Flores Víctor, Sepúlveda-Robles Omar, Cazares Adrián, Kameyama Luis, Guarneros Gabriel
Departamento de Genética y Biología Molecular, Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional (CINVESTAV-IPN), Mexico City, Mexico.
Catedrático CONACyT - Coordinación de Investigación en Salud, Instituto Mexicano del Seguro Social (IMSS), Centro Médico Nacional Siglo XXI, Mexico City, Mexico.
Arch Virol. 2017 Aug;162(8):2345-2355. doi: 10.1007/s00705-017-3366-5. Epub 2017 May 2.
Bacteriophages (phages) are estimated to be the most abundant and diverse entities in the biosphere harboring vast amounts of novel genetic information. Despite the genetic diversity observed, many phages share common features, such as virion morphology, genome size and organization, and can readily be associated with clearly defined phage groups. However, other phages display unique genomes or, alternatively, mosaic genomes composed of regions that share homology with those of phages of diverse origins; thus, their relationships cannot be easily assessed. In this work, we present a functional and comparative genomic analysis of Pseudomonas aeruginosa phage PaMx25, a virulent member of the Siphoviridae family. The genomes of PaMx25 and a highly homologous phage NP1, bore sequence homology and synteny with the genomes of phages that infect hosts different than Pseudomonas. In order to understand the relationship of the PaMx25 genome with that of other phages, we employed several computational approaches. We found that PaMx25 and NP1 effectively bridged several phage groups. It is expected that as more phage genomes become available, more gaps will be filled, blurring the boundaries that currently separate phage groups.
据估计,噬菌体是生物圈中数量最多、种类最丰富的实体,蕴藏着大量新的遗传信息。尽管观察到其遗传多样性,但许多噬菌体具有共同特征,如病毒体形态、基因组大小和组织方式,并且很容易与明确的噬菌体群体联系起来。然而,其他噬菌体则表现出独特的基因组,或者是由与不同来源噬菌体具有同源性的区域组成的嵌合基因组;因此,它们之间的关系不易评估。在这项工作中,我们对铜绿假单胞菌噬菌体PaMx25进行了功能和比较基因组分析,它是长尾噬菌体科的一种烈性噬菌体。PaMx25和高度同源的噬菌体NP1的基因组与感染非铜绿假单胞菌宿主的噬菌体基因组具有序列同源性和共线性。为了了解PaMx25基因组与其他噬菌体基因组的关系,我们采用了几种计算方法。我们发现PaMx25和NP1有效地连接了几个噬菌体群体。预计随着更多噬菌体基因组的可得,更多的空白将被填补,从而模糊目前分隔噬菌体群体的界限。