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Front Cell Infect Microbiol. 2018 Nov 23;8:414. doi: 10.3389/fcimb.2018.00414. eCollection 2018.
Potential Pandemic of H7N9 Avian Influenza A Virus in Human.
Pu Z1, Xiang D2, Li X1, Luo T1, Shen X1, Murphy RW3, Liao M1,4, Shen Y1,4.
Author information
Abstract
Since 2013, the H7N9 avian influenza A virus (AIV) has caused human infections and to the extent of now surpassing H5N1. This raises an alarm about the potential of H7N9 to become a pandemic problem. Our compilation of the amino acid changes required for AIVs to cross the species-barrier discovers 58 that have very high proportions in both the human- and avian-isolated H7N9 viruses. These changes correspond with sporadic human infections that continue to occur in regions of avian infections. Among the six internal viral genes, amino acid changes do not differ significantly between H9N2 and H7N9, except for V100A in PA, and K526R, D627K, and D701N in PB2. H9N2 AIVs provide internal genes to H7N9. Most of the amino acid changes in H7N9 appear to come directly from H9N2. Seventeen amino acid substitutions appear to have fixed quickly by the 5th wave. Among these, six amino acid sites in HA1 are receptor binding sites, and PB2-A588V was shown to promote the adaptation of AIVs to mammals. The accelerated fixation of mutations may promote the adaptation of H7N9 to human, but need further functional evidence. Although H7N9 AIVs still cannot efficiently transmit between humans, they have the genetic makeup associated with human infections. These viruses must be controlled in poultry to remove the threat of it becoming a human pandemic event.
KEYWORDS:
H7N9; avian influenza A virus; genetic marker; host barrier; human infection
PMID: 30533399 PMCID: PMC6265602 DOI: 10.3389/fcimb.2018.00414
Free PMC Article
Potential Pandemic of H7N9 Avian Influenza A Virus in Human.
Pu Z1, Xiang D2, Li X1, Luo T1, Shen X1, Murphy RW3, Liao M1,4, Shen Y1,4.
Author information
Abstract
Since 2013, the H7N9 avian influenza A virus (AIV) has caused human infections and to the extent of now surpassing H5N1. This raises an alarm about the potential of H7N9 to become a pandemic problem. Our compilation of the amino acid changes required for AIVs to cross the species-barrier discovers 58 that have very high proportions in both the human- and avian-isolated H7N9 viruses. These changes correspond with sporadic human infections that continue to occur in regions of avian infections. Among the six internal viral genes, amino acid changes do not differ significantly between H9N2 and H7N9, except for V100A in PA, and K526R, D627K, and D701N in PB2. H9N2 AIVs provide internal genes to H7N9. Most of the amino acid changes in H7N9 appear to come directly from H9N2. Seventeen amino acid substitutions appear to have fixed quickly by the 5th wave. Among these, six amino acid sites in HA1 are receptor binding sites, and PB2-A588V was shown to promote the adaptation of AIVs to mammals. The accelerated fixation of mutations may promote the adaptation of H7N9 to human, but need further functional evidence. Although H7N9 AIVs still cannot efficiently transmit between humans, they have the genetic makeup associated with human infections. These viruses must be controlled in poultry to remove the threat of it becoming a human pandemic event.
KEYWORDS:
H7N9; avian influenza A virus; genetic marker; host barrier; human infection
PMID: 30533399 PMCID: PMC6265602 DOI: 10.3389/fcimb.2018.00414
Free PMC Article