Smith N H, Selander R K
Department of Biology, Pennsylvania State University, University Park 16802.
J Bacteriol. 1990 Feb;172(2):603-9. doi: 10.1128/jb.172.2.603-609.1990.
Previous studies of the phase 1 flagellar filament protein (flagellin) in strains of five serovars of Salmonella indicated that the central region of the fliC gene encoding the antigenic part of the protein is hypervariable both between and within serovars. To explore the possible use of this variation as a source of information on the phylogenetic relationships of closely related strains, we used the polymerase chain reaction technique to sequence part of the central region of the phase 1 flagellar genes of seven strains of Salmonella typhimurium that were known to differ in chromosomal genotype, as indexed by multilocus enzyme electrophoresis. We found that the nucleotide sequences of the central region were identical in all seven strains and determined that both the previously published sequence of the fliC gene in S. typhimurium LT2 and a report of a marked difference in the amino acid sequence of the phase 1 flagellins of two isolates of this serovar are erroneous. Our finding that the fliC gene is not evolving by sequence drift at an unusually rapid rate is compatible with a model that invokes lateral transfer and recombination of the flagellin genes as a major evolutionary process generating new serovars (antigen combinations) of salmonellae.
先前对沙门氏菌五个血清型菌株中1期鞭毛丝蛋白(鞭毛蛋白)的研究表明,编码该蛋白抗原部分的fliC基因的中心区域在血清型之间和血清型内部均具有高度变异性。为了探索这种变异作为密切相关菌株系统发育关系信息来源的可能用途,我们使用聚合酶链反应技术对七株鼠伤寒沙门氏菌1期鞭毛基因的中心区域进行了测序,这些菌株已知在染色体基因型上存在差异,通过多位点酶电泳进行索引。我们发现所有七株菌株中心区域的核苷酸序列均相同,并确定先前发表的鼠伤寒沙门氏菌LT2中fliC基因序列以及该血清型两个分离株1期鞭毛蛋白氨基酸序列存在显著差异的报告都是错误的。我们发现fliC基因并非以异常快速的速率通过序列漂移进化,这与一种模型相符,该模型认为鞭毛蛋白基因的横向转移和重组是产生沙门氏菌新血清型(抗原组合)的主要进化过程。