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首页> 外文期刊>Applied and Environmental Microbiology >Rapid Microcystis Cyanophage Gene Diversification Revealed by Long- and Short-Term Genetic Analyses of the Tail Sheath Gene in a Natural Pond
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Rapid Microcystis Cyanophage Gene Diversification Revealed by Long- and Short-Term Genetic Analyses of the Tail Sheath Gene in a Natural Pond

机译:快速和微囊藻的噬菌体基因多样化揭示了天然池塘中尾鞘基因的长期和短期遗传分析。

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Viruses influence the abundance of host populations through virus-mediated host cell lysis. Viruses contribute to the generation and maintenance of host diversity, which also results in viral diversity throughout their coevolution. Here, to determine the phage gene diversification throughout the coevolution of host and phage in a natural environment, we investigated the genetic diversity and temporal changes in Microcystis cyanophage populations using a total of 810 sequences of the Ma-LMM01-type cyanophage tail sheath gene (g91) from 2006 to 2011 in a natural pond. The sequences obtained were highly diverse and assigned to 419 different genotypes (GT1 to GT419) clustered at 100% nucleotide sequence similarity. A maximum-parsimony network showed that the genotypes were largely divided into three sequence groups, which were dominated by major genotypes (more than 24 sequences: GT2, GT53, and GT163 in group I; GT25 in group II; and GT1 in group III). These major genotypes coexisted and oscillated throughout the sampling periods, suggesting that the Microcystis-cyanophage coevolution was partly driven by a negative frequency-dependent selection. Meanwhile, the high viral genetic diversity observed was derived from a large number of the variants of each major and moderately frequent genotype (including 7 to 18 sequences: GT7, GT26, GT56, GT149, and GT182 in group I; GT152 in group II) (1 or 2 nucleotide substitutions). The variants almost always co-occurred with their origin genotypes. This manner of variant emergence suggests that increased contact frequency within a host-phage population promotes rapid coevolution in a form of “arms race.”
机译:病毒通过病毒介导的宿主细胞裂解影响宿主种群的数量。病毒有助于宿主多样性的产生和维持,也导致病毒在整个进化过程中的多样性。在这里,为了确定整个宿主和噬菌体在自然环境中共同进化过程中的噬菌体基因多样性,我们使用总共810个Ma-LMM01型噬菌体尾鞘基因序列来调查微囊藻蓝藻种群的遗传多样性和时间变化( g91)从2006年到2011年在天然池塘中。获得的序列高度多样化,并被分配到以100%核苷酸序列相似性聚集的419个不同基因型(GT1至GT419)。最大简约网络显示该基因型大致分为三个序列组,以主要基因型为主(I组中的GT2,GT53和GT163超过24个序列; II组中的GT25; III组中的GT1)。 。这些主要基因型在整个采样期间共存并振荡,这表明微囊藻-噬菌体的协同进化部分是由负频率依赖性选择驱动的。同时,观察到的高病毒遗传多样性来自每种主要和中等频率基因型的大量变异(包括7至18个序列:I组中的GT7,GT26,GT56,GT149和GT182; II组中的GT152) (1或2个核苷酸取代)。这些变体几乎总是与它们的起源基因型同时出现。这种变异出现的方式表明,宿主噬菌体种群内部接触频率的增加促进了“军备竞赛”形式的快速协同进化。

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