Control of Gene Expression in Leptospira spp. by Transcription Activator-Like Effectors Demonstrates a Potential Role for LigA and LigB in Leptospira interrogans Virulence
Author(s) -
Christopher J. Pappas,
Mathieu Picardeau
Publication year - 2015
Publication title -
applied and environmental microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.552
H-Index - 324
eISSN - 1070-6291
pISSN - 0099-2240
DOI - 10.1128/aem.02202-15
Subject(s) - leptospira , biology , leptospira interrogans , virulence , gene , pathogen , microbiology and biotechnology , genetics , virology , leptospirosis
Leptospirosis is a zoonotic disease that affects ∼1 million people annually, with a mortality rate of >10%. Currently, there is an absence of effective genetic manipulation tools for targeted mutagenesis in pathogenic leptospires. Transcription activator-like effectors (TALEs) are a recently described group of repressors that modify transcriptional activity in prokaryotic and eukaryotic cells by directly binding to a targeted sequence within the host genome. To determine the applicability of TALEs withinLeptospira spp., two TALE constructs were designed. First, a constitutively expressed TALE gene specific for thelacO -like region upstream ofbgaL wastrans inserted in the saprophyteLeptospira biflexa (the TALEβgal strain). Reverse transcriptase PCR (RT-PCR) analysis and enzymatic assays demonstrated that BgaL was not expressed in the TALEβgal strain. Second, to study the role of LigA and LigB in pathogenesis, a constitutively expressed TALE gene with specificity for the homologous promoter regions ofligA andligB wascis inserted into the pathogenLeptospira interrogans (TALElig ). LigA and LigB expression was studied by using three independent clones: TALElig1 , TALElig2 , and TALElig3 . Immunoblot analysis of osmotically induced TALElig clones demonstrated 2- to 9-fold reductions in the expression levels of LigA and LigB, with the highest reductions being noted for TALElig1 and TALElig2 , which were avirulentin vivo and nonrecoverable from animal tissues. This study reconfirms galactosidase activity in the saprophyte and suggests a role for LigA and LigB in pathogenesis. Collectively, this study demonstrates that TALEs are effective at reducing the expression of targeted genes within saprophytic and pathogenic strains ofLeptospira spp., providing an additional genetic manipulation tool for this genus.
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