Departamento de Desarrollo Biotecnológico, Instituto de Higiene, Universidad de la República, Montevideo, Uruguay.
BMC Microbiol. 2009 Nov 18;9:237. doi: 10.1186/1471-2180-9-237.
Salmonella enterica serovar Enteritidis (S. Enteritidis) has caused major epidemics of gastrointestinal infection in many different countries. In this study we investigate genome divergence and pathogenic potential in S. Enteritidis isolated before, during and after an epidemic in Uruguay.
266 S. Enteritidis isolates were genotyped using RAPD-PCR and a selection were subjected to PFGE analysis. From these, 29 isolates spanning different periods, genetic profiles and sources of isolation were assayed for their ability to infect human epithelial cells and subjected to comparative genomic hybridization using a Salmonella pan-array and the sequenced strain S. Enteritidis PT4 P125109 as reference. Six other isolates from distant countries were included as external comparators.Two hundred and thirty three chromosomal genes as well as the virulence plasmid were found as variable among S. Enteritidis isolates. Ten out of the 16 chromosomal regions that varied between different isolates correspond to phage-like regions. The 2 oldest pre-epidemic isolates lack phage SE20 and harbour other phage encoded genes that are absent in the sequenced strain. Besides variation in prophage, we found variation in genes involved in metabolism and bacterial fitness. Five epidemic strains lack the complete Salmonella virulence plasmid. Significantly, strains with indistinguishable genetic patterns still showed major differences in their ability to infect epithelial cells, indicating that the approach used was insufficient to detect the genetic basis of this differential behaviour.
The recent epidemic of S. Enteritidis infection in Uruguay has been driven by the introduction of closely related strains of phage type 4 lineage. Our results confirm previous reports demonstrating a high degree of genetic homogeneity among S. Enteritidis isolates. However, 10 of the regions of variability described here are for the first time reported as being variable in S. Enteritidis. In particular, the oldest pre-epidemic isolates carry phage-associated genetic regions not previously reported in S. Enteritidis. Overall, our results support the view that phages play a crucial role in the generation of genetic diversity in S. Enteritidis and that phage SE20 may be a key marker for the emergence of particular isolates capable of causing epidemics.
肠炎沙门氏菌血清型肠炎(S. Enteritidis)已在许多不同国家引起了重大的胃肠道感染流行。在本研究中,我们调查了在乌拉圭流行前后分离的 S. Enteritidis 的基因组分化和致病潜力。
使用 RAPD-PCR 对 266 株 S. Enteritidis 进行了基因分型,选择了一些进行 PFGE 分析。从这些不同时期、遗传特征和分离源的 29 个分离株中,检测了它们感染人上皮细胞的能力,并使用沙门氏菌泛阵列和测序菌株 S. Enteritidis PT4 P125109 进行了比较基因组杂交作为参考。还包括来自遥远国家的另外 6 个分离株作为外部对照。在 S. Enteritidis 分离株中发现 233 个染色体基因和毒力质粒发生了变化。不同分离株之间发生变化的 16 个染色体区域中有 10 个对应于噬菌体样区域。最早的 2 个流行前分离株缺乏噬菌体 SE20,并携带在测序菌株中不存在的其他噬菌体编码基因。除了噬菌体的变异外,我们还发现了与代谢和细菌适应性相关的基因发生了变异。5 个流行株缺乏完整的沙门氏菌毒力质粒。重要的是,遗传模式相同的菌株在感染上皮细胞的能力上仍存在显著差异,这表明所使用的方法不足以检测这种差异行为的遗传基础。
乌拉圭最近发生的 S. Enteritidis 感染流行是由 4 型噬菌体亲缘关系密切的菌株引入引起的。我们的结果证实了先前的报告,表明 S. Enteritidis 分离株具有高度的遗传同质性。然而,这里描述的 10 个可变性区域是首次报道在 S. Enteritidis 中发生可变性。特别是,最早的流行前分离株携带以前未在 S. Enteritidis 中报道的噬菌体相关遗传区域。总体而言,我们的结果支持噬菌体在 S. Enteritidis 遗传多样性的产生中起着至关重要的作用的观点,并且噬菌体 SE20 可能是能够引起流行的特定分离株出现的关键标记。