Alke A, Schwantes A, Zemba M, Flügel R M, Löchelt M
Abteilung Retrovirale Genexpression, Forschungsschwerpunkt Angewandte Tumorvirologie, Deutsches Krebsforschungszentrum, Heidelberg, Germany.
Virology. 2000 Sep 15;275(1):170-6. doi: 10.1006/viro.2000.0537.
Cats were experimentally infected with cell culture-adapted feline foamy virus (FFV, spumaretrovirinae) isolate FUV. FFV was consistently recovered from peripheral blood leukocytes and throat samples of FFV-infected cats starting 2 to 3 weeks postinfection (p. i.), indicative of the establishment of persistent FFV infections. Viral persistence was established, even despite neutralizing antibodies that appeared early after infection. The humoral immune response toward FFV was quantitatively and qualitatively analyzed over time. FFV Gag-specific antibodies were first detected 2 weeks p. i. and increased further; reactivities to the other structural and nonstructural FFV proteins appeared slightly delayed. Reactivities against FFV Pol and Gag proteins were detectable by immunoblotting and radioimmunoprecipitation, whereas the latter techniques had to be employed for the unambiguous detection of FFV Env-, Bet-, and Bel 1-specific antibodies.
用细胞培养适应的猫泡沫病毒(FFV,泡沫逆转录病毒亚科)分离株FUV对猫进行实验性感染。从感染后2至3周开始,在FFV感染猫的外周血白细胞和咽喉样本中持续检测到FFV,这表明已建立持续性FFV感染。即使在感染后早期出现中和抗体,病毒持续性感染仍得以建立。随着时间的推移,对FFV的体液免疫反应进行了定量和定性分析。感染后2周首次检测到FFV Gag特异性抗体,且抗体水平进一步升高;对其他FFV结构和非结构蛋白的反应性出现时间稍晚。通过免疫印迹和放射免疫沉淀可检测到针对FFV Pol和Gag蛋白的反应性,而后者技术必须用于明确检测FFV Env、Bet和Bel 1特异性抗体。