Here, we present a simple and fast screening method to preselect candidate Dickeya solani Tn5 mutants which carry transposon insertions in plant tissueinduced genes for the follow-up studies. The described method is faster and cost-effective in comparison to standard IVET, expression microarrays and RNAseq, and it does not require any specialized laboratory equipment and/or technical assistance. The Tn5 mutants are generated using mini-Tn5 transposon carrying inducible reporter gene (promoterless gusA coding for β-glucuronidase) and are screened for the β-glucuronidase positive phenotypes under non-inductive conditions with X-gluc as a glucuronidase substrate. The bacterial mutants negative in the first screen are then screened for β-glucuronidase phenotypes in the presence of plant tissues, viz. roots, stems and leaves, suspended in liquid bacterial growth medium supplemented with X-gluc in a 48-well microtiter plate assay. The mutants that are positive in the screen with plant tissues are selected for sequencing of the Tn5 insertion sites directly from bacterial genome. This method allows generation of a number of ready-to-use Tn5 mutants showing up-regulation by plant tissue which can be later selected for further studies. We used this method to evaluate interaction of D. solani IPO2222 (type strain) with bittersweet nightshade (Solanum dulcamara L.) and potato (Solanum tuberosum L.) tissues.Keywords Gene fusion . Inducible reporter system . Screening . Promoterless gusAThe ability to cause infection in plants is a complex characteristic that occurs only in limited number of known bacterial species (Vidaver and Lambrecht 2004). Understanding the molecular background of pathogen adaptations which allows bacteria to invade and colonize plant tissues and/or subvert host metabolism remains therefore a substantial challenge (Guttman et al. 2014). A considerable number of genetic techniques have been developed for bacteria, leading to identification and further analyses of genes essential for bacteria-plant interactions in vivo (Handfield and Levesque 1999). These techniques, such as IVET (In Vitro Expression Technology), RIVET (Reverse IVET) and their modifications and adaptations, signature-tagged mutagenesis (STM) and difference fluorescent induction (DFI) as well as expression microarrays and RNAseq, are used with success to determine new bacterial virulence factors, genes involved in adaptation to the plant (micro-)environment and in bacterial fitness in specific host tissues during infection. Despite the great potential of all the mentioned techniques, they are often expensive and/or require specialized laboratory equipment and skillful technical assistance.We propose here an inexpensive, high-throughput system to preselect Dickeya solani genes involved in bacteria-plant interaction with the employment of random mutagenesis using a Tn5 transposon containing Eur