...
首页> 外文期刊>Frontiers in Microbiology >The Genomic Architecture of Novel Simulium damnosum Wolbachia Prophage Sequence Elements and Implications for Onchocerciasis Epidemiology
【24h】

The Genomic Architecture of Novel Simulium damnosum Wolbachia Prophage Sequence Elements and Implications for Onchocerciasis Epidemiology

机译:新型 damnosum damnosum Wolbachia 噬菌体序列元件的基因组结构及其对盘尾丝虫病流行病学的意义

获取原文
   

获取外文期刊封面封底 >>

       

摘要

Research interest in Wolbachia is growing as new discoveries and technical advancements reveal the public health importance of both naturally occurring and artificial infections. Improved understanding of the Wolbachia bacteriophages (WOs) WOcauB2 and WOcauB3 [belonging to a sub-group of four WOs encoding serine recombinases group 1 (sr1WOs)], has enhanced the prospect of novel tools for the genetic manipulation of Wolbachia . The basic biology of sr1WOs, including host range and mode of genomic integration is, however, still poorly understood. Very few sr1WOs have been described, with two such elements putatively resulting from integrations at the same Wolbachia genome loci, about 2 kb downstream from the FtsZ cell-division gene. Here, we characterize the DNA sequence flanking the FtsZ gene of w Dam, a genetically distinct line of Wolbachia isolated from the West African onchocerciasis vector Simulium squamosum E. Using Roche 454 shot-gun and Sanger sequencing, we have resolved >32 kb of WO prophage sequence into three contigs representing three distinct prophage elements. Spanning ≥36 distinct WO open reading frame gene sequences, these prophage elements correspond roughly to three different WO modules: a serine recombinase and replication module (sr1RRM), a head and base-plate module and a tail module. The sr1RRM module contains replication genes and a Holliday junction recombinase and is unique to the sr1 group WOs. In the extreme terminal of the tail module there is a SpvB protein homolog—believed to have insecticidal properties and proposed to have a role in how Wolbachia parasitize their insect hosts. We propose that these w Dam prophage modules all derive from a single WO genome, which we have named here sr1WOdamA1. The best-match database sequence for all of our sr1WOdamA1-predicted gene sequences was annotated as of Wolbachia or Wolbachia phage sourced from an arthropod. Clear evidence of exchange between sr1WOdamA1 and other Wolbachia WO phage sequences was also detected. These findings provide insights into how Wolbachia could affect a medically important vector of onchocerciasis, with potential implications for future control methods, as well as supporting the hypothesis that Wolbachia phages do not follow the standard model of phage evolution.
机译:随着新发现和技术进步揭示了自然感染和人工感染对公共卫生的重要性,人们对Wolbachia的研究兴趣与日俱增。对Wolbachia噬菌体(WOs)WOcauB2和WOcauB3的更好理解[属于四个编码丝氨酸重组酶组1(sr1WOs)的WOs的一个亚组],增强了对Wolbachia进行遗传操作的新工具的前景。 sr1WOs的基本生物学,包括宿主范围和基因组整合模式,仍然知之甚少。已经描述了很少的sr1WO,推定有两个这样的元件是由于在同一个Wolbachia基因组位点的整合而产生的,该位点位于FtsZ细胞分裂基因的下游约2 kb。在这里,我们表征了w Dam的FtsZ基因侧翼的DNA序列,w Dam是从西非盘尾丝虫病载体Simulium squamosum E分离的Wolbachia的遗传不同系。使用Roche 454 shot弹枪和Sanger测序,我们解析了> 32 kb的WO先知序列分成三个重叠群,代表三个不同的先知元素。这些传播因子跨越≥36个不同的WO开放阅读框基因序列,大致对应于三个不同的WO模块:丝氨酸重组酶和复制模块(sr1RRM),头部和基板模块以及尾部模块。 sr1RRM模块包含复制基因和霍利迪连接重组酶,并且是sr1组WO所特有的。在尾巴模块的末端,有一个SpvB蛋白同源物,据信具有杀虫特性,并建议在Wolbachia寄生昆虫宿主中发挥作用。我们建议这些w Dam传播模块全部来自单个WO基因组,在这里我们将其命名为sr1WOdamA1。我们所有sr1WOdamA1预测的基因序列的最佳匹配数据库序列均标有节肢动物的Wolbachia或Wolbachia噬菌体。 sr1WOdamA1和其他Wolbachia WO噬菌体序列之间交换的明确证据也被检测到。这些发现提供了关于沃尔巴氏菌如何影响盘尾丝虫病的医学上重要载体的见解,对将来的控制方法有潜在的影响,并支持了沃尔巴氏菌噬菌体不遵循噬菌体进化的标准模型的假设。

著录项

相似文献

  • 外文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号