Measles virus replication in lungs of hispid cotton rats after intranasal inoculation

• Published in: Proceedings of the Society for Experimental Biology and Medicine Vol. 201; no. 1; p. 80
• Main Authors: Wyde, P R, Ambrose, M W, Voss, T G, Meyer, H L, Gilbert, B E
• Format: Journal Article
• Language: English
• Published: United States 01.10.1992
• Subjects: Administration, Intranasal; Animals; Antibodies, Viral - biosynthesis; Disease Models, Animal; Female; Fluorescent Antibody Technique; Lung - microbiology; Lung - pathology; Male; Measles virus - pathogenicity; Rats; Time Factors; Virus Replication
• ISSN: 0037-9727
• DOI: 10.3181/00379727-201-43483

Hispid cotton rats were inoculated intranasally with either measles virus (MV) Edmonston, a multipassaged, tissue culture-adapted strain of MV, or with one of three clinical MV isolates that had limited passages (three to five times) in tissue culture cells. MV Edmonston was recovered from the lungs of every (n = 37) hispid cotton rat inoculated with this virus for at least 7 days after virus inoculation. Peak pulmonary titers occurred on Day +4 (3.3-4.4 log10/g lung). Scattered areas of inflammation were observed interstitially in lung sections from infected animals stained with hematoxylin and eosin, and a similar pattern of diffuse fluorescence was seen in cryostat sections stained with an indirect fluorescent antibody procedure specific for virus antigens. Fluorescent antibody and virus isolation studies on lung lavage cells both suggested that lung leukocytes were a primary target of the virus. In contrast to these findings, virus was isolated only sporadically from hispid cotton rats inoculated with any of the clinical measles virus isolates. Despite the restricted growth of MV in these animals, cotton rats may be useful for studying certain aspects of measles virus pathogenesis and for screening potential antiviral compounds in vivo.