RSV...Mumps & Rubella Viruses Flashcards
mumps virus
acute contagious disease characterized by non-suppurative enlargement of one or both of the salivary glands
mumps virus is mild in children, but causes meningitis and orchitis in adult
1/3 of mumps inf is asymptomatic
pathogenesis of mumps?
primary replication occurs in nasal or URT epithelial cell
viremia spread to the salivary gland and other organs
the incubation period is 2-4 but typically 14-18d
virus is shed in saliva 3 days b4 and 9d after the swelling of the salivary gland
it is difficult to control transmission of mumps because of the incubation period which means there is presence of
virus in saliva b4 clinical symptoms develop
mumps is a systemic virus and it replicates in visceral organs. virus frequently affect kidney and it can be detected in the urine
clinical findings
most characteristic features of symptomatic people is the swelling of the salivary gland which occurs in 50% of patient
malaise and anorexia followed by
enlargement of parotid and salivary gland
CNS involvement is common (10-30%)-aspetic meningitis
meaningoencephalitis
immunity
immunity is permanent after a single inf
Ab to HN glycoprotein (v antigen), f gp, internal NP nucleocapsid protein
subclinical inf also generate lifelong immunity
lab diagnosis
specimen: saliva, urine, cerebrospinal fluid…few days after onset
isolation: monkey kidney cells are preferred 3-4 incubation
other test: ELISA or HI, RT-PCR
Epidemiology: occurs endemically worldwide, cases occurs in hot climate and peak in winter/srping1
prevention and control
no specific therapy
attenuated live mumps virus vaccine
MMR live virus vaccine
2 doses are recommended for school entry
Rubella (german measles) virus
acute febrile illness characterized by rash and lymphadenopathy that affects children and young adults
incubation period - 12 days or longer
initial viral inf of rubella occurs?
respiratory tract followed by multiplication in d cervical lymph node
viremia of rubella occurs
7-9 days after inf and last until the appearance of AB on art 13-15 d
development of AB coincides with development of?
rash, suggesting immunological basis for the rash
clinical findings of rubella
after rash appears, virus remains detectable in the nasopharynx where it persist for weeks
20-50% primary inf is subclinical
rubella begins with malaise,
low-grade fever and
rash appearing on the same day
rash starts on face-trunk-extremities and rarely last more than 3 days
immunity of rubella
AB appears as the rash fades and AB titer rises over the next 1-3 weeks
initial AB is ism
one attack cover life long immunity
immune mother transfers AB to offspring and protect them for 4-6m
lab diagnosis
diagnosis is unreliable
nasopharyngeal or throat swab taken 6 days b4 and after onset of rash
monkey kidney cell line
other method HI, PCR,ELISA
prevention, treatment & control of rubella
peak incidence in spring
mild self limited illness with no specific treatment
immune globulin intravenous (IGIV)
Attenuated live rubella vaccines (MMR)
congenital rubella syndrome (CRS)
maternal viremia associated with rubella inf during pregnancy may result in inf of the placenta or fetus
only a limited number of fetal cells become inf
growth rate of infected cells is reduced resulting in number of cells in affected organs at birth
CRS inf may lead to
deranged (psychosis) and hypo plastic organ development, resulting in structural anomalies in the newborn
the earlier in pregnancy inf occurs the greater the ?
damage
fetal death and spontaneous abortion occurs in?
rubella inf
clinical finding of rubella
3 broad categories:
- transient effect in infants
- permanent manifestation that shows at birth or during 1st yr
- developmental abnormalities
classical traid of CRS
cataracts, cardiac abnormalities & deafness
transient symptoms of CRS
growth retardation rash hepatosplenomegaly jaundice meningoencephalitis
most common developmental manifestation of CRS
moderate to profound mental retardation
treatment of CRS
immunity: maternal rubella igG is transferred to infants and lost over a period of 4-6 m
no specific treatment
can be prevented by childhood immunization with rubella vaccine to ensure that women of child bearing age are immune
immune globulin intravenous (IGIV)- not helpful for fetus