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PRESENTATION
TITLE
Mirjam Nilsson​
AGENDA
Introduction​
Primary goals
​Areas of growth
Timeline
​Summary​
INTRODUCTION
Bacterial isolation, purification and identification are the first steps to
bacteriological studies. Isolation is done to obtain pure bacterial cultures.
Bacteria are
usually isolated from fish kidney and spleen; and from the hepatopancreas,
lymphoid
organ and muscles of shrimp. These tissues are monitor organs that usually
harbor
the disease-causing bacteria during infection.
To obtain a pure bacterial culture is the first step to bacterial identification.
Pure culture is essential in the study of the morphology, physiology,
biochemical
characteristics, and susceptibility to antimicrobial agents of a particular
bacterial
strain.
Presentation title 3
Pure cultures are best obtained by using solid
media, by streak plate or pour plate
method. Streak plate, if properly done, is the
most practical method. In the streak
plate method, a loopful of the inoculum is
placed near the periphery of the plate with
agar medium and spread or streaked on the
upper portion of the plate with parallel
overlapping strokes. The inoculum is streaked
over other portions of the plate so that
isolated colonies could be observed in the last
streaked area.
5
THE IDENTIFICATION OF A BACTERIAL PATHOGEN IS
IMPORTANT IN FISH DIAGNOSIS. TREATMENT
COULD BE IMPLEMENTED ONLY AFTER THE CAUSATIVE
AGENT OR THE BACTERIUM HAS BEEN
IDENTIFIED. BACTERIAL SPECIES DIFFER IN
MORPHOLOGICAL, PHYSIOLOGICAL AND BIOCHEMICAL
CHARACTERISTICS AND THOSE CAN BE USED WHEN
CODING OR LABELLING THEM (APPENDIX
1.1). THEREFORE, IDENTIFICATION IS ACCOMPLISHED
BY PERFORMING SEVERAL MORPHOLOGICAL,
PHYSIOLOGICAL AND BIOCHEMICAL TESTS. RESULTS
OF THESE TESTS ARE COMPARED TO ESTABLISHED
TAXA OR IDENTIFICATION SCHEMES
6
• Bacterial cultures should be preserved
for future study. Storing in appropriate
• medium preserves bacterial cultures.
The simplest method is by sub-
culturing or by
• transferring the organism to fresh solid
medium that has a minimal nutrient
content
• to prevent bacterial overgrowth. The
bacteria are allowed to grow before
storing in
• the refrigerator or are covered with
paraffin oil and stored at room
temperature in the
• dark. Another simple method is by deep-freezing of
the bacterial culture, stocked in a
• broth medium with glycerol. Glycerol is added to
prevent the dessication of bacterial
• cells. Bacterial cultures may also be preserved by
freeze-drying or lyophilization. In
• this method, water is removed from the frozen
bacterial suspension by sublimation
• under vacuum.
• Bacterial cultures should be properly labeled or
coded before storage. It is
• important to label the tube or vial for storing bacterial
cultures with an indelible
• ink. The label or code should include the reference
number and other pertinent
• information such as source of sample (host animal,
location), date of isolation,
• special properties, identification, name of the person
who isolated the organism and
• the date of preparation of the stock culture.
THANK YOU

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Isolation of bacteria.pptx

  • 2. AGENDA Introduction​ Primary goals ​Areas of growth Timeline ​Summary​
  • 3. INTRODUCTION Bacterial isolation, purification and identification are the first steps to bacteriological studies. Isolation is done to obtain pure bacterial cultures. Bacteria are usually isolated from fish kidney and spleen; and from the hepatopancreas, lymphoid organ and muscles of shrimp. These tissues are monitor organs that usually harbor the disease-causing bacteria during infection. To obtain a pure bacterial culture is the first step to bacterial identification. Pure culture is essential in the study of the morphology, physiology, biochemical characteristics, and susceptibility to antimicrobial agents of a particular bacterial strain. Presentation title 3
  • 4. Pure cultures are best obtained by using solid media, by streak plate or pour plate method. Streak plate, if properly done, is the most practical method. In the streak plate method, a loopful of the inoculum is placed near the periphery of the plate with agar medium and spread or streaked on the upper portion of the plate with parallel overlapping strokes. The inoculum is streaked over other portions of the plate so that isolated colonies could be observed in the last streaked area.
  • 5. 5 THE IDENTIFICATION OF A BACTERIAL PATHOGEN IS IMPORTANT IN FISH DIAGNOSIS. TREATMENT COULD BE IMPLEMENTED ONLY AFTER THE CAUSATIVE AGENT OR THE BACTERIUM HAS BEEN IDENTIFIED. BACTERIAL SPECIES DIFFER IN MORPHOLOGICAL, PHYSIOLOGICAL AND BIOCHEMICAL CHARACTERISTICS AND THOSE CAN BE USED WHEN CODING OR LABELLING THEM (APPENDIX 1.1). THEREFORE, IDENTIFICATION IS ACCOMPLISHED BY PERFORMING SEVERAL MORPHOLOGICAL, PHYSIOLOGICAL AND BIOCHEMICAL TESTS. RESULTS OF THESE TESTS ARE COMPARED TO ESTABLISHED TAXA OR IDENTIFICATION SCHEMES
  • 6. 6 • Bacterial cultures should be preserved for future study. Storing in appropriate • medium preserves bacterial cultures. The simplest method is by sub- culturing or by • transferring the organism to fresh solid medium that has a minimal nutrient content • to prevent bacterial overgrowth. The bacteria are allowed to grow before storing in • the refrigerator or are covered with paraffin oil and stored at room temperature in the • dark. Another simple method is by deep-freezing of the bacterial culture, stocked in a • broth medium with glycerol. Glycerol is added to prevent the dessication of bacterial • cells. Bacterial cultures may also be preserved by freeze-drying or lyophilization. In • this method, water is removed from the frozen bacterial suspension by sublimation • under vacuum. • Bacterial cultures should be properly labeled or coded before storage. It is • important to label the tube or vial for storing bacterial cultures with an indelible • ink. The label or code should include the reference number and other pertinent • information such as source of sample (host animal, location), date of isolation, • special properties, identification, name of the person who isolated the organism and • the date of preparation of the stock culture.