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作为抗鲍曼不动杆菌DNA疫苗候选物的nlpA基因的克隆与表达。

Cloning and expression of nlpA gene as DNA vaccine candidate against Acinetobacter baumannii.

作者信息

Hashemzehi Rassoul, Doosti Abbas, Kargar Mohammad, Jaafarinia Mojtaba

机构信息

Department of Molecular Genetics, Fars Science and Research Branch, Islamic Azad University, Shiraz, Islamic Republic of Iran.

Department of Molecular Genetics, Marvdasht Branch, Islamic Azad University, Marvdasht, Islamic Republic of Iran.

出版信息

Mol Biol Rep. 2018 Aug;45(4):395-401. doi: 10.1007/s11033-018-4167-y. Epub 2018 May 22.

Abstract

Acinetobacter baumannii is one of the highly antibiotic-resistant bacteria that cause infections with high rate of death. This bacterium is one the common causes of infection worldwide leading to endemic and epidemic nosocomial infections. Despite many efforts, there is no effective vaccine against A. baumannii. As NlpA is one of the important antigenic factors in biogenesis of outer membrane vesicles, and OMV-based reported vaccines in A. baumannii stimulated the immune responses, this study was aimed to clone and express nlpA gene in eukaryotic HDF cells and evaluate the induced immunization following the administration of resulting construct as DNA vaccine in BALB/c mice. The nlpA gene of A. baumannii was amplified using PCR. The PCR product was then cloned and subcloned into the pTZ57R/T and pEGFP-C2 vectors respectively. The cloning was confirmed by PCR, restriction enzyme digestion and DNA sequencing. The pEGFP-C2-nlpA recombinant plasmid was transferred into the HDF cells using electroporation and the expression of target gene was validated by RT-PCR. The recombinant construct was injected to BALB/c mice through three IM injections and the levels of IgG, IgM, INF-γ, IL-2, IL-4, and IL-12 were determined using ELISA assay. The A. baumannii nlpA gene was amplified during PCR as 867 bp band which was successfully cloned in pEGFP-C2-nlpA vector. Obtained data from RT-PCR and presence of the 867 bp fragment in transformed HDF cells confirmed the nlpA gene expression. Following the injection of pEGFP-C2-nlpA showed the increased level of IgG, IgM, INF-γ, IL-2, IL-4, and IL-12 in serum of immunized mice. Overall, through this study recombinant pEGFP-C2-nlpA was generated and successfully expressed the A. baumannii nlpA gene in eukaryotic cells. Additionally, our in vivo study confirmed that the recombinant construct capable to induce the immune response in immunized mice. These findings suggest the pEGFP-C2-nlpA may be considered as DNA vaccine candidate against A. baumannii.

摘要

鲍曼不动杆菌是一种具有高度抗生素耐药性的细菌,可导致感染,死亡率很高。这种细菌是全球感染的常见原因之一,可导致地方性和流行性医院感染。尽管付出了很多努力,但目前尚无针对鲍曼不动杆菌的有效疫苗。由于NlpA是外膜囊泡生物合成中的重要抗原因子之一,且基于外膜囊泡报道的鲍曼不动杆菌疫苗可刺激免疫反应,本研究旨在真核HDF细胞中克隆和表达nlpA基因,并在BALB/c小鼠中作为DNA疫苗给予所得构建体后评估诱导的免疫作用。使用PCR扩增鲍曼不动杆菌的nlpA基因。然后将PCR产物分别克隆并亚克隆到pTZ57R/T和pEGFP-C2载体中。通过PCR、限制性内切酶消化和DNA测序确认克隆。使用电穿孔法将pEGFP-C2-nlpA重组质粒转入HDF细胞,并通过RT-PCR验证靶基因的表达。通过三次肌肉注射将重组构建体注射到BALB/c小鼠体内,并使用ELISA测定法测定IgG、IgM、INF-γ、IL-2、IL-4和IL-12的水平。在PCR过程中扩增出867 bp条带的鲍曼不动杆菌nlpA基因,并成功克隆到pEGFP-C2-nlpA载体中。RT-PCR获得的数据以及转化的HDF细胞中867 bp片段的存在证实了nlpA基因的表达。注射pEGFP-C2-nlpA后,免疫小鼠血清中IgG、IgM、INF-γ、IL-2、IL-4和IL-12的水平升高。总体而言,通过本研究产生了重组pEGFP-C2-nlpA,并在真核细胞中成功表达了鲍曼不动杆菌nlpA基因。此外,我们的体内研究证实,重组构建体能够在免疫小鼠中诱导免疫反应。这些发现表明,pEGFP-C2-nlpA可被视为针对鲍曼不动杆菌的DNA疫苗候选物。

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