Department of Microbiology and Immunology, Jacobs School of Medicine and Biomedical Sciences, State University of New York at Buffalo, Buffalo, New York, USA.
Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, Michigan, USA.
mSphere. 2020 May 27;5(3):e00412-20. doi: 10.1128/mSphere.00412-20.
is a common cause of polymicrobial catheter-associated urinary tract infection (CAUTI), and yet literature describing the molecular mechanisms of its pathogenesis is limited. To identify factors important for colonization during single-species infection and during polymicrobial infection with a common cocolonizer, , we created a saturating library of ∼50,000 transposon mutants and conducted transposon insertion site sequencing (Tn-Seq) in a murine model of CAUTI. strain BE2467 carries 4,398 genes, 521 of which were identified as essential for growth in laboratory medium and therefore could not be assessed for contribution to infection. Using an input/output fold change cutoff value of 20 and values of <0.05, 340 genes were identified as important for establishing single-species infection only and 63 genes as uniquely important for polymicrobial infection with , and 168 genes contributed to both single-species and coinfection. Seven mutants were constructed for experimental validation of the primary screen that corresponded to flagella ( mutant), twin arginine translocation (), an ATP-dependent protease (), d-alanine-d-alanine ligase (), type 3 secretion ( and ), and type VI secretion (). Infection-specific phenotypes validated 6/7 (86%) mutants during direct cochallenge with wild-type and 3/5 (60%) mutants during coinfection with , for a combined validation rate of 9/12 (75%). Tn-Seq therefore successfully identified genes that contribute to fitness of within the urinary tract, determined the impact of coinfection on fitness requirements, and added to the identification of a collection of genes that may contribute to fitness of multiple urinary tract pathogens. is a common cause of polymicrobial catheter-associated urinary tract infections (CAUTIs), particularly during long-term catheterization. However, little is known regarding the pathogenesis of this organism. Using transposon insertion site sequencing (Tn-Seq), we performed a global assessment of fitness factors for CAUTI while simultaneously determining how coinfection with another pathogen alters fitness requirements. This approach provides four important contributions to the field: (i) the first global estimation of genes essential for growth in laboratory medium, (ii) identification of novel fitness factors for colonization of the catheterized urinary tract, (iii) identification of core fitness factors for both single-species and polymicrobial CAUTI, and (iv) assessment of conservation of fitness factors between common uropathogens. Genomewide assessment of the fitness requirements for common uropathogens during single-species and polymicrobial CAUTI thus elucidates complex interactions that contribute to disease severity and will uncover conserved targets for therapeutic intervention.
是一种常见的多微生物导管相关尿路感染(CAUTI)的原因,但描述其发病机制的文献有限。为了确定在单种感染和与常见共殖民者的混合感染期间定植的重要因素,我们创建了一个约 50,000 个转座子突变体的饱和文库,并在 CAUTI 的小鼠模型中进行了转座子插入位点测序(Tn-Seq)。BE2467 菌株携带 4398 个基因,其中 521 个被鉴定为在实验室培养基中生长所必需的,因此无法评估其对感染的贡献。使用输入/输出折叠变化截止值为 20 和 值 <0.05,鉴定出 340 个基因仅对建立单种感染很重要,63 个基因对与 的混合感染很重要,168 个基因对单种感染和共感染都有贡献。为了对初步筛选进行实验验证,构建了 7 个突变体,对应于鞭毛(突变体)、双精氨酸易位()、ATP 依赖性蛋白酶()、D-丙氨酸-D-丙氨酸连接酶()、III 型分泌(和)和 VI 型分泌()。直接与野生型共挑战时,7 个突变体中的 6/7(86%)在感染特异性表型中得到验证,在与共感染时,5 个突变体中的 3/5(60%)得到验证,总的验证率为 9/12(75%)。因此,Tn-Seq 成功地鉴定了在尿路中与 适应度相关的基因,确定了混合感染对适应度要求的影响,并增加了对可能与多种尿路病原体适应度相关的基因的鉴定。是多微生物导管相关尿路感染(CAUTI)的常见原因,尤其是在长期导管插入期间。然而,对于该生物体的发病机制知之甚少。使用转座子插入位点测序(Tn-Seq),我们对 引起 CAUTI 的适应性因素进行了全面评估,同时确定了与另一种病原体混合感染如何改变适应性要求。这种方法为该领域提供了四个重要贡献:(i)首次对实验室培养基中生长必需的 基因进行了全面估计,(ii)鉴定了用于导管化尿路定植的新型适应性因素,(iii)鉴定了单种和多微生物 CAUTI 的核心适应性因素,以及(iv)评估了常见尿路病原体之间适应性因素的保守性。因此,对单种和混合 CAUTI 期间常见尿路病原体的适应性要求进行全基因组评估,阐明了导致疾病严重程度的复杂相互作用,并将揭示用于治疗干预的保守靶标。