tetano
Editor, Senior Moderator
J Virol
. 2020 Nov 3;JVI.01172-20.
doi: 10.1128/JVI.01172-20. Online ahead of print.
Middle East Respiratory Syndrome Coronavirus Gene 5 Modulates Pathogenesis in Mice
Javier Gutierrez-Alvarez[SUP] 1 [/SUP], Li Wang[SUP] 1 [/SUP], Raul Fernandez-Delgado[SUP] 2 [/SUP], Kun Li[SUP] 3 [/SUP], Paul B McCray Jr[SUP] 3 [/SUP], Stanley Perlman[SUP] 4 5 [/SUP], Isabel Sola[SUP] 2 [/SUP], Sonia Zu?iga[SUP] 1 [/SUP], Luis Enjuanes[SUP] 1 [/SUP]
Affiliations
Abstract
Middle East respiratory syndrome coronavirus (MERS-CoV) causes a highly lethal pneumonia that emerged in 2012. There is limited information on MERS-CoV pathogenesis, as data from patients are scarce and the generation of animal models reproducing MERS clinical manifestations has been challenging. Human dipeptidyl peptidase 4 knock-in (hDPP4-KI) mice and a mouse-adapted MERS-CoV (MERSMA-6-1-2) were recently described. hDPP4-KI mice infected with MERSMA-6-1-2 show pathological signs of respiratory disease, high viral titers in the lung, and death. In this work, a mouse-adapted MERS-CoV infectious cDNA was engineered by introducing non-synonymous mutations contained in the MERSMA-6-1-2 genome into a MERS-CoV infectious cDNA, leading to a recombinant mouse-adapted virus (rMERS-MA) that was virulent in hDDP4-KI mice. MERS-CoV adaptation to cell culture or mouse lungs led to mutations and deletions in genus-specific gene 5 that prevented full-length protein expression. In contrast, analysis of 476 MERS-CoV field isolates showed that gene 5 is highly stable in vivo, both in humans and camels. To study the role of protein 5, two additional viruses were engineered expressing a full-length gene 5 (rMERS-MA-5FL), or containing a complete gene 5 deletion (rMERS-MA-Δ5). rMERS-MA-5FL virus was unstable, as deletions appeared during passage in different tissue culture cells, highlighting MERS-CoV instability. The virulence of rMERS-MA-Δ5 was analyzed in a sublethal hDPP4-KI mouse model. Unexpectedly, all mice died after infection with rMERS-MA-Δ5 in contrast to those infected with the parental virus, which contains a 17-nt deletion and a stop codon in protein 5 at position 108. Interferon and pro-inflammatory cytokine expression was delayed and dysregulated in the lungs of rMERS-MA-Δ5 infected mice. Overall, these data indicated that rMERS-MA-Δ5 virus was more virulent than the parental one and suggest that the residual gene 5 sequence present in the mouse-adapted parental virus had a function in ameliorating severe MERS-CoV pathogenesis.IMPORTANCE Middle East respiratory coronavirus (MERS-CoV) is a zoonotic virus causing human infections with high mortality rate (∼35%). Animal models together with reverse genetics systems are essential to understand MERS-CoV pathogenesis. We developed a reverse genetics system for a mouse-adapted MERS-CoV that reproduces the virus behavior observed in humans. This system is highly useful to investigate the role of specific viral genes in pathogenesis. In addition, we described a virus lacking gene 5 expression that is more virulent than the parental one. The data provide novel functions in IFN modulation for gene 5 in the context of viral infection, and will help to develop novel antiviral strategies.
. 2020 Nov 3;JVI.01172-20.
doi: 10.1128/JVI.01172-20. Online ahead of print.
Middle East Respiratory Syndrome Coronavirus Gene 5 Modulates Pathogenesis in Mice
Javier Gutierrez-Alvarez[SUP] 1 [/SUP], Li Wang[SUP] 1 [/SUP], Raul Fernandez-Delgado[SUP] 2 [/SUP], Kun Li[SUP] 3 [/SUP], Paul B McCray Jr[SUP] 3 [/SUP], Stanley Perlman[SUP] 4 5 [/SUP], Isabel Sola[SUP] 2 [/SUP], Sonia Zu?iga[SUP] 1 [/SUP], Luis Enjuanes[SUP] 1 [/SUP]
Affiliations
- PMID: 33144319
- DOI: 10.1128/JVI.01172-20
Abstract
Middle East respiratory syndrome coronavirus (MERS-CoV) causes a highly lethal pneumonia that emerged in 2012. There is limited information on MERS-CoV pathogenesis, as data from patients are scarce and the generation of animal models reproducing MERS clinical manifestations has been challenging. Human dipeptidyl peptidase 4 knock-in (hDPP4-KI) mice and a mouse-adapted MERS-CoV (MERSMA-6-1-2) were recently described. hDPP4-KI mice infected with MERSMA-6-1-2 show pathological signs of respiratory disease, high viral titers in the lung, and death. In this work, a mouse-adapted MERS-CoV infectious cDNA was engineered by introducing non-synonymous mutations contained in the MERSMA-6-1-2 genome into a MERS-CoV infectious cDNA, leading to a recombinant mouse-adapted virus (rMERS-MA) that was virulent in hDDP4-KI mice. MERS-CoV adaptation to cell culture or mouse lungs led to mutations and deletions in genus-specific gene 5 that prevented full-length protein expression. In contrast, analysis of 476 MERS-CoV field isolates showed that gene 5 is highly stable in vivo, both in humans and camels. To study the role of protein 5, two additional viruses were engineered expressing a full-length gene 5 (rMERS-MA-5FL), or containing a complete gene 5 deletion (rMERS-MA-Δ5). rMERS-MA-5FL virus was unstable, as deletions appeared during passage in different tissue culture cells, highlighting MERS-CoV instability. The virulence of rMERS-MA-Δ5 was analyzed in a sublethal hDPP4-KI mouse model. Unexpectedly, all mice died after infection with rMERS-MA-Δ5 in contrast to those infected with the parental virus, which contains a 17-nt deletion and a stop codon in protein 5 at position 108. Interferon and pro-inflammatory cytokine expression was delayed and dysregulated in the lungs of rMERS-MA-Δ5 infected mice. Overall, these data indicated that rMERS-MA-Δ5 virus was more virulent than the parental one and suggest that the residual gene 5 sequence present in the mouse-adapted parental virus had a function in ameliorating severe MERS-CoV pathogenesis.IMPORTANCE Middle East respiratory coronavirus (MERS-CoV) is a zoonotic virus causing human infections with high mortality rate (∼35%). Animal models together with reverse genetics systems are essential to understand MERS-CoV pathogenesis. We developed a reverse genetics system for a mouse-adapted MERS-CoV that reproduces the virus behavior observed in humans. This system is highly useful to investigate the role of specific viral genes in pathogenesis. In addition, we described a virus lacking gene 5 expression that is more virulent than the parental one. The data provide novel functions in IFN modulation for gene 5 in the context of viral infection, and will help to develop novel antiviral strategies.