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有助于脓肿和上皮细胞定植环境中适应性的基因。

Genes Contributing to Fitness in Abscess and Epithelial Cell Colonization Environments.

机构信息

Department of Oral Immunology and Infectious Diseases, University of LouisvilleLouisville, KY, United States.

Department of Microbiology, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian UniversityKrakow, Poland.

出版信息

Front Cell Infect Microbiol. 2017 Aug 28;7:378. doi: 10.3389/fcimb.2017.00378. eCollection 2017.

DOI:10.3389/fcimb.2017.00378
PMID:28900609
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5581868/
Abstract

is an important cause of serious periodontal diseases, and is emerging as a pathogen in several systemic conditions including some forms of cancer. Initial colonization by involves interaction with gingival epithelial cells, and the organism can also access host tissues and spread haematogenously. To better understand the mechanisms underlying these properties, we utilized a highly saturated transposon insertion library of , and assessed the fitness of mutants during epithelial cell colonization and survival in a murine abscess model by high-throughput sequencing (Tn-Seq). Transposon insertions in many genes previously suspected as contributing to virulence showed significant fitness defects in both screening assays. In addition, a number of genes not previously associated with virulence were identified as important for fitness. We further examined fitness defects of four such genes by generating defined mutations. Genes encoding a carbamoyl phosphate synthetase, a replication-associated recombination protein, a nitrosative stress responsive HcpR transcription regulator, and RNase Z, a zinc phosphodiesterase, showed a fitness phenotype in epithelial cell colonization and in a competitive abscess infection. This study verifies the importance of several well-characterized putative virulence factors of and identifies novel fitness determinants of the organism.

摘要

是严重牙周病的重要病因,并且作为一种病原体在包括某些形式癌症在内的几种系统性疾病中出现。最初的定植涉及与牙龈上皮细胞的相互作用,并且该生物体还可以进入宿主组织并通过血液传播。为了更好地理解这些特性的潜在机制,我们利用了 的高度饱和转座子插入文库,并通过高通量测序(Tn-Seq)评估了突变体在上皮细胞定植和在小鼠脓肿模型中存活期间的适应性。许多先前被怀疑与毒力有关的基因中的转座子插入在这两种筛选试验中都表现出明显的适应性缺陷。此外,还鉴定出一些以前与毒力无关的基因对适应性很重要。我们通过生成定义的突变进一步研究了四个这样的基因的适应性缺陷。编码氨甲酰磷酸合成酶、复制相关重组蛋白、硝化应激响应 HcpR 转录调节剂和锌磷酸二酯酶的基因在上皮细胞定植和竞争性脓肿感染中表现出适应性表型。这项研究验证了 的几个特征明确的假定毒力因子的重要性,并确定了该生物体的新适应性决定因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/495b/5581868/d95a9f145898/fcimb-07-00378-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/495b/5581868/a599cb88f4c5/fcimb-07-00378-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/495b/5581868/ef3644ef0490/fcimb-07-00378-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/495b/5581868/d5ec73aa7ddd/fcimb-07-00378-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/495b/5581868/d95a9f145898/fcimb-07-00378-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/495b/5581868/a599cb88f4c5/fcimb-07-00378-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/495b/5581868/ef3644ef0490/fcimb-07-00378-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/495b/5581868/d5ec73aa7ddd/fcimb-07-00378-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/495b/5581868/d95a9f145898/fcimb-07-00378-g0004.jpg

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