Smith Theresa J, Hill Karen K, Foley Brian T, Detter John C, Munk A Christine, Bruce David C, Doggett Norman A, Smith Leonard A, Marks James D, Xie Gary, Brettin Thomas S
Integrated Toxicology Division, United States Army Medical Institute of Infectious Diseases, Fort Detrick, Maryland, United States of America.
PLoS One. 2007 Dec 5;2(12):e1271. doi: 10.1371/journal.pone.0001271.
Clostridium botulinum and related clostridial species express extremely potent neurotoxins known as botulinum neurotoxins (BoNTs) that cause long-lasting, potentially fatal intoxications in humans and other mammals. The amino acid variation within the BoNT is used to categorize the species into seven immunologically distinct BoNT serotypes (A-G) which are further divided into subtypes. The BoNTs are located within two generally conserved gene arrangements known as botulinum progenitor complexes which encode toxin-associated proteins involved in toxin stability and expression.
METHODOLOGY/PRINCIPAL FINDINGS: Because serotype A and B strains are responsible for the vast majority of human botulism cases worldwide, the location, arrangement and sequences of genes from eight different toxin complexes representing four different BoNT/A subtypes (BoNT/A1-Ba4) and one BoNT/B1 strain were examined. The bivalent Ba4 strain contained both the BoNT/A4 and BoNT/bvB toxin clusters. The arrangements of the BoNT/A3 and BoNT/A4 subtypes differed from the BoNT/A1 strains and were similar to those of BoNT/A2. However, unlike the BoNT/A2 subtype, the toxin complex genes of BoNT/A3 and BoNT/A4 were found within large plasmids and not within the chromosome. In the Ba4 strain, both BoNT toxin clusters (A4 and bivalent B) were located within the same 270 kb plasmid, separated by 97 kb. Complete genomic sequencing of the BoNT/B1 strain also revealed that its toxin complex genes were located within a 149 kb plasmid and the BoNT/A3 complex is within a 267 kb plasmid.
CONCLUSIONS/SIGNIFICANCE: Despite their size differences and the BoNT genes they contain, the three plasmids containing these toxin cluster genes share significant sequence identity. The presence of partial insertion sequence (IS) elements, evidence of recombination/gene duplication events, and the discovery of the BoNT/A3, BoNT/Ba4 and BoNT/B1 toxin complex genes within plasmids illustrate the different mechanisms by which these genes move among diverse genetic backgrounds of C. botulinum.
肉毒梭菌及相关梭菌属表达一种极强的神经毒素,即肉毒杆菌神经毒素(BoNTs),可在人类和其他哺乳动物中引发持久且可能致命的中毒。BoNT内的氨基酸变异用于将该菌属分为七种免疫上不同的BoNT血清型(A - G),这些血清型又进一步分为亚型。BoNTs位于两种通常保守的基因排列中,称为肉毒杆菌祖代复合体,其编码参与毒素稳定性和表达的毒素相关蛋白。
方法/主要发现:由于血清型A和B菌株导致了全球绝大多数人类肉毒中毒病例,因此研究了代表四种不同BoNT/A亚型(BoNT/A1 - Ba4)和一株BoNT/B1的八个不同毒素复合体的基因位置、排列和序列。二价Ba4菌株同时包含BoNT/A4和BoNT/bvB毒素簇。BoNT/A3和BoNT/A4亚型的排列与BoNT/A1菌株不同,与BoNT/A2的排列相似。然而,与BoNT/A2亚型不同的是,BoNT/A3和BoNT/A4的毒素复合体基因存在于大质粒中,而非染色体中。在Ba4菌株中,两个BoNT毒素簇(A4和二价B)位于同一个270 kb的质粒中,间隔97 kb。BoNT/B1菌株的全基因组测序还显示,其毒素复合体基因位于一个149 kb的质粒中,而BoNT/A3复合体位于一个267 kb的质粒中。
结论/意义:尽管包含这些毒素簇基因的三个质粒大小不同且所含BoNT基因各异,但它们具有显著的序列同一性。部分插入序列(IS)元件的存在、重组/基因复制事件的证据以及在质粒中发现的BoNT/A3、BoNT/Ba4和BoNT/B1毒素复合体基因,说明了这些基因在肉毒梭菌不同遗传背景间移动的不同机制。