Literature DB >> 31053588

A Novel Cre Recombinase-Mediated In Vivo Minicircle DNA (CRIM) Vaccine Provides Partial Protection against Newcastle Disease Virus.

Yanlong Jiang1, Xing Gao1, Ke Xu1, Jianzhong Wang1, Haibin Huang1, Chunwei Shi1, Wentao Yang1, Yuanhuan Kang1, Roy Curtiss2, Guilian Yang3, Chunfeng Wang3.   

Abstract

Minicircle DNA (mcDNA), which contains only the necessary components for eukaryotic expression and is thus smaller than traditional plasmids, has been designed for application in genetic manipulation. In this study, we constructed a novel plasmid containing both the Cre recombinase under the phosphoglycerate kinase (PGK) promoter and recombinant lox66 and lox71 sites located outside the cytomegalovirus (CMV) expression cassette. The strictly controlled synthesis of Cre recombinase in vivo maintained the complete form of the plasmid in vitro, whereas the in vivo production of Cre transformed the parental plasmid to mcDNA after transfection. The newly designed Cre recombinase-mediated in vivo mcDNA platform, named CRIM, significantly increased the nuclear entry of mcDNA, followed by increased production of mRNA and protein, using enhanced green fluorescent protein (EGFP) as a model. Similar results were also observed in chickens when the vaccine was delivered by the regulated-delayed-lysis Salmonella strain χ11218, where significantly increased production of EGFP was observed in chicken livers. Then, we used the HN gene of genotype VII Newcastle disease virus as an antigen model to construct the traditional plasmid pYL43 and the novel mcDNA plasmid pYL47. After immunization, our CRIM vaccine provided significantly increased protection against challenge compared with that of the traditional plasmid, providing us with a novel mcDNA vaccine platform.IMPORTANCE Minicircle DNA (mcDNA) has been considered an attractive alternative to DNA vaccines; however, the relatively high cost and complicated process of purifying mcDNA dramatically restricts the application of mcDNA in the veterinary field. We designed a novel in vivo mcDNA platform in which the complete plasmid could spontaneously transform into mcDNA in vivo In combination with the regulated-delayed-lysis Salmonella strain, the newly designed mcDNA vaccine provides us with an elegant platform for veterinary vaccine development.
Copyright © 2019 American Society for Microbiology.

Entities:  

Keywords:  DNA vaccines; Salmonella-delivered vaccines; minicircle DNA

Mesh:

Substances:

Year:  2019        PMID: 31053588      PMCID: PMC6606863          DOI: 10.1128/AEM.00407-19

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  50 in total

1.  Nuclear-associated plasmid, but not cell-associated plasmid, is correlated with transgene expression in cultured mammalian cells.

Authors:  M B James; T D Giorgio
Journal:  Mol Ther       Date:  2000-04       Impact factor: 11.454

2.  MAGIC, an in vivo genetic method for the rapid construction of recombinant DNA molecules.

Authors:  Mamie Z Li; Stephen J Elledge
Journal:  Nat Genet       Date:  2005-01-30       Impact factor: 38.330

3.  Minicircle DNA immobilized in bacterial ghosts: in vivo production of safe non-viral DNA delivery vehicles.

Authors:  Wolfgang Jechlinger; Chakameh Azimpour Tabrizi; Werner Lubitz; Peter Mayrhofer
Journal:  J Mol Microbiol Biotechnol       Date:  2004

4.  Synapsis of loxP sites by Cre recombinase.

Authors:  Kaushik Ghosh; Feng Guo; Gregory D Van Duyne
Journal:  J Biol Chem       Date:  2007-06-15       Impact factor: 5.157

5.  An araC-controlled bacterial cre expression system to produce DNA minicircle vectors for nuclear and mitochondrial gene therapy.

Authors:  B W Bigger; O Tolmachov; J M Collombet; M Fragkos; I Palaszewski; C Coutelle
Journal:  J Biol Chem       Date:  2001-04-13       Impact factor: 5.157

6.  Expression of the fusion glycoprotein of Newcastle disease virus in transgenic rice and its immunogenicity in mice.

Authors:  Zhen-Quan Yang; Qiao-Quan Liu; Zhi-Ming Pan; Hen-Xiu Yu; Xin-An Jiao
Journal:  Vaccine       Date:  2006-08-28       Impact factor: 3.641

7.  Cre-lox-based system for multiple gene deletions and selectable-marker removal in Lactobacillus plantarum.

Authors:  Jolanda M Lambert; Roger S Bongers; Michiel Kleerebezem
Journal:  Appl Environ Microbiol       Date:  2006-12-01       Impact factor: 4.792

8.  A recombinant attenuated Salmonella enterica serovar Typhimurium vaccine encoding Eimeria acervulina antigen offers protection against E. acervulina challenge.

Authors:  Vjollca Konjufca; Soo-Young Wanda; Mark C Jenkins; Roy Curtiss
Journal:  Infect Immun       Date:  2006-09-18       Impact factor: 3.441

9.  Quantification of plasmid DNA copies in the nucleus after lipoplex and polyplex transfection.

Authors:  Richard N Cohen; Marieke A E M van der Aa; Nichole Macaraeg; Ai Ping Lee; Francis C Szoka
Journal:  J Control Release       Date:  2009-01-12       Impact factor: 9.776

10.  Regulated programmed lysis of recombinant Salmonella in host tissues to release protective antigens and confer biological containment.

Authors:  Wei Kong; Soo-Young Wanda; Xin Zhang; Wendy Bollen; Steven A Tinge; Kenneth L Roland; Roy Curtiss
Journal:  Proc Natl Acad Sci U S A       Date:  2008-07-07       Impact factor: 11.205

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  2 in total

1.  Improving therapeutic potential of non-viral minimized DNA vectors.

Authors:  Lirio M Arévalo-Soliz; Cinnamon L Hardee; Jonathan M Fogg; Nathan R Corman; Cameron Noorbakhsh; Lynn Zechiedrich
Journal:  Cell Gene Ther Insights       Date:  2020-11-19

2.  Lox'd in translation: contradictions in the nomenclature surrounding common lox-site mutants and their implications in experiments.

Authors:  Daniel Shaw; Luis Serrano; Maria Lluch-Senar
Journal:  Microbiology (Reading)       Date:  2020-12-07       Impact factor: 2.777

  2 in total

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