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WCMC
Opening in 2017
$50M ($25M+ secured) basic and translational research center focused on microbiome research
Multi-disciplinary areas of research: human & animal health, agriculture, energy & environment
Opportunities & Services
Dr. Paul Kubes • [email protected] | Dr. Shaunna Huston • [email protected]
Dr. Paul Kubes
Professor, Cumming School of Medicine, University of Calgary
Director, Western Canadian Microbiome Centre
Director, Snyder Institute for Chronic Diseases
Canada Research Chair, Leukocyte Recruitment in inflammatory disease
University of Calgary • Alberta • Canada
Imaging the Developing Immunobiome
and Microbiome
As the microbiome seeds a newborn some fun-
damental and critical events occur that ensure
a co-existence between the microbiome and
the immunobiome. If this does not happen
due to antibiotic use, C-section or poor diet the
microbiome and immunobiome may evolve in
an aberrant manner and the host is set up for
chronic inflammatory disease. We can image
the immunobiome in an unprecedented fash-
ion examining all of the immune cells dynami-
cally and seeing their behavior in germ free
mice and mice exposed to different microbi-
omes. We are elucidating the key strains that
can lead to inappropriate immunity.
PROFILE
MICROBIOME PROJECTS
Dr. Kubes is the director of the Snyder Institute for
Chronic Diseases at the University of Calgary. He
holds a Canada Research Chair in Leukocyte Recruit-
ment in Inflammatory Disease, and was named the
2011 Canada Researcher of the year by CIHR. He has
published over 290 peer-reviewed papers exploring
immune response in human disease in journals like
Cell, Science, Nature Immunology and Nature Medi-
cine.
Dr. Kubes lab is committed to understanding complex
immune responses in the context of human clinical
diseases. The primary focus is to directly visualize the
roles of immune cells during Inflammation, Infection
and tissue Injury. Dr. Kubes is leading the way in di-
rectly imaging the immune system using cutting edge
technology, including spinning-disk confocal and mul-
ti-photon microscopy. By imaging complex cellular be-
haviors in real time, both in vitro and in vivo, the lab
is characterizing how immune cells, such as neutro-
phils, monocytes, NKT cells and Kupffer cells function
under physiological and pathological disease states.
The work being done in Dr. Kubes lab sheds new light
on the immune system and new ways to study im-
mune mechanisms that are relevant to human dis-
eases. These diseases include sepsis, cellulitis, hepa-
titis, stroke and lyme disease.
CONTACT
Dr. Paul Kubes | (403)-220-8558 | [email protected]
http://www.ucalgary.ca/paulkubeslab/
SPECIALTIES
Intra-vital in vivo imaging
Spinning-disk confocal microscopy
2-Photon laser scanning fluorescence
Dr. Paul Kubes
SELECT PUBLICATIONS
Wang J, Kubes P. A Reservoir of Mature Cavity
Macrophages that Can Rapidly Invade Visceral
Organs to Affect Tissue Repair. Cell. 2016 Apr
21;165(3):668-78
Zeng Z, Surewaard BG, Wong CH, Geoghegan
JA, Jenne CN, Kubes P. CRIg Functions as a
Macrophage Pattern Recognition Receptor to
Directly Bind and Capture Blood-Borne Gram-
Positive Bacteria. Cell Host Microbe. 2016 Jul
13;20(1):99-106.
Kolaczkowska E, Jenne CN, Surewaard BG,
Thanabalasuriar A, Lee WY, Sanz MJ, Mowen
K, Opdenakker G, Kubes P. Molecular mecha-
nisms of NET formation and degradation re-
vealed by intravital imaging in the liver vascu-
lature. Nat Commun. 2015 Mar 26;6:6673.
Wong CH, Jenne CN, Petri B, Chrobok NL,
and Kubes P. Nucleation of platelets with
bloodborne pathogens on Kupffer cell pre-
cedes other innate immunity and contributes
to bacterial clearance. Nature Immunology 14
(8):785-92, 2013.
Yipp BG, Petri B, Salina D, Jenne CN, Scott BN,
Zbytnuik LD, Pittman K, Asaduzzaman M, Wu
K, Meijndert HC, Malawista SE, de Boisfleury
Chevance A, Zhang K, Conly J, Kubes P. Infec-
tion-induced NETosis is a dynamic process in-
volving neutrophil multitasking in vivo. Nat
Med. 2012 Sep;18(9):1386-93.
NOTABLE ACHIEVEMENTS
Seymour Heisler Memorial Lectureship
Award (2016)
Chair Gairdner Award MAB committees,
Member F1000 (2015)
Canadian Society for Immunology Cinader
Award (2012)
CIHR Researcher of the Year (2011)
Distinguished Scholar Award, Royal Society
of Canada (2009)
Alberta Science and Technology Award for
Outstanding Leadership in Science (2005)
American Physiological Society, Henry Pick-
ering Bowditch Lectureship (2003)
Faculty of Medicine Smith Distinguished
Achievement Award for Senior Faculty
(2001, 2003)
Dr. Kathy McCoy
Professor, Cumming School of Medicine, University of Calgary
Director, Germ-Free Facility, Western Canadian Microbiome Centre
University of Calgary • Alberta • Canada
Impact of commensal microbiota
on threshold of inflammasome
Impact of microbiota on develop-
ment of immune system in early
life
Maternal microbial imprinting on
neonatal innate immune system
PROFILE
MICROBIOME PROJECT
Dr. Kathy McCoy is interested in the dynamic inter-
play between the gut microbiota and the innate and
adaptive immune systems. Using germ-free and gno-
tobiotic mouse models her research group aims to
understand how exposure to intestinal microbes
early in life educates and regulates the developing
immune system and how this impacts on suscepti-
bility to immune-mediated diseases such as allergy
and autoimmunity.
Dr. McCoy obtained her PhD in Immunology from the
Malaghan Institute of Medical Research, Otago Uni-
versity, Wellington, New Zealand. She performed her
postdoctoral studies and was a junior group leader
at the Institute of Experimental Immunology in Zü-
rich, Switzerland. She then held Asst. Professor posi-
tions at McMaster University (2006-2010) and Uni-
versity of Bern, Switzerland (2010-2016).
Dr. McCoy was recently recruited to the University of
Calgary where she continues her research on micro-
biome-immune interactions while directing the new
germ-free/gnotobiotic facility of the Western Canadi-
an Microbiome Centre (WCMC).
SPECIALTIES
Axenic embryo transfer for re-derivation
of germ-free animals
Expertise in gnotobiology & mucosal im-
munology
In vivo animal models
Dr. Kathy McCoy
SELECT PUBLICATIONS
Gomez de Agüero M, Ganal-Vonarburg SC,
Fuhrer T, Rupp S, Uchimura Y, Steinert A, Heik-
enwälder M, Hapfelmeier S, Sauer U, McCoy
KD†, Macpherson AJ†. Early postnatal innate
immune development driven by the maternal
microbiota. Science 2016 Mar 18;351
(6279):1296-302. †Equal senior authors
Zaiss MM, Rapin A, Lebon L, Dubey LK, Mosco-
ni I, Sarter K, Piersigilli A, Menin L, Walker AW,
Rougemont J, Paerewijck O, Geldhof P, McCoy
KD, Macpherson AJ, Croese J, Giacomin PR,
Loukas A, Junt T, Marsland BJ, Harris NL. The
Intestinal Microbiota Contributes to the Ability
of Helminths to Modulate Allergic Inflamma-
tion. Immunity. 2015 Nov 17;43(5):998-1010.
Li H, Limenitakis JP, Fuhrer T, Geuking MB,
Lawson MA, Wyss M, Brugiroux S, Keller I,
Macpherson JA, Rupp S, Stolp B, Stein JV,
Stecher B, Sauer U, McCoy KD, Macpherson
AJ. The outer mucus layer hosts a distinct in-
testinal microbial niche. Nat Commun. 2015
Sep 22;6:8292.
Gollwitzer ES, Saglani S, Trompette A, Yadava
K, Sherburn R, McCoy KD, Nicod LP, Lloyd CM,
Marsland BJ. Lung microbiota promotes toler-
ance to allergens in neonates via PD-L1. Nat
Med. 2014 Jun;20(6):642-7.
NOTABLE ACHIEVEMENTS
European Commission-Research and Inno-
vation Action Operating Grant (2016-2020)
Swiss National Science Foundation Operat-
ing Grant (2014-2017)
European Research Council-ERC Starting
Grant (2011-2016)
ERC Consolidator Grant (2011)
Canada Research Chair in Gastrointestinal
Immunology (2008-2010)
CONTACT
Dr. Kathy McCoy | (403) 220-6139 | [email protected]
Dr. Markus Geuking
Assistant Professor, Cumming School of Medicine, University of Calgary
Nominated for Tier II Canada Research Chair
University of Calgary • Alberta • Canada
Microbiota-mediated modulation
of antigen-specific CD4+ T helper
cells
Impact of antigen-specific
antimicrobial T helper cell
responses on the function and
composition of the microbiota
PROFILE
MICROBIOME PROJECTS
Dr. Geuking was recruited to the University of Calgary
from the University of Bern, Switzerland. He has over
30-peer reviewed publications in journals such as Sci-
ence and Immunity. The Geuking lab investigates the
interaction between the intestinal microbiota and the
host immune system in health and disease.
The team uses axenic and gnotobiotic in vivo models
in combination with genetically modified commensal
species to interrogate whether and how the microbio-
ta can modulate T helper cell responses. This allows
for controlled and defined experiments to study how
the microbiota modulates T helper cell response, but
also how, in return, T helper cell responses directed
at the microbiota impact the microbiota at the level of
transcriptional or metabolic activity and microbiota
composition. These are important parameters re-
quired for designing therapies where the microbiota
is used as a tool to therapeutically modulate immune
responses in disease.
Dr. Geukings’ lab develops genetically modified mi-
crobes as tools to study antigen-specific T helper cell
responses in gnotobiotic situations using state-of-the-
art technologies including intravital microscopy, next
generation transcriptional profiling of individual sort-
ed species, and immunophenotyping using flow and
mass cytometry as readouts.
CONTACT
Dr. Markus Geuking | (403) 220-6840 | [email protected]
SPECIALTIES
Infrastructure for germ-free and gnotobi-
otic in vivo experiments.
Genetic modification of commensal bac-
teria.
Optimized bioinformatics pipelines for
gnotobiotic conditions.
Dr. Markus Geuking
SELECT PUBLICATIONS
Li, H, Limenitakis, JP, Fuhrer, T, Geuking, MB,
Lawson, MA, Wyss, M, Brugiroux, S, Keller, I,
Macpherson, JA, Rupp, S, et al. (2015). The
outer mucus layer hosts a distinct intestinal
microbial niche. Nat Commun. 2015 Sep
22;6:8292
Mosconi I, Geuking MB, Zaiss MM, Massacand
JC, Aschwanden C, Kwong Chung CK, McCoy
KD, and Harris NL. Intestinal bacteria induce
TSLP to promote mutualistic T-cell responses.
Mucosal Immunol. 2013 Nov;6(6):1157-67
Cahenzli J, Köller Y, Wyss M, Geuking MB, and
McCoy KD. Intestinal microbial diversity during
early-life colonization shapes long-term IgE lev-
els. Cell Host Microbe. 2013 Nov 13;14
(5):559-70.
Geuking MB, Cahenzli J, Lawson MA, Ng DC,
Slack E, Hapfelmeier S, McCoy KD, and Mac-
pherson AJ. Intestinal Bacterial Colonization
Induces Mutualistic Regulatory T Cell Respons-
es. Immunity 2011 May 27;34(5):794-806.
Geuking MB, Weber J, Dewannieux M, Gorelik
E, Heidmann T, Hengartner H, Zinkernagel RM,
and Hangartner L. Recombination of re-
trotransposon and exogenous RNA virus re-
sults in nonretroviral cDNA integration. Sci-
ence 2009 Jan 16;323(5912):393-6.
NOTABLE ACHIEVEMENTS
AbbVie IBD Grant (2015)
Lutz Zwillenberg Award (2012)
Swiss National Science Foundation Am-
bizione Grant (2010)
Dr. Marie-Claire Arrieta
Assistant Professor, Cumming School of Medicine, University of Calgary
University of Calgary • Alberta • Canada
The Alberta Kids At Risk (AKAR)
Study—how microbial inheritance
and early life exposures influence
metabolic and immune
development
Early life bacterial and fungal
signatures predictive of asthma
Role of early-life exposure of
intestinal lipopolysaccharide
(LPS) in lung inflammation
Early-life microbial metabolite-
host interactions in mouse
models
PROFILE
MICROBIOME PROJECTS
Marie-Claire Arrieta, PhD is an assistant professor at
the University of Calgary. She has been studying how
intestinal alterations lead to immune diseases since
2007. During her PhD she studied the role of intesti-
nal permeability in the pathogenesis of colitis and di-
abetes. She also worked in Brett Finlay’s lab as a
postdoctoral fellow for five years, where she com-
bined her knowledge of microbes and immunology to
lead a major clinical study on the role of the microbio-
ta in asthma. She played a central role in building the
bioinformatics techniques needed to analyze the mi-
crobiota from these clinical studies and has demon-
strated that certain species of the intestinal microbio-
ta from three-month-old children determine the risk
of that child to succumb to asthma later in life. She
has been published in leading scientific journals such
as Gut, PNAS, and Science Translational Medicine.
She also co-authored a forthcoming book aimed at
parents, “Let Them Eat Dirt”, which explores how the
microbiome influences childhood development and
how a microbial alterations can lead to several im-
mune-mediated diseases. Marie-Claire’s current re-
search interests lie in the role of the intestinal micro-
biota in pediatric health and disease.
CONTACT
Dr. Marie-Claire Arrieta | (403) 220-4566 | [email protected]
SPECIALTIES
16S and 18S analysis of microbiomes
Metabolomics
Mucosal immunology of the gut and the
lung
Dr. Marie-Claire Arrieta
SELECT PUBLICATIONS
Stiemsma L, Arrieta MC, Dimitriu P, Cheng J,
Thorson L, Lefebvre D, Azad MB, Subbarao P,
Mandhane P, Becker A, Sears M, Kollmann T,
Mohn W, Finlay B, Turvey S. Shifts in Lachno-
spira and Clostridium sp. in the 3-month
stool microbiome are associated with pre-
school-age asthma. Clin Sci (Lond). 2016 Sep
15
Arrieta MC, Walter J, Finlay BB. 2016. Human
Microbiota-Associated Mice: A Model with
Challenges. Cell Host and Microbe. 19(5):575-
8
Yurist-Doutsch S, Arrieta MC, Tupin A, Valdez Y,
Antunes LC, Yen R, Finlay BB. 2016. Nutrient
Deprivation Affects Salmonella Invasion and
Its Interaction with the Gastrointestinal Micro-
biota. PLoS One. Jul 20;11(7):e0159676
Arrieta MC*, Stiemsma LT*, Dimitriu PA,
Yurist-Doutsch S, Thorson L, Brandt R,
Lefebvre D, Sears M, Kollmann T, Mc.Nagny K,
CHILD Study Investigators, Mohn WW, Turvey
S, and Finlay BB. 2015. Early infancy microbial
and metabolic alterations impact risk of child-
hood asthma. Science Translational Medi-
cine. 2015 Sep 30;7(307):307 * equal contri-
bution.
Arrieta MC, Stiemsma LT, Amenyogbe N,
Brown EM, Finlay B. 2014. The intestinal mi-
crobiome in early life: health and disease.
Front Immunol. Sep 5;5:427
NOTABLE ACHIEVEMENTS
Brett Finlay and Marie-Claire Arrieta. “Let
Them Eat Dirt: How Our Quest For Clean Is
Making Our Children Sick”. Layperson book
to be published by Algonquin Books (USA)
and Greystone Books (Canada) in Septem-
ber 2016. Translated into 10 languages.
Dr. Laura K. Sycuro
Assistant Professor, Cumming School of Medicine, University of Calgary
University of Calgary • Alberta • Canada
Incident STIs in Kenyan girls: A
prospective cohort spanning
sexual debut
N o n - n u t r i t i v e s w e e t e n e r
consumption during pregnancy:
impact on infant gut microbiome
and metabolism in the CHILD
cohort
Iron acquisition pathways in the
u p p e r r e s p i r a t o r y t r a c t
microbiome: evaluating strategies
to prevent infections
PROFILE
MICROBIOME PROJECTS
Dr. Sycuro leads a highly interdisciplinary research
group with the broad goal of harnessing the maternal
microbiome to promote healthy pregnancies. Her
team aspires to advance the precision with which we
define the composition of the human microbiome and
mechanistically link its species, strains, and genes to
reproductive health outcomes. This work is unfolding
in two directions:
1) Technology development that deepens our under-
standing of the microbiome’s pan-genomic content
and fluidity
2) Identification of important genes that are fun-
neled into interdisciplinary functional studies
Dr. Sycuro’s lab is also working to better define the
microbial communities contributing to pregnancy loss
and preterm delivery. The long-term goal of this re-
search is to identify new diagnostic markers and
treatment strategies that safely correct microbial im-
balances before they trigger early labor.
The Sycuro Lab is advancing understanding of the
human microbiome through state-of-the-art applica-
tions of high throughput sequencing technologies.
Her team is developing methods of detecting and as-
sembling the genomes of uncultivated species and
strains.
CONTACT
Dr. Laura K. Sycuro | (403) 220-4453 | [email protected]
SPECIALTIES
Bacterial & Hi-C metagenomics, compara-
tive and functional genomics and cultiva-
tion of fastidious anaerobes
Software development for NGS microbi-
ome studies
Microfluidic models of biofilms and micro-
bial communities
Dr. Laura K. Sycuro
SELECT PUBLICATIONS
Herbst-Kralovetz MM, Pyles RB, Ratner AJ, Sy-
curo LK, and Mitchell C. (2016) New systems
for studying intercellular interactions in bacte-
rial vaginosis. Journal of Infectious Disease.
214 Suppl 1:S6–S13.
Gorgos LM*, Sycuro LK*, Srinivasan S, Fiedler
TL, Morgan MT, Balkus JE, McClelland SR,
Fredricks DN, and Marrazzo JM. (2015) Rela-
tionship of specific bacteria in the cervical and
vaginal microbiotas with cervicitis.
*Contributed equally to this work. Sexually
Transmitted Diseases. 42(9): 475–81.
Sycuro LK, Rule CS, Petersen TW, Wycoff TJ,
Sessler T, Nagarkar DB, Khalid F, Pincus Z,
Biboy J, Vollmer W, and Salama NR. (2013)
Flow cytometry based enrichment for cell
shape mutants identifies multiple genes that
influence Helicobacter pylori morphology. Mo-
lecular Microbiology. 90(4): 869–83.
Sycuro LK, Pincus Z, Gutierrez KD†, Born P,
Stern CA†, Vollmer W, Salama NR. (2010) Pep-
tidoglycan crosslinking relaxation promotes
Helicobacter pylori's helical shape and stom-
ach colonization. Cell. 141(5): 822–33.
NOTABLE ACHIEVEMENTS
University of Calgary Office of the Vice Presi-
dent of Research ( 2016-2019)
Fluxion Biosciences Innovation Award
(2010)
IP Declaration : AnPhIRL: An analytical pipe-
line for identification and evaluation of ge-
nomes obtained from metagenomes; dis-
closed filing date: 2016/06/06
Dr. Mark Swain
Professor, Cumming School of Medicine, University of Calgary
Cal Wenzel Family Foundation Chair in Hepatology
Head, Division of Gastroenterology and Hepatology, University of Calgary
Section Head, Section of Gastroenterology and Hepatology, Calgary
Zone, Alberta Health Services
University of Calgary • Alberta • Canada
Influence of the microbiome on sig-
naling pathways that link peripher-
al inflammation with changes in
behavior (i.e. sickness behaviors
including fatigue, cognitive impair-
ment, mood alterations)
Gut-brain axis as it relates to
the impact of changes in the
gut the microbiome on the brain in
inflammatory bowel disease and
irritable bowel disease
PROFILE
MICROBIOME PROJECTS
Dr. Mark Swain is currently a Professor of Medicine,
Hepatologist and Clinician-Scientist at the University
of Calgary.
Dr. Swain has basic bench research programs funded
by the Canadian Institutes of Health Research in 2
areas, namely: i) Mechanisms underlying the develop-
ment of fatigue in liver disease, and ii) the innate im-
mune response in the regulation of hepatic inflamma-
tion. Dr. Swain’s clinical research is focused in the
areas of viral hepatitis and autoimmune liver disease.
Dr. Swain has published more than 100 peer-
reviewed papers and book chapters and has served
on the Editorial Boards for the scientific journals Gut,
American Journal of Physiology and Clinical Sciences.
He has won many awards for teaching and research,
including the University of Calgary Watanabe Distin-
guished Achievement Award for Overall Excellence. He
is currently the Cal Wenzel Family Foundation Chair in
Hepatology, and the Head of the Translational Re-
search Core for the Snyder Institute for Chronic Dis-
eases at the University of Calgary.
CONTACT
Dr. Mark Swain | (403) 592-5011 | [email protected]
SPECIALTIES
Animal models of liver and bowel inflam-
mation
Intravital microscopy of the cerebral vas-
culature
Functional MRI
Animal sickness behavior assessment
Microglial isolation and characterization
Dr. Mark Swain
SELECT PUBLICATIONS
NOTABLE ACHIEVEMENTS
Appointed as a Fellow of the American Asso-
ciation for the Study of Liver Diseases
(2014-present)
Elected Executive Committee member, In-
ternational Society for Hepatic Encephalo-
pathy and Nitrogen Metabolism (2014-
present)
Invited member External Advisory Commit-
tee, University of Birmingham Liver Biomedi-
cal Research Unit (2012-present)
Canadian Institutes of Health Research/
Health Canada, Joint Advisory Committee -
Hepatitis C initiative (Expert Fatigue/Quality
of Life) (1999-2004)
Faculty of Medicine Watanabe Distin-
guished Achievement Award for Overall Ex-
cellence, University of Calgary (2003)
D'Mello C, Ronaghan N, Zaheer R, Dicay M,
LeT, MacNaughton WK, Surrette MG, Swain
MG. Probiotics attenuate immune-to-brain sig-
naling and improve sickness behaviors in
mice with experimental liver disease. J Neuro-
sci, 2015 Jul 29;35(30):10821-30
Almishri W, Deans J, Swain MG. Rapid activa-
tion and hepatic recruitment of innate-like reg-
ulatory B cells after invariant NKT cell stimula-
tion in mice. J Hepatol. 2015 Oct;63(4):943-
51.
Pang JX, Zimmer S, Niu S, Crotty P, Tracey J,
Pradhan F, Shaheen AA, Coffin CS, Heitman
SJ, Kaplan GG, Swain MG, Myers RP. Liver
stiffness by transient elastography predicts
liver-related complications and mortality in
patients with chronic liver disease. PLoS One.
2014 Apr 22;9(4)
D’Mello C, Swain MG. Liver-brain interactions
in inflammatory liver diseases: implications for
fatigue and mood disorders. Brain Behav Im-
mun, 2014 Jan; 35:9-20
Swain MG, Lai M-Y, Shiffman ML, Cooksley
WGE, Zeuzem S, Dieterich DT, Abergel A,
Pessôa MG, Lin A, Tietz A, Connell EV, Diago
M. A sustained virologic response is durable in
patients with chronic hepatitis C treated with
peginterferon alfa-2a and ribavirin. Gastroen-
terology 2010;139:1593-601
Dr. Raylene Reimer
Professor, Faculty of Kinesiology, University of Calgary
Full Scientist, Alberta Children's Hospital Research Institute
University of Calgary • Alberta • Canada
Prebiotic fiber supplementation
and gut microbiota in non-alcoholic
fatty liver disease
Dietary manipulation of gut microbi-
ota to manage obesity and insulin
resistance
Effect of Inulin and Other Fiber
Source(s) on the Microbiome in
Healthy Adults
A 12-week Exercise Program for
Adults with Celiac Disease: Effects
on Quality of Life and Gut Microbio-
ta
Nutrition optimization in malnour-
ished patients with Crohn’s disease
is associated with beneficial gut
microbiome changes
PROFILE
MICROBIOME PROJECTS
Dr. Raylene Reimer is a Registered Dietitian and Uni-
versity of Calgary Professor. Her research focuses on
the role of diet in regulating energy intake and gut mi-
crobiota in the context of obesity, type 2 diabetes, and
other chronic diseases such as fatty liver disease and
inflammatory bowel disease.
She has done extensive research in animal models to
study how maternal diet during pregnancy influences
offspring's gut microbiota, satiety hormone production
and ultimately obesity risk. Her studies have identified
prebiotic fibre as a potentially valuable dietary inter-
vention in establishing a new lower set point for energy
intake and adiposity in both obese and non-obese ani-
mal models. Translating findings from animal models
to human clinical studies is a key way in which Reimer
spans bench to bedside discovery and application. Her
research group is also making progress in understand-
ing how modifying the gut microbiota with prebiotics
and probiotics affects behavior in neuropsychiatric dis-
orders including autism-spectrum disorder and obses-
sive-compulsive disorder.
Dr. Reimer holds several industry research contracts
that help take evidence-based findings into applica-
tion. She was honored in May 2012 with the Centrum
New Scientist Award for Outstanding Research
(Canadian Nutrition Society).
CONTACT
Dr. Raylene Reimer | (403) 220-8218 | [email protected]
SPECIALTIES
Dietary manipulation of gut microbiota
Prebiotics and probiotics
Clinical trials
Rodent models of the 'Developmental
Origins of Health and Disease'
Obesity and chronic disease
Dr. Raylene Reimer
SELECT PUBLICATIONS
NOTABLE ACHIEVEMENTS
Strategic Clinical Network Research and In-
novation Advisory Committee (Diabetes,
Obesity and Nutrition) (2014-present)
CIHR Chair and Scientific Officer, Nutrition,
Food & Health Peer Review Committee
(2011; 2012; 2015)
Associate Dean Graduate Education, Facul-
ty of Kinesiology, University of Calgary
(2011-2012)
Researcher of the Month – Canadians for
Health Research (2015)
Fellow of The Obesity Society (2013)
BMO Co-Chair in Healthy Living – Alberta
Children’s Hospital Foundation (2010-
2015)
Abbott Nutrition, Prebiotics Advisory Board
(Abbott Canada, Saint-Laurent, Québec,
2010)
Canada’s Top 40 Under 40 Nominee (2009)
Ho J, Reimer RA, Doulla M, Huang C (2016)
Effect of prebiotic intake on gut microbiota,
intestinal permeability and glycemic control in
children with type 1 diabetes: study protocol
for a randomized controlled trial. Trials 17
(1):347
Paul HA, Bomhof MR, Vogel HJ, Reimer RA
(2016) Diet-induced changes in maternal gut
microbiota and serum metabolomic profiles
influence programming of offspring obesity
risk in rats. Scientific Reports, Feb
12;6:20683
Klein MS, Newell C, Bomhof MR, Reimer RA,
Hittel DS, Rho JM, Vogel HJ, Shearer J (2016)
Metabolomic modelling to monitor host re-
sponsiveness to gut microbiota manipulation
in the BTBR mouse. J Proteome Res 15
(4):1143-1150
Nicolucci AC, Reimer RA (2016) Prebiotics as a
modulator of gut microbiota in paediatric obe-
sity. Pediatric Obesity Apr 13. doi: 10.1111/
ijpo.12140.
Lambert JE, Myslicki J, Bomhof MR, Belke DD,
Shearer J, Reimer RA (2015) Exercise training
modifies gut microbiota in normal and diabetic
mice. Appl Physiol Nutr Metab. 40(7):749-752
Hallam MC, Barile D, Meyrand M, German JB,
Reimer RA (2014) Maternal high protein or
prebiotic fiber diets affect maternal milk com-
position and gut microbiota in rat dams and
their offspring. Obesity 22:2344-2351.
Dr. Joe Harrison
Assistant professor, Faculty of Science, University of Calgary
Canada Research Chair in Biofilm Microbiology and Genomics
Chair, University of Calgary Biofilm Research Group
University of Calgary • Alberta • Canada
The Bugs-to-Drugs Initiative
Dr. Harrison is leading a team of researchers
that are establishing the Alberta Microbiota
Repository (ABMR), a unique collection of bac-
teria and fungi that is serving as a platform to
discover bioactive natural products from micro-
biomes. This ambitious collaborative is ena-
bling new lines of discovery-driven investiga-
tion that will advance our fundamental under-
standing of host-microbe interactions in health
and disease, and is driving innovation by iden-
tifying new therapeutic strategies for treating
plant, animal and human diseases important
to Canadians.
PROFILE
MICROBIOME PROJECTS
Biofilms are slime-covered communities of microbes
that stick to surfaces, and biofilm formation is at the
root of many chronic and device-associated human
bacterial infections. The Harrison lab seeks to under-
stand – at a molecular level – how bacteria build bio-
films that resist drugs, evade immunity and cause
infection.
Dr. Harrison studies a process called signal transduc-
tion. All living cells use this process to sense external
stimuli and trigger a chain of chemical events inside
the cell, resulting in physiological adaptation to the
environment. In many bacteria, the signal transduc-
tion process that orchestrates biofilm growth and dis-
persion depends on a key intracellular molecule, cy-
clic diguanylate (c-di-GMP). While a lot is known about
how enzymes “make and break” c-di-GMP, little is
known about the environmental stimuli that activate
and inhibit these enzymes. This is a key research ar-
ea because bacteria must use c-di-GMP signaling to
sense and respond to host stimuli to build biofilms. C-
di-GMP is a promising therapeutic target because it is
absent in mammals.
Dr. Harrison had a lead role in developing the Calgary
Biofilm Device (commercially available as the
MBECTM assay), which is now sold worldwide, serves
as an ASTM method for regulated product claims, and
is used to develop anti-biofilm agents.
CONTACT
Dr. Joe Harrison | (403) 220-7627 | [email protected]
http://contacts.ucalgary.ca/info/bio/profiles/1-4173438
SPECIALTIES
Bacterial Genomics
Gene and protein engineering/synthetic
biology
Bacterial signal transduction; especial-
ly molecular sensory perception
Antimicrobial resistance (antibiotics and
metals)
High-throughput screening; especially as
it pertains to drug-discovery via the Bugs-
to-Drugs collaborative
Biofilm microbiology
Bacterial pathogenesis
Dr. Joe Harrison
SELECT PUBLICATIONS
NOTABLE ACHIEVEMENTS
CIHR Project Scheme Grant (2016-2020)
Gold Medal - Canadian Society for Microbiol-
ogists (CSM) Canadian Graduate Student
Microbiologist of the Year (2008)
Cohen, D, U. Mechold, H. Nevenzala, J. D.
Rich, D. C. Bay, M. R. Parsek, V. Kaever J. J.
Harrison* and E. Banin* (2015) Oligoribonu-
clease is a central feature of cyclic diguanyl-
ate signalling in Pseudomonas aeruginosa.
Proceedings of the National Academy of Sci-
ences USA 112:11359-64. *equal senior au-
thors
Hmelo, L. R., B. R. Borlee, H. Almblad, M. E.
Love, T. E. Randall, B. S. Tseng, C. Lin, Y. Irie,
K. M. Storek, J. J. Yang, R. J. Siehnel, P.L.
Howell, P.K. Singh, T. Tolker-Nielsen, M. R.
Parsek, H. P. Schweizer and J. J. Harrison
(2015) Precision-engineering the Pseudomo-
nas aeruginosa genome with two-step allelic
exchange. Nature Protocols 10(11):1820-41.
Almblad, H., J. J. Harrison, M. T. Rybtke, J.
Groizeleau, M. Givskov, M. R. Parsek and T.
Tolker-Nielsen (2015) The cAMP-Vfr signaling
pathway in Pseudomonas aeruginosa is inhib-
ited by c-di-GMP. Journal of Bacteriology
197:2190-2200.
Harrison, J. J., C. A. Stremick, R. J. Turner, N.
D. Allan, M. E. Olson and H. Ceri (2010). Mi-
crotiter susceptibility testing of microbes
growing on peg lids: A miniaturized biofilm
model for high-throughput screening. Nature
Protocols 5:1236-1254.