Origin and Spread of Syphilis
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LYME DISEASE Other Names: Borrelia Burgdorferi
LYME DISEASE Other names: Borrelia burgdorferi CAUSE Lyme disease is caused by a spirochete bacteria (Borrelia burgdorferi) that is transmitted through the bite from an infected arthropod vector, the black-legged or deer tick Ixodes( scapularis). SIGNIFICANCE Lyme disease can infect people and some species of domestic animals (cats, dogs, horses, and cattle) causing mild to severe illness. Although wildlife can be infected by the bacteria, it typically does not cause illness in them. TRANSMISSION The bacteria has been observed in the blood of a number of wildlife species including several bird species but rarely appears to cause illness in these species. White-footed mice, eastern chipmunks, and shrews serve as the primary natural reservoirs for Lyme disease in eastern and central parts of North America. Other species appear to have low competencies as reservoirs for the bacteria. The transmission of Lyme disease is relatively convoluted due to the complex life cycle of the black-legged tick. This tick has multiple developmental stages and requires three hosts during its life cycle. The life cycle begins with the eggs of the ticks that are laid in the spring and from which larval ticks emerge. Larval ticks do not initially carryBorrelia burgdorferi, the bacteria must be acquired from their hosts they feed upon that are carriers of the bacteria. Through the summer the larval ticks feed on the blood of their first host, typically small mammals and birds. It is at this point where ticks may first acquireBorrelia burgdorferi. In the fall the larval ticks develop into nymphs and hibernate through the winter. -
Geographically Tracking the Syphilis Outbreak in Houston/Harris County, TX
Stop the Spread: Geographically Tracking the Syphilis Outbreak in Houston/Harris County, TX Monica Branch MD Candidate 2017 Chicago Medical School at Rosalind Franklin University of Medicine & Science 2014 GE-National Medical Fellowships Primary Care Leadership Program Scholar Legacy Community Health Services, Houston, TX Abstract In 2012, the Houston Department of Health and Human Services (HDHHS) declared a syphilis outbreak in Houston/Harris County after observing a 97% increase in the number of primary and secondary syphilis infections compared to the same time period in 20112,3. The purpose of this project was to identify the prevalence of syphilis infections by zip code. Identifying these geographical areas will assist the S.E.A.C. and Legacy Community Health Services in deploying resources to these communities in efforts to provide education and screening to these high-risk populations. An inquiry of Legacy’s electronic medical records system (Centricity) was performed to identify the number of syphilis infections by zip code and by sex, race/ethnicity, and HIV co-infection in Houston/Harris County among all active patients at Legacy Community Health Services. A total of 1,282 syphilis cases were reported among active patients in Centricity. The majority (91%) was male; (88%) of those males were HIV+; and (41%) were Black. The overall prevalence of syphilis among the 97 zip codes in Houston/Harris County is 4.40%. The majority of the syphilis diagnoses (98 cases;7.64%) were within the 77006 zip code among white males with a prevalence of 0.5%. However, other areas outside of this zip code reported syphilis cases where 67-97% were among Black males. -
Phagocytosis of Borrelia Burgdorferi, the Lyme Disease Spirochete, Potentiates Innate Immune Activation and Induces Apoptosis in Human Monocytes Adriana R
University of Connecticut OpenCommons@UConn UCHC Articles - Research University of Connecticut Health Center Research 1-2008 Phagocytosis of Borrelia burgdorferi, the Lyme Disease Spirochete, Potentiates Innate Immune Activation and Induces Apoptosis in Human Monocytes Adriana R. Cruz University of Connecticut School of Medicine and Dentistry Meagan W. Moore University of Connecticut School of Medicine and Dentistry Carson J. La Vake University of Connecticut School of Medicine and Dentistry Christian H. Eggers University of Connecticut School of Medicine and Dentistry Juan C. Salazar University of Connecticut School of Medicine and Dentistry See next page for additional authors Follow this and additional works at: https://opencommons.uconn.edu/uchcres_articles Part of the Medicine and Health Sciences Commons Recommended Citation Cruz, Adriana R.; Moore, Meagan W.; La Vake, Carson J.; Eggers, Christian H.; Salazar, Juan C.; and Radolf, Justin D., "Phagocytosis of Borrelia burgdorferi, the Lyme Disease Spirochete, Potentiates Innate Immune Activation and Induces Apoptosis in Human Monocytes" (2008). UCHC Articles - Research. 182. https://opencommons.uconn.edu/uchcres_articles/182 Authors Adriana R. Cruz, Meagan W. Moore, Carson J. La Vake, Christian H. Eggers, Juan C. Salazar, and Justin D. Radolf This article is available at OpenCommons@UConn: https://opencommons.uconn.edu/uchcres_articles/182 INFECTION AND IMMUNITY, Jan. 2008, p. 56–70 Vol. 76, No. 1 0019-9567/08/$08.00ϩ0 doi:10.1128/IAI.01039-07 Copyright © 2008, American Society for Microbiology. All Rights Reserved. Phagocytosis of Borrelia burgdorferi, the Lyme Disease Spirochete, Potentiates Innate Immune Activation and Induces Apoptosis in Human Monocytesᰔ Adriana R. Cruz,1†‡ Meagan W. Moore,1† Carson J. -
Pre-Antibiotic Therapy of Syphilis Charles T
University of Kentucky UKnowledge Microbiology, Immunology, and Molecular Microbiology, Immunology, and Molecular Genetics Faculty Publications Genetics 2016 Pre-Antibiotic Therapy of Syphilis Charles T. Ambrose University of Kentucky, [email protected] Right click to open a feedback form in a new tab to let us know how this document benefits oy u. Follow this and additional works at: https://uknowledge.uky.edu/microbio_facpub Part of the Medical Immunology Commons Repository Citation Ambrose, Charles T., "Pre-Antibiotic Therapy of Syphilis" (2016). Microbiology, Immunology, and Molecular Genetics Faculty Publications. 83. https://uknowledge.uky.edu/microbio_facpub/83 This Article is brought to you for free and open access by the Microbiology, Immunology, and Molecular Genetics at UKnowledge. It has been accepted for inclusion in Microbiology, Immunology, and Molecular Genetics Faculty Publications by an authorized administrator of UKnowledge. For more information, please contact [email protected]. Pre-Antibiotic Therapy of Syphilis Notes/Citation Information Published in NESSA Journal of Infectious Diseases and Immunology, v. 1, issue 1, p. 1-20. © 2016 C.T. Ambrose This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. This article is available at UKnowledge: https://uknowledge.uky.edu/microbio_facpub/83 Journal of Infectious Diseases and Immunology Volume 1| Issue 1 Review Article Open Access PRE-ANTIBIOTICTHERAPY OF SYPHILIS C.T. Ambrose, M.D1* 1Department of Microbiology, College of Medicine, University of Kentucky *Corresponding author: C.T. Ambrose, M.D, College of Medicine, University of Kentucky Department of Microbiology, E-mail: [email protected] Citation: C.T. -
The False Narrative of Syphilis and Its Origin in Europe
Bowling Green State University ScholarWorks@BGSU HIST 4800 Early America in the Atlantic World (Herndon) HIST 4800 Summer 6-11-2014 Neither “Headache” Nor “Illness:” The False Narrative of Syphilis and its Origin in Europe Michael W. Horton Bowling Green State University, [email protected] Follow this and additional works at: https://scholarworks.bgsu.edu/hist4800_atlanticworld Part of the European History Commons, and the History of Science, Technology, and Medicine Commons Repository Citation Horton, Michael W., "Neither “Headache” Nor “Illness:” The False Narrative of Syphilis and its Origin in Europe" (2014). HIST 4800 Early America in the Atlantic World (Herndon). 2. https://scholarworks.bgsu.edu/hist4800_atlanticworld/2 This Student Project is brought to you for free and open access by the HIST 4800 at ScholarWorks@BGSU. It has been accepted for inclusion in HIST 4800 Early America in the Atlantic World (Herndon) by an authorized administrator of ScholarWorks@BGSU. Mike Horton HIST 4800: Research Seminar Dr. Ruth Herndon June 11, 2014 Neither “Headache” Nor “Illness:” The False Narrative of Syphilis and its Origin in Europe. Abstract In this paper I argue that the master narrative of the origin of syphilis in Europe, known as the Columbian Theory does not hold up to historical review since it does not contain enough concrete evidence for we as historians to be comfortable with as the master narrative. To form my argument I use the writings of Girolamo Fracastoro, an Italian physician known for coining the term “syphilis,” as the basis when I review the journal of Christopher Columbus. I review his journal, which chronicles the first voyage to the Americas, to see if there is any connection between the syphilis disease and him or his crew. -
Canine Lyme Borrelia
Canine Lyme Borrelia Borrelia burgdorferi bacteria are the cause of Lyme disease in humans and animals. They can be visualized by darkfild microscopy as "corkscrew-shaped" motile spirochetes (400 x). Inset: The black-legged tick, lxodes scapularis (deer tick), may carry and transmit Borrelia burgdorferi to humans and animals during feeding, and thus transmit Lyme disease. Samples: Blood EDTA-blood as is, purple-top tubes or EDTA-blood preserved in sample buffer (preferred) Body fluids Preserved in sample buffer Notes: Send all samples at room temperature, preferably preserved in sample buffer MD Submission Form Interpretation of PCR Results: High Positive Borrelia spp. infection (interpretation must be correlated to (> 500 copies/ml swab) clinical symptoms) Low Positive (<500 copies/ml swab) Negative Borrelia spp. not detected Lyme Borreliosis Lyme disease is caused by spirochete bacteria of a subgroup of Borrelia species, called Borrelia burgdorferi sensu lato. Only one species, B. burgdorferi sensu stricto, is known to be present in the USA, while at least four pathogenic species, B. burgdorferi sensu stricto, B. afzelii, B. garinii, B. japonica have been isolated in Europe and Asia (Aguero- Rosenfeld et al., 2005). B. burgdorferi sensu lato organisms are corkscrew-shaped, motile, microaerophilic bacteria of the order Spirochaetales. Hard-shelled ticks of the genus Ixodes transmit B. burgdorferi by attaching and feeding on various mammalian, avian, and reptilian hosts. In the northeastern states of the US Ixodes scapularis, the black-legged deer tick, is the predominant vector, while at the west coast Lyme borreliosis is maintained by a transmission cycle which involves two tick species, I. -
Borrelia Burgdorferi and Treponema Pallidum: a Comparison of Functional Genomics, Environmental Adaptations, and Pathogenic Mechanisms
PERSPECTIVE SERIES Bacterial polymorphisms Martin J. Blaser and James M. Musser, Series Editors Borrelia burgdorferi and Treponema pallidum: a comparison of functional genomics, environmental adaptations, and pathogenic mechanisms Stephen F. Porcella and Tom G. Schwan Laboratory of Human Bacterial Pathogenesis, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, NIH, Hamilton, Montana, USA Address correspondence to: Tom G. Schwan, Rocky Mountain Laboratories, 903 South 4th Street, Hamilton, Montana 59840, USA. Phone: (406) 363-9250; Fax: (406) 363-9445; E-mail: [email protected]. Spirochetes are a diverse group of bacteria found in (6–8). Here, we compare the biology and genomes of soil, deep in marine sediments, commensal in the gut these two spirochetal pathogens with reference to their of termites and other arthropods, or obligate parasites different host associations and modes of transmission. of vertebrates. Two pathogenic spirochetes that are the focus of this perspective are Borrelia burgdorferi sensu Genomic structure lato, a causative agent of Lyme disease, and Treponema A striking difference between B. burgdorferi and T. pal- pallidum subspecies pallidum, the agent of venereal lidum is their total genomic structure. Although both syphilis. Although these organisms are bound togeth- pathogens have small genomes, compared with many er by ancient ancestry and similar morphology (Figure well known bacteria such as Escherichia coli and Mycobac- 1), as well as by the protean nature of the infections terium tuberculosis, the genomic structure of B. burgdorferi they cause, many differences exist in their life cycles, environmental adaptations, and impact on human health and behavior. The specific mechanisms con- tributing to multisystem disease and persistent, long- term infections caused by both organisms in spite of significant immune responses are not yet understood. -
A Rare Case of Tabes Dorsalis
Journal of Gynecology and Women’s Health ISSN 2474-7602 Case Report J Gynecol Women’s Health Volume 17 Issue 2- November 2019 Copyright © All rights are reserved by Tobe S Momah DOI: 10.19080/JGWH.2019.17.555960 A Rare Case of Tabes Dorsalis Tobe S Momah*, Bhavsar Parth, Jones Shawntiah, Berry Kelsey and Duff David Department of Family Medicine, University of Mississippi Medical Center, USA Submission: November 05, 2019; Published: November 12, 2019 *Corresponding author: Tobe S Momah, Department of Family Medicine, University of Mississippi Medical Center, USA Background Tabes Dorsalis has become a rare clinical presentation in cases of neuro syphilis since the advent of antibiotics. The recent surge in syphilis cases [1], however, has once again raised interest in the diagnosis and treatment of this rare clinical entity. In this case report, a case of tabes dorsalis in an 82 year African American female is presented. She, also, had right peroneal nerve mono neuropathy that challenged the clinical diagnosis of tabes dorsalis and complicated its management. Keywords: Emergency room; Patient’s laboratory; Arterial duplex; Neurology; Magnetic Resonance; Cerebro Spinal; Serology returned; Physical therapy; Tabes dorsalis Abbreviatations: ER: Emergency Room; CT: Computerized Tomography; MRI: Magnetic Resonance Imaging; CSF: Cerebro Spinal Fluid; RPR: Rapid Plasma Reagin; EMG: Electromyography; PT: Physical Therapy Case Report ness of breath, chest pain or loss of consciousness. Patient’s lab- oratory values were significant for low copper (743mcg/l) and thrombocytopeniaPatient was assessed (64,000k/UL). in ER and determined to have impaired sensation in right lower extremity with inability to move the right leg in any direction. -
WO 2014/134709 Al 12 September 2014 (12.09.2014) 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 2014/134709 Al 12 September 2014 (12.09.2014) P O P C T (51) International Patent Classification: (81) Designated States (unless otherwise indicated, for every A61K 31/05 (2006.01) A61P 31/02 (2006.01) kind of national protection available): AE, AG, AL, AM, AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, (21) International Application Number: BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DK, DM, PCT/CA20 14/000 174 DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, (22) International Filing Date: HN, HR, HU, ID, IL, IN, IR, IS, JP, KE, KG, KN, KP, KR, 4 March 2014 (04.03.2014) KZ, LA, LC, LK, LR, LS, LT, LU, LY, MA, MD, ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, (25) Filing Language: English OM, PA, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, SA, (26) Publication Language: English SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, (30) Priority Data: ZW. 13/790,91 1 8 March 2013 (08.03.2013) US (84) Designated States (unless otherwise indicated, for every (71) Applicant: LABORATOIRE M2 [CA/CA]; 4005-A, rue kind of regional protection available): ARIPO (BW, GH, de la Garlock, Sherbrooke, Quebec J1L 1W9 (CA). GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, SZ, TZ, UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, RU, TJ, (72) Inventors: LEMIRE, Gaetan; 6505, rue de la fougere, TM), European (AL, AT, BE, BG, CH, CY, CZ, DE, DK, Sherbrooke, Quebec JIN 3W3 (CA). -
Introduction to Bacteriology and Bacterial Structure/Function
INTRODUCTION TO BACTERIOLOGY AND BACTERIAL STRUCTURE/FUNCTION LEARNING OBJECTIVES To describe historical landmarks of medical microbiology To describe Koch’s Postulates To describe the characteristic structures and chemical nature of cellular constituents that distinguish eukaryotic and prokaryotic cells To describe chemical, structural, and functional components of the bacterial cytoplasmic and outer membranes, cell wall and surface appendages To name the general structures, and polymers that make up bacterial cell walls To explain the differences between gram negative and gram positive cells To describe the chemical composition, function and serological classification as H antigen of bacterial flagella and how they differ from flagella of eucaryotic cells To describe the chemical composition and function of pili To explain the unique chemical composition of bacterial spores To list medically relevant bacteria that form spores To explain the function of spores in terms of chemical and heat resistance To describe characteristics of different types of membrane transport To describe the exact cellular location and serological classification as O antigen of Lipopolysaccharide (LPS) To explain how the structure of LPS confers antigenic specificity and toxicity To describe the exact cellular location of Lipid A To explain the term endotoxin in terms of its chemical composition and location in bacterial cells INTRODUCTION TO BACTERIOLOGY 1. Two main threads in the history of bacteriology: 1) the natural history of bacteria and 2) the contagious nature of infectious diseases, were united in the latter half of the 19th century. During that period many of the bacteria that cause human disease were identified and characterized. 2. Individual bacteria were first observed microscopically by Antony van Leeuwenhoek at the end of the 17th century. -
Treponema Pallidum, the Syphilis Spirochete: Making a Living As a Stealth Pathogen
HHS Public Access Author manuscript Author ManuscriptAuthor Manuscript Author Nat Rev Manuscript Author Microbiol. Author Manuscript Author manuscript; available in PMC 2017 June 01. Published in final edited form as: Nat Rev Microbiol. 2016 December ; 14(12): 744–759. doi:10.1038/nrmicro.2016.141. Treponema pallidum, the syphilis spirochete: making a living as a stealth pathogen Justin D. Radolf1, Ranjit K. Deka2, Arvind Anand3, David Šmajs4, Michael V. Norgard5, and X. Frank Yang6 1Departments of Medicine, Pediatrics, Genetics and Genomic Science, Molecular Biology and Biophysics, and Immunology, UConn Health, Farmington, CT, USA 2Department of Microbiology, The University of Texas Southwestern Medical Center, Dallas, TX, USA 3Department of Medicine, UConn Health, Farmington, CT, USA 4Department of Biology, Faculty of Medicine, Masaryk University, Brno, Czech Republic 5Department of Microbiology, The University of Texas Southwestern Medical Center, Dallas, TX, USA 6Department of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, IN Abstract The last two decades have seen a worldwide resurgence in infections caused by Treponema pallidum subsp. pallidum, the syphilis spirochete. The syphilis spirochete’s well-recognized capacity for early dissemination and immune evasion has earned it the designation ‘the stealth pathogen’. Despite the many hurdles to studying syphilis pathogenesis, most notably the inability to culture and to genetically manipulate T. pallidum, in recent years, considerable progress has been made in elucidating the structural, physiologic, and regulatory facets of stealth pathogenicity. In this Review, we integrate this eclectic body of information to garner fresh insights into the highly successful parasitic lifestyles of the syphilis spirochete and related pathogenic treponemes. Pathogenic treponemes cause venereal syphilis, yaws, endemic syphilis, and pinta—multi- stage, infections that, although similar, can be differentiated based on clinical, epidemiologic, and geographic criteria1,2. -
WHO GUIDELINES for the Treatment of Treponema Pallidum (Syphilis)
WHO GUIDELINES FOR THE Treatment of Treponema pallidum (syphilis) WHO GUIDELINES FOR THE Treatment of Treponema pallidum (syphilis) WHO Library Cataloguing-in-Publication Data WHO guidelines for the treatment of Treponema pallidum (syphilis). Contents: Web annex D: Evidence profiles and evidence-to-decision frameworks - Web annex E: Systematic reviews for syphilis guidelines - Web annex F: Summary of conflicts of interest 1.Syphilis – drug therapy. 2.Treponema pallidum. 3.Sexually Transmitted Diseases. 4.Guideline. I.World Health Organization. ISBN 978 92 4 154980 6 (NLM classification: WC 170) © World Health Organization 2016 All rights reserved. Publications of the World Health Organization are available on the WHO website (http://www.who.int) or can be purchased from WHO Press, World Health Organization, 20 Avenue Appia, 1211 Geneva 27, Switzerland (tel.: +41 22 791 3264; fax: +41 22 791 4857; email: [email protected]). Requests for permission to reproduce or translate WHO publications – whether for sale or for non-commercial distribution– should be addressed to WHO Press through the WHO website (http://www.who.int/about/licensing/ copyright_form/index.html). The designations employed and the presentation of the material in this publication do not imply the expression of any opinion whatsoever on the part of the World Health Organization concerning the legal status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. Dotted and dashed lines on maps represent approximate border lines for which there may not yet be full agreement. The mention of specific companies or of certain manufacturers’ products does not imply that they are endorsed or recommended by the World Health Organization in preference to others of a similar nature that are not mentioned.