Institute of Veterinary, Animal and Biomedical Sciences, Massey University, Palmerston North, New Zealand.
PLoS One. 2011;6(11):e27121. doi: 10.1371/journal.pone.0027121. Epub 2011 Nov 11.
Campylobacter jejuni ST-474 is the most important human enteric pathogen in New Zealand, and yet this genotype is rarely found elsewhere in the world. Insight into the evolution of this organism was gained by a whole genome comparison of two ST-474, flaA SVR-14 isolates and other available C. jejuni isolates and genomes. The two isolates were collected from different sources, human (H22082) and retail poultry (P110b), at the same time and from the same geographical location. Solexa sequencing of each isolate resulted in ~1.659 Mb (H22082) and ~1.656 Mb (P110b) of assembled sequences within 28 (H22082) and 29 (P110b) contigs. We analysed 1502 genes for which we had sequences within both ST-474 isolates and within at least one of 11 C. jejuni reference genomes. Although 94.5% of genes were identical between the two ST-474 isolates, we identified 83 genes that differed by at least one nucleotide, including 55 genes with non-synonymous substitutions. These covered 101 kb and contained 672 point differences. We inferred that 22 (3.3%) of these differences were due to mutation and 650 (96.7%) were imported via recombination. Our analysis estimated 38 recombinant breakpoints within these 83 genes, which correspond to recombination events affecting at least 19 loci regions and gives a tract length estimate of ~2 kb. This includes a ~12 kb region displaying non-homologous recombination in one of the ST-474 genomes, with the insertion of two genes, including ykgC, a putative oxidoreductase, and a conserved hypothetical protein of unknown function. Furthermore, our analysis indicates that the source of this recombined DNA is more likely to have come from C. jejuni strains that are more closely related to ST-474. This suggests that the rates of recombination and mutation are similar in order of magnitude, but that recombination has been much more important for generating divergence between the two ST-474 isolates.
空肠弯曲菌 ST-474 是新西兰最重要的人类肠道病原体,然而这种基因型在世界其他地方却很少见。通过对两株 ST-474、flaA SVR-14 分离株和其他可用的空肠弯曲菌分离株和基因组进行全基因组比较,我们对该生物的进化有了深入的了解。这两株分离株分别从不同的来源、人类(H22082)和零售家禽(P110b)、同一时间和同一地理位置采集。对每个分离株进行 Solexa 测序,得到约 1.659 Mb(H22082)和 1.656 Mb(P110b)的组装序列,由 28 个(H22082)和 29 个(P110b)contigs 组成。我们分析了 1502 个基因,这些基因在两个 ST-474 分离株中以及至少一个 11 个空肠弯曲菌参考基因组中都有序列。尽管两个 ST-474 分离株之间 94.5%的基因是相同的,但我们发现有 83 个基因至少有一个核苷酸不同,包括 55 个具有非同义突变的基因。这些基因覆盖了 101 kb,包含 672 个点差异。我们推断,这些差异中有 22 个(3.3%)是由于突变,650 个(96.7%)是通过重组导入的。我们的分析估计在这 83 个基因中存在 38 个重组断点,这些断点对应于影响至少 19 个基因座区域的重组事件,给出了约 2 kb 的片段长度估计。其中一个 ST-474 基因组中的一个约 12 kb 区域显示非同源重组,插入了两个基因,包括 ykgC,一个假定的氧化还原酶和一个未知功能的保守假定蛋白。此外,我们的分析表明,这种重组 DNA 的来源更有可能来自与 ST-474 关系更密切的空肠弯曲菌菌株。这表明重组和突变的速率在数量级上相似,但重组对两个 ST-474 分离株之间的差异产生更为重要。