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:'''HA''': ([[hemagglutinin]]): Avian influenza HA bind alpha 2-3 [[sialic acid]] receptors while human influenza HA bind alpha 2-6 sialic acid receptors. Swine influenza viruses have the ability to bind both types of sialic acid receptors. | :'''HA''': ([[hemagglutinin]]): Avian influenza HA bind alpha 2-3 [[sialic acid]] receptors while human influenza HA bind alpha 2-6 sialic acid receptors. Swine influenza viruses have the ability to bind both types of sialic acid receptors. | ||
== | ==Biology== | ||
===Genetics=== | |||
== | |||
"The physical structure of all influenza A viruses is similar. The virions or virus particles are enveloped and can be either spherical or filamentous in form. In clinical isolates that have undergone limited passages in eggs or tissue culture, there are more filamentous than spherical particles, whereas passaged laboratory strains consist mainly of spherical virions."<ref> [http://www.clinicalservicesjournal.com/print.asp?id=872 Clinical Services Journal] article ''Avian influenza issues analysed'' published March 2006</ref> | "The physical structure of all influenza A viruses is similar. The virions or virus particles are enveloped and can be either spherical or filamentous in form. In clinical isolates that have undergone limited passages in eggs or tissue culture, there are more filamentous than spherical particles, whereas passaged laboratory strains consist mainly of spherical virions."<ref> [http://www.clinicalservicesjournal.com/print.asp?id=872 Clinical Services Journal] article ''Avian influenza issues analysed'' published March 2006</ref> | ||
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The [[RNA]] synthesis and its assembly with the nucleoprotein takes place in the [[cell nucleus]], the synthesis of proteins takes place in the [[cytoplasm]]. The assembled virion cores leave the nucleus and migrate towards the [[cell membrane]], with patches of viral [[transmembrane protein]]s (hemagglutinin, neuraminidase and M2 proteins) and an underlying layer of the M1 protein, and [[budding|bud]] through these patches, releasing finished enveloped [[virus]]es into the [[extracellular fluid]]. | The [[RNA]] synthesis and its assembly with the nucleoprotein takes place in the [[cell nucleus]], the synthesis of proteins takes place in the [[cytoplasm]]. The assembled virion cores leave the nucleus and migrate towards the [[cell membrane]], with patches of viral [[transmembrane protein]]s (hemagglutinin, neuraminidase and M2 proteins) and an underlying layer of the M1 protein, and [[budding|bud]] through these patches, releasing finished enveloped [[virus]]es into the [[extracellular fluid]]. | ||
==Structure== | |||
==Tropism== | |||
==Natural Reservoir== | |||
== | |||
==References== | ==References== | ||
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[[Category:Disease]] | [[Category:Disease]] | ||
[[Category:Pulmonology]] | [[Category:Pulmonology]] | ||
[[Category:Influenza| ]] | [[Category:Influenza| ]] | ||
[[Category:Infectious disease]] | [[Category:Infectious disease]] | ||
[[Category:Primary care]] | [[Category:Primary care]] | ||
[[Category:H5N1]] | |||
[[Category:Orthomyxoviridae]] | |||
{{WH}} | {{WH}} | ||
{{WS}} | {{WS}} | ||
Revision as of 14:33, 3 November 2014
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Influenza Microchapters |
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Influenza causes On the Web |
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American Roentgen Ray Society Images of Influenza causes |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Taxonomy
- There are three types of influenza viruses: A, B and C.
- Human influenza A and B viruses cause seasonal epidemics of disease almost every winter in the United States.
- The emergence of a new and very different influenza virus to infect people can cause an influenza pandemic. Influenza type C infections cause a mild respiratory illness and are not thought to cause epidemics.
- Influenza A viruses are divided into subtypes based on two proteins on the surface of the virus: the hemagglutinin (H) and the neuraminidase (N). There are 18 different hemagglutinin subtypes and 11 different neuraminidase subtypes. (H1 through H18 and N1 through N11 respectively.)
- Influenza A viruses can be further broken down into different strains. Current subtypes of influenza A viruses found in people are influenza A (H1N1) and influenza A (H3N2) viruses. In the spring of 2009, a new influenza A (H1N1) virus (CDC 2009 H1N1 Flu website) emerged to cause illness in people. This virus was very different from the human influenza A (H1N1) viruses circulating at that time. The new virus caused the first influenza pandemic in more than 40 years. That virus (often called “2009 H1N1”) has now replaced the H1N1 virus that was previously circulating in humans.
- Influenza B viruses are not divided into subtypes, but can be further broken down into lineages and strains. Currently circulating influenza B viruses belong to one of two lineages: B/Yamagata and B/Victoria.
- The antigenic type (e.g., A, B, C)
- The host of origin (e.g., swine, equine, chicken, etc. For human-origin viruses, no host of origin designation is given.)
- Geographical origin (e.g., Denver, Taiwan, etc.)
- Strain number (e.g., 15, 7, etc.)
- Year of isolation (e.g., 57, 2009, etc.)
- For influenza A viruses, the hemagglutinin and neuraminidase antigen description in parentheses (e.g., (H1N1), (H5N1)
- Influenza A (H1N1), A (H3N2), and one or two influenza B viruses (depending on the vaccine) are included in each year’s influenza vaccine. Getting a flu vaccine can protect against flu viruses that are the same or related to the viruses in the vaccine. Information about this season’s vaccine can be found atPreventing Seasonal Flu with Vaccination. The seasonal flu vaccine does not protect against influenza C viruses. In addition, flu vaccines will NOT protect against infection and illness caused by other viruses that also can cause influenza-like symptoms. There are many other non-flu viruses that can result in influenza-like illness (ILI) that spread during flu season.
- Genetic factors in distinguishing between "human flu viruses" and "avian influenza viruses" include:
- PB2: (RNA polymerase): Amino acid (or residue) position 627 in the PB2 protein encoded by the PB2 RNA gene. Until H5N1, all known avian influenza viruses had a Glu at position 627, while all human influenza viruses had a lysine.
- HA: (hemagglutinin): Avian influenza HA bind alpha 2-3 sialic acid receptors while human influenza HA bind alpha 2-6 sialic acid receptors. Swine influenza viruses have the ability to bind both types of sialic acid receptors.
Biology
Genetics
"The physical structure of all influenza A viruses is similar. The virions or virus particles are enveloped and can be either spherical or filamentous in form. In clinical isolates that have undergone limited passages in eggs or tissue culture, there are more filamentous than spherical particles, whereas passaged laboratory strains consist mainly of spherical virions."[1]
The Influenza A virus genome is contained on eight single (non-paired) RNA strands that code for eleven proteins (HA, NA, NP, M1, M2, NS1, NEP, PA, PB1, PB1-F2, PB2). The segmented nature of the genome allows for the exchange of entire genes between different viral strains during cellular cohabitation. The eight RNA segments are:
- HA encodes hemagglutinin (about 500 molecules of hemagglutinin are needed to make one virion) "The extent of infection into host organism is determined by HA. Influenza viruses bud from the apical surface of polarized epithelial cells (e.g. bronchial epithelial cells) into lumen of lungs and are therefore usually pneumotropic. The reason is that HA is cleaved by tryptase clara which is restricted to lungs. However HAs of H5 and H7 pantropic avian viruses subtypes can be cleaved by furin and subtilisin-type enzymes, allowing the virus to grow in other organs than lungs." [2]
- NA encodes neuraminidase (about 100 molecules of neuraminidase are needed to make one virion).
- NP encodes nucleoprotein.
- M encodes two matrix proteins (the M1 and the M2) by using different reading frames from the same RNA segment (about 3000 matrix protein molecules are needed to make one virion).
- NS encodes two distinct non-structural proteins (NS1 and NEP) by using different reading frames from the same RNA segment.
- PA encodes an RNA polymerase.
- PB1 encodes an RNA polymerase and PB1-F2 protein (induces apoptosis) by using different reading frames from the same RNA segment.
- PB2 encodes an RNA polymerase.
The genome segments have common terminal sequences, and the ends of the RNA strands are partially complementary, allowing them to bond to each other by hydrogen bonds. After transcription from negative-sense to positive-sense RNA the +RNA strands get the cellular 5' cap added by cap snatching, which involves the viral protein NS1 binding to the cellular pre-mRNAs. The cap is then cleaved from the cellular pre-mRNA using a second viral protein, PB2. The short oligo cap is then added to the influenza +RNA strands, allowing its processing as messenger RNA by ribosomes. The +RNA strands also serve for synthesis of -RNA strands for new virions.
The RNA synthesis and its assembly with the nucleoprotein takes place in the cell nucleus, the synthesis of proteins takes place in the cytoplasm. The assembled virion cores leave the nucleus and migrate towards the cell membrane, with patches of viral transmembrane proteins (hemagglutinin, neuraminidase and M2 proteins) and an underlying layer of the M1 protein, and bud through these patches, releasing finished enveloped viruses into the extracellular fluid.
Structure
Tropism
Natural Reservoir
References
- ↑ Clinical Services Journal article Avian influenza issues analysed published March 2006
- ↑ UniProtKB/Swiss-Prot entry P09345 Complete sequence of a cDNA clone of the hemagglutinin gene of influenza A/Chicken/Scotland/59 (H5N1) virus: comparison with contemporary North American and European strains.