Fitzgerald Collette, Sherwood Rachel, Gheesling Linda L, Brenner Frances W, Fields Patricia I
Foodborne and Diarrheal Diseases Branch, Division of Bacterial and Mycotic Diseases, National Center for Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia 30333, USA.
Appl Environ Microbiol. 2003 Oct;69(10):6099-105. doi: 10.1128/AEM.69.10.6099-6105.2003.
The Kauffmann-White scheme for serotyping Salmonella recognizes 46 somatic (O) antigen groups, which together with detection of the flagellar (H) antigens form the basis for serotype identification. Although serotyping has become an invaluable typing method for epidemiological investigations of Salmonella, it does have some practical limitations. We have been characterizing the genes required for O and H antigen biosynthesis with the goal of developing a DNA-based system for the determination of serotype in Salmonella. The majority of the enzymes involved in O antigen biosynthesis are encoded by the rfb gene cluster. We report the sequencing of the rfb region from S. enterica serotype Sundsvall (serogroup O:6,14). The S. enterica serotype Sundsvall rfb region is 8.4 kb in length and comprises six open reading frames. When compared with other previously characterized rfb regions, the serogroup O:6,14 sequence is most related to serogroup C(1). On the basis of DNA sequence similarity, we identified two genes from the mannose biosynthetic pathway, two mannosyl transferase genes, the O unit flippase gene and, possibly, the O antigen polymerase. The whole cluster is derived from a low-G+C-content organism. Comparative sequencing of an additional serogroup O:6,14 isolate (S. enterica serotype Carrau) revealed a highly homologous sequence, suggesting that O antigen factors O:24 and O:25 (additional O factors associated with serogroup O:6,14) are encoded outside the rfb gene cluster. We developed a serogroup O:6,14-specific PCR assay based on a region of the putative wzx (O antigen flippase) gene. This provides the basis for a sensitive and specific test for the rapid identification of Salmonella serogroup O:6,14.
用于沙门氏菌血清分型的考夫曼-怀特方案识别出46个菌体(O)抗原组,这些抗原组与鞭毛(H)抗原的检测一起构成了血清型鉴定的基础。尽管血清分型已成为沙门氏菌流行病学调查中一种非常有价值的分型方法,但它确实存在一些实际局限性。我们一直在对O和H抗原生物合成所需的基因进行特征分析,目的是开发一种基于DNA的系统来确定沙门氏菌的血清型。参与O抗原生物合成的大多数酶由rfb基因簇编码。我们报告了肠炎沙门氏菌桑德瓦尔血清型(血清群O:6,14)rfb区域的测序结果。肠炎沙门氏菌桑德瓦尔血清型的rfb区域长度为8.4 kb,包含六个开放阅读框。与其他先前已特征化的rfb区域相比,血清群O:6,14序列与血清群C(1)的关系最为密切。基于DNA序列相似性,我们从甘露糖生物合成途径中鉴定出两个基因、两个甘露糖基转移酶基因、O单位翻转酶基因以及可能的O抗原聚合酶。整个基因簇来源于一种低G+C含量的生物体。对另一个血清群O:6,14分离株(肠炎沙门氏菌卡劳血清型)的比较测序显示出高度同源的序列,这表明O抗原因子O:24和O:25(与血清群O:6,14相关的额外O因子)是在rfb基因簇之外编码的。我们基于假定的wzx(O抗原翻转酶)基因区域开发了一种血清群O:6,14特异性PCR检测方法。这为快速鉴定沙门氏菌血清群O:6,14提供了一种灵敏且特异的检测方法的基础。