Meq缺失株马立克病毒SC9-1通过自然重组获得Meq基因的能力

Yankun Zhang, Ni Han, Peng Sun, Junxia Chen, Shuai Su, Peng Zhao, Zhizhong Cui
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摘要

我们希望探索meq缺失的马立克病病毒(MDV)疫苗株SC9-1通过重组从MDV野生株Md5中获得meq基因的能力。将鸡胚成纤维细胞(CEFs)与SC9-1疫苗病毒和Md5病毒共感染,传代至第三代,并在细胞培养中从单个斑块中提取病毒DNA。用SC9-1疫苗预免疫的特异性无病原体鸡感染Md5病毒。在不同的时间点从鸡中分离出病毒。然后,从单个空斑中提取病毒DNA,并通过聚合酶链反应进行扩增以鉴定分离的病毒。对翻转重组位点(FRT)残基区进行克隆和测序。结果表明,CEFs和鸡体内分离的病毒均为SC9-1或Md5病毒,未检出重组病毒。序列分析表明,分离的病毒与亲本病毒FRT残基序列同源性为100%。因此,SC9-1通过自然重组从Md5中获得meq基因的可能性很小。meq基因敲除区在体内和体外连续传代中具有良好的遗传稳定性。
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Capacity of the Meq-deleted Strain Marek's Virus SC9-1 to Acquire the Meq Gene by Natural Recombination.

We wished to explore the ability of the meq-deleted Marek's disease virus (MDV) vaccine strain SC9-1 to acquire the meq gene from the MDV wild strain Md5 by recombination. Chicken embryo fibroblast cells (CEFs) were co-infected with the SC9-1 vaccine virus and Md5 virus, passaged to third generation, and viral DNA was extracted from a single plaque in the cell culture. Specific pathogen-free chickens pre-immunized with the SC9-1 vaccine virus were infected with the Md5 virus. Viruses were isolated from chickens-at different time points. Then, viral DNA was extracted from a single plaque and amplification by polymerase chain reaction done to identify isolated viruses. The flip recombina-se sites (FRT) residue region was cloned and sequenced. Results showed that the isolated viruses in cultured CEFs or in chickens were the SC9-1 or Md5 virus, and recombinant viruses were not detected. Sequence analyses revealed that the homology of the FRT residue sequence between the isolated virus and parent virus was 100%. Therefore, there is little chance that SC9-1 can acquire the meq gene from Md5 by natural recombination. Also, the meq-gene knockout region had good genetic stability during serial passages in vivo and in vitro.

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