一种禽致癌疱疹病毒的染色体整合揭示了端粒偏好和淋巴瘤克隆性的证据。

Charmaine M Robinson, Henry D Hunt, Hans H Cheng, Mary E Delany
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引用次数: 30

摘要

背景:疱疹病毒是包括人类在内的许多生物体的主要健康问题,在个体的一生中引起急性和慢性反复感染。马立克氏病病毒(MDV)是一种高度传染性的疱疹病毒,可引起鸡群的肿瘤状况。一些脊椎动物感染的疱疹病毒已被证明在感染潜伏期以整合状态存在。然而,MDV在潜伏期的状态一直是一个有争议的话题。结果:本研究采用高分辨率多色荧光原位杂交技术(FISH)显示了MDV在鸡染色体端粒的整合。染色体整合的细胞基因组图谱使我们能够检查个体内淋巴瘤之间的克隆关系,而来自多个个体的肿瘤分析表明了染色体偏好的潜力。结论:我们的数据强调了病毒和宿主之间存在实质性的基因组水平相互作用,并且值得考虑它们在疱疹病毒病理生物学的关键方面的潜在影响和作用,包括感染、潜伏期、细胞转化、潜伏期破裂和病毒进化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Chromosomal integration of an avian oncogenic herpesvirus reveals telomeric preferences and evidence for lymphoma clonality.

Chromosomal integration of an avian oncogenic herpesvirus reveals telomeric preferences and evidence for lymphoma clonality.

Chromosomal integration of an avian oncogenic herpesvirus reveals telomeric preferences and evidence for lymphoma clonality.

Chromosomal integration of an avian oncogenic herpesvirus reveals telomeric preferences and evidence for lymphoma clonality.

Background: Herpesviruses are a major health concern for numerous organisms, including humans, causing both acute and chronic infections recurrent over an individual's lifespan. Marek's disease virus (MDV) is a highly contagious herpesvirus which causes a neoplastic condition in chicken populations. Several vertebrate-infecting herpesviruses have been shown to exist in an integrated state during latent periods of infection. However the status of MDV during latency has been a topic of debate.

Results: Here we employed high-resolution multi-color fluorescence in situ hybridization (FISH) to show integration of MDV at the telomeres of chicken chromosomes. Cytogenomic mapping of the chromosomal integrations allowed us to examine the clonal relationships among lymphomas within individuals, whereas analysis of tumors from multiple individuals indicated the potential for chromosomal preferences.

Conclusions: Our data highlight that substantive genome-level interactions between the virus and host exist, and merit consideration for their potential impact and role in key aspects of herpesvirus pathobiology including infection, latency, cellular transformation, latency-breaks and viral evolution.

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