首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Conjugative DNA transfer into human cells by the VirB/VirD4 type IV secretion system of the bacterial pathogen Bartonella henselae
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Conjugative DNA transfer into human cells by the VirB/VirD4 type IV secretion system of the bacterial pathogen Bartonella henselae

机译:细菌病原体汉氏巴尔通体的VirB / VirD4 IV型分泌系统将结合性DNA转移到人细胞中

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Bacterial type IV secretion systems (T4SS) mediate interbacterial conjugative DNA transfer and transkingdom protein transfer into eukaryotic host cells in bacterial pathogenesis. The sole bacterium known to naturally transfer DNA into eukaryotic host cells via a T4SS is the plant pathogen Agrobacterium tumefaciens. Here we demonstrate T4SS-mediated DNA transfer from a human bacterial pathogen into human cells. We show that the zoonotic pathogen Bartonella henselae can transfer a cryptic plasmid occurring in the bartonellae into the human endothelial cell line EA.hy926 via its T4SS VirB/VirD4. DNA transfer into EA.hy926 cells was demonstrated by using a reporter derivative of this Bartone//a-specific mobilizable plasmid generated by insertion of a eukaryotic egfp-expression cassette. Fusion of the C-terminal secretion signal of the endogenous VirB/VirD4 protein substrate BepD with the plasmid-encoded DNA-transport protein Mob resulted in a 100-fold increased DNA transfer rate. Expression of the delivered egfp gene in EA.hy926 cells required cell division, suggesting that nuclear envelope breakdown may facilitate passive entry of the transferred ssDNA into the nucleus as prerequisite for complementary strand synthesis and transcription of the egfp gene. Addition of an eukaryotic neomycin phosphotransferase expression cassette to the reporter plasmid facilitated selection of stable transgenic EA.hy926 cell lines that display chromosomal integration of the transferred plasmid DNA. Our data suggest that T4SS-dependent DNA transfer into host cells may occur naturally during human infection with Bartonella and that these chronically infecting pathogens have potential for the engineering of in vivo gene-delivery vectors with applications in DNA vaccination and therapeutic gene therapy.
机译:IV型细菌分泌系统(T4SS)在细菌发病机理中介导细菌间共轭DNA转移和transkingdom蛋白转移到真核宿主细胞中。已知可通过T4SS将DNA天然转移到真核宿主细胞中的唯一细菌是植物病原土壤杆菌。在这里,我们证明了T4SS介导的DNA从人类细菌病原体转移到人类细胞中。我们显示,人畜共患病原体汉氏巴尔通体可以通过其T4SS VirB / VirD4将发生在巴尔通体中的隐秘质粒转移到人内皮细胞系EA.hy926中。通过使用插入真核egfp表达盒而产生的该Bartone // a特异性可移动质粒的报道分子衍生物,证明了DNA转移到EA.hy926细胞中的过程。内源性VirB / VirD4蛋白底物BepD的C端分泌信号与质粒编码的DNA转运蛋白Mob融合,导致DNA转运速率提高了100倍。传递的egfp基因在EA.hy926细胞中的表达需要细胞分裂,这表明核被膜破裂可能促进转移的ssDNA被动进入核内,这是egfp基因互补链合成和转录的前提。向报道质粒中添加真核新霉素磷酸转移酶表达盒有助于选择稳定的转基因EA.hy926细胞系的选择,所述EA.hy926细胞系表现出转移质粒DNA的染色体整合。我们的数据表明,在人类感染巴尔通体的过程中,依赖T4SS的DNA转移到宿主细胞中可能会自然发生,并且这些长期感染的病原体具有体内基因传递载体工程化的潜力,可用于DNA疫苗接种和治疗性基因治疗。

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