Staphylococcal Enterotoxins in Scarlet Fever Complicating Chickenpox M
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The Role of Streptococcal and Staphylococcal Exotoxins and Proteases in Human Necrotizing Soft Tissue Infections
toxins Review The Role of Streptococcal and Staphylococcal Exotoxins and Proteases in Human Necrotizing Soft Tissue Infections Patience Shumba 1, Srikanth Mairpady Shambat 2 and Nikolai Siemens 1,* 1 Center for Functional Genomics of Microbes, Department of Molecular Genetics and Infection Biology, University of Greifswald, D-17489 Greifswald, Germany; [email protected] 2 Division of Infectious Diseases and Hospital Epidemiology, University Hospital Zurich, University of Zurich, CH-8091 Zurich, Switzerland; [email protected] * Correspondence: [email protected]; Tel.: +49-3834-420-5711 Received: 20 May 2019; Accepted: 10 June 2019; Published: 11 June 2019 Abstract: Necrotizing soft tissue infections (NSTIs) are critical clinical conditions characterized by extensive necrosis of any layer of the soft tissue and systemic toxicity. Group A streptococci (GAS) and Staphylococcus aureus are two major pathogens associated with monomicrobial NSTIs. In the tissue environment, both Gram-positive bacteria secrete a variety of molecules, including pore-forming exotoxins, superantigens, and proteases with cytolytic and immunomodulatory functions. The present review summarizes the current knowledge about streptococcal and staphylococcal toxins in NSTIs with a special focus on their contribution to disease progression, tissue pathology, and immune evasion strategies. Keywords: Streptococcus pyogenes; group A streptococcus; Staphylococcus aureus; skin infections; necrotizing soft tissue infections; pore-forming toxins; superantigens; immunomodulatory proteases; immune responses Key Contribution: Group A streptococcal and Staphylococcus aureus toxins manipulate host physiological and immunological responses to promote disease severity and progression. 1. Introduction Necrotizing soft tissue infections (NSTIs) are rare and represent a more severe rapidly progressing form of soft tissue infections that account for significant morbidity and mortality [1]. -
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. -
Staphylococcus Aureus Exfoliative Toxins: How They Cause Disease
View metadata, citation and similar papers at core.ac.uk brought to you by CORE To cite this article: JID 122:1070–1077, 2004 provided by Elsevier - Publisher Connector Published by the ology Progress in Dermatology Editor: Alan N. Moshell, M.D. Staphylococcus aureus exfoliative toxins: How they cause disease. Lisa R.W. Plano, M.D., Ph.D. Departments of Pediatrics and Microbiology & Immunology University of Miami School of Medicine, Miami, Florida Abbreviations: cell surface molecules associated with adhesion and BI- bullous impetigo multiple antibiotic resistances including methicillin and ET- exfoliative toxins vancomycin resistance (Centers for Disease Control and EDIN- epidermal cell differentiation inhibitor Prevention, 1997; 2000a; 2000b), all contributing to the ETA- exfoliative toxin A (epidermolysisn A, exfoliatin A) pathogenicity of these organisms. A minimum of 34 ETB- exfoliative toxin B (epidermolysisn B, exfoliatin B) different extracellular proteins are produced by S. ETD- exfoliative toxin D (epidermolysisn D, exfoliatin D) aureus, and many of these have defined roles in the PF- pemphigus foliaceus pathogenesis of their associated diseases (Iandolo, SSSS- Staphylococcal scalded skin syndrome, (pemphi- 1989). Infectious conditions caused by these organisms gus neonatorum, dermatitis exfoliativa neonatorum, can be divided into three major categories; (i) superficial Ritter’s disease) skin infections, skin abcesses and wound infections TEN- toxic epidermal necrolysis including bullous impetigo (BI) and furuncles, (ii) systemic or infections of deep seeded tissues including osteomyelitis, endocarditis, pneumonia and sepsis, and Introduction (iii) conditions caused by intoxication with one of the General Microbiology: Staphylococci are hardy excreted toxins. Among the conditions caused by intoxi- Gram-positive cocci found as bacterial pathogens or cation with an exotoxin are toxic shock syndrome caused commensal organisms in both humans and animals. -
Severe Orbital Cellulitis Complicating Facial Malignant Staphylococcal Infection
Open Access Austin Journal of Clinical Case Reports Case Report Severe Orbital Cellulitis Complicating Facial Malignant Staphylococcal Infection Chabbar Imane*, Serghini Louai, Ouazzani Bahia and Berraho Amina Abstract Ophthalmology B, Ibn-Sina University Hospital, Morocco Orbital cellulitis represents a major ophthalmological emergency. Malignant *Corresponding author: Imane Chabbar, staphylococcal infection of the face is a rare cause of orbital cellulitis. It is the Ophthalmology B, Ibn-Sina University Hospital, Morocco consequence of the infectious process extension to the orbital tissues with serious loco-regional and general complications. We report a case of a young diabetic Received: October 27, 2020; Accepted: November 12, child, presenting an inflammatory exophthalmos of the left eye with purulent 2020; Published: November 19, 2020 secretions with a history of manipulation of a facial boil followed by swelling of the left side of face, occurring in a febrile context. The ophthalmological examination showed preseptal and orbital cellulitis complicating malignant staphylococcal infection of the face. Orbito-cerebral CT scan showed a left orbital abscess with exophthalmos and left facial cellulitis. An urgent hospitalization and parenteral antibiotherapy was immediately started. Clinical improvement under treatment was noted without functional recovery. We emphasize the importance of early diagnosis and urgent treatment of orbital cellulitis before the stage of irreversible complications. Keywords: Orbital cellulitis, Malignant staphylococcal infection of the face, Management, Blindness Introduction cellulitis complicated by an orbital abscess with exophthalmos (Figure 2a, b), and left facial cellulitis with frontal purulent collection Malignant staphylococcal infection of the face is a serious skin (Figure 3a, b). disease. It can occur following a manipulation of a facial boil. -
Serine Proteases with Altered Sensitivity to Activity-Modulating
(19) & (11) EP 2 045 321 A2 (12) EUROPEAN PATENT APPLICATION (43) Date of publication: (51) Int Cl.: 08.04.2009 Bulletin 2009/15 C12N 9/00 (2006.01) C12N 15/00 (2006.01) C12Q 1/37 (2006.01) (21) Application number: 09150549.5 (22) Date of filing: 26.05.2006 (84) Designated Contracting States: • Haupts, Ulrich AT BE BG CH CY CZ DE DK EE ES FI FR GB GR 51519 Odenthal (DE) HU IE IS IT LI LT LU LV MC NL PL PT RO SE SI • Coco, Wayne SK TR 50737 Köln (DE) •Tebbe, Jan (30) Priority: 27.05.2005 EP 05104543 50733 Köln (DE) • Votsmeier, Christian (62) Document number(s) of the earlier application(s) in 50259 Pulheim (DE) accordance with Art. 76 EPC: • Scheidig, Andreas 06763303.2 / 1 883 696 50823 Köln (DE) (71) Applicant: Direvo Biotech AG (74) Representative: von Kreisler Selting Werner 50829 Köln (DE) Patentanwälte P.O. Box 10 22 41 (72) Inventors: 50462 Köln (DE) • Koltermann, André 82057 Icking (DE) Remarks: • Kettling, Ulrich This application was filed on 14-01-2009 as a 81477 München (DE) divisional application to the application mentioned under INID code 62. (54) Serine proteases with altered sensitivity to activity-modulating substances (57) The present invention provides variants of ser- screening of the library in the presence of one or several ine proteases of the S1 class with altered sensitivity to activity-modulating substances, selection of variants with one or more activity-modulating substances. A method altered sensitivity to one or several activity-modulating for the generation of such proteases is disclosed, com- substances and isolation of those polynucleotide se- prising the provision of a protease library encoding poly- quences that encode for the selected variants. -
Staphylococcal Infection Information for Daycare Facilities
Staphylococcal Infection Information for Daycare Facilities These guidelines are to help in developing a program to address managing children with methicillin-resistant Staphylococcus aureus (MRSA) infections and MRSA outbreaks specifically in the daycare setting. However, this information can be adapted to address the same problems in other settings and with almost all infectious diseases. Basic Information about MRSA The emergence of antibiotic resistant bacteria has become a significant public health concern. Due to the extensive use of antibiotics, the sharing of antibiotics, and/or the failure to complete a course of antibiotics, our current arsenal of antibiotics is becoming ineffective against common bacterial infections. Staphylococcus aureus (commonly referred to as “staph”) is a bacteria that can live on human skin of even the cleanest individuals. It can cause boils, wound infections, abscesses, cellulitis, impetigo, pneumonia, and even bloodstream infections. The Centers for Disease Control and Prevention estimate that 25-35% of children and adults in the United States have staph colonization— staph living on them, but not harming them. Staph like to live in the nose, groin, around the anus, armpits, finger tips, tracheostomy sites, wounds, and in the secretions of intubated patients. Staph spreads by direct skin-to-skin contact with an infected individual or a colonized individual or more rarely from objects contaminated by these individuals such as sheets soiled with infected wound drainage. Staph is not found in dirt or mud or carried through the air. The emergence of MRSA In the past, staph infections were easily treated with a short course of penicillin with very few complications. -
Studies of Staphylococcal Infections. I. Virulence of Staphy- Lococci and Characteristics of Infections in Embryonated Eggs * WILLIAM R
Journal of Clinical Investigation Vol. 43, No. 11, 1964 Studies of Staphylococcal Infections. I. Virulence of Staphy- lococci and Characteristics of Infections in Embryonated Eggs * WILLIAM R. MCCABE t (From the Research Laboratory, West Side Veterans Administration Hospital, and the Department of Medicine, Research and Educational Hospitals, University of Illinois College of Medicine, Chicago, Ill.) Many of the determinants of the pathogenesis niques still require relatively large numbers of and course of staphylococcal infections remain staphylococci to produce infection (19). Fatal imprecisely defined (1, 2) despite their increas- systemic infections have been equally difficult to ing importance (3-10). Experimental infections produce in animals and have necessitated the in- in suitable laboratory animals have been of con- jection of 107 to 109 bacteria (20-23). A few siderable assistance in clarifying the role of host strains of staphylococci have been found that are defense mechanisms and specific bacterial virulence capable of producing lethal systemic infections factors with a variety of other infectious agents. with inocula of from 102 to 103 bacteria (24) and A sensitive experimental model would be of value have excited considerable interest (25-27). The in defining the importance of these factors in virulence of these strains apparently results from staphylococcal infections, but both humans and an unusual antigenic variation (27, 28) which, the usual laboratory animals are relatively re- despite its interest, is of doubtful significance in sistant. Extremely large numbers of staphylo- human staphylococcal infection, since such strains cocci are required to produce either local or sys- have been isolated only rarely from clinical in- temic infections experimentally. -
Isolation and Identification of Bacteria Causing Arthritis in Chickens اﻟدﺟﺎج ﻲ
Iraqi Journal of Veterinary Sciences, Vol. 25, No. 2, 2011 (93-95) Isolation and identification of bacteria causing arthritis in chickens B. Y. Rasheed Department of Microbiology, College of Veterinary Medicine, University of Mosul, Mosul, Iraq (Received September 6, 2009; Accepted March 28, 2011) Abstract Sixty chickens 30-55 days old with arthritis symptoms, were collected from different broiler chickens farms, all samples were examined clinically, post mortem and bacterial isolation were done. The results revealed isolation of 26 (50.98%) of Staphylococcus aureus, which were found highly sensitive to amoxycillin. The experimental infection of 10 chickens was carried out on 35 days old by intravenous inoculated with 107 cfu/ml of isolated Staphylococcus aureus. Arthritis occurred in 8 (80%) chickens. Clinical signs and post mortem findings confined to depression, swollen joints, inability to stand. Keywords: Bacteria, Arthritis, Chicken. Available online at http://www.vetmedmosul.org/ijvs عزل وتشخيص المسببات الجرثومية ﻻلتھاب المفاصل في الدجاج بلسم يحيى رشيد فرع اﻻحياءالمجھرية، كلية الطب البيطري، جامعة الموصل، الموصل، العراق الخﻻصة جمعت ستون دجاجة بعمر٣٠-٥٥ يوم يظھر عليھا عﻻمات التھاب المفاصل من حقول فروج اللحم, وفحصت جميع العينات وسجلت العﻻمات المرضية والصفة التشريحية واجري العزل الجرثومي لھا. أظھرت النتائج عزل ٢٦ عزلة (٩٨، ٥٠ %) من جراثيم المكورات العنقودية وكانت ھذه العزﻻت عالية الحساسية لﻻموكسيسيلينز. أجري الخمج التجريبي على١٠ دجاجات وبعمر ٣٥ يوم حيث حقنت بالمكورات العنقودية المعزولة وبجرعة ٧١٠ مستعمرة/سم٣ في الوريد أدى ذلك إلى حصول التھاب المفاصل في ٨ (٨٠%) دجاجات بينت العﻻمات السريرية والصفة التشريحية حصول خمول وتورم المفاصل وعدم القدرة على الوقوف. Introduction (inflammation of tendon sheaths) and arthritis of the hock and stifle joints (1). -
Staphylococcal Infection in Meat Animals and Meat Workers
Staphylococcal Infection in Meat Animals and Meat Workers REIMERT T. RAVENHOLT, M.D., M.P.H., ROBERT C. EELKEMA, D.V.M., M.D., MARIE MULHERN, B.S., and RAY B. WATKINS, D.V.M. most of the serious and fatal ing an Acronizing process (chlortetracycline re¬ ALTHOUGHu cases of staphylococcal disease in Seattle HC1) about May 15, 1956. The antibiotic and King County, Wash., occur among hospital¬ placed chlorine in the ice water bath in which ized patients suffering from other diseases the chickens were immersed for 4-6 hours after (1-5), several recent incidents suggested that they were killed, cleaned, and eviscerated. It the community has nonhospital reservoirs of was claimed that the Acronizing process ex¬ staphylococcal infection which may be impor¬ tended the "shelf life" of the poultry, permit¬ tant in the ecology of staphylococci. ting the holding of chickens at ordinary refrig¬ One such incident was an outbreak of boils erator temperature for as long as 14 days. Most (pyoderma) among workers in a poultry-proc¬ of the workers, however, had little if any direct essing establishment in Seattle. An investiga¬ contact with the Acronizing process. tion in October 1956 revealed that from May Investigation of the outbreak also revealed through September of that year 19 (63 percent) that abscesses, especially along the keel bone, of the 30 poultry handlers in the establishment were sometimes observed in chickens. The plant developed boils and other suppurative skin le¬ manager and sanitary inspector were instructed sions. Most of the afflicted workers missed a to submit any abscessed poultry carcasses for few days from work, and several more than a culture. -
Targeting Staphylococcus Aureus Toxins: a Potential Form of Anti-Virulence Therapy
toxins Review Targeting Staphylococcus aureus Toxins: A Potential form of Anti-Virulence Therapy Cin Kong 1, Hui-min Neoh 2 and Sheila Nathan 1,* 1 School of Biosciences and Biotechnology, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, 43600 Bangi, Selangor Darul Ehsan, Malaysia; [email protected] 2 UKM Medical Molecular Biology Institute (UMBI), Universiti Kebangsaan Malaysia, 56000 Cheras, Kuala Lumpur, Malaysia; [email protected] * Correspondence: [email protected]; Tel.: +60-3-8921-3862 Academic Editor: Yinduo Ji Received: 18 February 2016; Accepted: 10 March 2016; Published: 15 March 2016 Abstract: Staphylococcus aureus is an opportunistic pathogen and the leading cause of a wide range of severe clinical infections. The range of diseases reflects the diversity of virulence factors produced by this pathogen. To establish an infection in the host, S. aureus expresses an inclusive set of virulence factors such as toxins, enzymes, adhesins, and other surface proteins that allow the pathogen to survive under extreme conditions and are essential for the bacteria’s ability to spread through tissues. Expression and secretion of this array of toxins and enzymes are tightly controlled by a number of regulatory systems. S. aureus is also notorious for its ability to resist the arsenal of currently available antibiotics and dissemination of various multidrug-resistant S. aureus clones limits therapeutic options for a S. aureus infection. Recently, the development of anti-virulence therapeutics that neutralize S. aureus toxins or block the pathways that regulate toxin production has shown potential in thwarting the bacteria’s acquisition of antibiotic resistance. In this review, we provide insights into the regulation of S. -
Pathology of Gangrene Yutaka Tsutsumi
Chapter Pathology of Gangrene Yutaka Tsutsumi Abstract Pathological features of gangrene are described. Gangrene is commonly caused by infection of anaerobic bacteria. Dry gangrene belongs to noninfectious gangrene. The hypoxic/ischemic condition accelerates the growth of anaerobic bacteria and extensive necrosis of the involved tissue. Clostridial and non-clostridial gangrene provokes gas formation in the necrotic tissue. Acute gangrenous inflammation happens in a variety of tissues and organs, including the vermiform appendix, gallbladder, bile duct, lung, and eyeball. Emphysematous (gas-forming) infection such as emphysematous pyelonephritis may be provoked by Escherichia coli and Klebsiella pneumoniae. Rapidly progressive gangrene of the extremities (so-called “flesh-eating bacteria” infection) is seen in fulminant streptococcal, Vibrio vulnificus, and Aeromonas hydrophila infections. Fournier gangrene is an aggressive and life-threatening gangrenous disease seen in the scrotum and rectum. Necrotiz- ing fasciitis is a subacute form of gangrene of the extremities. Of note is the fact that clostridial and streptococcal infections in the internal organs may result in a lethal hypercytokinemic state without association of gangrene of the arms and legs. Uncontrolled diabetes mellitus may play an important role for vulnerability of the infectious diseases. Pseudomonas-induced malignant otitis externa and craniofacial mucormycosis are special forms of the lethal gangrenous disorder. Keywords: anaerobic bacteria, clostridial gas gangrene, flesh-eating bacteria, necrotizing fasciitis, non-clostridial gas gangrene 1. Introduction Gangrene is a lesion of ischemic tissue death. Typically, the acral skin of the hand and foot accompanies numbness, pain, coolness, swelling, and the skin color changes to reddish black. When severe infection is associated, fever and sepsis may follow. -
Wednesday Slide Conference 2008-2009
PROCEEDINGS DEPARTMENT OF VETERINARY PATHOLOGY WEDNESDAY SLIDE CONFERENCE 2008-2009 ARMED FORCES INSTITUTE OF PATHOLOGY WASHINGTON, D.C. 20306-6000 2009 ML2009 Armed Forces Institute of Pathology Department of Veterinary Pathology WEDNESDAY SLIDE CONFERENCE 2008-2009 100 Cases 100 Histopathology Slides 249 Images PROCEEDINGS PREPARED BY: Todd Bell, DVM Chief Editor: Todd O. Johnson, DVM, Diplomate ACVP Copy Editor: Sean Hahn Layout and Copy Editor: Fran Card WSC Online Management and Design Scott Shaffer ARMED FORCES INSTITUTE OF PATHOLOGY Washington, D.C. 20306-6000 2009 ML2009 i PREFACE The Armed Forces Institute of Pathology, Department of Veterinary Pathology has conducted a weekly slide conference during the resident training year since 12 November 1953. This ever- changing educational endeavor has evolved into the annual Wednesday Slide Conference program in which cases are presented on 25 Wednesdays throughout the academic year and distributed to 135 contributing military and civilian institutions from around the world. Many of these institutions provide structured veterinary pathology resident training programs. During the course of the training year, histopathology slides, digital images, and histories from selected cases are distributed to the participating institutions and to the Department of Veterinary Pathology at the AFIP. Following the conferences, the case diagnoses, comments, and reference listings are posted online to all participants. This study set has been assembled in an effort to make Wednesday Slide Conference materials available to a wider circle of interested pathologists and scientists, and to further the education of veterinary pathologists and residents-in-training. The number of histopathology slides that can be reproduced from smaller lesions requires us to limit the number of participating institutions.