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MarTrack: A versatile toolbox of mariner transposon derivatives used for functional genetic analysis of bacterial genomes.

Authors :
Wei, Lifan
Qiao, Haoxian
Liu, Bing
Yin, Kaiyu
Liu, Qin
Zhang, Yuanxing
Ma, Yue
Wang, Qiyao
Source :
Microbiological Research. Feb2019, Vol. 219, p84-93. 10p.
Publication Year :
2019

Abstract

Abstract The mariner transposon family of Himar1 has been widely used for the random mutagenesis of bacteria to generate single insertions into the chromosome. Here, a versatile toolbox of mariner transposon derivatives was generated and applied to the functional genomics investigation of fish pathogen Edwardsiella piscicida. In this study, we combined the merits of the random mutagenesis of mariner transposon and common efficient reporter marker genes or regulatory elements, mcherry , gfp , luxAB , lacZ , sacBR , and P BAD and antibiotic resistance cassettes to construct a series of derivative transposon vectors, p Mmch , p MKGR , p MCGR , p MXKGR , p MLKGR , p MSGR , and p MPR , based on the initial transposon p Mar2xT7. The function and effectiveness of the modified transposons were verified by introducing them into E. piscicida EIB202. Based on the toolbox, a transposon insertion mutant library containing approximately 3.0 × 105 separated mutants was constructed to explore the upstream regulators of esrB , the master regulator of the type III and type VI secretion systems (T3/T6SS) in E. piscicida. Following analysis by Con-ARTIST, ETAE_2184 (renamed as EsrR) was screened out and identified as a novel regulator mediating T3SS expression. In addition, the esrR mutants displayed critical virulence attenuation. Due to the broad-range host compatibility of mariner transposons, the newly built transposon toolbox can be broadly applied for functional genomics studies in various bacteria. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09445013
Volume :
219
Database :
Academic Search Index
Journal :
Microbiological Research
Publication Type :
Academic Journal
Accession number :
134088738
Full Text :
https://doi.org/10.1016/j.micres.2018.11.008