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Neutrophil extracellular traps in sheep mastitis
Neutrophil extracellular traps (NETs) are structures composed of DNA, histones, and antimicrobial proteins that are released extracellularly by neutrophils and other immune cells as a means for trapping and killing invading pathogens. Here, we describe NET formation in milk and in mammary alveoli of...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4471908/ https://www.ncbi.nlm.nih.gov/pubmed/26088507 http://dx.doi.org/10.1186/s13567-015-0196-x |
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author | Pisanu, Salvatore Cubeddu, Tiziana Pagnozzi, Daniela Rocca, Stefano Cacciotto, Carla Alberti, Alberto Marogna, Gavino Uzzau, Sergio Addis, Maria Filippa |
author_facet | Pisanu, Salvatore Cubeddu, Tiziana Pagnozzi, Daniela Rocca, Stefano Cacciotto, Carla Alberti, Alberto Marogna, Gavino Uzzau, Sergio Addis, Maria Filippa |
author_sort | Pisanu, Salvatore |
collection | PubMed |
description | Neutrophil extracellular traps (NETs) are structures composed of DNA, histones, and antimicrobial proteins that are released extracellularly by neutrophils and other immune cells as a means for trapping and killing invading pathogens. Here, we describe NET formation in milk and in mammary alveoli of mastitic sheep, and provide a dataset of proteins found in association to these structures. Nucleic acid staining, immunomicroscopy and fluorescent in-situ hybridization of mastitic mammary tissue from sheep infected with Streptococcus uberis demonstrated the presence of extranuclear DNA colocalizing with antimicrobial proteins, histones, and bacteria. Then, proteomic analysis by LTQ-Orbitrap Velos mass spectrometry provided detailed information on protein abundance changes occurring in milk upon infection. As a result, 1095 unique proteins were identified, of which 287 being significantly more abundant in mastitic milk. Upon protein ontology classification, the most represented localization classes for upregulated proteins were the cytoplasmic granule, the nucleus, and the mitochondrion, while function classes were mostly related to immune defence and inflammation pathways. All known NET markers were massively increased, including histones, granule proteases, and antimicrobial proteins. Of note was the detection of protein arginine deiminases (PAD3 and PAD4). These enzymes are responsible for citrullination, the post-translational modification that is known to trigger NET formation by inducing chromatin decondensation and extracellular release of NETs. As a further observation, citrullinated residues were detected by tandem mass spectrometry in histones of samples from mastitic animals. In conclusion, this work provides novel microscopic and proteomic information on NETs formed in vivo in the mammary gland, and reports the most complete database of proteins increased in milk upon bacterial mastitis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13567-015-0196-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4471908 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44719082015-06-19 Neutrophil extracellular traps in sheep mastitis Pisanu, Salvatore Cubeddu, Tiziana Pagnozzi, Daniela Rocca, Stefano Cacciotto, Carla Alberti, Alberto Marogna, Gavino Uzzau, Sergio Addis, Maria Filippa Vet Res Research Article Neutrophil extracellular traps (NETs) are structures composed of DNA, histones, and antimicrobial proteins that are released extracellularly by neutrophils and other immune cells as a means for trapping and killing invading pathogens. Here, we describe NET formation in milk and in mammary alveoli of mastitic sheep, and provide a dataset of proteins found in association to these structures. Nucleic acid staining, immunomicroscopy and fluorescent in-situ hybridization of mastitic mammary tissue from sheep infected with Streptococcus uberis demonstrated the presence of extranuclear DNA colocalizing with antimicrobial proteins, histones, and bacteria. Then, proteomic analysis by LTQ-Orbitrap Velos mass spectrometry provided detailed information on protein abundance changes occurring in milk upon infection. As a result, 1095 unique proteins were identified, of which 287 being significantly more abundant in mastitic milk. Upon protein ontology classification, the most represented localization classes for upregulated proteins were the cytoplasmic granule, the nucleus, and the mitochondrion, while function classes were mostly related to immune defence and inflammation pathways. All known NET markers were massively increased, including histones, granule proteases, and antimicrobial proteins. Of note was the detection of protein arginine deiminases (PAD3 and PAD4). These enzymes are responsible for citrullination, the post-translational modification that is known to trigger NET formation by inducing chromatin decondensation and extracellular release of NETs. As a further observation, citrullinated residues were detected by tandem mass spectrometry in histones of samples from mastitic animals. In conclusion, this work provides novel microscopic and proteomic information on NETs formed in vivo in the mammary gland, and reports the most complete database of proteins increased in milk upon bacterial mastitis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13567-015-0196-x) contains supplementary material, which is available to authorized users. BioMed Central 2015-06-18 2015 /pmc/articles/PMC4471908/ /pubmed/26088507 http://dx.doi.org/10.1186/s13567-015-0196-x Text en © Pisanu et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Pisanu, Salvatore Cubeddu, Tiziana Pagnozzi, Daniela Rocca, Stefano Cacciotto, Carla Alberti, Alberto Marogna, Gavino Uzzau, Sergio Addis, Maria Filippa Neutrophil extracellular traps in sheep mastitis |
title | Neutrophil extracellular traps in sheep mastitis |
title_full | Neutrophil extracellular traps in sheep mastitis |
title_fullStr | Neutrophil extracellular traps in sheep mastitis |
title_full_unstemmed | Neutrophil extracellular traps in sheep mastitis |
title_short | Neutrophil extracellular traps in sheep mastitis |
title_sort | neutrophil extracellular traps in sheep mastitis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4471908/ https://www.ncbi.nlm.nih.gov/pubmed/26088507 http://dx.doi.org/10.1186/s13567-015-0196-x |
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