The Gram-negative bacterium Pseudomonas aeruginosa represents a prototype of multi-drug resistant opportunistic pathogens for which novel therapeutic options are urgently required. In order to identify new candidates as potential drug targets, we combined large-scale transposon mutagenesis data analysis and bioinformatics predictions to retrieve a set of putative essential genes which are conserved in P. aeruginosa and predicted to encode cell envelope or secreted proteins. By generating unmarked deletion or conditional mutants, we confirmed the in vitro essentiality of two periplasmic proteins, LptH and LolA, responsible for lipopolysaccharide and lipoproteins transport to the outer membrane respectively, and confirmed that they are important for cell envelope stability. LptH was also found to be essential for P. aeruginosa ability to cause infection in different animal models. Conversely, LolA-depleted cells appeared only partially impaired in pathogenicity, indicating that this protein likely plays a less relevant role during bacterial infection. Finally, we ruled out any involvement of the other six proteins under investigation in P. aeruginosa growth, cell envelope stability and virulence. Besides proposing LptH as a very promising drug target in P. aeruginosa, this study confirms the importance of in vitro and in vivo validation of potential essential genes identified through random transposon mutagenesis.

In vitro and in vivo screening for novel essential cell-envelope proteins in Pseudomonas aeruginosa / Fernandez Pinar, Regina; LO SCIUTO, Alessandra; Rossi, Alice; Ranucci, Serena; Bragonzi, Alessandra; Imperi, Francesco. - In: SCIENTIFIC REPORTS. - ISSN 2045-2322. - ELETTRONICO. - 5:(2015), pp. 1-11. [10.1038/srep17593]

In vitro and in vivo screening for novel essential cell-envelope proteins in Pseudomonas aeruginosa

Fernandez Pinar, Regina;LO SCIUTO, ALESSANDRA;IMPERI, FRANCESCO
2015

Abstract

The Gram-negative bacterium Pseudomonas aeruginosa represents a prototype of multi-drug resistant opportunistic pathogens for which novel therapeutic options are urgently required. In order to identify new candidates as potential drug targets, we combined large-scale transposon mutagenesis data analysis and bioinformatics predictions to retrieve a set of putative essential genes which are conserved in P. aeruginosa and predicted to encode cell envelope or secreted proteins. By generating unmarked deletion or conditional mutants, we confirmed the in vitro essentiality of two periplasmic proteins, LptH and LolA, responsible for lipopolysaccharide and lipoproteins transport to the outer membrane respectively, and confirmed that they are important for cell envelope stability. LptH was also found to be essential for P. aeruginosa ability to cause infection in different animal models. Conversely, LolA-depleted cells appeared only partially impaired in pathogenicity, indicating that this protein likely plays a less relevant role during bacterial infection. Finally, we ruled out any involvement of the other six proteins under investigation in P. aeruginosa growth, cell envelope stability and virulence. Besides proposing LptH as a very promising drug target in P. aeruginosa, this study confirms the importance of in vitro and in vivo validation of potential essential genes identified through random transposon mutagenesis.
2015
essential genes; infection; LPS; lipoproteins; outer membrane; Pseudomonas aeruginosa; virulence
01 Pubblicazione su rivista::01a Articolo in rivista
In vitro and in vivo screening for novel essential cell-envelope proteins in Pseudomonas aeruginosa / Fernandez Pinar, Regina; LO SCIUTO, Alessandra; Rossi, Alice; Ranucci, Serena; Bragonzi, Alessandra; Imperi, Francesco. - In: SCIENTIFIC REPORTS. - ISSN 2045-2322. - ELETTRONICO. - 5:(2015), pp. 1-11. [10.1038/srep17593]
File allegati a questo prodotto
File Dimensione Formato  
Fernandez-Pinar_Vitro_2015.pdf

accesso aperto

Tipologia: Versione editoriale (versione pubblicata con il layout dell'editore)
Licenza: Creative commons
Dimensione 855.09 kB
Formato Adobe PDF
855.09 kB Adobe PDF

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/843418
Citazioni
  • ???jsp.display-item.citation.pmc??? 11
  • Scopus 22
  • ???jsp.display-item.citation.isi??? 19
social impact