Pathway mapping of leukocyte transcriptome in influenza patients reveals distinct pathogenic mechanisms associated with progression to severe infection
Influenza infections produce a spectrum of disease severity, ranging from a mild respiratory illness to respiratory failure and death. The host-response pathways associated with the progression to severe influenza disease are not well understood. To gain insight into the disease mechanisms associate...
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Published in | BMC medical genomics Vol. 13; no. 1; pp. 28 - 13 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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BioMed Central Ltd
17.02.2020
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Abstract | Influenza infections produce a spectrum of disease severity, ranging from a mild respiratory illness to respiratory failure and death. The host-response pathways associated with the progression to severe influenza disease are not well understood.
To gain insight into the disease mechanisms associated with progression to severe infection, we analyzed the leukocyte transcriptome in severe and moderate influenza patients and healthy control subjects. Pathway analysis on differentially expressed genes was performed using a topology-based pathway analysis tool that takes into account the interaction between multiple cellular pathways. The pathway profiles between moderate and severe influenza were then compared to delineate the biological mechanisms underpinning the progression from moderate to severe influenza.
107 patients (44 severe and 63 moderate influenza patients) and 52 healthy control subjects were included in the study. Severe influenza was associated with upregulation in several neutrophil-related pathways, including pathways involved in neutrophil differentiation, migration, degranulation and neutrophil extracellular trap (NET) formation. The degree of upregulation in neutrophil-related pathways were significantly higher in severely infected patients compared to moderately infected patients. Severe influenza was also associated with downregulation in immune response pathways, including pathways involved in antigen presentation such as CD4+ T-cell co-stimulation, CD8+ T cell and Natural Killer (NK) cells effector functions. Apoptosis pathways were also downregulated in severe influenza patients compare to moderate and healthy controls.
These findings showed that there are changes in gene expression profile that may highlight distinct pathogenic mechanisms associated with progression from moderate to severe influenza infection. |
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AbstractList | Influenza infections produce a spectrum of disease severity, ranging from a mild respiratory illness to respiratory failure and death. The host-response pathways associated with the progression to severe influenza disease are not well understood. To gain insight into the disease mechanisms associated with progression to severe infection, we analyzed the leukocyte transcriptome in severe and moderate influenza patients and healthy control subjects. Pathway analysis on differentially expressed genes was performed using a topology-based pathway analysis tool that takes into account the interaction between multiple cellular pathways. The pathway profiles between moderate and severe influenza were then compared to delineate the biological mechanisms underpinning the progression from moderate to severe influenza. 107 patients (44 severe and 63 moderate influenza patients) and 52 healthy control subjects were included in the study. Severe influenza was associated with upregulation in several neutrophil-related pathways, including pathways involved in neutrophil differentiation, migration, degranulation and neutrophil extracellular trap (NET) formation. The degree of upregulation in neutrophil-related pathways were significantly higher in severely infected patients compared to moderately infected patients. Severe influenza was also associated with downregulation in immune response pathways, including pathways involved in antigen presentation such as CD4+ T-cell co-stimulation, CD8+ T cell and Natural Killer (NK) cells effector functions. Apoptosis pathways were also downregulated in severe influenza patients compare to moderate and healthy controls. These findings showed that there are changes in gene expression profile that may highlight distinct pathogenic mechanisms associated with progression from moderate to severe influenza infection. Background Influenza infections produce a spectrum of disease severity, ranging from a mild respiratory illness to respiratory failure and death. The host-response pathways associated with the progression to severe influenza disease are not well understood. Methods To gain insight into the disease mechanisms associated with progression to severe infection, we analyzed the leukocyte transcriptome in severe and moderate influenza patients and healthy control subjects. Pathway analysis on differentially expressed genes was performed using a topology-based pathway analysis tool that takes into account the interaction between multiple cellular pathways. The pathway profiles between moderate and severe influenza were then compared to delineate the biological mechanisms underpinning the progression from moderate to severe influenza. Results 107 patients (44 severe and 63 moderate influenza patients) and 52 healthy control subjects were included in the study. Severe influenza was associated with upregulation in several neutrophil-related pathways, including pathways involved in neutrophil differentiation, migration, degranulation and neutrophil extracellular trap (NET) formation. The degree of upregulation in neutrophil-related pathways were significantly higher in severely infected patients compared to moderately infected patients. Severe influenza was also associated with downregulation in immune response pathways, including pathways involved in antigen presentation such as CD4+ T-cell co-stimulation, CD8+ T cell and Natural Killer (NK) cells effector functions. Apoptosis pathways were also downregulated in severe influenza patients compare to moderate and healthy controls. Conclusions These findings showed that there are changes in gene expression profile that may highlight distinct pathogenic mechanisms associated with progression from moderate to severe influenza infection. Background Influenza infections produce a spectrum of disease severity, ranging from a mild respiratory illness to respiratory failure and death. The host-response pathways associated with the progression to severe influenza disease are not well understood. Methods To gain insight into the disease mechanisms associated with progression to severe infection, we analyzed the leukocyte transcriptome in severe and moderate influenza patients and healthy control subjects. Pathway analysis on differentially expressed genes was performed using a topology-based pathway analysis tool that takes into account the interaction between multiple cellular pathways. The pathway profiles between moderate and severe influenza were then compared to delineate the biological mechanisms underpinning the progression from moderate to severe influenza. Results 107 patients (44 severe and 63 moderate influenza patients) and 52 healthy control subjects were included in the study. Severe influenza was associated with upregulation in several neutrophil-related pathways, including pathways involved in neutrophil differentiation, migration, degranulation and neutrophil extracellular trap (NET) formation. The degree of upregulation in neutrophil-related pathways were significantly higher in severely infected patients compared to moderately infected patients. Severe influenza was also associated with downregulation in immune response pathways, including pathways involved in antigen presentation such as CD4+ T-cell co-stimulation, CD8+ T cell and Natural Killer (NK) cells effector functions. Apoptosis pathways were also downregulated in severe influenza patients compare to moderate and healthy controls. Conclusions These findings showed that there are changes in gene expression profile that may highlight distinct pathogenic mechanisms associated with progression from moderate to severe influenza infection. Keywords: Influenza, Transcriptome, Neutrophils, Neutrophil extracellular trap Influenza infections produce a spectrum of disease severity, ranging from a mild respiratory illness to respiratory failure and death. The host-response pathways associated with the progression to severe influenza disease are not well understood. To gain insight into the disease mechanisms associated with progression to severe infection, we analyzed the leukocyte transcriptome in severe and moderate influenza patients and healthy control subjects. Pathway analysis on differentially expressed genes was performed using a topology-based pathway analysis tool that takes into account the interaction between multiple cellular pathways. The pathway profiles between moderate and severe influenza were then compared to delineate the biological mechanisms underpinning the progression from moderate to severe influenza. 107 patients (44 severe and 63 moderate influenza patients) and 52 healthy control subjects were included in the study. Severe influenza was associated with upregulation in several neutrophil-related pathways, including pathways involved in neutrophil differentiation, migration, degranulation and neutrophil extracellular trap (NET) formation. The degree of upregulation in neutrophil-related pathways were significantly higher in severely infected patients compared to moderately infected patients. Severe influenza was also associated with downregulation in immune response pathways, including pathways involved in antigen presentation such as CD4+ T-cell co-stimulation, CD8+ T cell and Natural Killer (NK) cells effector functions. Apoptosis pathways were also downregulated in severe influenza patients compare to moderate and healthy controls. These findings showed that there are changes in gene expression profile that may highlight distinct pathogenic mechanisms associated with progression from moderate to severe influenza infection. Abstract Background Influenza infections produce a spectrum of disease severity, ranging from a mild respiratory illness to respiratory failure and death. The host-response pathways associated with the progression to severe influenza disease are not well understood. Methods To gain insight into the disease mechanisms associated with progression to severe infection, we analyzed the leukocyte transcriptome in severe and moderate influenza patients and healthy control subjects. Pathway analysis on differentially expressed genes was performed using a topology-based pathway analysis tool that takes into account the interaction between multiple cellular pathways. The pathway profiles between moderate and severe influenza were then compared to delineate the biological mechanisms underpinning the progression from moderate to severe influenza. Results 107 patients (44 severe and 63 moderate influenza patients) and 52 healthy control subjects were included in the study. Severe influenza was associated with upregulation in several neutrophil-related pathways, including pathways involved in neutrophil differentiation, migration, degranulation and neutrophil extracellular trap (NET) formation. The degree of upregulation in neutrophil-related pathways were significantly higher in severely infected patients compared to moderately infected patients. Severe influenza was also associated with downregulation in immune response pathways, including pathways involved in antigen presentation such as CD4+ T-cell co-stimulation, CD8+ T cell and Natural Killer (NK) cells effector functions. Apoptosis pathways were also downregulated in severe influenza patients compare to moderate and healthy controls. Conclusions These findings showed that there are changes in gene expression profile that may highlight distinct pathogenic mechanisms associated with progression from moderate to severe influenza infection. Influenza infections produce a spectrum of disease severity, ranging from a mild respiratory illness to respiratory failure and death. The host-response pathways associated with the progression to severe influenza disease are not well understood.BACKGROUNDInfluenza infections produce a spectrum of disease severity, ranging from a mild respiratory illness to respiratory failure and death. The host-response pathways associated with the progression to severe influenza disease are not well understood.To gain insight into the disease mechanisms associated with progression to severe infection, we analyzed the leukocyte transcriptome in severe and moderate influenza patients and healthy control subjects. Pathway analysis on differentially expressed genes was performed using a topology-based pathway analysis tool that takes into account the interaction between multiple cellular pathways. The pathway profiles between moderate and severe influenza were then compared to delineate the biological mechanisms underpinning the progression from moderate to severe influenza.METHODSTo gain insight into the disease mechanisms associated with progression to severe infection, we analyzed the leukocyte transcriptome in severe and moderate influenza patients and healthy control subjects. Pathway analysis on differentially expressed genes was performed using a topology-based pathway analysis tool that takes into account the interaction between multiple cellular pathways. The pathway profiles between moderate and severe influenza were then compared to delineate the biological mechanisms underpinning the progression from moderate to severe influenza.107 patients (44 severe and 63 moderate influenza patients) and 52 healthy control subjects were included in the study. Severe influenza was associated with upregulation in several neutrophil-related pathways, including pathways involved in neutrophil differentiation, migration, degranulation and neutrophil extracellular trap (NET) formation. The degree of upregulation in neutrophil-related pathways were significantly higher in severely infected patients compared to moderately infected patients. Severe influenza was also associated with downregulation in immune response pathways, including pathways involved in antigen presentation such as CD4+ T-cell co-stimulation, CD8+ T cell and Natural Killer (NK) cells effector functions. Apoptosis pathways were also downregulated in severe influenza patients compare to moderate and healthy controls.RESULTS107 patients (44 severe and 63 moderate influenza patients) and 52 healthy control subjects were included in the study. Severe influenza was associated with upregulation in several neutrophil-related pathways, including pathways involved in neutrophil differentiation, migration, degranulation and neutrophil extracellular trap (NET) formation. The degree of upregulation in neutrophil-related pathways were significantly higher in severely infected patients compared to moderately infected patients. Severe influenza was also associated with downregulation in immune response pathways, including pathways involved in antigen presentation such as CD4+ T-cell co-stimulation, CD8+ T cell and Natural Killer (NK) cells effector functions. Apoptosis pathways were also downregulated in severe influenza patients compare to moderate and healthy controls.These findings showed that there are changes in gene expression profile that may highlight distinct pathogenic mechanisms associated with progression from moderate to severe influenza infection.CONCLUSIONSThese findings showed that there are changes in gene expression profile that may highlight distinct pathogenic mechanisms associated with progression from moderate to severe influenza infection. |
ArticleNumber | 28 |
Audience | Academic |
Author | Meyers, Adrienne F. A. Ball, T. Blake Zerbib, Yoann Ho, John Shojaei, Maryam Pisipati, Amarnath Kumar, Aseem Jenkins, Emily K. McLean, Anthony Nalos, Marek Schughart, Klaus Kumar, Anand Tang, Benjamin M. Keynan, Yoav |
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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/32066441$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1084/jem.20180628 10.1371/journal.pone.0079217 10.1016/j.gpb.2014.10.002 10.1016/j.ajpath.2011.03.013 10.1186/cc8208 10.1182/blood-2006-06-031856 10.1016/j.virusres.2012.11.002 10.1016/j.coi.2015.12.002 10.1038/nm.4370 10.1038/sj.onc.1205324 10.1182/blood-2017-03-768507 10.1186/cc11477 10.1016/j.bbamcr.2013.06.028 10.3389/fphys.2013.00278 10.3389/fcimb.2017.00160 10.1016/j.clim.2012.05.005 10.1093/nar/gks1215 10.1371/journal.pone.0017186 10.1182/blood-2006-02-002477 10.1128/JVI.79.23.14933-14944.2005 10.1038/nm.3350 10.3389/fmicb.2017.00575 10.4049/jimmunol.0902497 10.1152/ajplung.00266.2007 10.1159/000345937 10.1016/j.chom.2009.07.006 10.1126/science.aaa1578 10.1164/rccm.200909-1420OC 10.1183/13993003.02098-2016 10.1038/s41590-018-0111-5 10.4049/jimmunol.0900252 10.1038/srep17809 10.1016/j.meegid.2018.08.007 10.1073/pnas.1322229111 10.1016/j.ajpath.2017.09.014 10.1182/blood-2002-04-1039 10.1038/s41467-019-11249-y |
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Keywords | Neutrophil extracellular trap Influenza Neutrophils Transcriptome |
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References | PC Rodriguez (672_CR35) 2007; 109 MOSAIC Investigators (672_CR12) 2018; 19 MJ Ciancanelli (672_CR10) 2016; 38 AK Zaas (672_CR11) 2009; 6 J-E Park (672_CR5) 2018; 65 N Hernandez (672_CR8) 2018; 215 O Ramilo (672_CR15) 2007; 109 D Damjanovic (672_CR26) 2012; 144 Y Keynan (672_CR6) 2013; 16 MR White (672_CR25) 2007; 293 L Jin (672_CR18) 2014; 12 S Quinones-Parra (672_CR34) 2014; 111 HK Ashar (672_CR31) 2018; 188 Z Zhang (672_CR32) 2015; 5 AD Friedman (672_CR21) 2002; 21 MD Tate (672_CR24) 2009; 183 B Drescher (672_CR28) 2013; 171 672_CR16 672_CR38 672_CR1 R Sano (672_CR37) 2013; 1833 GP Parnell (672_CR14) 2012; 16 A Nieto (672_CR4) 2017; 3 TP Rygiel (672_CR36) 2009; 183 672_CR19 EK Allen (672_CR9) 2017; 23 S Sridhar (672_CR33) 2013; 19 JF Bermejo-Martin (672_CR2) 2009; 13 T Mauad (672_CR3) 2010; 181 RD Pechous (672_CR27) 2017; 7 BM Tang (672_CR13) 2019; 10 C Mitrea (672_CR17) 2013; 4 M Bai (672_CR23) 2017; 130 I Rusinova (672_CR20) 2012; 41 T Narasaraju (672_CR30) 2011; 179 AF Gombart (672_CR22) 2003; 101 TM Tumpey (672_CR29) 2005; 79 MJ Ciancanelli (672_CR7) 2015; 348 |
References_xml | – volume: 215 start-page: 2567 issue: 10 year: 2018 ident: 672_CR8 publication-title: J Exp Med doi: 10.1084/jem.20180628 – ident: 672_CR19 doi: 10.1371/journal.pone.0079217 – volume: 12 start-page: 210 issue: 5 year: 2014 ident: 672_CR18 publication-title: Genomics Proteomics Bioinformatics doi: 10.1016/j.gpb.2014.10.002 – volume: 179 start-page: 199 issue: 1 year: 2011 ident: 672_CR30 publication-title: Am J Pathol doi: 10.1016/j.ajpath.2011.03.013 – volume: 13 start-page: R201 issue: 6 year: 2009 ident: 672_CR2 publication-title: Crit Care doi: 10.1186/cc8208 – volume: 109 start-page: 1568 issue: 4 year: 2007 ident: 672_CR35 publication-title: Blood doi: 10.1182/blood-2006-06-031856 – volume: 171 start-page: 1 issue: 1 year: 2013 ident: 672_CR28 publication-title: Virus Res doi: 10.1016/j.virusres.2012.11.002 – volume: 38 start-page: 109 year: 2016 ident: 672_CR10 publication-title: Curr Opin Immunol doi: 10.1016/j.coi.2015.12.002 – volume: 23 start-page: 975 issue: 8 year: 2017 ident: 672_CR9 publication-title: Nat Med doi: 10.1038/nm.4370 – volume: 21 start-page: 3377 issue: 21 year: 2002 ident: 672_CR21 publication-title: Oncogene doi: 10.1038/sj.onc.1205324 – volume: 130 start-page: 2092 issue: 19 year: 2017 ident: 672_CR23 publication-title: Blood doi: 10.1182/blood-2017-03-768507 – volume: 16 start-page: R157 issue: 4 year: 2012 ident: 672_CR14 publication-title: Crit Care doi: 10.1186/cc11477 – volume: 1833 start-page: 3460 issue: 12 year: 2013 ident: 672_CR37 publication-title: Biochim Biophys Acta BBA - Mol Cell Res doi: 10.1016/j.bbamcr.2013.06.028 – volume: 4 start-page: 278 year: 2013 ident: 672_CR17 publication-title: Front Physiol doi: 10.3389/fphys.2013.00278 – volume: 7 start-page: 160 year: 2017 ident: 672_CR27 publication-title: Front Cell Infect Microbiol doi: 10.3389/fcimb.2017.00160 – volume: 144 start-page: 57 issue: 1 year: 2012 ident: 672_CR26 publication-title: Clin Immunol doi: 10.1016/j.clim.2012.05.005 – volume: 41 start-page: D1040 issue: D1 year: 2012 ident: 672_CR20 publication-title: Nucleic Acids Res doi: 10.1093/nar/gks1215 – ident: 672_CR38 doi: 10.1371/journal.pone.0017186 – volume: 109 start-page: 2066 issue: 5 year: 2007 ident: 672_CR15 publication-title: Blood doi: 10.1182/blood-2006-02-002477 – volume: 79 start-page: 14933 issue: 23 year: 2005 ident: 672_CR29 publication-title: J Virol doi: 10.1128/JVI.79.23.14933-14944.2005 – volume: 19 start-page: 1305 issue: 10 year: 2013 ident: 672_CR33 publication-title: Nat Med doi: 10.1038/nm.3350 – volume: 3 start-page: 575 issue: 8 year: 2017 ident: 672_CR4 publication-title: Front Microbiol doi: 10.3389/fmicb.2017.00575 – volume: 183 start-page: 7441 issue: 11 year: 2009 ident: 672_CR24 publication-title: J Immunol doi: 10.4049/jimmunol.0902497 – volume: 293 start-page: L1293 issue: 5 year: 2007 ident: 672_CR25 publication-title: Am J Physiol-Lung Cell Mol Physiol doi: 10.1152/ajplung.00266.2007 – volume: 16 start-page: 9 issue: 1–2 year: 2013 ident: 672_CR6 publication-title: Public Health Genomics doi: 10.1159/000345937 – volume: 6 start-page: 207 issue: 3 year: 2009 ident: 672_CR11 publication-title: Cell Host Microbe doi: 10.1016/j.chom.2009.07.006 – volume: 348 start-page: 448 issue: 6233 year: 2015 ident: 672_CR7 publication-title: Science doi: 10.1126/science.aaa1578 – volume: 181 start-page: 72 issue: 1 year: 2010 ident: 672_CR3 publication-title: Am J Respir Crit Care Med doi: 10.1164/rccm.200909-1420OC – ident: 672_CR16 doi: 10.1183/13993003.02098-2016 – ident: 672_CR1 – volume: 19 start-page: 625 issue: 6 year: 2018 ident: 672_CR12 publication-title: Nat Immunol doi: 10.1038/s41590-018-0111-5 – volume: 183 start-page: 1990 issue: 3 year: 2009 ident: 672_CR36 publication-title: J Immunol doi: 10.4049/jimmunol.0900252 – volume: 5 start-page: 17809 year: 2015 ident: 672_CR32 publication-title: Sci Rep doi: 10.1038/srep17809 – volume: 65 start-page: 288 year: 2018 ident: 672_CR5 publication-title: Infect Genet Evol doi: 10.1016/j.meegid.2018.08.007 – volume: 111 start-page: 1049 issue: 3 year: 2014 ident: 672_CR34 publication-title: Proc Natl Acad Sci doi: 10.1073/pnas.1322229111 – volume: 188 start-page: 135 issue: 1 year: 2018 ident: 672_CR31 publication-title: Am J Pathol doi: 10.1016/j.ajpath.2017.09.014 – volume: 101 start-page: 3265 issue: 8 year: 2003 ident: 672_CR22 publication-title: Blood doi: 10.1182/blood-2002-04-1039 – volume: 10 start-page: 3422 issue: 1 year: 2019 ident: 672_CR13 publication-title: Nat Commun doi: 10.1038/s41467-019-11249-y |
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Snippet | Influenza infections produce a spectrum of disease severity, ranging from a mild respiratory illness to respiratory failure and death. The host-response... Background Influenza infections produce a spectrum of disease severity, ranging from a mild respiratory illness to respiratory failure and death. The... Abstract Background Influenza infections produce a spectrum of disease severity, ranging from a mild respiratory illness to respiratory failure and death. The... |
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Title | Pathway mapping of leukocyte transcriptome in influenza patients reveals distinct pathogenic mechanisms associated with progression to severe infection |
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