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Transcript
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