对16S rRNA基因序列的评估和基于基因组的分析,用于识别非致病性Yersinia
Angelina A Kislichkina1, Angelika A Sizova1, Yury P Skryabin2
1Department of Culture Collection, State Research Center for Applied Microbiology and Biotechnology, Obolensk, Russia.
Frontiers in microbiology
|January 23, 2025
概括
由于高度相似性和基因内变异性,16S rRNA基因测序难以识别非致病性Yersinia. 基于基因组的分析,使用核心SNP和平均核酸标识 (ANI),为准确的Yersinia物种识别提供了卓越的区分能力.
科学领域:
- 微生物学 微生物学
- 基因组学就是基因组学.
- 生物信息学是一种生物信息学.
背景情况:
- 16S rRNA基因测序是细菌识别的标准,但面临着局限性.
- 16S rRNA基因中的高序列相似性和基因内异质性可能会阻碍精确的物种歧视.
- 识别非致病性Yersinia物种对于公共卫生和研究至关重要.
研究的目的:
- 为了比较16S rRNA基因测序与基于基因组的分析用于识别非致病性Yersinia物种的区分能力.
- 为了评估核心单核酸多态 (SNP) 和平均核酸身份 (ANI) 对Yersinia分类学的实用性.
- 评估Yersinia基因组内的16S rRNA基因异质性的程度.
主要方法:
- 使用了来自NCBI的373个Yersinia菌株的完整和草稿基因组.
- 使用核心SNP和ANI进行基因组分析.
- 分析了16S rRNA基因序列,以查看菌株内部和跨菌株的同质性和变异性.
- 比较来自16S rRNA基因数据的分类学赋值与基于基因组的方法.
主要成果:
- 基于基因组的分析 (核心SNP和ANI) 揭示了与NCBI注释相比34个Yersinia基因组的分类学差异.
- 16S rRNA基因的基因内同质性在完整基因组中超过99.5%,超过50%的基因组表现出四种或更多的变异.
- 11%的基因组草案缺乏全长的16S rRNA基因,排除了基因内异质性评估.
- 在Y.intermedia和Y.rochesterensis的菌株中发现了相同的16SrRNA基因序列,这些菌株基于ANI和核心SNP而有所区别.
- 基于16S rRNA基因的家族遗传树并没有准确地反映Yersinia物种之间的基因组关系.
结论:
- 由于序列相似性和基因内异质性,16S rRNA基因测序不足以准确识别密切相关的非致病性Yersinia物种.
- 基于基因组的分析,特别是核心SNP和ANI,为Yersinia分类学提供了更高的分辨率和可靠性.
- 这项研究强调了需要基于基因组的方法来解决分类学模两可,并改善研究不足的Yersinia物种的表征.
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