Sheet1. Page 1. Supplementary table S1 Detailed information on the 67 phenotypes used in this study. Test GIDEON II. Bergey's Test description

Similar documents
Product Catalogue Clinical and Industrial Microbiology

SOP: API 20E Microbial Identification

(API 20E ) Analytical Profile Index System for Identification of Enterobacteriaceae. Manal AL khulaifi

Unusual Enterobacteriaceae: "Proteus rettgeri" That "Change" into Providencia stuartii

GENUS STAPHYLOCOCCUS: Isolation and Identification

320 MBIO Microbial Diagnosis. Aljawharah F. Alabbad Noorah A. Alkubaisi 2017

á62ñ MICROBIOLOGICAL EXAMINATION OF NONSTERILE PRODUCTS: TESTS FOR SPECIFIED MICROORGANISMS

Fate of Staphylococci and Enteric Microorganisms Introduced into Slurry of Frozen Pot Pies

DEPARTMENT OF CLINICAL LABORATORY SCIENCES SCHOOL OF HEALTH TECHNOLOGY AND MANAGEMENT THE UNIVERSITY AT STONY BROOK STONY BROOK, NEW YORK

Lab Exercise: Examining Water Quality: Most Probable Number & Colilert Test Kit Lab

International Journal Of Recent Scientific Research

Xylanase Enzyme Stability and Biochemical Characteristics Thermoxylanolytic Bacteria From Mudiak Sapan Hot Springs at Solok Selatan District

Neisseria lactamicus sp. n., a Lactose-fermenting Species Resembling Neisseria meningitidis

Inoculate: Media. Physical State of Media: Liquid. The Five I s: Basic Techniques to Culture Microbes Tools of the Microbiology Laboratory

Pet Microbe 1: Lab Guide

Bacterial Isolation, Identification, and Storage. Lila Ruangpan

Chapter 03 - Tools of the Laboratory: Methods for the Culturing of Microscopic Analysis of microorganisms

Anaerobic Bacteria from the Large Intestine of Mice1

Pre-Packaged Multi-Media for the Identification of Bacteria: The Enterotube II System. Introduction

BD Mac Conkey II Agar / Columbia CNA Agar with 5% Sheep Blood (Biplate)

Reisolation of Staphylococcus salivarius from the

Rapid Identification of Enterobacteriaceae with the Micro-ID

The Genus Aeromonas: Biochemical Characteristics, Atypical Reactions, and Phenotypic Identification Schemes

MICROBIOLOGICAL STUDY OF A BACILLUS MEGATENUM STRAIN WITH SOIL PHOSPHORUS SOLUBILIZATION POTENTIAL

Vanessa Cris D. Blancaflor 1, Jocelyn T. Zarate 2 and Celia B. Dela Viña 3 1, 3

This week's experiment focuses on bacterial growth and methods to control bacterial growth.

Micro Digital Media 2/e Copyright 2012, Intuitive Systems, Inc. Section: TABLE OF CONTENTS

QUALITY ASSURANCE IN MICROBIOLOGY

SCHEDULE. Friday: Pet Investigations: Plate counts - how to know how many clones of your pet you have (pg. 9-10)

Escherichia vulneris: a New Species of Enterobacteriaceae Associated with Human Wounds

BD CHROMagar Orientation Medium / Columbia CNA Agar (Biplate)

Thioglycolate Medium for Differentiating

STREPTOCOCCI' ANIMAL STRAINS OF HEMOLYTIC. hydrolyze sodium hippurate. Avery (1929) also demonstrated

Cell Biology Homework

Bacillus subtilis as an Alternative Source of Beta-glucosidase

Xylose Lysine Deoxycholate (XLD) Agar LI acc. EP/USP

Bacteriological Analytical Manual Online January 2001

Evaluation of the MS-2 System for Rapid Identification of Enterobacteriaceae

Chapter 6 Isolation and Identification of Vibrio cholerae Serogroups O1 and O139

BBL QualiSwab Quality Control Culture Devices

Isolation and characterization of Acetobacter aceti from rotten papaya

National Food Safety Standard Microbiological Examination of Food Hygiene - Examination of Shigella 食品安全国家标准食品微生物学检验志贺氏菌检验

BD Columbia CNA Agar with 5% Sheep Blood, Improved II

ACP601: Plant Mycology and Bacteriology Plant Bacteriology

LABORATORY HANDBOOK VETERINARY BACTERIOLOGY & MYCOLOGY VPM 201, 2011 ATLANTIC VETERINARY COLLEGE

2.1 Tryptone Soya Broth containing 4% Tween 80 (TSB + T), or another appropriate deactivating broth.

The Classification of Micrococci and Staphylococci Based on their DNA Base Composition and Adansonian Analysis

Laboratory Procedure October 1999 HEALTH PROTECTION BRANCH OTTAWA ANALYSIS OF SPROUTS FOR COLIFORMS, ESCHERICHIA COLI, AND KLEBSIELLA PNEUMONIAE..

MICROBIAL GROWTH. Dr. Hala Al-Daghistani

Bacteriological analysis of plastic and wood chopping boards

Characteristics of Pasteurella multocida of Human Origin

Implementation of the VITEK MS and Its Use in Microbial Identification

Biology 123 Microbiology Spring 2015

A r~g~rj JJl~ttu><:l Jp. Qu.~ntifY. b~tct.~ri. al on hatching eggs. 1. Correlation of optical density with initial bacterial count

Supplementary data: Morphology

ISO 6579 INTERNATIONAL STANDARD. Microbiology of food and animal feeding stuffs Horizontal method for the detection of Salmonella spp.

ACCEPTED. JCM Revised

NUTRITION, ISOLATION, CULTIVATION AND COUNTING OF BACTERIA. Dr. Jigar Shah IPNU

Project 7: Wound Cultures and Identification

Bacterial Classification and Identification. Kunle Kassim, PhD, MPH Professor, Microbiology August, 2010

Abstract. Mary Jane Ferraro, PhD, MPH Jana M. Swenson, MMSc

Streptomyces spinoverrucosus, a New Species from the Air of

International Journal of Systematic and Evolutionary Microbiology (2004), 54,

EVALUATION OF SALMONELLA TEST METHOD OF SRI LANKA STANDARDS INSTITUTION

The Domestic Student Kitchen: A Microbiological Hazard?

used plain agar to which sheep serum was added. Some authors' CULTURES OF THE MENINGOCOCCUSi

Simultaneous Determination of Inorganic Anions, Organic Acids, Amino Acids and Carbohydrates by Capillary Electrophoresis

Classification of Vibrio cholerae (Vibrio comma)

SUMMARY OF MICROBIOLOGY QC REQUIREMENTS Note: all procedures listed are eligible for the IQCP option described in S&C CLIA (effective 1/4/2016)

A NEW FACULTATIVE ANAEROBE CAPABLE OF GROWTH ON CHLOROBIPHENYLS MICHEL SYLVESTRE AND JOHANNE FAUTEUX

STUDIES ON PASTEURIZATION' instance, a disposition to prevent the sale of milk from these. small colonies may become pin-point in size if there are

REISOLATION AND EMENDATION OF DESCRIPTION OF VIBRIO MARINUS (RUSSELL) FORD'

Lab Notes for Exam 3 Section

Determination of Minimum Inhibitory Concentration (MIC) of Routinely used Disinfectants against Microflora Isolated from Clean Rooms

Int.J.Curr.Microbiol.App.Sci (2014) 3(10)

Methicillin resistant Staphylococcus aureus (MRSA)- Background and analysis

Section III Research Articles and Short Communications

Isolation and characterization of lactic acid bacteria from curd and cucumber

Microbial Nutrition and Growth

Ezy MIC Strip FEATURES AND ADVANTAGES

Exercise 24-A MICROBIAL CONTROL METHODS (Effects Of Temperature, Ultra Violet Light, Disinfectants And Antiseptics)

Impact of recharge sources on isotopic composition and microbiological quality of groundwater- a case study from Punjab, India

CLIA Complexity: MODERATE

Handbook of Microbiological Quality Control

Published on: 1 st June 2012 STUDY OF BACTERIAL DIVERSITY OF CRUDE OIL DEGRADING BACTERIA ISOLATED FROM CRUDE OIL CONTAMINATED SITES

Chapter 02 Tools of the Laboratory: Methods for the Culturing and Microscopic Analysis

IDENTIFICATION OF MORAXELLA SPECIES AND MORPHOLOGICALLY SIMILAR ORGANISMS

National Standards of the People s Republic of China GB xxxx. National Food Safety Standard. Microbiological Test of Food

Pseudomonas paucimobilis, a New Species Isolated from Human Clinical Specimens, the Hospital Environment, and Other Sources

possessed the H formula d - e, n.. which is known to exist in the Amersfoort as Salmonella salinatis, was identified by Dr. Welch as a member of the

ISSN (Online) ISSN (Print) *Corresponding author Rasel Barua.

Antimicrobial Susceptibility Testing

Characterization and Identification of Bacterial Flora from Infected Equine Hooves

BIOLOGY Principles of Microbiology LABORATORY MANUAL

A Discovery Laboratory Investigating Bacterial Gene Regulation

Bacterial Cytology 1 BACTERIAL CYTOLOGY

STUDIES ON PROTEOLYTIC THERMODURIC PSYCHROTROPHIC BACTERIA IN MILK AND FERMENTED MILK PRODUCTS

The Phylogenetic Characterization of a Bioluminescent Bacterium Isolated From Shrimp

Method Suitability Report Membrane Filtration Sterility Test with QTMicro Apparatus

Isolation and Characterization of Acidophilic Sulphur and Iron Oxidizing Acidithiobacillus ferrooxidans from Black Shale

Transcription:

Supplementary table S1 Detailed information on the 67 phenotypes used in this study Phenotype (a) Test GIDEON I GIDEON II Bergey's Test description type (c) GIDEON I+ (e) GIDEON I- (d) GIDEON II+ (b) total (h) GIDEON II- (g) Bergey's+ (f) total (k) Bergey's- (l) (i) total (m) Acetate utilization Aerobe Alkaline phosphatase Anaerobe Arginine dihydrolase Bacillus or coccobacillu s Beta hemolysis A variety of commercial kits are satisfactory. Includes late reactions for -positive and non-fermve negative rods Organisms which grow only in the presence of air. Most kits utilize p- nitrophenyl phosphate as substrate. Insure thorough washing if phosphate buffers are employed Organisms which do not grow in the presence of oxygen For most organisms, Moeller medium interpreted with control after 18 hours (or longer for -positive and non-fermve negative rods) 27 19 46 5 2 7 7 10 17 64 167 231 7 35 42 25 0 25 30 15 45 7 3 10 12 21 33 46 169 215 14 27 41 16 11 27 46 88 134 8 15 23 35 55 90 Bacilli predominate 160 48 208 28 12 40 0 0 0 Sheep blood 18 134 152 4 17 21 4 5 9 Page 1

Bilesusceptible Capnophilic Casein hydrolysis Catalase Cellobiose Media and bile concentrations vary according to the species ed; Presumpto Plates useful for anaerobes Exogenous carbon dioxide (5 to 7%) must be present for growth; Gas Pak or cylinder gas are preferred Standard skimmilk/nutrient agar halo ; Presumpto Plates useful for anaerobes Perform on young colonies (up to 24 hours) using 3% hydrogen peroxide (alternative technique for Mycobacteria); Presumpto Plates useful for anaerobes reactions for positive & nonfermve 16 35 51 2 7 9 0 0 0 22 175 197 2 33 35 0 0 0 13 47 60 2 7 9 19 19 38 123 91 214 18 20 38 34 32 66 33 63 96 4 7 11 42 50 92 Page 2

Citrate Coagulase production Simmons citrate medium using a light inoculum (avoid stabbing the agar). Includes late reactions for positive and nonfermve negative rods Standard or commercial slide plasma s acceptable; tube s may help differentiate Staphylococcus aureus from other taxa 35 81 116 11 16 27 16 19 35 30 45 75 3 7 10 2 3 5 Coccus Coccus - clusters or groups predominate Cocci predominate. 44 170 214 12 28 40 0 0 0 The predominant forms are cocci, in clusters or irregular groups. 12 204 216 2 39 41 0 0 0 Coccus - pairs or chains predominate The predominant forms are cocci in chains or pairs. 28 185 213 10 30 40 0 0 0 Colistin- Polymyxin susceptible Standard disk diffusion technique; recommended media and disk potency may vary for specific taxa 38 55 93 3 11 14 0 0 0 Page 3

D-Mannitol D-Mannose DNase reactions for positive & nonfermve reactions for positive & nonfermve Standard commercial agar s; Presumpto Plates useful for anaerobes 53 128 181 12 19 31 49 58 107 85 60 145 14 12 26 70 20 90 15 71 86 2 9 11 2 0 2 Page 4

D-Sorbitol D-Xylose Esculin hydrolysis Facultative reactions for positive & nonfermve reactions for positive & nonfermve For most organisms, Moeller medium interpreted with control after 18 hours (or longer for -positive and non-fermve negative rods) Organisms which grow both in the presence and absence of air. 18 127 145 5 24 29 18 60 78 44 118 162 10 22 32 32 77 109 52 93 145 17 12 29 49 31 80 97 130 227 19 23 42 0 0 0 Page 5

Gas from glucose Gelatin hydrolysis Gas produced from D- glucose; Durham tube or gas bubbles noted in commercial kits Commercial or self prepared (or X-ray film) s interpreted after 24-48 hours against control at lowered temperature; Presumpto Plates useful for anaerobes 22 106 128 3 15 18 4 6 10 30 111 141 3 19 22 30 31 61 Glucose fermenter techniques are generally producing more subtle ph changes; specific techniques applied for Neisseria; Presumpto Plates useful for anaerobes 131 78 209 26 9 35 0 0 0 Glucose oxidizer Hugh and Leifson method; in most cases 'positive' indicates nonfermve organism which oxidizes glucose 22 192 214 2 38 40 0 0 0 Page 6

Glycerol reactions for positive & nonfermve 24 86 110 8 14 22 28 31 59 Gram negative Gram positive Growth at 42 degrees C Gram-negative forms predominate Gram-positive forms predominate Media vary according to the species ed 117 110 227 17 24 41 0 0 0 100 127 227 23 18 41 14 8 22 43 27 70 10 2 12 0 4 4 Growth in 6.5% NaCl Media vary according to the species ed 29 67 96 6 9 15 0 0 0 Growth in KCN Growth on MacConkey agar Growth on ordinary blood agar Commercial kits based on 1:13,000 KCN are suggested Visible growth within 48 hours; or within 7 days for positive and non-fermve Visible growth on sheep blood agar within 48 hours 10 14 24 2 0 2 18 10 28 55 165 220 7 31 38 0 2 2 211 18 229 39 3 42 0 0 0 Page 7

Hydrogen sulfide Indole Lactose TSI for enterobacteriaceae and most other species; Presumpto Plates useful for anaerobes. Includes late appearance of hydrogen sulfide for -positive and nonfermve negative rods A spot is acceptable for most organisms; overnight ing with a paper strip is helpful in confirming negative reactions; Presumpto Plates useful for anaerobes reactions for positive & nonfermve 13 116 129 4 16 20 0 2 2 20 145 165 2 24 26 18 47 65 61 104 165 11 17 28 48 55 103 Page 8

L-Arabinose reactions for positive & nonfermve 44 114 158 8 23 31 24 84 108 Lipase L- Rhamnose Standard egg yolk agar ; Presumpto Plates useful for anaerobes reactions for positive & nonfermve 20 76 96 2 13 15 5 9 14 20 109 129 2 24 26 10 43 53 Lysine decarboxyla se For most organisms, Moeller medium interpreted with control after 18 hours (or longer for -positive and non-fermve negative rods) 11 63 74 4 5 9 6 20 26 Page 9

Malonate Maltose Melibiose Methyl red Standard based on maintenance of alkaline ph (bromthymol blue) in the presence of glucose and malonate; commercial kits are acceptable reactions for positive & nonfermve reactions for positive & nonfermve Commercial or selfprepared media are generally acceptable 11 29 40 1 4 5 0 0 0 105 66 171 18 9 27 86 32 118 25 88 113 9 18 27 18 45 63 23 29 52 2 5 7 5 7 12 Page 10

Motile Mucate utilization myo-inositol Nitrate to nitrite Nitrite to gas Standard hanging drop on fresh broth isolates for most purposes; perform at 22 to 25 degrees C if Listeria suspected A variety of commercial kits are satisfactory. Includes late reactions for -positive and non-fermve negative rods reactions for positive & nonfermve Commercial and selfprepared media are acceptable; alternative techniques used for mycobacteria Standard zinc dust applied to 'nitratenegative' organisms 70 144 214 11 26 37 60 32 92 11 23 34 2 6 8 3 8 11 10 107 117 5 16 21 3 29 32 75 92 167 8 19 27 31 43 74 14 76 90 1 11 12 0 0 0 Page 11

ONPG (beta galactosidas e) Ornithine decarboxyla se Oxidase Pyrrolidonylbetanaphthylami de Commercial kits are generally satisfactory; suggest a heavy inoculum in buffered medium; yellow pigmented organisms may not be suitable for ing For most organisms, Moeller medium interpreted with control after 18 hours (or longer for -positive and non-fermve negative rods) Paper strip from appropriate media L-pyrrolidonyl-betanaphthylamide - PYR (or pyrrolidonyl arylamidase - PYRA) - reagents commercially available; read color within 10 seconds (2 minutes for Carr-Scarborough reagent) 45 70 115 8 9 17 4 11 15 17 67 84 2 5 7 13 23 36 56 130 186 5 24 29 19 19 38 23 56 79 5 10 15 0 0 0 Page 12

Raffinose Salicin Spore formation Starch hydrolysis reactions for positive & nonfermve reactions for positive & nonfermve Note that spores may only appear in vitro, and may not be seen in clinical material Standard starch hydrolysis or Mueller- Hilton agar s developed with iodine solutions; Presumpto Plates useful for anaerobes 30 107 137 10 17 27 23 66 89 41 93 134 9 12 21 28 24 52 18 216 234 2 40 42 3 2 5 27 65 92 5 15 20 38 44 82 Page 13

Sucrose Tartrate utilization Trehalose reactions for positive & nonfermve A variety of commercial kits are satisfactory. Includes late reactions for -positive and non-fermve negative rods reactions for positive & nonfermve 84 93 177 20 11 31 85 44 129 10 18 28 2 3 5 4 3 7 75 63 138 14 15 29 66 42 108 Page 14

Urea hydrolysis Voges Proskauer Yellow pigment Christensen agar ing for most taxa; other techniques for mycobacteria, ureaplasma and other organisms as recommended. Includes late reactions for positive and nonfermve negative rods Commercial or selfprepared media are generally acceptable; the is most reliable when performed on cultures no older than three days Yellow pigment noted on sheep blood or other primary isolation agar. Includes late appearance of pigment for -positive and non-fermve negative rods (a) GIDEON phenotypes (b) Type of required for the phenotype determination in the wet lab according to GIDEON (c) Remarks on wet lab for determination of the phenotype according to GIDEON (d) Number of phenotype-positive bacteria in the GIDEON I dataset (e) Number of phenotype-negative bacteria in the GIDEON I dataset (f) Total number of bacteria with phenotype labels in the GIDEON I dataset (g) Number of phenotype-positive bacteria in the GIDEON II dataset (h) Number of phenotype-negative bacteria in the GIDEON II dataset (i) Total number of bacteria with phenotype labels in the GIDEON II dataset 28 127 155 7 22 29 15 56 71 28 68 96 8 8 16 10 19 29 13 161 174 1 28 29 1 4 5 Page 15

(j) Number of phenotype-positive bacteria in the Bergey dataset (k) Number of phenotype-negative bacteria in the Bergey dataset (l) Total number of bacteria with phenotype labels in the Bergey dataset Page 16