tetano
Editor, Senior Moderator
Gene. 2015 Jan 12. pii: S0378-1119(15)00032-3. doi: 10.1016/j.gene.2015.01.016. [Epub ahead of print]
[h=1]Analysis of the crow lung transcriptome in response to infection with highly pathogenic H5N1 avian influenza virus.[/h] Vijayakumar P[SUP]1[/SUP], Mishra A[SUP]2[/SUP], Ranaware PB[SUP]1[/SUP], Kolte AP[SUP]3[/SUP], Kulkarni DD[SUP]1[/SUP], Burt DW[SUP]4[/SUP], Raut AA[SUP]1[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] The highly pathogenic avian influenza (HPAI) H5N1 virus, currently circulating in Asia, causes severe disease in domestic poultry as well as wild birds like crow. However, the molecular pathogenesis of HPAIV infection in crows and other wild birds is not well known. Thus, as a step to explore it, a comprehensive global gene expression analysis was performed on crow lungs, infected with HPAI H5N1 crow isolate (A/Crow/India/11TI11/2011) using high throughput next generation sequencing (NGS) (GS FLX Titanium XLR70). The reference genome of crow is not available, so RNA seq analysis was performed on the basis of a de novo assembled transcriptome. The RNA seq result shows, 4052 genes were expressed uniquely in noninfected, 6277 genes were expressed uniquely in HPAIV infected sample and of the 6814 genes expressed in both samples, 2279 genes were significantly differentially expressed. Our transcriptome profile data allows for the ability to understand the molecular mechanism behind the recent lethal HPAIV outbreak in crows which was, until recently, thought to cause lethal infections only in gallinaceous birds such as chickens, but not in wild birds. The pattern of differentially expressed genes suggest that this isolate of H5N1 virus evades the host innate immune response by attenuating interferon (IFN)-inducible signalling possibly by down regulating the signalling from type I IFN (IFNAR1 and IFNAR2) and type II IFN receptors, upregulation of the signalling inhibitors suppressor of cytokine signalling 1 (SOCS1) and SOCS3 and altering the expression of toll-like receptors (TLRs). This may be the reason for disease and mortality in crows.
Copyright ? 2015. Published by Elsevier B.V.
[h=4]KEYWORDS:[/h] Avian influenza virus infection; De novo transcriptomics; High-throughput RNA sequencing; Host immune response; Jungle crows
PMID: 25592823 [PubMed - as supplied by publisher]
http://www.ncbi.nlm.nih.gov/pubmed/25592823
[h=1]Analysis of the crow lung transcriptome in response to infection with highly pathogenic H5N1 avian influenza virus.[/h] Vijayakumar P[SUP]1[/SUP], Mishra A[SUP]2[/SUP], Ranaware PB[SUP]1[/SUP], Kolte AP[SUP]3[/SUP], Kulkarni DD[SUP]1[/SUP], Burt DW[SUP]4[/SUP], Raut AA[SUP]1[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] The highly pathogenic avian influenza (HPAI) H5N1 virus, currently circulating in Asia, causes severe disease in domestic poultry as well as wild birds like crow. However, the molecular pathogenesis of HPAIV infection in crows and other wild birds is not well known. Thus, as a step to explore it, a comprehensive global gene expression analysis was performed on crow lungs, infected with HPAI H5N1 crow isolate (A/Crow/India/11TI11/2011) using high throughput next generation sequencing (NGS) (GS FLX Titanium XLR70). The reference genome of crow is not available, so RNA seq analysis was performed on the basis of a de novo assembled transcriptome. The RNA seq result shows, 4052 genes were expressed uniquely in noninfected, 6277 genes were expressed uniquely in HPAIV infected sample and of the 6814 genes expressed in both samples, 2279 genes were significantly differentially expressed. Our transcriptome profile data allows for the ability to understand the molecular mechanism behind the recent lethal HPAIV outbreak in crows which was, until recently, thought to cause lethal infections only in gallinaceous birds such as chickens, but not in wild birds. The pattern of differentially expressed genes suggest that this isolate of H5N1 virus evades the host innate immune response by attenuating interferon (IFN)-inducible signalling possibly by down regulating the signalling from type I IFN (IFNAR1 and IFNAR2) and type II IFN receptors, upregulation of the signalling inhibitors suppressor of cytokine signalling 1 (SOCS1) and SOCS3 and altering the expression of toll-like receptors (TLRs). This may be the reason for disease and mortality in crows.
Copyright ? 2015. Published by Elsevier B.V.
[h=4]KEYWORDS:[/h] Avian influenza virus infection; De novo transcriptomics; High-throughput RNA sequencing; Host immune response; Jungle crows
PMID: 25592823 [PubMed - as supplied by publisher]
http://www.ncbi.nlm.nih.gov/pubmed/25592823