Evaluation of the Cult-Dip Plusdip Slide Method for Urinary Tract Infection

Total Page:16

File Type:pdf, Size:1020Kb

Evaluation of the Cult-Dip Plusdip Slide Method for Urinary Tract Infection 7107 Clin Pathol 1995;48:710-713 Evaluation of the Cult-Dip Plus dip slide method for urinary tract infection J Clin Pathol: first published as 10.1136/jcp.48.8.710 on 1 August 1995. Downloaded from J M Blondeau, Y Yaschuk, D Galenzoski, D Hrabok, M Isaacson, L Lee, H Link, L Walshaw Abstract results comparable with those obtained using Aim-To evaluate the Cult-Dip Plus standard plate streaking methods.3'-Dip slides (Merck, Germany), a bacteriological cul- that incorporate substrates for the detection ture test for detecting uropathogens. of bacterial enzymes could result in the early Methods-Cult-Dip Plus consists of Bro- identification of uropathogens. Kilian and lacin (CLED) and MacConkey agar, each Bulow8 showed that E coli was one of the containing methylumbelliferylglucuronide few bacteria to produce the enzyme B-glu- (MUG). Using 1022 urine samples, this curonidase. Hydrolysis of 4-methylumbelliferyl- product was compared with the routine B-D-glucuronide (MUG) by B-glucuronidase method of calibrated loop inoculated produces 4-methylumbelliferon-a product CLED and blood agar for screening urine which fluoresces under ultraviolet light. for uropathogens. The MUG test for Cult-Dip Plus is a new urine dip slide con- identifying Escherichia coli was also eval- sisting of Brolacin (cystine, lactose, electrolyte uated. deficient (CLED)) and MacConkey agar, each Results-Compared with the routine containing MUG. We evaluated the Cult-Dip method, Cult-Dip Plus has a sensitivity, Plus for recovery of uropathogens and the specificity, positive predictive value and MUG test for rapid identification of E coli. negative predictive value of 88-3%, 98-0%, 91.90b, and 97*1%, respectively. The MUG test correctly identified 92% of E coli isol- Methods ates with a sensitivity, specificity and pos- The MUG test is based on detection of fluor- itive predictive value of91-6%, 95-2%, and escence from release of 4-methylumbelliferon 93-6%, respectively. following hydrolysis of the parent compound Conclusion-Cult-Dip Plus appears to be by B-glucuronidase. Cult-Dip Plus was sup- an alternative method to the calibrate loop plied by BDH (Toronto, Ontario, Canada). The method for detecting uropathogens. Blood and CLED agars were purchased from http://jcp.bmj.com/ MUG test permits rapid, reliable and in- PML Microbiologicals (Edmonton, Alberta, expensive identification of E coli. Canada). (J Clin Pathol 1995;48:710-713) We prospectively analysed 1022 urine samples from different patients submitted over Keywords: Dip slide, urinary tract infection, E coli. a two month period. The semiquantitative plate culture method described by Clarridge et al9 was used as the reference method for de- on October 1, 2021 by guest. Protected copyright. Acute urinary tract infections are a major health termining bacteriuria. For routine culture, problem affecting an estimated 10-20% of 0001 ml urine was delivered to each blood women at some point during their lifetime.' In and CLED agar plate using a calibrated dis- healthy men the prevalence of urinary tract posable loop (Simport, Quebec, Canada). This Division of method detects . 1000 colony forming units/ Microbiology, St infections is less than 0-1%. As many as 42% Paul's (Grey Nuns) of all hospital acquired infections are of the ml (cfu/ml). Hospital, 1702 20th urinary tract.2 Following this, the Cult-Dip Plus dip slide Street West, was inoculated by either immersing the slide Saskatoon, In both compromised and uncompromised Saskatchewan, Canada hosts Escherichia coliis the micro-organism most in the urine (minimum 30 ml required) or when S7M OZ9 commonly associated with urinary tract in- the volume of urine was such that the paddle J M Blondeau could not be immersed, by flooding both sides Y Yaschuk fections. Others, such as Staphylococcus sp, D Galenzoski Enterococcus sp, Pseudomonas sp, and other spe- of the slide with urine using a sterile disposable D Hrabok cies belonging to the Enterobacteriaceae are also pasteur pipette (5 ml). This method detects M Isaacson significant causes of urinary tract infections; 100 cfu/ml. Colony counts of 1-10 colonies L Lee Plus were considered H Link however, their prevalence may vary depending detected by Cult-Dip L Walshaw on the age and condition of the host. Isolation negative so as to standardise the colony count and rapid identification of micro-organisms comparisons between both methods. After in- Department of oculation, culture plates/dip slides were in- Microbiology, causing urinary tract infections is important University of for determining the causative organism and cubated for 18-24 hours at 35-37°C. Saskatchewan, because it affects the appropriate selection or Saskatoon J M Blondeau continuation, or both, ofantimicrobial therapy. Urine dip slides are immersible plastic IDENTIFICATION OF MICRO-ORGANISMS Correspondence to: on lactose colonies Dr J M Blondeau. paddles containing agar medium each side. Typical fermenting resembling been shown to be E coli were identified by using the Bactident E Accepted for publication Dip slides have previously 20 December 1994 cost-effective, easy to use devices that provide coli test (BDH, Toronto, Ontario, Canada), a Evaluation of the Cult-Dip Plus dip slide method for urinary tract infection 711 Table 1 Comparison of 1022 uine specimens isolated by Cult-Dip Plus and routine Compared with the calibrated loop method culture Cult-Dip Plus had a sensitivity of 88-3%, a Both methods Cult-Dip Plus Routine culture specificity of 98-0%, a positive predictive value J Clin Pathol: first published as 10.1136/jcp.48.8.710 on 1 August 1995. Downloaded from Negative' 761 24 16 of 91-9%, and a negative predictive value of Positive* 181 16 24 97'1% (table 1). * Pure isolates in quantities greater than 10 000 cfu/ml. There were 221 significant organisms iden- + Includes those with no visible growth and those with two or more species of micro-organism tified. Table 2 shows the frequency of uro- (mixed). pathogens detected by either Cult-Dip Plus, routine culture or both. As expected, E coli was the most frequently recovered pathogen. In Table 2 Frequency of uropathogens isolated by Cult-Dip Plus and routine culture all cases where a significant uropathogen was Micro-organism Both methods Cult-Dip Plus Routine method recovered by either Cult-Dip Plus or by routine Gram negative bacilli 131 13 11 culture but not by both, the corresponding Gram positive cocci 38 3 13 method had mixed organisms and was not Yeast 12 - - All genera 181 16 24 investigated further. Table 3 shows the results of the MUG test for identification ofE coli. Of the E coli isolates, 92% were MUG test positive compared with Table 3 Summary of uropathogens MUG test positive by either Cult-Dip Plus, 25% of K pneumoniae and 20% of P mirabilis Bacident, or both isolates recovered by Cult-Dip Plus. None of Cult-Dip Plus Isolates Routine culture the remaining isolates were MUG test positive. (No. positivelno. tested (%)) (No. positivelno. tested (%o)) In total, 105 E coli isolates were recovered Micro-organism Cult-Dip Plus Bactident Bactident as significant uropathogens. Of these, 88 were by both methods, eight by Cult-Dip E coli 88/96 (92) 64/68 (94) 70/77 (91) recovered Kpneumoniae 4/16 (25) NT NT Plus only and nine by routine culture only. Of Pmirabilis 2/10 (20) NT NT the 99 E coli isolates recovered by Cult-Dip NT=not tested. Plus, 96 underwent a MUG test (three were not viewed for fluorescence and were not analysed further) (table 3). Of the 96 tested, 88 (92%) were MUG test positive. Detection of fluor- two hour identification system for E coli based escence was similar for both media on the dip on indole formation and B-D-glucuronidase slide. Thirty one of the 99 isolates recovered (MUG test). If either of these tests were neg- by Cult-Dip Plus were identified by Vitek and ative, isolates were identified by Vitek (bio- 68 were identified by Bactident. Of the 68 Merieux Vitek Inc., Hazelwood, Missouri, isolates tested by Bactident, 64 (94%) were USA). All other significant micro-organisms MUG test positive. Of the eight E coli isolates recovered by either method were identified detected by Cult-Dip Plus only and which by Vitek or by a combination of individual were MUG test negative, five were tested by http://jcp.bmj.com/ biochemical and/or latex agglutination tests. Bactident and three were MUG test positive The dip slide MUG test was read by holding (see discussion). Overall, the Cult-Dip Plus dip slides with significant growth under long MUG test had a sensitivity of 91-6% and a wave ultraviolet light (360 nm). Presumptive specificity of 95-2% and a positive predictive identification of E coli was confirmed by Bac- value of 93-6% for identifying E coli. tident. The presence of fluorescence indicated Of the 95 E coli isolates recovered by routine on October 1, 2021 by guest. Protected copyright. a positive MUG test. Results for isolation of culture, 77 were tested by Bactident and 70 uropathogens and identification ofE coli by our (91%) were MUG test positive (table 3). Of routine method(s) and with the Cult-Dip Plus the 70 MUG test positive isolates, 63 (90%) were compared. were also positive by the Cult-Dip Plus MUG test. Of the seven remaining isolates, five were Cult-Dip Plus MUG test negative and the Results remaining two were untested. Ofthe 19 routine Of the 1022 urine samples analysed, 221 cultures that the Bactident MUG test were not (21 6%) had significant findings (>10 000 cfu/ performed on, 16 were Cult-Dip Plus MUG ml and pure) by one method or the other; 181 test positive and three were not tested.
Recommended publications
  • OSPE Renal Micro AA
    MICROBIOLOGY PRACTICAL TEAMWORK 437 URINARY TRACT INFECTION Objectives: 1- Know the important steps in specimen collection and transport to the lab. 2-How to process urine Specimens in the lab. – Urine microbiological and biochemical analysis. – Organisms culture and identification. – Antibiotic susceptibility testing. – Results interoperation. 3- Know the clinically important etiological Organisms associated with UTI, their identification and susceptibility testing. Done by : ABEER ALABDULJABBAR NOURA ALOTHAIM OMAR ALSUHAIBANI Important aspects of Microbiologic Examination of UTI SPECIMEN COLLECTION : -Urine collection SPECIMEN PROCESSING : -Urine analysis -Urine culture -Interpretation of microbiology -laboratory result 1- SPECIMEN COLLECTION Type of specimens Midstream urine (MSU): best for adult The urine collected in a wide mouthed container from patients a mid stream specimen is the most ideal for processing Female patients pass urine with a labia separated and mid stream sample is collected Adhesive bag best for child Suprapubic aspiration Catheter sample: (used with elderly) Urine specimens for laboratory investigations can be collected from catheterized patients as shown (left). The second port is for putting fluids into the bladder (right). Urine from the drainage bag should not be tested because it may have been standing for several hours. TRANSPORT MEDIA -Sterile urine container -Dip slide (one side is CLED media and the other is MacConkey agar or blood agar) 2- SPECIMEN PROCESSING B-Culture and C-Antimicrobial A-Urine analysis identification Susceptibility D-Results (ID) testing interpretation • Microbiological Disk diffusion Culture media test Macroscopic Urine inoculation and E test Microscopic reading of culture Biochemical Identification of cultured organisms A-Urine analysis v Biochemical : Biochemical Urine Examination (Dip stick) Testing for UTI : Midstream clean catch with dipstick analysis Dipstick results may be affected by medications/dyes, i.e.
    [Show full text]
  • Product List 2006
    94474 Product COVER 5/12/05 6:09 pm Page 1 [email protected] Данный документ является собственностью компании "СИМАС" www.simas.ru Product List 2006 т.ф. (495) 980-29-37, 781-21-58, 319-22-78, 311-22-09 Oxoid Price List 2006 International Orders UK Orders International Customer Services UK Customer Services Oxoid Limited Oxoid Limited Wade Road Wade Road Basingstoke Basingstoke Hampshire RG24 8PW Hampshire RG24 8PW UK Telephone: 01256 816566 Telephone: +44 (0) 1256 841144 Facsimile: 01256 334994 Facsimile: +44 (0) 1256 463388 e-mail: [email protected] e-mail: [email protected] Web: www.oxoid.com Web: www.oxoid.com Technical Support Helpline Technical Support Helpline Telephone: 01256 694281 Telephone: +44 (0) 1256 694287 Facsimile: 01256 329728 Facsimile: +44 (0) 1256 329728 e-mail: [email protected] e-mail: [email protected] For details of your local Oxoid distributor Telephone: +44 (0) 1256 694347 Facsimile: +44 (0) 1256 329728 www.oxoid.com ForFor.b:w9cee(e-bb@+5.b@b-wi,b9b@b-wlP Conditions of Sm9@Fb@@ndibil: [email protected] ec’ F,w.oph.:Support +5.b:xoi. +ee(e-bb@ 94474 Product Text 3/12/05 9:31 am Page 1 [email protected] Данный документ является собственностью компании "СИМАС" www.simas.ru Contents PAGE PAGE ❐ Important Information 2 ❐ AST 25 ❐ Products by Organism 3 Aura System 25 ❐ Worldwide Distributors 6 Disc Dispensers 25 Discs 28 ❐ Prepared Media 21 Diagnostic Discs 28 Dip Slides 21 ❐ Ready Bags 22 ID Biochemical Tests 29 Prepared Media 22 Microbact 29 Biochemical Reagents 28 OBIS Kits 28 ❐ Culture Media 9 Touch Sticks
    [Show full text]
  • OXOID MANUAL PRELIMS 16/6/06 12:18 Pm Page 1
    OXOID MANUAL PRELIMS 16/6/06 12:18 pm Page 1 The OXOID MANUAL 9th Edition 2006 Compiled by E. Y. Bridson (substantially revised) (former Technical Director of Oxoid) Price: £50 OXOID MANUAL PRELIMS 16/6/06 12:18 pm Page 2 The OXOID MANUAL 9th Edition 2006 Compiled by E. Y. Bridson (substantially revised) (former Technical Director of Oxoid) 9th Edition 2006 Published by OXOID Limited, Wade Road, Basingstoke, Hampshire RG24 8PW, England Telephone National: 01256 841144 International: +44 1256 841144 Email: [email protected] Facsimile National: 01256 463388 International: +44 1256 463388 Website http://www.oxoid.com OXOID SUBSIDIARIES AROUND THE WORLD AUSTRALIA DENMARK NEW ZEALAND Oxoid Australia Pty Ltd Oxoid A/S Oxoid NZ Ltd 20 Dalgleish Street Lunikvej 28 3 Atlas Place Thebarton, Adelaide DK-2670 Greve, Denmark Mairangi Bay South Australia 5031, Australia Tel: 45 44 97 97 35 Auckland 1333, New Zealand Tel: 618 8238 9000 or Fax: 45 44 97 97 45 Tel: 00 64 9 478 0522 Tel: 1 800 331163 Toll Free Email: [email protected] NORWAY Fax: 618 8238 9060 or FRANCE Oxoid AS Fax: 1 800 007054 Toll Free Oxoid s.a. Nils Hansen vei 2, 3 etg Email: [email protected] 6 Route de Paisy BP13 0667 Oslo BELGIUM 69571 Dardilly Cedex, France PB 6490 Etterstad, 0606 Oxoid N.V./S.A. Tel: 33 4 72 52 33 70 Oslo, Norway Industriepark, 4E Fax: 33 4 78 66 03 76 Tel: 47 23 03 9690 B-9031 Drongen, Belgium Email: [email protected] Fax: 47 23 09 96 99 Tel: 32 9 2811220 Email: [email protected] GERMANY Fax: 32 9 2811223 Oxoid GmbH SPAIN Email: [email protected] Postfach 10 07 53 Oxoid S.A.
    [Show full text]
  • Microbiology Program –Medical Faculty (5-Y
    MICROBIOLOGY PROGRAM – Medicine Faculty 2020/2021 Didactic hours: Seminars: 36 hrs, practical classes: 34 hrs S1. Basics of medical bacteriology: morphology of bacteria. Procaryotic cell structure: capsule, flagella, fimbriae, cell wall, cell membrane, LPS, cytoplasm components; spores. Morphology of bacteria: bacterial cell (structure, dimensions, shapes, arrangements – cocci, rods (bacilli), spirochetes. Differential characteristics of bacteria: differences of bacterial cell wall structure: Gram- positive, Gram negative -negative bacteria, mycobacteria. Classification of microorganisms: kingdom, phylum, class, order, family, genus, species (strain, biotype, serotype, serovar). Direct detection of bacteria: bacterial cell detection (microscopy; smears), bacterial component (antigen) detection in the specimen sample (serology) genetic material detection (molecular techniques). Types of slide preparation - unstained (wet mount) slide preparation, stained smear; direct smear, smear from culture. Types of microscopes: bright-field light microscopy, dark-field microscopy, fluorescent microscopy. Staining techniques and application: simple and differential staining, positive and negative staining; staining types: Gram staining, Ziehl-Neelsen (acid –fast) staining , Neisser staining, Giemsa staining, Loeffler staining. Major groups of Gram-positive bacteria – cocci: Staphylococcus, Streptococcus, Enterococcus; bacilli: Bacillus, Clostridium; Corynebacterium, Listeria, Lactobacillus, Mycobacterium, Nocardia, Actinomyces. Major groups of Gram-negative
    [Show full text]
  • Microbiologically-Influenced Corrosion (MIC) Or Biocorrosion
    MICROBIALLY INFLUENCED CORROSION OF INDUSTRIAL MATERIALS - BIOCORROSION NETWORK - (Brite-Euram III Thematic Network N° ERB BRRT-CT98-5084 Biocorrosion 00-02 Simple methods for the investigation of of the role of biofilms in corrosion September 2000 Task 1: Biofilms Publication by Iwona Beech, Alain Bergel, Alfonso Mollica, Hans-Curt Flemming (Task Leader), Vittoria Scotto and Wolfgang Sand SIMPLE METHODS FOR THE INVESTIGATION OF THE ROLE OF BIOFILMS IN CORROSION BRITE EURAM THEMATIC NETWORK ON MIC OF INDUSTRIAL MATERIALS TASK GROUP 1 BIOFILM FUNDAMENTALS IWONA BEECH ALAIN BERGEL ALFONSO MOLLICA HANS-CURT FLEMMING (TASK LEADER) VITTORIA SCOTTO WOLFGANG SAND 1 CONTENTS 1 MICROBIOLOGICAL FUNDAMENTALS 1.1 WHAT IS MIC? 1.2 PRINCIPLES OF MICROBIAL LIFE 1.3 SOME DETAILS OF MICROBIAL LIFE 1.4 MICROORGANISMS INVOLVED IN MIC 2 MICROBIOLOGICAL INVESTIGATION OF MIC 2.1 LIQUID SAMPLES 2.2 SOLID SAMPLES 2.3 PRE-TREATMENT OF SAMPLES 2.4 DETECTION AND IDENTIFICATION OF MICROORGANISMS 2.4.1 MICROSCOPICAL EXAMINATION 2.4.2 RAPID DETECTION 3 A GUIDE TO SIMPLE METHODS TO ASSESS THE PRESENCE OF BIOFILMS IN FIELD AND THE MIC RISK 3.1 INTRODUCTION 3.2 METHODS FOR BIOFILM EVALUATION 3.2.1 CARBOHYDRATE ANALYSIS 3.2.1.2 PROTEIN ANALYSIS 3.3.1 IS THE BIOFIL M COMPOSED OF OXYGEN PRODUCERS OR OXYGEN CONSUMERS? 3.4 THE CORROSION POTENTIAL MEASUREMENT: A TOOL FOR EVALUATING THE MIC RISK 2 1 MICROBIOLOGICAL FUNDAMENTALS Iwona Beech and Hans-Curt Flemming 1.1 What is MIC? MIC is the acronym for “Microbally Influenced Corrosion”. It refers to the possibility that microorganisms are involved in the deterioration of metallic (as well as non-metallic) materials.
    [Show full text]
  • European Urinalysis Guidelines SUMMARY
    Scand J Clin Lab Invest 2000; 60: 1 ± 96 European Urinalysis Guidelines SUMMARY These European Urinalysis Guidelines are given Classi®cation of examiniations under the auspices of the European Confedera- Examinations have been re-classi®ed into four tion of Laboratory Medicine (ECLM). hierarchical levels based on accuracy of mea- surements (chemistry on Page 12, particle Medical needs for urinalysis analysis on Page 23, microbiology on Page Urinalysis should always be performed on the 31). In addition, the previous literature on the basis of medical need, and appropriate exam- visual appearance and odour of urine is inations for various clinical populations and presented (Page 13). presentations should be determined by cost/ bene®t analysis. On this basis, selection indica- Chemical methods of examination tions for urinalysis are suggested for detecting Principles and performance criteria of multiple diseases of the kidneys or urinary tract (Page 6). test strips are reviewed (Page 13). A nitrite test The referral for detailed urine examinations should not be used alone in detecting urinary should include an adequate description of the tract infections because of its low sensitivity. specimen type, and should inform the labora- Quali®ed procedures for measurement are tory of the clinical need in order to facilitate recommended (Page 56). Pregnancy examina- correct selection of examination procedures and tions are reviewed brie¯y (Page 18). interpretation of results (Page 6). This medical Quantitative chemical measurements are dis- information is mandatory when the choice is cussed in detail, mainly with respect to protein being made between minimum and optimum measurements (Page 18). Measurements asses- procedures for different specimens.
    [Show full text]
  • Point-Of-Care Testing for Urinary Tract Infections Horizon Scan Report 0045 June 2016
    Diagnostic Evidence Co-operative Oxford Point-of-care testing for urinary tract infections Horizon Scan Report 0045 June 2016 Clinical Question: In diagnosing patients with suspected urinary tract infections, what is the accuracy and utility of point-of- care tests compared to the current standard of urine microscopy, culture and antibiotic sensitivity analysis? Background, Current Practice and Advantages over Existing Technology: Background Urinary tract infections (UTIs) are among the most common types of infections, with an estimated 92 million people affected worldwide in 2013.1 The global burden of this disease is rising, with 16.1% increase in age- standardised incidence between 1990 and 2013 and 58,000 years lost to disability (YLD) in 2003 alone.1 UTIs are also a significant cause of mortality especially among the elderly population with 4835 deaths in England and Wales reported in 2012.2 UTI symptoms accounted for 1-3% of all primary care consultations3 and it was the main indication for 13.7% of community antibiotic prescriptions.4 The 1994/5 cost estimates of treating UTIs in the National Health Service were £124 million.5 Two decades on, it can only be assumed that with the rising prevalence of UTIs combined with the emergence of antibiotic-resistant organisms, the health and economic burden of the disease is likely to have increased. UTIs are broadly defined as infection of the urethra, bladder, ureters or kidneys by non-commensal micro- organisms, most commonly Escherichia coli, Staphylococcus saprophyticus and Enterococcus faecalis.6 Other causative uropathogens include Enterobacteriaceae sp. (Proteus mirabilis and Klebsiella sp.), group B streptococci, Pseudomonas aeruginosa, and Citrobacter sp.
    [Show full text]
  • READY-TO-USE DIPSLIDE MEDIA DA-212115.03 Rev.: Aug 2005
    INSTRUCTIONS FOR USE – READY-TO-USE DIPSLIDE MEDIA DA-212115.03 Rev.: Aug 2005 BD™ BBL UROTUBE • BBL UROTUBE M • BBL UROTUBE E • BBL UROTUBE E. coli • BBL UROTUBE SXT INTENDED USE BBL UROTUBE products are dipslides used for the isolation and determination of the colony count of microorganisms isolated from urine specimens. The surfaces of the dipslides are coated with two or three different culture media. All BBL UROTUBE products contain CLED Agar for the determination of the total count of bacteria and/or yeasts, and MacConkey Agar for the detection of Gram negative bacteria, e.g., Enterobacteriaceae. The third medium, if available, is dependent on the respective product. PRINCIPLES AND EXPLANATION OF THE PROCEDURE Microbiological method. Dipslides are widely used today as a screening technique for the enumeration and isolation of microorganisms from routine urine specimens.1-5 After the dipslide is immersed into a properly collected fresh urine specimen and the slide is subsequently incubated, the colony number on the surface of CLED Agar is compared to a reference picture. CLED Agar was developed by Sandys in 1960 to prevent the swarming of Proteus by restricting the electrolytes in the culture medium which was modified later several times for use in urine culture.6 It was designated as Cystine-Lactose-Electrolyte-Deficient (CLED) medium and reported to be ideal for dip-inoculum techniques and for urinary bacteriology in general.6,7 The nutrients in CLED Agar are supplied by the gelatin and casein peptones, and beef extract. Lactose is included to provide an energy source for organisms capable of utilizing it by a fermentative mechanism.
    [Show full text]
  • Laboratory Manual of Microbiology
    Laboratory Manual of Microbiology Laboratory Manual of Microbiology Vivek Kumar Microbiology Section, Department of Soil and Water Research, Plant Wealth Sector, Public Authority of Agriculture and Fish Recourses, State of Kuwait Published by: Scientific Publishers (India) 5-A, New Pali Road, P.O. Box 91, Jodhpur – 342 001 (India) E-mail: [email protected] www.scientificpub.com © Scientific Publishers (India), 2011 All rights reserved. No part of this publication or the information contained herein may be reproduced, stored in a retrieval system, or transmitted in any form or by any means, electronic, mechanical, by photocopying, recording or otherwise, without written prior permission from the editor and the publishers. ISBN: 978-81-7233-706-3 (HB) 978-81-7233-707-0 (PB) Lasertype set : Rajesh Ojha Printed in India PREFACE The rapid expansion of microbiology has lad to proliferation of technical methods. This laboratory manual of microbiology is an attempt to form a comprehensive reference source for a common microbiologist. The manual is aimed at the graduate and advanced student and the research worker who studies or uses micro- organisms. Each exercise has been designed to be modular and with brevity. The exercises have also been designed to use commonly available microbiological tools and instruments to complete in short time period. This laboratory manual of microbiology has been written to meet the needs of students taking microbiology as major or subsid- iary subject. The intention is to provide the student with an organi- zed, user-friendly tool to better enable him or her to understand laboratory aspects of microbiology as well as to hopefully make learning laboratory material and preparing for independent player of a given experiment.
    [Show full text]
  • LIOFILCHEM® S.R.L
    Liofilchem® Product Catalogue 2019 Clinical and Industrial Microbiology ® ! Microbiology Products Est. 1983 MICROPLANET MICROPLANET 2 In memory of Dr. Santa Ruggieri 1962-2011 MICROPLANET 3 Visit www.liofilchem.com to be up to date with our product updates, latest news, special offers and information on products and services. The Liofilchem website offers a convenient and eco-friendly complete on-line Product Catalogue, fliers, brochures and video featured product pages. Liofilchem Quality Control Certificates, Technical Sheets, MSDS and much more are available for download at the on-line Technical Library." TheMICROPLANET Liofilchem on-line technical documentation service is convenient, quick and available 24/7. 4 LIOFILCHEM® s.r.l. Via Scozia, Zona Industriale 64026 Roseto degli Abruzzi (Te) Italy Tel.: +39 0858930745 Fax: +39 0858930330 www.liofilchem.com Since 1983 Liofilchem® s.r.l. has committed its Research and Development department to the production of reliable and high quality bacteriology products. Our dedication to Customer satisfaction and exceptional manufacturing versatility have granted Liofilchem® continuous growth, as a result of the increasing quality of our products and the worldwide distribution of the Liofilchem® brand name. Liofilchem® is present in over 130 countries with agents and distributors placing our products in clinical and industrial laboratories around the world. Our catalogue is comprised of approximately 6000 items basically classified into two main categories, clinical and industrial microbiology. Liofilchem® manufacturing
    [Show full text]
  • Practical UTI
    Lecture : Practical UTI important Extra notes "ﻻ ﺣول وﻻ ﻗوة إﻻ ﺑﺎ@ اﻟﻌﻠﻲ اﻟﻌظﯾم" وﺗﻘﺎل ھذه اﻟﺟﻣﻠﺔ إذا داھم اﻹﻧﺳﺎن أﻣر ﻋظﯾم ﻻ notes Doctors ﯾﺳﺗطﯾﻌﮫ ، أو ﯾﺻﻌب ﻋﻠﯾﮫ اﻟﻘﯾﺎم ﺑﮫ . Objectives: 1- to Know the important steps in specimen collection and transport to the lab. 2. How to process urine Specimens in the lab. – Urine microbiological and biochemical analysis. – Organisms culture and identification. – Antibiotic susceptibilitytesting. – Results interoperation. 3. Know the clinically important etiological Organisms associated with UTI, their identification and susceptibility testing. • اﻟﻌﻣل ﻣﻌﺗﻣد و ﺷﺎﻣل ﻋﻠﻰ ﻣﺣﺎﺿرات اﻟدﻛﺎﺗرة : Overview • ﻻ ﺗﺧﺎﻓون ﻣن ﻋدد اﻟﺳﻼﯾدز , اﻟﺳﻼﯾدز ﺧﻔﯾﻔﺔ و ﻏﺎﻟﺑﯾﺔ اﻟﻣﻌﻠوﻣﺎت ﻣﻌروﻓﺔ وﺳﮭﻠﺔ اﻟﻣﺣﺎﺿرة ﺗﺗﻛﻠم ﻋن أرﺑﻊ ﻣﺣﺎور أﺳﺎﺳﯾﺔ : إن ﺷﺎء ﷲ collecting urine 1- • ﻓﻲ ﻧﮭﺎﯾﺔ اﻟﻣﺣﺎﺿرة ﻓﯾﮫ ﻛﯾﺳﯾز ﻣن ﺳﻼﯾد اﻟدﻛﺎﺗرة , ﻟﻛن اﻟﺣل ﻣن اﻟﺗﯾم analysis urine 2- • رﻛزوا ﻋﻠﻰ .. groth + stain + culture their and microorganism microorganisms the 3- (وﺑﺎﻟﺗوﻓﯾﯾق اﺟﻣﻌﯾﯾن) Testing Susceptibility Antimicrobial 4- Important aspects of Microbiologic Examination of UTI: • Urine collection • Urine analysis • Interpretation of microbiology • laboratory result 1- Urine collection Midstream urine (MSU): • The urine collected in a wide mouthed container from patients a mid stream specimen is the most ideal for processing • Female patients pass urine with a labia separated and mid stream sample is collected Adhesive bag Types of specimens: Suprapubic aspiration (for children) Clean catch Catheter sample: (used with elderly) • Urine specimens for laboratory investigations can be collected from catheterized patients as shown (left). The second port is for putting fluids into the bladder (right). • Urine from the drainage bag should not be tested because it may have been standing for several hours.
    [Show full text]
  • 1 Methicillin-Resistant Staphylococcus Aureus On
    Methicillin-Resistant Staphylococcus aureus on Public Transportation Vehicles: Sampler Performance, Prevalence, and Epidemiology DISSERTATION Presented in Partial Fulfillment of the Requirements for the Degree Doctor of Philosophy in the Graduate School of The Ohio State University By Jonathan Kyle Lutz, M.P.H. Graduate Program in Public Health The Ohio State University 2011 Dissertation Committee: J. Mac Crawford, Advisor Armando E.S. Hoet Jiyoung Lee John R. Wilkins III 1 Copyright by Jonathan Kyle Lutz 2011 i Abstract Methicillin-resistant Staphylococcus aureus (MRSA) is an important public health threat, with significant disease burden. Of particular concern are the growing number of cases that have origins in the community (CA-MRSA); these infections often affect individuals without underlying risk factors for disease. Because MRSA colonizes a large number of people, can be easily spread by fomites, and survives on surfaces for months, the environment is an important element in MRSA transmission. Public transportation vehicles, which have high levels of crowding and significant hand-to-fomite contact, may represent an important site for MRSA transmission. This study determined the background prevalence of MRSA on buses from a large transportation agency. Prior to vehicle sampling, a laboratory-based study was conducted to evaluate the performance of four sampling methods for recovery of S. aureus from a stainless steel surface. Results indicate that overall, the electrostatic wipe resulted in the greatest performance across all inoculating concentrations ([relative sampling efficiency=SE; 2 analytical sensitivity=Sn] SE48h=17.8%; Sn48h=7 CFU/100cm ). However, the swab sampler performed well when corrected for area actually sampled (SE48h=24.3%; 2 Sn48h=76 CFU/100cm ), but is greatly limited by the surface area which can be effectively sampled.
    [Show full text]