Division of Infectious Diseases, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
J Bacteriol. 2012 Sep;194(18):5101-9. doi: 10.1128/JB.00932-12. Epub 2012 Jul 20.
Members of the histone-like nucleoid-structuring (H-NS) family of proteins have been shown to play important roles in silencing gene expression and in nucleoid compaction. In Pseudomonas aeruginosa, the two H-NS family members MvaT and MvaU are thought to bind the same AT-rich regions of the chromosome and function coordinately to control a common set of genes. Here we present evidence that the loss of both MvaT and MvaU cannot be tolerated because it results in the production of Pf4 phage that superinfect and kill cells or inhibit their growth. Using a ClpXP-based protein depletion system in combination with transposon mutagenesis, we identify mutants of P. aeruginosa that can tolerate the depletion of MvaT in an ΔmvaU mutant background. Many of these mutants contain insertions in genes encoding components, assembly factors, or regulators of type IV pili or contain insertions in genes of the prophage Pf4. We demonstrate that cells that no longer produce type IV pili or that no longer produce the replicative form of the Pf4 genome can tolerate the loss of both MvaT and MvaU. Furthermore, we show that the loss of both MvaT and MvaU results in an increase in expression of Pf4 genes and that cells that cannot produce type IV pili are resistant to infection by Pf4 phage. Our findings suggest that type IV pili are the receptors for Pf4 phage and that the essential activities of MvaT and MvaU are to repress the expression of Pf4 genes.
组蛋白样核小体结构(H-NS)家族的成员已被证明在基因表达沉默和核小体紧缩中发挥重要作用。在铜绿假单胞菌中,两个 H-NS 家族成员 MvaT 和 MvaU 被认为结合染色体的相同 AT 丰富区域,并协调作用以控制一组共同的基因。在这里,我们提供的证据表明,同时缺失 MvaT 和 MvaU 是不能容忍的,因为它会导致 Pf4 噬菌体的产生,该噬菌体超感染和杀死细胞或抑制它们的生长。我们使用基于 ClpXP 的蛋白耗竭系统结合转座子诱变,鉴定出可以在 ΔmvaU 突变体背景下耐受 MvaT 耗竭的铜绿假单胞菌突变体。这些突变体中的许多都含有插入到编码 IV 型菌毛组件、组装因子或调节剂的基因中,或者插入到 Pf4 噬菌体的基因中。我们证明不再产生 IV 型菌毛或不再产生 Pf4 基因组复制形式的细胞可以耐受 MvaT 和 MvaU 的缺失。此外,我们表明,同时缺失 MvaT 和 MvaU 会导致 Pf4 基因的表达增加,并且不能产生 IV 型菌毛的细胞对 Pf4 噬菌体的感染具有抗性。我们的发现表明 IV 型菌毛是 Pf4 噬菌体的受体,并且 MvaT 和 MvaU 的基本活性是抑制 Pf4 基因的表达。