Siobhán Mcclean

Dr. Siobhán Mcclean


Research Focus & Metrics

Academic Career Length

37Years (1990-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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IMIrene Jurado Martín
Irene Jurado Martín
MSMaite Sainz
Maite Sainz
SMSiobhán Mcclean
Siobhán Mcclean
Pseudomonas aeruginosa is a dominant pathogen in people with cystic fibrosis (CF) contributing to morbidity and mortality. Its tremendous ability to adapt greatly facilitates its capacity to cause chronic infections. The adaptability and flexibility of the pathogen are afforded by the extensive number of virulence factors it has at its disposal, providing P. aeruginosa with the facility to tailor its response against the different stressors in the environment. A deep understanding of these virulence mechanisms is crucial for the design of therapeutic strategies and vaccines against this multi-resistant pathogen. Therefore, this review describes the main virulence factors of P. aeruginosa and the adaptations it undergoes to persist in hostile environments such as the CF respiratory tract. The very large P. aeruginosa genome (5 to 7 MB) contributes considerably to its adaptive capacity; consequently, genomic studies have provided significant insights into elucidating P. aeruginosa evolution and its interactions with the host throughout the course of infection.


1 April 1998 in European Journal of Pharmaceutical Sciences
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Journal Article
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SMSiobhán Mcclean
Siobhán Mcclean
EPEna Prosser
Ena Prosser
EMEucharia Meehan
Eucharia Meehan
DODenise O'Malley
Denise O'Malley
NCNuala Clarke
Nuala Clarke
David BraydenDavid Brayden
David Brayden

2 March 2015 in Pathogens
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LCLouise Cullen
Louise Cullen
SMSiobhán Mcclean
Siobhán Mcclean
Chronic lung infections are associated with increased morbidity and mortality for individuals with underlying respiratory conditions such as cystic fibrosis (CF) and chronic obstructive pulmonary disease (COPD). The process of chronic colonisation allows pathogens to adapt over time to cope with changing selection pressures, co-infecting species and antimicrobial therapies. These adaptations can occur due to environmental pressures in the lung such as inflammatory responses, hypoxia, nutrient deficiency, osmolarity, low pH and antibiotic therapies. Phenotypic adaptations in bacterial pathogens from acute to chronic infection include, but are not limited to, antibiotic resistance, exopolysaccharide production (mucoidy), loss in motility, formation of small colony variants, increased mutation rate, quorum sensing and altered production of virulence factors associated with chronic infection. The evolution of Pseudomonas aeruginosa during chronic lung infection has been widely studied. More recently, the adaptations that other chronically colonising respiratory pathogens, including Staphylococcus aureus, Burkholderia cepacia complex and Haemophilus influenzae undergo during chronic infection have also been investigated. This review aims to examine the adaptations utilised by different bacterial pathogens to aid in their evolution from acute to chronic pathogens of the immunocompromised lung including CF and COPD.


11 November 2013 in Microbiologyopen
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Journal Article
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ASAnthony De Soyza
Anthony De Soyza
AHAmanda J. Hall
Amanda J. Hall
EMEshwar Mahenthiralingam
Eshwar Mahenthiralingam
PDPavel Drevinek
Pavel Drevinek
WKWiesław Kaca
Wiesław Kaca
EPEu Fp7 Funded Cost Action Bm1003 “Cell Surface Virulence Determinants Of Cystic Fibrosis Pathogens”
Eu Fp7 Funded Cost Action Bm1003 “Cell Surface Virulence Determinants Of Cystic Fibrosis Pathogens”
Pseudomonas aeruginosa is a major opportunistic pathogen in cystic fibrosis (CF) patients and causes a wide range of infections among other susceptible populations. Its inherent resistance to many antimicrobials also makes it difficult to treat infections with this pathogen. Recent evidence has highlighted the diversity of this species, yet despite this, the majority of studies on virulence and pathogenesis focus on a small number of strains. There is a pressing need for a P. aeruginosa reference panel to harmonize and coordinate the collective efforts of the P. aeruginosa research community. We have collated a panel of 43 P. aeruginosa strains that reflects the organism's diversity. In addition to the commonly studied clones, this panel includes transmissible strains, sequential CF isolates, strains with specific virulence characteristics, and strains that represent serotype, genotype or geographic diversity. This focussed panel of P. aeruginosa isolates will help accelerate and consolidate the discovery of virulence determinants, improve our understanding of the pathogenesis of infections caused by this pathogen, and provide the community with a valuable resource for the testing of novel therapeutic agents.