期刊
JOURNAL OF BACTERIOLOGY
卷 203, 期 3, 页码 -出版社
AMER SOC MICROBIOLOGY
DOI: 10.1128/JB.00548-20
关键词
Legionella pneumophila; cell viability; genetic competence; genome analysis; natural transformation systems
类别
资金
- LABEX ECOFECT of Universite de Lyon [ANR-11-LABX-0048, ANR-11-IDEX-0007]
- Centre International de Recherche en Infectiologie
Legionella pneumophila, a pathogenic bacterium causing severe pneumonia in humans, has environmental life traits crucial to its infectiousness. Transposon insertion sequencing (TIS) can be used to identify essential genes and genetic basis of life traits, though its application in L. pneumophila has been limited. Successful implementation of TIS in clinical isolates of L. pneumophila has provided insights into essential genes, potential drug targets, and genes involved in horizontal gene transfer. This represents a significant step towards understanding the genetic basis of this pathogenic species.
Legionella pneumophila is a Gram-negative bacterium ubiquitous in freshwater environments which, if inhaled, can cause a severe pneumonia in humans. The emergence of L. pneumophila is linked to several traits selected in the environment, the acquisition of some of which involved intra- and interkingdom horizontal gene transfer events. Transposon insertion sequencing (TIS) is a powerful method to identify the genetic basis of selectable traits as well as to identify fitness determinants and essential genes, which are possible antibiotic targets. TIS has not yet been used to its full power in L. pneumophila, possibly because of the difficulty of obtaining a high-saturation transposon insertion library. Indeed, we found that isolates of sequence type 1 (ST1), which includes the commonly used laboratory strains, are poorly permissive to saturating mutagenesis by conjugation-mediated transposon delivery. In contrast, we obtained high-saturation libraries in non-ST1 clinical isolates, offering the prospect of using TIS on unaltered L. pneumophila strains. Focusing on one of them, we then used TIS to identify essential genes in L. pneumophila. We also revealed that TIS could be used to identify genes controlling vertical transmission of mobile genetic elements. We then applied TIS to identify all the genes required for L. pneumophila to develop competence and undergo natural transformation, defining the set of major and minor type IV pilins that are engaged in DNA uptake. This work paves the way for the functional exploration of the L. pneumophila genome by TIS and the identification of the genetic basis of other life traits of this species. IMPORTANCE Legionella pneumophila is the etiologic agent of a severe form of nosocomial and community-acquired pneumonia in humans. The environmental life traits of L. pneumophila are essential to its ability to accidentally infect humans. A comprehensive identification of their genetic basis could be obtained through the use of transposon insertion sequencing. However, this powerful approach had not been fully implemented in L. pneumophila. Here, we describe the successful implementation of the transposon-sequencing approach in a clinical isolate of L. pneumophila. We identify essential genes, potential drug targets, and genes required for horizontal gene transfer by natural transformation. This work represents an important step toward identifying the genetic basis of the many life traits of this environmental and pathogenic species.
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