Abstract
After inoculation with JHM strain into DBT cell monolayers, a persistently infected DBT cell culture was established without producing typical cytopathic changes after about 15th passages. By immunofluorescence virus specific antigen was demonstrated in 10 to 15% DBT cells. This persistently infected culture (JHM-CC) was resistant to superinfection with parental JHM, but such resistance was not shown against vesicular stomatitis virus. JHM-CC virus produced small plaques on DBT cell monolayers. Temperature sensitive (TS) mutant, defective interfering (DI) particle or interferon was not detected in the JHM-CC. To intracerebral inoculation with JHM-CC virus, cortisone treated ICR mice survived without showing clinical signs, however, demyelinating lesions were produced in the brain and spinal cord of them.
Original language | English (US) |
---|---|
Pages (from-to) | 301-308 |
Number of pages | 8 |
Journal | Advances in Experimental Medicine and Biology |
Volume | 142 |
State | Published - 1981 |
Externally published | Yes |
Fingerprint
ASJC Scopus subject areas
- Biochemistry, Genetics and Molecular Biology(all)
Cite this
Persistent infection with mouse hepatitis virus, JHM strain in DBT cell culture. / Hirano, N.; Goto, N.; Makino, Shinji; Fujiwara, K.
In: Advances in Experimental Medicine and Biology, Vol. 142, 1981, p. 301-308.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Persistent infection with mouse hepatitis virus, JHM strain in DBT cell culture.
AU - Hirano, N.
AU - Goto, N.
AU - Makino, Shinji
AU - Fujiwara, K.
PY - 1981
Y1 - 1981
N2 - After inoculation with JHM strain into DBT cell monolayers, a persistently infected DBT cell culture was established without producing typical cytopathic changes after about 15th passages. By immunofluorescence virus specific antigen was demonstrated in 10 to 15% DBT cells. This persistently infected culture (JHM-CC) was resistant to superinfection with parental JHM, but such resistance was not shown against vesicular stomatitis virus. JHM-CC virus produced small plaques on DBT cell monolayers. Temperature sensitive (TS) mutant, defective interfering (DI) particle or interferon was not detected in the JHM-CC. To intracerebral inoculation with JHM-CC virus, cortisone treated ICR mice survived without showing clinical signs, however, demyelinating lesions were produced in the brain and spinal cord of them.
AB - After inoculation with JHM strain into DBT cell monolayers, a persistently infected DBT cell culture was established without producing typical cytopathic changes after about 15th passages. By immunofluorescence virus specific antigen was demonstrated in 10 to 15% DBT cells. This persistently infected culture (JHM-CC) was resistant to superinfection with parental JHM, but such resistance was not shown against vesicular stomatitis virus. JHM-CC virus produced small plaques on DBT cell monolayers. Temperature sensitive (TS) mutant, defective interfering (DI) particle or interferon was not detected in the JHM-CC. To intracerebral inoculation with JHM-CC virus, cortisone treated ICR mice survived without showing clinical signs, however, demyelinating lesions were produced in the brain and spinal cord of them.
UR - http://www.scopus.com/inward/record.url?scp=0019766098&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0019766098&partnerID=8YFLogxK
M3 - Article
C2 - 6278888
AN - SCOPUS:0019766098
VL - 142
SP - 301
EP - 308
JO - Advances in Experimental Medicine and Biology
JF - Advances in Experimental Medicine and Biology
SN - 0065-2598
ER -