Cottell Jennifer L, Saw Howard T H, Webber Mark A, Piddock Laura J V
Institute of Microbiology and Infection, School of Immunity and Infection, The College of Medical and Dental Sciences, The University of Birmingham, Birmingham B15 2TT, UK.
BMC Microbiol. 2014 Jun 24;14:168. doi: 10.1186/1471-2180-14-168.
The spread of bacterial plasmids is an increasing global problem contributing to the widespread dissemination of antibiotic resistance genes including β-lactamases. Our understanding of the details of the biological mechanisms by which these natural plasmids are able to persist in bacterial populations and are able to establish themselves in new hosts via conjugative transfer is very poor. We recently identified and sequenced a globally successful plasmid, pCT, conferring β-lactam resistance.
Here, we investigated six plasmid encoded factors (tra and pil loci; rci shufflon recombinase, a putative sigma factor, a putative parB partitioning gene and a pndACB toxin-antitoxin system) hypothesised to contribute to the 'evolutionary success' of plasmid pCT. Using a functional genomics approach, the role of these loci was investigated by systematically inactivating each region and examining the impact on plasmid persistence, conjugation and bacterial host biology. While the tra locus was found to be essential for all pCT conjugative transfer, the second conjugation (pil) locus was found to increase conjugation frequencies in liquid media to particular bacterial host recipients (determined in part by the rci shufflon recombinase). Inactivation of the pCT pndACB system and parB did not reduce the stability of this plasmid.
Our findings suggest the success of pCT may be due to a combination of factors including plasmid stability within a range of bacterial hosts, a lack of a fitness burden and efficient transfer rates to new bacterial hosts rather than the presence of a particular gene or phenotype transferred to the host. The methodology used in our study could be applied to other 'successful' globally distributed plasmids to discover the role of currently unknown plasmid backbone genes or to investigate other factors which allow these elements to persist and spread.
细菌质粒的传播是一个日益严重的全球性问题,它导致了包括β-内酰胺酶在内的抗生素抗性基因的广泛传播。我们对这些天然质粒能够在细菌群体中持续存在并通过接合转移在新宿主中定殖的生物学机制细节了解甚少。我们最近鉴定并测序了一个在全球范围内成功传播的质粒pCT,它赋予β-内酰胺抗性。
在此,我们研究了六个假定有助于质粒pCT“进化成功”的质粒编码因子(tra和pil位点;rci洗牌重组酶、一个假定的sigma因子、一个假定的parB分配基因和一个pndACB毒素-抗毒素系统)。使用功能基因组学方法,通过系统地使每个区域失活并检查对质粒持久性、接合作用和细菌宿主生物学的影响,来研究这些位点的作用。虽然发现tra位点对于所有pCT接合转移都是必需的,但发现第二个接合(pil)位点可增加在液体培养基中对特定细菌宿主受体的接合频率(部分由rci洗牌重组酶决定)。pCT pndACB系统和parB的失活并未降低该质粒的稳定性。
我们的研究结果表明,pCT的成功可能归因于多种因素的组合,包括在一系列细菌宿主中的质粒稳定性、缺乏适应性负担以及向新细菌宿主的高效转移率,而不是转移到宿主中的特定基因或表型的存在。我们研究中使用的方法可应用于其他全球分布的“成功”质粒,以发现目前未知的质粒骨干基因的作用,或研究使这些元件持续存在和传播的其他因素。