The interferon-induced dynamin-like MxA GTPase restricts the replication of influenza A viruses. We identified adaptive mutations in the nucleoprotein (NP) of pandemic strains A/Brevig Mission/1/1918 (1918) and A/Hamburg/4/2009 (pH1N1) that confer MxA resistance. These resistance-associated amino acids in NP differ between the two strains but form a similar discrete surface-exposed cluster in the body domain of NP, indicating that MxA resistance evolved independently. The 1918 cluster was conserved in all descendent strains of seasonal influenza viruses. Introduction of this cluster into the NP of the MxA-sensitive influenza virus A/Thailand/1(KAN-1)/04 (H5N1) resulted in a gain of MxA resistance coupled with a decrease in viral replication...
The influenza pandemic that emerged in 2009 provided an unprecedented opportunity to study adaptatio...
The threat of viral pandemics demands a comprehensive understanding of evolution at the host-pathoge...
The threat of viral pandemics demands a comprehensive understanding of evolution at the host–pathoge...
textabstractThe interferon-induced dynamin-like MxA GTPase restricts the replication of influenza A ...
<div><p>The interferon-induced dynamin-like MxA GTPase restricts the replication of influenza A viru...
The interferon-induced dynamin-like MxA GTPase restricts the replication of influenza A viruses. We ...
Host restriction factors play a crucial role in preventing trans-species transmission of viral patho...
<div><p>The innate-immune restriction factor MxA inhibits influenza replication by targeting the vir...
The innate-immune restriction factor MxA inhibits influenza replication by targeting the viral nucle...
Interferon-induced Mx proteins show strong antiviral activity against influenza A viruses (IAVs). We...
To establish a new lineage in the human population, avian influenza A viruses (AIV) must overcome th...
To establish a new lineage in the human population, avian influenza A viruses (AIV) must overcome th...
The human MxA protein, encoded by the interferon-inducible MX1 gene, is an intracellular influenza A...
International audienceInfluenza A viruses (IAVs) can cause zoonotic infections with pandemic potenti...
<p>Bold letters indicate amino acids in NP shown to increase significantly MxA resistance, whereas a...
The influenza pandemic that emerged in 2009 provided an unprecedented opportunity to study adaptatio...
The threat of viral pandemics demands a comprehensive understanding of evolution at the host-pathoge...
The threat of viral pandemics demands a comprehensive understanding of evolution at the host–pathoge...
textabstractThe interferon-induced dynamin-like MxA GTPase restricts the replication of influenza A ...
<div><p>The interferon-induced dynamin-like MxA GTPase restricts the replication of influenza A viru...
The interferon-induced dynamin-like MxA GTPase restricts the replication of influenza A viruses. We ...
Host restriction factors play a crucial role in preventing trans-species transmission of viral patho...
<div><p>The innate-immune restriction factor MxA inhibits influenza replication by targeting the vir...
The innate-immune restriction factor MxA inhibits influenza replication by targeting the viral nucle...
Interferon-induced Mx proteins show strong antiviral activity against influenza A viruses (IAVs). We...
To establish a new lineage in the human population, avian influenza A viruses (AIV) must overcome th...
To establish a new lineage in the human population, avian influenza A viruses (AIV) must overcome th...
The human MxA protein, encoded by the interferon-inducible MX1 gene, is an intracellular influenza A...
International audienceInfluenza A viruses (IAVs) can cause zoonotic infections with pandemic potenti...
<p>Bold letters indicate amino acids in NP shown to increase significantly MxA resistance, whereas a...
The influenza pandemic that emerged in 2009 provided an unprecedented opportunity to study adaptatio...
The threat of viral pandemics demands a comprehensive understanding of evolution at the host-pathoge...
The threat of viral pandemics demands a comprehensive understanding of evolution at the host–pathoge...