Next Generation of Tn7-Based Single-Copy Insertion Elements for Use in Multi- and Pan-Drug-Resistant Strains of Acinetobacter baumannii

被引:27
作者
Ducas-Mowchun, Kaleigh [1 ]
De Silva, P. Malaka [1 ]
Crisostomo, Leandro [1 ]
Fernando, Dinesh M. [1 ]
Chao, Tzu-Chiao [2 ]
Pelka, Peter [1 ]
Schweizer, Herbert P. [3 ]
Kumar, Ayush [1 ,4 ]
机构
[1] Univ Manitoba, Dept Microbiol, Winnipeg, MB, Canada
[2] Univ Regina, Dept Biol, Regina, SK, Canada
[3] Univ Florida, Coll Med, Dept Mol Genet & Microbiol, Emerging Pathogens Inst, Gainesville, FL USA
[4] Univ Manitoba, Manitoba Chemosensory Biol Grp, Winnipeg, MB, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
single copy; apramycin; cloning; gene expression; zeocin; ANTIBIOTIC-RESISTANCE; MINI-TN7; INSERTION; GENETIC TOOLS; ATTTN7; SITES; EXPRESSION; REPLICATION; BACTERIA; VECTORS; CLONING; ORIGIN;
D O I
10.1128/AEM.00066-19
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The purpose of this study was to create single-copy gene expression systems for use in genomic manipulations of multidrug-resistant (MDR) and extensively drug-resistant (XDR) clinical isolates of Acinetobacter baumannii. In this study, mini-Tn7 vectors with zeocin and apramycin selection markers were created by cloning the We and aac(3)-IV genes, respectively, enabling either inducible gene expression (pUC18T-mini-Tn7T-Zeo-LAC and pUC18T-mini-Tn7T-Apr-LAC) or expression from native or constitutive promoters (pUC18T-mini-Tn7T-Zeo and pUC18T-mini-Tn7T-Apr). The selection markers of these plasmids are contained within a Flp recombinase target (FRT) cassette, which can be used to obtain unmarked mini-Tn7 insertions upon introduction of a source of Flp recombinase. To this end, site-specific excision vectors pFLP2A and pFLP2Z (containing apramycin and zeocin selection markers, respectively) were created in this study as an accessory to the mini-Tn7 vectors described above. Combinations of these novel mini-Tn7 plasmids and their compatible pFLP2Z or pFLP2A accessory plasmid were used to generate unmarked insertions in MDR clinical isolates of A. baumannii. In addition, several fluorescent markers were cloned and inserted into MDR and XDR clinical isolates of A. baumannii via these apramycin and zeocin mini-Tn7 constructs to demonstrate their application. IMPORTANCE Acinetobacter baumannii is a high-priority pathogen for which research on mechanisms of resistance and virulence is a critical need. Commonly used antibiotic selection markers are not suitable for use in MDR and XDR isolates of A. baumannii due to the high antibiotic resistance of these isolates, which poses a barrier to the study of this pathogen. This study demonstrates the practical potential of using apramycin and zeocin mini-Tn7- and Flp recombinase-encoded constructs to carry out genomic manipulations in clinical isolates of A. baumannii displaying MDR and XDR phenotypes.
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页数:10
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