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细菌在宿主中基因组还原进化的早期阶段。

The early stage of bacterial genome-reductive evolution in the host.

机构信息

Department of Medicine, College of Medicine, Korea University, Anam-Dong, Seongbuk-Gu, Seoul, Korea.

出版信息

PLoS Pathog. 2010 May 27;6(5):e1000922. doi: 10.1371/journal.ppat.1000922.

DOI:10.1371/journal.ppat.1000922
PMID:20523904
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2877748/
Abstract

The equine-associated obligate pathogen Burkholderia mallei was developed by reductive evolution involving a substantial portion of the genome from Burkholderia pseudomallei, a free-living opportunistic pathogen. With its short history of divergence (approximately 3.5 myr), B. mallei provides an excellent resource to study the early steps in bacterial genome reductive evolution in the host. By examining 20 genomes of B. mallei and B. pseudomallei, we found that stepwise massive expansion of IS (insertion sequence) elements ISBma1, ISBma2, and IS407A occurred during the evolution of B. mallei. Each element proliferated through the sites where its target selection preference was met. Then, ISBma1 and ISBma2 contributed to the further spread of IS407A by providing secondary insertion sites. This spread increased genomic deletions and rearrangements, which were predominantly mediated by IS407A. There were also nucleotide-level disruptions in a large number of genes. However, no significant signs of erosion were yet noted in these genes. Intriguingly, all these genomic modifications did not seriously alter the gene expression patterns inherited from B. pseudomallei. This efficient and elaborate genomic transition was enabled largely through the formation of the highly flexible IS-blended genome and the guidance by selective forces in the host. The detailed IS intervention, unveiled for the first time in this study, may represent the key component of a general mechanism for early bacterial evolution in the host.

摘要

马源专性需氧病原体鼻疽伯克霍尔德菌是通过还原进化形成的,其基因组的很大一部分来自自由生活的机会性病原体鼻疽伯克霍尔德菌。由于其分化的历史较短(约 350 万年),鼻疽伯克霍尔德菌为研究细菌在宿主中基因组还原进化的早期步骤提供了极好的资源。通过检查 20 株鼻疽伯克霍尔德菌和鼻疽伯克霍尔德菌的基因组,我们发现,在鼻疽伯克霍尔德菌的进化过程中,IS(插入序列)元件 ISBma1、ISBma2 和 IS407A 逐步大规模扩张。每个元件在其靶标选择偏好得到满足的地方增殖。然后,ISBma1 和 ISBma2 通过提供次级插入位点,促进了 IS407A 的进一步传播。这种传播增加了基因组缺失和重排,主要由 IS407A 介导。大量基因也存在核苷酸水平的破坏。然而,这些基因尚未出现明显的侵蚀迹象。有趣的是,所有这些基因组修饰并没有严重改变从鼻疽伯克霍尔德菌继承的基因表达模式。这种高效而精细的基因组转变在很大程度上是通过形成高度灵活的 IS 混合基因组和宿主中选择压力的指导来实现的。本研究首次揭示了详细的 IS 干预,可能代表了细菌在宿主中早期进化的一般机制的关键组成部分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f57f/2877748/4818dfcfba5c/ppat.1000922.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f57f/2877748/d9b9f49c24ca/ppat.1000922.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f57f/2877748/ae3ca1f4eb3d/ppat.1000922.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f57f/2877748/a26e960fef65/ppat.1000922.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f57f/2877748/976d3a955266/ppat.1000922.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f57f/2877748/02b751fccc33/ppat.1000922.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f57f/2877748/4818dfcfba5c/ppat.1000922.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f57f/2877748/d9b9f49c24ca/ppat.1000922.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f57f/2877748/ae3ca1f4eb3d/ppat.1000922.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f57f/2877748/a26e960fef65/ppat.1000922.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f57f/2877748/976d3a955266/ppat.1000922.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f57f/2877748/02b751fccc33/ppat.1000922.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f57f/2877748/4818dfcfba5c/ppat.1000922.g006.jpg

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