The document discusses several RNA viruses including influenza viruses, which are type A, B, or C orthomyxoviruses. Influenza A viruses can be further divided into subtypes based on surface proteins and have caused past pandemics in humans. Antigenic drift and shifts of these proteins allow influenza to evade immunity. The viruses are transmitted through respiratory droplets and cause flu symptoms. Diagnosis involves virus isolation, antigen detection, or PCR. Treatment is with neuraminidase inhibitors and vaccination helps prevent infection.
The document discusses several RNA viruses including influenza viruses, which are type A, B, or C orthomyxoviruses. Influenza A viruses can be further divided into subtypes based on surface proteins and have caused past pandemics in humans. Antigenic drift and shifts of these proteins allow influenza to evade immunity. The viruses are transmitted through respiratory droplets and cause flu symptoms. Diagnosis involves virus isolation, antigen detection, or PCR. Treatment is with neuraminidase inhibitors and vaccination helps prevent infection.
The document discusses several RNA viruses including influenza viruses, which are type A, B, or C orthomyxoviruses. Influenza A viruses can be further divided into subtypes based on surface proteins and have caused past pandemics in humans. Antigenic drift and shifts of these proteins allow influenza to evade immunity. The viruses are transmitted through respiratory droplets and cause flu symptoms. Diagnosis involves virus isolation, antigen detection, or PCR. Treatment is with neuraminidase inhibitors and vaccination helps prevent infection.
Orthomyxoviruses Influenza viruses Paramyxoviruses Measles, mumps, RSV and parainfluenza virus Togaviruses Rubella Rhabdoviruses Rabies virus Retroviruses HIV Coronaviruses Coronavirus, MERS-virus and SARS Filoviruses Ebola virus Flaviviruses Yellow Fever virus, dengue virus and HCV. Deltaviruses HDV Orthomyxoviruses
Dr. Muna. M. A. Yousif
M.D clinical Microbiology Structure • Orthomyxoviruses are enveloped viruses with a helical nucleocapsid and a single-stranded, segmented genome (usually 8 pieces) of negative polarity. • The envelope contains haemagglutinin (HA) and neuraminidase (NA) spikes. • Matrix proteins are found and are important for structural integrity and as an ion channel. • The most important member in this family is the influenza virus. Structure • Orthomyxoviruses include different influenza viruses (types A, B and C). • They are a group of highly contagious human pathogens and outbreaks of influenza are a major cause of morbidity and mortality to humans each year. • Influenza pandemics have killed thousands of people through out the centuries. Classification • Antigenic differences in the nucleocapsid proteins and matrix proteins are used to divide influenza viruses into types A, B and C. • Influenza type A has different subtypes, based on antigenic variation in the surface proteins (HA and NA) • There are 16 types of HA and 9 types of NA. • Influenza A virus contains both human and animal strains. • Influenza B contains only human strains. • Influenza C contains human and swine strains. History of influenza • 1889 (Asiatic or Russian pandemic): killed 1 million. • 1918 (Spanish flu pandemic) (H1N1): killed 20 million. • 1957 Asian flu (H2N2) killed 1.5 million • 1968 Hong Kong flu (H3N2)killed 1 million • 1977 Russian flu(H1N1) killed • 2009 flu pandemic (H1N1)killed 18,000- 280,000 • 2013 avian flu (H7N9) killed more than 24 Epidemiology • Antigenic changes occur continuously in influenza A virus and to a lesser extent in influenza B. Influenza C virus is a stable virus and no change in it’s antigenicity is known to occur. • Aquatic birds, chickens, ducks, pigs, horses are affected by animal influenza virus type A. • Changes in the antigenicity of HA and NA of influenza viruses (type A) is responsible for causing devastating world-wide epidemics. Types of antigenic changes 1. Antigenic shift: is due to major changes that result from reassortment of the eight RNA genome segments. These reassortments result in the formation of a new viral strain that infects a susceptible population giving a pandemic. Aquatic birds act as a source of new genes but the reassortment which leads to the appearance of the new strain occurs in pigs. 2. Antigenic drift: results from only minor antigenic changes resulting from point mutations in the viral HA and NA glycoproteins • Because influenza B virus is only infects humans, there is no animal source of new RNA segments and therefore, antigenic shift does NOT occur in influenza B. Pathogenesis • The virus is transmitted from person to person by respiratory secretions. Patients secrete the virus 24 hours before becoming symptomatic and 48 hours after. • Attachment of the virus occurs in the mucosal epithelial cells of the upper respiratory tract by HA and infection is initiated. • Neuraminidase breaks down neuraminic acid (sialic acid) before the release of progeny virus from the infected cell. Clinical disease • After an incubation period of 1-3 days the patient develops sudden fever, headache, chills, myalgia, sore throat and a dry cough. • These symptoms last for 10 days up to 2 weeks. • Secondary bacterial infection by Staphylococcus aureus is common. Diagnosis • Infection maybe diagnosed clinically or in the lab by: 1. Virus isolation 2. Fluorescent antibody staining can be used to demonstrate the virus in nasal or throat washings, swabs or sputum 3. PCR 4. Rapid tests (used by physicians and detect viral antigens) 5. Antibody detection in patients serum. Treatment • Neuraminidase inhibitors:Oseltamivir (Tamiflu) and zanamivir (Relenza) can be used for both treating and preventing infection. Are effective against both influenza A and B. • Amantadine stops viral replication by preventing entry or uncoating of the virus. It can be used to prevent and treat influenza A virus ONLY. • Most strains of influenza have now become resistant to amantadine and it has CNS side-effects. • Rimantadine is a derivative of amantadine with fewer side-effects. Prevention • Vaccine against influenza A and B viruses is available .It is composed of the two most recent A strains (H1N1 and H3N2) and the most recent B strain. • There are two types of vaccines present; 1. Killed vaccine. Given intramuscularly. 2. Live vaccine containing temperature sensitive mutants of influenza A and B virus. Given by nasal spray ‘nasal mist’ Avian influenza virus • Avian influenza virus in humans is caused by influenza A virus (H5N1). • Avian influenza infects primarily chickens but in 1997 an aggressive human type appeared in Hong Kong. • In 2003 an outbreak of avian influenza virus appeared in Asia and killed thousands of birds. • In March 2013 an outbreak, the World Health Organization (WHO) reported 132 human H7N9 infections, with 44 deaths • Avian influenza virus rarely spreads among humans because human mucous membranes do not have the specific receptor required for binding of the virus to occur. This receptor is only present in the alveoli of humans, therefore, although infection is uncommon in human, when it does happen infection is severe. • Avian flu is sensitive only to neuraminidase inhibitors and not to amantidine. • There is no human vaccine. Swine flu • Is caused by S-OIV (swine-origin influenza virus) H1N1 virus. • S-OIV first appeared in Mexico, then the United States and a few months later a pandemic occurred. • Is caused by a quadruple reassortment (with genes from N. American and Eurasian swine viruses and from avian and human influenza viruses) • Swine flu is readily transmitted among humans and presents with symptoms of the seasonal flu. • Is diagnosed using PCR. • Treatment is by using Oseltamivir and zanamivir. • Two types of vaccines are present (killed and live-attenuated vaccine).
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International Journal of Innovative Science and Research Technology