• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

年龄依赖性小鼠对辛德比斯病毒感染的抵抗力:病毒复制作为宿主年龄的函数。

Age-dependent resistance of mice to sindbis virus infection: viral replication as a function of host age.

机构信息

Department of Microbiology, The University of Texas at Austin, Austin, Texas 78712.

出版信息

Infect Immun. 1971 Feb;3(2):268-73. doi: 10.1128/iai.3.2.268-273.1971.

DOI:10.1128/iai.3.2.268-273.1971
PMID:16557964
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC416142/
Abstract

The development of resistance of outbred white mice to two plaque size variants of Sindbis virus was studied as a function of host age. A sudden drop in mortality occurred over a 3-day period. As little as 1 plaque-forming unit (PFU) per mouse was lethal in 1-day-old animals, whereas inocula of 10(9) PFU per mouse failed to produce high mortality in weanlings. A comparison of viral growth kinetics shows that early replication was similar in newborns and weanlings but that after 6 to 8 hr the production rate and, therefore, the maximal viral titer were suppressed in weanlings. The data demonstrate a lethal viral threshold. Titers in excess of this level lead to mortality, whereas those below it allow survival.

摘要

本研究旨在探讨年龄因素对野白化鼠抵抗两种辛德比斯病毒噬菌斑大小变体能力的影响。结果发现,死亡率在 3 天内突然下降。在 1 日龄动物中,每只老鼠只需 1 个噬菌斑形成单位(PFU)即可致命,而在 10(9)PFU 每只老鼠的接种物未能在断奶幼鼠中产生高死亡率。病毒生长动力学的比较表明,新生儿和断奶幼鼠的早期复制相似,但在 6 至 8 小时后,断奶幼鼠的产率(因此,最大病毒滴度)受到抑制。数据表明存在致命的病毒阈值。超过此水平的滴度会导致死亡,而低于此水平的滴度则允许存活。

相似文献

1
Age-dependent resistance of mice to sindbis virus infection: viral replication as a function of host age.年龄依赖性小鼠对辛德比斯病毒感染的抵抗力:病毒复制作为宿主年龄的函数。
Infect Immun. 1971 Feb;3(2):268-73. doi: 10.1128/iai.3.2.268-273.1971.
2
Pathogenesis of encephalitis induced in newborn mice by virulent and avirulent strains of Sindbis virus.由辛德毕斯病毒强毒株和无毒株诱导新生小鼠发生脑炎的发病机制。
J Virol. 1990 May;64(5):2041-6. doi: 10.1128/JVI.64.5.2041-2046.1990.
3
Age-dependent resistance to lethal alphavirus encephalitis in mice: analysis of gene expression in the central nervous system and identification of a novel interferon-inducible protective gene, mouse ISG12.小鼠中年龄依赖性对致死性甲病毒脑炎的抗性:中枢神经系统基因表达分析及一种新型干扰素诱导保护性基因——小鼠ISG12的鉴定
J Virol. 2002 Nov;76(22):11688-703. doi: 10.1128/jvi.76.22.11688-11703.2002.
4
Sindbis Virus Can Exploit a Host Antiviral Protein To Evade Immune Surveillance.辛德毕斯病毒可利用宿主抗病毒蛋白逃避免疫监视。
J Virol. 2016 Oct 28;90(22):10247-10258. doi: 10.1128/JVI.01487-16. Print 2016 Nov 15.
5
Growth and release of several alphaviruses in chick and BHK cells.几种甲病毒在鸡胚细胞和BHK细胞中的生长与释放
J Gen Virol. 1980 Aug;49(2):297-307. doi: 10.1099/0022-1317-49-2-297.
6
[Biological characteristics and genomic information of a bacteriophage against pan-drug resistant in a burn patient and its effects on bacterial biofilm].[烧伤患者中一株抗泛耐药菌噬菌体的生物学特性、基因组信息及其对细菌生物膜的影响]
Zhonghua Shao Shang Za Zhi. 2020 Jan 20;36(1):14-23. doi: 10.3760/cma.j.issn.1009-2587.2020.01.004.
7
Bunyamwera virus replication in cultured Aedes albopictus (mosquito) cells: establishment of a persistent viral infection.布尼亚姆韦拉病毒在培养的白纹伊蚊(蚊子)细胞中的复制:持续性病毒感染的建立。
J Virol. 1981 Jun;38(3):1015-24. doi: 10.1128/JVI.38.3.1015-1024.1981.
8
Sindbis virus infection of two model insect cell systems--a comparative study.两种模式昆虫细胞系统的辛德毕斯病毒感染——一项比较研究。
Virus Res. 2006 Dec;122(1-2):28-34. doi: 10.1016/j.virusres.2006.06.007. Epub 2006 Jul 18.
9
Mutagenesis of the in-frame opal termination codon preceding nsP4 of Sindbis virus: studies of translational readthrough and its effect on virus replication.辛德毕斯病毒nsP4之前的框内乳白终止密码子诱变:翻译通读及其对病毒复制影响的研究
J Virol. 1989 Mar;63(3):1326-37. doi: 10.1128/JVI.63.3.1326-1337.1989.
10
Role of the immune response in age-dependent resistance of mice to encephalitis due to Sindbis virus.免疫反应在小鼠对辛德毕斯病毒所致脑炎的年龄依赖性抵抗力中的作用。
J Infect Dis. 1976 Apr;133(4):456-64. doi: 10.1093/infdis/133.4.456.

引用本文的文献

1
Production of Noncapped Genomic RNAs Is Critical to Sindbis Virus Disease and Pathogenicity.非帽状基因组 RNA 的产生对辛德比斯病毒疾病和致病性至关重要。
mBio. 2020 Dec 1;11(6):e02675-20. doi: 10.1128/mBio.02675-20.
2
Death and gastrointestinal bleeding complicate encephalomyelitis in mice with delayed appearance of CNS IgM after intranasal alphavirus infection.在经鼻感染甲病毒后中枢神经系统IgM出现延迟的小鼠中,死亡和胃肠道出血使脑脊髓炎复杂化。
J Gen Virol. 2018 Mar;99(3):309-320. doi: 10.1099/jgv.0.001005.
3
Age has a role in driving host immunopathological response to alphavirus infection.年龄在驱动宿主对甲病毒感染的免疫病理反应中起作用。
Immunology. 2017 Dec;152(4):545-555. doi: 10.1111/imm.12799. Epub 2017 Aug 23.
4
Sindbis Virus Can Exploit a Host Antiviral Protein To Evade Immune Surveillance.辛德毕斯病毒可利用宿主抗病毒蛋白逃避免疫监视。
J Virol. 2016 Oct 28;90(22):10247-10258. doi: 10.1128/JVI.01487-16. Print 2016 Nov 15.
5
Cellular responses to Sindbis virus infection of neural progenitors derived from human embryonic stem cells.源自人类胚胎干细胞的神经祖细胞对辛德毕斯病毒感染的细胞反应。
BMC Res Notes. 2014 Oct 24;7:757. doi: 10.1186/1756-0500-7-757.
6
Possible role of a cell surface carbohydrate in evolution of resistance to viral infections in old world primates.细胞表面碳水化合物在旧世界灵长类动物对病毒感染的抗性进化中的可能作用。
J Virol. 2013 Aug;87(15):8317-26. doi: 10.1128/JVI.01118-13. Epub 2013 Jun 5.
7
Activation of the type I interferon pathway is enhanced in response to human neuronal differentiation.针对人类神经元分化,I 型干扰素通路的激活得到增强。
PLoS One. 2013;8(3):e58813. doi: 10.1371/journal.pone.0058813. Epub 2013 Mar 7.
8
Alpha/beta interferon protects adult mice from fatal Sindbis virus infection and is an important determinant of cell and tissue tropism.α/β干扰素可保护成年小鼠免受致命性辛德毕斯病毒感染,并且是细胞和组织嗜性的重要决定因素。
J Virol. 2000 Apr;74(7):3366-78. doi: 10.1128/jvi.74.7.3366-3378.2000.
9
A single nucleotide change in the 5' noncoding region of Sindbis virus confers neurovirulence in rats.辛德毕斯病毒5'非编码区的单核苷酸变化赋予大鼠神经毒性。
J Virol. 1999 Dec;73(12):10440-6. doi: 10.1128/JVI.73.12.10440-10446.1999.
10
A single amino acid change in the E2 glycoprotein of Sindbis virus confers neurovirulence by altering an early step of virus replication.辛德毕斯病毒E2糖蛋白中的单个氨基酸变化通过改变病毒复制的早期步骤赋予神经毒性。
J Virol. 1997 Aug;71(8):6100-5. doi: 10.1128/JVI.71.8.6100-6105.1997.

本文引用的文献

1
Influence of age of mice on the recovery from experimental Sendal virus infection.小鼠年龄对实验性仙台病毒感染恢复的影响。
Nature. 1961 Dec 30;192:1258-9. doi: 10.1038/1921258a0.
2
AGE-DEPENDENCE OF SUSCEPTIBILITY OF WHITE MICE TO VARIOLA VIRUS.小白鼠对天花病毒易感性的年龄依赖性
Acta Virol. 1965 May;9:230-4.
3
VIRUS INVASION OF THE CENTRAL NERVOUS SYSTEM: A STUDY OF SINDBIS VIRUS INFECTION IN THE MOUSE USING FLUORESCENT ANTIBODY.病毒对中枢神经系统的侵袭:利用荧光抗体对小鼠辛德毕斯病毒感染的研究
Am J Pathol. 1965 Jun;46(6):929-43.
4
DIFFERENCES IN INTERFERON CONTENT IN TISSUES OF MICE OF VARIOUS AGES INFECTED WITH COXSACKIE B1 VIRUS.感染柯萨奇B1病毒的不同年龄小鼠组织中干扰素含量的差异
Proc Soc Exp Biol Med. 1964 Apr;115:947-53. doi: 10.3181/00379727-115-29086.
5
PRODUCTION OF INTERFERON BY NEWBORN AND ADULT MICE INFECTED WITH SINDBIS VIRUS.感染辛德毕斯病毒的新生小鼠和成年小鼠产生干扰素的情况。
Virology. 1964 Apr;22:651-2. doi: 10.1016/0042-6822(64)90091-1.
6
ASPECTS OF THE PATHOGENESIS OF VIRUS DISEASES.病毒疾病的发病机制方面
Bacteriol Rev. 1964 Mar;28(1):30-71. doi: 10.1128/br.28.1.30-71.1964.
7
Techniques for hemagglutination and hemagglutination-inhibition with arthropod-borne viruses.节肢动物传播病毒的血凝及血凝抑制技术。
Am J Trop Med Hyg. 1958 Sep;7(5):561-73. doi: 10.4269/ajtmh.1958.7.561.
8
Nutrition needs of mammalian cells in tissue culture.组织培养中哺乳动物细胞的营养需求。
Science. 1955 Sep 16;122(3168):501-14. doi: 10.1126/science.122.3168.501.
9
Influence of age on susceptibility to virus infections with particular reference to laboratory animals.年龄对病毒感染易感性的影响,特别提及实验动物
Annu Rev Microbiol. 1952;6:247-80. doi: 10.1146/annurev.mi.06.100152.001335.
10
Pathogenesis of type 1 dengue virus infection in suckling, weanling and adult mice. 1. The relation of virus replication to interferon and antibody formation.1型登革病毒在乳鼠、断奶小鼠和成年小鼠中的感染发病机制。1. 病毒复制与干扰素及抗体形成的关系。
Am J Epidemiol. 1969 Jun;89(6):669-80. doi: 10.1093/oxfordjournals.aje.a120981.