School of Biological Sciences, University of Canterbury, Christchurch 8140, New Zealand.
División de Biología Molecular, Instituto Potosino de Investigación Científica y Tecnológica, Camino a la Presa San José 2055, 78216 San Luis Potosí, S.L.P., Mexico.
Infect Genet Evol. 2014 Mar;22:134-41. doi: 10.1016/j.meegid.2014.01.013. Epub 2014 Jan 23.
Recent advances in sequencing and metagenomics have enabled the discovery of many novel single stranded DNA (ssDNA) viruses from various environments. We have previously demonstrated that adult dragonflies, as predatory insects, are useful indicators of ssDNA viruses in terrestrial ecosystems. Here we recover and characterise 13 viral genomes which represent 10 novel and diverse circular replication associated protein (Rep)-encoding single stranded (CRESS) DNA viruses (1628-2668nt) from Procordulia grayi and Xanthocnemis zealandica dragonfly larvae collected from four high-country lakes in the South Island of New Zealand. The dragonfly larvae associated CRESS DNA viruses have different genome architectures, however, they all encode two major open reading frames (ORFs) which either have bidirectional or unidirectional arrangement. The 13 viral genomes have a conserved NAGTATTAC nonanucleotide motif and in their predicted Rep proteins we identified the rolling circle replication (RCR) motif 1, 2 and 3, as well as superfamily 3 (SF3) helicase motifs. Maximum likelihood phylogenetic and pairwise identity analysis of the Rep amino acid sequences reveal that the dragonfly larvae novel CRESS DNA viruses share <63% pairwise amino acid identity to the Reps of other CRESS DNA viruses whose complete genomes have been determined and available in public databases and that these viruses are novel. CRESS DNA viruses are circulating in larval dragonfly populations; however, we are unable to ascertain whether these viruses are infecting the larvae directly or are transient within dragonflies via their diet.
近年来,测序和宏基因组学的进展使得人们能够从各种环境中发现许多新型的单链 DNA(ssDNA)病毒。我们之前已经证明,蜻蜓作为捕食性昆虫,是陆地生态系统中 ssDNA 病毒的有用指示物。在这里,我们从新西兰南岛四个高海拔湖泊中采集的成年大蜻蜓和黄蜻蜓幼虫中回收并鉴定了 13 种病毒基因组,它们代表了 10 种新型和多样化的圆形复制相关蛋白(Rep)编码的单链(CRESS)DNA 病毒(1628-2668nt)。与蜻蜓幼虫相关的 CRESS DNA 病毒具有不同的基因组结构,但它们都编码两个主要的开放阅读框(ORF),这些 ORF 具有双向或单向排列。这 13 种病毒基因组具有保守的 NAGTATTAC 九聚体基序,并且在它们预测的 Rep 蛋白中,我们鉴定了滚环复制(RCR)基序 1、2 和 3,以及超级家族 3(SF3)解旋酶基序。Rep 氨基酸序列的最大似然系统发育和成对身份分析表明,这些新型 CRESS DNA 病毒与其他 CRESS DNA 病毒的 Rep 之间的共享<63%的成对氨基酸身份,这些病毒的完整基因组已经确定并在公共数据库中可用,并且这些病毒是新型的。CRSS DNA 病毒在幼虫蜻蜓种群中循环;然而,我们无法确定这些病毒是否直接感染幼虫,或者是否通过它们的饮食在蜻蜓体内短暂存在。