Li Jihong, Miyamoto Kazuaki, McClane Bruce A
Department of Molecular Genetics and Biochemistry, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USA.
Infect Immun. 2007 Apr;75(4):1811-9. doi: 10.1128/IAI.01981-06. Epub 2007 Jan 29.
Clostridium perfringens type E isolates produce iota-toxin, which is encoded by iap and ibp genes. Using Southern blot analyses, the current study identified iap/ibp plasmids of approximately 97 or approximately 135 kb among eight type E isolates. For most of these isolates, their iap/ibp plasmid also encoded urease and lambda-toxin. However, the beta2-toxin gene, if present, was on a different plasmid from the iap/ibp plasmid. For all isolates, the iap/ibp plasmid carried a tcp locus, strongly suggesting that these plasmids are conjugative. Overlapping PCR analyses demonstrated some similarity between the iap/ibp plasmids and enterotoxin-encoding plasmids of type A isolates. Additional PCR analyses demonstrated that the iap/ibp locus is located near dcm sequences, an apparent plasmid hot spot for toxin gene insertion, and that two IS1151-related sequences are present in the iap/ibp locus. To begin testing whether those IS1151-like sequences can mobilize iap/ibp genes, a PCR assay was performed that amplifies a product only from circular DNA forms that could represent transposition intermediates. This PCR assay detected circular forms containing iap/ibp genes and silent enterotoxin gene sequences, with or without an IS1151-like sequence. Collectively, these results suggest that a mobile genetic element carrying iap/ibp has inserted onto a tcp-carrying enterotoxin plasmid in a type A isolate, creating a progenitor iap/ibp plasmid. That plasmid then spread via conjugation to other isolates, converting them to type E. Further iap/ibp plasmid diversity occurred when either the iap/ibp genes later remobilized and inserted onto other conjugative plasmids or some iap/ibp plasmids acquired additional DNA sequences.
E 型产气荚膜梭菌分离株可产生埃塔毒素,该毒素由 iap 和 ibp 基因编码。通过 Southern 印迹分析,本研究在 8 株 E 型分离株中鉴定出约 97 kb 或约 135 kb 的 iap/ibp 质粒。对于这些分离株中的大多数,其 iap/ibp 质粒还编码脲酶和 λ 毒素。然而,β2 毒素基因(如果存在)位于与 iap/ibp 质粒不同的质粒上。对于所有分离株,iap/ibp 质粒携带一个 tcp 位点,强烈表明这些质粒是可接合的。重叠 PCR 分析表明,iap/ibp 质粒与 A 型分离株的肠毒素编码质粒之间存在一些相似性。进一步的 PCR 分析表明,iap/ibp 基因座位于 dcm 序列附近,dcm 序列是毒素基因插入的明显质粒热点,并且在 iap/ibp 基因座中存在两个与 IS1151 相关的序列。为了开始测试那些 IS1151 样序列是否能移动 iap/ibp 基因,进行了一项 PCR 检测,该检测仅从可能代表转座中间体的环状 DNA 形式扩增产物。该 PCR 检测检测到含有 iap/ibp 基因和沉默肠毒素基因序列的环状形式,无论是否有 IS1151 样序列。总体而言,这些结果表明,携带 iap/ibp 的可移动遗传元件已插入 A 型分离株中携带 tcp 的肠毒素质粒上,产生了一个原始的 iap/ibp 质粒。然后该质粒通过接合传播到其他分离株,将它们转化为 E 型。当 iap/ibp 基因后来重新移动并插入到其他接合质粒上,或者一些 iap/ibp 质粒获得额外的 DNA 序列时,会出现进一步的 iap/ibp 质粒多样性。