Reinhart Alexandria A, Nguyen Angela T, Brewer Luke K, Bevere Justin, Jones Jace W, Kane Maureen A, Damron F Heath, Barbier Mariette, Oglesby-Sherrouse Amanda G
University of Maryland, School of Medicine, Department of Microbiology and Immunology, Baltimore, Maryland, USA.
University of Maryland, School of Pharmacy, Department of Pharmaceutical Sciences, Baltimore, Maryland, USA.
Infect Immun. 2017 Apr 21;85(5). doi: 10.1128/IAI.00764-16. Print 2017 May.
is a Gram-negative opportunistic pathogen that requires iron for virulence. Iron homeostasis is maintained in part by the PrrF1 and PrrF2 small RNAs (sRNAs), which block the expression of iron-containing proteins under iron-depleted conditions. The PrrF sRNAs also promote the production of the quinolone signal (PQS), a quorum sensing molecule that activates the expression of several virulence genes. The tandem arrangement of the genes allows for expression of a third sRNA, PrrH, which is predicted to regulate gene expression through its unique sequence derived from the intergenic (IG) sequence (the PrrH sequence). Previous studies showed that the locus is required for acute lung infection. However, the individual functions of the PrrF and PrrH sRNAs were not determined. Here, we describe a system for differentiating PrrF and PrrH functions by deleting the PrrH sequence [(ΔH)]. Our analyses of this construct indicate that the PrrF sRNAs, but not PrrH, are required for acute lung infection by Moreover, we show that the virulence defect of the Δ mutant is due to decreased bacterial burden during acute lung infection. analysis of gene expression in lung homogenates shows that PrrF-mediated regulation of genes for iron-containing proteins is disrupted in the Δ mutant during infection, while the expression of genes that mediate PrrF-regulated PQS production are not affected by deletion Combined, these studies demonstrate that regulation of iron utilization plays a critical role in 's ability to survive during infection.
是一种革兰氏阴性机会致病菌,其毒力需要铁元素。铁稳态部分由PrrF1和PrrF2小RNA(sRNA)维持,它们在缺铁条件下阻断含铁蛋白的表达。PrrF sRNA还促进喹诺酮信号(PQS)的产生,PQS是一种群体感应分子,可激活多个毒力基因的表达。这些基因的串联排列允许第三种sRNA PrrH的表达,预计它通过源自基因间(IG)序列的独特序列(PrrH序列)来调节基因表达。先前的研究表明,该基因座是急性肺部感染所必需的。然而,PrrF和PrrH sRNA的个体功能尚未确定。在这里,我们描述了一种通过删除PrrH序列[(ΔH)]来区分PrrF和PrrH功能的系统。我们对该构建体的分析表明,PrrF sRNA而非PrrH是急性肺部感染所必需的。此外,我们表明Δ突变体的毒力缺陷是由于急性肺部感染期间细菌载量降低。对肺匀浆中基因表达的分析表明,在感染期间,PrrF介导的含铁蛋白基因调控在Δ突变体中被破坏,而介导PrrF调控的PQS产生的基因表达不受缺失的影响。综合这些研究表明,铁利用的调节在感染期间的生存能力中起着关键作用。