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Classification of Bacteria

This presentation provides information about the different methods of classification of bacteria.

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Classification of Bacteria

  1. 1. Classification of Bacteria Presented By:- Zeeshan Mazhar Md. Mahtab Rashid M.Sc Ag (Mycology & Plant Pathology) I.Ag.Sc , B.H.U.
  2. 2. Why do we need Bacterial Classification? • A reliable classification system is a prerequisite for scientists and professionals dealing with microorganisms in order to keep track of their tremendous variety. • The ultimate objective of biological classification is the characterization and orderly arrangement of organisms into groups. • Classification is often confused with identification but, as a matter of fact, classification is a prerequisite for identification. • Many bacteriologists think that Bergey's Manual represents the official classification but this is a misunderstanding. The editors of Bergey's Manual try to provide a classification that is as accurate and up-to-date as possible but it is not official, in contrast to bacterial nomenclature where each taxon has one valid name. The closest to an official classification system is the one that is widely accepted by the community
  3. 3. History of Classification of Bacteria & Archea • The history of the classification of bacteria clearly demonstrates that changes were caused by the availability of new techniques. • The late 19th century was the beginning of bacterial taxonomy and Ferdinand Cohn in 1872 was the first to classify six genera of bacteria (as members of the plants) mainly based on their morphology. • At the beginning of the 20th century more and more physiological and biochemical data were used, in addition to morphology, as important markers for the classification and identification of microorganisms. • The first edition of Bergey's Manual of Determinative Bacteriology classified the Bacteria in 1923 on the basis of these phenotypic properties as “typically unicellular plants”, the so- called Schizomycetes. Even in the 7th edition of Bergey's Manual, published in 1957, Bacteria were still classified as members of plants (Protophyta, primitive plants). Based on the partial sequences of 16S ribosomal RNA (rRNA) genes, Archaea (originally named Archaebacteria) were first classified as a separate kingdom in 1977. • In the 8th edition of Bergey's Manual, which was published in 1974, Bacteria were no longer considered as plants and were recognized as members of the kingdom Procaryotae.
  4. 4. Time span Classification mainly based on Late 19th century Morphology, Growth Requirements, Pathogenic potential 1900–1960 Morphology, Physiology, Biochemistry 1960–1980 Chemotaxonomy, Numerical Taxonomy, DNA–DNA Hybridization 1980–today Genotypic Analyses, Multi-locus Sequence Analyses, Average Nucleotide Identity, Whole Genome Analysis
  5. 5. Basis of Classification A. Phentoypic Classification i. Gram stain and bacterial morphology: Of all the different classification systems the Gram stain has withstood the test of time. Discovered by H.C. Gram in 1884 it remains an important and useful technique to this day. It allows a large proportion of clinically important bacteria to be classified as either Gram positive or negative based on their morphology and differential staining properties. Slides are sequentially stained with crystal violet, iodine, then destained with alcohol and counter-stained with safranin. Gram positive bacteria stain bluepurple and Gram negative bacteria stain red. The difference between the two groups is believed to be due to a much larger peptidoglycan (cell wall) in Gram positives. As a result the iodine and crystal violet precipitate in the thickened cell wall and are not eluted by alcohol in contrast with the Gram negatives where the crystal violet is readily eluted from the bacteria. As a result bacteria can be distinguished based on their morphology and staining properties. Some bacteria such as mycobacteria (the cause of tuberculosis) are not reliably stained due to the large lipid content of the peptidoglycan. Alternative staining techniques (Kinyoun or acid fast stain) are therefore used that take advantage of the resistance to destaining after lengthier initial staining. ii. Growth Requirements: Microorganisms can be grouped on the basis of their need for oxygen to grow. Facultatively anaerobic bacteria can grow in high oxygen or low oxygen content and are among the more versatile bacteria. In contrast, strictly anaerobic bacteria grow only in conditions where there is minimal or no oxygen present in the environment. Bacteria such as bacteroides found in the large bowel are examples of anaerobes. Strict aerobes only grow in the presence of significant quantities of oxygen. Pseudomonas aeruginosa, an opportunistic pathogen, is an example of a strict aerobe. Microaerophilic bacteria grow under conditions of reduced oxygen and sometimes also require increased levels of carbon dioxide. Neisseria species (e.g., the cause of gonorrhea) are examples of micraerophilic bacteria.
  6. 6. iii. Biochemical reactions: Clinical microbiology laboratories typically will identify a pathogen in a clinical sample, purify the microorganism by plating a single colony of the microorganism on a separate plate, and then perform a series of biochemical studies that will identify the bacterial species. iv. Serologic systems: Selected antisera can be used to classify different bacterial species. This may be based on either carbohydrate or protein antigens from the bacterial cell wall or the capsular polysaccharide. (Group A streptococcal M proteins or O and H polysaccharide antigens of salmonella). v. Environmental Reservoirs: When considering likely pathogens it is also important to know which of the different species are found in different locations. Environmental reservoirs are generally divided into those that are endogenous (i.e., on or within the human body) and exogenous (somewhere in the environment). When considering the likely cause of an infection the likely source of the infection is important in your differential diagnosis. For example an abscess that develops after large bowel surgery is likely caused by an anaerobic organism that is resident in the large bowel. A skin rash developing in a hiker with a history of multiple tick bites is more likely to be borrelia, the agent of Lyme disease. An outbreak of food poisoning traced to imported unpasteurized cheese might be due to listeria. Endogenous reservoirs account for a large proportion of human infections. Many parts of the body have their own normal flora. S. epidermidis is found on the skin. Viridans streptococci are a part of the normal oropharyngeal flora and S. aureus is a commensal of the anterior nares.
  7. 7. B. Genotypic Classification i. Ribosomal RNA (rRNA) sequence analysis: This has emerged as a major method for classification. It has been used (as described above) to establish a phylogenetic tree. In addition it is now also used to rapidly diagnose the pathogen responsible for an infection, to help select appropriate therapy and to identify noncultivatable microorganisms. ii. Universal Phylogenetic Tree: Woese has developed a “universal phylogenetic tree” for all living organisms that establishes a tripartite division of all living organisms– bacteria, archaea and eucarya. His work is based on a comparison of 16s ribosomal RNA sequences. These sequences are highly conserved and undergo change at a slow, gradual and consistent rate. They are therefore useful for making comparisons among the different living organisms. iii. DNA-DNA hybridization iv. G+C content
  8. 8. Morphological classification • Bacteria can be classified into six major groups on morphological basis. 1. TRUE BACTERIA • Cocci – These are spherical or oval cells. On the basis of arrangement of individual organisms they can be described as – Monococci (Cocci in singles) – Monococcus spp. – Diplococci (Cocci in pairs) – Streptococcus pneumoniae – Staphylococci (Cocci in grape-like clusters) – Staphylococcus aureus – Streptococci (Cocci in chains) – Streptococcus pyogenes – Tetrad (Cocci in group of four) - Micrococcus spp. – Sarcina (Cocci in group of eight)
  9. 9. • Bacilli – These are rod-shaped bacteria. On the basis of arrangement of organisms, they can be described as – Diplobacilli – Streptobacilli – Palisades – Chinese-letter form – Coccobacilli – Comma-shaped
  10. 10. 2. ACTINOMYCETES (actin- ray, mykes-fungus) These are rigid organisms like true bacteria but they resemble fungi in that they exhibit branching and tend to form filaments. They are termed such because of their resemblance to sun rays when seen in tissue sections.
  11. 11. 3. Spirochaetes These are relatively longer, slender, non- branched microorganisms of spiral shape having several coils.
  12. 12. 4. Mycoplasmas These bacteria lack in rigid cell wall (cell wall lacking) and are highly pleomorphic and of indefinite shape. They occur in round or oval bodies and in interlacing filaments. 5. Rickettsiae and Chlamydiae These are very small, obligate parasites, and at one time were considered closely related to the viruses. Now, these are regarded as bacteria.
  13. 13. Based on Anatomical features • Capsule • Capsulate– Streptococcus pneumoniae • Non-capsulate – Viridans streptococci • Flagella • Flagellate – • Monotrichous • Lophotrichous • Amphitrichous • Peritrichous • Aflagellate – Shigella spp. • Spore • Spore-forming – Bacillus spp. • Non-sporing – Escherichia coli 15
  14. 14. Based on Staining reaction • GRAM’S STAIN • Gram-positive cocci – Staphylococcus aureus • Gram-negative cocci – Neisseria gonorrhoeae • Gram-positive rods – Clostridium spp. • Gram-negative rods – E. coli • ACID FAST STAIN • Acid-fast bacilli –Mycobacterium tuberculosis • Non-acid-fast bacilli – Staphylococcus aureus
  15. 15. Based on Cultural characteristics • Extra growth factors requirements • Fastidious – Hemophilus influenzae • Non-fastidious – Escherichia coli • Hemolysis on Sheep Blood Agar • Alpha-hemolysis – Streptococcus pneumoniae • Beta-hemolysis – Streptococcus pyogenes • Utilization of carbohydrates • Oxidative - Micrococcus • Fermentative – Escherichia coli 17
  16. 16. Based on Cultural characteristics • Growth rate • Rapid growers– Vibrio cholerae • Slow growers – Mycobacterium tuberculosis • Pigment production • Pigment producer – Staphylococcus aureus • Pigment non-producer – Escherichia coli 18 Based on Nutrition • Autotrophs • Heterotrophs
  17. 17. Based on environmental factors A. Temperature • Psychrophiles (15-200C) – Pseudomonas fluorescens • Mesophiles (20-400C) – Escherichia coli, Salmonella enterica, Staphylococcus aureus • Thermophiles (50-600C)- Bacillus stearothermophilus • Extremely thermophiles (as high as 2500C) 19
  18. 18. B. Oxygen dependence • Aerobe (grow in ambient temperature, which contains 21% O2 and a small amount of CO2, 0.03%) • Obligate aerobes – Strictly require O2 for their growth (Pseudomonas aeruginosa) • Micro-aerophilic (grow under reduced O2, 5-10% and increased CO2, 8-10%)- Campylobacter jejuni, Helicobacter pylori • Facultative anaerobe (capable of growing either in presence or absence of O2)- E. coli • Obligate anaerobe – Clostridium spp. • Capnophilic (require increased concentration of CO2, i.e., 5-10%) – H. influenzae, N. gonorrhoeae • Aerotolerant 20
  19. 19. 21 C. pH • Acidophiles (Lactobacillus acidophilus) • Alkaliphiles (Vibrio) • Neutralophiles (pH 6-8) Majority of the medically important bacteria grow best at neutral or slightly alkaline reaction (pH 7.2-7.6) D. Salt concentration • Halophiles • Non-halophiles
  20. 20. Other ways of classification • Motile/Non-motile • Pathogenic/Non-pathogenic • Sensitive/Resistant (to particular antibiotic/ chemicals) • Lactose fermenter/Lactose non-fermenter • Bergey’s Manual of Determinative Bacteriology • Gram-negative eubacteria that have cell walls • Gram-positive eubacteria that have cell walls • Cell wall-less eubacteria: Mycoplasma • Archaeobacteria 22
  21. 21. Thanks for having patience with me.

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This presentation provides information about the different methods of classification of bacteria.

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