Issue 6 , December 2012 - CRIP
Transcription
Issue 6 , December 2012 - CRIP
A Message from the Director 2012 was a busy year which was rich in emotion for the Centre! First, we hosted two events during the spring: the Café-CRIP in April with the valued collaboration of the Centre québécois de valorisation des biotechnologies and our annual Symposium in May. These activities are important for the CRIP for several reasons. It encourages networking between our members, our students and our partners in the agri-food industry; it demonstrates our expertise and ability to lead innovative projects that generate solutions for the industry; and it exposes the Centre to national and international scientific community. Our calendar for 2013 is already completely booked. As expected, everyone will be asked to participate and collaborate at our future meetings. The road towards CRIPA During the summer, the preparation of our application to renew our Fonds de recherche du Québec-Nature et technologies (FRQ_NT) Strategic Cluster funding has kept us busy. First and foremost, we have a new name: CRIPA! And following this great team effort, I would like to sincerely thank all the members for their involvement and constructive comments. This renewal will breathe new life into our group by the addition of the poultry production to our scientific program. This will add 10 new members to CRIPA and will raise our total regular and associated membership to 40. The application was submitted on November 1st and will be presented in January 2013 to the FRQ_NT visiting committee. We will then patiently wait for their decision. With all these changes, I would like to sincerely thank some members that have left for other positions or endeavours and those that have retired! Their scientific contribution, promotion of the CRIP and participation in CRIP activities was remarkable and appreciated. Thank you! I invite you to read this 6th edition of the Info-CRIP that highlights the activities of our research group and its members. This is an edition that marks a new historical direction for our Centre. Have a good read, Josée Harel, director Welcome to Our New Members During the preparation of our application for renewal, we recruited several individuals to become members of our strategic cluster. These new recruits will enrich and diversify the expertise in the CRIPA. For some (*), their mandate will begin only with the renewal of CRIPA. We welcome them and here is a brief description of the new members. Maryse Boucher*, professor, CEGEP de Saint-Hyacinthe. She is the only college researcher and is a microbiologist-immunologist. She teaches biology in several programs including: nursing, animal health, dental hygiene, biotechnology, dietetic and natural sciences. Since October 2012, her research has taken place at Cintech agroalimentaire where she provides technical support in microbiology. Email: [email protected]. Martine Boulianne*, full professor, Faculté de médecine vétérinaire, Université de Montréal. Her research interest is poultry: with feathers, carcass and eggs. She investigates the risk associated with Salmonella and Campylobacter contamination. Alternatives to antibiotic use are also part of her research priorities. Email: [email protected]. Web page: www.medvet.umontreal.ca/sciences_cliniques/boulianne.htm. Younès Chorfi*, assistant professor, Faculté de médecine vétérinaire, Université de Montréal. His research interests focus on the effect of mycotoxins on the health and performance of animals, the immune system and susceptibility to infectious diseases. He is also interested in improving animal health through improved nutrition and feed. Email: [email protected]. Caroline Duchaine, full professor, Université Laval. She has an interest in environmental microbiology, specifically in the domains of aerobiology and aerovirology. These domains study air-born particles of biologic and viral origin. Email:[email protected]. Web Page: http://www.bioaerosols.ulaval.ca/equipe/ Sébastien P. Faucher, assistant professor, McGill University, Macdonald Campus. His research interests are focused on host-pathogen interactions, more specifically in the virulence factors and regulatory networks that are involved in these interactions. His favorite bacterium is Legionella pneumophila. Email: [email protected]. Web page: http://www.faucherlab.com/ Ismail Fliss*, full professor, Faculté des sciences de l’agriculture et de l’alimentation, Université Laval. He is interested in the role of probiotics and probiotic bacteria in the prevention and resistance to enteric infections. The use of rapid detection methods of pathogenic microflora (DNA probes, PCR, RT-PCR, NASBA) and in vitro simulation of the human digestive system are also part of his research. Email: [email protected]. Web page: www2.ulaval.ca/ulaval_ca/recherche/chercheur/fiche/241602.html Info-CRIP No 6 – December 2012 2 Philippe Fravalo, associate professor, Faculté de médecine vétérinaire, Université de Montréal. His main research interests are important pathogens associated with food-borne infections and food-borne pathogen surveillance in the poultry and porcine industries. Email: [email protected]. Web page: www.medvet.umontreal.ca/professeurs/pfravalo.htm Frédéric Guay*, full professor, Faculté des sciences de l’agriculture et de l’alimentation, Université Laval. His research focuses on the management and nutrition of pigs, vitamin and mineral nutrition, organic swine production and mycotoxins. Email: [email protected]. Web page: www2.ulaval.ca/ulaval_ca/recherche/chercheur/fiche/364523.html. Yvan L’Homme, researcher, Canadian Food Inspection Agency, Saint-Hyacinthe. He works on the discovery, characterization and classification of new viruses, and on epidemiology and control of enteric viruses in production animals and humans. He is also interested in virology and food-borne viruses, vaccines, zoonotic pathogens, viral indicators of contamination and microbial synergy. Email: [email protected]. Nicholas Ogden, researcher, Public Health Agency of Canada. His interests are on the ecology of Lyme disease and of other vector-borne diseases and zoonosis. He is also interested in risk prediction associated with climate changes, and the development of methods to improve surveillance and control of infectious diseases. Email: [email protected]. Xin Zhao*, full professor, McGill University. His research interests are focused on microbial virulence factors that affect the host immune system, mechanisms used by bacterial pathogens to initiate intestinal infections and the development of vaccines, prebiotics and probiotics as alternatives to antibiotics. Email: [email protected]. Web page: http://www.mcgill.ca/animal/staff/faculty/zhao. News from Our Members In the last year, several members have had outstanding news and here is some of the news that made it to us: Denis Archambault, UQAM Dr. Archambault and Andrea Gomez Corredor, a postdoctoral fellow at the Institut de Recherches Cliniques de Montréal, published novel results in May in the prestigious Journal of Virology. Their work characterized the pathway involved in the Rev uptake pathways involved in the regulation of viral genes. This discovery also identified new drug targets that could be developed to fight AIDS. Steve Charette, Université Laval Dr. Charette was awarded third place in the “La Preuve par l’image 2012” contest hosted by Acfas with his picture entitled “La forêt des affamés”. Info-CRIP No 6 – December 2012 3 Martin Chénier, McGill University The work published in Microbial Ecology by Dr. Chénier and his team was the subject of an opinion piece in Science on the persistence of antibiotic resistance in the environmental microflora of pig farms. news.sciencemag.org/sciencenow/2011/drug-resistance-loiters-on-antib.html. Martine Denicourt, Université de Montréal Dr. Denicourt was appointed Vice-president of the executive committee for the Association des vétérinaires en industrie animale, AVIA. J. Daniel Dubreuil, Université de Montréal "The Whole Shebang: The Gastrointestinal Tract, Escherichia coli Enterotoxins and Secretion". Dr. Dubreuil just published an extensive review on diarrhea caused by E. coli. This review explores the interaction between pathogenic E. coli and the intestinal system which includes the nervous system and the diverse factors leading to diarrhea. The review is available for those interested in understanding the mechanisms involved in E. coli infection, the different toxins produced and their effect on the gastro-intestinal system in clicking to this link: http://www.horizonpress.com/cimb/v/v14/71.pdf. Marcelo Gottschalk, Université de Montréal Dr. Gottschalk is co-author of a clinical study on cirrhotic adults that have eaten uncooked pork meat and showed S. suis infection that involved two new serotypes. In September 2011, the research team published the results of this study entitled: "Sepsis and spontaneous bacterial peritonitis in Thailand" in The Lancet, vol 378: 960. The team of Dr. Gottschalk has secured funding from the Association of Universities and Colleges of Canada for an International Development project between Canada, Latin America and the Antilles. The funded project will collect data regarding infections caused by Streptococcus suis, a pathogen of human and pig. John M. Fairbrother and Éric Nadeau, Université de Montréal Prevtec microbial is a spin-off business from the Escherichia coli Laboratory (Ecl) and is lead by Drs. John M. Fairbrother and Éric Nadeau. Coliprotec, a vaccine developed by the company, has been approved in Brazil. Prevtec has also signed an agreement with the French multinational corporation, Virbac, to distribute the vaccine in France. « Prevtec Microbia : Chez les tsars ou chez l'Oncle Sam ? ». lapresseaffaires.cyberpresse.ca/prevtecmicrobia-chez-les-tsars-ou-chez-loncle-sam-.php. Prevtec was also the subject of a new report in La Presse as for an emerging innovative company: affaires.lapresse.ca/prevtec-microbia-visele-monde.php. In July, Dr. Fairbrother received the ALUMNI Award 2012 from the University of Sydney in Australia that recognised his exceptional contribution to the international scientific community. Ann Letellier, Université de Montréal Dr. Letellier has received the Vétoquinol award for research which recognises the contribution of a member of the teaching staff to train graduated veterinary science students. Mariela Segura, Université de Montréal The article “Streptococcus suis Capsular Polysaccharide Inhibits Phagocytosis through Destabilization of Lipid Microdomains and Prevents Lactosylceramide-Dependent Recognition” by Mariela Segura and her research team which includes two other members of the CRIP, Dr. Marcelo Gottschalk and Dr. Marie-Rose Van Calsteren, was published in the February edition of Info-CRIP No 6 – December 2012 4 Infection and Immunity of the American Society for Microbiology. This article was selected for a spotlight which highlights research of great scientific interest especially for the novelty of the discovery and its scientific merit. In September, Dr. Segura received a Women of Distinction award, a prestigious award from the Women’s Y Foundation of Montréal. The award recognizes her involvement in the domain of sciences and technologies. Congratulation Mariela! News from the Administrative Center Good retirement Manon Coutellier! Last June, the GREMIP honored Manon Coutellier, also secretary at the CRIP, for her well-deserved retirement. Everyone thanks her for her good advice, her meticulous and keen work, and her attention to detail that simplified the life of GREMIP and CRIP members without forgetting numerous hours worked behind the scenes. Her departure left a vacancy that has been occupied since June by Isabelle Flibotte. Welcome Isabelle! A birth at the CRIP! At the beginning of June, Cécile Crost, coordinator at the CRIP, left for her maternity leave. Since then, the birth of her son Paul has kept her busy! Cécile is back since December 10. Anne-Marie Christen took over Cécile’s job during her leave. Anne-Marie’s mandate with the CRIP will be done at the end of January 2013. It’s official, the egg comes from the chicken! On October 10th 2012, the Fédération des producteurs d’œufs de consommation du Québec (FPOCQ) invited their partners to participate in a guided tour to learn about all the branches of their industry. As a new partner, the CRIP was represented by the author and, as a witness, she can now confirm that the egg comes from the chicken. First, a bus brought around fifty participants to Ferme avicole Marie Pierre which is located in Roxton Pond. This family-owned farm produces eggs for human consumption. At the farm, we were able to see all the equipment and facilities required for egg production, including the heating system, automatic feeders, egg collectors, manure management, biosecurity and the preparation of the eggs to be shipped to the grading station. About two days after the eggs are laid, the eggs are sent by refrigerated truck to Nutri-Oeuf in Saint-Hyacinthe. At the plant, the eggs are washed, candled, graded, cartoned, packaged and sent to different supermarket chains and grocery stores. Several operations are automated but a pair of eyes is always needed at the grading station to spot and remove the cracked eggs. The guided tour ended at Vitoeuf Inc, a family-owned business that transforms eggs into its liquid and hard boiled forms. We would like to thank the FPOCQ for this interesting visit and initiative! Anne-Marie Christen, CRIP coordinator Info-CRIP No 6 – December 2012 5 CRIP Activities in 2012 During the last year, several activities were organized by the CRIP to create networking opportunities for students, members and our partners. Here is a summary of the events highlighting the work of several CRIP members. The 5th Symposium Our 5th Annual Symposium was held on May 16 and 17 at the Faculté de médecine vétérinaire (FMV) of the Université de Montréal. The event was possible due to the generous financial support of PFIZER animal health, OLYMEL, ELANCO, MIA CELLAVIE Inc, BIOAMERICA, QIAGEN and the FMV. High quality conferences A total of 125 participants were present for four presentations that covered the field of immunology, bacterial pathogenesis, virology and public health which were presented by Drs. Volker Gerdts from the University of Saskatchewan (VIDO), David Francis of South Dakota University (USA), Hans Nauwynck from Ghent University (Belgium) and Wondwossen Gebreyes of Ohio State University (USA), respectively. Left to Right : David Francis, Hans Nauwynck, Josée Harel, Volker Gerdts, Wondwossen Gebreyes et Carl A. Gagnon Dr. Martin Lessard from the Dairy and Swine Research and Development Centre of Agriculture and Agri-Food Canada in Sherbrooke presented his latest results regarding the use of chitosan as an antigen transporter in the intestinal tract. Our Trainees We were impressed by the quality of the oral presentations given by 14 students in the CRIP. The 27 poster presentations were also of a high scientific calibre. A workshop on careers associated with animal health was also given by Jean-François Marquis (Vertex Pharmaceutical) and Sébastien Faucher (McGill University). This workshop was a success and appreciated by the students. Dr. Pascal Dubreuil, Vice-dean for Clinical Affairs of the FMV, presented the awards for the best and second best oral and poster presentations. Best oral presentations: 1st place: Damian Clarke, a FMV student supervised by Dr. Mariela Segura, for his presentation entitled “Role of CD4+ T cells in the immune response against encapsulated Group B Streptococcus”. 2nd place: Rémi Lavoie, a FMV student supervised by Drs. Josée Harel and Christine Martin, for his presentation entitled “Single‐cell measurement of F165.1 and Pap phase variation in real‐time”. Best Posters: 1st place: Bruno Haas a Université Laval student supervised by Dr. Daniel Grenier for his poster entitled “DNase activity of Streptococcus suis: Left to right : Pascal Dubreuil, Damian Clarke, Josée Harel, Rémi Lavoie, Chan Wu and Bruno Haas Info-CRIP No 6 – December 2012 6 Characterization and possible roles in virulence”. 2nd place: Chan Wu, a FMV student supervised by Dr. Mario Jacques, for her poster entitled “Zinc as an agent for the prevention of biofilm formation by pathogenic bacteria”. Café-CRIP Why and how to control biofilms in the agri-food industry? Dr Mario Jacques from the CRIP teamed up with the Centre québécois de valorisation des biotechnologies (CQVB) and its dynamic animal health Director, Mrs Dora Rodriguez, to host its second Café-CRIP on April 24th. More than 80 participants from universities and the agri-food sector interested in the impact of biofilms in the agri-food industry learned about the efficacy of equipment disinfection and the treatment of infections with antibiotics. Left to Right: MM. Michel Pouliot, Merle E. Olson, Mario Jacques, Sylvain Fournaise, Phil Stewart, Luc Lagacé and Dora Rodriguez from CQVB The five speakers were Mr. Phil Stewart (Center for Biofilm Engineering, Montana State University, USA), Mr. Luc Lagacé (Centre ACER inc., Québec), Mr. Merle E. Olson (Innovotech inc., Alberta), Mr. Michel Pouliot (Agropur, Québec) and Mr. Sylvain Fournaise (Olymel, Québec). They presented on the challenges, surveillance, innovation and protocols associated with the control of biofilms in different agri-food industries including the maple, milk and meat transformation. The take home message was that biofilms can be controlled but may not always be eradicated. A summary was prepared by the CQVB and is available on CRIP’s web site (in French only). To learn more about biofilms, you can obtain the French publication « BioTendance®: Les biofilms: s'en préoccupe-t-on assez dans l'industrie agroalimentaire ? » produced by CQVB by clicking the following hyperlink: Pourquoi et comment contrôler les biofilms dans l'industrie agroalimentaire ? - Publication. Lunch-Conferences of the GREMIP/CRIP In the last year, the students, members and guests of the CRIP have had the opportunity to acquire new knowledge during the nine lunch conferences hosted by the GREMIP/CRIP. These interesting presentations offered an opportunity to explore new research field, and to chat in a relaxed atmosphere with high level researchers. A renowned visitor – Dr. Roy Curtiss III In October, Dr. Roy Curtiss III presented a talk entitled “Induction of Cellular Immunity and Delivery of DNA Vaccines by Recombinant Salmonella” during the FMV research day in association with the 30 year anniversary of the GREMIP. Dr. Curtiss is the director of the Center for Infectious Diseases and Vaccinology and Microbial Genetic Engineering at the Dr Roy Curtiss III, professor at Biodesign Institute and he is also a leader in the field of genetic Arizona State University and molecular pathogenicity of bacteria. The research goals of the Center for Infectious Diseases and Vaccinology and Microbial Genetic Engineering are to Info-CRIP No 6 – December 2012 7 develop vaccines to prevent enteric and respiratory infectious disease in humans and animals, including poultry. Dr. Curtiss III’s work and discoveries have resulted in the publication of more than 250 scientific articles and the creation of several patents. Presentations given in the previous year are summarized in the following table: Invited Speakers Date Titles 2011 Jean-Pierre Vaillancourt, FMV, UdeM November 17 Les Belles soirées de l’Université de Montréal Recherche en biosécurité à la ferme / Orientations futures Steve Charette, U Laval December 8 Modèle infectieux amibe et Streptococcus suis 2012 Luke Masson, IRB, CRNC February 16 Ken Dewar, U McGill April 12 Michel Desjardins, UdeM May 10 Christian Baron, UdeM June 5 Guy-Pierre Martineau, École nationale vétérinaire de Toulouse, France June 8 Timothy Geary, U McGill October 4 Roy Curtiss III, U of Arkansas October 17 Customized DNA Microarrays: Handy tools for pathogen detection and source tracking Intestinal microbiome variation in vervet monkeys in a common environment with a controlled diet La contribution de la protéomique à la connaissance des fonctions du phagosome Développement d’inhibiteurs des systèmes de sécrétion comme médicaments antimicrobiens Le GREMIP et les pathocénoses Resistance to macrocyclic lactone preventatives in the dog heartworm Dirofilaria immitis Induction of Cellular Immunity and Delivery of DNA Vaccines by Recombinant Salmonella Workshops for Students In addition to the annual symposium and the lunch-conferences, several workshops are organised for students to help them acquire new knowledge and diversify their skill sets. Technical Workshops of the CRIP Two technical workshops were held this year, one in statistics and one in microscopy. March 30 – Comprendre et appliquer les statistiques paramétriques en biologie By Gabriel Perron, Ph. D., Department of System Biology, Harvard University Twenty-two students and members of the CRIP benefited from Dr. Perron’s teaching during this biostatics workshop. The t-test, the general linear models and linear regression models are no longer mysterious for these students! Info-CRIP No 6 – December 2012 8 September 27 2012 - Microscopie de fluorescence quantitative : aspects pratiques By Judith Lacoste, Ph. D., MIA CELLAVIE Inc. This interesting and practical workshop gave an overview of the proper use of microscope. Dr. Lacoste presented several practical tricks to ensure that good quality images are acquired with a microscope. A PDF file is available on the CRIP website for those that unfortunately missed this workshop. The file can be obtained by clicking here: www.crip.umontreal.ca/documents/documents/MicFluoAspectsPrat27sep2012_JLacoste.pdf Bursaries from FPPQ, CRIP and FRQ_NT Gaël Auray was awarded a $25,000 study grant from the Fédération des producteurs de porcs du Québec! Gaël is a post-doctoral fellow in the laboratory of Dr. Marcelo Gottschalk at the FMV. He won a contest held by the FPPQ and he was awarded a $25,000 study grant. Congratulation Gaël! And a sincere thank for the financial support of the FPPQ! Gaël Auray receiving his grant from Mr. Normand Martineau of the FFPQ In 2011, this study grant was awarded to Fernando Alvarez, master candidate student in the laboratory of Dr. Carl A. Gagnon, FMV, UdeM. Need-based Bursaries Master: Maryline Bouchard (UdeM), Guillaume Goyette-Desjardins (UdeM), Cristelle Karam, (UQAM) and Jean-Philippe Auger (UdeM) were each awarded a $5,000 bursary. Doctoral: Sébastien Crépin (IAF, INRS), Alexandre Thibodeau (UdeM), Virginie Lachapelle (UdeM) and Bruno Haas (U Laval) were each awarded a $6,000 bursary. Travel Grants Eleven travel grants were awarded to the following students: Clément Muzika (UdeM), Mohammed Chekabab, (UdeM), Jean-Philippe Côté (UdeM), Devin Holman (U McGill), Claude Lachance (UdeM), Amélie Garénaux (IAF, INRS), Yannick Tremblay (UdeM), Skander Hathroubi (UdeM), Christian Savard (UdeM), Fernando Alvarez (UdeM) and Yenney Hernandez Reyes (UdeM). The next contest will be organised in February 2013. FRQ_NT Postdoctoral Grant In May 2012, Christian Savard, postdoctoral fellow in the laboratory of Dr. Carl A. Gagnon, was awarded a $60,000 grant from FRQ_NT for a period of two years. Congratulations to all our students! Info-CRIP No 6 – December 2012 9 An international internship bursary from FRQ_NT An internship in Japan Why not? “I greatly encourage student to learn about the international internship bursary. Several interesting bursaries are offered every year by different agencies including the FRQ_NT. This is a unique opportunity to have a great learning experience for students that they will remember all their lives.” David Roy, student at the Faculté de médecine vétérinaire, Université de Montréal. First and foremost, the choice of Japan for my internship was based on a desire to acquire new technical knowledge and to develop a new collaboration between the laboratory of Dr. Mariela Segura and the Japanese team of Dr. Takamatsu. I have to say that for a first international internship, Japan was the best destination to get me out of my comfort zone because Japan is the opposite of Quebec. I jumped at the opportunity to do an international internship because it offered a great professional development opportunity and allowed me to discover a country and a culture that is greatly different than my own. When I arrived, the first thing I noticed was the cleanliness and the effort people put into maintaining the country clean and, also their attention to detail. I then began to experience homesickness and, the most difficult aspect, the language barrier. Few Japanese people speak English. However, they were welcoming and their cheerfulness was contagious. These aspects helped overcome the language barrier and the homesickness and this made the integration into the research team and Japanese culture easier. During my stay, I lived in the international student residence and this gave me the opportunity to meet other international students and make new friends, including individuals from Thailand and India. Training Received Since my first internship at the GREMIP, I have worked with several genetic tools developed by Dr. Takamatsu’s group. My internship in Japan gave me the opportunity to meet our collaborators. I sought to benefit from their expertise in order to clarify several aspects of their protocol and to ask for advice to help me navigate the future steps of my research project. While I was there, I tried to learn as much as possible about the genetic tools the Japanese laboratory developed, which I use on a regular basis in Quebec. Given that I had a basic knowledge of the mutation vector developed by Dr. Takamatsu, I was able to learn different applications for the vector series that are available. During my internship, I developed plasmids to be used for interspecies gene-exchange for genes located in the polysaccharide capsule encoding locus. Info-CRIP No 6 – December 2012 10 Thus, this training reinforced my knowledge but also added value to the genetic tools I will be using for different projects in Dr. Segura’s laboratory. When I had free time, I was also able to work on Dr. Takamatsu’s personal project which involves a pathogen of bees. The advantages of an international internship Of course, an international internship is not limited to working. Although Japanese are dedicated and hard workers, I was able to use my free time to visit their beautiful country. In Japan, 2-3 days is enough time to visit several cities because their public transit is extraordinary. However, certain places or islands are only reachable by plane or boat and to visit these several days off are required. Despite the limited time to travel, I visited several cities with different attractions and features. This allowed me to appreciate the different aspects of Japan. Kyoto is the old capital that has ancestral architecture worth seeing. The current capital of Japan, Tokyo, is an urban jungle especially the “electric” district of Asakusa. The town that I will remember the most is the small coastal town of Hitachi. This town had a nice view of the sea, ports, boats and a few homes devastated by the tsunami of 2011. The town also has a beautiful fish market with several seafood restaurants. I loved the place because you could feel the passion that the Japanese have for fishing and the products of sea. Despite the language barrier, I was well received in Japan. The Japanese are very welcoming people and are always happy to share their customs and traditions. Japan is country with a rich history and it was interesting to talk to people about their culture. You can feel their pride in their values. If you can learn a few Japanese words and some of their customs, your effort will be greatly appreciated. What surprised me the most was the number of time people were surprised that I used chop-stick to eat and how often I was complimented on my dexterity with the chopsticks. This international internship was the first time I worked in an environment abroad. This gave me the opportunity to develop both personally and professionally. Working with a Japanese research team helped me learn to adapt to new environments by integrating myself in a new team that has different working norms and cultures. Being able to adapt is an important research skill because science is a field where collaboration, exchange of ideas and networking is a must. David Roy The Fonds de recherche du Québec-Nature et technologies is acknowledged for his financial support of this internship. Info-CRIP No 6 – December 2012 11 CRIP 2011-2012 Graduates Doctorat Assaad Elias, 2011/11. Carboxyméthyl amidon et son complexe avec du chitosane comme excipients pour des formulations pharmaceutiques; Director Mircea Alexandru Mateescu; Collaborator Martin Lessard. Chantal Forest, 2011/11. Étude fonctionnelle de l’opéron fimbriaire stg de Salmonella enterica serovar Typhi; Director France Daigle. Rima Habib, 2011/11. Rôle des régulateurs de fer pour la virulence chez Escherichia coli; Director Charles M. Dozois. Andrea Gomez Corredor, 2011/11. Caractérisation moléculaire et fonctionnelle de la protéine REV du virus de l’immunodéficience bovine (VIB); Director Denis Archambault. Richard Graveline, 2012/02. Étude des mécanismes moléculaires influençant la variation de phase des adhésines P, F1651 et CS31A présentes chez des souches d’Escherichia coli pathogènes; Directors Josée Harel and Christine Martin. Marc Lemieux, 2012/06. Le carboxyméthyl amidon de faible à haut degré de substitution : Excipient multifonctionnel pour des formes pharmaceutiques à administration orale; Director Mircea Alexandru Mateescu and Patrick Gosselin. Wilfried Saron, 2012/06. Expression chez les plantes de protéines recombinantes pour des procédures vaccinales : Cas de l’artévirus porcin et de la flagelline de Salmonella typhimurium; Director Denis Archambault and Fathey Sarhan. Marie-Ève Charbonneau, 2012/08. Étude de la biogenèse de l’autotransporteur AIDA-1 d’Escherichia coli; Director Michael Mourez. Sébastien Crépin, 2012/10. Role of the Pho regulon for virulence and gene regulation in pathogenic E. coli; Director Charles M. Dozois and Josée Harel. Master Paul Kiswendsida Kaboré, 2012/02. Étude de prévalence et associations des gènes de virulence et résistance aux antimicrobiens d’Escherichia coli de la flore intestinale du poulet sain; Director John M. Fairbrother and Ann Letellier. Claudia Hamida Syed, 2012/05. Escherichia coli STb toxin induces apoptosis in intestinal epithelial cell lines; Director J. Daniel Dubreuil. Info-CRIP No 6 – December 2012 12 New Initiatives Since 2006, a total of 18 projects New Initiatives have been funded by CRIP. They allowed the training of about 30 students and postdoctoral fellows and some research assistants. These projects have generated scientific publications, presentation of conferences and posters to national and international congresses, new research collaboration, new research proposals and patent registration. And as these New Initiatives projects have an important impact on CRIP research, they will maintain under our next 2013-2019 funding period. The table below presents titles and investigators involved in New Initiatives projects in 2011 and 2012. Investigator Co-investigators Project Titles 2012 La portion C-terminale de la protéine d’adhésion P97 de Mycoplasma hyopneumoniae : Une molécule adjuvante à des fins vaccinales Evaluation of a new treatment to control the exacerbated proinflammatory response in Streptococcus suis infected hosts Rôle des biofilms bactériens dans la persistance de virus pathogènes du porc dans l’environnement de la ferme D. Archambault, UQAM M. Segura, UdeM C. A. Gagnon, UdeM M. G. Gottschalk, UdeM M. Segura, UdeM M. Jacques, UdeM C. A. Gagnon, UdeM D. Grenier, U Laval 2011 Identification de facteurs de virulence chez le pathogène Streptococcus suis à l’aide d’un modèle alternatif d’hôte D. Grenier, U Laval M. G. Gottschalk, UdeM S. Charette, U Laval Relation entre protozoaires aquatiques et survie d’Escherichia coli producteur de Shiga toxines dans l’environnement : Implication du régulon Pho J. Harel, UdeM F. Daigle, UdeM C. M. Dozois, IAF, INRS Results for the 2010 Competition – New initiatives Zinc as an agent for the prevention of biofilm formation by pathogenic bacteria Principal investigator: Co-investigators: Dr. Mario Jacques, FMV, Université de Montréal Dr. Marie Archambault, FMV, UdeM Dr. Daniel Grenier, Université Laval Trainees: Chan Wu, MSc student, FMV, UdeM Dr. Yannick Tremblay, postdoctoral fellow, FMV, UdeM Research Assistant: Josée Labrie, FMV, UdeM Biofilms are a structured community of micro-organisms enclosed in an extracellular matrix. Biofilms are associated with the persistence of several infectious diseases. The extracellular matrix of biofilms protects bacteria against the host immune system, antibiotics and disinfectants. Recently, the laboratory of Dr Jacques demonstrated that zinc could inhibit the formation of biofilms by Actinobacillus pleuropneumoniae, a bacterial pathogen of swine. Based on this observation, the authors wanted to investigate the effect of zinc on the growth and biofilm Info-CRIP No 6 – December 2012 13 formation of different swine pathogens including Bordetella bronchiseptica, Escherichia coli, Haemophilus parasuis, Salmonella, Staphylococcus aureus et Streptococcus suis. Bacteria were grown in 96-well plates under optimal biofilm formation conditions. The biofilms were then stained with crystal violet. The presence of a biofilm was confirmed using confocal laser scanning microscopy and the fluorescent stain FilmTracerTM FM® 1-43. At micromolar concentrations, zinc weakly inhibited bacterial growth and blocked biofilm formation in a dosedependent manner for A. pleuropneumoniae, Salmonella Typhimurium and H. parasuis. Additionally, biofilm formation by E. coli, S. aureus and S. suis was weakly inhibited by zinc. "Confocal laser scanning microscopy images of Salmonella biofilms grown in the presence of different ZnCl2 concentrations. Biofilms were stained with FilmTracer FM 1-43, a fluoresecent marker." Image A indicates less presence of biofilm and image C indicates a strong biofilm formation. Our results indicate that zinc has an inhibitory effect on biofilm formation of several bacterial pathogens of porcine origin. However, the mechanism behind the antibiofilm properties of zinc has yet to be characterized. Structure determination of Streptococcus suis type 14 capsular polysaccharide Principal investigator: Co-investigators: Dr. Mariela Segura, FMV, Université de Montréal Dr. Marcelo Gottschalk, FMV, UdeM Dr. Marie-Rose Van Calsteren, CRDA, AAC Dr. Nahuel Fittipaldi, Methodist Hospital Research Institute, USA Trainees: David Roy, MSc student, FMV, UdeM Guillaume Goyette-Desjardins, MSc student, FMV, UdeM Cynthia Calzas, PhD student, FMV, UdeM Streptococcus suis is a major swine pathogen responsible for important economic losses to the swine industry worldwide and an emerging zoonotic agent of meningitis and streptococcal toxic shock-like syndrome. In Southeast and East Asia, this bacterium affects not only people working in the pig industry but also the general population, and it represents a significant public health concern. In the very last years, as a direct consequence of intensified research efforts, large amounts of data on putative virulence factors have appeared in the literature. Among them, the capsular polysaccharide (CPS) is considered as the most critical for bacterial virulence. Of the 35 serotypes described based on CPS composition, most studies have been done on S. suis serotype 2, which is classically associated with swine and human disease. In addition to serotype 2, S. suis serotype 14 has been described as being an important swine pathogen and an emerging zoonotic agent. Human cases of meningitis and severe sepsis with Info-CRIP No 6 – December 2012 14 shock and multiple organ failure have been described in Western countries, including Canada, and many strains are isolated each year from diseased pigs. Our knowledge on pathogenesis of the disease induced by S. suis serotype 14 or on the virulence factors involved is scarce. The complete genome sequence of this serotype has recently been published and we report here for the first time the structure determination of S. suis serotype 14 CPS using chemical, chromatographic, and spectroscopic methods. Lectin binding, physicochemical properties and biosynthesis were also investigated. The CPS structure was compared with that of other streptococcal antigens. The CPS of S. suis serotype 14 was purified, chemically modified, and characterized. Sugar and absolute configuration analyses gave the following CPS composition: D-Gal, 3; D-Glc, 1; D-GlcNAc, 1; D-Neu5Ac, 1. The Sambucus nigra lectin, which recognizes the Neu5Ac(α2– 6)Gal/GalNAc sequence, showed binding to the native CPS. Sialic acid was found to be terminal, and the CPS was quantitatively desialylated by mild acid hydrolysis. It was also submitted to periodate oxidation followed by borohydride reduction and Smith degradation. Sugar and methylation analyses, 1H and 13C nuclear magnetic resonance, and mass spectrometry of the native CPS or of its specifically modified products allowed to determine the repeating unit sequence: [6)[Neu5Ac(α2–6)Gal(β1–4)GlcNAc(β1–3)]Gal(β1– 3)Gal(β1-4)Glc(β1]n. S. suis serotype 14 CPS has an identical sialic acid-containing side chain as serotype 2 CPS, but differs by the absence of rhamnose in its composition. The same side chain is also present in group B Streptococcus type Ia CPS, except that in the latter sialic acid is 2,3- rather than 2,6-linked to the following galactose. A correlation between the S. suis CPS sequence and genes of the serotype 14 cps locus encoding putative glycosyltransferases and polymerase responsible for the biosynthesis of the repeating unit is proposed. Info-CRIP No 6 – December 2012 15 Advances in Research Laboratoire d’épidémiologie et de médecine porcine (LEMP) Sylvie D’Allaire, Benjamin Delisle and Marie-Ève Lambert Collaborators: Julie Arsenault and Martine Denicourt, FMV, UdeM Tools to improve PRRS control Porcine reproductive and respiratory syndrome (PRRS) costs the Canadian swine industry approximately 130 Million CAD annually. Increasing our knowledge of PRRS virus (PRRSV) epidemiology is one of the best investments to improve disease management in the field and to reduce production costs. Rapid advancement in molecular biology as led to the development of molecular diagnosis tools that are readily available to the practitioners. The challenge is now to integrate the molecular-based data with traditional epidemiological data to gain a maximum knowledge on PRRSV transmission to facilitate herd and regional control of the disease. The LEMP continuously updates and maintains a Quebec PRRSV database of more than 2600 sequences, collected over the past 15 years, combined with geographical and demographical herd information, serving both field and research purposes. Through this database, the laboratory provides active and constant support to participating veterinarians for several Quebec ARC&E initiatives. Reports on circulating PRRSV strains are produced using phylogenetic, spatial and statistical software to facilitate the interpretation of sequencing results and to maximize its use in the field. Also, members of the LEMP currently investigate various reporting and analysis tools integrating sequence data for area regional control and elimination (ARC&E) projects in Canada in order to propose optimal methods of reporting circulating strains in support to these initiatives. This project aims to compile existing reporting methodologies and outputs available, to describe and prioritize the applications of PRRSV sequencing data in ARC&E and to evaluate current and potential analysis options to meet identified priorities. The value, limitations, and ongoing feasibility of delivering these reports on a timely basis to current and future projects will be presented as well as the objectives and feasibility of comparing sequence data between different ARC&E projects. From a research perspective, several direct and indirect transmission pathways of the virus have been reported, but their relative importance remains to be established. The LEMP is currently developing a methodology integrating traditional and molecular data in order to assess various aspects of PRRSV transmission dynamic using a multidisciplinary approach. More specifically, several methods available for classifying PRRSV strains into genetic clusters are and will be evaluated as well as the potential for generating automatically the classification to manage more efficiently incoming PRRSV sequence submissions on a timely basis. Recombination events will also be examined in order to avoid phylogenetic misclassification of strains, to gain insight into molecular structures involved in sequence cross over and to describe herd and neighbourhood characteristics of farms involved in these events. Spatial and temporal dispersal of PRRSV strains will be evaluated to understand dynamic of PRRSV populations as a part of a global assessment of the importance of various sources of contamination. Members of the LEMP are also interested in developing a methodological approach to identify the most likely source of virus introduction into a herd by analyzing the likelihood of herd Info-CRIP No 6 – December 2012 16 contacts through various pathways (e.g. animal source, employees, airborne transmission…) among herds sharing genetically similar PRRSV strains. This could serve as guidelines to prioritize interventions on specific risk factors to limit introduction of a new PRRSV strain taking into account the different herd characteristics such as production type, flow of animals, etc. All the information gained through these latter research projects will be helpful in decision making and risk assessment. For further information, please contact: Dr. Sylvie D’Allaire, [email protected] Benjamin Delisle, [email protected] Dr. Marie-Ève Lambert, [email protected] Following is a list of LEMP articles published during the last year. Epidemiological investigations in regard to porcine reproductive and respiratory syndrome (PRRS) in Quebec, Canada. Part 1: Biosecurity practices and their geographical distribution in two areas of different swine density Lambert ME, Poljak Z, Arsenault J, D’Allaire S Prev Vet Med. 2012 April; 104 (1-2): 74-83. Porcine reproductive and respiratory syndrome virus (PRRSV) is a considerable threat to the swine industry and implementing biosecurity measures is essential for the control of its transmission. The aims of this study were: (1) to describe biosecurity practices in production sites located in a moderate density (MD) and a high density (HD) pig area according to production type; (2) to group sites in different patterns according to their biosecurity practices; and (3) to determine the geographical distribution of sites according to biosecurity patterns. Biosecurity practices were selected based on PRRS epidemiology. A questionnaire was completed on 125 breeding sites (MD = 54; HD = 71) and 120 growing (HD) sites, between 2005 and 2008. Depending on area and production type, the frequency of biosecurity practices used ranged from 0 to 2% for barrier at site entrance, 0 to 19% for use of shower, 25 to 35% for washing truck between loads of pigs, 51 to 57% for absence of rendering or rendering without access to the site, and 26 to 51% for absence of gilt purchase or purchase with quarantine. Better practices pertaining to entrance protocol (i.e. “no-entry” sign, shower, ≥24 h downtime) were reported more frequently on breeding sites in the MD than the HD area (P < 0.05). In the HD area, growing sites had in general a lower level of biosecurity than breeding sites. Using a two-step clustering procedure performed separately for breeding and growing sites, two different patterns were obtained for each production type, which corresponded to a high and low level of biosecurity. For breeding sites, a higher biosecurity level was observed at sites located away from other pig sites, set at more than 300 m from the public road, having higher sow inventory, or being part of an integrated production (P < 0.05). Spatial clusters of sites for each biosecurity pattern were detected. This study identified some shortcomings regarding biosecurity that should be addressed before implementing any PRRSV regional control. Vicinity of sites with different biosecurity levels also suggests difficulties in planning priorities of intervention based on geographical distribution of sites. Info-CRIP No 6 – December 2012 17 Epidemiological investigations in regard to porcine reproductive and respiratory syndrome (PRRS) in Quebec, Canada. Part 2: Prevalence and risk factors in breeding sites Lambert ME, Arsenault J, Poljak Z, D’Allaire S Prev Vet Med. 2012 April; 104 (1-2): 84-93. Porcine reproductive and respiratory syndrome virus (PRRSV) is a major threat for swine industry and understanding factors involved in its epidemiology is undoubtedly essential for disease control. As a part of larger project, a cross-sectional study was performed on breeding sites in a moderate density area of swine production in Quebec to estimate the prevalence of PRRSV infected sites and to evaluate if characteristics of sites and biosecurity practices, either as specific measures or as a global score, were associated with PRRSVstatus. A questionnaire and diagnostic procedures were performed on 54 breeding sites between September 2006 and August 2008. A biosecurity score that had been previously computed using two-step clustering procedure was used, classifying breeding sites into two biosecurity patterns (high vs. low) according to 21 specific biosecurity measures. The apparent prevalence of PRRSV infected sites was 74.0% (95% CI, 60.3–85.0). Univariable and multivariable logistic regression models with robust standard errors adjusting for potential clustering of sites due to same ownership were computed. In a first multivariable model evaluating characteristics of sites and specific biosecurity variables, four main effects were significantly associated (P < 0.05) with PRRSV positive status: large pig inventory (OR: 10.7), proximity to closest pig site (OR: 7.3), absence of shower (OR: 8.7) and free access to the main entrance of the site by the rendering truck (OR: 7.0). In a second multivariable model including a global biosecurity score as a surrogate for a specific pattern of biosecurity measures, this score was not retained in the final model. The adjusted population attributable fractions were 16% for the proximity to closest pig site variable, 27% for the absence of shower variable, and 10% for the free access to main entrance of the site by the rendering truck. These two latter biosecurity measures, manageable directly on the site, should be prioritized and be part of any intervention strategy designed for PRRSV control. Correlation among genetic, Euclidean, temporal, and herd ownership distances of porcine reproductive and respiratory syndrome virus strains in Quebec, Canada Lambert ME, Arsenault J, Poljak Z, D’Allaire S BMC Veterinary Research 2012 June, 8:76. Porcine reproductive and respiratory syndrome (PRRS) is a viral disease that has a major economic impact for the swine industry. Its control is mostly directed towards preventing its spread which requires a better understanding of the mechanisms of transmission of the virus between herds. The objectives of this study were to describe the genetic diversity and to assess the correlation among genetic, Euclidean and temporal distances and ownership to better understand pathways of transmission. A cross-sectional study was conducted on sites located in a high density area of swine production in Quebec. Geographical coordinates (longitude/latitude), date of submission and ownership were obtained for each site. ORF5 sequencing was attempted on PRRSV positive sites. Proportion of pairwise combinations of strains having ≥98% genetic homology were analysed according to Euclidean distances and ownership. Correlations between genetic, Euclidean and temporal distances and ownership were assessed using Mantel tests on continuous and binary matrices. Sensitivity of the correlations between genetic and Euclidean as well as temporal distances was evaluated for different Euclidean and temporal distance thresholds. An ORF5 sequence was identified for 132 of the 176 (75%) PRRSV positive sites; 122 were wild-type strains. The mean (min-max) genetic, Euclidean and temporal pairwise distances were 11.6% (0–18.7), 15.0 km (0.04-45.7) and 218 days (0–852), respectively. Significant positive correlations were observed between genetic and ownership, genetic and Euclidean and between genetic and temporal binary Info-CRIP No 6 – December 2012 18 distances. The relationship between genetic and ownership suggests either common sources of animals or semen, employees, technical services or vehicles, whereas that between genetic and Euclidean binary distances is compatible with area spread of the virus. The latter correlation was observed only up to 5 km. This study suggests that transmission of PRRSV is likely to occur between sites belonging to the same owner or through area spread within a 5 km distance. Both should be considered in the perspective of prevention. Porcine reproductive and respiratory syndrome virus diversity of Eastern Canada swine herds in a large sequence dataset reveals two hypervariable regions under positive selection Delisle B, Gagnon CA, Lambert ME, D’Allaire S Infect Genet Evol. 2012 Jul;12(5):1111-1119. Porcine reproductive and respiratory syndrome virus (PRRSV) is known to be genetically highly variable, but knowledge of sequence diversity from Eastern Canada and its degree of genetic plasticity in or near the principal neutralizing epitope (PNE) in association with evolutionary selective pressure is limited. The purposes of our study were to investigate the extent of strain diversity, the existing glycotypes and the amino acid sites under selective evolutionary pressure in its encoded protein, GP5, for a dataset of 1301 sequences (1998 to 2009). This was addressed by partitioning and clustering into subgenotypes a large number of open reading frame 5 sequences from the province of Quebec and analyzing the content of these subgenotypes. The overall pairwise diversity was 12% and was comparable to what has been reported around the world. The mean diversity for sequences within subgenotypes was around 7%. No marked variations in subgenotype emergence could be observed through time. Thirtyeight GP5 glycotype patterns were observed which included a newly identified site at position N57 which was already present in 1998. These patterns possessed one to six N-glycosylation sites in total and could be located in eight different positions. No obvious grouping of glycotypes could be established in relation to subgenotypes. Positions N44 and N51 were confirmed to be fixed N-glycosylation positions, whereas other positions where found to be shifting and located in or near hypervariable regions (HVR) 1 and 2. Both HVR were under selective evolutionary pressure in half of all subgenotypes including vaccine-like groups. Conversely, the PNE flanked by both HVR was well conserved amongst most subgenotypes demonstrating potential molecular constraint in a probable viral binding region. The analysis of this dataset increased knowledge of evolutionary change inferred from genetic data, more specifically regarding the implications of both HVRs in PRRSV diversity. Gilt replacement strategies used in two swine production areas in Quebec in regard to porcine reproductive and respiratory syndrome virus Lambert ME, Denicourt M, Poljak Z, D’Allaire S J Swine Health Prod. 2012;20(5):223–230. The objectives of this study was to describe gilt replacement strategies in regard to porcine reproductive and respiratory syndrome virus (PRRSV) and to assess differences between high density (HD) and moderate density (MD) pig areas. A cross-sectional study was conducted in breeding sites located in an HD (n = 68) and an MD area (n = 52) in Quebec between May 2005 and August 2008. A questionnaire on strategies used to introduce replacement gilts was completed and PRRSV status was assessed by enzyme-linked immunosorbent assay or reverse-transcription polymerase chain reaction. Sites housing at least one pig positive by either test were classified as PRRSV-positive. Strategies were described according to herd characteristics, PRRSV status, and area. Self-replacement and purchase of mature or immature gilts were observed on 37%, 35%, and 28% of sites, respectively. In positive sites purchasing mature gilts, 18% had a PRRSV-positive supplier, and gilts were introduced either directly into Info-CRIP No 6 – December 2012 19 the sow herd (15%) or after isolation (41%) or acclimatization (44%). Most positive sites purchasing immature gilts practiced acclimatization (93%), either by commingling gilts with commercial pigs (93%) or inoculating serum (7%). Acclimatization processes were rarely monitored through diagnostic procedures. Lower sow inventory, higher prevalence of PRRSV infection, and higher frequency of self-replacement were observed in the HD compared to the MD area. Negative and positive sites practicing voluntary exposure to PRRSV both clustered spatially within the MD area. Replacement strategies may have weaknesses that should be addressed to facilitate PRRSV management at the herd and regional levels. Alopecia areata and humpy-back syndrome in suckling piglets Drolet R, Denicourt M, D’Allaire S Can Vet J. 2012; 53: 865-869. This report describes in several nursing piglets an uncommon variant of humpy-back syndrome associated with multiple rib fractures and multisystemic vasculitis and for the first time in swine a skin disease consistent with alopecia areata. Both conditions were observed concurrently on the farm and even in some piglets. Possible causes are discussed. 2013 CRIPA Scientific Communications We invite you to participate to our next scientific communications for 2013! Place these important dates on your agenda and keep an eye on the CRIPA Bulletin for further information and registration. May 8th CRIPA Scientific Colloquium organized in the frame of the "81ième congrès de l’Acfas" at Université Laval, Québec: "Le microbiote animal : Une question d’équilibre!" May 9th CRIPA 6th Annual Symposium We thank Yannick Tremblay and Jenny-Lee Thomassin for the translation of the Info-CRIP 6. Info-CRIP No 6 – December 2012 20