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使用四重奏扫描在人类和灵长类免疫缺陷病毒序列比对中识别重组体。

Identifying recombinants in human and primate immunodeficiency virus sequence alignments using quartet scanning.

作者信息

Lemey Philippe, Lott Martin, Martin Darren P, Moulton Vincent

机构信息

Rega Institute, Katholieke Universiteit Leuven, Minderbroedersstraat 10, 3000 Leuven, Belgium.

出版信息

BMC Bioinformatics. 2009 Apr 27;10:126. doi: 10.1186/1471-2105-10-126.

Abstract

BACKGROUND

Recombination has a profound impact on the evolution of viruses, but characterizing recombination patterns in molecular sequences remains a challenging endeavor. Despite its importance in molecular evolutionary studies, identifying the sequences that exhibit such patterns has received comparatively less attention in the recombination detection framework. Here, we extend a quartet-mapping based recombination detection method to enable identification of recombinant sequences without prior specifications of either query and reference sequences. Through simulations we evaluate different recombinant identification statistics and significance tests. We compare the quartet approach with triplet-based methods that employ additional heuristic tests to identify parental and recombinant sequences.

RESULTS

Analysis of phylogenetic simulations reveal that identifying the descendents of relatively old recombination events is a challenging task for all methods available, and that quartet scanning performs relatively well compared to the triplet based methods. The use of quartet scanning is further demonstrated by analyzing both well-established and putative HIV-1 recombinant strains. In agreement with recent findings, we provide evidence that the presumed circulating recombinant CRF02_AG is a 'pure' lineage, whereas the presumed parental lineage subtype G has a recombinant origin. We also demonstrate HIV-1 intrasubtype recombination, confirm the hybrid origin of SIV in chimpanzees and further disentangle the recombinant history of SIV lineages in a primate immunodeficiency virus data set.

CONCLUSION

Quartet scanning makes a valuable addition to triplet-based methods for identifying recombinant sequences without prior specifications of either query and reference sequences. The new method is available in the VisRD v.3.0 package http://www.cmp.uea.ac.uk/~vlm/visrd.

摘要

背景

重组对病毒进化具有深远影响,但在分子序列中表征重组模式仍是一项具有挑战性的工作。尽管其在分子进化研究中很重要,但在重组检测框架中,识别呈现此类模式的序列受到的关注相对较少。在此,我们扩展了一种基于四重奏映射的重组检测方法,以能够在无需预先指定查询序列和参考序列的情况下识别重组序列。通过模拟,我们评估了不同的重组识别统计量和显著性检验。我们将四重奏方法与基于三联体的方法进行比较,后者采用额外的启发式检验来识别亲本序列和重组序列。

结果

系统发育模拟分析表明,对于所有可用方法而言,识别相对古老重组事件的后代都是一项具有挑战性的任务,并且与基于三联体的方法相比,四重奏扫描表现相对较好。通过分析既定的和假定的HIV-1重组毒株,进一步证明了四重奏扫描的用途。与最近的发现一致,我们提供证据表明,假定的流行重组型CRF02_AG是一个“纯”谱系,而假定的亲本谱系亚型G具有重组起源。我们还展示了HIV-1亚型内重组,证实了黑猩猩中SIV的杂交起源,并在一个灵长类免疫缺陷病毒数据集中进一步理清了SIV谱系的重组历史。

结论

四重奏扫描是对基于三联体的方法的有价值补充,可在无需预先指定查询序列和参考序列的情况下识别重组序列。新方法可在VisRD v.3.0软件包http://www.cmp.uea.ac.uk/~vlm/visrd中获取。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b77c/2684544/47f51b538279/1471-2105-10-126-1.jpg

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