Subashchandrabose Sargurunathan, Smith Sara, DeOrnellas Valerie, Crepin Sebastien, Kole Monica, Zahdeh Carina, Mobley Harry L T
Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, Michigan, USA.
mSphere. 2015 Nov 4;1(1). doi: 10.1128/mSphere.00013-15. eCollection 2016 Jan-Feb.
Acinetobacter baumannii is emerging as a leading global multiple-antibiotic-resistant nosocomial pathogen. The identity of genes essential for pathogenesis in a mammalian host remains largely unknown. Using transposon-directed insertion-site sequencing (TraDIS), we identified A. baumannii genes involved in bacterial survival in a leukopenic mouse model of bloodstream infection. Mice were inoculated with a pooled transposon mutant library derived from 109,000 mutants, and TraDIS was used to map transposon insertion sites in the genomes of bacteria in the inoculum and of bacteria recovered from mouse spleens. Unique transposon insertion sites were mapped and used to calculate a fitness factor for every insertion site based on its relative abundance in the inoculum and postinfection libraries. Eighty-nine transposon insertion mutants that were underrepresented after experimental infection in mice compared to their presence in the inocula were delineated as candidates for further evaluation. Genetically defined mutants lacking feoB (ferrous iron import), ddc (d-ala-d-ala-carboxypeptidase), and pntB (pyridine nucleotide transhydrogenase subunit) exhibited a fitness defect during systemic infection resulting from bacteremia. In vitro, these mutants, as well as a fepA (ferric enterobactin receptor) mutant, are defective in survival in human serum and within macrophages and are hypersensitive to killing by antimicrobial peptides compared to the survival of the parental strain under these conditions. Our data demonstrate that FepA is involved in the uptake of exogenous enterobactin in A. baumannii. Genetic complementation rescues the phenotypes of mutants in assays that emulate conditions encountered during infection. In summary, we have determined novel A. baumannii fitness genes involved in the pathogenesis of mammalian infection. IMPORTANCE A. baumannii is a significant cause of bacterial bloodstream infection in humans. Since multiple antibiotic resistance is becoming more common among strains of A. baumannii, there is an urgent need to develop novel tools to treat infections caused by this dangerous pathogen. To develop knowledge-guided treatment approaches for A. baumannii, a thorough understanding of the mechanism by which this pathogen causes bloodstream infection is required. Here, using a mouse model of infection, we report the identification of A. baumannii genes that are critical for the ability of this pathogen to cause bloodstream infections. This study lays the foundation for future research on A. baumannii genes that can be targeted to develop novel therapeutics against this emerging human pathogen.
鲍曼不动杆菌正成为全球主要的多重耐药医院病原体。在哺乳动物宿主中,其致病必需基因的身份仍大多未知。我们利用转座子定向插入位点测序(TraDIS),在白细胞减少的血流感染小鼠模型中鉴定出了鲍曼不动杆菌中参与细菌存活的基因。用来自109,000个突变体的混合转座子突变体文库接种小鼠,并使用TraDIS来绘制接种物中细菌以及从小鼠脾脏中回收的细菌基因组中转座子插入位点的图谱。绘制独特的转座子插入位点,并根据其在接种物和感染后文库中的相对丰度计算每个插入位点的适应度因子。与接种物中相比,在小鼠实验感染后代表性不足的89个转座子插入突变体被划定为进一步评估的候选对象。缺乏feoB(亚铁离子转运蛋白)、ddc(d-丙氨酰-d-丙氨酸羧肽酶)和pntB(吡啶核苷酸转氢酶亚基)的基因定义突变体在由菌血症引起的全身感染期间表现出适应度缺陷。在体外,与亲本菌株在这些条件下的存活情况相比,这些突变体以及fepA(铁载体肠杆菌素受体)突变体在人血清中和巨噬细胞内的存活存在缺陷,并且对抗菌肽杀伤高度敏感。我们的数据表明,FepA参与了鲍曼不动杆菌中外源肠杆菌素的摄取。基因互补在模拟感染过程中遇到的条件的实验中挽救了突变体的表型。总之,我们确定了鲍曼不动杆菌中与哺乳动物感染发病机制相关的新的适应度基因。重要性鲍曼不动杆菌是人类细菌性血流感染的重要病因。由于多重耐药性在鲍曼不动杆菌菌株中越来越普遍,迫切需要开发新的工具来治疗由这种危险病原体引起的感染。为了开发针对鲍曼不动杆菌的基于知识的治疗方法,需要深入了解这种病原体引起血流感染的机制。在此,我们利用感染小鼠模型报告了鲍曼不动杆菌中对该病原体引起血流感染能力至关重要的基因的鉴定。本研究为未来针对鲍曼不动杆菌基因的研究奠定了基础,这些基因可作为靶点来开发针对这种新出现的人类病原体的新型疗法。