Tracz Dobryan M, Tabor Helen, Jerome Morganne, Ng Lai-King, Gilmour Matthew W
National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Manitoba, Canada.
J Clin Microbiol. 2006 Jun;44(6):2007-18. doi: 10.1128/JCM.02630-05.
Salmonella enterica serovars Typhi, Paratyphi A, and Sendai are human-adapted pathogens that cause typhoid (enteric) fever. The acute prevalence in some global regions and the disease severity of typhoidal Salmonella have necessitated the development of rapid and specific detection tests. Most of the methodologies currently used to detect serovar Typhi do not identify serovars Paratyphi A or Sendai. To assist in this aim, comparative sequence analyses were performed at the loci of core bacterial genetic determinants and Salmonella pathogenicity island 2 genes encoded by clinically significant S. enterica serovars. Genetic polymorphisms specific for serovar Typhi (at trpS), as well as polymorphisms unique to human-adapted typhoidal serovars (at sseC and sseF), were observed. Furthermore, entire coding sequences unique to human-adapted typhoidal Salmonella strains (i.e., serovar-specific genetic loci rather than polymorphisms) were observed in publicly available comparative genomic DNA microarray data sets. These polymorphisms and loci were developed into real-time PCR, standard PCR, and liquid microsphere suspension array-based molecular protocols and tested for with a panel of clinical and reference subspecies I S. enterica strains. A proportion of the nontyphoidal Salmonella strains hybridized with the allele-specific oligonucleotide probes for sseC and sseF; but the trpS allele was unique to serovar Typhi (with a singular serovar Paratyphi B strain as an exception), and the coding sequences STY4220 and STY4221 were unique among serovars Typhi, Paratyphi A, and Sendai. These determinants provided phylogenetic data on the genetic relatedness of serovars Typhi, Paratyphi A, and Sendai; and the protocols developed might allow the rapid identification of these Salmonella serovars that cause enteric fever.
伤寒沙门氏菌、甲型副伤寒沙门氏菌和仙台沙门氏菌是适应人类的病原体,可引起伤寒(肠)热。在一些全球区域的急性流行情况以及伤寒沙门氏菌的疾病严重程度使得快速和特异性检测试验的开发成为必要。目前用于检测伤寒血清型的大多数方法无法识别甲型副伤寒血清型或仙台血清型。为了实现这一目标,在核心细菌遗传决定因素位点以及由具有临床意义的肠炎沙门氏菌血清型编码的沙门氏菌致病岛2基因处进行了比较序列分析。观察到伤寒血清型特异的基因多态性(在trpS处),以及适应人类的伤寒血清型特有的多态性(在sseC和sseF处)。此外,在公开可用的比较基因组DNA微阵列数据集中观察到适应人类的伤寒沙门氏菌菌株特有的完整编码序列(即血清型特异的基因位点而非多态性)。这些多态性和位点被开发成实时PCR、标准PCR以及基于液体微球悬浮阵列的分子方案,并使用一组临床和参考肠炎沙门氏菌亚种I菌株进行了测试。一部分非伤寒沙门氏菌菌株与sseC和sseF的等位基因特异性寡核苷酸探针杂交;但trpS等位基因是伤寒血清型特有的(有一个甲型副伤寒B血清型菌株为例外),编码序列STY4220和STY4221在伤寒血清型、甲型副伤寒血清型和仙台血清型中是独特的。这些决定因素提供了关于伤寒血清型、甲型副伤寒血清型和仙台血清型遗传相关性的系统发育数据;并且所开发的方案可能允许快速鉴定这些引起肠热的沙门氏菌血清型。