Medical Microbiology

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RNAviruses 467

&RSvirusescausebronchiolitisorpneumonia,mainlyinchildrenuptosix
monthsofage,orrarelyuptotwoyears.Immunestatusappearstoplayan
importantroleinthecourseoftheinfection.Ithasbeendeterminedthatthe
courseofthediseaseismoresevereinchildrenwhohavereceiveddeadvac-
cinematerial(similarlytomeasles).Thisispresumablyduetoantibodies,in
thecaseofsmallchildrenthemother’santibodiesacquiredbydiaplacental
transport.Immunosuppressedpatients,forinstance,bonemarrowrecipi-
ents,arealsoatriskforRSV.
Diagnosis.Inadditiontoserodiagnosticmethods,directdetectiontestsbased
onimmunofluorescenceorenzymeimmunoassayareavailableforpara-
myxoviruses,someofthemquitesensitive.Paramyxovirusesreplicatereadily
incellculturesfromhumantissues.
Epidemiology.Paramyxovirusesaretransmittedbydropletinfection.Gener-
alizedcontaminationlevelsinthepopulation(exceptforNipahandHendra)
arealreadyveryhighinchildhood(90%in 1 0-year-oldchildrenforparain-
fluenzavirustypes 1 – 3).
NipahandHendravirusesarezoonosesthataretransmittedtohumans
fromanimals(Nipah:pigs,Hendra:horses).Variousdifferentanimalscanbe
infectedbythesepathogens,butbats(Pteropus)appeartobethenaturalre-
servoirforbothviruses.
Prevention.Attenuatedlivevaccinesareavailableformeaslesandmumps.The
deadvaccineshouldnotbeusedduetotheaggravatingeffectmentionedabove.
Novaccineshaveasyetbeendevelopedfortheotherparainfluenzaviruses.

Rhabdoviruses


&Amongtherhabdoviruses,thelyssaviruses,genotypes 1 – 7 ,arehuman
pathogens.Theyaretransmittedbythebiteofaninfectedanimalinits
salivaandinfections,oncefullymanifest,arealwayslethal(rabies,hydro-
phobia).Thereservoirfortype 1 isprovidedbywildanimalsingeneral
(foxes,etc.),bats(sylvaticrabies),and,inAsia,dogs(urbanrabies).Types
2 – 7 arerestrictedtoEurope,Asia,Africa,andAustraliawiththeirmain
reservoirinbats.
Diagnosis:directdetectionwithIFincorneacellsandskinbiopsies,post-
mortemisolationfrombraintissues.
Prevention:duetotheweek-longandevenmonth-longincubationperiod
(exceptintypes 2 – 4),postexposureprophylacticvaccinationwithcombined
active(deadvaccine)andpassive(humanimmunoglobulin)vaccinesis
possible.Pre-exposureprophylaxisintheformofdeadvaccineisadminis-
teredtopersonsathighrisk. &

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Kayser, Medical Microbiology © 2005 Thieme

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