Ventura Marco, Lee Ju-Hoon, Canchaya Carlos, Zink Ralf, Leahy S, Moreno-Munoz J A, O'Connell-Motherway M, Higgins D, Fitzgerald Gerald F, O'Sullivan Daniel J, van Sinderen Douwe
Alimentary Pharmabiotic Centre and Department of Microbiology, Biosciences Institute, National University of Ireland, Western Road, Cork, Ireland.
Appl Environ Microbiol. 2005 Dec;71(12):8692-705. doi: 10.1128/AEM.71.12.8692-8705.2005.
So far, there is only fragmentary and unconfirmed information on bacteriophages infecting the genus Bifidobacterium. In this report we analyzed three prophage-like elements that are present in the genomes of Bifidobacterium breve UCC 2003, Bifidobacterium longum NCC 2705, and Bifidobacterium longum DJO10A, designated Bbr-1, Bl-1, and Blj-1, respectively. These prophagelike elements exhibit homology with genes of double-stranded DNA bacteriophages spanning a broad phylogenetic range of host bacteria and are surprisingly closely related to bacteriophages infecting low-G+C bacteria. All three prophage-like elements are integrated in a tRNA(Met) gene, which appears to be reconstructed following phage integration. Analysis of the distribution of this integration site in many bifidobacterial species revealed that the attB sites are well conserved. The Blj-1 prophage is 36.9 kb long and was induced when a B. longum DJO10A culture was exposed to mitomycin C or hydrogen peroxide. The Bbr-1 prophage-like element appears to consist of a noninducible 28.5-kb chimeric DNA fragment composed of a composite mobile element inserted into prophage-like sequences, which do not appear to be widely distributed among B. breve strains. Northern blot analysis of the Bbr-1 prophage-like element showed that large parts of its genome are transcriptionally silent. Interestingly, a gene predicted to encode an extracellular beta-glucosidase carried within the Bbr-1 prophage-like element was shown to be transcribed.
到目前为止,关于感染双歧杆菌属的噬菌体仅有零散且未经证实的信息。在本报告中,我们分析了存在于短双歧杆菌UCC 2003、长双歧杆菌NCC 2705和长双歧杆菌DJO10A基因组中的三个类前噬菌体元件,分别命名为Bbr-1、Bl-1和Blj-1。这些类前噬菌体元件与双链DNA噬菌体的基因具有同源性,宿主细菌的系统发育范围广泛,并且令人惊讶地与感染低G+C含量细菌的噬菌体密切相关。所有这三个类前噬菌体元件都整合在一个tRNA(Met)基因中,该基因在噬菌体整合后似乎被重建。对许多双歧杆菌物种中该整合位点分布的分析表明,attB位点高度保守。Blj-1前噬菌体长36.9 kb,当长双歧杆菌DJO10A培养物暴露于丝裂霉素C或过氧化氢时可被诱导。Bbr-1类前噬菌体元件似乎由一个不可诱导的28.5 kb嵌合DNA片段组成,该片段由插入类前噬菌体序列的复合移动元件组成,这些序列似乎在短双歧杆菌菌株中分布不广泛。对Bbr-1类前噬菌体元件的Northern印迹分析表明,其基因组的大部分在转录上是沉默的。有趣的是,预测在Bbr-1类前噬菌体元件中携带的一个编码细胞外β-葡萄糖苷酶的基因被证明可以转录。