bta-miR-378 and bta-miR-185 were also validated. RESULTS: Total RNA from milk exosomes was collected from healthy cows (n = 3, the control group) and S. aureus infected cows (n = 6, the SA group). Two hundred ninety miRNAs (221 known and 69 novel ones) were identified. Among them, 22 known and 15 novel miRNAs were differentially expressed. Target genes of DE miRNAs were significantly enriched in intracellular protein transport, endoplasmic reticulum and identical protein binding. The expression of two miRNAs (bta-miR-378 and bta-miR-185) with high read counts and log(2) fold changes (> 3.5) was significantly higher in mastitic milk infected with S. aureus. One target gene (VAT1L) of bta-miR-378 and five target genes (DYRK1B, MLLT3, HP1BP3, NPR2 and PGM1) of bta-miR-185 were validated. CONCLUSION: DE miRNAs in exosomes from normal and S. aureus infected milk were identified. The predicted targets for two DE miRNAs (bta-miR-378 and bta-miR-185) were further validated. The linkage between the validated target genes and diseases suggested that we should pay particular attention to exosome miRNAs from mastitic milk in terms of milk safety. BioMed Central 2019-12-05 /pmc/articles/PMC6896338/ /pubmed/31805863 http://dx.doi.org/10.1186/s12864-019-6338-1 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Ma, Shaoyang
Tong, Chao
Ibeagha-Awemu, Eveline M.
Zhao, Xin
Identification and characterization of differentially expressed exosomal microRNAs in bovine milk infected with Staphylococcus aureus
title Identification and characterization of differentially expressed exosomal microRNAs in bovine milk infected with Staphylococcus aureus
title_full Identification and characterization of differentially expressed exosomal microRNAs in bovine milk infected with Staphylococcus aureus
title_fullStr Identification and characterization of differentially expressed exosomal microRNAs in bovine milk infected with Staphylococcus aureus
title_full_unstemmed Identification and characterization of differentially expressed exosomal microRNAs in bovine milk infected with Staphylococcus aureus
title_short Identification and characterization of differentially expressed exosomal microRNAs in bovine milk infected with Staphylococcus aureus
title_sort identification and characterization of differentially expressed exosomal micrornas in bovine milk infected with staphylococcus aureus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6896338/
https://www.ncbi.nlm.nih.gov/pubmed/31805863
http://dx.doi.org/10.1186/s12864-019-6338-1
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