(TEM) of the reconstructed 1918 pandemic influenza virus. The bottom structure represents membrane debris from the cells used to amplify the virus. Avian influenza is caused by the
influenza A virus which principally affects birds but can also infect humans and other mammals. Influenza A is an
RNA virus with a genome comprising a
negative-sense, RNA segmented genome that encodes 11 viral genes. The virus particle (also called the virion) is 80–120 nanometers in diameter and elliptical or filamentous in shape. There is evidence that the virus can survive for long periods in freshwater after being excreted in feces by its avian host, and can withstand prolonged freezing. There are two
proteins on the surface of the
viral envelope; hemagglutinin and neuraminidase.
Hemagglutinin (H) is an
antigenic glycoprotein which binds to sialic acid receptors on the surface of the host cell, thereby mediating the entry of the virus into the host cell.
Neuraminidase (N) is an antigenic glycosylated
enzyme which facilitates the release of progeny viruses from infected cells. There are 18 known types of hemagglutinin, of which H1 thru H16 have been found in birds, and 11 types of neuraminidase. Further variations exist within the subtypes and can lead to very significant differences in the virus's ability to infect and cause disease.
Influenza virus nomenclature To unambiguously describe a specific
isolate of virus, researchers use the internationally accepted
Influenza virus nomenclature, which describes, among other things, the species of animal from which the virus was isolated, and the place and year of collection. As an example,
A/chicken/Nakorn-Patom/Thailand/CU-K2/04(H5N1): •
A stands for the genus of influenza (
A,
B or
C) •
chicken is the animal species the isolate was found in (note: human isolates lack this component term and are thus identified as human isolates by default) •
Nakorn-Patom/Thailand is the place this specific virus was isolated •
CU-K2 is the laboratory reference number that identifies it from other influenza viruses isolated at the same place and year •
04 represents the year of isolation 2004 •
H5 stands for the fifth of several known types of the protein
hemagglutinin •
N1 stands for the first of several known types of the protein
neuraminidase. Other examples include: A/duck/Hong Kong/308/78(H5N3), A/avian/NY/01(H5N2), A/chicken/Mexico/31381-3/94(H5N2), and A/shoveler/Egypt/03(H5N2).
Genetic characterization Analysis of the virus' genome enables researchers to determine the order of its nucleotides. Comparison of the genome of a virus with that of a different virus can reveal differences between the two viruses.
Genetic variations are important because they can change amino acids that make up the influenza virus’ proteins, resulting in structural changes to the proteins, and thereby altering properties of the virus. Some of these properties include the ability to evade immunity and the ability to cause severe disease. There are a number of factors that generally prevent avian influenza viruses from causing epidemics in humans or other mammals. • The viral HA protein of avian influenza binds to alpha-2,3
sialic acid receptors, which are present in the
respiratory tract and intestines of avian species, while human influenza HA binds to alpha-2,6 sialic acid receptors, which are present in the human upper respiratory tract. • The myxovirus resistance protein (
Mx1) is an important antiviral restriction factor that inhibits the replication of avian influenza viruses in particular. Human-adapted strains of IAV display reduced sensitivity to human Mx1 compared with avian strains. Influenza viruses are constantly changing as small genetic
mutations accumulate, a process known as
antigenic drift. Over time, mutation may lead to a change in antigenic properties such that host
antibodies (acquired through vaccination or prior infection) do not provide effective protection, causing a fresh outbreak of disease. The segmented genome of influenza viruses facilitates
genetic reassortment. This can occur if a host is infected simultaneously with two different strains of influenza virus; then it is possible for the viruses to interchange genetic material as they reproduce in the host cells. Thus, an avian influenza virus can acquire characteristics, such as the ability to infect humans, from a different virus strain. The presence of both alpha 2,3 and alpha 2,6 sialic acid receptors in
pig tissues allows for co-infection by avian influenza and human influenza viruses. This susceptibility makes pigs a potential "melting pot" for the reassortment of influenza A viruses. == Epidemiology ==