Clark Clifford G, Kropinski Andrew M, Parolis Haralambos, Grant Christopher C R, Trout-Yakel Keri M, Franklin Kristyn, Ng Lai-King, Paramonov Nikolay A, Parolis Lesley A S, Rahn Kris, Tabor Helen
Department of Medical Microbiology, 510 Medical Sciences Building, University of Manitoba, 730 William Avenue, Winnipeg, MB R3T 2N2, Canada.
Enteric Diseases Program, Bacteriology and Enteric Diseases Program, National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, MB R3E 3R2, Canada.
J Med Microbiol. 2009 Jul;58(Pt 7):884-894. doi: 10.1099/jmm.0.007187-0. Epub 2009 Jun 5.
The serotyping of O and H antigens is an important first step in the characterization of Salmonella enterica. However, serotyping has become increasingly technically demanding and expensive to perform. We have therefore sequenced additional S. enterica O antigen gene clusters to provide information for the development of DNA-based serotyping methods. Three S. enterica isolates had O antigen gene clusters with homology to the Escherichia coli O123 O antigen region. O antigen clusters from two serogroup O58 S. enterica strains had approximately 85 % identity with the E. coli O123 O antigen region over their entire length, suggesting that these Salmonella and E. coli O antigen regions evolved from a common ancestor. The O antigen cluster of a Salmonella serogroup O41 isolate had a lower level of identity with E. coli O123 over only part of its O antigen DNA cluster sequence, suggesting a different and more complex evolution of this gene cluster than those in the O58 strains. A large part of the Salmonella O41 O antigen DNA cluster had very close identity with the O antigen cluster of an O62 strain. This region of DNA homology included the wzx and wzy genes. Therefore, molecular serotyping tests using only the O41 or O62 wzx and wzy genes would not differentiate between the two serogroups. The E. coli O123 O-antigenic polysaccharide and its repeating unit were characterized, and the chemical structure for E. coli O123 was entirely consistent with the O antigen gene cluster sequences of E. coli O123 and the Salmonella O58 isolates. An understanding of both the genetic and structural composition of Salmonella and E. coli O antigens is necessary for the development of novel molecular methods for serotyping these organisms.
对O抗原和H抗原进行血清型鉴定是肠炎沙门氏菌特征描述的重要第一步。然而,血清型鉴定在技术上的要求越来越高,执行成本也越来越高。因此,我们对额外的肠炎沙门氏菌O抗原基因簇进行了测序,以提供信息用于开发基于DNA的血清型鉴定方法。三株肠炎沙门氏菌分离株具有与大肠杆菌O123 O抗原区域同源的O抗原基因簇。来自两株O58血清型肠炎沙门氏菌菌株的O抗原簇在其全长上与大肠杆菌O123 O抗原区域具有约85%的同一性,这表明这些沙门氏菌和大肠杆菌的O抗原区域是由一个共同祖先进化而来的。一株O41血清型沙门氏菌分离株的O抗原簇仅在其O抗原DNA簇序列的一部分上与大肠杆菌O123具有较低水平的同一性,这表明该基因簇的进化与O58菌株中的基因簇不同且更为复杂。沙门氏菌O41 O抗原DNA簇的很大一部分与一株O62菌株的O抗原簇具有非常接近的同一性。该DNA同源区域包括wzx和wzy基因。因此,仅使用O41或O62的wzx和wzy基因进行分子血清型检测无法区分这两个血清型。对大肠杆菌O123 O抗原多糖及其重复单元进行了表征,大肠杆菌O123的化学结构与大肠杆菌O123和沙门氏菌O58分离株的O抗原基因簇序列完全一致。对于开发用于对这些生物体进行血清型鉴定的新型分子方法而言,了解沙门氏菌和大肠杆菌O抗原的遗传和结构组成是必要的。