Graduate Program in Immunology, MERGE-ID Track, Graduate School of Biomedical Sciences, Tufts University School of Medicine, Boston, Massachusetts, USA.
Department of Molecular Biology and Microbiology, Tufts University School of Medicine, Boston, Massachusetts, USA.
Infect Immun. 2020 Mar 23;88(4). doi: 10.1128/IAI.00034-20.
is a Gram-negative bacterial pathogen that causes a range of infections, including pneumonias, urinary tract infections, and septicemia, in otherwise healthy and immunocompromised patients. has become an increasing concern due to the rise and spread of antibiotic-resistant and hypervirulent strains. However, its virulence determinants remain understudied. To identify novel virulence factors needed to cause pneumonia, a high-throughput screen was performed with an arrayed library of over 13,000 transposon insertion mutants in the lungs of wild-type (WT) and neutropenic mice using transposon sequencing (Tn-seq). Insertions in 166 genes resulted in mutants that were significantly less fit in the lungs of WT mice than in those of neutropenic mice. Of these, mutants with insertions in 51 genes still had significant defects in neutropenic mice, while mutants with insertions in 52 genes recovered significantly. screens using a minilibrary of transposon mutants identified putative functions for a subset of these genes, including in capsule content and resistance to reactive oxygen and nitrogen species. Lung infections in mice confirmed roles in virulence for the Δ, Δ, Δ, Δ, Δ, and Δ mutants, all of which were defective in either capsule content or growth in reactive oxygen or nitrogen species. The fitness of the Δ, Δ, Δ, Δ, and Δ mutants was higher in neutropenic mouse lungs, indicating that these genes encode proteins that protect against neutrophil-related effector functions.
是一种革兰氏阴性细菌病原体,可引起多种感染,包括肺炎、尿路感染和败血症,尤其是在健康和免疫功能低下的患者中。由于抗生素耐药性和高毒性菌株的出现和传播,已成为一个日益令人关注的问题。然而,其毒力决定因素仍研究不足。为了确定引起肺炎所需的新型毒力因子,我们使用转座子测序(Tn-seq),在野生型(WT)和中性粒细胞减少症小鼠的肺部,对超过 13000 个转座子插入突变体的阵列文库进行了高通量筛选。在 166 个基因中有插入的突变体在 WT 小鼠肺部的适应性明显低于中性粒细胞减少症小鼠肺部的适应性。在这些基因中,插入 51 个基因的突变体在中性粒细胞减少症小鼠中仍然存在显著缺陷,而插入 52 个基因的突变体则显著恢复。使用转座子突变体的 mini-library 进行的筛选确定了其中一些基因的可能功能,包括荚膜内容物和对活性氧和氮物种的抗性。在小鼠肺部的感染证实了 Δ、Δ、Δ、Δ、Δ 和 Δ 突变体在 毒力中的作用,所有这些突变体在荚膜内容物或在活性氧或氮物种中的生长方面都存在缺陷。Δ、Δ、Δ、Δ、和 Δ 突变体在中性粒细胞减少症小鼠肺部的适应性更高,表明这些基因编码的蛋白质可保护免受中性粒细胞相关效应功能的影响。