Cargando…
Metatranscriptomics reveals metabolic adaptation and induction of virulence factors by Haemophilus parasuis during lung infection
Haemophilus parasuis is a common inhabitant of the upper respiratory tract of pigs, and the causative agent of Glässer’s disease. This disease is characterized by polyserositis and arthritis, produced by the severe inflammation caused by the systemic spread of the bacterium. After an initial coloniz...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4580352/ https://www.ncbi.nlm.nih.gov/pubmed/26395877 http://dx.doi.org/10.1186/s13567-015-0225-9 |
_version_ | 1782391381505867776 |
---|---|
author | Bello-Ortí, Bernardo Howell, Kate J. Tucker, Alexander W. Maskell, Duncan J. Aragon, Virginia |
author_facet | Bello-Ortí, Bernardo Howell, Kate J. Tucker, Alexander W. Maskell, Duncan J. Aragon, Virginia |
author_sort | Bello-Ortí, Bernardo |
collection | PubMed |
description | Haemophilus parasuis is a common inhabitant of the upper respiratory tract of pigs, and the causative agent of Glässer’s disease. This disease is characterized by polyserositis and arthritis, produced by the severe inflammation caused by the systemic spread of the bacterium. After an initial colonization of the upper respiratory tract, H. parasuis enters the lung during the early stages of pig infection. In order to study gene expression at this location, we sequenced the ex vivo and in vivo H. parasuis Nagasaki transcriptome in the lung using a metatranscriptomic approach. Comparison of gene expression under these conditions with that found in conventional plate culture showed generally reduced expression of genes associated with anabolic and catabolic pathways, coupled with up-regulation of membrane-related genes involved in carbon acquisition, iron binding and pathogenesis. Some of the up-regulated membrane genes, including ABC transporters, virulence-associated autotransporters (vtaAs) and several hypothetical proteins, were only present in virulent H. parasuis strains, highlighting their significance as markers of disease potential. Finally, the analysis also revealed the presence of numerous antisense transcripts with possible roles in gene regulation. In summary, this data sheds some light on the scarcely studied in vivo transcriptome of H. parasuis, revealing nutritional virulence as an adaptive strategy for host survival, besides induction of classical virulence factors. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13567-015-0225-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4580352 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-45803522015-09-24 Metatranscriptomics reveals metabolic adaptation and induction of virulence factors by Haemophilus parasuis during lung infection Bello-Ortí, Bernardo Howell, Kate J. Tucker, Alexander W. Maskell, Duncan J. Aragon, Virginia Vet Res Research Article Haemophilus parasuis is a common inhabitant of the upper respiratory tract of pigs, and the causative agent of Glässer’s disease. This disease is characterized by polyserositis and arthritis, produced by the severe inflammation caused by the systemic spread of the bacterium. After an initial colonization of the upper respiratory tract, H. parasuis enters the lung during the early stages of pig infection. In order to study gene expression at this location, we sequenced the ex vivo and in vivo H. parasuis Nagasaki transcriptome in the lung using a metatranscriptomic approach. Comparison of gene expression under these conditions with that found in conventional plate culture showed generally reduced expression of genes associated with anabolic and catabolic pathways, coupled with up-regulation of membrane-related genes involved in carbon acquisition, iron binding and pathogenesis. Some of the up-regulated membrane genes, including ABC transporters, virulence-associated autotransporters (vtaAs) and several hypothetical proteins, were only present in virulent H. parasuis strains, highlighting their significance as markers of disease potential. Finally, the analysis also revealed the presence of numerous antisense transcripts with possible roles in gene regulation. In summary, this data sheds some light on the scarcely studied in vivo transcriptome of H. parasuis, revealing nutritional virulence as an adaptive strategy for host survival, besides induction of classical virulence factors. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13567-015-0225-9) contains supplementary material, which is available to authorized users. BioMed Central 2015-09-23 2015 /pmc/articles/PMC4580352/ /pubmed/26395877 http://dx.doi.org/10.1186/s13567-015-0225-9 Text en © Bello-Ortí et al. 2015 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 Bello-Ortí, Bernardo Howell, Kate J. Tucker, Alexander W. Maskell, Duncan J. Aragon, Virginia Metatranscriptomics reveals metabolic adaptation and induction of virulence factors by Haemophilus parasuis during lung infection |
title | Metatranscriptomics reveals metabolic adaptation and induction of virulence factors by Haemophilus parasuis during lung infection |
title_full | Metatranscriptomics reveals metabolic adaptation and induction of virulence factors by Haemophilus parasuis during lung infection |
title_fullStr | Metatranscriptomics reveals metabolic adaptation and induction of virulence factors by Haemophilus parasuis during lung infection |
title_full_unstemmed | Metatranscriptomics reveals metabolic adaptation and induction of virulence factors by Haemophilus parasuis during lung infection |
title_short | Metatranscriptomics reveals metabolic adaptation and induction of virulence factors by Haemophilus parasuis during lung infection |
title_sort | metatranscriptomics reveals metabolic adaptation and induction of virulence factors by haemophilus parasuis during lung infection |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4580352/ https://www.ncbi.nlm.nih.gov/pubmed/26395877 http://dx.doi.org/10.1186/s13567-015-0225-9 |
work_keys_str_mv | AT belloortibernardo metatranscriptomicsrevealsmetabolicadaptationandinductionofvirulencefactorsbyhaemophilusparasuisduringlunginfection AT howellkatej metatranscriptomicsrevealsmetabolicadaptationandinductionofvirulencefactorsbyhaemophilusparasuisduringlunginfection AT tuckeralexanderw metatranscriptomicsrevealsmetabolicadaptationandinductionofvirulencefactorsbyhaemophilusparasuisduringlunginfection AT maskellduncanj metatranscriptomicsrevealsmetabolicadaptationandinductionofvirulencefactorsbyhaemophilusparasuisduringlunginfection AT aragonvirginia metatranscriptomicsrevealsmetabolicadaptationandinductionofvirulencefactorsbyhaemophilusparasuisduringlunginfection |