Antiviral drug susceptibility of influenza viruses essay

Additional NAIs licensed outside the United States include the intravenous peramivir, which is approved in Japan, South Korea, and China, while inhaled laninamivir is licensed only in Japan; the oral prodrug of A A was dropped from development For nitazoxanide, cell culture supernatants were collected at 48 h postinfection hpi and viral titers were determined in MDCK cells and expressed as log10 of tissue culture infectious dose TCID90 per ml.

Search our thousands of essays: Human infections resulting from swine influenza viruses are relatively rare; between andonly 27 such infections were documented in the United States 4.

Oseltamivir is recommended for hospitalized, critically ill, or immunocompromised patients, in whom viral replication may be protracted; in such patients, a longer treatment course e. Therefore, it is critical to comprehend the epidemiological and molecular mechanisms by which influenza A viruses acquire the capability to cross species barriers.

Of People Infected Estimated No. All recombinant NA recNA proteins contained a His tag at the N terminus followed by a tetramerization domain, from human vasodilator-stimulated phosphoprotein, and a thrombin site Longer durations of prophylaxis are often recommended for institutional and community outbreaks see Table 1.

Zanamivir may be preferred for prophylaxis because of its limited systemic absorption, but oseltamivir is a reasonable alternative, especially for women at increased risk for respiratory problems. Meanwhile, animals are a source of panzootics which largely contribute to influenza pandemics.

It can be considered after exposure for persons at high risk for complications who cannot receive the influenza vaccine or received it within the last 2 weeks, and for those who are unlikely to respond to vaccination.

Address correspondence to Larisa V. Prophylaxis is recommended to help control confirmed influenza outbreaks in nursing homes; antiviral medication should be given to residents and to unvaccinated healthcare workers.

Diarrhea, nausea, sinusitis, fever, and arthralgia have been reported with zanamivir. Zanamivir Antiviral drugs can be used for treatment and prophylaxis of influenza. MDCK cells were used for experiments using nitazoxanide according to previously published protocols 25 and as recommended by the manufacturer.

An Introduction to Established and Emerging Zoonotic Diseases In general, the transfer of viruses to new hosts requires contact between a host and virus and amplification initiated by the infection of an individual which may lead to an outbreak.

Virus inoculum at a multiplicity of infection MOI of 0. Essay UK - http: Antiviral treatment can be considered for previously healthy persons with suspected or confirmed influenza if it can be started within 48 hours of illness onset.

Peramivir for at least 5 days may be considered for those who cannot take oseltamivir. Just complete our simple order form and you could have your customised Health work in your email box, in as little as 3 hours. The major source of these onsets per annum is the emergence of an antigenically novel virus which the human population lack protective immunity against.

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Briefly, cell monolayers were pretreated for 2 h with fludase at concentrations ranging from 0. Unadsorbed virus was removed and nitazoxanide added at final concentrations of 0.

However, the production of variable viral features with the capacity to effectively extend throughout the new host population is critical. Using a fluorescent NA inhibition NI assay, a single variant virus that carried a naturally occurring change affecting inhibition of the NA activity by oseltamivir and zanamivir, but not by other NAIs, was identified.

Using cell culture assays, the investigational antiviral drugs nitazoxanide, favipiravir, and fludase were shown to inhibit the replication of A H3N2 v viruses, including the virus with the SP substitution in the NA.

So-called swine triple reassortants containing genes of influenza viruses from three different species avian, human, and swine became widespread in North American swine populations circa and pose a constant threat to human health.

Human infection with a novel influenza type A virus is a disease reportable to the World Health Organization WHO under International Health Regulations 2 and has been a nationally notifiable condition in the United States since 3.

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Influenza A viruses that circulate in swine but infect humans are called variant viruses 5. There were 12 confirmed cases of A H3N2 v infection in the United States in and inwith additional cases occurring in 9 ; nearly all infections have resulted from exposure to swine at state and local fairs Due to the limited therapeutic options, it was essential to monitor susceptibilities of the A H3N2 v viruses to available and investigational antiviral drugs.

This article has been cited by other articles in PMC. Reduction of infectious virus yield in the presence of nitazoxanide 25favipiravir 26and ribavirin 26 was assessed essentially as previously described. Neuropsychiatric events, including self-injury and delirium, have been reported in patients taking neuraminidase inhibitors, but a cause-and-effect relationship has not been established, and neuropsychiatric dysfunction is a known complication of influenza illness itself.

Nucleotide sequence accession numbers. They are active against both influenza A and B viruses. Oral oseltamivir Tamiflu, and generics and inhaled zanamivir Relenza are FDA-approved for treatment and prophylaxis of influenza.Antiviral Drugs for Seasonal Influenza Download PDF: US English.

Show Related Terms Hide Related Antiviral drugs can be used for treatment and prophylaxis of influenza. LV Gubareva et al. Global update on the susceptibility of human influenza viruses to neuraminidase inhibitors, Antiviral Res ;. Influenza viruses resistant to one or more antiviral drugs can emerge and spread rapidly (28, 34, 35), and active virological surveillance is essential to accurately and timely identify such changes in circulating viruses.

To combat antiviral resistance acquired either naturally or under drug selection, new antivirals that target different molecular and. resistant influenza viruses, alternative antiviral strategies have been developed.

The sialidase activity in the virus neuramindase (NA) protein plays a critical role in the influenza virus replication cycle, and the design of NA protein inhibitors is currently one of the most common approaches in the development of anti-influenza virus drugs.

In light of the high levels of resistance shown toward these two drugs, however, the threat to human health from influenza A viruses remains a significant problem (Laohpongspaisan et al., ; Rungrotmongkol et al., ; Cox and Subbarao, ). With a huge number of victims, 80 to million, sincethe influenza is considered as one of the most pandemic diseases ever.

There are three types of influenza virus: influenza virus A, influenza virus B, and influenza virus c. These are a subtypes of the virus family orthomyx-oviride. The Composition of Influenza A Viruses Influenza A viruses are of the Orthomyxoviridae genera and are all enveloped, negative-sense, single-stranded, segmented RNA viruses.

Within the lipid envelope of influenza A is an M2 protein, functioning as an ion channel, NA and HA molecules.

Antiviral drug susceptibility of influenza viruses essay
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