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J Med Microbiol 57 (2008), 563-569; DOI: 10.1099/jmm.0.47705-0
© 2008 Society for General Microbiology
ISSN 1473-5644

Signal-mediated interactions between Pseudomonas aeruginosa and Candida albicans

Gordon McAlester1, Fergal O'Gara1,2 and John P. Morrissey1

1 Department of Microbiology, University College Cork, Ireland

2 BIOMERIT Research Centre, Biosciences Institute, University College Cork, Ireland

Correspondence
John P. Morrissey
j.morrissey{at}ucc.ie

Received 18 October 2007
Accepted 29 January 2008

Pseudomonas aeruginosa causes infections in a wide variety of hosts and is the leading cause of mortality in cystic fibrosis (CF) patients. Although most clinical isolates of P. aeruginosa share common virulence determinants, it is known that strains evolve and change phenotypically during CF lung infections. These changes can include alterations in the levels of N-acyl homoserine lactones (HSLs), which are secreted signal molecules. In the CF lung, fungi, especially Candida albicans and Aspergillus fumigatus, may coexist with P. aeruginosa but the implications for disease are not known. Recent studies have established that signalling can occur between P. aeruginosa and C. albicans, with the bacterial molecule 3-oxo-C12HSL affecting Candida morphology, and the fungal metabolite farnesol reducing levels of the Pseudomonas quinolone signal and pyocyanin in Pseudomonas. Whether these interactions are common and typical in clinical strains of P. aeruginosa was addressed using CF isolates that produced varied levels of HSLs. It was found that, whereas some clinical P. aeruginosa strains affected C. albicans morphology, others did not. This correlated closely with the amounts of 3-oxo-C12HSL produced by the isolates. Furthermore, it was established that signalling is bidirectional and that the C. albicans molecule farnesol inhibits swarming motility in P. aeruginosa CF strains. This work demonstrates that clinical isolates of these opportunistic pathogens can interact in strain-specific ways via secreted signals and illustrates the importance of studying these interactions to fully understand the microbial contribution to disease in polymicrobial infections.

Abbreviations: CF, cystic fibrosis; HSL, N-acyl homoserine lactone; PQS, Pseudomonas quinolone signal; PVC, polyvinyl chloride; QS, quorum sensing.






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