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RNA Viruses 1 M.Tvorko RNA Viruses • Diverse group of microbes • Assigned to one of 12 families based on envelope, capsid, and nature of RNA genome 2 3 Enveloped Segmented Single-Stranded RNA Viruses 4 The Biology of Orthomyxoviruses: Influenza • 3 distinct influenza virus types: A, B, C; Type A causes most infections • Viral infection – Virus attaches to, and multiplies in, the cells of the respiratory tract – Segments of RNA genome enter the nucleus (transcribed/translated) – Finished viruses are assembled and budded off the cell with an envelope 5 ОRTHOMYXOVIRUSES HA - hemagglutinin NA - neuraminidaze helical nucleocapsid (RNA minus NP protein Bilayer lipid membrane polymerase complex M1 protein types A, B, C : NP, M1 protein subtypes: HA or NA 7 • Key to influenza are glycoprotein spikes – – Hemagglutinin (H) – 15 different subtypes; most important virulence factor; binds to host cells – Neuraminidase (N) – 9 subtypes – hydrolyzes mucus and assists viral budding and release 8 Hemagglutinin (HA) 9 10 Influenza virus cycle 11 12 Influenza A • In Birds – 16 HA A variants – 9 NA A variants • In Humans – 3 HA A variants • (H1, H2, and H3) – 2 NA A variants • (N1 and N2 • Both glycoproteins frequently undergo genetic changes decreasing the effectiveness of the host immune response • Constant mutation is called antigenic drift – gradually change their amino acid composition • Antigenic shift – one of the genes or RNA strands is substituted with a gene or strand from another influenza virus from a different animal host – Genome of virus consists of 10 genes encoded on 8 separate RNA strands 14 Antigenic shift event 15 Influenza B • Only undergo antigenic drift • Not known to undergo antigenic shift Influenza C • Known to cause only minor respiratory disease; probably not involved in epidemics 16 Influenza A • Acute, highly contagious respiratory illness • Seasonal, pandemics; among top 10 causes of death in U.S. – most commonly among elderly and small children • Binds to ciliated cells of respiratory mucosa • Causes rapid shedding of cells, stripping the respiratory epithelium; severe inflammation • Fever, headache, myalgia, pharyngeal pain, shortness of breath, coughing • Weakened host defenses predispose patients to secondary bacterial infections, especially pneumonia 17 Diagnosis, Treatment, Prevention • Rapid immunofluorescence tests to detect antigens in a pharyngeal specimen; serological testing to screen for antibody titer • Treatment: control symptoms; amantadine, rimantadine, zanamivir (Relenza), and oseltamivir (Tamiflu) • Flu virus has developed high rate of resistance to amantadine and rimantadine • Annual trivalent vaccine recommended 18 Influenza Vaccines • Whole virus vaccine: inactivated virus vaccine grown in embryonated eggs; 70-90% effective in healthy persons <65 years of age, 30-70% in persons ≥65 years • Split virus vaccine: previously associated with fewer systemic reactions among the elderly and children <12 years • Subunit vaccine: composed of HA and NA • Live, attenutated influenza virus vaccines under development Enveloped Nonsegmented ssRNA Viruses 20 Paramyxoviruses Paramyxoviruses (parainfluenza, mumps virus) Morbillivirus (measles virus) Pneumovirus (respiratory syncytia virus) • Respiratory transmission • Envelope has glycoprotein and F spikes that initiate cell-to-cell fusion • Fusion with neighboring cells – syncytium or multinucleate giant cells form 21 PARAMYXOVIRUSES • HN/H/G glycoprotein F glycoprotein SPIKES helical nucleocapsid (RNA minus NP protein) polymerase complex M protein The effects of paramyxoviruses Insert figure 25.5 Effects of paramyxoviruses 23 Parainfluenza • • • • Widespread as influenza but more benign Respiratory transmission Seen mostly in children Minor cold, bronchitis, bronchopneumonia, croup • No specific treatment available; supportive therapy 24 Mumps • Epidemic parotitis; self-limited, associated with painful swelling of parotid salivary glands • Humans are the only reservoir • 40% of infections are subclinical; long-term immunity • 300 cases in U.S./year • Incubation 2-3 weeks fever, muscle pain and malaise, classic swelling of one or both cheeks • Usually uncomplicated invasion of other organs; in 20-30% of infected adult males, epididymis and testes become infected; sterility is rare • Symptomatic treatment • Live attenuated vaccine MMR 25 Mumps 26 Measles • • • • • • • • • Caused by Morbillivirus Also known as red measles and rubeola Different from German measles Very contagious; transmitted by respiratory aerosols Humans are the only reservoir Less than 100 cases/yr in U.S.; frequent cause of death worldwide Virus invades respiratory tract Sore throat, dry cough, headache, conjunctivitis, lymphadenitis, fever, Koplik spots – oral lesions Exanthem 27 Signs and symptoms of measles Measles • Most serious complication is subacute sclerosing panencephalitis (SSPE), a progressive neurological degeneration of the cerebral cortex, white matter, and brain stem – 1 case in a million infections – Involves a defective virus spreading through the brain by cell fusion and destroys cells – Leads to coma and death in months or years • Attenuated viral vaccine MMR 30 RESPIRATORY SYNCYTIAL (RS) VIRUS It is the single most serious cause of bronchiolitis and pneumonitis in infants. The particle is slightly smaller (80-120 nm) than other paramyxoviruses, and the nucleocapsid measures 1115 nm. Although RS is one of the most labile of viruses. RS virus does not hemagglutinate. RSV Bronchiolitis- clinical features Symptoms for this disease are: sneezing runny nose sore throat low fever common cold symptoms just more severe. • • • • • RSV is a viral disease. Respiratory Syncytial Virus (RSV)is a very serious virus often found in children and infants under the age of three. Adults are at very low risk of catching RSV. Rabies • • • • Rhabdovirus family; genus Lyssavirus Enveloped, bullet-shaped virions Slow, progressive zoonotic disease Primary reservoirs are wild mammals; it can be spread by both wild and domestic mammals by bites, scratches, and inhalation of droplets 34 Structure of the rabies virus Insert figure 25.8 Structure of rabies virus 35 Rabies • Virus enters through bite, grows at trauma site for a week and multiplies, then enters nerve endings and advances toward the ganglia, spinal cord and brain • Infection cycle completed when virus replicates in the salivary glands Clinical phases of rabies: • Prodromal phase – fever, nausea, vomiting, headache, fatigue; some experience pain, burning, tingling sensations at site of wound • Furious phase – agitation, disorientation, seizures, twitching, hydrophobia • Dumb phase – paralyzed, disoriented, stuporous • Progress to coma phase, resulting in death 36 Pathologic pictures of rabies 37 • Often diagnosed at autopsy – intracellular inclusions (Negri bodies) in nervous tissue • Bite from wild or stray animals demands assessment of the animal, meticulous wound care, and specific treatment • Preventive therapy initiated if signs of rabies appear • Treatment – passive and active post exposure immunization – Infuse the wound with human rabies immune globulin (HRIG) and globulin; vaccination with human diploid cell vaccine (HDCV), an inactivated vaccine given in 6 doses with 2 boosters • Control – vaccination of domestic animals, elimination of strays, and strict quarantine practices – Live oral vaccine incorporated into bait for wild animals 38 Arboviruses • viruses that spread by arthropod vectors – mosquitoes, ticks, flies, & gnats • 400 viruses The Influence of the Vector • Vectors and viruses tend to be clustered in the tropics and subtropics – many temperate zones have periodic epidemics • life cycles are closely tied to the ecology of the vectors • peak incidence when the arthropod is actively feeding and reproducing • Humans can serve as dead-end, accidental hosts or they can be a maintenance reservoir • Controlling the vector controls the disease Characteristics of Arbovirus Infections • Viral encephalitis – brain, meninges, and spinal cord are involved – convulsions, tremor, paralysis, loss of coordination, memory deficits, changes in speech and personality, coma – survivors may experience permanent brain damage • Treatment is supportive 42 Togaviruses • Enveloped virion containing non-segmented, ssRNA (both + an – sense) ~11.7kb • Subspecies (i.e.: Rubella virus) causes Rubella or German Measles • Symptoms include low grade fever, sore throat, rash, and lymphoadenopathy • Viral RNA is complimented by the host cells machinery and the –’ve sense strand produced serves as a template for more +’ve sense strands Rubella • Caused by Rubivirus, a Togavirus • ssRNA with a loose envelope • German measles • Endemic disease • Most cases reported are adolescents and young adults • Transmitted through contact with respiratory secretions Rubella Two clinical forms: • Postnatal rubella – generally mild – malaise, fever, sore throat, lymphadenopathy, rash – lasting about 3 days • Congenital rubella – infection during 1st trimester most likely to induce miscarriage or multiple defects • Diagnosis based on serological testing • No specific treatment available • Attenuated viral vaccine MMR Hemorrhagic Fevers Yellow fever eliminated in U.S. – Two patterns of transmission: • urban cycle – humans and mosquitoes • sylvan cycle – forest monkeys and mosquitoes – South America – Acute fever, headache, muscle pain • may progress to oral hemorrhage, nosebleed, vomiting, jaundice, and liver and kidney damage – significant mortality rate Hemorrhagic Fevers Dengue fever flavivirus carried by Aedes mosquito usually mild infection – dengue hemorrhagic shock syndrome, breakbone fever • extreme muscle and joint pain • can be fatal Bunyavirus • Spread by infected animals • Hantavirus pulmonary syndrome (HPS) – caused by a strain of hantavirus named “Sin Nombre” – deer mouse is the host • sheds the virus in saliva, urine, and feces Model of Human Hepatitis C Virus Lipid Envelope Capsid Protein Nucleic Acid Envelope Glycoprotein E2 Envelope Glycoprotein E1 HCV - Epidemiology Prevalence In Groups at Risk Recipients of clotting factors before 1987 75 - 90% Injection drug users 70 - 85% Long-term hemodialysis patients 10% Individuals with > 50 sexual partners 10% Recipients of blood prior to 1990 5% Infants born to infected mothers 5% Long-term sexual partners of HCV positive 1 - 5% Health workers after random needlesticks 1 - 2% HCV • ACCOUNTS FOR 90-95% OF POST TRANSFUSION HEPATITIS • RISK OF SEXUAL TRANSMISSION LOWER THAN FOR HBV • RISK THROUGH CASUAL CONTACT LOW HCV • VERTICAL TRANSMISSION POSSIBLE – RISK INCREASED IF MOTHER IS POSITIVE FOR HCV RNA – RISK INCREASED IF MOTHER IS HIV POSITIVE • OVERALL PREVALENCE ESTIMATED AT 1.4% WHO IS AT GREATEST RISK FOR HCV INFECTION? • DRUG ABUSERS • BLOOD PRODUCT RECIPIENTS (ANTI-HCV SCREENING HAS GREATLY REDUCED RISK) • HEMODIALYSIS PATIENTS • LAB PERSONNEL WORKING WITH BLOOD PRODUCTS WHO IS AT GREATEST RISK FOR HCV INFECTION? • SEXUALLY ACTIVE HOMOSEXUALS • PERSONS WITH MULTIPLE AND FREQUENT SEXUAL CONTACTS • MEDICAL/DENTAL PERSONNEL (3-10% VIA NEEDLESTICK FROM INFECTED PATIENT) HDV INFECTION PATTERNS COINFECTION ACUTE SIMULTANEOUS INFECTION WITH HBV AND HDV OFTEN RESULTS IN FULMINANT INFECTION (70% CIRRHOSIS) SURVIVORS RARELY DEVELOP CHRONIC INFECTION (< 5%) HDV INFECTION PATTERNS • SUPERINFECTION – RESULTS IN HDV SUPERINFECTION IN AN HBsAg CARRIER (CHRONIC HBV) – CAN OCCUR ANYTIME DURING CHRONIC DISEASE – USUALLY RESULTS IN RAPIDLY PROGRESSIVE SUBACUTE OR CHRONIC HEPATITIS Nonenveloped Nonsegmented ssRNA Viruses: Picornaviruses and Caliciviruses • Picornaviruses – Enterovirus – poliovirus, HAV – Rhinovirus – rhinovirus – Cardiovirus – infects heart and brain 57 Poliovirus and Poliomyelitis • naked capsid • can survive stomach acids when ingested Poliomyelitis (polio) acute enteroviral infection of the spinal cord can cause neuromuscular paralysis • Worldwide vaccination programs have reduced the number of cases – eradication is expected Poliovirus • Pretty tough virus: resistant to acid, bile, & detergents, survives stomach acids • virus is ingested (food, water, contaminated objects) • most infections are mild • grows in oropharynx & intestine, then enters blood (viremia) • if viremia persists, virus spreads to spinal cord & brain • invasion of motor neurons causes flaccid paralysis • decades later post-polio syndrome (PPS) of muscle deterioration can develop 59 Diseases of the Enteroviruses • Coxsackie A viruses – Infection occurs via the fecal-oral route – Produce lesion and fever • Herpangina • Hand-foot-and-mouth disease Human Rhinovirus (HRV) • More than 110 serotypes (strains) associated with the common cold • Sensitive to acidic environments – optimum temperature is 33oC • Unique molecular surface makes development of a vaccine unlikely • Endemic with many strains circulating in the population at one time – acquired from contaminated hands and fomites Hepatitis A virus particles found in fecal extracts by immunoelectron microscopy. Both full and empty particles are present. The virus is 27 to 29 nm in diameter. (X 125,000.) Hepatitis A Transmission Close personal contact Household or sexual contact Daycare centers Fecal-oral contamination of food or water Food handlers Raw shellfish Travel to endemic areas Blood-borne (rare) Injecting drug users 64 Hepatitis A Vaccine Efficacy Studies Vaccine Site/Age Group N Vaccine Efficacy (95% CI) HAVRIX (SKB) 2 doses 360 EL.U. Thailand 1-16 yrs 38,157 94% (79%-99%) VAQTA (Merck) 1 dose 25 units New York 2-16 yrs 1,037 100% (85%-100%) Epidemiology of Hepatitis E Fecal-oral transmission (human to human) Contaminated water supplies in tropical or subtropical developing countries Structural model of the Hepatitis E virus Mainly young adults Can infect primates, swine, sheep, rats Swine may be reservoir of infection in North America (attenuated virus) Maternal-infant transmission occurs and is often fatal Nonenveloped Segmented dsRNA Viruses: Reoviruses Unusual double-stranded RNA genome Two best known: • Rotavirus – oral-fecal transmission; primary viral cause of mortality and morbidity resulting from diarrhea in infants and children – Treatment with rehydration and electrolyte replacement • Reovirus – cold-like upper respiratory infection, enteritis 67 RETROVIRUSES HIV and AIDS History of an infectious agent In Los Angeles 1967-1978: only two cases of Pneumocystis carinii pneumonia • 1979 - 5 cases of Pneumocystis carinii pneumonia All Homosexual Dot-like intracystic bodies of Pneumocystis carinii in lung Cytologic preparation from a bronchoalveolar lavage – Giemsa stain Pneumocystis jiroveci 69 HIV and AIDS an infectious agent – Kaposi’s Sarcoma Early 1981 MMWR: 5 cases of Kaposi’s sarcoma Hitherto: rare (immunocompromization) Elderly - Non-aggressive 1981 - 26 cases of Kaposi’s sarcoma • Young • Male • San Francisco and New York • All Homosexuals 70 HIV HIV - Life History HIV chemokine CD4 CD4 CCR5 CCR5 CD4 Mutant CCR5 Chemokine receptors are macrophage necessary co-receptors along with CD4 antigen 73 Позавузлова лімфома шиї Саркома Капоші Toxoplasma gondii Candidosis Anti-HIV Strategies Highly Active AntiRetroviral Therapy HAART: Two nucleoside analog RT inhibitors and 1 protease inhibitor Now also: Two nucleoside analog RT inhibitors and 1 non nucleoside 80 81 82