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. Maculopapular RashMeasles virus Rubella virus Parvovirus Human Herpes 6. Vesicular RashHerpes simplex virusVaricella zoster virus Coxsakievirus. Measles. Measles virus is a paramyxovirusParamyxoviruses :Enveloped virus, ssRNA genome as a single piece.The family includes parainfluenza
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1. Viral Infections of the Skin and Mucus Membranes
2. Maculopapular Rash
Measles virus
Rubella virus
Parvovirus
Human Herpes 6
Vesicular Rash
Herpes simplex virus
Varicella zoster virus
Coxsakievirus
3. Measles
Measles virus is a paramyxovirus
Paramyxoviruses :
Enveloped virus, ssRNA genome as a single piece.
The family includes parainfluenza virus, mumps virus, measles virus and respiratory syncytial virus.
Parainfluenza and mumps virus have a surface hemagglutinin and neuraminidase, while measles have a hemagglutinin, but not neuraminidase.
The virion structure includes:
Spikes
F protein
Matrix protein M, below the envelope
Only one serotype
4. Measles Disease
Acute febrile illness, mostly in childhood
Incubation period: 10 – 12 days
Onset is flu-like: high fever, cough, conjunctivitis
Koplik's spots: red spots with bluish-white centre on the buccal mucosa
1 – 2 days later, acute symptoms decline with appearance of a widespread maculopapular rash
Over 10 – 14 days, recovery is usually complete as the rash fades
6. Complications Giant cell pneumonia, more common in adults
Otitis media
Post-measles encephalitis
Subacute sclerosing panencephalitis (SSPE):
progressive and fatal degenerative disease
within the infected cells, there is a defective form of the virus which because it can not produce functional M protein, is not released as complete virus from the cells.
7. Laboratory Diagnosis Most cases are diagnosed clinically
NPA, immunofluorescence
8. Epidemiology
Transmission: person to person by respiratory droplets. Malnutrition contributes to high mortality. Control
Live attenuated vaccine, combined with mumps and rubella (MMR)
Administration: between 12 – 18 months.
9. Rubella (German Measles) Rubella Virus
Classified as togavirus
ssRNA virus with an envelope
pleomorphic in appearance, 50 – 60 nm in diameter
nucleocapsid is icosahedral in symmetry
ssRNA is infective and replication occurs in the cytoplasm
three major polypeptides: C and envelope glycoproteins E1 and E2
single serotype
10. Postnatal Rubella Incubation period: 12 – 21 days
Macular rash, appears first on the face, then spreads to the trunk and limbs
Minor pyrexia, malaise and lymphadenopathy with suboccipital nodes most commonly enlarged and tender
Arthralgia is uncommon in children, but may occur in up to 60% of adult females, involving the fingers, wrists, ankles and knees
Encephalitis and thrombocytopenia are rare complications
11. Pathogenesis Virus is transmitted by air-borne route URT Viremia
Skin, joints, placenta cross the barrier
Infect fetal differentiating cells
Early in pregnancy: this will cause congenital abnormalities
12. Laboratory Diagnosis Clinical diagnosis is unreliable
Investigation by virus isolation is not indicated (unreliable and time-consuming)
Serological diagnosis is the method of choice, detecting rubella specific IgG and rubella specific IgM. These tests are also used for screening to ascertain susceptibility and whether rubella immunization is indicated.
Congenital rubella syndrome: serological testing for specific IgM. Maternal IgM does not cross the placenta so detection of specific IgM is diagnostic of intrauterine infection
13. Control Attenuated live vaccine (MMR)
Seroconversion occurs in over 95%
Protection persists for more than 20 years
Administration in pregnancy is contra-indicated
Pregnancy should be avoided for the month following vaccination
14. Human Parvovirus Only parvovirus B19 is the cause of diseases in humans
Genus: Erythrovirus
15. The Virus 20 – 25 nm in diameter
icosahedral symmetry, no envelope
the capsid consists of two proteins, VP1 and VP2
specific viral receptors such as blood group P antigen; explains narrow host range
infection is followed by life-long immunity
Genome: ssDNA
16. Replication Dependent on cellular factors expressed transiently in the cell during late S or early G2 phase of mitosis.
All parvoviruses require dividing cells for replication
17. Clinical Diseases Rash illness (Erythema infectiosum)
Erythematous maculopapular rash
Common in children aged 4 – 11 years
Very similar to rubella
Joint disease
80% in adult females
10% in childhood cases
arthritis involving small joints of the hands with wrists, knees and ankles affected in some cases
18. Aplastic crisis
A transient acute event which complicates chronic hemolytic anemia
Fall in hemoglobin
Disappearance of reticulocytes from peripheral blood
Erythropoiesis cessation lasts for 5 – 7 days
Symptoms of worsening anemia
B19 infection is responsible for 90% of the cases
Occurs most commonly in children with sickle cell anemic
B19 in the immunocompromized
Persistent infection that leads to persistent anemia
19. Laboratory Diagnosis Virus detection
Serum,
detecting viral antigens using ELISA
detecting viral genome using nucleic acid hybridization and PCR
Antibody detection
Recent infection can be diagnosed by detecting B19-specific IgM or increasing amounts of specific IgG.
20. Epidemiology
Endemic throughout the year in temperate climates
Transmission occurs by respiratory route
High-titre viremia enables transmission by blood
Congenital transmission (vertical)
Treatment
Most cases are mild and self-limiting
Aplastic crisis: blood transfusion
Immunosuppressed: blood transfusion and human normal immunoglobulin
Intrauterine infection: intrauterine blood transfusion
21. Human Herpesvirus 6 (HHV 6) Sequence analysis revealed two variants:
HHV 6A: no clear disease association
HHV 6B: exanthema subitum or roseola infantum
22. Roseola Infantum The disease is common between 6 months and 3 years
Sudden onset of fever
Throat congestion and cervical lymphadenopathy
Widespread macular rash occurs in 10% of the cases
Some cases are associated with HHV-7 infection
HHV-6 and -7, both infect T lymphocytes
23. Vesicular Rash Herpes simplex virus
Varicella zoster virus
Coxsakievirus
24. Herpes Simplex Viruses Ubiquitous virus, infecting the majority of world’s population
Two types: HSV-1 and HSV-2
Type 1 is associated primarily with mouth, eye and CNS
Type 2 is found mostly in the genital tract
Transmission: direct contact
25. Herpes Simplex Structure Icosahedral virus
Lipoprotein envelope, derived from the nuclear membrane
Genome: linear, ds DNA
Replicate in the nucleus
26. HSV Glycoproteins At least 11 glycoproteins are known
Three are essential for production of infectious virus:
gB and gD : penetration into the cells
gH: release of the virus
27. Pathogenesis Primary Infection
The typical lesion is the vesicle; ballooning degeneration of intra-epithelial cells. The roof of the vesicle breaks down, forming ulcer
During the replication phase at the site of entery in the epithelium, virus particles enter through the sensory nerve endings and transported along the axon to the nerve body (neurone) in the sensory (dorsal root) ganglion by retrograde axonal flow. Latent infection occurs in the survived neurons that still harbor the viral genome
Antibodies reduce the severity of the infections, although it does not prevent recurrences.
28. Latent Infection About 1% of cells in the affected ganglion carry the viral genome.
Viral DNA exists as free circular episomes (20 copies / cell).
Latency-associated transcripts (LAT) are present
HSV-1: causes latency in trigeminal ganglion
HSV-2: causes latency in sacral ganglion
29. Reactivation Known triggers for recurrences are accompanied by a local increase in prostaglandin levels and depression of cell-mediated immunity.
Reactivation can be induced by
UV light
Fever
Trauma
Stress
Interval between the stimulus and lesion appearance is 2 – 5 days.
31. Clinical Features Oral infection
Acute febrile gingivostomatitis in preschool children
Vesicular lesions ulcerate rapidly
Skin infections
Herpetic whitlow: primary lesion on the fingers or thumb of the toddler with herpetic stomatitis, due to autoinoculation. It also occurs as accidental inoculation in health care workers.
Eczema herpeticum: severe form of cutaneous herpes. It may occur in children with atopic eczema.
32. Clinical Features Eye infection
Conjunctivitis or keratoconjunctivitis associated with corneal ulceration. This will result in corneal scarring and vision impairment.
The majority are caused by HSV-1
Most patients with recurring eye disease are aged over 50 years
CNS infection
The most likely route of infection is central spread from trigeminal ganglion
HSV encephalitis
CSF collected in the acute stage should be used for PCR amplification of HSV DNA.
More commonly due to HSV-1
33. Clinical Features Genital tract infection
Both types can infect genital tract, but HSV-2 is more common. The lesions are vesicular at first but rapidly ulcerate
Male: affects the glans and shaft of the penis
Female: affects the labia and vagina or cervix
Fever and malaise are accompanied by regional lymphadenopathy, urethritis and vaginal discharge
34. Clinical Features Recurrent genital herpes
Can be as frequent as six or more episodes a year.
Attacks are milder and shorter than first episodes
HSV-1 genital infection recurs less often than HSV-2
Either type is capable of transmission from mother to infant. Transplacental passage has been recorded but is very rare. Ascending infection from the cervix is more significant especially when the membranes are ruptured prematurely.
35. Laboratory Diagnosis Isolation of HSV in cultures of human diploid fibroblast cells. Growth is rapid. CPE includes rounded, ballooned cells in foci and giant cell formation
Detection of viral antigens in cell (by immunofluorescence), scraped from the base of lesions
Detection of amplified viral DNA by PCR in CSF
36. Giant cell formation induced by Herpes simplex infection
37. Treatment Acyclovir: inhibits viral DNA synthesis
Acute HSV infections
Latency is not eradicated by this agent
Prophylactic to prevent reactivation in the immunocompromized (transplant recipients)
Available for topical, oral and intravenous route
38. Varicella Zoster Virus Two forms
Primary infection is a generalized eruption (chicken pox)
Reactivation is localized to one or few dermatomes (shingles, Varicella Zoster)
Only one antigenic type
39. Pathogenesis of Chicken Pox Children, vesicular skin eruption
Virus enters through URT or conjunctiva
The virus causes viremia
The vesicles lie in the middle of the epidermis. The fluid becomes cloudy with the influx of leucocytes. These pustules dry up, scabs form and desquamate.
Lesions in all stages are present at any time while new ones are appearing.
40. Pathogenesis of Varicella Zoster VZV stays latent in the sensory ganglia
Reactivation can occur at any age but the rate is much increased in persons aged 60 years or over.
Zoster is usually limited to one dermatome; in adults most commonly in the thoracic or upper lumbar region.
42. Clinical FeaturesChicken Pox Incubation period: 14 – 15 days
The patient is infectious for 2 days before and up to 5 days after onset
The rash is most dense on the trunk and head
Macules ---- Papules ---- Vesicles ---- Pustules
43. Chicken Pox
44. Complications Secondary bacterial infection (commonest)
Pneumonia
CNS
cerebellar ataxia syndrome
acute encephalitits
45. Herpes Zoster Reactivated VZV infection
Localized eruption, unilateral, typically confined to one dermatome
Prodromal paraesthesia and pain in the area supplied by affected nerve are common before skin lesions develop
Postherpetic neuralgia
Most common complication of zoster
50% risk in patients aged over 60 years
pain persisting for 1 month or more after the rash
46. Herpes Zoster
47. Ophthalmic zoster
Involvement of ophthalmic division of the trigeminal nerve
corneal ulceration, stromal keratitis
permanent scarring and loss of sight
48. Laboratory Diagnosis Early vesicular lesions are the best diagnostic material
Virus isolation takes from 5 days to 3 weeks
More rapid detection is possible with centrifugation-enhanced cultures (shell vials)
Direct immunofluorescence
VZV DNA amplification by PCR
49. Treatment Acyclovir
Given to high-risk of complication
Neonates (first 3 weeks of life)
Ophthalmic zoster
Immunocompromized
50. Epidemiology Spread: respiratory route, in winter and early spring
Varicella is highly infectious to susceptible close contacts
Mortality is high in normal adults, particularly smokers who develop pneumonia
Zoster is associated with decreased T cell function:
Old age
Pre-AIDS phase
Organ transplant recipients
51. Control Passive immunization: varicella zoster immunoglobulin (VZIG):
Neonates
Non-immune pregnant contacts
Immunocompromized contacts
A live attenuated vaccine, IM injection
52. Coxsackieviruses Picornavirus
Icosahedral, positive sense, linear, ssRNA
Two groups: A and B
Group A:
Herpangina (vesicular pharyngitis)
Hand – Foot – and – Mouth disease
Acute hemorrhagic conjunctivitis
Group B:
Pleurodynia (epidemic myalgia)
Myocarditis
Meningoencephalitis
53. Herpangina
Severe febrile pharyngitis
The pharynx is usually hyperemic and discrete vesicles occur on the posterior half of the palate, pharynx, tonsils or tongue
Self-limited and most frequent in small children
Hand – Foot – and – Mouth disease
Oral and pharyngeal ulcerations
Vesicular rash on the palm and soles
54. Hand – Foot – and – Mouth disease