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菌株YH002的甲基化组比较分析揭示了一个假定的新基序和毒力基因的多种表观遗传调控。

Comparative Methylome Analysis of Strain YH002 Reveals a Putative Novel Motif and Diverse Epigenetic Regulations of Virulence Genes.

作者信息

Ghatak Sandeep, Armstrong Cheryl M, Reed Sue, He Yiping

机构信息

Division of Animal Health, ICAR Research Complex for NEH Region, Umiam, India.

Molecular Characterization of Foodborne Pathogens Research Unit, Eastern Regional Research Center, Agricultural Research Service, United States Department of Agriculture, Wyndmoor, PA, United States.

出版信息

Front Microbiol. 2020 Dec 23;11:610395. doi: 10.3389/fmicb.2020.610395. eCollection 2020.

Abstract

is a major cause of foodborne gastroenteritis worldwide inflicting palpable socioeconomic costs. The ability of this pathogen to successfully infect its hosts is determined not only by the presence of specific virulence genes but also by the pathogen's capacity to appropriately regulate those virulence genes. Therefore, DNA methylation can play a critical role in both aspects of this process because it serves as both a means to protect the integrity of the cellular DNA from invasion and as a mechanism to control transcriptional regulation within the cell. In the present study we report the comparative methylome data of YH002, a multidrug resistant strain isolated from retail beef liver. Investigation into the methylome identified a putative novel motif (CGCG) of a type II restriction-modification (RM) system. Comparison of methylomes of the strain to well-studied strains highlighted non-uniform methylation patterns among the strains though the existence of the typical type I and type IV RM systems were also observed. Additional investigations into the existence of DNA methylation sites within gene promoters, which may ultimately result in altered levels of transcription, revealed several virulence genes putatively regulated using this mode of action. Of those identified, a flagella gene (), a RNA polymerase sigma factor (), a capsular polysaccharide export protein (), and a multidrug efflux pump were highly notable.

摘要

是全球食源性肠胃炎的主要病因,造成了明显的社会经济成本。这种病原体成功感染宿主的能力不仅取决于特定毒力基因的存在,还取决于病原体适当调控这些毒力基因的能力。因此,DNA甲基化在这一过程的两个方面都可以发挥关键作用,因为它既是保护细胞DNA完整性免受入侵的一种手段,也是控制细胞内转录调控的一种机制。在本研究中,我们报告了从零售牛肝中分离出的多重耐药菌株YH002的比较甲基化组数据。对甲基化组的研究确定了一种II型限制修饰(RM)系统的推定新基序(CGCG)。将该菌株的甲基化组与深入研究的菌株进行比较,突出了菌株之间甲基化模式的不一致,不过也观察到了典型的I型和IV型RM系统的存在。对基因启动子内DNA甲基化位点的存在进行的进一步研究,这最终可能导致转录水平的改变,揭示了几个可能使用这种作用方式调控的毒力基因。在这些已鉴定的基因中,一个鞭毛基因()、一个RNA聚合酶sigma因子()、一个荚膜多糖输出蛋白()和一个多重耐药外排泵非常值得注意。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1719/7785942/daed348a1420/fmicb-11-610395-g001.jpg

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