Departamento de Bioquímica y Biología Molecular, Facultad de Ciencias Químicas y Farmacéuticas, Universidad de Chile, P.O. Box 174, Correo 22, Santiago, Chile.
J Bacteriol. 2010 Apr;192(8):2246-54. doi: 10.1128/JB.00270-09. Epub 2010 Feb 19.
Salmonella enterica serovar Enteritidis has emerged as a major health problem worldwide in the last few decades. DNA loci unique to S. Enteritidis can provide markers for detection of this pathogen and may reveal pathogenic mechanisms restricted to this serovar. An in silico comparison of 16 Salmonella genomic sequences revealed the presence of an approximately 12.5-kb genomic island (GEI) specific to the sequenced S. Enteritidis strain NCTC13349. The GEI is inserted at the 5' end of gene ydaO (SEN1377), is flanked by 308-bp imperfect direct repeats (attL and attR), and includes 21 open reading frames (SEN1378 to SEN1398), encoding primarily phage-related proteins. Accordingly, this GEI has been annotated as the defective prophage SE14 in the genome of strain NCTC13349. The genetic structure and location of phiSE14 are conserved in 99 of 103 wild-type strains of S. Enteritidis studied here, including reference strains NCTC13349 and LK5. Notably, an extrachromosomal circular form of phiSE14 was detected in every strain carrying this island. The presence of attP sites in the circular forms detected in NCTC13349 and LK5 was confirmed. In addition, we observed spontaneous loss of a tetRA-tagged version of phiSE14, leaving an empty attB site in the genome of strain NCTC13349. Collectively, these results demonstrate that phiSE14 is an unstable genetic element that undergoes spontaneous excision under standard growth conditions. An internal fragment of phiSE14 designated Sdf I has been used as a serovar-specific genetic marker in PCR-based detection systems and as a tool to determine S. Enteritidis levels in experimental infections. The instability of this region may require a reassessment of its suitability for such applications.
在过去的几十年中,肠炎沙门氏菌血清型肠炎亚种已成为全球范围内的一个主要健康问题。肠炎沙门氏菌特有的 DNA 基因座可为该病原体的检测提供标记,并可能揭示仅限于该血清型的致病机制。对 16 株沙门氏菌基因组序列的计算机比较显示,在测序的肠炎沙门氏菌 NCTC13349 菌株中存在一个约 12.5kb 的基因组岛(GEI)。该 GEI 插入基因 ydaO(SEN1377)的 5'端,两侧为 308bp 的不完全直接重复序列(attL 和 attR),并包含 21 个开放阅读框(SEN1378 至 SEN1398),主要编码噬菌体相关蛋白。因此,该 GEI 在 NCTC13349 菌株的基因组中被注释为缺陷型前噬菌体 SE14。phiSE14 的遗传结构和位置在本研究中 103 株野生型肠炎沙门氏菌中的 99 株中得到保守,包括参考菌株 NCTC13349 和 LK5。值得注意的是,在携带该岛的每一株菌中都检测到了phiSE14 的染色体外环状形式。在 NCTC13349 和 LK5 中检测到的环状形式中存在 attP 位点得到了证实。此外,我们观察到 phiSE14 的一个 tetRA 标记版本自发丢失,导致 NCTC13349 菌株基因组中出现一个空的 attB 位点。这些结果表明,phiSE14 是一个不稳定的遗传元件,在标准生长条件下会自发切除。phiSE14 的一个内部片段被指定为 Sdf I,已被用作基于 PCR 的检测系统中的血清型特异性遗传标记,以及确定实验感染中肠炎沙门氏菌水平的工具。该区域的不稳定性可能需要重新评估其在这些应用中的适用性。