Paul Deepjyoti, Bhattacharjee Amitabha, Bhattacharjee Dibyojyoti, Dhar Debadatta, Maurya Anand Prakash, Chakravarty Atanu
Department of Microbiology, Assam University, Silchar, India.
Department of Statistics, Assam University, Silchar, India.
Antimicrob Resist Infect Control. 2017 Feb 20;6:26. doi: 10.1186/s13756-017-0183-2. eCollection 2017.
New Delhi metallo beta-lactamase is known to compromise carbapenem therapy and leading to treatment failure. However, their response to carbapenem stress is not clearly known. Here, we have investigated the transcriptional response of and plasmid copy number alteration under carbapenem exposure.
Three harboring plasmids representing three incompatibility types (IncFIC, IncA/C and IncK) were inoculated in LB broth with and without imipenem, meropenem and ertapenem. After each 1 h total RNA was isolated, immediately reverse transcribed into cDNA and quantitative real time PCR was used for transcriptional expression of . Horizontal transferability and stability of the plasmids encoding were also determined. Changes in copy number of harboring plasmids under the exposure of different carbapenems were determined by real time PCR. Clonal relatedness among the isolates was determined by pulsed field gel electrophoresis.
Under carbapenem stress over an interval of time there was a sharp variation in the transcriptional expression of although it did not follow a specific pattern. All carrying plasmids were transferable by conjugation. These plasmids were highly stable and complete loss was observed between 92 to 96 serial passages when antibiotic pressure was withdrawn. High copy number of was found for IncF type plasmids compared to the other replicon types.
This study suggests that the single dose of carbapenem pressure does not significantly influence the expression of and also focus on the stability of this gene as well as the change in copy number with respect to the incompatible type of plasmid harboring resistance determinant.
已知新德里金属β-内酰胺酶会影响碳青霉烯类药物治疗效果并导致治疗失败。然而,它们对碳青霉烯类药物应激的反应尚不清楚。在此,我们研究了在碳青霉烯类药物暴露下的转录反应以及质粒拷贝数的变化。
将携带代表三种不相容类型(IncFIC、IncA/C和IncK)质粒的三株菌接种于含和不含亚胺培南、美罗培南和厄他培南的LB肉汤中。每1小时后分离总RNA,立即反转录为cDNA,并使用定量实时PCR检测的转录表达。还测定了编码的质粒的水平转移性和稳定性。通过实时PCR测定不同碳青霉烯类药物暴露下携带质粒的拷贝数变化。通过脉冲场凝胶电泳确定分离株之间的克隆相关性。
在一段时间的碳青霉烯类药物应激下,的转录表达虽无特定模式但有急剧变化。所有携带质粒的菌均可通过接合转移。这些质粒高度稳定,在撤除抗生素压力后,92至96次连续传代之间观察到质粒完全丢失。与其他复制子类型相比,IncF型质粒的拷贝数较高。
本研究表明单剂量碳青霉烯类药物压力不会显著影响的表达,同时也关注了该基因的稳定性以及携带耐药决定簇的不相容类型质粒的拷贝数变化。