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1
Comparative effects of host and viral factors on early pathogenesis of Marek's disease.宿主和病毒因素对马立克氏病早期发病机制的比较影响。
Infect Immun. 1977 Apr;16(1):136-44. doi: 10.1128/iai.16.1.136-144.1977.
2
Comparative pathogenesis studies with oncogenic and nononcogenic Marek's disease viruses and turkey herpesvirus.致癌性和非致癌性马立克氏病病毒与火鸡疱疹病毒的比较发病机制研究。
Am J Vet Res. 1979 Apr;40(4):541-8.
3
Influence of the bursa of Fabricius on the pathogenesis of Marek's disease.法氏囊对马立克氏病发病机制的影响。
Infect Immun. 1981 Jan;31(1):199-207. doi: 10.1128/iai.31.1.199-207.1981.
4
The mechanism of genetic resistance to Marek's disease in chickens.鸡对马立克氏病的遗传抗性机制。
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5
Marek's disease tumor-associated surface antigen (MATSA) in resistant versus susceptible chickens.抗性与易感鸡体内的马立克氏病肿瘤相关表面抗原(MATSA)
Avian Dis. 1979 Oct-Dec;23(4):831-7.
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Relationship between the immunosuppressive potential and the pathotype of Marek's disease virus isolates.马立克氏病病毒分离株的免疫抑制潜力与致病型之间的关系。
Avian Dis. 1998 Jan-Mar;42(1):124-32.
7
RNA-seq analysis of viral gene expression in the skin of Marek's disease virus infected chickens.马立克氏病病毒感染鸡皮肤中病毒基因表达的RNA测序分析
Vet Immunol Immunopathol. 2019 Jul;213:109882. doi: 10.1016/j.vetimm.2019.109882. Epub 2019 Jun 18.
8
Effect of cyclophosphamide on the response of chickens to a virulent strain of Marek's disease virus.环磷酰胺对鸡对强毒株马立克氏病病毒反应的影响。
Infect Immun. 1975 Nov;12(5):1058-64. doi: 10.1128/iai.12.5.1058-1064.1975.
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Pathogenesis of Marek's disease: early appearance of Marek's disease tumor-associated surface antigen in infected chickens.马立克氏病的发病机制:感染鸡中马立克氏病肿瘤相关表面抗原的早期出现。
J Natl Cancer Inst. 1978 Sep;61(3):849-54.
10
Characterization of four very virulent Argentinian strains of Marek's disease virus and the influence of one of those isolates on synergism between Marek's disease vaccine viruses.四株阿根廷超强毒马立克氏病病毒的特性以及其中一株分离株对马立克氏病疫苗病毒间协同作用的影响
Avian Pathol. 2004 Apr;33(2):190-5. doi: 10.1080/03079450310001652103.

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BG1 has a major role in MHC-linked resistance to malignant lymphoma in the chicken.BG1在鸡对恶性淋巴瘤的MHC连锁抗性中起主要作用。
Proc Natl Acad Sci U S A. 2009 Sep 29;106(39):16740-5. doi: 10.1073/pnas.0906776106. Epub 2009 Sep 11.
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Sequence determination of a mildly virulent strain (CU-2) of Gallid herpesvirus type 2 using 454 pyrosequencing.利用454焦磷酸测序法对鸡疱疹病毒2型的一种弱毒株(CU-2)进行序列测定。
Virus Genes. 2008 Jun;36(3):479-89. doi: 10.1007/s11262-008-0213-5. Epub 2008 Mar 20.
3
Differential cytokine responses following Marek's disease virus infection of chickens differing in resistance to Marek's disease.对马立克氏病抵抗力不同的鸡感染马立克氏病病毒后细胞因子的差异反应
J Virol. 2003 Jan;77(1):762-8. doi: 10.1128/jvi.77.1.762-768.2003.
4
Influence of the bursa of Fabricius on the pathogenesis of Marek's disease.法氏囊对马立克氏病发病机制的影响。
Infect Immun. 1981 Jan;31(1):199-207. doi: 10.1128/iai.31.1.199-207.1981.
5
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Virus-induced atherosclerosis.病毒诱导的动脉粥样硬化。
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7
Genetics of neoplasia--impact of ecogenetics on oncogenesis. A review.肿瘤形成的遗传学——生态遗传学对肿瘤发生的影响。综述。
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本文引用的文献

1
Genetic Control of Lymphomatosis in the Fowl.家禽淋巴瘤病的遗传控制
Science. 1947 Oct 24;106(2756):379-84. doi: 10.1126/science.106.2756.379.
2
Studies on genetic resistance to Marek's disease.马立克氏病的遗传抗性研究。
Avian Dis. 1968 Feb;12(1):9-28.
3
Course of infection in tissues of susceptible chickens after exposure to strains of Marek's disease virus and turkey herpesvirus.易感鸡暴露于马立克氏病病毒株和火鸡疱疹病毒株后在组织中的感染过程。
J Natl Cancer Inst. 1972 Nov;49(5):1367-73.
4
Pathogenesis of Marek's disease in chicks with and without maternal antibody.有或无母源抗体雏鸡马立克氏病的发病机制
J Natl Cancer Inst. 1973 Nov;51(5):1559-73. doi: 10.1093/jnci/51.5.1559.
5
Influence of age at exposure on the pathogenesis of Marek's disease.暴露时的年龄对马立克氏病发病机制的影响。
J Natl Cancer Inst. 1973 Sep;51(3):929-39. doi: 10.1093/jnci/51.3.929.
6
Effects of passive antibody on early pathogenesis of Marek's disease.被动抗体对马立克氏病早期发病机制的影响。
Infect Immun. 1972 Aug;6(2):193-8. doi: 10.1128/iai.6.2.193-198.1972.
7
T lymphoblastoid cell lines from Marek's disease lymphomas.来自马立克氏病淋巴瘤的T淋巴母细胞系
Nature. 1974 Sep 6;251(5470):79-80. doi: 10.1038/251079a0.
8
Initial lesions in chickens infected with JM strain of Marek's disease virus.感染马立克氏病病毒JM株的鸡的初期病变。
Jpn J Vet Res. 1974 Jul;22(3):80-94.
9
Marek's disease herpesvirus particles in tissues from chickens free of precipitating antibodies.来自无沉淀抗体鸡组织中的马立克氏病疱疹病毒颗粒
J Natl Cancer Inst. 1972 May;48(5):1519-23.
10
Viral antigen, virus particles, and infectivity of tissues from chickens with Marek's disease.
J Natl Cancer Inst. 1970 Aug;45(2):341-51.

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.

DOI:10.1128/iai.16.1.136-144.1977
PMID:194836
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC421500/
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。