A NEW- OR DELTA-TYPE STREPTOCOCCUS

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

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

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

SKIN INFECTION OF RABBITS WITH HEMOLYTIC STREP- TOCOCCI ISOLATED FROM A PATIENT WITH ERYSIPELAS.

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

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

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

37.50C. for 3, 4, or 5 days, together with uninoculated control. Histological examination of the sections of kidney grown with

Identifying Enterobacter aerogenes from a Mixed Culture of Unknown Gram Positive and Gram Negative Bacteria Kevin Le November 13, 2013

THE TECHNIC OF THE KOLMER COMPLEMENT FIXATION TESTS FOR SYPHILIS EMPLOYING ONE-FIFTH AMOUNTS OF REAGENTS JOHN A. KOLMER

GENUS STAPHYLOCOCCUS: Isolation and Identification

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

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

obtained from the infected and treated tissues, Fleming's2 technic of hemolytic streptococcus B. Immediately following the infection, 1.0 ml.

ON THE DEVELOPMENT OF STRAINS OF BACTERIA RESIS-

THE ISOLATION AND IDENTIFICATION OF BETA- HEMOLYTIC STREPTOCOCCI

Pet Microbe 1: Lab Guide

Group A Streptococcal L Forms

Escherichia-Aerobacter group, have been studied recently at the SPECIES OF ESCHERICHIA-AEROBACTER ORGANISMS

Discussion. Objectives:

MICROBIOLOGICAL TOOLS FOR QUALITY ASSURANCE IN HATCHERY: Laboratory Methods

Diagnostic Microbiology

Activity 5.1.4: Gram Staining

Effect of Storage of Mueller-Hinton Agar Plates on

Chapter 6: Microbial Growth

Thioglycolate Medium for Differentiating

WeldingAL-6XN. General Welding Recommendations

PURE CULTURE TECHNIQUES

LECTURE: 26 SIMPLE SEROLOGICAL LABORATORY TECHNIQUES LEARNING OBJECTIVES:

CONTROL OF MICROBIAL GROWTH - DISINFECTANTS AND ANTISEPTICS

Microbial Biotechnology agustin krisna wardani

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

Urine Monovette with Boric Acid

THE INTERNATION RESEARCH GROUP ON WOOD PRESERVATION. Vina W. Yang and Barbara L. Illman

BACTERIAL FLORA OF THE NORMAL AND INFECTED SKIN: A EVALUATION OF VARIOUS METHODS OF PERFORMING SKIN CULTURES*

Isolation & Characterization of Bacteria

Project 7: Wound Cultures and Identification

Isolation of Lac+ Mutants from a Lac- Strain of Escherichia coli, by the Replica Plating Technique

INTRODUCTION water-soluble Figure 1.

SIDEWALL CORE DESCRIPTIONS

INDIAN SCHOOL MUSCAT SENIOR SECTION DEPARTMENT OF CHEMISTRY CLASS X- PRACTICAL WORKSHEET

ercenta by Dr. Kim D. Coder, Professor of Tree Biology & Health Care Warnell School of Forestry & Natural Resources, University of Georgia

Methods of Culturing Microorganisms. Chapter 3. Five Basic Techniques of Culturing Bacteria. Topics

LactobaciUus acidophilus. The bacteria were cultivated at 30'C. juice was added). After twenty-four to thirty-six hours, the

Ti-a-dianges from the first to the second and from the second. ina which there is little or no multiplication, or the multiplication

CLIA Complexity: MODERATE

Evaluation of Microbial Contamination of Cutting Fluids with Nano Graphite Inclusions

BD CHROMagar Orientation Medium / Columbia CNA Agar (Biplate)

(From the Laboratories of The Rockefeller Institute for Medic~al Research, Princeton, New Jersey)

LAB. Interpretation Guide. Lactic Acid Bacteria Count Plate

Microbiological Quality: Understanding Drinking Water Quality and Management

Exercise 19. Fungi: Molds and Yeasts F10 Or The Rotten World Around Us

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

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

Cell Biology Homework

OXIDATION/FERMENTATION OF GLUCOSE TEST

Microbial Growth. PowerPoint Lecture Presentations prepared by Bradley W. Christian, McLennan Community College C H A P T E R

Bacterial Isolation, Identification, and Storage. Lila Ruangpan

TRYPTIC SOY AGAR (TSA) WITH LECITHIN AND TWEEN 80

ADVANCED ELECTROPHORESIS

(Sackett) Bergey et al. var. phaseolicola Burkholder. A convoluted

Stay or Go: A Study on Oxygen Tension on the Biofilm Formation of Cystic Fibrosis Bacteria. Honors Project. In fulfillment of the Requirements for

ON THE FORMATION OF SPECIFIC ANTI-BODIES IN THE BLOOD, FOLLOWING UPON TREATMENT WITH THE SERA OF DIFFERENT ANIMALS.

Creating a Culture of Data Integrity Using an Automated Detection and Enumeration Method

Protocol Reference: Verification Protocol

number Done by Corrected by Doctor

Table of Contents. A Culture of Service

Streptococci: the Bile-Esculin Test

Transmission Electron Microscopic Study of Antibiotic Action on Klebsiella pneumoniae Biofilm

Partner: Cathy 22 March Separation and Qualitative Determination of Cations and Anions

EZ-CFU Microorganisms

BACTERIA SENSITIVE TO NUTRIENT BROTH MEDIUM IN TERRESTRIAL ENVIRONMENTS

Worms and their environment

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

SOP: API 20E Microbial Identification

Lab Notes for Exam 3 Section

2.4 TYPES OF MICROBIAL CULTURE

EVALUATION OF SALMONELLA TEST METHOD OF SRI LANKA STANDARDS INSTITUTION

PREPARATION OF HISTOLOGICAL SPECIMENS

Electron Microscopy of Proteus vulgaris Exposed to

Antimicrobial susceptibility testing. EUCAST disk diffusion method

IQCP for Commercially Prepared CLSI-Exempt Media

AEROBIC AND ANAEROBIC BACTERIAL COUNTS OF NASAL WASHINGS:

BD Mueller Hinton Chocolate Agar

PHYTOSANITARY PROCEDURES

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

BBL CHROMagar Orientation and BBL Trypticase Soy Agar with 5% Sheep Blood (TSA II) I Plate Rev. 01 October 2008

VIII HEATING PATES FOR LOGS, PUTS, AND FLITCHES TO IBE CUT INTO VENEER. June No UNITED SLATES DEPARTMENT OF AGRICULTURE FOREST SERVICE

Automated methods in the Microbiology Lab-Issues and Troubleshooting! Presented By: Dr B. Oboudi

Microbial Growth. Phases of Growth. Pariporina: Bakteerien kasvukäyrä kuvaajana - Piirrä bakteerien klassinen kasvukäyrä - Nimeä kasvun eri vaiheet

26 January Fungus resistance.

Automation Supporting Single Cell Cloning Experiments and QbD-Based Bioprocess Development

lactic Acid Production by Streptococcus thermo phi/us and Lactobacillus bulgaricus in Milk Precultured with Psychrotrophic Bacteria

<51> Uji Batas Mikroba Farmakope Indonesia ed.4 (<61>Microbial Limit Test) and Identification method. Marlia Singgih Wibowo School of Pharmacy ITB

Cell Culture Flasks DATA SHEET

Experiment A: Solidification and Casting

Analysis of Corynebacterium vaginale by an Immunodiffusion

its present name, Clostridium Welchii. Many investigators have studied this organism and have

PROCEDURE MANUAL. Prepared By Date Adopted Supersedes Procedure # Review Date Revision Date Signature

LESSON ASSIGNMENT. After completing this lesson, you should be able to: Identify principles for maintaining a "working" stock culture.

Transcription:

A NEW- OR DELTA-TYPE STREPTOCOCCUS CARRIE KIRK BRYANT Prom the Department of Microbiology and Bacteriopathology oj the Thomas W. Evans Museum and Dental Institute School of Dentistry, University of Pennsylvania, Philadelphia Received for publication June 27, 1924 INTRODUCTION In making some routine studies of streptococci isolated from root canals of pulpless teeth at the Evans Institute, I have found a type which can not be classified as any one of the four outlined by Brown (1919). The following description taken from Brown's work, will give the general characteristics of these four types. Type a... at the end of approximately 48 hours incubation... To the eye the deep colonies appeared as small biconvex greenish colonies.... surrounded by zones in which the blood corpuscles were distinctly greenish in color. Under the low power of the microscope.... the greenish zone was less apparent, but in the outer portion of the zone there was possibly a slight hemolysis After refrigeration for forty-eight hours.... Examined under the low power of the microscope the deep colonies were seen to be surrounded by what may be called "double zones".... composed of a distinct inner collection of... greenish nonhemolyzed corpuscles next to the colony and an outer more or less hemolyzed ring.... Apparently the greenish discoloration of the corpuscles was accompanied by a fixation against hemolysis for (1) it preceded hemolysis, (2) the hemolytic substance must have passed out from the colony through the collection of corpuscles, and (3) it must have been present in greater concentration among these corpuscles next to the colony than farther out where hemolysis did occur.. As it has been noted that the zone of greenish corpuscles was formed during incubation and that hemolysis took place during refrigeration, 53

54 CARRIE KIRK BRYANT the blood agar plate was replaced into the incubator for another period of forty-eight hours. There appeared outside the hemolyzed zone another ring of greenish corpuscles.... Still another exposure to the temperature of the refrigerator resulted in the formation of a second ring of partial hemolysis.... Apparently the alternate throwing off of rings of fixed corpuscles and of hemolysis in response to alternate incubation and refrigeration is limited only by the exhaustion of the medium and the accumulation of metabolic products which inhibit further growth and activity. Type j3. This type of appearance in blood agar may be described as a colony surrounded by a perfectly clear, colorless zone of hemolysis. *... There is no trace of discoloration and when viewed microscopically no corpuscles are seen in the medium surrounding the colony. The colony itself is grayish by transmitted or reflected light.... after refrigeration for forty-eight hours they showed no change.... nor did they change during a second period of incubation and refrigeration. The difference in behavior of the two types in respect to refrigeration is so great as to suggest different hemolytic substances or processes. Type a'.... It can scarcely be called anything but a hemolytic streptococcus for there are distinct hemolyzed zones and no apparent discoloration... colonies of the alpha prime type appear somewhat hazy or poorly defined within the hemolyzed zones. Under the microscope... the reason for this haziness is apparent; a few corpuscles are seen to remain throughout the zone but are most numerous next to the colony. After forty-eight hours incubation the plate.... was refrigerated for forty-eight hours. The zones were noticeably enlarged.... Placed into the incubator for another period of forty-eight hours the zones became still larger and rather diffuse but no multiple zones of concentric rings were formed. Type y. By the gamma type is meant the growth of the streptococcus colonies within and on the blood agar plate without the production of any perceptible hemolysis or discoloration of the surrounding medium during incubation or refrigeration. ORIGINAL OBSERVATIONS Grown in 5 per cent blood agar plates, using defibrinated horse blood, the surface colonies of the type under consideration produce no visible change in the surrounding medium. The deep

NEW- OR DELTA-TYPE STREPTOCOCCUS colonies after forty-eight hours incubation appear macroscopically, irregularly shaped, olive green in color and about 0.75 mm. in diameter. Each is surrounded by a pale green zone slightly narrower than the diameter of the colony. The illdefined outer margin of this green zone is not surrounded by a clear colorless zone, but merges directly into the unchanged blood agar beyond. This appearance is unchanged by forty-eight FIG. 1. PLATE COLONIES OF ORGANism GROWN IN 5 PER' CENT BLOOD AGAR,) DRAWN AFTER FORTY-EIGHT HOURS INCUBATION AND FORTY-EiG;HT HOURS IN ICE Box SUBSEQUENTLY There were approximately 175 colonies on the plate. Naked eye study seen by transmitted light andx ea. 8 diam. hours subsequent subjection to refrigeration (fig. 1). Under the, low power of the microscope in the zone immediately surrounding the colony the blood cells are seen to have lost all their pink color and to appear as minute pale grey-brown dots or when seen! in clumps, as slightly darker grey-brown masses. There is no apparent decrease in their number, and they lie on an absolutely clear colorless back ground. The outer margin of this zone is very ill-defined and merges gradually into the unchanged medium where the agar is tinted a distinct pink from the laked hemoglobin 55

~~~~~~* ';';;.....h...'*. 60~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~1 56 CARRIE KIRK BRYANT and the blood cells have retained their normal tone-the clumps especially being seen as definitely red masses (fig. 2). The colonies resemble Brown's alpha type in that they are immediately surrounded by a zone, greenish to the naked eye, in which the blood cells still persist but without their normal color. But they differ from the alpha type in that refrigeration fails to produce an outer zone of hemolysis. They differ FIG. 2. COLONY TAKEN FRom FIo.1AS SEEN THROUGH Low POWER OF THE MICROSCOPE, SHOWING COLONY &ND ZOE IMMEDIATELY SURROUNDING- IT, WITH SINGLE AND SMALL CLUMPS OF ERYTHROCYTES, GREY-BROWN IN COLOR, IN A CLEAR COLO'RLEss BACKGROUND Beyond this and merging into it are to be seen the erythrocytes as they appear throughout the rest of the plate, single ones as brownish or red-brown, and clumps always red, lying in a pale pink backgro.und. X ca. 30 actual size of colony. from, both the alpha prime and the beta types in that there 'is no decrease in the number of blood cells in the zone surrounding the colony. That the action of these delta-type streptococci on blood -agar is characteristic, and is not due to some environmental peculiarity, is proven by the fact that they have been found present in plates showing typical colonies of the alph'a type in mixed cub-

.. NEW- OR DELTA-TYPE STREPTOCOCCUS 57 0~~~~~ 9- S.op404 eq 9 +~~~~~ z z 0~~~~~~" PoX - - 4i~~~~~4 CO~~~~~~~~~< 0~~~~~ co~~~~~~~~~c -~ ~ Iq4qC) cq~ c @5 _s~ 0 0' 4.. Q Q.. -.. 0)94 *... *)....4*...4...^* - @ @405 Ps... O..... i 0 0) 4~ 0 0 4aQ9. 0 O~~~~~~~~~~~~~'-

58 CARRIE KRKI BRYANT ture. When isolated and replated in pure culture they have retained their characteristic action in blood agar plates through repeated generations. The morphological study was made from the water of condensation of an agar slant which had been incubated for twentyfour hours after inoculation with a typical deep colony picked from a blood plate. The surface growth on agar was frail, effused and filmy. The organism appeared as a Gram-positive micrococcus about 0.75 micron in diameter, in short chains varying from four to about fifteen elements and in irregular clumps. By reference to chart 1 it will be seen that of the four strains isolated, all acidified and coagulated milk, all were bile insoluble, and none fermented inulin, raffinose, or sucrose. They varied in their proteolytic action on milk and gelatin. We seem then, in these organisms, to be dealing with true streptococci which are of a type until now undescribed as to their behavior in blood agar plates. REFERENCE BRowN, JAmms HowARD 1919 The use of blood agar for the study of streptococci. Monographs of The Rockefeller Institute for Medical Research, January 21, No. 9.