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乳酸脱氢酶升高病毒对小鼠的持续感染:病毒在脾脏巨噬细胞中的短暂复制

Persistent infection of mice by lactate dehydrogenase-elevating virus: transient virus replication in macrophages of the spleen.

作者信息

Chan S P, Onyekaba C O, Harty J T, Plagemann P G

机构信息

Department of Microbiology, Medical School, University of Minnesota, Minneapolis 55455.

出版信息

Virus Res. 1989 Dec;14(4):317-26. doi: 10.1016/0168-1702(89)90024-5.

DOI:10.1016/0168-1702(89)90024-5
PMID:2623945
Abstract

In order to assess whether the spleen is the major site of replication of lactate dehydrogenase-elevating virus (LDV) in mice during the acute phase of infection, LDV replication in the spleen was measured by electron microscopy and fluorescent antibody staining of tissue sections and northern hybridization of total spleen RNA with an LDV-specific cDNA probe, and the effect of splenectomy on LDV replication was determined. LDV RNA and antigens and infected cells, presumably macrophages, were present in the spleen in high concentrations 18-25 h post infection, but then rapidly disappeared to undetectable levels during the next 1-2 days. Thus, LDV clearly replicates in the spleen during the initial phase of infection, but LDV replication in the spleen is transient due to the cytocidal nature of LDV replication and destruction of all permissive macrophages in the spleen. Furthermore, spleen macrophages do not seem to represent the major source of LDV released into the circulation, since LDV viremia as well as anti-LDV antibody production were the same in splenectomized and control animals for at least 28 days postinfection.

摘要

为了评估在感染急性期乳酸脱氢酶升高病毒(LDV)在小鼠体内复制的主要部位是否为脾脏,通过电子显微镜、组织切片的荧光抗体染色以及用LDV特异性cDNA探针进行脾脏总RNA的Northern杂交来检测脾脏中LDV的复制情况,并确定脾切除对LDV复制的影响。感染后18 - 25小时,脾脏中存在高浓度的LDV RNA、抗原以及被感染的细胞(推测为巨噬细胞),但在接下来的1 - 2天内迅速消失至检测不到的水平。因此,LDV在感染初期确实在脾脏中复制,但由于LDV复制的杀细胞特性以及脾脏中所有允许其感染的巨噬细胞被破坏,脾脏中LDV的复制是短暂的。此外,脾脏巨噬细胞似乎并非循环中释放的LDV的主要来源,因为在感染后至少28天内,脾切除动物和对照动物的LDV病毒血症以及抗LDV抗体产生情况相同。

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Persistent infection of mice by lactate dehydrogenase-elevating virus: transient virus replication in macrophages of the spleen.乳酸脱氢酶升高病毒对小鼠的持续感染:病毒在脾脏巨噬细胞中的短暂复制
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Lactate dehydrogenase-elevating virus replication persists in liver, spleen, lymph node, and testis tissues and results in accumulation of viral RNA in germinal centers, concomitant with polyclonal activation of B cells.乳酸脱氢酶升高病毒的复制持续存在于肝脏、脾脏、淋巴结和睾丸组织中,并导致生发中心病毒RNA的积累,同时伴有B细胞的多克隆激活。
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Extensive cytocidal replication of lactate dehydrogenase-elevating virus in cultured peritoneal macrophages from 1-2-week-old mice.乳酸脱氢酶升高病毒在1至2周龄小鼠培养的腹腔巨噬细胞中进行广泛的杀细胞性复制。
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Replication of lactate dehydrogenase-elevating virus in cells infected with murine leukaemia viruses in vitro.体外培养的感染鼠白血病病毒的细胞中乳酸脱氢酶升高病毒的复制
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Cytotoxic T cells are elicited during acute infection of mice with lactate dehydrogenase-elevating virus but disappear during the chronic phase of infection.细胞毒性T细胞在小鼠感染乳酸脱氢酶升高病毒的急性期被激活,但在感染的慢性期消失。
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Lactate dehydrogenase-elevating virus entry into the central nervous system and replication in anterior horn neurons.乳酸脱氢酶升高病毒进入中枢神经系统并在前角神经元中复制。
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Replication of lactate dehydrogenase-elevating virus in macrophages. 1. Evidence for cytocidal replication.乳酸脱氢酶升高病毒在巨噬细胞中的复制。1. 细胞杀伤性复制的证据。
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引用本文的文献

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Multiplex fluorescent immunoassay for detection of mice infected with lactate dehydrogenase elevating virus.用于检测感染乳酸脱氢酶升高病毒小鼠的多重荧光免疫测定法。
J Am Assoc Lab Anim Sci. 2013;52(3):253-8.
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The level of virus-specific T-cell and macrophage recruitment in porcine reproductive and respiratory syndrome virus infection in pigs is independent of virus load.猪繁殖与呼吸综合征病毒感染猪时,病毒特异性T细胞和巨噬细胞的募集水平与病毒载量无关。
J Virol. 2004 Jun;78(11):5923-33. doi: 10.1128/JVI.78.11.5923-5933.2004.
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Lactate dehydrogenase-elevating virus (LDV): subgenomic mRNAs, mRNA leader and comparison of 3'-terminal sequences of two LDV isolates.
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Virus Res. 1992 Apr;23(1-2):55-72. doi: 10.1016/0168-1702(92)90067-j.
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Lactate dehydrogenase-elevating virus, equine arteritis virus, and simian hemorrhagic fever virus: a new group of positive-strand RNA viruses.乳酸脱氢酶升高病毒、马动脉炎病毒和猴出血热病毒:一组新的正链RNA病毒。
Adv Virus Res. 1992;41:99-192. doi: 10.1016/s0065-3527(08)60036-6.