Difference between revisions of "Influenza A"

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These two proteins are a target of interest for antiviral drugs. Furthermore, they are also the antigen proteins to which a host antibodies can bind and trigger an immune response. Influenza type A viruses are categorized into different subtypes, or strains, based on which type of these two proteins is present on the surface of the virion. Currently, there are 16 subtypes of HA and 9 subtypes of NA known to exist. The most prevalent form of the different subtypes is H1N1. Single hemagglutinin-neuraminidase proteins, in which both HA and NA are found in a single protein, also exist. However, these will not be used in SensUs 2021.
 
These two proteins are a target of interest for antiviral drugs. Furthermore, they are also the antigen proteins to which a host antibodies can bind and trigger an immune response. Influenza type A viruses are categorized into different subtypes, or strains, based on which type of these two proteins is present on the surface of the virion. Currently, there are 16 subtypes of HA and 9 subtypes of NA known to exist. The most prevalent form of the different subtypes is H1N1. Single hemagglutinin-neuraminidase proteins, in which both HA and NA are found in a single protein, also exist. However, these will not be used in SensUs 2021.
  
==Mechanism of Action==
+
==Mechanism of Infection==
 
The involvement of the hemagglutinin and neuraminidase proteins in the infection of H1N1 is essential for the virus reproduction, and a more specific mechanism is discussed below.  
 
The involvement of the hemagglutinin and neuraminidase proteins in the infection of H1N1 is essential for the virus reproduction, and a more specific mechanism is discussed below.  
 
The hemagglutinin protein (HA) has the role of searching for the sialic acid receptors in respiratory-lining cell membranes. (figure _). Upon binding of this protein and the receptor, fusion of the virus and the cell membrane is facilitated with the help of glycan proteins. The virus then enters the cell where it sheds its shell and approaches the cell’s nucleus. Using the host replication mechanisms, the virus makes copies of itself. At this step of the infection process, important viral proteins are synthesized. These newly replicated viral elements subsequently attempt to leave through the cell membrane and infect other cells. To inhibit the exit of the viral components, sialic acid receptors on the cell membrane attempt to bind the HA glycoproteins. This is where viral evolution/mutability can play a role in the expansion of the capabilities of the virus.   
 
The hemagglutinin protein (HA) has the role of searching for the sialic acid receptors in respiratory-lining cell membranes. (figure _). Upon binding of this protein and the receptor, fusion of the virus and the cell membrane is facilitated with the help of glycan proteins. The virus then enters the cell where it sheds its shell and approaches the cell’s nucleus. Using the host replication mechanisms, the virus makes copies of itself. At this step of the infection process, important viral proteins are synthesized. These newly replicated viral elements subsequently attempt to leave through the cell membrane and infect other cells. To inhibit the exit of the viral components, sialic acid receptors on the cell membrane attempt to bind the HA glycoproteins. This is where viral evolution/mutability can play a role in the expansion of the capabilities of the virus.   
 
The neuraminidase glycoprotein (N) has the role of cleaving the sialic acid receptors, allowing the exit of the viral components which then go in search of a new host.  
 
The neuraminidase glycoprotein (N) has the role of cleaving the sialic acid receptors, allowing the exit of the viral components which then go in search of a new host.  
 
After infection is complete, the H1N1 virus triggers cell apoptosis, leading to the death of the cell and spread of the virions.
 
After infection is complete, the H1N1 virus triggers cell apoptosis, leading to the death of the cell and spread of the virions.
 +
'''pictures'''
  
 +
===Medical Application===
 +
Optimal dose and effects are achieved with upper limit of 60 mg/kg/day.  If the desired effects are not achieved (in other words, the seizures are not gone or the The influenza virus spreads when people with the flu cough, sneeze or talk. Infected people transfer tiny droplets to people close to them and infect them by the handover of droplets (Influenza (Flu) 2019). During an outbreak, it is important to be able to control and prevent the virus from spreading further, for example, by implementing control measures. Those control measures can be determined based on the reproduction number. The reproduction number is defined as: “the expected number of secondary cases produced by a single infection in a completely susceptible population”(https://web.stanford.edu/~jhj1/teachingdocs/Jones-on-R0.pdf). A clear overview of the number of infected people is needed to calculate the reproduction number.
 +
For disease control, it is crucial to know the infection rate in a specific region. The results may influence critical decisions such as whether to perform other diagnostic testing or to implement infection prevention and control measures for influenza (Overview of Influenza testing methods 2020). Furthermore, manpower can be in short supply during a pandemic and the speed at which someone can be tested and receive the result is of vital importance.
 +
Biosensors that will be developed in SensUs 2021 are envisioned to be used outside the hospital in a point-of-care (POC) setting. Inside the hospital there is not a big advantage, as there are already very specific and accurate tests available for that setting (Diagnosis, 2020). Important applications are fast testing at the GP and at home. Therefore the test should be easy to use. The biosensors will be designed to enable a fast yes/no answer, based on measuring the concentration of viral particles in the sample. The biosensors will not distinguish between different virus subtypes, as the subtype causing the pandemic is assumed to be known.
  
===Efficacy and influence on hepatic function===
+
===State of the Art===
Optimal dose and effects are achieved with upper limit of 60 mg/kg/day.  If the desired effects are not achieved (in other words, the seizures are not gone or the side effects are too strong), testing for blood levels of VPA needs to be executed in order to determine whether they fall within the optimal range of total VPA 50-100 µg/mL. Otherwise, the dose is altered in agreement with the doctor according to the individual state of the patient, his/her other conditions or other medication that they take. The toxicity level of valproate in blood, although not very conclusive, is taken as 150 µg/mL<ref name=”[19]”> valproic Acid Dosage Guide with Precautions. (2019, March 28), at [https://www.drugs.com/dosage/valproic-acid.html “https://www.drugs.com/dosage/valproic-acid.html”].</ref>
+
'''Still paste some tables'''
.
 
  
VPA impacts the hepatic drug metabolism by inhibiting it and displacing other strongly bound drugs from proteins, which implies that dosage changes need to be considered when using it in combination with other drugs. <ref name=”[20]”> Valproic Acid (2018, October 1)  , at [https://labtestsonline.org/tests/valproic-acid“https://labtestsonline.org/tests/valproic-acid”].</ref> The normal limits of valproate in blood of 70-100 kg person is 1000-3000 mg/day  <ref name=”[46]”> Farmacotherapeutisch Kompas. Retrieved December 19, 2019, at [https://www.farmacotherapeutischkompas.nl/bladeren/preparaatteksten/v/valproinezuur“https://www.farmacotherapeutischkompas.nl/bladeren/preparaatteksten/v/valproinezuur”].</ref>
 
 
==Number of patients==
 
Epilepsy affects around 50 million people worldwide. This includes people having less than one seizure per year. The prevalence of active epilepsy (i.e. patients who have frequent seizures or use medication) is between 0.4% and 1%. On a global scale, an estimated five million people are diagnosed with epilepsy each year.
 
Epileptic seizures can be controlled by using anti-epileptic drugs (AEDs). About 70% of epileptic patients becomes free of seizures by appropriate AEDs. Low-cost treatments are available, with daily medication that costs as little as US$ 5 per year.<ref name=”[21]”>  WHO. (2019, June 20). Epilepsy. Retrieved October 30, 2019 , at [https://www.who.int/news-room/fact-sheets/detail/epilepsy “https://www.who.int/news-room/fact-sheets/detail/epilepsy”].</ref>
 
 
==Medical use and TDM==
 
 
Valproate (VPA) is usually taken as tablets of 250 mg or as a syrup with 250 mg per ml, but this may vary per product <ref name=”[39]”> Valproic Acid Capsules - FDA prescribing information, side effects and uses. (2018, June 1).Retrieved November 26, 2019, at [https://www.drugs.com/pro/valproic-acid-capsules.html“https://www.drugs.com/pro/valproic-acid-capsules.html”].</ref>.The dose of VPA is at first taken in small amounts and is then gradually increased until the satisfactory dose is reached.
 
Testing for valproate levels is important to check if the blood levels are within normal therapeutic range <ref name=”[20]”> Valproic Acid (2018, October 1)  , at [https://labtestsonline.org/tests/valproic-acid“https://labtestsonline.org/tests/valproic-acid”].</ref>
 
. The test should measure  the free concentration (i.e. the concentration of unbound valproate) as this fraction is pharmacologically active.
 
The recommended levels of unbound valproate are 6-22 µg/mL in blood <ref name=”[20]”> Valproic Acid (2018, October 1)  , at [https://labtestsonline.org/tests/valproic-acid“https://labtestsonline.org/tests/valproic-acid”].</ref>. For epilepsy patients, the range for the treatment of total valproate should be 50-100 µg/mL. Overall, if a patient has a VPA concentration that falls within this range, does not have recurrent seizures and has minimal side effects, then the dose is said to be suitable<ref name=”[20]”> Valproic Acid (2018, October 1)  , at [https://labtestsonline.org/tests/valproic-acid“https://labtestsonline.org/tests/valproic-acid”].</ref>
 
. To provide a patient their right amount of medication, therapeutic drug monitoring (TDM) is implemented in hospitals, because every patient responds differently to a certain dose of medication.
 
VPA is a conventional drug that is used as first line monotherapy for idiopathic generalized epilepsies. Its effectiveness is not clearly conclusive and varies between different patients. The doses are not generalized and depend on patient’s age and weight. Doses are taken every day, with some patients even two times a day. It is not advised, but sometimes necessary, to take VPA in combination with other seizure drugs (e.g., ethosuximide, lamotrigine, phenytoin, rufinamide, topira mate), some antidepressants or certain antibiotics<ref name=”[20]”> Valproic Acid (2018, October 1)  , at [https://labtestsonline.org/tests/valproic-acid“https://labtestsonline.org/tests/valproic-acid”].</ref>. Medications based on VPA are harmful for the unborn child. If valproate is taken during pregnancy, research has shown that up to 4 in 10 babies are at risk of developmental disorders, and approximately 1 in 10 are at risk of birth defects. <ref name=”[22]”>  gov.uk. (2018, March 23), at [https://www.gov.uk/guidance/valproate-use-by-women-and-girls“https://www.gov.uk/guidance/valproate-use-by-women-and-girls”].</ref>
 
 
==Safety & Lab protocols==
 
 
===Safety===
 
===Safety===
All anti-epileptic drugs have side-effects, including VPA. The risk of hyperammonemia is nearly 40% in patients ingesting intravenous VPA in the ICU setting <ref name=”[4]”>  Lind, J., & Nordlund, P. (2019, July). Intravenous use of valproic acid in status epilepticus is associated with high risk of hyperammonemia, Seizure Vol. 69. Retrieved October 23, 2019, at [https://doi.org/10.1016/j.seizure.2019.03.020“https://doi.org/10.1016/j.seizure.2019.03.020”].</ref>
 
. Other adverse effects include thrombocytopenia and endocrine effects of women. Valproate is associated with a dose-related teratogenicity rate, with risk of major malformation higher than 30% at doses greater than 1100 mg/d. In utero exposure is also linked to dose-dependent reduced verbal IQ and autism<ref name=”[6]”>  Abou-Khalil, & Bassel, W. (2019). Update on Antiepileptic Drugs 2019. Retrieved November 6, 2019, at [ https://insights.ovid.com/crossref?an=00132979-201904000-00014“ https://insights.ovid.com/crossref?an=00132979-201904000-00014”].</ref>
 
.
 
Children, who were exposed to VPA during birth, have a possible chance of a major congenital malformation (MCM) <ref name=”[7]”>  Morrow , J., Russell, A., Guthrie, E., Parsons, L., Robertson, I., Waddell, R., … Craig, J. (2006, January 17). Malformation risks of antiepileptic drugs in pregnancy: a prospective study from the UK Epilepsy and Pregnancy Register. Retrieved October 23, 2019, at [https://jnnp.bmj.com/content/77/2/193“https://jnnp.bmj.com/content/77/2/193”].</ref>
 
. The risk of having severe consequences for these infants exposed to sodium valproate in utero has been estimated between 6% and 12%<ref name=”[8]”>  Use of Sodium Valproate in Pregnancy. (2014, December 15). Retrieved October 23, 2019, at [https://www.medsafe.govt.nz/profs/PUArticles/December2014SodiumValproate.htm“https://www.medsafe.govt.nz/profs/PUArticles/December2014SodiumValproate.htm”].</ref>
 
. This can be prevented by reducing the dose of the drug. An example of endocrine effects might be idiosyncratic liver toxicity <ref name=”[9]”> Stewart, J. D., Horvath, R., Baruffini, E., Ferrero, I., Bulst, S., Watkins, P. B., … Chinnery, P. F. (2010, November). POLG determines the risk of sodium valproate induced liver toxicity. Retrieved October 23, 2019, at [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841971/“https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841971/”].</ref>
 
 
===Lab Protocols===
 
 
VPA is considered thermodynamically stable, which indicates that it is not reactive under normal environmental conditions. It should be stored in a metal can or drum and kept away from incompatible materials such as oxidizing agents, bases and strong reducing agents as ignition may result.
 
 
Working with VPA can be irritating when inhaled or when getting directly in contact with the yes. To prevent this, VPA needs to be handled in a fume hood, safety goggles, lab coats, and gloves need to worn. Direct skin contact or ingestion of VPA should be avoided. In case of contact, flush the specific body part and go to the doctor without delay <ref name=”[10]”> Chemwatch: 15242 Version No: 7.1.1.1 Safety Data Sheet (Conforms to Regulation (EU) No 2015/830)</ref>
 
 
==State of the art==
 
 
 
 
 
 
{| class="wikitable" style="margin-bottom:0"
 
!Company
 
!Product
 
!Test name
 
!Sample Volume (μL)
 
!Reportable range
 
!Dilution
 
!Precision
 
!Incubation time
 
!Measuring Technique
 
|-
 
|Beckman Coulter<ref name=”[23]”>Emit 2000 Valproic Acid Assay (2010, September) Retrieved from November 7, 2019''. Beckman.</ref> <ref name=”[24]”>Beckman Coulter system Reagent, AU400/AU400e (2012, February) Retrieved from November 7, 2019''. Beckman.</ref>
 
|AU2700/AU5400
 
|VALPROIC ACID EMIT® 2000
 
|3.5 μL
 
|< 150 μg/mL
 
|1:1
 
|Total CV < 4.3%<br /> Inter-assay: CV < 3.2%
 
|15-75 min.
 
|ELISA<sup>1</sup>
 
|-
 
|Roche COBAS<ref name=”[25]”>Cobas 8000 modular analyzer series (last update: 2019, November 8).</ref> <ref name=”[26]”>van Eckardstein, A et al. (2013). cobas 8000 Modular Analyzer Series Evaluated under Routine-like Conditions at 14 Sites in Australia, Europe, and the United States. Retrieved from October 23., at [https://pdfs.semanticscholar.org/beb9/eaea6d45ba8fec2f3049cc5e242d9d2cfb13.pdf
 
“https://pdfs.semanticscholar.org/beb9/eaea6d45ba8fec2f3049cc5e242d9d2cfb13.pdf
 
”].</ref>
 
|Cobas 8000
 
|Cobas 8000
 
|1.5–35
 
|3.15 – 150 mg/L <ref name=”[27]”>Therapeutic drug monitoring (2011). Retrieved from November 8, 2019.'' R-Biopharm AG.</ref>
 
|1:(3-121)
 
|Inter-assay: CV < 0.7% ~ 2.9%<br />Total CV<3%
 
|9 min – 27 min
 
|ELISA<sup>1</sup>
 
|-
 
|ABBOTT LABORATORIES DIAGNOSTIC DIVISION<ref name=”[28]”>iValproic Acid B1P350 (2009,August).</ref>
 
<ref name=”[29]”> Free Valproic Acid Assay (2014, April). Retrieved from November 3, 2019, at [https://www.cadth.ca/sites/default/files/pdf/lab-tests/06_Free_Valproic_Acid_Assay_e.pdf/“https://www.cadth.ca/sites/default/files/pdf/lab-tests/06_Free_Valproic_Acid_Assay_e.pdf”].</ref>
 
 
|B1P350
 
|ARCHITECT iValproic Acid
 
|10
 
|2 - 150 μg/mL
 
|1:10
 
|Total CV≤ 7%
 
|29 min
 
|CMIA<sup>2</sup>
 
|-
 
|SIEMENS HEALTHCARE DIAGNOSTICS INC.<ref name=”[30]”> ADVIA 1900 Chemistry system</ref>
 
|67070
 
|ADVIA 1200 CHEMISTRYSYSTEM -VALPROIC ACID (VPA) ASSAY
 
|2-3
 
|NA
 
|1:5
 
|Inter-assay: CV = 0.2% - 5.3 %<br /> Total CV= 0.4%-5.3% <ref name=”[31]”> American Association for Clinical Chemistry, 70th AACC Annual Scientific Meeting (July, August, 2018). Retrieved from November 7, 2019</ref>
 
 
|3-21 min
 
|ELISA<sup>1</sup>
 
|-
 
|MICROGENICS CORPORATION<ref name=”[32]”>CEDIA Valproic Acid II Assay (2018, November). Retrieved from November 7, 2019</ref>
 
|62390
 
|CEDIA TDM ASSAY -VALPROIC ACID
 
|NA
 
|3.0-150 μg/mL
 
|NA
 
|Inter-assay: CV = 1.3% - 2.4 %<br /> Total CV= 1.8%-3.4%
 
|Reagent 1 : 2-5 min <br/>Reagent 2: 4-8 min
 
|ELISA<sup>1</sup>
 
 
 
  
|}<div style="margin-bottom:1em"><sub>''1 ELISA: Enzyme Linked Immunosorbent Assay''<br />Note: 2.CMIA: Chemiluminescent Microparticle Immunoassay
+
When working with the influenza virus, influenza infection in humans can occur following a laboratory accident. For safety reasons, inactivated virus particles will be used in SensUs 2021, as a substitute for infectious influenza virus particles.  
</sub></div>
 
  
To measure unbound VPA, blood samples are treated by ultrafiltration, followed by an immunoassay, also referred to as ELISA. By performing the ultrafiltration, the protein-bound form of VPA is separated from its unbound form. After that, the level of the unbound fraction can  be measured by an immunoassay, e.g. an ELISA kit. Alternatively, LC-MS can be used to measure VPA.<ref name=”[40]”> ao, S., Miao, H., Tao, X., Jiang, B., Xiao, Y., Cai, F., … Chen, W. (2011, July 1). LC–MS/MS method for simultaneous determination of valproic acid and major metabolites in human plasma, Journal of Chromatography B
+
==Lab Protocols==
Volume 879, Retrieved November 28, 2019, at [https://www.sciencedirect.com/science/article/pii/S1570023211003278?via=ihub“https://www.sciencedirect.com/science/article/pii/S1570023211003278?via=ihub”].</ref>
+
The use of safety equipment combined with good practices is fundamental to laboratory safety and in helping to reduce the risks involved in dealing with biosafety hazards.
Steps such as solvent extraction or derivation must be executed prior to a HPLC assay, which takes significant time<ref name=”[29]”> Free Valproic Acid Assay (2014, April). Retrieved from November 3, 2019, at [https://www.cadth.ca/sites/default/files/pdf/lab-tests/06_Free_Valproic_Acid_Assay_e.pdf/“https://www.cadth.ca/sites/default/files/pdf/lab-tests/06_Free_Valproic_Acid_Assay_e.pdf”].</ref>
+
According to Article 4.84 of the Working Conditions Decree, the inactivated virus particles can be classified as category 1 of the biological agents, as they are unlikely to cause disease in humans.  
. CMIA is a special type of ELISA <ref name=”[34]”> Ilyas M., Ahmad. I (2014, July 12), Chemiluminescent microparticle immunoassay based detection and prevalence of HCV infection in district Peshawar Pakistan, third alinea Background, Retrieved from November 7, 2019, at [https://virologyj.biomedcentral.com/articles/10.1186/1743-422X-11-127“https://virologyj.biomedcentral.com/articles/10.1186/1743-422X-11-127”].</ref>
+
Therefore, only the biosafety guidelines as defined in the ML-1 (minimum containment level) have to be followed. It is stipulated in the guidelines that general laboratory protocols such as the usage of barrier protection (lab coats, gloves and face protection) when handling the samples are to be followed. The protection barriers are not always necessary from a microbiological perspective. However, it is compulsory when handling disinfectants or solvents.  
.
 
Several innovations are being investigated for VPA testing. For example, 2D-LC system (two-dimensional chromatography) was studied, allowing large volume injection, reducing interfering components, and reducing the analysis time and preventing most interference components by selecting useful sections in the “heart-cut” column(1D) from entering the analysis column (2D).<ref name=”[11]”>  Liu, W., Shang, X., Yao, S., & Wang, F. (2019, August 20). A novel and nonderivatization method for the determination of valproic acid in human serum by two‐dimensional liquid chromatography. Retrieved October 17, 2019, at [https://doi.org/10.1002/bmc.4695.“https://doi.org/10.1002/bmc.4695.”].</ref>
 
. Another example is dried blood spot (DBS) followed by gas chromatography mass spectrometry (GC–MS), which does not require solvent extraction or elution. The limit of quantitation was 200 ng/mL. <ref name=”[12]”> Guo, M., Shao, L., Chen, X., Li, H., Wang, L., Pan, Y., & Tang, D. (2019, September 13). Assay of dried blood spot from finger prick for sodium valproate via ink auxiliary headspace gas chromatography mass spectrometry, Journal of Chromatography A Vol. 1601 p. 335-339. Retrieved October 24, 2019, at [ https://doi.org/10.1016/j.chroma.2019.05.039“ https://doi.org/10.1016/j.chroma.2019.05.039”].</ref>
 
  
 
== References ==
 
== References ==
  
 
<references />
 
<references />

Revision as of 14:58, 17 December 2020

This wiki page is not yet finished

General Information

The theme of SensUs 2021 is acute respiratory viruses. The current Covid-19 pandemic has made it apparent that large virus outbreaks can cause immense harm to human health and can disrupt society as a whole. The most common respiratory virus is influenza A. Therefore, the influenza virus serves as an interesting biomarker for this year’s Competition.

The influenza A virus is known to cause influenza in birds and some mammals, like humans. Different subtypes of the influenza A virus have been isolated from wild birds. Some subtypes of the influenza A virus can cause severe symptoms both in domestic poultry and (rarely) in humans and can even lead to death. Occasionally, viruses can be transmitted from wild birds to domestic animals, like chickens or pigs. This may give rise to human influenza. Influenza A viruses are negative-sense, single-stranded RNA viruses. Different subtypes of influenza A exist, these are characterized by proteins on the outermost membrane of the virus, called hemagglutinin (H or HA) and neuraminidase (N or NA). H and N are the antigens of the virus, and play an important role in the interaction between the host’s immunological response and the virus. Recently, researchers have reported the discovery of an antibody which is generally effective against all types of the influenza A virus. The subtype which will be used in SensUs 2021 is H1N1. Historically, H1N1 has been responsible for most deaths due to influenza. It is a popular influenza strain for research purposes [link, link, link] . Due to its popularity among researchers, antigens and antibodies are commercially available, making H1N1 suitable as a target for the SensUs competition. Influenza A vaccines for humans have been developed. New versions of the vaccines are developed twice per year for use all over the world, which is necessary due to rapid mutations of the influenza virus. Every year during flu season, a large part of the population is vaccinated in order to protect individuals against the virus. However, due to unforeseen mutations of the virus, it might be possible that in a certain year a vaccine will prove ineffective. In that case large portions of the population would be at risk and a pandemic could occur. The probability of a major influenza A pandemic is estimated to be around 0.5-1% each year.

History of influenza (A)

A lack of data up until 1500 AC complicates the research on influenza before that period.[206] Possibly the first influenza pandemic occurred around 6000 BC in China. The symptoms of human influenza seem to have been clearly described by Hippocrates, roughly 2,400 years ago[207][208]. Although the virus seems to have caused epidemics throughout human history, historical data on influenza is difficult to interpret, due to the fact that symptoms of influenza are similar to those found in other respiratory diseases, like RSV (respiratory syncytial virus). The most infamous and lethal outbreak was the 1918 flu pandemic (Spanish flu) (type A influenza, H1N1 subtype), which lasted into 1920. The number of deaths is unknown, but estimates range from 17 to 100 million people. This pandemic has been described as "the greatest medical holocaust in history" and may have killed as many people as the plague (Black Death). This huge death toll was caused by an extremely high infection rate of up to 50% and the severity of the symptoms, suspected to be caused by cytokine storms in which the innate immune system causes an uncontrolled and excessive release of pro-inflammatory signaling molecules called cytokines. One of the most recent outbreaks of influenza was the 2009 Swine Flu. Similar to the Spanish Flu, it was also of the subtype H1N1. The death toll of the 2009 pandemic is estimated to be around 150,000 to 575,000.

Structure of the influenza virus

The virus particle (virion) is 80–120 nanometers in diameter. The virion shape can be spherical, elliptical, or even filamentous with a length of tens of micrometers. The virion is made up of a viral envelope containing two main types of proteins, wrapped around a central core. The two large proteins found on the outside of viral particles are hemagglutinin (HA) and neuraminidase (NA). HA is a protein that mediates binding of the virion to target cells and entry of the viral genome into the target cell, and therefore plays an important role in infecting healthy cells. NA is involved in releasing the progeny viruses once a cell has been infected and has started producing the virus itself. These two proteins are a target of interest for antiviral drugs. Furthermore, they are also the antigen proteins to which a host antibodies can bind and trigger an immune response. Influenza type A viruses are categorized into different subtypes, or strains, based on which type of these two proteins is present on the surface of the virion. Currently, there are 16 subtypes of HA and 9 subtypes of NA known to exist. The most prevalent form of the different subtypes is H1N1. Single hemagglutinin-neuraminidase proteins, in which both HA and NA are found in a single protein, also exist. However, these will not be used in SensUs 2021.

Mechanism of Infection

The involvement of the hemagglutinin and neuraminidase proteins in the infection of H1N1 is essential for the virus reproduction, and a more specific mechanism is discussed below. The hemagglutinin protein (HA) has the role of searching for the sialic acid receptors in respiratory-lining cell membranes. (figure _). Upon binding of this protein and the receptor, fusion of the virus and the cell membrane is facilitated with the help of glycan proteins. The virus then enters the cell where it sheds its shell and approaches the cell’s nucleus. Using the host replication mechanisms, the virus makes copies of itself. At this step of the infection process, important viral proteins are synthesized. These newly replicated viral elements subsequently attempt to leave through the cell membrane and infect other cells. To inhibit the exit of the viral components, sialic acid receptors on the cell membrane attempt to bind the HA glycoproteins. This is where viral evolution/mutability can play a role in the expansion of the capabilities of the virus. The neuraminidase glycoprotein (N) has the role of cleaving the sialic acid receptors, allowing the exit of the viral components which then go in search of a new host. After infection is complete, the H1N1 virus triggers cell apoptosis, leading to the death of the cell and spread of the virions. pictures

Medical Application

Optimal dose and effects are achieved with upper limit of 60 mg/kg/day. If the desired effects are not achieved (in other words, the seizures are not gone or the The influenza virus spreads when people with the flu cough, sneeze or talk. Infected people transfer tiny droplets to people close to them and infect them by the handover of droplets (Influenza (Flu) 2019). During an outbreak, it is important to be able to control and prevent the virus from spreading further, for example, by implementing control measures. Those control measures can be determined based on the reproduction number. The reproduction number is defined as: “the expected number of secondary cases produced by a single infection in a completely susceptible population”(https://web.stanford.edu/~jhj1/teachingdocs/Jones-on-R0.pdf). A clear overview of the number of infected people is needed to calculate the reproduction number. For disease control, it is crucial to know the infection rate in a specific region. The results may influence critical decisions such as whether to perform other diagnostic testing or to implement infection prevention and control measures for influenza (Overview of Influenza testing methods 2020). Furthermore, manpower can be in short supply during a pandemic and the speed at which someone can be tested and receive the result is of vital importance. Biosensors that will be developed in SensUs 2021 are envisioned to be used outside the hospital in a point-of-care (POC) setting. Inside the hospital there is not a big advantage, as there are already very specific and accurate tests available for that setting (Diagnosis, 2020). Important applications are fast testing at the GP and at home. Therefore the test should be easy to use. The biosensors will be designed to enable a fast yes/no answer, based on measuring the concentration of viral particles in the sample. The biosensors will not distinguish between different virus subtypes, as the subtype causing the pandemic is assumed to be known.

State of the Art

Still paste some tables

Safety

When working with the influenza virus, influenza infection in humans can occur following a laboratory accident. For safety reasons, inactivated virus particles will be used in SensUs 2021, as a substitute for infectious influenza virus particles.

Lab Protocols

The use of safety equipment combined with good practices is fundamental to laboratory safety and in helping to reduce the risks involved in dealing with biosafety hazards. According to Article 4.84 of the Working Conditions Decree, the inactivated virus particles can be classified as category 1 of the biological agents, as they are unlikely to cause disease in humans. Therefore, only the biosafety guidelines as defined in the ML-1 (minimum containment level) have to be followed. It is stipulated in the guidelines that general laboratory protocols such as the usage of barrier protection (lab coats, gloves and face protection) when handling the samples are to be followed. The protection barriers are not always necessary from a microbiological perspective. However, it is compulsory when handling disinfectants or solvents.

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