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高度减毒痘苗病毒MVA基因组中缺失区域的定位及其对毒力的影响。

Mapping of deletions in the genome of the highly attenuated vaccinia virus MVA and their influence on virulence.

作者信息

Meyer H, Sutter G, Mayr A

机构信息

Institute of Medical Microbiology, Infectious and Epidemic Diseases, Veterinary Faculty, Ludwig-Maximilians Universität, München, Germany.

出版信息

J Gen Virol. 1991 May;72 ( Pt 5):1031-8. doi: 10.1099/0022-1317-72-5-1031.

Abstract

Different passages of the vaccinia virus strain Ankara (CVA wild-type) during attenuation to MVA (modified vaccinia virus Ankara) have been analysed to detect alterations in the genome. Physical maps for the restriction enzymes HindIII and XhoI have been established. Six major deletions relative to the wild-type strain CVA could be localized. They reduce the size of the entire genome from 208 kb (CVA wild-type) to 177 kb for the MVA strain. Four deletions occurred during the first 382 passages and the resulting variant (CVA 382) displays an attenuated phenotype similar to that of the MVA strain. The deletions are located in both terminal fragments, affect two-thirds of the host range gene K1L and eliminate 3.5 kb of a highly conserved region in the HindIII A fragment. During the next 190 passages leading to MVA two additional deletions appeared. Again, one is located in the left terminal fragment, and the other includes the A-type inclusion body gene. Neither of the deletions appear to participate in further attenuation of the virus. Rescue of the partially deleted host range region with the corresponding wild-type DNA restored the ability of the attenuated strains MVA and CVA 382 to grow in some non-permissive tissue cultures. Nevertheless, the complete host range of the wild-type strain was not recovered. Also, plaque-forming behaviour and reduced virulence were not influenced. From the data presented it may be concluded that the partially deleted host range gene is not solely responsible for attenuation.

摘要

对痘苗病毒安卡拉株(CVA野生型)减毒为MVA(改良痘苗病毒安卡拉株)过程中的不同传代进行了分析,以检测基因组中的改变。已建立了限制性内切酶HindIII和XhoI的物理图谱。相对于野生型毒株CVA,可定位六个主要缺失。它们使整个基因组的大小从208 kb(CVA野生型)减少到MVA毒株的177 kb。在前382次传代过程中出现了四个缺失,产生的变体(CVA 382)表现出与MVA毒株相似的减毒表型。这些缺失位于两个末端片段中,影响宿主范围基因K1L的三分之二,并消除了HindIII A片段中一个高度保守区域的3.5 kb。在导致MVA的接下来190次传代中,又出现了另外两个缺失。同样,一个位于左末端片段,另一个包括A型包涵体基因。这些缺失似乎都没有参与病毒的进一步减毒。用相应的野生型DNA拯救部分缺失的宿主范围区域,恢复了减毒株MVA和CVA 382在一些非允许性组织培养物中生长的能力。然而,野生型毒株的完整宿主范围并未恢复。此外,蚀斑形成行为和毒力降低也未受影响。根据所提供的数据可以得出结论,部分缺失的宿主范围基因并非减毒的唯一原因。

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