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      A decade of advances in transposon-insertion sequencing

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          Abstract

          It has been 10 years since the introduction of modern transposon-insertion sequencing (TIS) methods, which combine genome-wide transposon mutagenesis with high-throughput sequencing to estimate the fitness contribution or essentiality of each genetic component in a bacterial genome. Four TIS variations were published in 2009: transposon sequencing (Tn-Seq), transposon-directed insertion site sequencing (TraDIS), insertion sequencing (INSeq) and high-throughput insertion tracking by deep sequencing (HITS). TIS has since become an important tool for molecular microbiologists, being one of the few genome-wide techniques that directly links phenotype to genotype and ultimately can assign gene function. In this Review, we discuss the recent applications of TIS to answer overarching biological questions. We explore emerging and multidisciplinary methods that build on TIS, with an eye towards future applications.

          Abstract

          In this Review, several experts discuss progress in the decade since the development of transposon-based approaches for bacterial genetic screens. They describe how advances in both experimental technologies and analytical strategies are resulting in insights into diverse biological processes.

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          Most cited references119

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          Tn-seq; high-throughput parallel sequencing for fitness and genetic interaction studies in microorganisms

          Biological pathways are structured in complex networks of interacting genes. Solving the architecture of such networks may provide valuable information, such as how microorganisms cause disease. Here we present a method (Tn-seq) for accurately determining quantitative genetic interactions on a genome-wide scale in microorganisms. Tn-seq is based on the assembly of a saturated Mariner transposon insertion library. After library selection, changes in frequency of each insertion mutant are determined by sequencing of the flanking regions en masse. These changes are used to calculate each mutant’s fitness. Fitness was determined for each gene of the gram-positive bacterium Streptococcus pneumoniae, a causative agent of pneumonia and meningitis. A genome-wide screen for genetic interactions identified both alleviating and aggravating interactions that could be further divided into seven distinct categories. Due to the wide activity of the Mariner transposon, Tn-seq has the potential to contribute to the exploration of complex pathways across many different species.
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            Identifying genetic determinants needed to establish a human gut symbiont in its habitat.

            The human gut microbiota is a metabolic organ whose cellular composition is determined by a dynamic process of selection and competition. To identify microbial genes required for establishment of human symbionts in the gut, we developed an approach (insertion sequencing, or INSeq) based on a mutagenic transposon that allows capture of adjacent chromosomal DNA to define its genomic location. We used massively parallel sequencing to monitor the relative abundance of tens of thousands of transposon mutants of a saccharolytic human gut bacterium, Bacteroides thetaiotaomicron, as they established themselves in wild-type and immunodeficient gnotobiotic mice, in the presence or absence of other human gut commensals. In vivo selection transforms this population, revealing functions necessary for survival in the gut: we show how this selection is influenced by community composition and competition for nutrients (vitamin B(12)). INSeq provides a broadly applicable platform to explore microbial adaptation to the gut and other ecosystems.
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              Simultaneous assay of every Salmonella Typhi gene using one million transposon mutants.

              Very high-throughput sequencing technologies need to be matched by high-throughput functional studies if we are to make full use of the current explosion in genome sequences. We have generated a very large bacterial mutant pool, consisting of an estimated 1.1 million transposon mutants and we have used genomic DNA from this mutant pool, and Illumina nucleotide sequencing to prime from the transposon and sequence into the adjacent target DNA. With this method, which we have called TraDIS (transposon directed insertion-site sequencing), we have been able to map 370,000 unique transposon insertion sites to the Salmonella enterica serovar Typhi chromosome. The unprecedented density and resolution of mapped insertion sites, an average of one every 13 base pairs, has allowed us to assay simultaneously every gene in the genome for essentiality and generate a genome-wide list of candidate essential genes. In addition, the semiquantitative nature of the assay allowed us to identify genes that are advantageous and those that are disadvantageous for growth under standard laboratory conditions. Comparison of the mutant pool following growth in the presence or absence of ox bile enabled every gene to be assayed for its contribution toward bile tolerance, a trait required of any enteric bacterium and for carriage of S. Typhi in the gall bladder. This screen validated our hypothesis that we can simultaneously assay every gene in the genome to identify niche-specific essential genes.
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                Author and article information

                Contributors
                amy.cain@mq.edu.au
                vanopijn@bc.edu
                Journal
                Nat Rev Genet
                Nat. Rev. Genet
                Nature Reviews. Genetics
                Nature Publishing Group UK (London )
                1471-0056
                1471-0064
                12 June 2020
                : 1-15
                Affiliations
                [1 ]ISNI 0000 0001 2158 5405, GRID grid.1004.5, ARC Centre of Excellence in Synthetic Biology, Department of Molecular Sciences, , Macquarie University, ; Sydney, NSW Australia
                [2 ]ISNI 0000 0001 2238 295X, GRID grid.7490.a, Helmholtz Institute for RNA-based Infection Research, , Helmholtz Centre for Infection Research, ; Würzburg, Germany
                [3 ]ISNI 0000 0001 1958 8658, GRID grid.8379.5, Faculty of Medicine, , University of Würzburg, ; Würzburg, Germany
                [4 ]ISNI 0000000419368710, GRID grid.47100.32, Department of Microbial Pathogenesis, , Yale University School of Medicine, ; New Haven, CT USA
                [5 ]ISNI 0000000419368710, GRID grid.47100.32, Microbial Sciences Institute, , Yale University, ; New Haven, CT USA
                [6 ]ISNI 0000000121885934, GRID grid.5335.0, Department of Veterinary Medicine, , University of Cambridge, ; Cambridge, UK
                [7 ]ISNI 0000 0004 0444 7053, GRID grid.208226.c, Department of Biology, , Boston College, ; Boston, MA USA
                Author information
                http://orcid.org/0000-0002-4230-6572
                http://orcid.org/0000-0003-4732-2667
                http://orcid.org/0000-0001-7599-3471
                http://orcid.org/0000-0002-7069-5958
                http://orcid.org/0000-0001-6895-6795
                Article
                244
                10.1038/s41576-020-0244-x
                7291929
                32533119
                e42905df-5810-4ffd-81e4-422093897140
                © Springer Nature Limited 2020

                This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.

                History
                : 24 April 2020
                Categories
                Review Article

                bacterial genetics,mutagenesis,high-throughput screening,mobile elements

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