Hydrocephalus in Suckling Rats Infected Intracerebrally with Mouse Hepatitis Virus, MHV‐A59
Identifieur interne : 001725 ( Main/Exploration ); précédent : 001724; suivant : 001726Hydrocephalus in Suckling Rats Infected Intracerebrally with Mouse Hepatitis Virus, MHV‐A59
Auteurs : Norio Hirano [Japon] ; Naoaki Goto [Japon] ; Tetsuo Ogawa [Japon] ; Katsuhiko Ono [Japon] ; Toshiaki Murakami [Japon] ; Kosaku Fujiwara [Japon]Source :
- Microbiology and Immunology [ 0385-5600 ] ; 1980-09.
English descriptors
- Teeft :
- Acta neuropathol, Animals inoculated, Anomaly, Brain days, Brain lesions, Cancer inst, Cell cultures, Cerebral cortex, Cerebral lesions, Cerebrospinal fluid, Encephalitis, Extensive destruction, Fujiwara, Gesamte virusforsch, Hamster, Hepatitis, Hepatitis virus, High frequency, Hirano, Hydrocephalus, Immunofluorescence, Inoculated, Inoculation, Intracerebral inoculation, Lesion, Measles virus, Mouse, Mouse cell line, Mouse hepatitis virus, Mouse leukemia, Murine virus, Neuron, Numerous neurons, Oligodendroglia cells, Present study, Rat, Reovirus type, Respiratory infection, Rhesus monkeys, Sialodacryoadenitis virus, Subacute encephalitis, Suckling, Suckling rats, Survivors inoculated, Uninfected control, Virus, Virus antigen, Virus assay, Virus titer, Wistar rats.
Abstract
After intracerebral inoculation of mouse hepatitis virus, MHV‐A59 strain, into 3‐ to 5‐day‐old Wistar rats, some survivors at 14 days postinoculation (p.i.) were found to lack the cerebral cortex and to have an accumulation of a considerable amount of cerebrospinal fluid. The virus titer in the brain increased exponentially after inoculation, reaching a maximum 4 to 6 days p.i. when immunofluorescence revealed virus‐specific antigen within neurons in the cerebral cortex. A small amount of infectious virus was also detectable 14 days p.i. when the cerebral anomaly was evident. This brain malformation causing hydrocephalus was due to cerebral damage by viral infection.
Url:
DOI: 10.1111/j.1348-0421.1980.tb02887.x
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: 000408
- to stream Istex, to step Curation: 000388
- to stream Istex, to step Checkpoint: 000832
- to stream Main, to step Merge: 001754
- to stream Main, to step Curation: 001725
Le document en format XML
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<profileDesc><textClass><keywords scheme="Teeft" xml:lang="en"><term>Acta neuropathol</term>
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<term>Anomaly</term>
<term>Brain days</term>
<term>Brain lesions</term>
<term>Cancer inst</term>
<term>Cell cultures</term>
<term>Cerebral cortex</term>
<term>Cerebral lesions</term>
<term>Cerebrospinal fluid</term>
<term>Encephalitis</term>
<term>Extensive destruction</term>
<term>Fujiwara</term>
<term>Gesamte virusforsch</term>
<term>Hamster</term>
<term>Hepatitis</term>
<term>Hepatitis virus</term>
<term>High frequency</term>
<term>Hirano</term>
<term>Hydrocephalus</term>
<term>Immunofluorescence</term>
<term>Inoculated</term>
<term>Inoculation</term>
<term>Intracerebral inoculation</term>
<term>Lesion</term>
<term>Measles virus</term>
<term>Mouse</term>
<term>Mouse cell line</term>
<term>Mouse hepatitis virus</term>
<term>Mouse leukemia</term>
<term>Murine virus</term>
<term>Neuron</term>
<term>Numerous neurons</term>
<term>Oligodendroglia cells</term>
<term>Present study</term>
<term>Rat</term>
<term>Reovirus type</term>
<term>Respiratory infection</term>
<term>Rhesus monkeys</term>
<term>Sialodacryoadenitis virus</term>
<term>Subacute encephalitis</term>
<term>Suckling</term>
<term>Suckling rats</term>
<term>Survivors inoculated</term>
<term>Uninfected control</term>
<term>Virus</term>
<term>Virus antigen</term>
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<front><div type="abstract">After intracerebral inoculation of mouse hepatitis virus, MHV‐A59 strain, into 3‐ to 5‐day‐old Wistar rats, some survivors at 14 days postinoculation (p.i.) were found to lack the cerebral cortex and to have an accumulation of a considerable amount of cerebrospinal fluid. The virus titer in the brain increased exponentially after inoculation, reaching a maximum 4 to 6 days p.i. when immunofluorescence revealed virus‐specific antigen within neurons in the cerebral cortex. A small amount of infectious virus was also detectable 14 days p.i. when the cerebral anomaly was evident. This brain malformation causing hydrocephalus was due to cerebral damage by viral infection.</div>
</front>
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<tree><country name="Japon"><region name="Région de Kantō"><name sortKey="Hirano, Norio" sort="Hirano, Norio" uniqKey="Hirano N" first="Norio" last="Hirano">Norio Hirano</name>
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<name sortKey="Fujiwara, Kosaku" sort="Fujiwara, Kosaku" uniqKey="Fujiwara K" first="Kosaku" last="Fujiwara">Kosaku Fujiwara</name>
<name sortKey="Goto, Naoaki" sort="Goto, Naoaki" uniqKey="Goto N" first="Naoaki" last="Goto">Naoaki Goto</name>
<name sortKey="Murakami, Toshiaki" sort="Murakami, Toshiaki" uniqKey="Murakami T" first="Toshiaki" last="Murakami">Toshiaki Murakami</name>
<name sortKey="Ogawa, Tetsuo" sort="Ogawa, Tetsuo" uniqKey="Ogawa T" first="Tetsuo" last="Ogawa">Tetsuo Ogawa</name>
<name sortKey="Ono, Katsuhiko" sort="Ono, Katsuhiko" uniqKey="Ono K" first="Katsuhiko" last="Ono">Katsuhiko Ono</name>
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