Title: ReoViruses Characteristics
1ReoViruses - Characteristics
- non-enveloped, double stranded RNA, segmented
- double layered capsid, icosahedral
- outer capsid consists of mostly structural
proteins - this capsid in removed by proteolytic enzymes
within the GI tract - thus forming intermediate/infectious subviral
particles - inner capsid binds the enzymes required for
transcription and replication - capping enzymes
- RNA dependent RNA polymerase
- Reo Respiratory, Enteric, Orphan
- for many years there was not human diseases
associated with these viruses - now viruses have been associated with UR T
infections and GI infections - very resistant to environment and
gastrointestinal conditions - remain active within the host and outside of the
host - of the three orders of Reoviruses only the
Rotaviruses cause significant human diseases most
in the form of acute gastroenteritis
2ReoViruses - Characteristics
- non-enveloped, double stranded RNA, segmented
- double layered capsid, icosahedral
- outer capsid consists of mostly structural
proteins - this capsid in removed by proteolytic enzymes
within the GI tract - thus forming intermediate/infectious subviral
particles - inner capsid binds the enzymes required for
transcription and replication - capping enzymes
- RNA dependent RNA polymerase
- Reo Respiratory, Enteric, Orphan
- for many years there was not human diseases
associated with these viruses - now viruses have been associated with UR T
infections and GI infections - very resistant to environment and
gastrointestinal conditions - remain active within the host and outside of the
host - of the three orders of Reoviruses only the
Rotaviruses cause significant human diseases most
in the form of acute gastroenteritis
3Rotavirus - Cycle
- Adsorption
- Intestinal protease cleave and remove portions of
the outer capsid - this creates an infectious subviral particle
with an exposed VP4 that binds the virus to
sialic acid receptors on intestinal epithelial
cells - VP4 is antigenic
- Penetration
- the ISVP penetrates the cells directly via the
fusion action of VP4 - the remainder of the outer capsid is removed
during penetration - the inner capsid/nucleic acid is released into
the cytoplasm - virus transcription and replication occur via the
nucleoprotein core
4Rotavirus - Cycle
- Transcription and Replication
- double stranded RNA strands(10 - 12) are
transcribed within the core producing a
m-RNA(from the negative sense template) which
leaves the core and associates with the
ribosomes setting the stage for early and late
proteins - viral glycoproteins are incorporated into the
membrane of the ER - within the core, the positive sense RNA strands
serve as templates for the negative sense
strands - Assembly
- the double stranded RNA replicas are released
from the core and associate with late structural
proteins giving nucleocapsids - these nucleocapsid bud through the ER membrane
thus acquiring outer capsid and a temporary
membrane which is cleaved within the ER. - Release
- Since early proteins shut down the cellular
macromolecular synthesis, the cell dies and
lysis thus releasing the viruses
5RotaVirus Clinical Disease
- Gastroenteritis mostly in infants and children
- diarrhea, vomiting, fever, dehydration
- no fecal leucocytes or blood
- follows a 48 hour incubation period
- Due to gastrointestinal mucosal cell death
- Due to adenylate cyclase activation by viral
products
6RotaVirus - Diagnosis
- symptoms cannot be distinguished from other viral
diarrheas - laboratory
- antigen detection large quantities of rotavirus
particles are present with the feces and can
easily be found via antigen detection methods - EIA
- Latex agglutination
- Electron microscopy
- serology
- since most people have antibody against
rotavirus, this is not always diagnostic but a
detectable four fold increase in serum antibody
is diagnostic
7RotaVirus - Epidemiology
- Reservoir infected humans symptomatic and
asymptomatic - Sources fomites in developed countries i.e.US,
etc - also contaminated water in under developed
countries - mode of transmission
- person-to-person, indirect, fecal-oral,
food-water, fomites - statistics
- rotaviruses account for 50 of all cases of
diarrhea in children requiring hospitalization - 70,00 cases in the U.S. annually
- gt 1 million cases worldwide annually
8RotaVirus - Control
- Sanitation
- Sewage Disposal
- Water Treatment
- Fomite Disinfection
- Immunization
- Active Attenuated Vaccine
- RotaTeq pentavalent five serotypes
9Reoviruses - ColtiVirus
- Colorado Tick Fever
- Clinical Disease
- sudden onset of fever, chill, headache,
photophobia, myalgia, arthralgia, and lethargy
acute disease many mild or subclincal infections - accompanied by biphasic fever, conjunctivitis,
lymphadenopathy, hepatospenomegaly, and
maculopapular rash - must be distinguished from Rocky Mountain Spotted
Fever - Pathogenesis
- CTF virus infected the erythroid precusor cells,
which mature into RBC that are released into the
circuclation the virus is protected from immune
clearance within the cells (viremia) for weeks or
months - the infected RBCs seed the vascular endothelial
and smooth muscle cells which often results in
hemorrhage
10ReoViruses - ColtiVirus
- Diagnosis
- detection of viral antigens on the surface of
erythrocytes with immunofluorence - fourfold increase in IgM for 45 days following
infection - Epidemiology Many mammalian reservoirs through
the western U.S. serve to infect wood tick
vectors to humans
11Rhabdoviruses - Characteristics
- bullet shaped, enveloped, virions containing a
helical nucleocapsid - envelope contains a glycoprotein spike composed
of G protein - G protein in the viral attachment protein
(VAP) - G protein is antigenic
- nucleocapsid contains
- one single stranded negative sense RNA
- L and NS proteins RNA dependent RNA polymerase
- N protein major caspid structural protein
which protect the RNA - M(matrix) protein between the envelope and the
capsid - Lyssavirus is the major pathogen in the family
- etiological agent of rabies
- virus replication occurs in the cytoplasm
12Rhabdoviruses Viral Cycle
- Adsorption
- G protein attaches virus to the host cell
- virus is primarily neurotrophic but also
replicates in muscle cells - Penetration
- virus enter the host cell by endocytosis
- viral envelope then fuses with the endosomal
membrane via acidification - nucleoprotein is released into the cytoplasm
- Replication
- transcription of the viral RNA occurs through the
action of viral RNA dependent RNA polymerase - five m-RNAs are transcribed each translated
into a different protein - the polymerase also produces the positive sense
RNA template required for the replication of new
negative sense RNA strands - the G protein is process by the Golgi and
delivered to the cell membrane - Matrix protein is also bound to the membrane
13RhabdoViruses Viral Cycle
- Assembly
- replicas of the genome associate with the
N(structural) and L/NS (polymerase) to form the
nucleocapsid - nucleoprotein bind to the Matrix protein at the
cell membrane this caused condensation and
coiling of the particle - Release
- Virus buds through the cell membrane and acquires
its envelope
14Rhadoviruses - Pathogenesis
- most cells infected with rhabdoviruses exhibit
cell death and lysis - the major exception to this is rabies virus
which causes little discernible cell damage - virus has affinity for nicotinic acetylcholine
receptors on nerve cells - virus also multiples in muscles cells at
inoculation site - virus remains at inoculation site for several
days to weeks - virus reaches the CNS by retrograde axoplasmic
transport to the dorsal root ganglia and the
spinal cord virus moves from the spinal cord to
the brain
15LyssaVirus Clinical Disease
- Rabies - neurological disease manifested by
hydrophobia, generalized seizures,
disorientation, and hallucinations accompanied by
various degrees of paralysis these symptoms lead
to coma, respiratory paralysis, and death (
disease is 100 fatal in humans and animals) - long incubation period ( 60 - 365 day) avg about
80 days - prodromal period consist of fever, malaise,
headache, paresthesia, gastrointestinal upset,
fatigue, and anorexia - the disease itself is an Encephalitis accompanied
by neuron degeneration - symptoms are due to the replication of virus
within cells of the hippocampus, brainstem,
cerebellum(Purkinjes cells) and pons - virus disseminates from the CNS via afferent
neurons to skin of the head and neck, salivary
glands, retina, cornea, nasal mucosa, etc
16LyssaVirus - Diagnosis
- Diagnosis of Rabies is to late for clinical
intervention - Symptoms the neurological pattern gives a
presumptive diagnosis confirmed if recent
history of animal bite - Laboratory Confirmation both animal and human
- cytopathology hallmark of rabies is the
observation of intracytoplasmic
inclusions(composed of viral nucleocapsids) in
affected neurons - Negri Bodies found in brain of infected animals
and 70 -90 of humans - inflammatory lesions characteristic of
encephalitis are not observed from humans who
have died of rabies - antigen detection viral antigens in CNS and Skin
- immunofluorescence reveals rabies antigens
within and upon cells - viral isolation cell cultures or infant mice
- serology
- antibody is not detectable until late in the
disease when its found in cerebrospinal fluid and
serum rapid fluorescent focus inhibition - cell mediated immunity plays little or no role in
protection and recovery from rabies
17LyssaVirus - Epidemiology
- Reservoir domestic and wild mammals
- Urban Rabies
- the dog is the principal reservoir of rabies
virus in the world - rabies control programs in the U.S have reduced
the significance of dogs - Sylvatic Rabies
- wild animal reservoirs account for most rabies in
the U.S. - Source the bite of infected animals
- Incidence the distribution of human rabies
parallels the distribution of animal rabies
therefore countries like India and South America
that have high incidence of animal rabies have
high incidence of human rabies - 1 - 5 cases of human rabies per year in the U.S.
- 20,000 humans bitten by animals annually
18LyssaVirus (Rabies) - Control
- Since antibody does prevent the spread of virus
to the CNS and the brain, the induction of both
active and passive immunity forms the basis of
control in humans and domestic animals - Rabies Post Exposure Prophylaxis in the U.S
there are several cases (20,000) of human
exposure to rabies each year, but very few cases
of human rabies this is due to post-exposure
prophylaxis - Treatment of the Bite (Wound)
- Active immunization with HDCV
- Five doses of HDCV days 0, 3, 7, 14, 28,
- One large dose of anti-rabies hyper-immune
globulin - One-half in the bite Other half in the buttocks
- Immunization Human and Animal
- Basis of Pre-exposure Control in high risk humans
- inactive rabies virus grown in human diploid
cells(HDCV) is used in humans - various active and attenuated vaccines grown in
eggs or tissue culture are available for animal
use
19Rotavirus - Cycle
- Adsorption
- Intestinal protease cleave and remove portions of
the outer capsid - this creates an infectious subviral particle
with an exposed VP4 that binds the virus to
sialic acid receptors on intestinal epithelial
cells - VP4 is antigenic
- Penetration
- the ISVP penetrates the cells directly via the
fusion action of VP4 - the remainder of the outer capsid is removed
during penetration - the inner capsid/nucleic acid is released into
the cytoplasm - virus transcription and replication occur via the
nucleoprotein core
20Rotavirus - Cycle
- Transcription and Replication
- double stranded RNA strands(10 - 12) are
transcribed within the core producing a
m-RNA(from the negative sense template) which
leaves the core and associates with the
ribosomes setting the stage for early and late
proteins - viral glycoproteins are incorporated into the
membrane of the ER - within the core, the positive sense RNA strands
serve as templates for the negative sense
strands - Assembly
- the double stranded RNA replicas are released
from the core and associate with late structural
proteins giving nucleocapsids - these nucleocapsid bud through the ER membrane
thus acquiring outer capsid and a temporary
membrane which is cleaved within the ER. - Release
- Since early proteins shut down the cellular
macromolecular synthesis, the cell dies and
lysis thus releasing the viruses
21RotaVirus Clinical Disease
- Gastroenteritis mostly in infants and children
- diarrhea, vomiting, fever, dehydration
- no fecal leucocytes or blood
- follows a 48 hour incubation period
- Due to gastrointestinal mucosal cell death
- Due to adenylate cyclase activation by viral
products
22RotaVirus - Diagnosis
- symptoms cannot be distinguished from other viral
diarrheas - laboratory
- antigen detection large quantities of rotavirus
particles are present with the feces and can
easily be found via antigen detection methods - EIA
- Latex agglutination
- Electron microscopy
- serology
- since most people have antibody against
rotavirus, this is not always diagnostic but a
detectable four fold increase in serum antibody
is diagnostic
23RotaVirus - Epidemiology
- Reservoir infected humans symptomatic and
asymptomatic - Sources fomites in developed countries i.e.US,
etc - also contaminated water in under developed
countries - mode of transmission
- person-to-person, indirect, fecal-oral,
food-water, fomites - statistics
- rotaviruses account for 50 of all cases of
diarrhea in children requiring hospitalization - 70,00 cases in the U.S. annually
- gt 1 million cases worldwide annually
24RotaVirus - Control
- Sanitation
- Sewage Disposal
- Water Treatment
- Fomite Disinfection
- Immunization
- Active Attenuated Vaccine
- RotaTeq pentavalent five serotypes
25Reoviruses - ColtiVirus
- Colorado Tick Fever
- Clinical Disease
- sudden onset of fever, chill, headache,
photophobia, myalgia, arthralgia, and lethargy
acute disease many mild or subclincal infections - accompanied by biphasic fever, conjunctivitis,
lymphadenopathy, hepatospenomegaly, and
maculopapular rash - must be distinguished from Rocky Mountain Spotted
Fever - Pathogenesis
- CTF virus infected the erythroid precusor cells,
which mature into RBC that are released into the
circuclation the virus is protected from immune
clearance within the cells (viremia) for weeks or
months - the infected RBCs seed the vascular endothelial
and smooth muscle cells which often results in
hemorrhage
26ReoViruses - ColtiVirus
- Diagnosis
- detection of viral antigens on the surface of
erythrocytes with immunofluorence - fourfold increase in IgM for 45 days following
infection - Epidemiology Many mammalian reservoirs through
the western U.S. serve to infect wood tick
vectors to humans
27Rhabdoviruses - Characteristics
- bullet shaped, enveloped, virions containing a
helical nucleocapsid - envelope contains a glycoprotein spike composed
of G protein - G protein in the viral attachment protein
(VAP) - G protein is antigenic
- nucleocapsid contains
- one single stranded negative sense RNA
- L and NS proteins RNA dependent RNA polymerase
- N protein major caspid structural protein
which protect the RNA - M(matrix) protein between the envelope and the
capsid - Lyssavirus is the major pathogen in the family
- etiological agent of rabies
- virus replication occurs in the cytoplasm
28Rhabdoviruses Viral Cycle
- Adsorption
- G protein attaches virus to the host cell
- virus is primarily neurotrophic but also
replicates in muscle cells - Penetration
- virus enter the host cell by endocytosis
- viral envelope then fuses with the endosomal
membrane via acidification - nucleoprotein is released into the cytoplasm
- Replication
- transcription of the viral RNA occurs through the
action of viral RNA dependent RNA polymerase - five m-RNAs are transcribed each translated
into a different protein - the polymerase also produces the positive sense
RNA template required for the replication of new
negative sense RNA strands - the G protein is process by the Golgi and
delivered to the cell membrane - Matrix protein is also bound to the membrane
29RhabdoViruses Viral Cycle
- Assembly
- replicas of the genome associate with the
N(structural) and L/NS (polymerase) to form the
nucleocapsid - nucleoprotein bind to the Matrix protein at the
cell membrane this caused condensation and
coiling of the particle - Release
- Virus buds through the cell membrane and acquires
its envelope
30Rhadoviruses - Pathogenesis
- most cells infected with rhabdoviruses exhibit
cell death and lysis - the major exception to this is rabies virus
which causes little discernible cell damage - virus has affinity for nicotinic acetylcholine
receptors on nerve cells - virus also multiples in muscles cells at
inoculation site - virus remains at inoculation site for several
days to weeks - virus reaches the CNS by retrograde axoplasmic
transport to the dorsal root ganglia and the
spinal cord virus moves from the spinal cord to
the brain
31LyssaVirus Clinical Disease
- Rabies - neurological disease manifested by
hydrophobia, generalized seizures,
disorientation, and hallucinations accompanied by
various degrees of paralysis these symptoms lead
to coma, respiratory paralysis, and death (
disease is 100 fatal in humans and animals) - long incubation period ( 60 - 365 day) avg about
80 days - prodromal period consist of fever, malaise,
headache, paresthesia, gastrointestinal upset,
fatigue, and anorexia - the disease itself is an Encephalitis accompanied
by neuron degeneration - symptoms are due to the replication of virus
within cells of the hippocampus, brainstem,
cerebellum(Purkinjes cells) and pons - virus disseminates from the CNS via afferent
neurons to skin of the head and neck, salivary
glands, retina, cornea, nasal mucosa, etc
32LyssaVirus - Diagnosis
- Diagnosis of Rabies is to late for clinical
intervention - Symptoms the neurological pattern gives a
presumptive diagnosis confirmed if recent
history of animal bite - Laboratory Confirmation both animal and human
- cytopathology hallmark of rabies is the
observation of intracytoplasmic
inclusions(composed of viral nucleocapsids) in
affected neurons - Negri Bodies found in brain of infected animals
and 70 -90 of humans - inflammatory lesions characteristic of
encephalitis are not observed from humans who
have died of rabies - antigen detection viral antigens in CNS and Skin
- immunofluorescence reveals rabies antigens
within and upon cells - viral isolation cell cultures or infant mice
- serology
- antibody is not detectable until late in the
disease when its found in cerebrospinal fluid and
serum rapid fluorescent focus inhibition - cell mediated immunity plays little or no role in
protection and recovery from rabies
33LyssaVirus - Epidemiology
- Reservoir domestic and wild mammals
- Urban Rabies
- the dog is the principal reservoir of rabies
virus in the world - rabies control programs in the U.S have reduced
the significance of dogs - Sylvatic Rabies
- wild animal reservoirs account for most rabies in
the U.S. - Source the bite of infected animals
- Incidence the distribution of human rabies
parallels the distribution of animal rabies
therefore countries like India and South America
that have high incidence of animal rabies have
high incidence of human rabies - 1 - 5 cases of human rabies per year in the U.S.
- 20,000 humans bitten by animals annually
34LyssaVirus (Rabies) - Control
- Since antibody does prevent the spread of virus
to the CNS and the brain, the induction of both
active and passive immunity forms the basis of
control in humans and domestic animals - Rabies Post Exposure Prophylaxis in the U.S
there are several cases (20,000) of human
exposure to rabies each year, but very few cases
of human rabies this is due to post-exposure
prophylaxis - Treatment of the Bite (Wound)
- Active immunization with HDCV
- Five doses of HDCV days 0, 3, 7, 14, 28,
- One large dose of anti-rabies hyper-immune
globulin - One-half in the bite Other half in the buttocks
- Immunization Human and Animal
- Basis of Pre-exposure Control in high risk humans
- inactive rabies virus grown in human diploid
cells(HDCV) is used in humans - various active and attenuated vaccines grown in
eggs or tissue culture are available for animal
use