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减毒马立克氏病病毒Bam HI-L片段内缺失对vIL-8表达及新鉴定的开放阅读框LORF4转录本的影响

Impact of deletions within the Bam HI-L fragment of attenuated Marek's disease virus on vIL-8 expression and the newly identified transcript of open reading frame LORF4.

作者信息

Jarosinski Keith William, O'Connell Priscilla Helene, Schat Karel Antoni

机构信息

Unit of Avian Health, Department of Microbiology and Immunology, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853, USA.

出版信息

Virus Genes. 2003 May;26(3):255-69. doi: 10.1023/a:1024447230464.

Abstract

Marek's disease (MD) in chickens is caused by MD herpesvirus (MDV), which induces T cell lymphomas. The early pathogenesis of MDV infection is characterized by a primary infection in B lymphocytes followed by infection of activated T lymphocytes. It has been speculated that a MDV-encoded homologue of interleukin-8 (vIL-8) may be important to attract activated T lymphocytes to infected B lymphocytes. Recently, more virulent strains of MDV have emerged, named very virulent plus (vv+)MDV, that cause earlier and more prolonged cytolytic infections compared to less virulent strains. In this report, it was found that vIL-8 mRNA expression in vivo was increased in very virulent (vv) and vv+MDV strains compared to mild (m) and virulent (v) strains, and could not be detected in two attenuated MDV strains examined using very sensitive real-time quantitative reverse transcription-polymerase chain reaction (qRT-PCR) assays. In order to identify potential mechanisms for the increased vIL-8 mRNA expression in more virulent strains, and lack thereof in attenuated strains, the vIL-8 gene and putative promoter sequences upstream of the vIL-8 gene were compared from 10 different MDV strains, including attenuated derivatives. Only the JM-16 strain (both non-attenuated and attenuated) and attenuated 584A (584Ap80C) encoded a predicted vIL-8 gene sequence different from all other strains examined. Within the putative vIL-8 gene promoter sequence, there was little difference among the non-attenuated strains; however significant deletions were identified in the attenuated JM-16/p71, Md11 (R2/23), and 584Ap80C strains. Additionally, these deletions were located within a previously hypothetical open reading frame (ORF) named LORF4. Rapid amplification of cDNA ends identified a full-length transcript of LORF4 in the MDV-transformed lymphoblastoid cell line MSB-1, and deletions within this ORF caused truncated predicted proteins in 4 out of 6 attenuated MDV strains examined.

摘要

鸡马立克氏病(MD)由马立克氏病疱疹病毒(MDV)引起,该病毒可诱发T细胞淋巴瘤。MDV感染的早期发病机制的特征是首先在B淋巴细胞中发生原发性感染,随后感染活化的T淋巴细胞。据推测,MDV编码的白细胞介素-8同源物(vIL-8)可能对于吸引活化的T淋巴细胞至受感染的B淋巴细胞很重要。最近,出现了毒性更强的MDV毒株,称为超强毒(vv+)MDV,与毒性较弱的毒株相比,它们会引发更早且持续时间更长的溶细胞性感染。在本报告中,发现与温和型(m)和强毒型(v)毒株相比,超强毒(vv)和vv+MDV毒株在体内的vIL-8 mRNA表达增加,并且使用非常灵敏的实时定量逆转录-聚合酶链反应(qRT-PCR)检测法在检测的两种减毒MDV毒株中未检测到vIL-8 mRNA表达。为了确定在毒性更强的毒株中vIL-8 mRNA表达增加以及在减毒株中缺乏该表达的潜在机制,对包括减毒衍生物在内的10种不同MDV毒株的vIL-8基因及其上游的假定启动子序列进行了比较。只有JM-16毒株(包括非减毒株和减毒株)以及减毒的584A(584Ap80C)编码的预测vIL-8基因序列与所检测的所有其他毒株不同。在假定的vIL-8基因启动子序列内,非减毒株之间差异不大;然而,在减毒的JM-16/p71、Md11(R2/23)和584Ap80C毒株中发现了明显的缺失。此外,这些缺失位于一个先前假定的名为LORF4的开放阅读框(ORF)内。通过cDNA末端快速扩增在MDV转化的淋巴母细胞系MSB-1中鉴定出LORF4的全长转录本,并且在所检测的6种减毒MDV毒株中有4种在该ORF内的缺失导致预测的蛋白质截短。

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