Department of Microbiology, University College Cork, Cork, Ireland.
Appl Environ Microbiol. 2013 Aug;79(16):4786-98. doi: 10.1128/AEM.01197-13. Epub 2013 May 31.
Here we present an entire temporal transcriptional profile of Lactococcus lactis subsp. cremoris UC509.9 undergoing lytic infection with two distinct bacteriophages, Tuc2009 and c2. Furthermore, corresponding high-resolution whole-phage genome tiling arrays of both bacteriophages were performed throughout lytic infection. Whole-genome microarrays performed at various time points postinfection demonstrated a rather modest impact on host transcription. The majority of changes in the host transcriptome occur during late infection stages; few changes in host gene transcription occur during the immediate and early infection stages. Alterations in the L. lactis UC509.9 transcriptome during lytic infection appear to be phage specific, with relatively few differentially transcribed genes shared between cells infected with Tuc2009 and those infected with c2. Despite the apparent lack of a coordinated general phage response, three themes common to both infections were noted: alternative transcription of genes involved in catabolic flux and energy production, differential transcription of genes involved in cell wall modification, and differential transcription of genes involved in the conversion of ribonucleotides to deoxyribonucleotides. The transcriptional profiles of both bacteriophages during lytic infection generally correlated with the findings of previous studies and allowed the confirmation of previously predicted promoter sequences. In addition, the host transcriptional response to lysogenization with Tuc2009 was monitored along with tiling array analysis of Tuc2009 in the lysogenic state. Analysis identified 44 host genes with altered transcription during lysogeny, 36 of which displayed levels of transcription significantly reduced from those for uninfected cells.
我们在这里展示了乳球菌乳亚种 UC509.9 在受到两种不同噬菌体 Tuc2009 和 c2 的裂解感染时的完整时间转录谱。此外,还在裂解感染过程中对这两种噬菌体的相应高分辨率全噬菌体基因组平铺阵列进行了相应的研究。在感染后不同时间点进行的全基因组微阵列显示,宿主转录的影响相当小。宿主转录组的大多数变化发生在晚期感染阶段;在即时和早期感染阶段,宿主基因转录的变化很少。在裂解感染过程中,乳球菌 UC509.9 转录组的改变似乎是噬菌体特异性的,感染 Tuc2009 的细胞和感染 c2 的细胞之间共享的差异转录基因相对较少。尽管噬菌体似乎没有协调的一般反应,但在两种感染中都注意到了三个共同的主题:参与分解代谢通量和能量产生的基因的替代转录、参与细胞壁修饰的基因的差异转录以及参与将核糖核苷酸转化为脱氧核糖核苷酸的基因的差异转录。两种噬菌体在裂解感染过程中的转录谱通常与先前研究的结果一致,并允许确认先前预测的启动子序列。此外,还监测了 Tuc2009 溶原化时宿主的转录反应,并对溶原状态下的 Tuc2009 进行了平铺阵列分析。分析确定了 44 个在溶原化过程中转录发生改变的宿主基因,其中 36 个基因的转录水平与未感染细胞相比显著降低。