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Molecular Evolution and Life Cycle of Wolbachia Bacteriohage

Molecular Evolution and Life Cycle of Wolbachia Bacteriohage
沃尔巴克氏菌噬菌体的分子进化和生命周期
批准号:
8288780
负责人:
SETH R BORDENSTEIN
金额:
$24.07万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-09-01 至 2014-06-30

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Project Summary: Wolbachia pipientis is one of the most prevalent obligate, intracellular bacteria in multicellular animals. By causing a diverse array of reproductive alterations in arthropods that favor the fitness of infected females, this bacterium has spread worldwide through hundreds of thousands of species. One of the unique genomic features to Wolbachia is an overabundance of mobile DNA including a temperate double-stranded DNA bacteriophage, called WO-B, that has no known function. Our long term goal is to elucidate the mechanisms, relevance, and applications of this bacteriophage to the biology of Wolbachia. The specific hypothesis is that the bacteriophage is a mobile genetic parasite of Wolbachia, capable of integrating into and killing Wolbachia to ensure its own replication as a selfish element. We base that hypothesis on four observations: First, WO-B is widespread and infects 89% of all strains in the two major Wolbachia lineages that infect arthropods. Second, sequence analyses specify WO-B recombination and horizontal transmission between Wolbachia that coinfect the same host. Third, the presence of WO-B does not correlate with the capacity to induce reproductive alterations. Fourth, observations of WO-B particles from purified insect homogenates and from within lysed Wolbachia cells demonstrate that WO-B is active and may kill Wolbachia. Based on these observations, the experimental focus of this proposal is on the molecular evolution and predation of Wolbachia phage WO-B. The specific aims are to: 1. Determine the molecular evolutionary forces shaping Wolbachia bacteriophage. By completing this aim, we will answer three related questions: (Aim 1A) How does an obligate intracellular niche affect phage genome evolution? We will determine how the distinctive ecological conditions of an obligate intracellular bacterium affect genetic diversity in WO-B and we will compare this to the rules of phage genome evolution in free-living bacteria. (Aim 1B) What classes of phage genes are under selection and do they correlate with gene functions such as integration, lysis, lysogeny, virulence, or structure? (Aim 1C) What are the number, diversity, and functions of phage genes that laterally transfer to and from Wolbachia coinfections? Our preliminary results suggest rampant horizontal phage transfer coupled with strong purifying selection. 2. Determine if bacteriophage kill Wolbachia and thereby regulate intrahost densities and Wolbachia's effects on hosts. Here, we will answer two questions related to phage function: (Aim 2A) In a controlled laboratory environment, do lytic phages prey on Wolbachia endosymbionts? (Aim 2B) Does environmental stress trigger phage lysis and does this variation in lysis correspond to variation in Wolbachia densities and interactions with the host? We propose these subaims as an alternative to the prevailing view that phage may be adaptive to Wolbachia's ability to modify arthropod reproduction. Our preliminary studies suggest their principal role is predation of Wolbachia. Project Narrative: The study of Wolbachia pipientis phage may impact public health by increasing knowledge on how to employ the phage as (i) a conduit for spreading transgenic traits into arthropod-borne vectors and (ii) as a therapeutic tool for removing filarial Wolbachia and associated human pathologies
期刊论文(18)
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科研奖励(0)
会议论文
DOI: 10.7554/elife.04266
发表时间: 2014-11-25
期刊: eLife
影响因子: 7.7
作者: [Metcalf JA, Funkhouser-Jones LJ, Brileya K, Reysenbach AL, Bordenstein SR]
通讯作者: Bordenstein SR
DOI: 10.7717/peerj.529
发表时间: 2014
期刊: PeerJ
影响因子: 2.7
作者: [Metcalf JA, Jo M, Bordenstein SR, Jaenike J, Bordenstein SR]
通讯作者: Bordenstein SR
DOI: 10.1038/ncomms13155
发表时间: 2016-10-11
期刊: NATURE COMMUNICATIONS
影响因子: 16.6
作者: [Bordenstein, Sarah R., Bordenstein, Seth R.]
通讯作者: Bordenstein, Seth R.
DOI: 10.1371/journal.pone.0024984
发表时间: 2011
期刊: PloS one
影响因子: 3.7
作者: [Kent BN, Funkhouser LJ, Setia S, Bordenstein SR]
通讯作者: Bordenstein SR
11
    The Mechanism of Cytoplasmic Incompatibility
    • 批准号:
      10078245
    • 项目类别:
    • 资助金额:
      $39.56万
    • 财政年份:
      2020
    • 负责人:
      SETH R BORDENSTEIN
    • 依托单位:
    The Mechanism of Cytoplasmic Incompatibility
    • 批准号:
      9885060
    • 项目类别:
    • 资助金额:
      $38.63万
    • 财政年份:
      2020
    • 负责人:
      SETH R BORDENSTEIN
    • 依托单位:
    The Mechanism of Cytoplasmic Incompatibility
    • 批准号:
      10322407
    • 项目类别:
    • 资助金额:
      $39.63万
    • 财政年份:
      2020
    • 负责人:
      SETH R BORDENSTEIN
    • 依托单位:
    The Mechanism of Cytoplasmic Incompatibility
    海外基金