Desiere F, McShan W M, van Sinderen D, Ferretti J J, Brüssow H
Nestlé Research Center, Nestec Ltd., Vers-chez-les-Blanc, CH Lausanne 26, Switzerland.
Virology. 2001 Sep 30;288(2):325-41. doi: 10.1006/viro.2001.1085.
The genome of the highly pathogenic M1 serotype Streptococcus pyogenes isolate SF370 contains eight prophage elements. Only prophage SF370.1 could be induced by mitomycin C treatment. Prophage SF370.3 showed a 33.5-kb-long genome that closely resembled the genome organization of the cos-site temperate Siphovirus r1t infecting the dairy bacterium Lactococcus lactis. The two-phage genomes shared between 60 and 70% nucleotide sequence identity over the DNA packaging, head and tail genes. Analysis of the SF370.3 genome revealed mutations in the replisome organizer gene that may prevent the induction of the prophage. The mutated phage replication gene was closely related to a virulence marker identified in recently emerged M3 serotype S. pyogenes strains in Japan. This observation suggests that prophage genes confer selective advantage to the lysogenic host. SF370.3 encodes a hyaluronidase and a DNase that may facilitate the spreading of S. pyogenes through tissue planes of its human host. Prophage SF370.2 showed a 43-kb-long genome that closely resembled the genome organization of pac-site temperate Siphoviridae infecting the dairy bacteria S. thermophilus and L. lactis. Over part of the structural genes, the similarity between SF370.2 and S. thermophilus phage O1205 extended to the nucleotide sequence level. SF370.2 showed two probable inactivating mutations: one in the replisome organizer gene and another in the gene encoding the portal protein. Prophage SF370.2 also encodes a hyaluronidase and in addition two very likely virulence factors: prophage-encoded toxins acting as superantigens that may contribute to the immune deregulation observed during invasive streptococcal infections. The superantigens are encoded between the phage lysin and the right attachment site of the prophage genome. The genes were nearly sequence identical with a DNA segment in S. equi, suggesting horizontal gene transfer. The trend for prophage genome inactivation was even more evident for the remaining five prophage sequences that showed massive losses of prophage DNA. In these prophage remnants only 13-0.3 kb of putative prophage DNA was detected. We discuss the genomics data from S. pyogenes strain SF370 within the framework of Darwinian coevolution of prophages and lysogenic bacteria and suggest elements of genetic cooperation and elements of an arms race in this host-parasite relationship.
高致病性M1血清型化脓性链球菌分离株SF370的基因组包含8个前噬菌体元件。只有前噬菌体SF370.1可通过丝裂霉素C处理诱导。前噬菌体SF370.3显示出一个33.5 kb长的基因组,与感染乳杆菌属乳酸乳球菌的cos位点温和性肌尾噬菌体r1t的基因组组织极为相似。这两个噬菌体基因组在DNA包装、头部和尾部基因上的核苷酸序列同一性为60%至70%。对SF370.3基因组的分析揭示了复制体组织者基因中的突变,这可能会阻止前噬菌体的诱导。突变的噬菌体复制基因与日本最近出现的M3血清型化脓性链球菌菌株中鉴定出的一种毒力标记密切相关。这一观察结果表明,前噬菌体基因赋予溶原性宿主选择性优势。SF370.3编码一种透明质酸酶和一种DNA酶,这可能有助于化脓性链球菌在其人类宿主的组织平面中扩散。前噬菌体SF370.2显示出一个43 kb长的基因组,与感染嗜热链球菌和乳酸乳球菌的pac位点温和性肌尾噬菌体科的基因组组织极为相似。在部分结构基因上,SF370.2与嗜热链球菌噬菌体O1205之间的相似性延伸至核苷酸序列水平。SF370.2显示出两个可能的失活突变:一个在复制体组织者基因中,另一个在编码门蛋白的基因中。前噬菌体SF370.2还编码一种透明质酸酶,此外还有两个极有可能的毒力因子:作为超抗原的前噬菌体编码毒素,这可能导致侵袭性链球菌感染期间观察到的免疫失调。这些超抗原在前噬菌体基因组的噬菌体溶菌酶和右附着位点之间编码。这些基因与马链球菌中的一个DNA片段几乎序列相同,表明存在水平基因转移。对于其余五个显示出大量前噬菌体DNA缺失的前噬菌体序列,前噬菌体基因组失活的趋势更为明显。在这些前噬菌体残余物中,仅检测到13 - 0.3 kb的假定前噬菌体DNA。我们在噬菌体和溶原性细菌的达尔文共同进化框架内讨论化脓性链球菌菌株SF370的基因组学数据,并提出这种宿主 - 寄生虫关系中遗传合作的要素和军备竞赛的要素。