Billington S J, Wieckowski E U, Sarker M R, Bueschel D, Songer J G, McClane B A
Department of Veterinary Science and Microbiology, University of Arizona, Tucson, Arizona 85721, USA.
Infect Immun. 1998 Sep;66(9):4531-6. doi: 10.1128/IAI.66.9.4531-4536.1998.
Several Clostridium perfringens genotype E isolates, all associated with hemorrhagic enteritis of neonatal calves, were identified by multiplex PCR. These genotype E isolates were demonstrated to express alpha and iota toxins, but, despite carrying sequences for the gene (cpe) encoding C. perfringens enterotoxin (CPE), were unable to express CPE. These silent cpe sequences were shown to be highly conserved among type E isolates. However, relative to the functional cpe gene of type A isolates, these silent type E cpe sequences were found to contain nine nonsense and two frameshift mutations and to lack the initiation codon, promoters, and ribosome binding site. The type E animal enteritis isolates carrying these silent cpe sequences do not appear to be clonally related, and their silent type E cpe sequences are always located, near the iota toxin genes, on episomal DNA. These findings suggest that the highly conserved, silent cpe sequences present in most or all type E isolates may have resulted from the recent horizontal transfer of an episome, which also carries iota toxin genes, to several different type A C. perfringens isolates.
通过多重聚合酶链反应(PCR)鉴定出几株产气荚膜梭菌E型分离株,所有这些分离株均与新生犊牛的出血性肠炎有关。这些E型分离株被证明能表达α毒素和埃托毒素,但尽管携带了编码产气荚膜梭菌肠毒素(CPE)的基因(cpe)序列,却无法表达CPE。这些沉默的cpe序列在E型分离株中显示出高度保守性。然而,相对于A型分离株的功能性cpe基因,发现这些沉默的E型cpe序列包含9个无义突变和2个移码突变,并且缺乏起始密码子、启动子和核糖体结合位点。携带这些沉默cpe序列的E型动物肠炎分离株似乎没有克隆相关性,并且它们的沉默E型cpe序列总是位于附加体DNA上靠近埃托毒素基因的位置。这些发现表明,大多数或所有E型分离株中存在的高度保守的沉默cpe序列可能是由于最近一个携带埃托毒素基因的附加体水平转移到了几种不同的A型产气荚膜梭菌分离株中。