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TnSeq analysis reveals genetic determinant involved in the sensitivity of Pseudomonas towards tailocins

ABSTRACT: Identification by Tranposon Sequencing (TnSeq) of genetic determinants involved in Pseudomonas protegens sensitivity towards tailocins.

PROVIDER: PRJEB41502 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	ERR4976650_1.fastq.gz	Fastqsanger.gz
	ERR4976650_2.fastq.gz	Fastqsanger.gz
	ERR4976660_1.fastq.gz	Fastqsanger.gz
	ERR4976660_2.fastq.gz	Fastqsanger.gz
	ERR4976651_1.fastq.gz	Fastqsanger.gz

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Project description:As transposon sequencing (TnSeq) assays have become prolific in the microbiology field, it is of interest to scrutinize their potential drawbacks. TnSeq results are determined by counting transposon insertions following the PCR-based enrichment and subsequent deep sequencing of transposon insertions. Here we explore the possibility that PCR amplification of transposon insertions in a TnSeq library skews the results by introducing bias into the detection and/or enumeration of insertions. We compared the detection and frequency of mapped insertions when altering the number of PCR cycles in the enrichment step. In addition, we devised and validated a novel, PCR-free TnSeq method where the insertions are enriched via CRISPR/Cas9-targeted transposon cleavage and subsequent Oxford Nanopore sequencing. These PCR-based and PCR-free experiments demonstrate that, overall, PCR amplification does not significantly bias the results of the TnSeq assay insofar as insertions in the majority of genes represented in our library were similarly detected regardless of PCR cycle number and whether or not PCR amplification was employed. However, the detection of a small subset of genes which had been previously described as essential is indeed sensitive to the number of PCR cycles. We conclude that PCR-based enrichment of transposon insertions in a TnSeq assay is reliable but researchers interested in profiling essential genes should carefully weigh the number of amplification cycles employed in their library preparation protocols. In addition, we present a PCR-free TnSeq alternative that is comparable to traditional PCR-based methods although the latter remain superior owing to their accessibility and high sequencing depth.

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