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宿主和病毒因素对马立克氏病早期发病机制的比较影响。

Comparative effects of host and viral factors on early pathogenesis of Marek's disease.

作者信息

Fabricant J, Ianconescu M, Calnek B W

出版信息

Infect Immun. 1977 Apr;16(1):136-44. doi: 10.1128/iai.16.1.136-144.1977.

Abstract

A series of experiments on the early pathogenesis of Marek's disease was conducted according to a uniform scheme. In each experiment, there was a single variable-age, genetic strain, or virus strain. Virus assays from spleen, buffy coat, and bone marrow, and fluorescent antibody tests on spleen, bursa of Fabricius, and thymus were conducted on five birds per group daily from the 3rd through the 10th day postinoculation. From these data, it was apparent that the response could be divided into two periods: 4 to 6 days = early; 8 to 10 days = late. Serological tests showed all groups except the 1-day-old group to have neutralizing antibody by the end of the 10-day period. With few exceptions, none of the variables tested exerted any appreciable influence on the level of virus growth in spleen, bursa, or thymus during the early period. High levels of infection occurred in all birds during that period. Changes in infection pattern which occurred during the late period were significant and could be correlated with occurrence of Marek's disease in test samples of birds held until 7 weeks after infection. Infectivity levels dropped appreciably in the case of resistant N-line birds given JM virus, and, during the late period, infection levels were significantly higher in GA-infected birds than in those given viruses of lower virulence. Whereas the virus titers during the 8- to 10-day period usually reflected the eventual clinical pattern of Marek's disease, the levels of viral antigen (fluorescent antibody tests) were much less consistent. One further experiment conducted by the same uniform scheme demonstrated no significant effects on early pathogenesis or course of Marek's disease in birds given continuous oral medication with amino-ureido-sulfone.

摘要

按照统一方案进行了一系列关于马立克氏病早期发病机制的实验。在每个实验中,只有一个变量——年龄、遗传品系或病毒株。在接种后第3天至第10天,每天对每组5只鸟进行脾脏、血沉棕黄层和骨髓的病毒检测,以及脾脏、法氏囊和胸腺的荧光抗体检测。从这些数据可以明显看出,反应可分为两个阶段:4至6天为早期;8至10天为晚期。血清学检测显示,除1日龄组外,所有组在10天结束时都有中和抗体。除少数例外,在早期,所测试的变量对脾脏、法氏囊或胸腺中的病毒生长水平均未产生明显影响。在此期间,所有鸟类均发生了高水平感染。晚期发生的感染模式变化显著,且与感染后饲养至7周的鸟类测试样本中马立克氏病的发生相关。给抗性N系鸟接种JM病毒后,感染性水平明显下降,并且在晚期,感染GA病毒的鸟类的感染水平显著高于接种低毒力病毒的鸟类。虽然在8至10天期间的病毒滴度通常反映了马立克氏病最终的临床模式,但病毒抗原水平(荧光抗体检测)则不太一致。按照相同的统一方案进行的另一项实验表明,给鸟类连续口服氨基脲基砜对马立克氏病的早期发病机制或病程没有显著影响。

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