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牛组织的体外干扰素产生:用牛传染性鼻气管炎病毒诱导

In vitro interferon production by bovine tissues: induction with infectious bovine rhinotracheitis virus.

作者信息

Fulton R W, Rosenquist B D

出版信息

Am J Vet Res. 1976 Dec;37(12):1497-502.

PMID:187093
Abstract

The interferon-inducing ability of infectious bovine rhinotracheitis (IBR) virus was determined in tissue cultures of bovine origin inoculated with untreated and ultraviolet (UV) irradiated IBR viruses. Interferon was assayed by the plaque-reduction method in bovine fetal kidney (BFK) cell cultures, using vesicular stomatitis virus as challenge virus. Highest interferon concentrations were produced by cultures of bovine fetal (BF) spleen cells and aveolar macrophage cultures derived from adult cattle. Moderate interferon concentrations were produced by peripheral blood leukocyte (PBL) suspension cultures from adult cattle with serum-neutralizing antibodies against IBR virus. Cultures of PBL from 1 cow without detectable serum-neutralizing antibodies against IBR virus did not produce detectable interferon in response to IBR virus. Cultures of PBL from cattle with or without detectable serum-neutralizing antibodies against IBR virus produced interferon when stimulated with phytohemagglutinin (PHA). Low levles of viral inhibitors were detected infrequently in monolayer cultures of BFK and BF nasal mucosa inoculated with UV-irradiated IBR virus and in BF tracheal organ cultures inoculated with untreated IBR virus. Interferon was not detected in fluids collected from IBR virus-exposed monolayer cultures of primary and secondary BF lung, secondary BF tracheal mucosa, secondary BF liver, secondary BF adrenal, and PBL in the 4th and 7th passages. The antiviral inhibitors from BF spleen, bovine alveolar macrophage, and PBL cultures induced with IBR virus, as well as inhibitors from PBL cultures induced with PHA, had the usual properties of interferon.

摘要

在接种未处理的和紫外线(UV)照射的传染性牛鼻气管炎(IBR)病毒的牛源组织培养物中,测定了IBR病毒的干扰素诱导能力。使用水疱性口炎病毒作为攻击病毒,通过噬斑减少法在牛胎肾(BFK)细胞培养物中测定干扰素。最高的干扰素浓度是由牛胎(BF)脾细胞培养物和成年牛的肺泡巨噬细胞培养物产生的。来自具有抗IBR病毒血清中和抗体的成年牛的外周血白细胞(PBL)悬浮培养物产生中等浓度的干扰素。来自1头未检测到抗IBR病毒血清中和抗体的奶牛的PBL培养物在接触IBR病毒时未产生可检测到的干扰素。来自有或没有可检测到的抗IBR病毒血清中和抗体的奶牛的PBL培养物在用植物血凝素(PHA)刺激时产生干扰素。在用紫外线照射的IBR病毒接种的BFK和BF鼻黏膜单层培养物以及用未处理的IBR病毒接种的BF气管器官培养物中,很少检测到低水平的病毒抑制剂。在第4代和第7代原代和二代BF肺、二代BF气管黏膜、二代BF肝、二代BF肾上腺和PBL的IBR病毒暴露单层培养物收集的液体中未检测到干扰素。来自用IBR病毒诱导的BF脾、牛肺泡巨噬细胞和PBL培养物的抗病毒抑制剂,以及用PHA诱导的PBL培养物的抑制剂,具有干扰素的通常特性。

相似文献

1
In vitro interferon production by bovine tissues: induction with infectious bovine rhinotracheitis virus.牛组织的体外干扰素产生:用牛传染性鼻气管炎病毒诱导
Am J Vet Res. 1976 Dec;37(12):1497-502.
2
In vitro interferon production by bovine tissues: effects of hydrocortisone.牛组织的体外干扰素产生:氢化可的松的作用。
Am J Vet Res. 1976 Dec;37(12):1493-5.
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Duration of protection of calves against rhinovirus challenge exposure by infectious bovine rhinotracheitis virus-induced interferon in nasal secretions.传染性牛鼻气管炎病毒诱导的鼻腔分泌物中的干扰素对犊牛抵抗鼻病毒攻击暴露的保护持续时间。
Am J Vet Res. 1982 Feb;43(2):289-93.
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In utero infection of swine fetuses with infectious bovine rhinotracheitis virus (bovine herpesvirus-1).传染性牛鼻气管炎病毒(牛疱疹病毒1型)对猪胎儿的子宫内感染。
Am J Vet Res. 1984 Oct;45(10):1924-7.
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[The effectiveness of the paramunity inducer Baypamun (PIND-ORF) for the prevention and metaphylaxis of an experimental infection with the infectious bovine rhinotracheitis virus in cattle].[副免疫诱导剂拜朋(PIND-ORF)对预防和群体预防牛传染性鼻气管炎病毒实验性感染的有效性]
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Characteristics of the polyriboinosinic acid:polyribocytidylic acid assay for noncytopathogenic bovine viral diarrhea virus.聚肌苷酸:聚胞苷酸法检测非致细胞病变性牛病毒性腹泻病毒的特点
Am J Vet Res. 1983 Oct;44(10):1916-9.
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Response of bovine viruses to interferon.牛病毒对干扰素的反应。
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Effect of infectious bovine rhinotracheitis virus infection of calves on cell populations recovered by lung lavage.犊牛感染牛传染性鼻气管炎病毒对通过肺灌洗回收的细胞群体的影响。
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Effect of human leukocyte A interferon on prevention of infectious bovine rhinotracheitis virus infection of cattle.人白细胞A干扰素对预防牛传染性鼻气管炎病毒感染牛的作用。
Am J Vet Res. 1985 Jun;46(6):1251-5.
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Identification of a mutant bovine herpesvirus-1 (BHV-1) in post-arrival outbreaks of IBR in feedlot calves and protection with conventional vaccination.育肥牛犊抵达后发生传染性牛鼻气管炎(IBR)疫情时突变型牛疱疹病毒1型(BHV-1)的鉴定及常规疫苗接种的保护作用
Can J Vet Res. 2001 Apr;65(2):81-8.

引用本文的文献

1
Macrophages infected with cytopathic bovine viral diarrhea virus release a factor(s) capable of priming uninfected macrophages for activation-induced apoptosis.感染致细胞病变型牛病毒性腹泻病毒的巨噬细胞释放一种(或多种)因子,该因子能够使未感染的巨噬细胞致敏,从而引发激活诱导的细胞凋亡。
J Virol. 1997 Apr;71(4):3255-8. doi: 10.1128/JVI.71.4.3255-3258.1997.
2
Properties of bovine interferons.牛干扰素的特性。
Experientia. 1984 Dec 15;40(12):1410-2. doi: 10.1007/BF01951916.
3
Antiviral effects of bovine interferons on bovine respiratory tract viruses.牛干扰素对牛呼吸道病毒的抗病毒作用。
J Clin Microbiol. 1984 Apr;19(4):492-7. doi: 10.1128/jcm.19.4.492-497.1984.
4
Interferon induction in bovine and feline monolayer cultures by four bluetongue virus serotypes.四种蓝舌病毒血清型在牛和猫单层培养物中诱导干扰素的情况。
Can J Comp Med. 1982 Jan;46(1):100-2.
5
Interferon production by bovine tracheal organ cultures infected with bovid herpesvirus 1 strains.感染牛疱疹病毒1型毒株的牛气管器官培养物中干扰素的产生
Can J Comp Med. 1980 Oct;44(4):447-52.
6
Levels of interferon in blood serum and toxicity studies of bacteria-derived bovine alpha I1 interferon in dairy calves.血清中干扰素水平以及细菌衍生的牛αI1干扰素对奶牛犊牛的毒性研究
J Clin Microbiol. 1986 Aug;24(2):240-4. doi: 10.1128/jcm.24.2.240-244.1986.
7
Effects of immunopotentiating agents on alveolar macrophage properties.免疫增强剂对肺泡巨噬细胞特性的影响。
Comp Immunol Microbiol Infect Dis. 1986;9(2-3):155-9. doi: 10.1016/0147-9571(86)90007-x.
8
In vitro protective effect of bacteria-derived bovine alpha interferon I1 against selected bovine viruses.细菌衍生的牛α干扰素I1对特定牛病毒的体外保护作用
J Clin Microbiol. 1985 Dec;22(6):912-4. doi: 10.1128/jcm.22.6.912-914.1985.
9
Bovine interferon: its biology and application in veterinary medicine.牛干扰素:其生物学特性及其在兽医学中的应用。
Antiviral Res. 1987 May;7(4):187-210. doi: 10.1016/0166-3542(87)90028-3.
10
Susceptibility of feline herpesvirus 1 and a feline calicivirus to feline interferon and recombinant human leukocyte interferons.猫疱疹病毒1型和一种猫杯状病毒对猫干扰素及重组人白细胞干扰素的敏感性。
Antimicrob Agents Chemother. 1985 Nov;28(5):698-9. doi: 10.1128/AAC.28.5.698.