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相关概念视频

Lytic Cycle of Bacteriophages01:30

Lytic Cycle of Bacteriophages

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Bacteriophages, also known as phages, are specialized viruses that infect bacteria. A key characteristic of phages is their distinctive “head-tail” morphology. A phage begins the infection process (i.e., lytic cycle) by attaching to the outside of a bacterial cell. Attachment is accomplished via proteins in the phage tail that bind to specific receptor proteins on the outer surface of the bacterium. The tail injects the phage’s DNA genome into the bacterial cytoplasm. In the...
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Lysogenic Cycle of Bacteriophages00:43

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In contrast to the lytic cycle, phages infecting bacteria via the lysogenic cycle do not immediately kill their host cell. Instead, they combine their genome with the host genome, allowing the bacteria to replicate the phage DNA along with the bacterial genome. The incorporated copy of the phage genome is called the prophage. Some prophages can re-activate and enter the lytic cycle. This often occurs in response to a perturbation, such as DNA damage, but can also transpire in the absence of...
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Viral Recombination00:57

Viral Recombination

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Cells are sometimes infected by more than one virus at once. When two viruses disassemble to expose their genomes for replication in the same cell, similar regions of their genomes can pair together and exchange sequences in a process called recombination. Alternatively, viruses with segmented genomes can swap segments in a process called reassortment.
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Conservative Site-specific Recombination and Phase Variation02:53

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Because the DNA segments are cut and reorganized in a direction-specific manner, site-specific recombination has emerged as an efficient genetic engineering technique. Flippase and Cyclization recombinases or Flp and Cre, respectively, are two members of the tyrosine recombinase family derived from bacteriophages, that are used to mediate site-specific DNA insertions, deletions, and targeted expression of proteins in mammalian cell lines.
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CRISPR and crRNAs02:53

CRISPR and crRNAs

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Bacteria and archaea are susceptible to viral infections just like eukaryotes; therefore, they have developed a unique adaptive immune system to protect themselves. Clustered regularly interspaced short palindromic repeats and CRISPR-associated proteins (CRISPR-Cas) are present in more than 45% of known bacteria and 90% of known archaea.
The CRISPR-Cas system stores a copy of foreign DNA in the host genome and uses it to identify the foreign DNA upon reinfection. CRISPR-Cas has three different...
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Viral Mutations00:36

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A mutation is a change in the sequence of bases of DNA or RNA in a genome. Some mutations occur during replication of the genome due to errors made by the polymerase enzymes that replicate DNA or RNA. Unlike DNA polymerase, RNA polymerase is prone to errors because it is not capable of “proofreading” its work. Viruses with RNA-based genomes, like HIV, therefore accrue mutations faster than viruses with DNA-based genomes. Because mutation and recombination provide the raw material...
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相关实验视频

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Phage-Mediated Genetic Manipulation of the Lyme Disease Spirochete Borrelia burgdorferi
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控制重组来进化菌体的控制

James J Bull1,2, Holly A Wichman1,2, Stephen M Krone2,3

  • 1Department of Biological Sciences, University of Idaho, Moscow, ID 83844, USA.

Cells
|April 12, 2024
PubMed
概括

引导菌体宿主范围进化用于菌体治疗需要使复合成为可能. 高感染力和多重感染 (MOI) 促进共感染,这是重组的一个关键步骤,尽管微调野生菌体重组具有挑战性.

关键词:
计算模型是一种计算模型.数学模型是一个数学模型.菌体疗法是一种菌体疗法.协议 协议 协议 协议 协议

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科学领域:

  • 微生物学 微生物学
  • 进化生物学 进化生物学
  • 计算生物学 计算生物学

背景情况:

  • 菌体重组可以增强宿主范围的扩张.
  • 菌体治疗应用可能受益于促进菌体重组的协议.
  • 了解重组机制对于工程菌体至关重要.

研究的目的:

  • 研究实验协议如何影响菌体重组率.
  • 确定最大限度地增加共感染的条件,这是重组的先决条件.
  • 模拟不同生长条件下的重组剂的积累.

主要方法:

  • 数学和计算模型. 数学和计算模型.
  • 使用菌体T3和T7的实验进化.
  • 基于感染的多重性 (MOI) 和感染的强度,分析共感染动态.
  • 一个四个基因位置模型来评估重组水平.

主要成果:

  • 感染的高多重性 (MOI > 1) 和高感染力对于实现高 coinfection 水平至关重要.
  • 重组菌体在几代人中积累,但如果一个菌体谱系占主导地位,这种情况可以减少.
  • 补充低适应性菌体可以部分恢复丢失的重组.
  • 在野生菌体中微调重组很困难,但质量增强是可能的.

结论:

  • 同感染水平受到MOI和感染力的影响,而不仅仅是MOI.
  • 可以设计协议以提高菌体重组的质量,用于菌体治疗等应用.
  • 虽然精确的控制是难以捉摸的,但基本的程序可以促进有益的菌体进化.