tetano
Editor, Senior Moderator
Viruses. 2019 Nov 5;11(11). pii: E1028. doi: 10.3390/v11111028. [h=1]Aptamer Profiling of A549 Cells Infected with Low-Pathogenicity and High-Pathogenicity Influenza Viruses.[/h]
Coombs KM[SUP]1,[/SUP][SUP]2,[/SUP][SUP]3[/SUP], Simon PF[SUP]1,[/SUP][SUP]4[/SUP], McLeish NJ[SUP]1[/SUP], Zahedi-Amiri A[SUP]1,[/SUP][SUP]2[/SUP], Kobasa D[SUP]1,[/SUP][SUP]4[/SUP].
[h=3]Author information[/h] 1 Department of Medical Microbiology & Infectious Diseases, University of Manitoba, Winnipeg, MB R3E 0J9, Canada. 2 Manitoba Centre for Proteomics & Systems Biology, University of Manitoba, Winnipeg, MB R3E 3P4, Canada. 3 Children's Hospital Research Institute of Manitoba, University of Manitoba, Winnipeg, MB R3E 3P4, Canada. 4 Special Pathogen Program, National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, MB R3E 3R2, Canada.
[h=3]Abstract[/h] Influenza A viruses (IAVs) are important animal and human emerging and re-emerging pathogens that are responsible for yearly seasonal epidemics and sporadic pandemics. IAVs cause a wide range of clinical illnesses, from relatively mild infections by seasonal strains, to acute respiratory distress during infections with highly pathogenic avian IAVs (HPAI). For this study, we infected A549 human lung cells with lab prototype A/PR/8/34 (H1N1) (PR8), a seasonal H1N1 (RV733), the 2009 pandemic H1N1 (pdm09), or with two avian strains, an H5N1 HPAI strain or an H7N9 strain that has low pathogenicity in birds but high pathogenicity in humans. We used a newly-developed aptamer-based multiplexed technique (SOMAscan[SUP]?[/SUP]) to examine >1300 human lung cell proteins affected by the different IAV strains, and identified more than 500 significantly dysregulated cellular proteins. Our analyses indicated that the avian strains induced more profound changes in the A549 global proteome compared to all tested low-pathogenicity H1N1 strains. The PR8 strain induced a general activation, primarily by upregulating many immune molecules, the seasonal RV733 and pdm09 strains had minimal effect upon assayed molecules, and the avian strains induced significant downregulation, primarily in antimicrobial response, cardiovascular and post-translational modification systems.
[h=4]KEYWORDS:[/h] RNA virus infection; SOMAScan?; aptamers; emerging viruses; proteomics
PMID: 31694171 DOI: 10.3390/v11111028
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Coombs KM[SUP]1,[/SUP][SUP]2,[/SUP][SUP]3[/SUP], Simon PF[SUP]1,[/SUP][SUP]4[/SUP], McLeish NJ[SUP]1[/SUP], Zahedi-Amiri A[SUP]1,[/SUP][SUP]2[/SUP], Kobasa D[SUP]1,[/SUP][SUP]4[/SUP].
[h=3]Author information[/h] 1 Department of Medical Microbiology & Infectious Diseases, University of Manitoba, Winnipeg, MB R3E 0J9, Canada. 2 Manitoba Centre for Proteomics & Systems Biology, University of Manitoba, Winnipeg, MB R3E 3P4, Canada. 3 Children's Hospital Research Institute of Manitoba, University of Manitoba, Winnipeg, MB R3E 3P4, Canada. 4 Special Pathogen Program, National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, MB R3E 3R2, Canada.
[h=3]Abstract[/h] Influenza A viruses (IAVs) are important animal and human emerging and re-emerging pathogens that are responsible for yearly seasonal epidemics and sporadic pandemics. IAVs cause a wide range of clinical illnesses, from relatively mild infections by seasonal strains, to acute respiratory distress during infections with highly pathogenic avian IAVs (HPAI). For this study, we infected A549 human lung cells with lab prototype A/PR/8/34 (H1N1) (PR8), a seasonal H1N1 (RV733), the 2009 pandemic H1N1 (pdm09), or with two avian strains, an H5N1 HPAI strain or an H7N9 strain that has low pathogenicity in birds but high pathogenicity in humans. We used a newly-developed aptamer-based multiplexed technique (SOMAscan[SUP]?[/SUP]) to examine >1300 human lung cell proteins affected by the different IAV strains, and identified more than 500 significantly dysregulated cellular proteins. Our analyses indicated that the avian strains induced more profound changes in the A549 global proteome compared to all tested low-pathogenicity H1N1 strains. The PR8 strain induced a general activation, primarily by upregulating many immune molecules, the seasonal RV733 and pdm09 strains had minimal effect upon assayed molecules, and the avian strains induced significant downregulation, primarily in antimicrobial response, cardiovascular and post-translational modification systems.
[h=4]KEYWORDS:[/h] RNA virus infection; SOMAScan?; aptamers; emerging viruses; proteomics
PMID: 31694171 DOI: 10.3390/v11111028
Free full text