A Pilot Study of the Effects of Mycoplasma Ovipneumoniae Exposure on Domestic Lamb Growth And

Total Page:16

File Type:pdf, Size:1020Kb

A Pilot Study of the Effects of Mycoplasma Ovipneumoniae Exposure on Domestic Lamb Growth And bioRxiv preprint doi: https://doi.org/10.1101/459628; this version posted November 1, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. 1 Full title: 2 A pilot study of the effects of Mycoplasma ovipneumoniae exposure on domestic lamb growth and 3 performance. 4 5 Thomas E. Besser1*, Jessica Levy1, Melissa Ackerman2, Danielle Nelson1, Kezia Manlove3, Kathleen A. 6 Potter1, Jan Busboom4, Margaret Benson4 7 8 Short title: 9 Sub-clinical Mycoplasma ovipneumoniae infection 10 11 1 Department of Veterinary Microbiology and Pathology, Washington State University College of 12 Veterinary Medicine, Pullman WA, United States of America 13 2 Department of Veterinary Clinical Sciences, Washington State University College of Veterinary 14 Medicine, Pullman WA, United States of America 15 3 Department of Wildland Resources, Utah State University College of Natural Resources, Logan UT, 16 United States of America 17 4 Department of Animal Sciences, Washington State University College of Agricultural, Human, and 18 Natural Resource Sciences, Pullman WA, United States of America. 19 * Corresponding author 20 E-mail: [email protected] 1 bioRxiv preprint doi: https://doi.org/10.1101/459628; this version posted November 1, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. 21 Abstract 22 Mycoplasma ovipneumoniae is a globally distributed pathogen that has been associated with 23 pneumonia in both domestic and wild Caprinae. It is closely related to M. hyopneumoniae, a respiratory 24 pathogen of swine that is associated with decreased growth rates of pigs as well as clinical respiratory 25 disease. In order to assess the effects of M. ovipneumoniae on lamb performance, we generated a 26 cohort of lambs free of M. ovipneumoniae by segregation of test negative ewes after lambing, then 27 compared the growth and carcass quality traits of M. ovipneumoniae-free and -colonized lambs from 28 weaning to harvest. Some signs of respiratory disease were observed during the feeding trial in both 29 lamb groups, but the M. ovipneumoniae-exposed group included more affected lambs and higher 30 average disease scores. At harvest, lungs of lambs in both groups showed few grossly visible lesions, 31 although the M. ovipneumoniae-exposed group did exhibit increased microscopic lung lesions (P<0.05). 32 In addition, M. ovipneumoniae exposed lambs produced lower average daily gains (P<0.05), and lower 33 yield grade carcasses (P<0.05) compared to those of non-exposed lambs. The results demonstrated the 34 feasibility of test and segregation for elimination of M. ovipneumoniae from groups of sheep and 35 suggested that this pathogen may impair lamb growth and productivity even in the absence of overt 36 respiratory disease. 37 2 bioRxiv preprint doi: https://doi.org/10.1101/459628; this version posted November 1, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. 38 Introduction 39 The bacterium Mycoplasma ovipneumoniae was originally isolated and described from a 40 Australian sheep flock experiencing a high incidence of pneumonia in lambs [1]. Lesions associated with 41 the disease included proliferative interstitial pneumonia with septal and bronchiolar epithelial cell 42 hyperplasia and proliferation, with additional infiltration in some cases by lymphocytes or neutrophils. 43 This disease has since been observed to have a global distribution, a variable but generally low severity, 44 and has been variously termed enzootic pneumonia, chronic non-progressive pneumonia, or interstitial 45 pneumonia [2]. In severe cases, enzootic pneumonia may involve co-infection with multiple genetic 46 strain types of M. ovipneumoniae and also other bacterial respiratory pathogens, including prominently 47 Mannheimia haemolytica [3, 4]. Enzootic pneumonia has been associated with adverse effects on lamb 48 growth and productivity [5-9]. 49 M. ovipneumoniae is a member of the neurolyticum/hyopneumoniae subgroup of mycoplasmas, 50 which also includes M. hyopneumoniae of swine, M. dispar of cattle, and M. conjunctivae of sheep and 51 goats [10, 11]. M. hyopneumoniae is recognized as an important pathogen contributing to respiratory 52 disease and unthriftiness in pigs [12, 13]. The combined impacts of M. hyopneumoniae on respiratory 53 disease and impaired growth have led to the recent development and adoption of methods to eliminate 54 this pathogen from large swine herds through the use of breeding management combined with 55 antibiotic therapy [14, 15]. If the effects of M. ovipneumoniae on lamb growth and productivity are 56 similar to those of M. hyopneumoniae in swine, similar efforts at flock-level elimination of this pathogen 57 may be merited. 58 M. ovipneumoniae is widespread in US sheep operations. The USDA National Animal Health 59 Monitoring Service included diagnostics for M. ovipneumoniae in its Sheep 2011 survey of 450 US 60 domestic sheep operations [16]. Evidence of M. ovipneumoniae colonization was detected in 3 bioRxiv preprint doi: https://doi.org/10.1101/459628; this version posted November 1, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. 61 approximately 90% of operations. M. ovipneumoniae has also recently been identified as the primary 62 pathogen initiating severe epizootics of pneumonia in bighorn sheep [17, 18]. Further complicating the 63 picture, M. ovipneumoniae may also be detected in the lungs of lambs in the absence of overt clinical 64 signs or grossly visible lesions of enzootic pneumonia [2, 19]. These sub-clinical infections may also play 65 a role in impaired lamb growth and productivity that would not be detected in studies that rely solely on 66 grossly visible lung lesions as a marker for infection. 67 While previous studies of enzootic pneumonia have generally compared groups of lambs that 68 differed in the extent of grossly visible lung lesions, our approach was designed to evaluate the effects 69 of M. ovipneumoniae infection regardless of the extent of visible pneumonia lesions. Therefore, the 70 objective of this study was to determine the feasibility of producing a cohort of lambs unexposed to M. 71 ovipneumoniae on an infected premises in order to evaluate the effects of M. ovipneumoniae infection 72 or colonization of domestic lambs from weaning to harvest. 73 Materials and Methods 74 Ethics statement 75 This study was carried out in accordance with the recommendations in the Guide for the Care 76 and Use of Laboratory Animals of the National Institutes of Health and in conformance with 77 United States Department of Agriculture animal research guidelines, under protocol #04482 approved 78 by the Washington State University Institutional Animal Care and Use Committee (WSU IACUC). Parts of 79 this study were conducted at the University of Idaho Sheep Center under that same Washington State 80 University IACUC protocol under a memorandum of understanding with the University of Idaho 81 Laboratory Animal Research office. 82 Animals and husbandry 4 bioRxiv preprint doi: https://doi.org/10.1101/459628; this version posted November 1, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. 83 The study was conducted using lambs from a cross-bred production flock of approximately 100 84 ewes located at the University of Idaho Sheep Center. Carrier and non-carrier ewes were identified by 85 longitudinal testing using nasal swab samples tested by realtime polymerase chain reactions (PCR). After 86 lambing, lambs were supplemented with selenium and vitamin E (0.5 ml Bo-Se, Merck Animal Health, 87 Madison NJ) and carrier and non-carrier ewes with their lambs were separated and housed in non- 88 adjacent pens to prevent nose-to-nose contact. During this period, the pre-weaned lambs had access to 89 the feed available to the ewes, which consisted of a 50:50 mix of rolled corn and whole barley (1 90 kg/ewe/day) plus long-stemmed dairy-quality alfalfa hay (2 kg/ewe/day). At approximately 65 days of 91 age the lambs were weaned, weighed, and vaccinated with Clostridial CDT bacterin/toxoid. A second 92 dose of CDT vaccine was administered 30 d later during the feeding trial. 93 Microbiology 94 M. ovipneumoniae was detected in nasal swab and lung samples using realtime PCR. Swabs (BBL 95 CultureSwabEZ, Fisher Scientific, Waltham, MA) were serially inserted into both nares of each sampled 96 animal, replaced in the swab sheath, and maintained at 4C for up to 3 hrs before storage at -20C until 97 DNA extraction. At harvest, separate swabs from each principal bronchus (left, right, tracheal) were 98 handled and stored similarly. Swabs were eluted by vigorous agitation in 400 ul of phosphate-buffered 99 saline,
Recommended publications
  • Margaret A. Highland, DVM Washington State University
    Bacterial Pneumonia in Sheep, The Domestic – Bighorn Sheep Interface, and Research at ADRU USAHA Committee on Sheep and Goats Providence, RI October 27, 2015 PLC M. A. Highland, DVM, DACVP, PhD candidate PhD Veterinary Training Program USDA-ARS ADRU Veterinary Microbiology and Pathology Washington State University Pullman, WA DS – BHS Interface Issue Captive/penned commingling studies & anecdotal field reports associate BHS and DS contact with BHS pneumonia Removal of DS public land grazing allotments - profound economic impacts Pneumonia continues to afflict BHS herds - despite decades of research and intense management practices Anecdotal field reports also associate DG with BHS pneumonia - pack goat restrictions on public lands DS and BHS Pneumonia DS . Lambs > Adults . Etiology • Polymicrobial (bacteria +/- viruses) or Unimicrobial • Multifactorial (colostrum, air quality, environmental stressors) BHS (wild) . Reports of respiratory disease date back to the 1920’s . All age outbreaks +/- subsequent years of disease in lambs → population-limiting disease . Etiology • Long been debated • Evidence for polymicrobial (bacterial) and multifactorial • Viruses occasionally reported (no current indication for primary role) What do we know about BHS (and DS) pneumonia? Polymicrobial and Multifactorial (the presence of the bacteria in BHS alone does NOT = disease/death) Incompletely understood disease phenomenon DS and BHS pneumonia-associated bacteria Mycoplasma ovipneumoniae (M ovi) Pasteurellaceae (“Pasteurellas”) . Mannheimia haemolytica
    [Show full text]
  • Engineering the Genome of Minimal Bacteria Using CRISPR/Cas9 Tools Iason Tsarmpopoulos
    Engineering the genome of minimal bacteria using CRISPR/Cas9 tools Iason Tsarmpopoulos To cite this version: Iason Tsarmpopoulos. Engineering the genome of minimal bacteria using CRISPR/Cas9 tools. Mi- crobiology and Parasitology. Université de Bordeaux, 2017. English. NNT : 2017BORD0787. tel- 01834971 HAL Id: tel-01834971 https://tel.archives-ouvertes.fr/tel-01834971 Submitted on 11 Jul 2018 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. THÈSE PRÉSENTÉE POUR OBTENIR LE GRADE DE DOCTEUR DE L’UNIVERSITÉ DE BORDEAUX ÉCOLE DOCTORALE Science de la vie et de la Santé SPÉCIALITÉ Microbiologie and Immunologie Par Iason TSARMPOPOULOS Ingénierie de génome de bactéries minimales par des outils CRISPR/Cas9 Sous la direction de : Monsieur Pascal SIRAND-PUGNET Soutenue le jeudi 07 décembre 2017 à 14h00 Lieu : INRA, 71 avenue Edouard Bourlaux 33882 Villenave d'Ornon salle Amphithéâtre Josy et Colette Bové Membres du jury : Mme Cécile BEBEAR Université de Bordeaux et CHU de Bordeaux Président Mme Florence TARDY Anses-Laboratoire de Lyon Rapporteur M. Matthieu JULES Institut Micalis, INRA and AgroParisTech Rapporteur M. David BIKARD Institut Pasteur Examinateur M. Fabien DARFEUILLE INSERM U1212 - CNRS UMR 5320 Invité Mme Carole LARTIGUE-PRAT INRA - Université de Bordeaux Invité M.
    [Show full text]
  • Examining the Risk of Disease Transmission Between Wild Dall's
    Examining the Risk of Disease Transmission between Wild Dall’s Sheep and Mountain Goats, and Introduced Domestic Sheep, Goats, and Llamas in the Northwest Territories Prepared for: The Northwest Territories Agricultural Policy Framework and Environment and Natural Resources Government of the Northwest Territories, Canada August 20, 2005 Examining the Risk of Disease Transmission between Wild Dall’s Sheep and Mountain Goats, and Introduced Domestic Sheep, Goats, and Llamas in the Northwest Territories Elena Garde 1,2 , Susan Kutz 1,3 , Helen Schwantje 4, Alasdair Veitch 5, Emily Jenkins 1,6 , Brett Elkin 7 1 Research Group for Arctic Parasitology and the Canadian Cooperative Wildlife Health Centre, Western College of Veterinary Medicine, University of Saskatchewan, 52 Campus Drive, Saskatoon, SK, S7N 5B4. 2 Associate Wildlife Veterinarian, Biodiversity Branch, Ministry of Environment, PO Box 9338, Stn Prov Govt, 2975 Jutland Road, Victoria, BC, V8W 9M1, (250) 953-4285 [email protected] 3 Associate Professor, Faculty of Veterinary Medicine, University of Calgary, 3330 Hospital Dr. NW, Calgary AB, T2N 4N1 Ph: (306) 229-6110 4 Wildlife Veterinarian, Biodiversity Branch, Ministry of Environment, PO Box 9338, Stn Prov Govt, 2975 Jutland Road, Victoria, BC, V8W 9M1, (250) 953-4285 [email protected] 5 Supervisor, Wildlife Management, Environment and Natural Resources, Sahtu Region, P.O. Box 130, Norman Wells, NT X0E 0V0, Ph: (867) 587-2786; Fax: (867) 587-2359 [email protected] 6 Wildlife Disease Specialist / Research Scientist, Canadian Wildlife Service, 115 Perimeter Rd. Saskatoon, SK S7N 0X4 (306) 975-5357, (306) 966-7246 7 Disease & Contaminants Specialist, Environment and Natural Resources, 500 – 6102 50 th Ave.
    [Show full text]
  • Genomes Published Outside of SIGS, June
    Standards in Genomic Sciences (2011) 5:154-167 DOI:10.4056/sigs.2324675 Genome sequences of Bacteria and Archaea published outside of Standards in Genomic Sciences, June – September 2011 Oranmiyan W. Nelson1 and George M. Garrity1 1Editorial Office, Standards in Genomic Sciences and Department of Microbiology, Michigan State University, East Lansing, MI, USA The purpose of this table is to provide the community with a citable record of publications of ongoing genome sequencing projects that have led to a publication in the scientific literature. While our goal is to make the list complete, there is no guarantee that we may have omitted one or more publications appearing in this time frame. Readers and authors who wish to have publications added to this subsequent versions of this list are invited to provide the bib- liometric data for such references to the SIGS editorial office. Phylum Crenarchaeota Phylum Euryarchaeota Pyrococcus yayanosii CH1, sequence accession CP002779 [1] Methanocella paludicola, sequence accession AP011532 [2] Halorhabdus tiamatea, sequence accession AFNT00000000 [3] Thermococcus sp. Strain 4557, sequence accession CP002920 [4] Phylum Chloroflexi Phylum Proteobacteria Ralstonia solanacearum strain Po82, sequence accession CP002819 (chromosome) and CP002820 (megaplasmid) [5 Desulfovibrio alaskensis G20, sequence accession CP000112 [6] Methylophaga aminisulfidivorans MPT, sequence accession AFIG00000000 [7] Acinetobacter sp. P8-3-8, sequence accession AFIE00000000 [8] Sphingomonas strain KC8, sequence accession AFMP01000000
    [Show full text]
  • Mycoplasma Ovipneumoniae Rotter ML, Hirschl AM
    RESEARCH LETTERS Figure. Direct examination with dark-field microscopy of specimens from a patient with agammaglobulinemia who had Spiroplasma apis infection, France. A) Helical and motile bacteria in blood culture. B) Elongated and coccoid bacteria in joint fluid. C) Helical and motile bacteria in culture from joint fluid in modified SP4 broth medium. Scale bar indicates 10 µm. than honeybees. The insect stings in this patient are a likely 7. Mueller NJ, Tini GM, Weber A, Gaspert A, Husmann L, gateway of the reported infection. Bloemberg G, et al. Hepatitis from Spiroplasma sp. in an immunocompromised patient. Am J Transplant. 2015;15:2511–6. In summary, clinicians and microbiologists should be http://dx.doi.org/10.1111/ajt.13254 aware of fastidious organisms in atypical infections in im- 8. Lorenz B, Schroeder J, Reischl U. First evidence of an endogenous munocompromised patients. Our findings indicate a need Spiroplasma sp. infection in humans manifesting as unilateral for prolonged culture on specific agar on all joint fluids in cataract associated with anterior uveitis in a premature baby. Graefes Arch Clin Exp Ophthalmol. 2002;240:348–53. patients with agammaglobulinemia and targeted molecular http://dx.doi.org/10.1007/s00417-002-0453-3 methods to identify S. apis organisms. 9. Aquilino A, Masiá M, López P, Galiana AJ, Tovar J, Andrés M, et al. First human systemic infection caused by Spiroplasma. J Clin Microbiol. 2015;53:719–21. http://dx.doi.org/10.1128/JCM.02841-14 Acknowledgments We thank Anne Laurence Thomi Georgelin, who referred the Address for correspondence: Olivier Lortholary, Necker-Enfants Malades patient to the Necker-Pasteur Center for Infectious Diseases and University Hospital, 149 rue de Sevre 75743, Paris CEDEX, France; Tropical Medicine; Valérie Zeller for the management of septic email: [email protected] polyarthritis; and Philippe Lanotte and Marie-Pierre Dubrana, who participated in molecular analysis.
    [Show full text]
  • Attachment 1 .PLOS ONE
    Attachment 1 .PLOS ONE CORRECTION Correction: Exposure of bighorn sheep to domestic goats colonized with Mycoplasma ovipneumoniae induces sub-lethal pneumonia Thomas E. Besser, E. Frances Cassirer, Kathleen A. Potter, William J. Foreyt Tn response to queries raised after publication, the authors, the authors’ institution (Office of Research Assurance, Washington State University) and a member of PLOS ONE’s Editorial Board have reviewed the findings in this article, and as a consequence the authors provide an update to the Competing Interests statement and clarifications regarding the results: The competing interests declaration is updated to acknowledge additional sources of fund ing received by the authors. This specific study was supported by funding competitively awarded by the Wild Sheep Foundation and by revenue from the WSU Rocky Crate Endow ment for Wild Sheep Disease Research. Additional research funding for the authors’ bighorn sheep pneumonia-related research has been received from the US Department of Agriculture (including the Animal Plant Health Inspection Service and the US Forest Service), the US Geo logic Survey, numerous chapters and affiliates of the Wild Sheep Foundation, and the WSU Fowler Emerging Infectious Diseases endowment. Regarding the pneumonia diagnosis reported in the article, the authors re-assessed the pri mary data and solicited and received a second opinion from a veterinary pathologist at Wash ington Animal Disease Diagnostic Lab (WADDL) unassociated with the original project. Following this reassessment, the authors confirmed the descriptions and diagnoses as reported in the article, but they noted that the consulted pathologist advised, “some pathologists might describe the histopathologic lesions seen in the least severely affected animal as ‘bronchiolitis’ rather than ‘pneumonia’ due to the preponderance of that lesion in that animal”.
    [Show full text]
  • ( 12 ) United States Patent
    US009956282B2 (12 ) United States Patent ( 10 ) Patent No. : US 9 ,956 , 282 B2 Cook et al. (45 ) Date of Patent: May 1 , 2018 ( 54 ) BACTERIAL COMPOSITIONS AND (58 ) Field of Classification Search METHODS OF USE THEREOF FOR None TREATMENT OF IMMUNE SYSTEM See application file for complete search history . DISORDERS ( 56 ) References Cited (71 ) Applicant : Seres Therapeutics , Inc. , Cambridge , U . S . PATENT DOCUMENTS MA (US ) 3 ,009 , 864 A 11 / 1961 Gordon - Aldterton et al . 3 , 228 , 838 A 1 / 1966 Rinfret (72 ) Inventors : David N . Cook , Brooklyn , NY (US ) ; 3 ,608 ,030 A 11/ 1971 Grant David Arthur Berry , Brookline, MA 4 ,077 , 227 A 3 / 1978 Larson 4 ,205 , 132 A 5 / 1980 Sandine (US ) ; Geoffrey von Maltzahn , Boston , 4 ,655 , 047 A 4 / 1987 Temple MA (US ) ; Matthew R . Henn , 4 ,689 ,226 A 8 / 1987 Nurmi Somerville , MA (US ) ; Han Zhang , 4 ,839 , 281 A 6 / 1989 Gorbach et al. Oakton , VA (US ); Brian Goodman , 5 , 196 , 205 A 3 / 1993 Borody 5 , 425 , 951 A 6 / 1995 Goodrich Boston , MA (US ) 5 ,436 , 002 A 7 / 1995 Payne 5 ,443 , 826 A 8 / 1995 Borody ( 73 ) Assignee : Seres Therapeutics , Inc. , Cambridge , 5 ,599 ,795 A 2 / 1997 McCann 5 . 648 , 206 A 7 / 1997 Goodrich MA (US ) 5 , 951 , 977 A 9 / 1999 Nisbet et al. 5 , 965 , 128 A 10 / 1999 Doyle et al. ( * ) Notice : Subject to any disclaimer , the term of this 6 ,589 , 771 B1 7 /2003 Marshall patent is extended or adjusted under 35 6 , 645 , 530 B1 . 11 /2003 Borody U .
    [Show full text]
  • Isolation and Molecular Characterization of Mycoplasma Spp
    Veterinary World, EISSN: 2231-0916 RESEARCH ARTICLE Available at www.veterinaryworld.org/Vol.12/May-2019/6.pdf Open Access Isolation and molecular characterization of Mycoplasma spp. in sheep and goats in Egypt Mounier M. Abdel Halium1, Fayez A. Salib1, S. A. Marouf2 and Emil S. Abdel Massieh1 1. Department of Medicine and Infectious Diseases, Faculty of Veterinary Medicine, Cairo University, Giza, Egypt; 2. Department of Microbiology and Mycology, Faculty of Veterinary Medicine, Cairo University, Giza, Egypt. Corresponding author: Emil S. Abdel Massieh, e-mail: [email protected] Co-authors: MMAH: [email protected], FAS: [email protected], SAM: [email protected] Received: 04-12-2018, Accepted: 15-03-2019, Published online: 13-05-2019 doi: 10.14202/vetworld.2019.664-670 How to cite this article: Abdel Halium MM, Salib FA, Marouf SA, Abdel Massieh ES (2019) Isolation and molecular characterization of Mycoplasma spp. in sheep and goats in Egypt, Veterinary World, 12(5): 664-670. Abstract Background and Aim: Different species of Mycoplasma are associated with many pathological problems in small ruminants including respiratory manifestation, this problem results in significant losses, especially in African countries. This study aimed to (I) study some epidemiological aspects of Mycoplasma species infections in Egyptian sheep and goats at Giza Governorate, (II) diagnosis of Mycoplasma species affections using bacterial isolation and identification, (III) apply the polymerase chain reaction (PCR) for typing of different Mycoplasma species, and (IV) illustrate the phylogenetic tree for the isolated Mycoplasma species and other species from GenBank using the purified PCR product. Materials and Methods: A total of 335 samples were collected from sheep and goats from Giza Governorate in Egypt as 142 nasal swabs from clinically affected animals, 167 pneumonic lungs, 18 samples from tracheal bifurcation, and 8 samples by bronchial wash were cultured on pleuropneumonia-like organisms (PPLOs) media for cultivation of Mycoplasma species.
    [Show full text]
  • 2017 National Veterinary Scholars Symposium 18Th Annual August 4
    2017 National Veterinary Scholars Symposium 18th Annual August – 4 5, 2017 Natcher Conference Center, Building 45 National Institutes of Health Bethesda, Maryland Center for Cancer Research National Cancer Institute with The Association of American Veterinary Medical Colleges https://www.cancer.gov/ Table of Contents 2017 National Veterinary Scholars Symposium Program Booklet Welcome .............................................................................................................................. 1 NIH Bethesda Campus Visitor Information and Maps .........................................................2 History of the National Institutes of Health ......................................................................... 4 Sponsors ............................................................................................................................... 5 Symposium Agenda .......................................................................................................6 Bios of Speakers ................................................................................................................. 12 Bios of Award Presenters and Recipients ........................................................................... 27 Training Opportunities at the NIH ...................................................................................... 34 Abstracts Listed Alphabetically .......................................................................................... 41 Symposium Participants by College of Veterinary Medicine
    [Show full text]
  • Post-Translational Protein Deimination Signatures in Plasma and Plasma Evs of Reindeer (Rangifer Tarandus)
    biology Article Post-Translational Protein Deimination Signatures in Plasma and Plasma EVs of Reindeer (Rangifer tarandus) Stefania D’Alessio 1, Stefanía Thorgeirsdóttir 2, Igor Kraev 3 , Karl Skírnisson 2 and Sigrun Lange 1,* 1 Tissue Architecture and Regeneration Research Group, School of Life Sciences, University of Westminster, London W1W 6UW, UK; [email protected] 2 Institute for Experimental Pathology at Keldur, University of Iceland, Keldnavegur 3, 112 Reykjavik, Iceland; [email protected] (S.T.); [email protected] (K.S.) 3 Electron Microscopy Suite, Faculty of Science, Technology, Engineering and Mathematics, Open University, Milton Keynes MK7 6AA, UK; [email protected] * Correspondence: [email protected]; Tel.: +44-(0)207-911-5000 (ext. 64832) Simple Summary: Reindeer are an important wild and domesticated species of the Arctic, Northern Europe, Siberia and North America. As reindeer have developed various strategies to adapt to extreme environments, this makes them an interesting species for studies into diversity of immune and metabolic functions in the animal kingdom. Importantly, while reindeer carry natural infections caused by viruses (including coronaviruses), bacteria and parasites, they can also act as carriers for transmitting such diseases to other animals and humans, so called zoonosis. Reindeer are also affected by chronic wasting disease, a neuronal disease caused by prions, similar to scrapie in sheep, mad cows disease in cattle and Creutzfeldt-Jakob disease in humans. The current study assessed a specific protein modification called deimination/citrullination, which can change how proteins Citation: D’Alessio, S.; function and allow them to take on different roles in health and disease processes.
    [Show full text]
  • Biosafety Guidelines for Contained Use of Genetically Modified Microorganisms at Pilot and Industrial Scales
    Biosafety Guidelines for Contained Use of Genetically Modified Microorganisms at Pilot and Industrial Scales TECHNICAL BIOSAFETY COMMITTEE (TBC) NATIONAL CENTER FOR GENETIC ENGINEERING AND BIOTECHNOLOGY (BIOTEC) NATIONAL SCIENCE AND TECHNOLOGY DEVELOPMENT AGENCY (NSTDA) MINISTRY OF SCIENCE AND TECHNOLOGY (MOST) 2015 Biosafety Guidelines for Contained Use of Genetically Modified Microorganisms at Pilot and Industrial Scales TECHNICAL BIOSAFETY COMMITTEE (TBC) NATIONAL CENTER FOR GENETIC ENGINEERING AND BIOTECHNOLOGY (BIOTEC) NATIONAL SCIENCE AND TECHNOLOGY DEVELOPMENT AGENCY (NSTDA) MINISTRY OF SCIENCE AND TECHNOLOGY (MOST) 2015 Biosafety Guidelines for Contained Use of Genetically Modified Microorganisms at Pilot and Industrial Scales Technical Biosafety Committee National Center for Genetic Engineering and Biotechnology National Science and Technology Development Agency (NSTDA) © National Center for Genetic Engineering and Biotechnology 2015 ISBN : 978-616-12-0386-3 Tel : +66(0)2-564-6700 Fax : +66(0)2-564-6703 E-mail : [email protected] URL : http://www.biotec.or.th Printing House : P.A. Living Printing Co.,Ltd 4 Soi Sirintron 7 Road Sirintron District Bangplad Province Bangkok 10700 Tel : +66(0)2-881 9890 Fax : +66(0)2-881 9894 Preface Genetically Modified Microorganisms (GMMs) were first used in B.E. 2525 to produce insulin in industrial medicine. Currently, GMMs are used in various industries, such as the food, pharmaceutical and bioplastic industries, to manufacture a number of important consumer products. To ensure operator and environmental safety, the Technical Biosafety Committee (TBC) of the National Center for Genetic Engineering and Biotechnology (BIOTEC), the National Science and Technology Development Agency (NSTDA), has prepared guidelines for GMM work, publishing “Biosafety Guidelines for Contained Use of Genetically Modified Microorganisms at Pilot and Industrial Scales” in B.E.
    [Show full text]
  • WO 2014/121298 A2 7 August 2014 (07.08.2014) P O P C T
    (12) INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property Organization International Bureau (10) International Publication Number (43) International Publication Date WO 2014/121298 A2 7 August 2014 (07.08.2014) P O P C T (51) International Patent Classification: VULIC, Marin; c/o Seres Health, Inc., 161 First Street, A61K 39/02 (2006.01) Suite 1A, Cambridge, MA 02142 (US). (21) International Application Number: (74) Agents: HUBL, Susan, T. et al; Fenwick & West LLP, PCT/US2014/014738 Silicon Valley Center, 801 California Street, Mountain View, CA 94041 (US). (22) International Filing Date: 4 February 2014 (04.02.2014) (81) Designated States (unless otherwise indicated, for every kind of national protection available): AE, AG, AL, AM, English (25) Filing Language: AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, (26) Publication Language: English BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DK, DM, DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, (30) Priority Data: HN, HR, HU, ID, IL, IN, IR, IS, JP, KE, KG, KN, KP, KR, 61/760,584 4 February 2013 (04.02.2013) US KZ, LA, LC, LK, LR, LS, LT, LU, LY, MA, MD, ME, 61/760,585 4 February 2013 (04.02.2013) US MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, 61/760,574 4 February 2013 (04.02.2013) us OM, PA, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, SA, 61/760,606 4 February 2013 (04.02.2013) us SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, 61/926,918 13 January 2014 (13.01.2014) us TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, (71) Applicant: SERES HEALTH, INC.
    [Show full text]