Avian Mycoplasmosis (Mycoplasma Gallisepticum)
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Development of a Seroprevalence Map for Mycoplasma Gallisepticum
Original Paper Veterinarni Medicina, 61, 2016 (3): 136–140 doi: 10.17221/8764-VETMED Development of a seroprevalence map for Mycoplasma gallisepticum in broilers and its application to broilers from Comunidad Valenciana (Spain) over the course of two years (2009–2010) C. Garcia1, J.M. Soriano2, P. Catala-Gregori1 1Poultry Quality and Animal Nutrition Center of Comunidad Valenciana (CECAV), Castellon, Spain 2Faculty of Pharmacy, University of Valencia, Burjassot, Spain ABSTRACT: The aim of this study was to design and implement a Seroprevalence Map based on Business Intelligence for Mycoplasma gallisepticum (M. gallisepticum) in broilers in Comunidad Valenciana (Spain). To obtain the sero- logical data we analysed 7363 samples from broiler farms over 30 days of age over the course of two years (3813 and 3550 samples in 2009 and 2010, respectively, from 189 and 193 broiler farms in 2009 and 2010, respectively). Data were represented on a map of Comunidad Valenciana to include geographical information of flock location and to facilitate the monitoring. Only one region presented with average ELISA titre values of over 500 in the 2009 period, indicating previous contact with M. gallisepticum in broiler flocks. None of the other regions showed any pressure of infection, indicating a low seroprevalence for M. gallisepticum. In addition, data from this study represent a novel tool for easy monitoring of the serological response that incorporates geographical information. Keywords: Mycoplasma gallisepticum; broiler; seroprevalence map; ELISA, Comunidad Valenciana Mycoplasma gallisepticum (M. gallisepticum) is a matic for several days or months before experiencing bacterium causing poultry disease that is listed by stress (Dingfelder et al. -
Bacterial Communities of the Upper Respiratory Tract of Turkeys
www.nature.com/scientificreports OPEN Bacterial communities of the upper respiratory tract of turkeys Olimpia Kursa1*, Grzegorz Tomczyk1, Anna Sawicka‑Durkalec1, Aleksandra Giza2 & Magdalena Słomiany‑Szwarc2 The respiratory tracts of turkeys play important roles in the overall health and performance of the birds. Understanding the bacterial communities present in the respiratory tracts of turkeys can be helpful to better understand the interactions between commensal or symbiotic microorganisms and other pathogenic bacteria or viral infections. The aim of this study was the characterization of the bacterial communities of upper respiratory tracks in commercial turkeys using NGS sequencing by the amplifcation of 16S rRNA gene with primers designed for hypervariable regions V3 and V4 (MiSeq, Illumina). From 10 phyla identifed in upper respiratory tract in turkeys, the most dominated phyla were Firmicutes and Proteobacteria. Diferences in composition of bacterial diversity were found at the family and genus level. At the genus level, the turkey sequences present in respiratory tract represent 144 established bacteria. Several respiratory pathogens that contribute to the development of infections in the respiratory system of birds were identifed, including the presence of Ornithobacterium and Mycoplasma OTUs. These results obtained in this study supply information about bacterial composition and diversity of the turkey upper respiratory tract. Knowledge about bacteria present in the respiratory tract and the roles they can play in infections can be useful in controlling, diagnosing and treating commercial turkey focks. Next-generation sequencing has resulted in a marked increase in culture-independent studies characterizing the microbiome of humans and animals1–6. Much of these works have been focused on the gut microbiome of humans and other production animals 7–11. -
The Mysterious Orphans of Mycoplasmataceae
The mysterious orphans of Mycoplasmataceae Tatiana V. Tatarinova1,2*, Inna Lysnyansky3, Yuri V. Nikolsky4,5,6, and Alexander Bolshoy7* 1 Children’s Hospital Los Angeles, Keck School of Medicine, University of Southern California, Los Angeles, 90027, California, USA 2 Spatial Science Institute, University of Southern California, Los Angeles, 90089, California, USA 3 Mycoplasma Unit, Division of Avian and Aquatic Diseases, Kimron Veterinary Institute, POB 12, Beit Dagan, 50250, Israel 4 School of Systems Biology, George Mason University, 10900 University Blvd, MSN 5B3, Manassas, VA 20110, USA 5 Biomedical Cluster, Skolkovo Foundation, 4 Lugovaya str., Skolkovo Innovation Centre, Mozhajskij region, Moscow, 143026, Russian Federation 6 Vavilov Institute of General Genetics, Moscow, Russian Federation 7 Department of Evolutionary and Environmental Biology and Institute of Evolution, University of Haifa, Israel 1,2 [email protected] 3 [email protected] 4-6 [email protected] 7 [email protected] 1 Abstract Background: The length of a protein sequence is largely determined by its function, i.e. each functional group is associated with an optimal size. However, comparative genomics revealed that proteins’ length may be affected by additional factors. In 2002 it was shown that in bacterium Escherichia coli and the archaeon Archaeoglobus fulgidus, protein sequences with no homologs are, on average, shorter than those with homologs [1]. Most experts now agree that the length distributions are distinctly different between protein sequences with and without homologs in bacterial and archaeal genomes. In this study, we examine this postulate by a comprehensive analysis of all annotated prokaryotic genomes and focusing on certain exceptions. -
MIB–MIP Is a Mycoplasma System That Captures and Cleaves Immunoglobulin G
MIB–MIP is a mycoplasma system that captures and cleaves immunoglobulin G Yonathan Arfia,b,1, Laetitia Minderc,d, Carmelo Di Primoe,f,g, Aline Le Royh,i,j, Christine Ebelh,i,j, Laurent Coquetk, Stephane Claveroll, Sanjay Vasheem, Joerg Joresn,o, Alain Blancharda,b, and Pascal Sirand-Pugneta,b aINRA (Institut National de la Recherche Agronomique), UMR 1332 Biologie du Fruit et Pathologie, F-33882 Villenave d’Ornon, France; bUniversity of Bordeaux, UMR 1332 Biologie du Fruit et Pathologie, F-33882 Villenave d’Ornon, France; cInstitut Européen de Chimie et Biologie, UMS 3033, University of Bordeaux, 33607 Pessac, France; dInstitut Bergonié, SIRIC BRIO, 33076 Bordeaux, France; eINSERM U1212, ARN Regulation Naturelle et Artificielle, 33607 Pessac, France; fCNRS UMR 5320, ARN Regulation Naturelle et Artificielle, 33607 Pessac, France; gInstitut Européen de Chimie et Biologie, University of Bordeaux, 33607 Pessac, France; hInstitut de Biologie Structurale, University of Grenoble Alpes, F-38044 Grenoble, France; iCNRS, Institut de Biologie Structurale, F-38044 Grenoble, France; jCEA, Institut de Biologie Structurale, F-38044 Grenoble, France; kCNRS UMR 6270, Plateforme PISSARO, Institute for Research and Innovation in Biomedicine - Normandie Rouen, Normandie Université, F-76821 Mont-Saint-Aignan, France; lProteome Platform, Functional Genomic Center of Bordeaux, University of Bordeaux, F-33076 Bordeaux Cedex, France; mJ. Craig Venter Institute, Rockville, MD 20850; nInternational Livestock Research Institute, 00100 Nairobi, Kenya; and oInstitute of Veterinary Bacteriology, University of Bern, CH-3001 Bern, Switzerland Edited by Roy Curtiss III, University of Florida, Gainesville, FL, and approved March 30, 2016 (received for review January 12, 2016) Mycoplasmas are “minimal” bacteria able to infect humans, wildlife, introduced into naive herds (8). -
Common Poultry Diseases 1 G
PS47 Common Poultry Diseases 1 G. D. Butcher, J. P. Jacob, and F. B. Mather2 Respiratory Diseases respiratory distress by obstructing the upper air passages. Chickens may be affected with either or both forms of fowl There are many common and important diseases which can pox at one time. affect the respiratory system (air passages, lungs, air sacs) of poultry (see Table 1). Poultry refers to birds that people Transmission: Fowl pox is transmitted by direct contact keep for their use and generally includes the chicken, between infected and susceptible birds or by mosquitos. turkey, duck, goose, quail, pheasant, pigeon, guinea fowl, Virus-containing scabs also can be sloughed from affected pea fowl, ostrich, emu, and rhea. Due to modern systems birds and serve as a source of infection. The virus can of management, usually with high poultry densities, these enter the blood stream through the eye, skin wounds, or diseases are able to readily spread. respiratory tract. Mosquitos become infected from feeding on birds with fowl pox in their blood stream. There is Fowl Pox some evidence that the mosquito remains infective for life. Synonyms: chicken pox (not to be confused with chicken Mosquitos are the primary reservoir and spreaders of fowl pox in humans; the human disease does not affect poultry pox on poultry ranges. Several species of mosquito can and vice versa), sore head, avian diphtheria, bird pox transmit fowl pox. Often mosquitos winter-over in poultry houses so, outbreaks can occur during winter and early Species affected: Most poultry—chickens, turkeys, pheas- spring. ants, quail, ducks, psittacine, and ratites—of all ages are susceptible. -
Resident Microbiome Disruption with Antibiotics Enhances Virulence of a Colonizing Pathogen Received: 13 June 2017 Courtney A
www.nature.com/scientificreports OPEN Resident Microbiome Disruption with Antibiotics Enhances Virulence of a Colonizing Pathogen Received: 13 June 2017 Courtney A. Thomason 1, Nathan Mullen2, Lisa K. Belden1, Meghan May2 & Dana M. Accepted: 13 November 2017 Hawley1 Published: xx xx xxxx There is growing evidence that symbiotic microbes play key roles in host defense, but less is known about how symbiotic microbes mediate pathogen-induced damage to hosts. Here, we use a natural wildlife disease system, house fnches and the conjunctival bacterial pathogen Mycoplasma gallisepticum (MG), to experimentally examine the impact of the ocular microbiome on host damage and pathogen virulence factors during infection. We disrupted the ocular bacterial community of healthy fnches using an antibiotic that MG is intrinsically resistant to, then inoculated antibiotic- and sham-treated birds with MG. House fnches with antibiotic-disrupted ocular microbiomes had more severe MG-induced conjunctival infammation than birds with unaltered microbiomes, even after accounting for diferences in conjunctival MG load. Furthermore, MG cultures from fnches with disrupted microbiomes had increased sialidase enzyme and cytadherence activity, traits associated with enhanced virulence in Mycoplasmas, relative to isolates from sham-treated birds. Variation in sialidase activity and cytadherence among isolates was tightly linked with degree of tissue infammation in hosts, supporting the consideration of these traits as virulence factors in this system. Overall, our results suggest that microbial dysbiosis can result in enhanced virulence of colonizing pathogens, with critical implications for the health of wildlife, domestic animals, and humans. Animals harbor diverse symbiotic microbes that serve key roles in host defense against pathogens1. -
Ectoparasites of the Laughing Dove Streptopelia Senegalensis (Linnaeus, 1766) (Aves: Columbidae) in Zaria, Nigeria
Lundiana 9(1):67-71, 2008 © 2009 Instituto de Ciências Biológicas - UFMG ISSN 1676-6180 Ectoparasites of the Laughing Dove Streptopelia senegalensis (Linnaeus, 1766) (Aves: Columbidae) in Zaria, Nigeria 1Lucas K. Adang, 2Sonnie J. Oniye, 2Augustine U. Ezealor, 3Paul A. Abdu, 4Joseph O. Ajanusi & 1Kennedy P. Yoriyo 1 Department of Biological Sciences, Gombe State University, Gombe, Nigeria. E-mail: [email protected] 2 Department of Biological Sciences, 3 Department of Surgery and Medicine, 4 Department of Veterinary Parasitology and Entomology, Ahmadu Bello University, Zaria, Nigeria. Abstract A survey of ectoparasites of the Laughing Dove (Streptopelia senegalensis Linnaeus, 1766) was carried out in Zaria, Nigeria, to determine the prevalence, intensity and mean intensity of infestation. A total of 382 (231 males and 151 females) doves trapped from different locations in Zaria, Nigeria, were examined through plumage brushing. Eighty-eight (23.0%) of the birds were infested by the following six species of ectoparasites: lice – 32 (8.4%) Menopon gallinae Linnaeus, 1758, 37 (9.7%) Columbicola columbae Linnaeus, 1758, and 18(4.7%) Goniodes sp.; flies – 19 (5.0%) Pseudolynchia canariensis Macquart, 1840; ticks – 12 (3.1%) Argas persicus Oken, 1818; and mite: 1 (0.23%) Dermanyssus gallinae (Degeer, 1778). The frequency of single infestations (59 – 15.4%), was higher than that of double (27 – 7.1%) and triple (2 – 0.52%) infestations, though the difference was not statistically significant (p > 0.05). The males had a higher prevalence (55 – 23.8%) than the females (33 – 21.9%). However, this difference was also not significant (p > 0.05). Ectoparasites were collected from the birds through out the year, with highest prevalence (60.0%) in November. -
Genomic Islands in Mycoplasmas
G C A T T A C G G C A T genes Review Genomic Islands in Mycoplasmas Christine Citti * , Eric Baranowski * , Emilie Dordet-Frisoni, Marion Faucher and Laurent-Xavier Nouvel Interactions Hôtes-Agents Pathogènes (IHAP), Université de Toulouse, INRAE, ENVT, 31300 Toulouse, France; [email protected] (E.D.-F.); [email protected] (M.F.); [email protected] (L.-X.N.) * Correspondence: [email protected] (C.C.); [email protected] (E.B.) Received: 30 June 2020; Accepted: 20 July 2020; Published: 22 July 2020 Abstract: Bacteria of the Mycoplasma genus are characterized by the lack of a cell-wall, the use of UGA as tryptophan codon instead of a universal stop, and their simplified metabolic pathways. Most of these features are due to the small-size and limited-content of their genomes (580–1840 Kbp; 482–2050 CDS). Yet, the Mycoplasma genus encompasses over 200 species living in close contact with a wide range of animal hosts and man. These include pathogens, pathobionts, or commensals that have retained the full capacity to synthesize DNA, RNA, and all proteins required to sustain a parasitic life-style, with most being able to grow under laboratory conditions without host cells. Over the last 10 years, comparative genome analyses of multiple species and strains unveiled some of the dynamics of mycoplasma genomes. This review summarizes our current knowledge of genomic islands (GIs) found in mycoplasmas, with a focus on pathogenicity islands, integrative and conjugative elements (ICEs), and prophages. Here, we discuss how GIs contribute to the dynamics of mycoplasma genomes and how they participate in the evolution of these minimal organisms. -
Ehrlichiosis in Brazil
Review Article Rev. Bras. Parasitol. Vet., Jaboticabal, v. 20, n. 1, p. 1-12, jan.-mar. 2011 ISSN 0103-846X (impresso) / ISSN 1984-2961 (eletrônico) Ehrlichiosis in Brazil Erliquiose no Brasil Rafael Felipe da Costa Vieira1; Alexander Welker Biondo2,3; Ana Marcia Sá Guimarães4; Andrea Pires dos Santos4; Rodrigo Pires dos Santos5; Leonardo Hermes Dutra1; Pedro Paulo Vissotto de Paiva Diniz6; Helio Autran de Morais7; Joanne Belle Messick4; Marcelo Bahia Labruna8; Odilon Vidotto1* 1Departamento de Medicina Veterinária Preventiva, Universidade Estadual de Londrina – UEL 2Departamento de Medicina Veterinária, Universidade Federal do Paraná – UFPR 3Department of Veterinary Pathobiology, University of Illinois 4Department of Veterinary Comparative Pathobiology, Purdue University, Lafayette 5Seção de Doenças Infecciosas, Hospital de Clínicas de Porto Alegre, Universidade Federal do Rio Grande do Sul – UFRGS 6College of Veterinary Medicine, Western University of Health Sciences 7Department of Clinical Sciences, Oregon State University 8Departamento de Medicina Veterinária Preventiva e Saúde Animal, Universidade de São Paulo – USP Received June 21, 2010 Accepted November 3, 2010 Abstract Ehrlichiosis is a disease caused by rickettsial organisms belonging to the genus Ehrlichia. In Brazil, molecular and serological studies have evaluated the occurrence of Ehrlichia species in dogs, cats, wild animals and humans. Ehrlichia canis is the main species found in dogs in Brazil, although E. ewingii infection has been recently suspected in five dogs. Ehrlichia chaffeensis DNA has been detected and characterized in mash deer, whereas E. muris and E. ruminantium have not yet been identified in Brazil. Canine monocytic ehrlichiosis caused by E. canis appears to be highly endemic in several regions of Brazil, however prevalence data are not available for several regions. -
Sexually Transmitted Infections: Diagnosis and Management
SEXUALLY TRANSMITTED INFECTIONS: DIAGNOSIS AND MANAGEMENT STEPHANIE N. TAYLOR, MD LSUHSC SECTION OF INFECTIOUS DISEASES MEDICAL DIRECTOR, DELGADO CENTER PERSONAL HEALTH CENTER NEW ORLEANS, LA INTRODUCTION Ê Tremendous Public Health Problem Ê AtitdAn estimated 15 m illion AiAmericans acqu ire an STD each year Ê $10 billion dollars in healthcare costs per year Ê Substantial morbidity/mortality Ê Ulcerative and non-ulcerative STDs associated with increased HIV transmission STI PRINCIPLES Ê Counseling – HIV infection, abstinence, and “safer sex” practices Ê STD Screening of asymptomatic individuals and those with symptoms Ê Patients with one STD often have another Ê Partners should be evaluated and treated empirically at the time of presentation STI PRINCIPLES Ê Serologic testing for syphilis should be done in all patients Ê HIV t esti ng sh ould be s trong ly encouraged in all patients (New CDC Recommendation for “Opt-Out” testing) Ê STDs are associated with HIV transmission Major STI Pathogens Ê Bacteria Ê Viruses Ê HSV I & II, HPV, Ê Neisseria HBV, HIV , gonorrhoeae, molluscum Haemophilus ducreyi, Ê Protozoa GdGardnere lla vag inali s Ê Trichomonas Ê Spirochetes vaginalis Ê Fungi Ê Treponema pa llidum Ê Candida albicans Ê Chlamydia Ê Ectoparasites Ê Chlamy dia Ê Phthiris pubis, trachomatis Sarcoptes scabei MAJOR STI SYNDROMES Ê GENITAL ULCER DISEASE Ê URETHRITIS/CERVICITIS Ê PELVIC INFLAMMATORY DISEASE Ê VAGINITIS Ê OTHER VIRAL STDs Ê ECTOPARASITES GENITAL ULCER DISEASE Differential Diagnosis: Ê STIs Ê Syphilis, Herpes, Chancroid Ê LGV, -
Tick-Borne Disease Working Group 2020 Report to Congress
2nd Report Supported by the U.S. Department of Health and Human Services • Office of the Assistant Secretary for Health Tick-Borne Disease Working Group 2020 Report to Congress Information and opinions in this report do not necessarily reflect the opinions of each member of the Working Group, the U.S. Department of Health and Human Services, or any other component of the Federal government. Table of Contents Executive Summary . .1 Chapter 4: Clinical Manifestations, Appendices . 114 Diagnosis, and Diagnostics . 28 Chapter 1: Background . 4 Appendix A. Tick-Borne Disease Congressional Action ................. 8 Chapter 5: Causes, Pathogenesis, Working Group .....................114 and Pathophysiology . 44 The Tick-Borne Disease Working Group . 8 Appendix B. Tick-Borne Disease Working Chapter 6: Treatment . 51 Group Subcommittees ...............117 Second Report: Focus and Structure . 8 Chapter 7: Clinician and Public Appendix C. Acronyms and Abbreviations 126 Chapter 2: Methods of the Education, Patient Access Working Group . .10 to Care . 59 Appendix D. 21st Century Cures Act ...128 Topic Development Briefs ............ 10 Chapter 8: Epidemiology and Appendix E. Working Group Charter. .131 Surveillance . 84 Subcommittees ..................... 10 Chapter 9: Federal Inventory . 93 Appendix F. Federal Inventory Survey . 136 Federal Inventory ....................11 Chapter 10: Public Input . 98 Appendix G. References .............149 Minority Responses ................. 13 Chapter 11: Looking Forward . .103 Chapter 3: Tick Biology, Conclusion . 112 Ecology, and Control . .14 Contributions U.S. Department of Health and Human Services James J. Berger, MS, MT(ASCP), SBB B. Kaye Hayes, MPA Working Group Members David Hughes Walker, MD (Co-Chair) Adalbeto Pérez de León, DVM, MS, PhD Leigh Ann Soltysiak, MS (Co-Chair) Kevin R. -
POULTRY INDUSTRY OVERVIEW Chicken Is a Multi-Billion Dollar Business (For a Few)
POULTRY INDUSTRY OVERVIEW Chicken is a multi-billion dollar business (for a few) America’s favorite meat is a gold mine. In 2014, chicken generated revenues of $ 32.7 billion in the US alone. The three biggest companies control almost 60% of the production, concentrating power in the hands of a few corporations. Poultry companies are called Top Five Poultry Companies INTEGRATORS and they CONTRACT Soy Bean (Ready-To-Cook chicken - mil lb/week) farmers to raise their chickens Tyson Foods 176.64 Pilgrim’s Pride INTEGRATED =owned by the company Corn/Soybean 138.36 The integrator purchases the grains Perdue 56.49 to produce feed Sanderson Farms 58.80 Koch Foods 48.00 Others 159.79 Breeder Company Feed Mill Breeds are developed and owned by 27.6% The integrator creates their own secret feed mixes a firm, oen a subsidiary that they deliver to the farmers 21.7% SUBSIDIARY INTEGRATED 25% 9% 9.2% 7.5% Hatchery Chicks are hatched and sent to broiler farmers Breeder Farm These farms raise chickens who lay INTEGRATED eggs for the hatchery UNDER CONTRACT Broiler Farm Slaughter House Chicks and feed that are owned by the company are delivered to broiler farmers In 2014, chicken farmers raised UNDER CONTRACT Tyson Foods 8.5 billion chickens in the USA 33Processing Plants 33Million/week There are almost 30,000 poultry farmers in the US Pilgrim’s Pride 97% of the chicken we eat is produced under contract 24 Processing Plants 28Million/week INTEGRATED UNDER CONTRACT Tyson Foods produced 1.8 billion chickens Further Processing Pilgrim’s Pride produced 1.5 billion chickens Raw carcasses are turned into frozen or pre-cooked products and packaged for consumers Chicks are raised into slaughter INTEGRATED weight broiler chickens in less than 5 weeks MON TUE WED THU FRI SAT SUN Own Brand Food Services Pilgrim’s Pride as well as most of the poultry companies have contracts with retailers and food services to provide a predictable amount of products with a Many companies like Tyson own their own brands that standardized quality.