A Mathematical Model for Coinfection of Listeriosis and Anthrax Diseases

Total Page:16

File Type:pdf, Size:1020Kb

A Mathematical Model for Coinfection of Listeriosis and Anthrax Diseases Hindawi International Journal of Mathematics and Mathematical Sciences Volume 2018, Article ID 1725671, 14 pages https://doi.org/10.1155/2018/1725671 Research Article A Mathematical Model for Coinfection of Listeriosis and Anthrax Diseases Shaibu Osman 1 and Oluwole Daniel Makinde 2 1 Department of Mathematics, Pan African University, Institute for Basic Sciences, Technology and Innovations, Box 62000-00200, Nairobi, Kenya 2Faculty of Military Science, Stellenbosch University, Private Bag X2, Saldanha 7395, South Africa Correspondence should be addressed to Shaibu Osman; [email protected] Received 8 April 2018; Accepted 9 July 2018; Published 2 August 2018 Academic Editor: Ram N. Mohapatra Copyright © 2018 Shaibu Osman and Oluwole Daniel Makinde. Tis is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Listeriosis and Anthrax are fatal zoonotic diseases caused by Listeria monocytogene and Bacillus Anthracis, respectively. In this paper, we proposed and analysed a compartmental Listeriosis-Anthrax coinfection model describing the transmission dynamics of Listeriosis and Anthrax epidemic in human population using the stability theory of diferential equations. Our model revealed that the disease-free equilibrium of the Anthrax model only is locally stable when the basic reproduction number is less than one. Sensitivity analysis was carried out on the model parameters in order to determine their impact on the disease dynamics. Numerical simulation of the coinfection model was carried out and the results are displayed graphically and discussed. We simulate the Listeriosis-Anthrax coinfection model by varying the human contact rate to see its efects on infected Anthrax population, infected Listeriosis population, and Listeriosis-Anthrax coinfected population. 1. Introduction in animals cases only. Anthrax disease is caused by bacteria infections and it afects both humans and animals. Our model Listeriosis and Anthrax are fatal zoonotic diseases caused by is an improvement of the two models as we considered Listeria monocytogene and Bacillus Anthracis, respectively. Anthrax as a zoonotic disease and also looked at sensitivity Listeriosis in infants can be acquired in two forms. Mothers analysis and the efects of the contact rate on the disease usually acquire it afer eating foods that are contaminated transmissions. with Listeria monocytogenes and can develop sepsis resulting Authorsin[4]publishedapaperontheefectiveness in chorioamnionitis and delivering a septic infant or fetus. of constant and pulse vaccination policies using SIR model. Moreover, mothers carrying the pathogens in the gastroin- Te analysis of their results under constant vaccination testinal tract can infect the skin and respiratory tract of showed that the dynamics of the disease model is similar their babies during childbirth. Listeria monocytogenes are to the dynamics without vaccination [5, 6]. Tere are some among the commonest pathogens responsible for bacterial fndings on the spread of zoonotic diseases but a number meningitis among neonates. Responsible factors for the of these researches focused on the efect of vaccination on disease include induced immune suppression linked with the spread and transmission of the diseases as in the case HIV infection, hemochromatosis hematologic malignancies, of the authors in [7]. Moreover, authors in [8] investigated cirrhosis, diabetes, and renal failure with hemodialysis [1]. a disease transmission model by considering the impact of Authorsin[2]developedamodelforAnthraxtransmis- a protective vaccine and came up with the optimal vaccine sion but never considered the transmissions in both animal coveragethresholdrequiredfordiseaseeradication.However, and human populations. Our model is an improvement of authors in [9] employed optimal control to study a nonlinear the work done by authors in [2, 3]. Both formulated Anthrax SIR epidemic model with a vaccination strategy. Several models but only concentrated on the disease transmissions mathematical modeling techniques have been employed to 2 International Journal of Mathematics and Mathematical Sciences ℎIa Ω I R I a Ra ℎ a a Ia S S Ia kRa ℎSℎ Ia +Ial (1-)ΥIal Ral Ωℎ S I S R ℎ al I Ial al ℎRal ℎSℎ +ℎIal (1-)(1-Υ)Ial I Ial Sh R l Rl Cp Il Il Il R C ℎ l p p ℎIl Figure 1: Flowchart for the coinfection model. study the role of optimal control using SIR epidemic model infections determines the efects of the contact rate on the [10–12]. Authors in [13] formulated an SIR epidemic model disease transmissions. by considering vaccination as a control measure in their model analysis. Authors in [14] developed a mathematical model for the transmission dynamics of Listeriosis in animal 2. Model Formulation and human populations but did not use optimal control as In this section, we divide the model into subcompartments a control measure in fghting the disease. Tey divided the (groups)asshowninFigure1.Tetotalhumanpopula- animal population into four compartments by introducing tion (�ℎ) is divided into subcompartments consisting of the vaccination compartment. susceptible humans (�ℎ),individualsthatareinfectedwith Authors in [15] formulated a model and employed opti- Anthrax(��), individuals that are infected with Listeriosis mal control to investigate the impact of chemotherapy on (��),individualsthatareinfectedwithbothAnthraxand malaria disease with infection immigrants and [16] applied Listeriosis (���), and those that have recovered from Anthrax, optimal control methods associated with preventing exoge- Listeriosis, and both Anthrax and Listeriosis, respectively, nous reinfection based on a exogenous reinfection tubercu- (��), (��),and(���). Te total vector population is repre- losis model. Authors in [17] conducted a research on the sented by �V;thisisdividedintosubcompartmentsthat identifcation and reservoirs of pathogens for efective control consist of susceptible animals (�V) and animals infected with of sporadic disease and epidemics. Listeria monocytogenes Anthrax (�V),where(��) is population of carcasses of animals is among the major zoonotic food borne pathogen that is in the soil that may have diet of Anthrax. Carcasses of responsible for approximately twenty-eight percent of most animals which may have not been properly disposed of have food-related deaths in the United States annually and a major the tendency of generating pathogens. Te total vector and cause of serious product recalls worldwide. Te dairy farm humanpopulationsarerepresentedas has been observed as a potential point and reservoir for Listeria monocytogenes. Models are widely used in the study of transmission �ℎ =�ℎ +�� +�� +��� +�� +�� +���. (1) dynamics of infectious diseases. In recent times, the appli- � =� +�, cation of mathematical models in the study of infectious ℎ V V diseases has increased tremendously. Hence the emergence of a branch called mathematical epidemiology. Frequent where �=��V/(�+��). diagnostic tests, the availability of clinical data, and electronic Te concentration of carcasses and ingestion rate are surveillance have facilitated the applications of mathematical denoted as � and V, respectively. Listeriosis related death rates models to critical examining of scientifc hypotheses and the are � and �, respectively, and Anthrax related death rates are design of real-life strategies of controlling diseases [18, 19]. � and �, respectively. Waning immunity rates are given by Authors in [20] constructed a coinfection model of �, �,and�.�, �,and� are the recovery rates, respectively, and malaria and cholera diseases with optimal control but never �(1 − �) are the bi-infected persons who have recovered from considered sensitivity analysis and analysis of the force of Anthrax only. Te natural death rates of human and vector infection. Sensitivity analysis determines the most sensitive populations are �ℎ and �V, respectively, and the modifcation parameters to the model and the analysis of the force of parameter is given by �.Tecoinfectedpersonswhohave International Journal of Mathematics and Mathematical Sciences 3 recovered from Listeriosis are denoted by (1 − �)(1 − �).Tis 3.2. Basic Reproduction Number. In this section, the concept implies that of the Next-Generation Matrix would be employed in com- puting the basic reproduction number. Using the theorem �+�(1−�) + (1−�)(1−�) =1. (2) in Van den Driessche and Watmough [21] on the Listeriosis Te following diferential equations were obtained from the model in (4), the basic reproduction number of the Listeriosis fowchart diagram of the coinfection model in Figure 1: only model, (R0�),isgivenby ��ℎ V�Ωℎ =Ωℎ +��� +��� +���� −�ℎ�V�ℎ −��ℎ −�ℎ�ℎ R0� = (6) �� ���ℎ�(�+�ℎ +�) �� � =�� � −�� −(�+� +�)� �� ℎ V ℎ � ℎ � 3.3. Existence of the Disease-Free Equilibrium �� � =�� −�� � −(�+� +�+�)� 3.4. Endemic Equilibrium. Te endemic equilibrium points �� ℎ � V � ℎ � are computed by setting the system of diferential equations �� �� in the Listeriosis only model (4) to zero. Te endemic =�ℎ�V�� +��� +(�+�ℎ +�+�)��� �� equilibrium points are as follows: �� ∗ � ∗ Ωℎ +��� =��� −(�+�ℎ)�� + (1−�) ����� � = , �� ℎ ∗ �ℎ +� �� � (3) �∗�∗ =��� −(�+�ℎ)�� + (1−�) (1 − �) ���� ∗ ℎ �� �� = , (� + �ℎ +�) �� �� ∗ =����� −(�+�ℎ)��� �� �� ∗ � �� = , �+�ℎ ��� (7) =��� +���� −���� ∗ �� ∗ ��� �� = . �� �� V =Ω −� (� +� )� −�� �� V V � �� V V V ∗ ∗ ∗ ∗ �0� =(�ℎ ,�� ,�� ,��) �� V ∗ ∗ ∗ ∗ ∗ =�V (�� +��)�V −�V�V Ω +�� �
Recommended publications
  • Amerithrax Investigative Summary
    The United States Department of Justice AMERITHRAX INVESTIGATIVE SUMMARY Released Pursuant to the Freedom of Information Act Friday, February 19, 2010 TABLE OF CONTENTS I. THE ANTHRAX LETTER ATTACKS . .1 II. EXECUTIVE SUMMARY . 4 A. Overview of the Amerithrax Investigation . .4 B. The Elimination of Dr. Steven J. Hatfill as a Suspect . .6 C. Summary of the Investigation of Dr. Bruce E. Ivins . 6 D. Summary of Evidence from the Investigation Implicating Dr. Ivins . .8 III. THE AMERITHRAX INVESTIGATION . 11 A. Introduction . .11 B. The Investigation Prior to the Scientific Conclusions in 2007 . 12 1. Early investigation of the letters and envelopes . .12 2. Preliminary scientific testing of the Bacillus anthracis spore powder . .13 3. Early scientific findings and conclusions . .14 4. Continuing investigative efforts . 16 5. Assessing individual suspects . .17 6. Dr. Steven J. Hatfill . .19 7. Simultaneous investigative initiatives . .21 C. The Genetic Analysis . .23 IV. THE EVIDENCE AGAINST DR. BRUCE E. IVINS . 25 A. Introduction . .25 B. Background of Dr. Ivins . .25 C. Opportunity, Access and Ability . 26 1. The creation of RMR-1029 – Dr. Ivins’s flask . .26 2. RMR-1029 is the source of the murder weapon . 28 3. Dr. Ivins’s suspicious lab hours just before each mailing . .29 4. Others with access to RMR-1029 have been ruled out . .33 5. Dr. Ivins’s considerable skill and familiarity with the necessary equipment . 36 D. Motive . .38 1. Dr. Ivins’s life’s work appeared destined for failure, absent an unexpected event . .39 2. Dr. Ivins was being subjected to increasing public criticism for his work .
    [Show full text]
  • Investigation of Anthrax Associated with Intentional Exposure
    October 19, 2001 / Vol. 50 / No. 41 889 Update: Investigation of Anthrax Associated with Intentional Exposure and Interim Public Health Guidelines, October 2001 893 Recognition of Illness Associated with the Intentional Release of a Biologic Agent 897 Weekly Update: West Nile Virus Activity — United States, October 10–16, 2001 Update: Investigation of Anthrax Associated with Intentional Exposure and Interim Public Health Guidelines, October 2001 On October 4, 2001, CDC and state and local public health authorities reported a case of inhalational anthrax in Florida (1 ). Additional cases of anthrax subsequently have been reported from Florida and New York City. This report updates the findings of these case investigations, which indicate that infections were caused by the intentional release of Bacillus anthracis. This report also includes interim guidelines for postexposure pro- phylaxis for prevention of inhalational anthrax and other information to assist epidemi- ologists, clinicians, and laboratorians responding to intentional anthrax exposures. For these investigations, a confirmed case of anthrax was defined as 1) a clinically compatible case of cutaneous, inhalational, or gastrointestinal illness* that is laboratory confirmed by isolation of B. anthracis from an affected tissue or site or 2) other labora- tory evidence of B. anthracis infection based on at least two supportive laboratory tests. A suspected case was defined as 1) a clinically compatible case of illness without isola- tion of B. anthracis and no alternative diagnosis, but with laboratory evidence of B. anthracis by one supportive laboratory test or 2) a clinically compatible case of an- thrax epidemiologically linked to a confirmed environmental exposure, but without cor- roborative laboratory evidence of B.
    [Show full text]
  • 2001 Anthrax Letters
    Chapter Five: 2001 Anthrax Letters Author’s Note: The analysis and comments regarding the communication efforts described in this case study are solely those of the authors; this analysis does not represent the official position of the FDA. This case was selected because it is one of the few major federal efforts to distribute medical countermeasures in response to an acute biological incident. These events occurred more than a decade ago and represent the early stages of US biosecurity preparedness and response; however, this incident serves as an excellent illustration of the types of communication challenges expected in these scenarios. Due in part to the extended time since these events and the limited accessibility of individual communications and messages, this case study does not provide a comprehensive assessment of all communication efforts. In contrast to the previous case studies in this casebook, the FDA’s role in the 2001 anthrax response was relatively small, and as such, this analysis focuses principally on the communication efforts of the CDC and state and local public health agencies. The 2001 anthrax attacks have been studied extensively, and the myriad of internal and external assessments led to numerous changes to response and communications policies and protocols. The authors intend to use this case study as a means of highlighting communication challenges strictly within the context of this incident, not to evaluate the success or merit of changes made as a result of these events. Abstract The dissemination of Bacillus anthracis via the US Postal Service (USPS) in 2001 represented a new public health threat, the first intentional exposure to anthrax in the United States.
    [Show full text]
  • Global Burden of Norovirus and Prospects for Vaccine Development
    Global Burden of Norovirus and Prospects for Vaccine Development Primary author Ben Lopman Centers for Disease Control and Prevention Contributors and Reviewers Robert Atmar, Baylor College of Medicine Ralph Baric, University of North Carolina Mary Estes, Baylor College of Medicine Kim Green, NIH; National Institute of Allergy and Infectious Diseases Roger Glass, NIH; Fogarty International Center Aron Hall, Centers for Disease Control and Prevention Miren Iturriza-Gómara, University of Liverpool Cherry Kang, Christian Medical College Bruce Lee, Johns Hopkins University Umesh Parashar, Centers for Disease Control and Prevention Mark Riddle, Naval Medical Research Center Jan Vinjé, Centers for Disease Control and Prevention The findings and conclusions in this report are those of the authors and do not necessarily represent the official position of the Centers for Disease Control and Prevention, or the US Department of Health and Human Services. This work was funded in part by a grant from the Bill & Melinda Gates Foundation to the CDC Foundation. GLOBAL BURDEN OF NOROVIRUS AND PROSPECTS FOR VACCINE DEVELOPMENT | 1 Table of Contents 1. Executive summary ....................................................................3 2. Burden of disease and epidemiology 7 a. Burden 7 i. Global burden and trends of diarrheal disease in children and adults 7 ii. The role of norovirus 8 b. Epidemiology 9 i. Early childhood infections 9 ii. Risk factors, modes and settings of transmission 10 iii. Chronic health consequences associated with norovirus infection? 11 c. Challenges in attributing disease to norovirus 12 3. Norovirus biology, diagnostics and their interpretation for field studies and clinical trials..15 a. Norovirus virology 15 i. Genetic diversity, evolution and related challenges for diagnosis 15 ii.
    [Show full text]
  • Lessons from the Anthrax Attacks Implications for US
    Lessons from the Anthrax Attacks Implications for US. Bioterrorism Preparedness A Report on a National Forum on Biodefense Author David Heymart Research Assistants Srusha Ac h terb erg, L Joelle Laszld Organized by the Center for Strategic and International Studies and the Defense Threat Reduction Agency --CFr”V? --.....a DlSTRf BUTION This report ISfor official use only; distribution authorized to U S. government agencies, designated contractors, and those with an official need Contains information that may be exempt from public release under the Freedom of Information Act. exemption number 2 (5 USC 552); exemption number 3 (’lo USC 130).Approvalof the Defense Threat Reduction Agency prior to public release is requrred Contract Number OTRAM-02-C-0013 For Official Use Only About CSIS For four decades, the Center for Stravgic and Internahonal Studies (CSIS)has been dedicated 10 providing world leaders with strategic insights on-and pohcy solubons tcurrentand emergtng global lssues CSIS IS led by John J Hamre, former L S deputy secretary of defense It is guided by a board of trustees chaired by former U S senator Sam Nunn and consistlng of prominent individuals horn both the public and private sectors The CSIS staff of 190 researchers and support staff focus pnrnardy on three subjecr areas First, CSIS addresses the fuU spectrum of new challenges to national and mternabonal security Second, it maintains resident experts on all of the world's myor geographical regions Third, it IS committed to helping to develop new methods of governance for the global age, to this end, CSIS has programs on technology and pubhc policy, International trade and finance, and energy Headquartered in Washington, D-C ,CSIS IS pnvate, bipartlsan, and tax-exempt CSIS docs not take specific policy positions, accordygly, all views expressed herein should be understood to be solely those ofthe author Spousor.
    [Show full text]
  • African Meningitis Belt
    WHO/EMC/BAC/98.3 Control of epidemic meningococcal disease. WHO practical guidelines. 2nd edition World Health Organization Emerging and other Communicable Diseases, Surveillance and Control This document has been downloaded from the WHO/EMC Web site. The original cover pages and lists of participants are not included. See http://www.who.int/emc for more information. © World Health Organization This document is not a formal publication of the World Health Organization (WHO), and all rights are reserved by the Organization. The document may, however, be freely reviewed, abstracted, reproduced and translated, in part or in whole, but not for sale nor for use in conjunction with commercial purposes. The views expressed in documents by named authors are solely the responsibility of those authors. The mention of specific companies or specific manufacturers' products does no imply that they are endorsed or recommended by the World Health Organization in preference to others of a similar nature that are not mentioned. CONTENTS CONTENTS ................................................................................... i PREFACE ..................................................................................... vii INTRODUCTION ......................................................................... 1 1. MAGNITUDE OF THE PROBLEM ........................................................3 1.1 REVIEW OF EPIDEMICS SINCE THE 1970S .......................................................................................... 3 Geographical distribution
    [Show full text]
  • Anthrax Reporting and Investigation Guideline
    Anthrax Signs and Symptoms depend on the type of infection; all types can cause severe illness: Symptoms • Cutaneous: painless, pruritic papules or vesicles which form black eschars, often surrounded by edema or erythema. Fever and lymphadenopathy may occur. • Ingestion: Oropharyngeal: mucosal lesion in the oral cavity or oropharynx, sore throat, difficulty swallowing, and swelling of neck. Fever, fatigue, shortness of breath, abdominal pain, nausea/vomiting may occur. Gastrointestinal: abdominal pain, nausea, vomiting/diarrhea, abdominal swelling. Fever, fatigue, and headache are common. • Inhalation: Biphasic, presenting with fever, chills, fatigue, followed by cough, chest pain, shortness of breath, nausea/vomiting, abdominal pain, headache, diaphoresis, and altered mental status. Pleural effusion or mediastinal widening on imaging. • Injection: Severe soft tissue infection; no apparent eschar. Fever, shortness of breath, nausea may occur. Occasional meningeal or abdominal involvement. Incubation Usually < 1 week but as long as 60 days for inhalational anthrax Case Clinical criteria: An illness with at least one specific OR two non-specific symptoms and signs classification that are compatible with one of the above 4 types, systemic involvement, or anthrax meningitis; OR death of unknown cause and consistent organ involvement Confirmed: Clinically Probable: Clinically consistent with Suspect: Clinically consistent with isolation, consistent Gram-positive rods, OR positive consistent with positive IHC, 4-fold rise in test from CLIA-accredited laboratory, OR anthrax test ordered antibodies, PCR, or LF MS epi evidence relating to anthrax but no epi evidence Differential Varies by form; mononucleosis, cat-scratch fever, tularemia, plague, sepsis, bacterial or viral diagnosis pneumonia, mycobacterial infection, influenza, hantavirus Treatment Appropriate antibiotics and supportive care; anthrax antitoxin if spores are activated.
    [Show full text]
  • Bioterrorism, Biological Weapons and Anthrax
    Bioterrorism, Biological Weapons and Anthrax Part IV Written by Arthur H. Garrison Criminal Justice Planning Coordinator Delaware Criminal Justice Council Bioterrorism and biological weapons The use of bio-terrorism and bio-warfare dates back to 6th century when the Assyrians poisoned the well water of their enemies. The goal of using biological weapons is to cause massive sickness or death in the intended target. Bioterrorism and biological weapons The U.S. took the threat of biological weapons attack seriously after Gulf War. Anthrax vaccinations of U.S. troops Investigating Iraq and its biological weapons capacity The Soviet Union manufactured various types of biological weapons during the 1980’s • To be used after a nuclear exchange • Manufacturing new biological weapons – Gene engineering – creating new types of viruses/bacteria • Contagious viruses – Ebola, Marburg (Filoviruses) - Hemorrhagic fever diseases (vascular system dissolves) – Smallpox The spread of biological weapons after the fall of the Soviet Union •Material • Knowledge and expertise •Equipment Bioterrorism and biological weapons There are two basic categories of biological warfare agents. Microorganisms • living organic germs, such as anthrax (bacillus anthrax). –Bacteria –Viruses Toxins • By-products of living organisms (natural poisons) such as botulism (botulinum toxin) which is a by- product of growing the microorganism clostridium botulinum Bioterrorism and biological weapons The U.S. was a leader in the early research on biological weapons Research on making
    [Show full text]
  • Antibacterial Photosensitization Through Activation of PNAS PLUS Coproporphyrinogen Oxidase
    Antibacterial photosensitization through activation of PNAS PLUS coproporphyrinogen oxidase Matthew C. Surdela, Dennis J. Horvath Jr.a, Lisa J. Lojeka, Audra R. Fullena, Jocelyn Simpsona, Brendan F. Dutterb,c, Kenneth J. Sallenga, Jeremy B. Fordd, J. Logan Jenkinsd, Raju Nagarajane, Pedro L. Teixeiraf, Matthew Albertollec,g, Ivelin S. Georgieva,e,h, E. Duco Jansend, Gary A. Sulikowskib,c, D. Borden Lacya,d, Harry A. Daileyi,j,k, and Eric P. Skaara,1 aDepartment of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, TN 37232; bDepartment of Chemistry, Vanderbilt University, Nashville, TN 37232; cVanderbilt Institute for Chemical Biology, Nashville, TN 37232; dDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN 37232; eVanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN 37232; fBiomedical Informatics, Vanderbilt University School of Medicine, Nashville, TN 37203; gDepartment of Biochemistry, Vanderbilt University, Nashville, TN 37232; hDepartment of Electrical Engineering and Computer Science, Vanderbilt University, Nashville, TN 37232; iBiomedical and Health Sciences Institute, University of Georgia, Athens, GA 30602; jDepartment of Microbiology, University of Georgia, Athens, GA 30602; and kDepartment of Biochemistry and Molecular Biology, University of Georgia, Athens, GA 30602 Edited by Ferric C. Fang, University of Washington School of Medicine, Seattle, WA, and accepted by Editorial Board Member Carl F. Nathan June 26, 2017 (received for review January 10, 2017) Gram-positive bacteria cause the majority of skin and soft tissue Small-molecule VU0038882 (‘882) was previously identified in infections (SSTIs), resulting in the most common reason for clinic a screen for activators of the S. aureus heme-sensing system two- visits in the United States.
    [Show full text]
  • Novel Risk Factors for Coronavirus Disease-Associated Mucormycosis (CAM): a Case Control Study During the Outbreak in India
    medRxiv preprint doi: https://doi.org/10.1101/2021.07.24.21261040; this version posted July 26, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license . Novel risk factors for Coronavirus disease-associated mucormycosis (CAM): a case control study during the outbreak in India Umang Arora1, Megha Priyadarshi1, Varidh Katiyar2, Manish Soneja1, Prerna Garg1, Ishan Gupta1,- Vishwesh Bharadiya1, Parul Berry1, Tamoghna Ghosh1, Lajjaben Patel1 , Radhika Sarda1, Shreya Garg3, Shubham Agarwal1, Veronica Arora4, Aishwarya Ramprasad1, Amit Kumar1, Rohit Kumar Garg1, Parul Kodan1, Neeraj Nischal1, Gagandeep Singh5, Pankaj Jorwal1, Arvind Kumar1, Upendra Baitha1, Ved Prakash Meena1, Animesh Ray1, Prayas Sethi1, , Immaculata Xess5, Naval Vikram1, Sanjeev Sinha1, Ashutosh Biswas1,Alok Thakar3, Sushma Bhatnagar6, Anjan Trikha7, Naveet Wig1 1Department of Medicine, AIIMS, Delhi, India 2Department of Neurosurgery, AIIMS, Delhi, India 3Department of Otolaryngology & Head-Neck Surgery, AIIMS, Delhi, India 4Department of Medical Genetics, Sir Ganga Ram Hospital, Delhi, India 5Department of Microbiology, AIIMS, Delhi, India 6Department of Onco-anaesthesia and Palliative Medicine, AIIMS, Delhi, India 7Department of Anaesthesiology, Pain Medicine and Critical Care, AIIMS, Delhi, India 1. Umang Arora, MD (Medicine), Junior Resident, Department of Medicine, AIIMS, Delhi, India. E-mail ID: [email protected] 2. Megha Priyadarshi, DM (Infectious disease), Junior Resident, Department of Medicine, AIIMS, Delhi, India. E-mail ID: [email protected] 3. Varidh Katiyar, MCh (Neurosurgery), Chief Resident, Department of Neurosurgery AIIMS, Delhi, India. E-mail ID: [email protected] 4.
    [Show full text]
  • Gao-15-80, Anthrax
    United States Government Accountability Office Report to Congressional Requesters December 2014 ANTHRAX Agency Approaches to Validation and Statistical Analyses Could Be Improved GAO-15-80 December 2014 ANTHRAX Agency Approaches to Validation and Statistical Analyses Could Be Improved Highlights of GAO-15-80, a report to congressional requesters Why GAO Did This Study What GAO Found In 2001, the FBI investigated an After the 2001 Anthrax attacks, the genetic tests that were conducted by the intentional release of B. anthracis, a Federal Bureau of Investigation’s (FBI) four contractors were generally bacterium that causes anthrax, which scientifically verified and validated, and met the FBI’s criteria. However, GAO was identified as the Ames strain. found that the FBI lacked a comprehensive approach—or framework—that could Subsequently, FBI contractors have ensured standardization of the testing process. As a result, each of the developed and validated several contractors developed their tests differently, and one contractor did not conduct genetic tests to analyze B. anthracis verification testing, a key step in determining whether a test will meet a user’s samples for the presence of certain requirements, such as for sensitivity or accuracy. Also, GAO found that the genetic mutations. The FBI had contractors did not develop the level of statistical confidence for interpreting the previously collected and maintained testing results for the validation tests they performed. Responses to future these samples in a repository. incidents could be improved by using a standardized framework for achieving GAO was asked to review the FBI’s minimum performance standards during verification and validation, and by genetic test development process and incorporating statistical analyses when interpreting validation testing results.
    [Show full text]
  • The Interaction Between Human Antimicrobial Use and the Risk of Foodborne Zoonotic Bacteria
    Downloaded from orbit.dtu.dk on: Dec 20, 2017 The interaction between human antimicrobial use and the risk of foodborne zoonotic bacteria Koningstein, Maike; Hald, Tine; Mølbak, Kåre Publication date: 2014 Document Version Peer reviewed version Link back to DTU Orbit Citation (APA): Koningstein, M., Hald, T., & Mølbak, K. (2014). The interaction between human antimicrobial use and the risk of foodborne zoonotic bacteria. National Food Institute, Technical University of Denmark. General rights Copyright and moral rights for the publications made accessible in the public portal are retained by the authors and/or other copyright owners and it is a condition of accessing publications that users recognise and abide by the legal requirements associated with these rights. • Users may download and print one copy of any publication from the public portal for the purpose of private study or research. • You may not further distribute the material or use it for any profit-making activity or commercial gain • You may freely distribute the URL identifying the publication in the public portal If you believe that this document breaches copyright please contact us providing details, and we will remove access to the work immediately and investigate your claim. The interaction between human antimicrobial use and the risk of foodborne zoonotic bacteria Maike Koningstein, M.Sc. PhD Thesis 2013 Statens Serum Institute Department of Infectious Disease Epidemiology Artillerivej 5, 2300 Copenhagen, Denmark and National Food Institute, DTU Department for Microbiology
    [Show full text]