Monday, February 24, 2014

mcb2010L Chapter 15 - 17 (due feb. 27th)

 Chapter 15 page 121, page 122, 123, 124  
Yoslaine Albelo
Pg. 121
Generation Time
Direct Method: Requires enumeration of Viable cells in serially diluted samples of the test culture taken at 30 Min intervals.
Direct Method: Monitors bacterial growth by estimating Turbidity. This measurements is done by using a spectrophotometer where a beam of light is transmitted through a bacterial suspension to a light sensitive detector. This change of light would be the percentage of transmission and will also give you the logarithmic expression called absorbance. This method is more useful in measuring contamination of liquids by large numbers, rather than small numbers, of bacteria. This is done at a 30 min intervals as well.

Pg. 122
Review Questions
1. Does the term growth convey the same meaning when applied to bacteria and to multicellular organism?
 - No, Growth when referring to bacteria, it means an increase in the number of individual organism or and increase in the size of a population.  When referring to the growth in multicellular organism, its referring to an increase in the number of cells in a single individual organism.
2. Why do Variations in generation time exist?
 A) Among different species of microorganisms?
       - Because in any given environment, the optimal conditions will vary between species. A fast growing bacteria have generation times of 15-20 min under optimum growth conditions, in the other hand slow growing bacteria can take up to 24 hrs under  optimum condition.
 B) Within a single microbial species?
       - Because generation time depends on several factors, temperature, PH, etc. Growth medium can influence growth within a single microbial species.
3. The generation time and growth rate of an organism grown in the laboratory can be each determined by constructing a typical growth curve.
   A) Would you expect the growth rate of the infectious organisms found in an abscess that developed from a wound to mimic the growth curve obtain in the laboratory? Explain.
       No. Lab conditions usually have plentiful nutrients and ideal growth temperature. In an abscess from a wound, the fact that the bacteria has our immune system fighting them, and that they have to search for nutrients, would definitely slow down their rate of growth.
  B) Would you expect antibiotic therapy to be effective without any other concurrent treatment of the abscess?
       - In most cases no. Antibiotic are often unable to get into the abscess due to the abscess wall formed by adjacent uninfected cells around the abscess to prevent the spread of infection. Usually incision and/or drainage is required.
  C) Is generation time a useful parameter to indicate the types of media best suited to support the growth of a specific organism? Explain.
        - Yes. Organisms with a faster generation time can often grow quickly due to their non-specific requirements for growth and will be able to grow in a variety of different media. Slow growing organisms often have very specific nutritional requirements and will need a more complex media. This can be determined by using generation time measurements. 

page 123, 124 (Indy Graph)



  Chapter 16  page  139

Page 140 (Lupe)

Page 140

Chemotherapeutic Agent
Spectrum of Activity
Type(s) of Microorganisms
Penicillin
Narrow Spectrum
Gram Negative
Streptomycin
Broad Spectrum
Gram Negative and Gram Positive Bacteria
Tetracycline
Broad Spectrum
Gram Negative and Gram Positive
Chloramphenicol
Broad Spectrum
Gram Negative and Gram Positive
Gentamicin
Broad Spectrum
Gram Negative and Gram Positive
Vancomycin
Narrow Spectrum
Gram Positive
Sulfanilamide
Broad Spectrum
Gram Negative and Gram Positive


Review Questions


1.       Antibiotic specially function to destroy the peptide cross-bridge of peptidoglycan (the cell wall of bacteria). Since fungi cell wall compose of chitin, antibiotic won't affect fungi.



Chapter 17  page 147 (Done), 148
Janelly Carrasco, page 148


4. Which of the experimental chemical compounds appear to have the broadest range of microbicidal activity? The narrowest range of microbicidal activity?
The chemical compounds that appear to have the broadest range of microbicidal activity is bleach and hydrogen peroxide. The narrowest range was LT.

Review Questions

1. Evaluate the effectiveness of a disinfectant with a phenol coefficient of 40.
It would be 40x more effective than phenol.

2. Can the disinfection period (exposure time) be arbitrarily increased? Explain.
No, not without considering the toxicity of the chemical and environmental conditions that have to be considered before altering exposure time.

3. A household cleaner is labeled germicidal. Explain what this means to you.
This means that the antimicrobial agent is microbial. However, it does not indicate the type or types of microbes that the agent will kill effectively.

Thursday, February 6, 2014

chapter 11-13 lab

Chapter 11 - 
 page 95
Purpose : 
The purpose  of acid-fast staining  is to identify acid-fast organisms that belongs to genus mycobacterium.

pg 96 (Yoli)
Questions
1. What are the large stained areas on the sputum slide?
 - Mainly white blood cells and non acid-fast organisms
2. What is the decolorizing agent in the gram stain?-Ethanol2b. In the acid-fast stain?
- Acid alcohol
3. What diseases are diagnosed using the acid-fast stain?
-Tuberculosis (caused by Mycobacterium tuberculosis), Leprosy, Nacordiosis.
4. What is phenol (carbolic acid), and what is its usual application?
-Phenol is an alcohol with a benzene ring attached.  It s an aromatic compound and it is used as a disinfectant because it controls the growth microorganisms.

 Critical Thinking!
1. Assuming you could stain any cell, would an acid-fast organism be gram-positive or gram-negative? Explain.
-It would be gram positive (a weak or abnormal gram positive) because acid-fast organism have a wax-like lipid called mycolic acid that makes them impermeable to most stains, it won't pick up the blue/purple color correctly but the color that it does pick up it won't be decolorized at all by the decolorizing agent so it would give a weak positive gram result.
2. How do the acid-fast properties relate to the gram stain?
-Acid-fast organism retain the primary stain even after the decolorizing agent, Gram-positive also retains the primary stain after the decolorizing agent and Gram-negative would lose the primary stain when washed with the ethanol. Acid-fast staining is used to differentiate between different types of bacteria, which is the same use of the gram stain.
3.Clinical specimens suspected of containing Mycobacterium are digested with sodium hydroxide (NaOH) for 30 minutes prior to staining. Why is this technique used? Why isn't this technique used for staining other bacteria?
-Its used to remove debris and contaminating bacterias. This technique cannot be used for staining other bacterias because they would be killed in the process, acid-fast bacteria have a really strong and impermeable wall and it won't be killed with the sodium hydroxide.


Chapter 12 - page 102, 103 Janelly
PAGE 102 & 103

1. Why is heat necessary in spore staining?
Heat is necessary in spore staining because it is important that heat penetrates the endospore wall. Therefore, the imperiate coat that spores contain around them can loosen up the cortex and allow it to accept the stain.

2. Explain the function of water in spore staining.
The function of water in spore staining is to decolorize the vegative components. It also washes off the excess primary stain, but not the spore.

3. A.) Tap water is normally used as the decolorizing agent to wash off excess stain. When using acid-alcohol, it decolorizes the cells and results in removing the stain.

B.) When you use safranin as the primary stain and malachite green as the secondary stain, the cells will stain green.

C.) When heat is not applied during the primary stain, the spores are not stained and t hey appear colorless.

4. Explain the medical significance of a capsule.
Capsules essentially “hide” the bacteria. Encapsulated bacterial cells generally have greater pathogenicity because capsules protect the bacteria against phagocytes, so that the WBC's can't attack it. It is also used for biofilms, which can form on non-living materials in catheters, IUD's and pacemakers.

5. Explain the function of copper sulfate in this procedure.
The function of copper sulfate in this procedure is that it is used as a decolorizing agent that washes away the purple primary stain out of the capsule.
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Chapter 113 - page 107 Lupe
2. The microscopic appearance of S. aureus is a dark purple color hue and it's shape and appearance is considered coccobacillus (a cluster of irregular cells). The appearance of E. coli is of white color hue and it is single bacillus (irregular single cells). The last one, B. cereus is of dark purple color hue and its arrangement is single bacillus.

1. No methylene blue cannot be used in place of nigrosin for negative staining. Methylene blue is is a basic stain that is positively charged. Negative staining requires an acidic stain that is negatively charged.

2. The advantages of negative staining are that it does not require heat fixing, cell is highlighted which makes it easier to see, and it is simple and quick.

3. The bacteria remains unstained, because with negative staining, the staining will occur around the organism.