R. Paul Ross

Prof. R. Paul Ross

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Research Focus & Metrics

Academic Career Length

36Years (1991-Present)

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

Representative Publications

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13 July 2012 in Nature
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Journal Article
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MCMarcus J. Claesson
Marcus J. Claesson
IJIan Jeffery
Ian Jeffery
SCSusana Conde
Susana Conde
SPSusan E. Power
Susan E. Power
EOEibhlís O'connor
Eibhlís O'connor
POPaul W. O’toole
Paul W. O’toole

1 October 2005 in Nature Reviews Microbiology
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PCPaul Cotter
Paul Cotter
CHColin Hill
Colin Hill
RRR. Paul Ross
R. Paul Ross

24 December 2012 in Nature Reviews Microbiology
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PCPaul Cotter
Paul Cotter
RRR. Paul Ross
R. Paul Ross
CHColin Hill
Colin Hill

22 June 2010 in Proceedings of the National Academy of Sciences
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Journal Article
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MCMarcus J. Claesson
Marcus J. Claesson
SCSiobhán Cusack
Siobhán Cusack
Orla O'sullivanOrla O'sullivan
Orla O'sullivan
RGRachel Greene-Diniz
Rachel Greene-Diniz
HWHeleen de Weerd
Heleen de Weerd
POPaul O'Toole
Paul O'Toole
Alterations in the human intestinal microbiota are linked to conditions including inflammatory bowel disease, irritable bowel syndrome, and obesity. The microbiota also undergoes substantial changes at the extremes of life, in infants and older people, the ramifications of which are still being explored. We applied pyrosequencing of over 40,000 16S rRNA gene V4 region amplicons per subject to characterize the fecal microbiota in 161 subjects aged 65 y and older and 9 younger control subjects. The microbiota of each individual subject constituted a unique profile that was separable from all others. In 68% of the individuals, the microbiota was dominated by phylum Bacteroides , with an average proportion of 57% across all 161 baseline samples. Phylum Firmicutes had an average proportion of 40%. The proportions of some phyla and genera associated with disease or health also varied dramatically, including Proteobacteria , Actinobacteria , and Faecalibacteria . The core microbiota of elderly subjects was distinct from that previously established for younger adults, with a greater proportion of Bacteroides spp. and distinct abundance patterns of Clostridium groups. Analyses of 26 fecal microbiota datasets from 3-month follow-up samples indicated that in 85% of the subjects, the microbiota composition was more like the corresponding time-0 sample than any other dataset. We conclude that the fecal microbiota of the elderly shows temporal stability over limited time in the majority of subjects but is characterized by unusual phylum proportions and extreme variability.

21 May 2012 in Journal of Applied Microbiology
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EBE. Barrett
E. Barrett
RRR. Paul Ross
R. Paul Ross
POPaul O'Toole
Paul O'Toole
GFG.F. Fitzgerald
G.F. Fitzgerald
CSCatherine Stanton
Catherine Stanton
Aims To assess the ability of human intestinally derived strains of Lactobacillus and Bifidobacterium to produce γ‐aminobutyric acid (GABA). Methods and Results Strains of Lactobacillus and Bifidobacterium were grown in medium containing monosodium glutamate (MSG). Growth of the bacteria and conversion of MSG to GABA were measured. Of 91 intestinally derived bacteria assessed, one Lactobacillus strain and four strains of Bifidobacterium produced GABA. Lactobacillus brevis DPC6108 was the most efficient of the strains tested, converting up to 100% of MSG to GABA. The ability of the cultured intestinal strains to produce GABA was investigated using a simple pH‐controlled anaerobic faeces‐based fermentation, supplemented with 30 mg ml−1 MSG. The addition of Lact. brevis DPC6108 to a faeces‐based fermentation significantly increased the GABA concentration (P < 0·001), supporting the notion that this biosynthesis could occur in vivo. Conclusions The production of GABA by bifidobacteria exhibited considerable interspecies variation. Lactobacillus brevis and Bifidobacterium dentium were the most efficient GABA producers among the range of strains tested. The addition of Lact. brevis DPC6108 to the culturable gut microbiota increased the GABA concentration in fermented faecal slurry at physiological pH. Significance and Impact of the Study Identification of optimal MSG conversion to GABA by particular cultured elements of the commensal intestinal microbiota and the demonstration that this can occur under simulated in vivo conditions offer new prospects for microbiota modulation to promote health.

2 February 2015 in Microbial Ecology in Health and Disease
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Journal Article
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JRJuan Miguel Rodríguez
Juan Miguel Rodríguez
KMKiera Murphy
Kiera Murphy
CSCatherine Stanton
Catherine Stanton
RRR. Paul Ross
R. Paul Ross
OKOlivia I. Kober
Olivia I. Kober
MCMaria Carmen Collado
Maria Carmen Collado
The intestinal microbiota has become a relevant aspect of human health. Microbial colonization runs in parallel with immune system maturation and plays a role in intestinal physiology and regulation. Increasing evidence on early microbial contact suggest that human intestinal microbiota is seeded before birth. Maternal microbiota forms the first microbial inoculum, and from birth, the microbial diversity increases and converges toward an adult-like microbiota by the end of the first 3-5 years of life. Perinatal factors such as mode of delivery, diet, genetics, and intestinal mucin glycosylation all contribute to influence microbial colonization. Once established, the composition of the gut microbiota is relatively stable throughout adult life, but can be altered as a result of bacterial infections, antibiotic treatment, lifestyle, surgical, and a long-term change in diet. Shifts in this complex microbial system have been reported to increase the risk of disease. Therefore, an adequate establishment of microbiota and its maintenance throughout life would reduce the risk of disease in early and late life. This review discusses recent studies on the early colonization and factors influencing this process which impact on health.