Fergal O'gara

Prof. Fergal O'gara

orcid

Research Focus & Metrics

Academic Career Length

56Years (1971-Present)

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

Representative Publications

View All Publications
18 August 2015 in Nature Chemical Biology
Verified
Journal Article
Open access
PDF file
MMMarnix H. Medema
Marnix H. Medema
RKRenzo Kottmann
Renzo Kottmann
PYPelin Yilmaz
Pelin Yilmaz
MCMatthew Cummings
Matthew Cummings
JBJohn B Biggins
John B Biggins
FGFrank Oliver Glöckner
Frank Oliver Glöckner
A wide variety of enzymatic pathways that produce specialized metabolites in bacteria, fungi and plants are known to be encoded in biosynthetic gene clusters. Information about these clusters, pathways and metabolites is currently dispersed throughout the literature, making it difficult to exploit. To facilitate consistent and systematic deposition and retrieval of data on biosynthetic gene clusters, we propose the Minimum Information about a Biosynthetic Gene cluster (MIBiG) data standard.

1 February 2000 in Molecular Plant-Microbe Interactions®
Verified
Journal Article
Open access
SHStephan Heeb
Stephan Heeb
YIYoshifumi Itoh
Yoshifumi Itoh
TNTakayuki Nishijyo
Takayuki Nishijyo
USUrsula Schnider
Ursula Schnider
CKChristoph Keel
Christoph Keel
DHDieter Haas
Dieter Haas
The minimal replicon of the Pseudomonas plasmid pVS1 was genetically defined and combined with the Escherichia coli p15A replicon, to provide a series of new, oligocopy cloning vectors (5.3 to 8.3 kb). Recombinant plasmids derived from these vectors were stable in growing and nongrowing cells of root-colonizing P. fluorescens strains incubated under different environmental conditions for more than 1 month.

4 December 2012 in Biology and Fertility of Soils
Verified
Journal Article
Open access
PDF file
Hao TanHao Tan
Hao Tan
MBMatthieu Barret
Matthieu Barret
MMMarlies J. Mooij
Marlies J. Mooij
OROlivia Rice
Olivia Rice
JMJohn P. Morrissey
John P. Morrissey
FOFergal O'gara
Fergal O'gara
Fertilisers, especially nitrogen (N) and phosphorus (P) supplies, are frequently used in agricultural soil management to attain high crop yields. However, the intensive application of these chemical inputs can decrease the quality of agricultural soils and increase the probability of environmental pollution. In this study, the impact of P fertilisation on the diversity of the soil bacterial community was assessed. For this, a culture-independent approach targeting 16 rRNA and phoD genes was used on DNA extracted from pasture soils subjected to three different P fertilisation regimes for a long-term (42 years). As alkaline phosphomonoesterase (ALP) is necessary for mineralisation of organic P, an inverse relationship between the level of potential ALP activity and soil available P was expected. Indeed, a lower ALP activity was observed in soil subjected to higher chemical P fertiliser input. Analysis of the prevalence of three divergent families of ALP (PhoA, PhoD and PhoX) in metagenomic datasets revealed that PhoD is the most frequent ALP in soil samples and was selected as the most representative ALP possessed by the soil bacterial communities. Diversity of the phoD phosphorus mineraliser group, as well as the total bacterial community, was both increased in response to long-term P fertilisation. Specifically, phosphorus fertilisation decreased the relative abundance of certain taxa, including Acidobacteria and Pseudomonas fluorescens. In conclusion, this study shows that P fertilisation affects the microbial diversity of soil ecosystems, which might potentially modulate the soil biogeochemical cycle.

1 April 1994 in Trends in Biotechnology
Verified
Journal Article
Closed access
DDDavid N. Dowling
David N. Dowling
FOFergal O'gara
Fergal O'gara

1 June 2001 in Current Opinion in Biotechnology
Verified
Journal Article
Closed access
UWUltan F Walsh
Ultan F Walsh
JMJohn P Morrissey
John P Morrissey
FOFergal O'gara
Fergal O'gara

21 November 2005 in Proceedings of the National Academy of Sciences
Verified
Journal Article
Closed access
PDF file
GMG. Louise Mark
G. Louise Mark
JDJ. Maxwell Dow
J. Maxwell Dow
PKPatrick D. Kiely
Patrick D. Kiely
HHHazel Higgins
Hazel Higgins
JHJill Haynes
Jill Haynes
FOFergal O'gara
Fergal O'gara
Molecules exuded by plant roots are thought to act as signals to influence the ability of microbial strains to colonize the roots and to survive in the rhizosphere. Differential bacterial responses to signals from different plant species may mediate the selection of specific rhizosphere populations. Very little, however, is known about the effects of plant exudates on patterns of bacterial gene expression. Here, we have tested the concept that plant root exudates modulate expression of bacterial genes involved in establishing microbe-plant interactions. We have examined the influence on the Pseudomonas aeruginosa PA01 transcriptome of exudates from two varieties of sugarbeet that select for genetically distinct pseudomonad populations in the rhizosphere. The response to the two exudates showed only a partial overlap; the majority of those genes with altered expression was regulated in response to only one of the two exudates. Genes with altered expression included those with functions previously implicated in microbe-plant interactions, such as aspects of metabolism, chemotaxis and type III secretion, and a subset with putative or unknown function. Use of a panel of mutants with targeted disruptions allowed us to identify previously uncharacterized genes with roles in the competitive ability of P. aeruginosa in the rhizosphere within this subset. No genes with host-specific effects were identified. Homologues of the genes identified occur in the genomes of both beneficial and pathogenic root-associated bacteria, suggesting that this strategy may help to elucidate molecular interactions that are important for biocontrol, plant growth promotion, and plant pathogenesis.