De Boever E H, Clewell D B, Fraser C M
Department of Biologic and Materials Sciences, School of Dentistry, The University of Michigan, Ann Arbor, MI 48109, USA.
Mol Microbiol. 2000 Sep;37(6):1327-41. doi: 10.1046/j.1365-2958.2000.02072.x.
pAM373 is a 36.7 kb conjugative plasmid in Enterococcus faecalis that encodes a response to a peptide sex pheromone, cAM373, secreted by plasmid-free (recipient) strains of enterococci. It was identified over 15 years ago as one of five plasmids in E. faecalis strain RC73 and was of interest because a related pheromone activity could be detected in culture supernatants of Staphylococcus aureus and Streptococcus gordonii. Because of increased clinical concern relating to the possibility of mobilizing vancomycin resistance determinants from enterococci, where they are becoming common, into pathogens such as S. aureus, efforts were initiated to characterize pAM373 further. The results of a complete nucleotide sequence determination of pAM373, as well as a genetic analysis of key genes related to regulation of the pheromone response, are reported here. With regard to determinants related to conjugation, the plasmid has a structural organization similar to other known pheromone-responsive plasmids such as pAD1, pCF10 and pPD1; however, there are several unique features. Although there are significant homologues relating to a pheromone-binding surface protein (TraC) and a negatively regulating protein (TraA), there is an absence of a determinant equivalent to traB of pAD1 (reduces endogenous pheromone) and a determinant for surface-exclusion protein. The precursor structure of the inhibitor peptide iAM373 was identified, and its determinant (iam373) was found to be about 500 nt upstream of an apparent transcription terminator t1. Tn917-lac insertion analyses provided interesting insights into aspects of control of the pheromone response and showed that, although the traA product is sensitive to pheromone, it appears to act differently from the traA homologue of pAD1.
pAM373是粪肠球菌中一个36.7 kb的接合性质粒,它编码对一种肽性信息素cAM373的应答,cAM373由无质粒(受体)的肠球菌菌株分泌。15多年前,它被鉴定为粪肠球菌菌株RC73中的5个质粒之一,因其在金黄色葡萄球菌和戈登链球菌的培养上清液中可检测到相关的信息素活性而受到关注。由于临床对将万古霉素耐药决定簇从肠球菌(其在肠球菌中变得普遍)转移到病原体(如金黄色葡萄球菌)的可能性日益关注,因此开始努力进一步表征pAM373。本文报道了pAM373完整核苷酸序列测定的结果,以及与信息素应答调节相关的关键基因的遗传分析。关于与接合相关的决定簇,该质粒的结构组织与其他已知的信息素应答质粒(如pAD1、pCF10和pPD1)相似;然而,存在几个独特的特征。虽然存在与信息素结合表面蛋白(TraC)和负调控蛋白(TraA)相关的显著同源物,但不存在与pAD1的traB(降低内源性信息素)等效的决定簇和表面排斥蛋白的决定簇。鉴定了抑制肽iAM373的前体结构,发现其决定簇(iam373)位于明显的转录终止子t1上游约500 nt处。Tn917-lac插入分析为信息素应答控制的各个方面提供了有趣的见解,并表明,虽然traA产物对信息素敏感,但其作用方式似乎与pAD1的traA同源物不同。