Difference between revisions of "Category:Bacteria - Overview"

From WikiVet English
Jump to navigation Jump to search
Line 11: Line 11:
  
  
==Bacterial Genetics==
+
==[[Bacterial Genetics]]==
===Replication of Bacteria===
 
Bacteria  are haploid and have one circular chromosome of double stranded DNA.  Bacteria replicate through binary fission producing genetically  identical daughter cells. Each molecule of DNA in the daughter cells is  composed of a strand from the parent and a newly synthesised  complementary strand. This process of DNA replication is called  semiconservative replication.<br />
 
===Plasmids===
 
Plasmids  are small pieces of genetic material found in the cytoplasm and these  plasmids are able to replicate independantly of the bacterial  chromosome. Most species of bacteria contain plasmids that are composed  of double stranded DNA which are circular in shape. In pathogenic  bacteria it is often the plasmid that encodes virulence factors and  traits such as antibiotic resistance. <br />
 
Replication of  most plasmids is not directly related to the replication of the host  bacterium and it has been found that the distribution of plasmids to  daughter cells is a random process as plasmids in the cytoplasm may or  may not be transferred when the cytoplasm of the cell is seperated prior  to forming the daughter cells. <br />
 
Bacterial plasmids  can not only be transferred during bacterial replication but also via  processes called conjugation and transformation (although the  transformation process rarely occurs in nature).
 
===Bacteriophages===
 
A  bacteriophage is a term used to describe a virus that is able to infect  a bacterial cell and they can be either virulent or temperate depending  on their method of replication. Virulent bacteriophages undergo a lytic  cycle within the bacterium which eventually results in the production  of bacteriophage progeny from the cell and the lysis of the bacterium.  <br />
 
A bacteriophage can be composed of either DNA or RNA  and iehter single or double stranded. The capsid (outer protective  layer) of the bacteriophage often remains outside the bacterial cell  after the viral nucleic material has entered the cell cytoplasm. The  host specificity of bacteriophages is related to the chemical affinity  between attachment structures on the surface of the bacteriophage capsid  and the receptors on the surface of the bacterium. <br />
 
===Genetic Variation===
 
Genetic  variation can occur in a number of ways and the genotype of the  bacteria determines its inheritable potential. Below are the main ways  that genetic mutation can occur in bacteria;
 
<br />
 
<br />
 
'''Mutation'''
 
<br />
 
A  mutation is a stable inheritable alteration in the bacterial genome.  This means that base pairs within a gene are altered. Genes with altered  base pairs may, or may not, depending on the mutation be functional or  can incorrectly code for an amino acid in a protein resulting in a  phenotypic change rather than simply a gene alteration. The type of  mutations occurring in bacteria are silent, non-sense, mis-sense, frame  shift, deletion of base pairs, insertions, translocations and  inversions.
 
<br />
 
<br />
 
'''Genetic Recombination'''
 
<br />
 
Genetic  recombination occurs when sequences of DNA from seperate sources become  integrated. This new genetic material can be introduced via  conjugation, transduction and transformation.
 
<br />
 
<br />
 
''Conjugation''
 
<br />
 
Conjugation  represents the process whereby DNA is transferred from a donor cell to a  recipient cell. The donor cell synthesises a modified "pilus" which the  donor cell inserts into the recipient cell. This is often called a sex  pilus. Genetic material is then transferred through the pilus to the  recipient. During conjugation, plasmid genetic material is mostly  transferred, although chromosomal DNA can also be transferred via this  process. Conjugation is most frequently associated with gram negative  bacteria, but can occur in some gram positive bacteria. A sex pilus is  not formed in gram positive bacteria and instead plasmid DNA is  transferred when the bacteria are in close physical contact.
 
<br />
 
<br />
 
''Tranduction''
 
<br />
 
During  transduction, DNA from a donor bacterium is incorporated into the  nucleic acid of a bacteriophage and it is the progeny of the  bacteriophage infecting another bacterium that allows the transfer of  the genetic material.
 
<br />
 
<br />
 
''Transformation''
 
<br />
 
The  process of transformation involves the transfer of genes from a segment  of chromosomal DNA from a lysed donor bacterium to a fully functional  recipient. Natural transformation is uncommon and is usually restricted  to propcedures carried out in the lab.
 
<br />
 
  
[[Category:Bacteria - Overview]]
 
  
  

Revision as of 10:27, 5 August 2010

Introduction

A typical bacterial cell is composed of an outer capsule, a cell wall, a cell membrane, cytoplasm containing nuclear material and ifmotile, appendages such as flagella and fimbrae or pili. Some species of bacteria are more resistant to environmental influences than others, particularly those species of bacteria that are able to produce spores which can remain inactive until the appropriate environmental conditions prevail allowing the bacteria to resist conditions such as freezing, wet, dry or hot conditions.
The structural features of pathogenic bacteria are important in the production of disease and also very useful for the identification and diagnosis of infection in veterinary medicine.
Bacterial Cell Structure


Bacterial Growth and Measurement

Bacterial Genetics

Laboratory Diagnosis of Bacterial Disease

Laboratory techniques are often required for identifying the aetiological agent and/or the antimicrobial susceptibility of pathogens. It should be noted that any laboratory analysis should be accompanied by a full clinical examination and history.

Identification of Pathogenic Bacteria

Pathogenic bacteria can be identified by the examination of stained smears, cultural and biochemical characteristics and detection by immunological and molecular methods.

Stained Smears

There are a number of different routine methods used to stain bacteria for examination on a microscope slide. Gram stain smears are rapid and able to detect bacteria in large numbers and is often used for a 'rough and ready' analysis of tissue samples. Below is a table showing most of the main stains;


Staining Method Comments
Gram Stain Most common in bacterial smears. The stain contains crystal violet which is retained in the cell wall of the bacterium. Gram positive bacteria are blue and gram negative bacteria do not retain the crystal violet and appear red, the colour of the counterstain.
Giemsa Used to identify Dermatophilus congolensis, rickettsiae and Borrelia species which stain blue.
Dilute carbol fuchsin Used for identifying Campylobacter species, Brachyspira species and Fusobacterium species which stain red.
Polychrome methylene blue Used to identify Bacillus anthracis in blood smears which stain blue with distinctive pink capsules
Ziehl-Neelsen stain Red staining bacteria are described as acid-fast or Ziehl-Neelsen positive
Quinn et al., P.J.. (2002) Veterinary Microbiology and Microbial Disease. Oxford: Blackwell Science Limited. pp.Bacterial Counting Techniques, P23.


Bacterial Culture

As noted above, the selection of the culture medium, atmospheric conditions and pH are among many variables that need to be considered for the successful culture of bacteria in the lab. A routine culture undertaken involves using a combination of blood agar (see below) and MacConkey agar (see below) together with incubation for between 24-48hours. Blood agar is able top support most pathogenic species of bacteria and is usually appropriate for routine primary isolation. Selective media is then normally used for particular organisms.

Agar plates should be inoculated using a streaking technique facilitating growth of isolated colonies. The aseptic technique of inoculation should also be used to prevent contamination.

Below is a table detailing the main types of medium used in bacterial culture;

Medium Comments
Nutrient Agar Most commonly used basic medium. Non-fastidious bacteria (unable to produce their own vitamins) can grow on this medium. This medium is also suitable for demonstrating colonial morphology and pigment production. This type of agar is also commonly used as part of bacterial counting techniques as described above.
Blood Agar This medium contains blood and is able to support the growth of pathogenic bacteria. This medium also allows the recognition of bacterial haemolysin production
MacConkey Agar A selective medium containing bile which is useful for the isolation of enterobacteria and other gram negative bacteria. This medium also allows differentiation of lactose and non-lactose fermenting species. Colonies of lactose fermenters turn the surrounding medium pink as the medium also has a pH indicator.
Selenite broth, Rappaport-Vassiliadis Broth Selective enriched medium used to isolate salmonellae from samples containing other gram negative enteric organisms
Edwards Medium A blood agar based selective medium used for the isolation and recognition of steptococci
Chocolate Agar Heat-treated chocolate agar which provides special growth factors for the isolation of Haemophilus species and for the culture of Taylorella equigenitalis.
Brilliant green agar Indicator medium for the presumptive identification of Salmonella species. Salmonella colonies and surrounding medium have a pink appearence.
Buffered peptone water Non-selective medium used for isolation of pathogens when present in low numbers in samples collected from foods and environmental sources
Quinn et al., P.J.. (2002) Veterinary Microbiology and Microbial Disease. Oxford: Blackwell Science Limited. pp.Bacterial Counting Techniques, P24.


Biochemical techniques

Biochemical tests relate to the catabolic activities of bacteria and use this to demonstrate the utilisation of particular substrates. The range of sugars utilised by bacteria is relatively small and therefore catabolism of sugars is often used as a method of identification. Commercial testing kits are available which usually consist of a strip of plastic cupules containing a test to which a suspension of the bacterium is added. The identity of the bacteria is then deduced from the pattern of the various cupules.

Below is a table of the commonly used biochemical tests;

Test Pathogens Comments
CAMP Reaction Steptococcus agalactiae, Rhodococcus equi, Actinobacillus pleuropneumoniae, Listeria monocytogenes Haemolysis caused by Staphylococcus aureus is enhanced by pathogenic bacteria growing close to staphylococcal colonies
Pitting of Loeffler's serum slope Arcanobacterium pyogenes Proteolytic digestion of the medium around colonies
Haem-agglutination Bordetella bronchiseptica Agglutination of suspended ovine red blood cells by the bacteria
Nagler Test Clostridium perfringens Breakdown of lecithin in egg yolk agar by alpha toxin (lecithinase) produced by the organism. Surface application of antitoxin inhibits the alpha toxin activity
Quinn et al., P.J.. (2002) Veterinary Microbiology and Microbial Disease. Oxford: Blackwell Science Limited. pp.Bacterial Counting Techniques, P25.



Immunological Techniques

Immunological identification or serotyping uses the surface antigens on bacteria. Fluorescent antibody staining, antigen capture and direct enzyme-linked immunosorbent assays (ELISA) have been developed to identify bacterial pathogens. In all of these techniques the bacteria is bound by a specific antibody which has some form of indicator attached such as colour change enzymes or fluorescence.

Bacteriophage Typing

Some bacteriophages are very species specific and therefore phage typing represents another method that can be used to identify species of bacteria. This method allows bacterial species to be sub-divided into subtypes which are defined by their susceptibility to particular phages. Phage typing is commonly used to differentiate between Staphylococcus aureus and Salmonella enterica sub species.

Molecular Techniques

The most common molecular technique used to identify species of pathogenic bacteria are nucleic acid hybridisation and polymerase chain reactions (PCR). Nucleic acid hybridisation uses synthetic nucleic acid probes (specific for a particular species) that are applied to genetic material extracted from the pathogen. Probes can be used to detect DNA and RNA.

This category currently contains no pages or media.