PATHOGENESIS OF RIFT VALLEY FEVER VIRUS (RVFv) IN SWISS-ALBINO MICE : VIROLOGICAL ASSAY OF THE VIRUS CONTENT IN INTERNAL ORGANS
EL-NIMR, M., MOHSEN, A., EL-DEBEGY, A., EL-NAKASHLY, S., TAHA, M., EL-AZZAWY, M. (1986). PATHOGENESIS OF RIFT VALLEY FEVER VIRUS (RVFv) IN SWISS-ALBINO MICE : VIROLOGICAL ASSAY OF THE VIRUS CONTENT IN INTERNAL ORGANS. EKB Journal Management System, 17.1(33), 34-43. doi: 10.21608/avmj.1986.189963
M.M.H. EL-NIMR; A.Y.A MOHSEN; AIDA EL-DEBEGY; S. EL-NAKASHLY; M.M. TAHA; M. EL-AZZAWY. "PATHOGENESIS OF RIFT VALLEY FEVER VIRUS (RVFv) IN SWISS-ALBINO MICE : VIROLOGICAL ASSAY OF THE VIRUS CONTENT IN INTERNAL ORGANS". EKB Journal Management System, 17.1, 33, 1986, 34-43. doi: 10.21608/avmj.1986.189963
EL-NIMR, M., MOHSEN, A., EL-DEBEGY, A., EL-NAKASHLY, S., TAHA, M., EL-AZZAWY, M. (1986). 'PATHOGENESIS OF RIFT VALLEY FEVER VIRUS (RVFv) IN SWISS-ALBINO MICE : VIROLOGICAL ASSAY OF THE VIRUS CONTENT IN INTERNAL ORGANS', EKB Journal Management System, 17.1(33), pp. 34-43. doi: 10.21608/avmj.1986.189963
EL-NIMR, M., MOHSEN, A., EL-DEBEGY, A., EL-NAKASHLY, S., TAHA, M., EL-AZZAWY, M. PATHOGENESIS OF RIFT VALLEY FEVER VIRUS (RVFv) IN SWISS-ALBINO MICE : VIROLOGICAL ASSAY OF THE VIRUS CONTENT IN INTERNAL ORGANS. EKB Journal Management System, 1986; 17.1(33): 34-43. doi: 10.21608/avmj.1986.189963

PATHOGENESIS OF RIFT VALLEY FEVER VIRUS (RVFv) IN SWISS-ALBINO MICE : VIROLOGICAL ASSAY OF THE VIRUS CONTENT IN INTERNAL ORGANS

Assiut Veterinary Medical Journal
Article 5, Volume 17.1, Issue 33, May 1986, Page 34-43  XML PDF (3.48 MB)
Document Type: Research article
DOI: 10.21608/avmj.1986.189963
View on SCiNiTO View on SCiNiTO
Authors
M.M.H. EL-NIMR; A.Y.A MOHSEN; AIDA EL-DEBEGY; S. EL-NAKASHLY; M.M. TAHA; M. EL-AZZAWY
Abstract
One hundred and thirty swiss-albino mice of 3-4 weeks old were each inoculated intraperitoneally (1/p) with a fixed dose of RVE virus.
The first symptoms started to appear after 42 hours. The course of the disease progressed and the symptoms became apparent between 54 to 102 hors, then started to decline by 114 hours. Mice surviving at the end of the experiment did not manifest any clinical symptoms.
Livers, spleens, brains, kidneys, hearts, lungs, intestines and skeletal muscles were collected at predetermined intervals for quantitative assay of the virus content in the verious organs. Virus content as detected by titration in CER cell cultrues was higher in the liver than the heart, spleen, lung, kidney and less in the brain. Yet, virus could not be isolated from the intestines and skeletal muscles of infected mice.
Statistics
Article View: 135
PDF Download: 87