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Transcriptome Analysis Reveals New Insight of Fowl Adenovirus Serotype 4 Infection

Since 2015, Fowl adenovirus serotype 4 (FAdV-4) infection has caused serious economic losses to the poultry industry worldwide. We isolated and identified the FAdV-4 strain NP, from infected chickens on a layer farm, using chicken embryo allantoic cavity inoculation, electron microscopy, viral genom...

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Autores principales: Chen, Yuan, Huang, Ruiling, Qu, Guishu, Peng, Yaoshun, Xu, Lihui, Wang, Changkang, Huang, Cuiqin, Wang, Quanxi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7026491/
https://www.ncbi.nlm.nih.gov/pubmed/32117165
http://dx.doi.org/10.3389/fmicb.2020.00146
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author Chen, Yuan
Huang, Ruiling
Qu, Guishu
Peng, Yaoshun
Xu, Lihui
Wang, Changkang
Huang, Cuiqin
Wang, Quanxi
author_facet Chen, Yuan
Huang, Ruiling
Qu, Guishu
Peng, Yaoshun
Xu, Lihui
Wang, Changkang
Huang, Cuiqin
Wang, Quanxi
author_sort Chen, Yuan
collection PubMed
description Since 2015, Fowl adenovirus serotype 4 (FAdV-4) infection has caused serious economic losses to the poultry industry worldwide. We isolated and identified the FAdV-4 strain NP, from infected chickens on a layer farm, using chicken embryo allantoic cavity inoculation, electron microscopy, viral genome sequencing, and regression analysis. To explore the pathogenesis of FAdV-4 infection, we conducted transcriptome sequencing analysis of the liver in chickens infected with FAdV-4, using the Illumina® HiSeq 2000 system. Two days after infection with the FAdV-4 NP strain, 13,576 differentially expressed genes (DEGs) were screened in the liver, among which, 7,480 were up-regulated and 6,096 were down-regulated. Gene ontology (GO) analysis indicated that these genes were involved in 52 biological functions. Furthermore, Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis showed that those DEGs were involved in 33 pathways. We then focused on the KEGG pathway of phagosome and found that mRNA levels of the 25 DEGs in that pathway were up-regulated, and seven DEGs were down-regulated. Real-time quantitative polymerase chain reaction (qPCR) confirmed the accuracy and reliability of these findings. Moreover, 24 h after LMH cells were infected with FAdV-4, the mRNA levels of F-actin, Rab7, TUBA, and DVnein were significantly increased. These four genes were all subsequently silenced by RNA interference, and viral replication of FAdV-4 was then significantly down-regulated. These findings demonstrate the isolation and identification of the FAdV-4 NP strain, and the DEGs in KEGG pathway of phagosome were utilized by FAdV-4 to benefit its infection.
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spelling pubmed-70264912020-02-28 Transcriptome Analysis Reveals New Insight of Fowl Adenovirus Serotype 4 Infection Chen, Yuan Huang, Ruiling Qu, Guishu Peng, Yaoshun Xu, Lihui Wang, Changkang Huang, Cuiqin Wang, Quanxi Front Microbiol Microbiology Since 2015, Fowl adenovirus serotype 4 (FAdV-4) infection has caused serious economic losses to the poultry industry worldwide. We isolated and identified the FAdV-4 strain NP, from infected chickens on a layer farm, using chicken embryo allantoic cavity inoculation, electron microscopy, viral genome sequencing, and regression analysis. To explore the pathogenesis of FAdV-4 infection, we conducted transcriptome sequencing analysis of the liver in chickens infected with FAdV-4, using the Illumina® HiSeq 2000 system. Two days after infection with the FAdV-4 NP strain, 13,576 differentially expressed genes (DEGs) were screened in the liver, among which, 7,480 were up-regulated and 6,096 were down-regulated. Gene ontology (GO) analysis indicated that these genes were involved in 52 biological functions. Furthermore, Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis showed that those DEGs were involved in 33 pathways. We then focused on the KEGG pathway of phagosome and found that mRNA levels of the 25 DEGs in that pathway were up-regulated, and seven DEGs were down-regulated. Real-time quantitative polymerase chain reaction (qPCR) confirmed the accuracy and reliability of these findings. Moreover, 24 h after LMH cells were infected with FAdV-4, the mRNA levels of F-actin, Rab7, TUBA, and DVnein were significantly increased. These four genes were all subsequently silenced by RNA interference, and viral replication of FAdV-4 was then significantly down-regulated. These findings demonstrate the isolation and identification of the FAdV-4 NP strain, and the DEGs in KEGG pathway of phagosome were utilized by FAdV-4 to benefit its infection. Frontiers Media S.A. 2020-02-11 /pmc/articles/PMC7026491/ /pubmed/32117165 http://dx.doi.org/10.3389/fmicb.2020.00146 Text en Copyright © 2020 Chen, Huang, Qu, Peng, Xu, Wang, Huang and Wang. 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) and the copyright owner(s) 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
Chen, Yuan
Huang, Ruiling
Qu, Guishu
Peng, Yaoshun
Xu, Lihui
Wang, Changkang
Huang, Cuiqin
Wang, Quanxi
Transcriptome Analysis Reveals New Insight of Fowl Adenovirus Serotype 4 Infection
title Transcriptome Analysis Reveals New Insight of Fowl Adenovirus Serotype 4 Infection
title_full Transcriptome Analysis Reveals New Insight of Fowl Adenovirus Serotype 4 Infection
title_fullStr Transcriptome Analysis Reveals New Insight of Fowl Adenovirus Serotype 4 Infection
title_full_unstemmed Transcriptome Analysis Reveals New Insight of Fowl Adenovirus Serotype 4 Infection
title_short Transcriptome Analysis Reveals New Insight of Fowl Adenovirus Serotype 4 Infection
title_sort transcriptome analysis reveals new insight of fowl adenovirus serotype 4 infection
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7026491/
https://www.ncbi.nlm.nih.gov/pubmed/32117165
http://dx.doi.org/10.3389/fmicb.2020.00146
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