Causative Agents of Mycoses Basic Principles of Laboratory Diagnostics of Mycoses
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Subcutaneous Phycomycosis: a Review of 31 Cases Seen in Uganda
27 June 1964 Myelomatosis-Speed et al. BRITISH 1669 Case 10 (19 October 1962); Case 12 (24 February 1964); REFERNCES Case 14 (9 September 1962); and Case 16 (17 February 1963). N. (1947). Lancet, 2, 388. Alwall, Campgn, Case 5 received 10 further courses of melphalan, and the disease Bergel, F., and Stock, J. A. (1953). A.R. Brit. Emp. Cancer Br Med J: first published as 10.1136/bmj.1.5399.1669 on 27 June 1964. Downloaded from 31, 6. remained well controlled until the last 10 weeks of life, when Bergsagel, D. E. (1962). Cancer Chemother. Rep., No. 16, p. 261. the growth extended extremely rapidly. He received one further - Sprague, C. C., Austin, C., and Griffith, K. M. (1962). Ibid., No. 21, p. 87. course of radiotherapy for local pain. Case 9 received eight Bernard, J., Seligmann, M., and Danon, F. (1962). Nouv. Rev. franc. further courses of melphalan, and the disease was well controlled Himat., 2, 611. of ribs which Blokhin, N., Larionov, L., Perevodchikova, N., Chebotareva, L., and except for local pain from pathological fractures Merkulova, N. (1958). Ann. N.Y. Acad. Sci., 68, 1128. was relieved by irradiation. At post-mortem examination a Innes, J. (1963). Proc. roy. Soc. Med., 56, 648. gastric carcinoma, suspected in the last three months of life, - and Rider, W. D. (1955). Blood, 10, 252. Larionov, L. F., Khokhlov, A. S., Shkodinskaja, E. N., Vasina, 0. S., was found. Cases 8, 9, 12, 14, and 16 did not benefit from Troosheikina, V. I., and Novikova, M. A. (1955). Bull. -
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. -
Boards' Fodder
boards’ fodder Medical Mycology By Adriana Schmidt, MD, and Natalie M. Curcio, MD, MPH. (Updated July 2015*) SUPERFICIAL ORGANISM CLINICAL HISTO/KOH TREATMENT MYCOSES* Pityriasis Malessezia furfur Hypo- or hyper-pigmented Spaghetti & meatballs: Antifungal shampoos and/or versicolor macules short hyphae + yeast PO therapy Tinea nigra Hortaea werneckii (formerly Brown-black non-scaly Branching septate hyphae Topical imidazoles or palmaris Phaeoannellomyces werneckii) macules + budding yeast allylamines Black piedra Piedraia hortae Hard firm black Dark hyphae around concretions acrospores Cut hair off, PO terbinafine, White piedra Trichosporon ovoides or inkin Soft loose white Blastoconidia, imidazoles, or triazoles (formely beigelii) concretions arthroconidia Fluorescent small Microsporum Canis KOH: spores on outside spore ectothrix: M. audouinii of the hair shaft; “Cats And Dogs M. distortum Wood’s lamp --> yellow Sometimes Fight T. schoenleinii fluorescence & Growl” M. ferrugineum+/- gypseum Large spore Trichophyton spp. (T. tonsurans in North America; T. violaceum in KOH: spores within hair Topical antifungals; PO endothrix Europe, Asia, parts of Africa). shaft antifungals for T. manuum, Tinea corporis T. rubrum > T. mentag. Majocchi’s granuloma: T. rubrum capitis, unguium T. pedis Moccasin: T. rubrum, E. floccosum. Interdigital/vesicular: T. mentag T. unguium Distal lateral, proximal and proximal white subungual: T. rubrum. White superficial: T. mentag. HIV: T. rubrum SUBQ MYCOSES** ORGANISM TRANSMISSION CLINICAL HISTO/KOH TREATMENT -
Clinical and Laboratory Profile of Chronic Pulmonary Aspergillosis
Original article 109 Clinical and laboratory profile of chronic pulmonary aspergillosis: a retrospective study Ramakrishna Pai Jakribettua, Thomas Georgeb, Soniya Abrahamb, Farhan Fazalc, Shreevidya Kinilad, Manjeshwar Shrinath Baligab Introduction Chronic pulmonary aspergillosis (CPA) is a type differential leukocyte count, and erythrocyte sedimentation of semi-invasive aspergillosis seen mainly in rate. In all the four dead patients, the cause of death was immunocompetent individuals. These are slow, progressive, respiratory failure and all patients were previously treated for and not involved in angio-invasion compared with invasive pulmonary tuberculosis. pulmonary aspergillosis. The predisposing factors being Conclusion When a patient with pre-existing lung disease compromised lung parenchyma owing to chronic obstructive like chronic obstructive pulmonary disease or old tuberculosis pulmonary disease and previous pulmonary tuberculosis. As cavity presents with cough with expectoration, not many studies have been conducted in CPA with respect to breathlessness, and hemoptysis, CPA should be considered clinical and laboratory profile, the study was undertaken to as the first differential diagnosis. examine the profile in our population. Egypt J Bronchol 2019 13:109–113 Patients and methods This was a retrospective study. All © 2019 Egyptian Journal of Bronchology patients older than 18 years, who had evidence of pulmonary Egyptian Journal of Bronchology 2019 13:109–113 fungal infection on chest radiography or computed tomographic scan, from whom the Aspergillus sp. was Keywords: chronic pulmonary aspergillosis, immunocompetent, laboratory isolated from respiratory sample (broncho-alveolar wash, parameters bronchoscopic sample, etc.) and diagnosed with CPA from aDepartment of Microbiology, Father Muller Medical College Hospital, 2008 to 2016, were included in the study. -
Fungal Diseases
Abigail Zuger Fungal Diseases For creatures your size I offer a free choice of habitat, so settle yourselves in the zone that suits you best, in the pools of my pores or the tropical forests of arm-pit and crotch, in the deserts of my fore-arms, or the cool woods of my scalp Build colonies: I will supply adequate warmth and moisture, the sebum and lipids you need, on condition you never do me annoy with your presence, but behave as good guests should not rioting into acne or athlete's-foot or a boil. from "A New Year Greeting" by W.H. Auden. Introduction Most of the important contacts between human beings and the fungi occur outside medicine. Fungi give us beer, bread, antibiotics, mushroom omelets, mildew, and some devastating crop diseases; their ability to cause human disease is relatively small. Of approximately 100,000 known species of fungi, only a few hundred are human pathogens. Of these, only a handful are significant enough to be included in medical texts and introductory courses like this one. On the other hand, while fungal virulence for human beings is uncommon, the fungi are not casual pathogens. In the spectrum of infectious diseases, they can cause some of the most devastating and stubborn infections we see. Most human beings have a strong natural immunity to the fungi, but when this immunity is breached the consequences can be dramatic and severe. As modern medicine becomes increasingly adept in prolonging the survival of some patients with naturally-occurring immunocompromise (diabetes, cancer, AIDS), and causing iatrogenic immunocompromise in others (antibiotics, cytotoxic and MID 25 & 26 immunomodulating drugs), fungal infections are becoming increasingly important. -
1. Oral Infections.Pdf
ORAL INFECTIONS Viral infections Herpes Human Papilloma Viruses Coxsackie Paramyxoviruses Retroviruses: HIV Bacterial Infections Dental caries Periodontal disease Pharyngitis and tonsillitis Scarlet fever Tuberculosis - Mycobacterium Syphilis -Treponema pallidum Actinomycosis – Actinomyces Gonorrhea – Neisseria gonorrheae Osteomyelitis - Staphylococcus Fungal infections (Mycoses) Candida albicans Histoplasma capsulatum Coccidioides Blastomyces dermatitidis Aspergillus Zygomyces CDE (Oral Pathology and Oral Medicine) 1 ORAL INFECTIONS VIRAL INFECTIONS • Viruses consist of: • Single or double strand DNA or RNA • Protein coat (capsid) • Often with an Envelope. • Obligate intracellular parasites – enters host cell in order to replicate. • 3 most commonly encountered virus families in the oral cavity: • Herpes virus • Papovavirus (HPV) • Coxsackie virus (an Enterovirus). DNA Viruses: A. HUMAN HERPES VIRUS (HHV) GROUP: 1. HERPES SIMPLEX VIRUS • Double stranded DNA virus. • 2 types: HSV-1 and HSV-2. • Lytic to human epithelial cells and latent in neural tissue. Clinical features: • May penetrate intact mucous membrane, but requires breaks in skin. • Infects peripheral nerve, migrates to regional ganglion. • Primary infection, latency and recurrence occur. • 99% of cases are sub-clinical in childhood. • Primary herpes: Acute herpetic gingivostomatitis. • 1% of cases; severe symptoms. • Children 1 - 3 years; may occur in adults. • Incubation period 3 – 8 days. • Numerous small vesicles in various sites in mouth; vesicles rupture to form multiple small shallow punctate ulcers with red halo. • Child is ill with fever, general malaise, myalgia, headache, regional lymphadenopathy, excessive salivation, halitosis. • Self limiting; heals in 2 weeks. • Immunocompromised patients may develop a prolonged form. • Secondary herpes: Recurrent oral herpes simplex. • Presents as: a) herpes labialis (cold sores) or b) recurrent intra-oral herpes – palate or gingiva. -
Therapies for Common Cutaneous Fungal Infections
MedicineToday 2014; 15(6): 35-47 PEER REVIEWED FEATURE 2 CPD POINTS Therapies for common cutaneous fungal infections KENG-EE THAI MB BS(Hons), BMedSci(Hons), FACD Key points A practical approach to the diagnosis and treatment of common fungal • Fungal infection should infections of the skin and hair is provided. Topical antifungal therapies always be in the differential are effective and usually used as first-line therapy, with oral antifungals diagnosis of any scaly rash. being saved for recalcitrant infections. Treatment should be for several • Topical antifungal agents are typically adequate treatment weeks at least. for simple tinea. • Oral antifungal therapy may inea and yeast infections are among the dermatophytoses (tinea) and yeast infections be required for extensive most common diagnoses found in general and their differential diagnoses and treatments disease, fungal folliculitis and practice and dermatology. Although are then discussed (Table). tinea involving the face, hair- antifungal therapies are effective in these bearing areas, palms and T infections, an accurate diagnosis is required to ANTIFUNGAL THERAPIES soles. avoid misuse of these or other topical agents. Topical antifungal preparations are the most • Tinea should be suspected if Furthermore, subsequent active prevention is commonly prescribed agents for dermatomy- there is unilateral hand just as important as the initial treatment of the coses, with systemic agents being used for dermatitis and rash on both fungal infection. complex, widespread tinea or when topical agents feet – ‘one hand and two feet’ This article provides a practical approach fail for tinea or yeast infections. The pharmacol- involvement. to antifungal therapy for common fungal infec- ogy of the systemic agents is discussed first here. -
Tinea Capitis: Current Concepts in Clinical Practice
CONTINUING MEDICAL EDUCATION Tinea Capitis: Current Concepts in Clinical Practice Matthew J. Trovato, MD; Robert A. Schwartz, MD, MPH; Camila K. Janniger, MD GOAL To understand tinea capitis to better treat patients with the condition OBJECTIVES Upon completion of this activity, dermatologists and general practitioners should be able to: 1. Describe the etiology of tinea capitis. 2. Recognize and diagnose tinea capitis. 3. Effectively treat tinea capitis. CME Test on page 88. This article has been peer reviewed and is accredited by the ACCME to provide continuing approved by Victor B. Hatcher, PhD, Professor of medical education for physicians. Medicine, Albert Einstein College of Medicine. Albert Einstein College of Medicine designates Review date: January 2006. this educational activity for a maximum of 1 This activity has been planned and implemented category 1 credit toward the AMA Physician’s in accordance with the Essential Areas and Policies Recognition Award. Each physician should of the Accreditation Council for Continuing Medical claim only that credit that he/she actually spent Education through the joint sponsorship of Albert in the activity. Einstein College of Medicine and Quadrant This activity has been planned and produced in HealthCom, Inc. Albert Einstein College of Medicine accordance with ACCME Essentials. Drs. Trovato, Schwartz, and Janniger report no conflict of interest. The authors discuss off-label use of fluconazole, itraconazole, ketoconazole, and terbinafine. Dr. Hatcher reports no conflict of interest. Tinea capitis is a common infection, particularly seen in Europe and many other countries, which among young children in urban regions. The emit a green fluorescence. However, T tonsurans, infection often is seen in a form with mild scaling like other fungi, also may less often produce an and little hair loss, a result of the prominence of intense inflammatory reaction, which is sugges- Trichophyton tonsurans (the most frequent cause tive of an acute bacterial infection. -
STUDIES on INVASIVE KERATINOPHILIC DERMATOPHYTES of HUMAN HAIR *Brajesh Kumar Jha1, S
Brajesh et al Journal of Drug Delivery & Therapeutics; 2013, 3(2), 70-74 70 Available online at http://jddtonline.info RESEARCH ARTICLE STUDIES ON INVASIVE KERATINOPHILIC DERMATOPHYTES OF HUMAN HAIR *Brajesh Kumar Jha1, S. Mahadeva Murthy2 1Research Scholar, Department of Microbiology, Yubraja College, Mysore, India 2Associate Professor, Department of Microbiology, Yubraja College, Mysore, India *Corresponding Author’s Email: [email protected] Phone: +977- 9845087892 ABSTRACT: Background: Tinea Capitis (TC) is a dermatophyte infection of the scalp hair follicles and intervening skin. TC is mainly caused by anthropohilic and zoophilic species of the genera Trichophyton and Microsporum. On the basis of the type of hair invasion, dermatophytes are also classified as endothrix, ectothrix or favus. Despite the availability of effective antifungal agents, dermatophytic infections continue to be one of the principal dermatological diseases in Mysore. Objectives: To study the genus and species variants, of fungus causing Tinea Capitis infection and epidemiological factors responsible for the disease in Central Mysore. Materials and methods: Clinically suspected 527 patients with dermatophytes infection cases were included in our study, where 58 cases were diagnosed and confirmed as a Tinea Capitis patients only selected for our study. Suspected lesion like scalp skin scraping and hair plucking samples were collected after disinfecting the site with 70% of ethyl alcohol. Samples were collected in a sterile thick black envelope, folded, labelled and brought to the laboratory for further processing according to slandered Mycological protocol. Results: A total of 527 patients with dermatophytes infection suspected cases were included in our study, where 58 cases (11.0%) were confirmed as a Tinea Capitis. -
Utilization of the Internal Transcribed Spacer Regions As Molecular Targets
Medical Mycology 2002, 40, 87±109 Accepted 9July 2001 Review article Utilizationof the internaltranscribed spacer regions as molecular targets to detect andidentify human fungal pathogens P.C.IWEN*, S.H.HINRICHS* & M.E.RUPP Downloaded from https://academic.oup.com/mmy/article/40/1/87/961355 by guest on 29 September 2021 y *Department ofPathology and Microbiology,University ofNebraska MedicalCenter, Omaha, Nebraska, USA; Internal Medicine, y University ofNebraska MedicalCenter, Omaha, Nebraska, USA Advancesin molecular technology show greatpotential for the rapiddetection and identication of fungifor medical,scienti c andcommercial purposes. Numerous targetswithin the fungalgenome have been evaluated, with much of the current work usingsequence areas within the ribosomalDNA (rDNA) gene complex. This sectionof the genomeincludes the 18S,5 8Sand28S genes which codefor ribosomal ¢ RNA(rRNA) andwhich havea relativelyconserved nucleotide sequence among fungi.It alsoincludes the variableDNA sequence areas of the interveninginternal transcribedspacer (ITS) regionscalled ITS1 and ITS2. Although not translatedinto proteins,the ITScoding regions have a criticalrole in the developmentof functional rRNA,with sequencevariations among species showing promiseas signature regionsfor molecularassays. This review of the current literaturewas conducted to evaluateclinical approaches for usingthe fungalITS regions as molecular targets. Multipleapplications using the fungalITS sequences are summarized here including those for cultureidenti cation, phylogenetic -
DERMATOPHYTOSIS ( Ti Ri ) ( Ti Ri ) (=Tinea = Ringworm)
DERMATOPHYTOSIS (Ti(=Tinea = Ringworm) IInfection of the skin, hair or nails caused by a group of keratinophilic fungi, called dermatophytes ¨ Microsporum Hair, skin ¨ Epidermophyton Skin, nail ¨ TTihrichoph htyton HHiair, skin, nail DERMATOPHYTES IDigest keratin by their keratinases IResistant to cycloheximide IClassified into three groups depending on their usual habitat All three dermatoppyhytes contain virulence factors that allow them to invade the skin, hair, and nails Keratinases Elastase Proteinases DERMATOPHYTES IANTROPOPHILIC Trichophyton rubrum... IGEOPHILIC Microsporum gypseum... IZOOPHILIC Microsporum canis: cats and dogs Microsporum nanum: swine Trichophyton verrucosum: horse and swine… Zoophilic dermatophytes Microscopic characteristics of dermatophyte genera Microsporum Epidermophyton Trichophyton DERMATOPHYTOSIS PhPathogenesi s and Immuni ty IContact and trauma IMoisture ICrowded living conditions ICellular immunodeficiency Æ(()chronic inf.) IReRe--infectioninfection is possible (but, larger inoculum is needed, the course is shorter ) DERMATOPHYTOSIS Clllinical Cllfassification IInfection is named according to the anatomic location involved: a. Tinea barbae e. Tinea pedis (Athlete’ s foot) b. Tinea corporis f. Tinea manuum c. Tinea capitis g. Tinea unguium d. Tinea cruris (Jock itch) DERMATOPHYTOSIS Clini ca l manifestat ions ISkin: Circular, dry, erythematous, scaly, itchy lesions IHair: Typical lesions,”kerion”, scarring, “l“alopeci i”a” INail: Thickened,,fm, deformed, friable, discolored nails, subungual debris accumulation IFavus (Tinea favosa) DERMATOPHYTOSIS TiiTransmission IClose human contact ISharing clothes, combs, brushes, towels, bedsheets... (Indirect ) IAnimalAnimal--toto--humanhuman contact (Zoophilic) DERMATOPHYTOSIS Diagnos is I. Clllinical Appearance Wood lamp (UV, 365 nm) II. Lab A. Direct microscopic examination ((1010--2525%% KOH) Ectothrix/endothrix/favic hair DERMATOPHYTOSIS Diagnos is B. Culture Mycobiotic agar Sabdbouraud dextrose agar DERMATOPHYTES Iden tifica tion A. Colony characteristics B. -
Mucormycosis: Botanical Insights Into the Major Causative Agents
Preprints (www.preprints.org) | NOT PEER-REVIEWED | Posted: 8 June 2021 doi:10.20944/preprints202106.0218.v1 Mucormycosis: Botanical Insights Into The Major Causative Agents Naser A. Anjum Department of Botany, Aligarh Muslim University, Aligarh-202002 (India). e-mail: [email protected]; [email protected]; [email protected] SCOPUS Author ID: 23097123400 https://www.scopus.com/authid/detail.uri?authorId=23097123400 © 2021 by the author(s). Distributed under a Creative Commons CC BY license. Preprints (www.preprints.org) | NOT PEER-REVIEWED | Posted: 8 June 2021 doi:10.20944/preprints202106.0218.v1 Abstract Mucormycosis (previously called zygomycosis or phycomycosis), an aggressive, liFe-threatening infection is further aggravating the human health-impact of the devastating COVID-19 pandemic. Additionally, a great deal of mostly misleading discussion is Focused also on the aggravation of the COVID-19 accrued impacts due to the white and yellow Fungal diseases. In addition to the knowledge of important risk factors, modes of spread, pathogenesis and host deFences, a critical discussion on the botanical insights into the main causative agents of mucormycosis in the current context is very imperative. Given above, in this paper: (i) general background of the mucormycosis and COVID-19 is briefly presented; (ii) overview oF Fungi is presented, the major beneficial and harmFul fungi are highlighted; and also the major ways of Fungal infections such as mycosis, mycotoxicosis, and mycetismus are enlightened; (iii) the major causative agents of mucormycosis