Large Scale Immune Profiling of Infected Humans & Goats Reveals Differential Recognition of Brucella melitensis Antigens Video by Kathryn Dullard

Slides:



Advertisements
Similar presentations
Applications of Biotechnological Processes Antibody Production.
Advertisements

Zoonotic infection. Causative agents of the plague, tularemia, brucellosis and anthrax. Laboratory diagnostics and prophylaxis of diseases. Vinnitsa National.
Welcome to Journal club Dr. Md. Abul Hossain Khan Honorary Trainee Department of microbiology, MMC A Comparative Study of Typhidot and Widal Test in Patients.
Brucellosis Sung Chul Hwang, M.D. Dept of Pulmonary and Critical Care Medicine Ajou University School of Medicine.
Molecular Diagnosis of Infectious Diseases. Why use a molecular test to diagnose an infectious disease? Need an accurate and timely diagnosis Important.
Microarrays: Tools for Proteomics
21/1/2008Dr. Salwa Tayel (Brucellosis)1. 21/1/2008Dr. Salwa Tayel (Brucellosis)2 Associate Professor Family and Community Medicine Department King Saud.
Brucellosis Eradication Program 4-H Veterinary Science Extension Veterinary Medicine Texas AgriLife Extension Service College of Veterinary Medicine and.
Brucella Six species of Brucella
Brucellosis By: Leah Kasheta.
Carlee Holden Shay Mueller
Dr. drh. Maxs U.E. Sanam, M.Sc. Brucellosis. Brucellosis, is also known as “undulant fever”, “Mediterranean fever” or “Malta fever” is a zoonosis and.
Brianna Wyble Lacey Clarke
Comparison of the Diagnostic Value of the Standard Tube Agglutination Test and the ELISA IgG and IgM in Patients with Brucellosis Presented by Dr. Md.
Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, Al Jouf University.
BIOT 307 Kuby, Ch. 3, Antigens March, General Introduction Specificity due to recognition of antigenic determinants or epitopes Epitopes = immunologically.
DEPARTMENT OF HEALTH RESEARCH INSTITUTE FOR TROPICAL MEDICINE Ebola Reston in the Philippines Catalino S. Demetria, DVM.
Comparison of the diagnostic value of STA test and ELISA IgG and IgM in patients with Brucellosis Mustafa Ertek, Halil Yzgi, Zulal Ozkart et al. Turk.
Bioterrorist Agents: Brucellosis. Learning Objectives Become familiar with the following aspects of Brucellosis: Become familiar with the following aspects.
Update on Assay Development George J. Dawson, Ph.D. Infectious Diseases: Core R & D Abbott Laboratories West Nile Virus.
Brucellosis A zoonosis. Center for Food Security and Public Health Iowa State University Brucella spp. Gram negative, coccobacilli bacteria Facultative,
Brucellosis The disease and Panbio product training.
Comparison of the diagnostic value of STA test and ELISA IgG and IgM in patients with Brucellosis Mustafa Ertek, Halil Yzgi, Zulal Ozkart et al. Turk J.
GENUS: BRUCELLA Prof. Khalifa Sifaw Ghenghesh بسم الله الرحمن الرحيم.
Hepatitis. Hepatitis is an inflammation of the liver. Hepatitis is caused by several types of viruses as well as drug and chemical toxicity.
Generation of mAbs to FMDV/A and application in a cELISA for the detection of FMDV/A antibodies Dr. M. Yang National Center for Foreign Animal diseases.
Brucellosis Dr. Zahoor.
John R. LaMontagne Memorial Symposium on Pandemic Influenza Research April 4-5, 2005 Institute of Medicine Working Group Five: Immunology, Assay Standardization,
Enterically transmitted hepatitis (Water-borne hepatitis)
MINISTRY OF AGRICULTURE OF AZERBAIJAN REPUBLIC STATE VETERINARY CONTROL SERVICE BRUCELLOSIS IN AZERBAIJAN and REGIONAL PERSPECTIVES (CENTRAL ASIA) Sixth.
PPR Roadmap meeting for the Middle East, Qatar, 1 – 3 December 2015 Feuille de route PPR pour l’Afrique Central, 25 – 25 Aout 2015 PPR situation in Lebanon.
RESULTS Division of Arboviruses, Center for Immunology and Pathology, National Institute of Health, Korea Centers for disease control, Osong, Korea BACKGROUND.
References 1. Ames G.F., Kustu S.G., “Method for obtaining periplasmic proteins from bacterial cells using chloroform”. Patent Number:
Brucella Objectives Describe the general structure, biochemical, Antigenic structures and diagnostic criteria of Brucella. Illustrate the pathogenesis.
Invasive Enteritis and systemic infections: Four clinical syndromes, plus the carrier state, are associated with the genus Salmonella. 1-Gastroenteritis.
Brucella Antibody titers among cattle handlers in a rural community of Bangladesh.
BRUCELLOSIS DR. AREEJ M. N.. EPIDEMIOLOGY Epidemiology Worldwide zoonosisWorldwide zoonosis Only 17 countries declared brucellosis free1986Only 17 countries.
department < clinical chemistry, microbiology and immunology >
DIAGNOSIS OF DISEASES AND GENE THERAPY
Evaluation of Immune Protection Elicited by Recombinant Antigen EtsC
C- reactive protein (CRP)
VIRAL INFLUENZA.
Brucellae.
RICKETTSIA This is a bacterial It resembles viruses in:
The Optimization of a Novel qPCR Assay for Brucellosis
Serological test M.Sc. Sarah Ahmed.
[Undulant fever, Malta fever, Mediterranean fever]
Improving Rev.1 Vaccine Stability Produced in Iran
Laboratory Diagnosis of Infectious Diseases
BRUCELLOSIS Sir David Bruce ( )
Helminths (Trematoda)
Dept. Infectious Disease 2nd Affiliated Hospital CMU
Introduction Brucellosis is an infectious disease caused by bacteria.
بسم الله الرحمن الرحیم Majid Avijgan MD,
Diagnosing Infections
Hepatitis Primary Care: Clinics in Office Practice
Hepatitis B Hepatitis B is a pathogen, which causes liver disease and inflammation of the liver.
ELISA Immuno ExlorerTM HIV/AIDS Diagnostic Tool
Autoantibody Signature in Human Ductal Pancreatic Adenocarcinoma
1/17/ Zoonotic bacteria Capnocytophaga Erysipelothrix Francisella Listeria Pasteurella Spirillum Streptobacillus Yersinia Brucella.
M. Koopmans, E. de Bruin, G. -J. Godeke, I. Friesema, R
Mustansiriyah University College of science Biology Dept
ImmunoWELL Zika Virus Serology.
Asst. Prof. Dr. Dalya Basil Hanna
Volume 92, Issue 4, Pages (February 1998)
Brucellosis control programme in Turkey: Mass vaccination with strains S-19 and Rev-1 administered by conjunctival route Dr. Ahmet Murat SAYTEKİN Brucellosis.
Lecture 14 Antibody-Antigen Reactions
Unit 7: Infectious Diseases
Brucellosis Dr. Salma.
Volume 10, Issue 2, Pages (August 2011)
Presentation transcript:

Large Scale Immune Profiling of Infected Humans & Goats Reveals Differential Recognition of Brucella melitensis Antigens Video by Kathryn Dullard

Brucellosis Zoonotic infectious disease endemic in regions especially in Peru and the Middle East The reservoirs of Brucella melitensis: goats and sheep Brucellosis typically begins with a flu-like illness Inflammation of the liver and spleen, &gastrointestinal or respiratory symptoms can occur. Commonly used screening tests Problematic for differentiate between vaccination & infection in goats Problematic in differentiating acute, chronic and relapsing forms of brucellosis in humans living in endemic regions

Hypothesis The immune response to B.melitensis infection of the natural reservoir host (goat) & the accidental host (human) is similar despite potentially different routes of infection. Current Knowledge of Protein Antigens Relatively small number of immunogenic Brucella abortus protein – recognized by cattle, sheep & mice. Limited studies on recognition of Brucella melitensis in goats & sheep. No individual antigen has proven to be of sufficient diagnostic utility

Materials & Methods Current serological assays to diagnose human brucellosis are based on detection of agglutinating anti-LPS antibodies. Protein microarray A set of 1406 Open Reading Frames from B. melitensis, 1009 antigens selected based on the prediction of protein localization sites, and 397 Open Reading Frames were randomly selected. The array was probed with sera from experimentally infected goats and naturally infected humans from an endemic region in Peru. Data analysis Serodominant antigens = antigens with mean signal intensity > mean + 2 standard deviations above the negative controls.

B. melitensis Serum Samples Human sera: 42 serums = Blood Culture +, Rose Bengal + 18 serums = Blood Culture -, Rose Bengal + 18 serums = Blood Culture -, Rose Bengal – 57 serums = Control Goat sera: Positive and negative (uninfected) controls from a previously conducted vaccine safety study 15 serum samples = specific pathogen-free goat flock as an additional negative control Dose & Route of Inoculum: Humans infected by ingestion of infected goat’s milk products containing a small inoculum the goats were infected with a high dose (107 CFU) of B. melitensis strain 16M via the conjunctiva.

Goat Serodiagnostic Antigens 49 serodominant antigens were identified among 1406 antigens tested. 18 of those antigens were serodiagnostic The remaining 31 cross reactive antigens reacted similarly among all goats samples Human Serodiagnostic Antigens 33 serodominant identified from the 1406 tested 13 of those antigens were serodiagnostic 20 cross reactive antigens reacted similarly amoung all human samples Validation of serodiagnostic accuracy was conducted with immunostrips

Comparing Antigenic Proteins among Humans & Goats 2 common serodiagnostic antigens between humans and goats Top Antigen = Bp26 protein 26KD periplasmic immunogenic protein Immunodominant antigen in infected cattle, sheep, goats & humans 2 nd Antigen = Protease DO (HtrA) Antigens useful for brucellosis diagnosis 11 exclusively for humans 16 exclusively for goats 8 common cross reactive antigens 12 exclusively for humans 23 exclusively for goats

The natural reservoir host (goat) & the accidental host (human) have fundamentally different immune responses against B. melitensis

Discussion Identified several novel serodiagnostic antigens specific for human infection; Useful for the practical development of diagnostics Current assays – Identification of antibodies to LPS Brucella LPS is cross-reavtive with several other species; E. coli, Y. enterocolitica, F. tularensis Identification of diagnostic protein antigens may facilitate the development of more specific serodiagnostic assays Serodiagnostic Antigens for Humans & Goats

Serodiagnostic Antigens Specific for Humans Identified several novel serodiagnostic antigens specific for human infection; Useful for the practical development of diagnostics Current assays – Identification of antibodies to LPS Brucella LPS is cross-reavtive with several other species; E. coli, Y. enterocolitica, F. tularensis Identification of diagnostic protein antigens may facilitate the development of more specific serodiagnostic assays

Serodiagnostic Antigens Specific for Goats

Conclusion Seroreactive & metabolic pathways expressed during infection in these hosts. B. melitensis utilization of peptides and amino acids for growth during infection. Immune responses may be related to species further comment on this possibility is limited by the lack of available data. Both dose and route of inoculum may have contributed to the differential antigen recognition Humans are assumed to have been infected by ingestion of infected goat’s milk products containing a small inoculum the goats were infected with a high dose (107 CFU) of B. melitensis strain 16M via the conjunctiva. Protein expression differences by different strains of B. melitensis unlikely but must be considered as well.