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宿主年龄对小鼠实验性K病毒感染的影响。

Effect of host age on experimental K virus infection in mice.

作者信息

Greenlee J E

出版信息

Infect Immun. 1981 Jul;33(1):297-303. doi: 10.1128/iai.33.1.297-303.1981.

DOI:10.1128/iai.33.1.297-303.1981
PMID:7263066
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC350689/
Abstract

Mice were inoculated by the oral route with K virus at 4, 8, 12, and 23 days and at 4 months of age. The effect of host age on the pathogenesis of infection was studied by immunofluorescence, virus assay, and histopathology. K virus produced a systemic infection in all animals, although the infection because progressively more limited as animals matured. In mice inoculated at 4 days of age, K virus infection resulted in a fatal interstitial pneumonia identical to that seen in newborn animals and was characterized by the presence of virus and viral antigen in pulmonary and extrapulmonary vascular endothelia, reticuloendothelial organs, and brains. In older animals, K virus infection was clinically inapparent; organ involvement was similar in distribution to that seen in fatally infected suckling ice, but cells exhibiting specific viral fluorescence were fewer in number and viral titers were lower. Although animals surviving K virus infection developed high titers of hemagglutination inhibition antibody to the virus, positive cells and infectious virus could still be detected in intestines 2 months after inoculation. In animals inoculated at 8 and 12 days of age, in which K virus produced an extensive initial infection, virus could also be detected 56 days after inoculation in lungs, livers, spleens, and brains. The present study indicates that murine K virus produces a systemic infection throughout the life of its host and that the maturation of host defenses and the development of specific humoral immunity, although they limit dissemination of virus during acute infection, may not eliminate viral persistence in intestines or other organs once infection has occurred.

摘要

在4日龄、8日龄、12日龄、23日龄以及4月龄时,通过口服途径给小鼠接种K病毒。通过免疫荧光、病毒检测和组织病理学研究宿主年龄对感染发病机制的影响。K病毒在所有动物中引发了全身性感染,尽管随着动物成熟,感染逐渐受到更多限制。在4日龄接种的小鼠中,K病毒感染导致了与新生动物中所见相同的致命性间质性肺炎,其特征是在肺和肺外血管内皮、网状内皮器官及大脑中存在病毒和病毒抗原。在年龄较大的动物中,K病毒感染在临床上不明显;器官受累的分布与在致命感染的乳鼠中所见相似,但显示特异性病毒荧光的细胞数量较少且病毒滴度较低。尽管在K病毒感染中存活下来的动物产生了高滴度的针对该病毒的血凝抑制抗体,但在接种后2个月,仍可在肠道中检测到阳性细胞和传染性病毒。在8日龄和12日龄接种的动物中,K病毒引发了广泛的初始感染,在接种后56天,在肺、肝、脾和脑中也能检测到病毒。本研究表明,鼠K病毒在其宿主的整个生命过程中都会引发全身性感染,并且宿主防御机制的成熟和特异性体液免疫的发展,尽管它们在急性感染期间限制了病毒的传播,但一旦感染发生,可能无法消除病毒在肠道或其他器官中的持续存在。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8757/350689/35f9126315c3/iai00159-0309-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8757/350689/1357f7207952/iai00159-0307-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8757/350689/7a82aea8f712/iai00159-0307-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8757/350689/1def1465d8b5/iai00159-0307-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8757/350689/35f9126315c3/iai00159-0309-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8757/350689/1357f7207952/iai00159-0307-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8757/350689/7a82aea8f712/iai00159-0307-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8757/350689/1def1465d8b5/iai00159-0307-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8757/350689/35f9126315c3/iai00159-0309-a.jpg

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