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在单核细胞增生李斯特氏菌流行克隆 I 和选定的 1/2a 血清型菌株中,Sau3AI 样限制修饰基因盒的基因组定位和序列内容的保守性。

Conservation of genomic localization and sequence content of Sau3AI-like restriction-modification gene cassettes among Listeria monocytogenes epidemic clone I and selected strains of serotype 1/2a.

机构信息

North Carolina State University, Department of Food Science, Raleigh, North Carolina 27695-7624, USA.

出版信息

Appl Environ Microbiol. 2010 Aug;76(16):5577-84. doi: 10.1128/AEM.00648-10. Epub 2010 Jun 25.

Abstract

Listeria monocytogenes is a food-borne pathogen with a clonal population structure and apparently limited gene flow between strains of different lineages. Strains of epidemic clone I (ECI) have been responsible for numerous outbreaks and invariably have DNA that is resistant to digestion by Sau3AI, suggesting methylation of cytosine at GATC sites. A putative restriction-modification (RM) gene cassette has been identified in the genome of the ECI strain F2365 and all other tested ECI strains but is absent from other strains of the same serotype (4b). Homologous RM cassettes have not been reported among L. monocytogenes isolates of other serotypes. Furthermore, conclusive evidence for the involvement of this RM cassette in the Sau3AI resistance phenotype of ECI strains has been lacking. In this study, we describe a highly conserved RM cassette in certain strains of serotypes 1/2a and 4a that have Sau3AI-resistant DNA. In these strains the RM cassette was in the same genomic location as in the ECI reference strain F2365. The cassette included a gene encoding a putative recombinase, suggesting insertion via site-specific recombination. Deletion of the RM cassette in the ECI strain F2365 and the serotype 1/2a strain A7 rendered the DNA of both strains susceptible to Sau3AI digestion, providing conclusive evidence that the cassette includes a gene required for methylation of cytosine at GATC sites in both strains. The findings suggest that, in addition to its presence in ECI strains, this RM cassette and the accompanying genomic DNA methylation is also encountered among selected strains of other lineages.

摘要

单增李斯特菌是一种食源性病原体,具有克隆种群结构,不同谱系菌株之间的基因流动显然受到限制。流行克隆 I(ECI)菌株曾引发过多次暴发,其 DNA 始终对 Sau3AI 的消化具有抗性,这表明 GATC 位点的胞嘧啶发生了甲基化。在 ECI 菌株 F2365 的基因组以及所有其他测试的 ECI 菌株中都发现了一个假定的限制修饰(RM)基因盒,但在同一血清型(4b)的其他菌株中却不存在。在其他血清型的李斯特菌分离株中尚未报道过同源 RM 盒。此外,一直缺乏该 RM 盒参与 ECI 菌株 Sau3AI 抗性表型的确凿证据。在这项研究中,我们描述了某些血清型 1/2a 和 4a 菌株中 RM 盒的高度保守,这些菌株的 DNA 对 Sau3AI 具有抗性。在这些菌株中,RM 盒位于与 ECI 参考菌株 F2365 相同的基因组位置。盒内包含一个编码假定重组酶的基因,这表明通过位点特异性重组插入。在 ECI 菌株 F2365 和血清型 1/2a 菌株 A7 中缺失 RM 盒,使这两种菌株的 DNA 对 Sau3AI 的消化敏感,这提供了确凿的证据表明该盒包含了两种菌株中 GATC 位点胞嘧啶甲基化所需的基因。这些发现表明,除了在 ECI 菌株中存在外,该 RM 盒及其伴随的基因组 DNA 甲基化也存在于其他谱系的选定菌株中。

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