Repository logo
 

Pathogenicity and virulence of <i>Pseudomonas aeruginosa</i>: Recent advances and under-investigated topics.

Accepted version
Peer-reviewed

Loading...
Thumbnail Image

Change log

Abstract

Pseudomonas aeruginosa is a model for the study of quorum sensing, protein secretion, and biofilm formation. Consequently, it has become one of the most intensely reviewed pathogens, with many excellent articles in the current literature focusing on these aspects of the organism's biology. Here though, we aim to take a slightly different approach and consider some of the less well appreciated (but nonetheless important) factors that affect P. aeruginosa virulence. We start by reminding the reader of the global importance of P. aeruginosa infection, and that the "virulome" is very niche - specific. Overlooked but obvious questions such as "what prevents secreted protein products from being digested by co-secreted proteases?" are discussed, and we suggest how the nutritional preference(s) of the organism might dictate its environmental reservoirs. Recent studies identifying host genes associated with genetic predisposition towards P. aeruginosa infection (and even infection by specific P. aeruginosa strains), and the role(s) of intracellular P. aeruginosa are introduced. We also discuss the fact that virulence is a high-risk strategy, and touch on how expression of the two main classes of virulence factor is regulated. A particular focus is on recent findings highlighting how nutritional status and metabolism are as important as quorum sensing in terms of their impact on virulence, and how co-habiting microbial species at the infection site impact on P. aeruginosa virulence (and vice versa). It is our view that investigation of these issues are likely to dominate many aspects of research into this WHO-designated priority pathogen over the next decade.

Description

Journal Title

Virulence

Conference Name

Journal ISSN

2150-5594
2150-5608

Volume Title

Publisher

Informa UK Limited

Rights and licensing

Except where otherwised noted, this item's license is described as Attribution 4.0 International
Sponsorship
Cystic Fibrosis Trust (SRC-017)
MRC (APP26290)
Leverhulme Trust (RPG-2023-074)
Work in the MW laboratory is supported by grants from the Leverhulme Trust, the MRC, and the UK Cystic Fibrosis Trust. Work in the CG laboratory is funded by an Academy of Medical Sciences springboard grant and the Isaac Newton Trust (Cambridge). JEVS and ICS are supported by studentships from the BBSRC. RRN is a recipient of the Benn W. Levy Vice Chancellor Award (SBS DTP). EL is recipient of a Harding Distinguished Scholarship award. LM is recipient of a Herchel Smith postdoctoral Fellowship. ASAA is recipient of the Queens’ College Alexander Crummell studentship (SBSDTP).