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Transcriptomic Analysis on Responses of Murine Lungs to Pasteurella multocida Infection
Pasteurella multocida infection in cattle causes serious epidemic diseases and leads to great economic losses in livestock industry; however, little is known about the interaction between host and P. multocida in the lungs. To explore a fully insight into the host responses in the lungs during P. mu...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5476747/ https://www.ncbi.nlm.nih.gov/pubmed/28676843 http://dx.doi.org/10.3389/fcimb.2017.00251 |
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author | Wu, Chenlu Qin, Xiaobin Li, Pan Pan, Tingting Ren, Wenkai Li, Nengzhang Peng, Yuanyi |
author_facet | Wu, Chenlu Qin, Xiaobin Li, Pan Pan, Tingting Ren, Wenkai Li, Nengzhang Peng, Yuanyi |
author_sort | Wu, Chenlu |
collection | PubMed |
description | Pasteurella multocida infection in cattle causes serious epidemic diseases and leads to great economic losses in livestock industry; however, little is known about the interaction between host and P. multocida in the lungs. To explore a fully insight into the host responses in the lungs during P. multocida infection, a mouse model of Pasteurella pneumonia was established by intraperitoneal infection, and then transcriptomic analysis of infected lungs was performed. P. multocida localized and grew in murine lungs, and induced inflammation in the lungs, as well as mice death. With transcriptomic analysis, approximately 10(7) clean reads were acquired. 4236 differently expressed genes (DEGs) were detected during P. multocida infection, of which 1924 DEGs were up-regulated. By gene ontology (GO) and Kyoto encyclopedia of genes and genomes (KEGG) enrichments, 5,303 GO enrichments and 116 KEGG pathways were significantly enriched in the context of P. multocida infection. Interestingly, genes related to immune responses, such as pattern recognition receptors (PRRs), chemokines and inflammatory cytokines, were significantly up-regulated, suggesting the key roles of these genes in P. multocida infection. Transcriptomic data showed that IFN-γ/IL-17-related genes were increased, which were validated by qRT-PCR, ELISA, and immunoblotting. Our study characterized the transcriptomic profile of the lungs in mice upon Pasteurella infection, and our findings could provide valuable information with respect to better understanding the responses in mice during P. multocida infection. |
format | Online Article Text |
id | pubmed-5476747 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-54767472017-07-04 Transcriptomic Analysis on Responses of Murine Lungs to Pasteurella multocida Infection Wu, Chenlu Qin, Xiaobin Li, Pan Pan, Tingting Ren, Wenkai Li, Nengzhang Peng, Yuanyi Front Cell Infect Microbiol Microbiology Pasteurella multocida infection in cattle causes serious epidemic diseases and leads to great economic losses in livestock industry; however, little is known about the interaction between host and P. multocida in the lungs. To explore a fully insight into the host responses in the lungs during P. multocida infection, a mouse model of Pasteurella pneumonia was established by intraperitoneal infection, and then transcriptomic analysis of infected lungs was performed. P. multocida localized and grew in murine lungs, and induced inflammation in the lungs, as well as mice death. With transcriptomic analysis, approximately 10(7) clean reads were acquired. 4236 differently expressed genes (DEGs) were detected during P. multocida infection, of which 1924 DEGs were up-regulated. By gene ontology (GO) and Kyoto encyclopedia of genes and genomes (KEGG) enrichments, 5,303 GO enrichments and 116 KEGG pathways were significantly enriched in the context of P. multocida infection. Interestingly, genes related to immune responses, such as pattern recognition receptors (PRRs), chemokines and inflammatory cytokines, were significantly up-regulated, suggesting the key roles of these genes in P. multocida infection. Transcriptomic data showed that IFN-γ/IL-17-related genes were increased, which were validated by qRT-PCR, ELISA, and immunoblotting. Our study characterized the transcriptomic profile of the lungs in mice upon Pasteurella infection, and our findings could provide valuable information with respect to better understanding the responses in mice during P. multocida infection. Frontiers Media S.A. 2017-06-20 /pmc/articles/PMC5476747/ /pubmed/28676843 http://dx.doi.org/10.3389/fcimb.2017.00251 Text en Copyright © 2017 Wu, Qin, Li, Pan, Ren, Li and Peng. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Wu, Chenlu Qin, Xiaobin Li, Pan Pan, Tingting Ren, Wenkai Li, Nengzhang Peng, Yuanyi Transcriptomic Analysis on Responses of Murine Lungs to Pasteurella multocida Infection |
title | Transcriptomic Analysis on Responses of Murine Lungs to Pasteurella multocida Infection |
title_full | Transcriptomic Analysis on Responses of Murine Lungs to Pasteurella multocida Infection |
title_fullStr | Transcriptomic Analysis on Responses of Murine Lungs to Pasteurella multocida Infection |
title_full_unstemmed | Transcriptomic Analysis on Responses of Murine Lungs to Pasteurella multocida Infection |
title_short | Transcriptomic Analysis on Responses of Murine Lungs to Pasteurella multocida Infection |
title_sort | transcriptomic analysis on responses of murine lungs to pasteurella multocida infection |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5476747/ https://www.ncbi.nlm.nih.gov/pubmed/28676843 http://dx.doi.org/10.3389/fcimb.2017.00251 |
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