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毁灭褶翅小蜂杆状病毒的基因组片段丰度各异,并分别包装在病毒粒子中。

Microplitis demolitor bracovirus genome segments vary in abundance and are individually packaged in virions.

作者信息

Beck Markus H, Inman Ross B, Strand Michael R

机构信息

Department of Entomology and Center for Tropical and Emerging Global Diseases, University of Georgia, Athens, GA 30602, USA.

出版信息

Virology. 2007 Mar 1;359(1):179-89. doi: 10.1016/j.virol.2006.09.002. Epub 2006 Oct 10.

Abstract

Polydnaviruses (PDVs) are distinguished by their unique association with parasitoid wasps and their segmented, double-stranded (ds) DNA genomes that are non-equimolar in abundance. Relatively little is actually known, however, about genome packaging or segment abundance of these viruses. Here, we conducted electron microscopy (EM) and real-time polymerase chain reaction (PCR) studies to characterize packaging and segment abundance of Microplitis demolitor bracovirus (MdBV). Like other PDVs, MdBV replicates in the ovaries of females where virions accumulate to form a suspension called calyx fluid. Wasps then inject a quantity of calyx fluid when ovipositing into hosts. The MdBV genome consists of 15 segments that range from 3.6 (segment A) to 34.3 kb (segment O). EM analysis indicated that MdBV virions contain a single nucleocapsid that encapsidates one circular DNA of variable size. We developed a semi-quantitative real-time PCR assay using SYBR Green I. This assay indicated that five (J, O, H, N and B) segments of the MdBV genome accounted for more than 60% of the viral DNAs in calyx fluid. Estimates of relative segment abundance using our real-time PCR assay were also very similar to DNA size distributions determined from micrographs. Analysis of parasitized Pseudoplusia includens larvae indicated that copy number of MdBV segments C, B and J varied between hosts but their relative abundance within a host was virtually identical to their abundance in calyx fluid. Among-tissue assays indicated that each viral segment was most abundant in hemocytes and least abundant in salivary glands. However, the relative abundance of each segment to one another was similar in all tissues. We also found no clear relationship between MdBV segment and transcript abundance in hemocytes and fat body.

摘要

多分DNA病毒(PDVs)的独特之处在于它们与寄生蜂有着独特的关联,以及其分段的双链(ds)DNA基因组,这些基因组在丰度上是非等摩尔的。然而,实际上对于这些病毒的基因组包装或片段丰度了解相对较少。在这里,我们进行了电子显微镜(EM)和实时聚合酶链反应(PCR)研究,以表征毁灭褶翅小蜂杆状病毒(MdBV)的包装和片段丰度。与其他PDVs一样,MdBV在雌性卵巢中复制,病毒粒子在那里积累形成一种称为萼液的悬浮液。然后,黄蜂在将卵产入宿主时会注入一定量的萼液。MdBV基因组由15个片段组成,大小从3.6 kb(片段A)到34.3 kb(片段O)不等。EM分析表明,MdBV病毒粒子包含一个单一的核衣壳,该核衣壳包裹着一个大小可变的环状DNA。我们使用SYBR Green I开发了一种半定量实时PCR检测方法。该检测方法表明,MdBV基因组的五个片段(J、O、H、N和B)占萼液中病毒DNA的60%以上。使用我们的实时PCR检测方法对相对片段丰度的估计也与从显微照片确定的DNA大小分布非常相似。对被寄生的粉纹夜蛾幼虫的分析表明,MdBV片段C、B和J的拷贝数在宿主之间有所不同,但它们在一个宿主内的相对丰度与它们在萼液中的丰度几乎相同。组织间检测表明,每个病毒片段在血细胞中最丰富,在唾液腺中最不丰富。然而,每个片段彼此之间的相对丰度在所有组织中都是相似的。我们还发现MdBV片段与血细胞和脂肪体中的转录本丰度之间没有明显的关系。

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