BACTERIAL IDENTIFICATION TESTS

BACTERIAL IDENTIFICATION TESTS 11.1 INTRODUCTION In the previous chapter we have discussed various methods of isolation of bacteria. The bacteria thus isolated needs to be further identified to genus and species level. The identification is required so as to cure the illness or the infection caused due to the bacteria by using appropriate antibiotics. Identification also holds significance for epidemiological purposes. OBJECTIVES After reading this chapter, you will be able to : describe the processes involved in the identification of bacteria. explain the significance of microscopy in the process of identification of bacteria. explain the significance of biochemical test in the process of identification of bacteria. describe the significance of serology in the process of identification of bacteria. describe the significance of phage typing in the process of identification of bacteria. explain the significance of antimicrobial susceptibility testing in the process of identification of bacteria 11.2 BACTERIAL IDENTIFICATION The isolated bacteria are further processed through one or few of the procedures mentioned below so as to identify the bacteria Staining of the isolated bacteria Motility testing MICROBIOLOGY Bacterial Identification Tests Biochemical testing Serological tests Phage typing Identification disc testing Semiautomated and Automated identification systems Molecular techniques (i) Staining of the isolated bacteria Staining of the bacteria forms the foremost and the most important step in the identification of bacteria. The isolated bacteria are stained by various methods depending upon the bacteria in focus. Various staining techniques are as follow 1. Gram staining: differentiates bacteria into two types Gram positive and Gram negative bacteria Gram positive bacteria can be either cocci or bacilli or vibrios. Gram positive pathogenic bacteria are staphylococci, streptococci, pneumococci, etc Gram negative bacteria can be either cocci or bacilli. Gram negative pathogenic bacteria commonly encountered are E.coli, Klebsiella, Salmonella spp, shigella, etc 2. Albert staining: is performed in case if one suspects a Corynebacterium spp. 3. Acid fast staining: is performed in cases suspected of Mycobacterial infection. Eg. Tuberculosis, leprosy, etc. 4. Special staining is necessary in case of spirochetes and other organisms. INTEXT QUESTIONS 11.1 1. ......................... of bacteria is the important step in identification of bacteria 2. Gram stain differentiates bacteria as ......................... & ......................... 3. ......................... staining is used in Identification of Corynebacterium spp 4. ......................... staining is used in identification of Mycobacterial infection 5. ........................., ......................... & ......................... are examples of Gram Positive Bacteria 6. ........................., ......................... & ......................... are examples of Gram Negative Bacteria MICROBIOLOGY MODULE Microbiology Notes 123 MODULE Microbiology 124 Notes Bacterial Identification Tests (ii) Motility testing Motility testing is performed by preparing a wet mount and is then observed under the microscope. Motility of bacteria can also be tested by inoculating the bacteria in the semisolid motility medium. (iii) Biochemical tests The staining is followed by use of various biochemical reagents and tests to get closer to the identification of bacteria. There are many biochemical tests available for bacterial identification. Few of them are required to be carried out depending upon the bacteria. The commonly used biochemical tests are as mentioned below (a) Catalase test (b) Coagulase test (c) Oxidase test (d) Sugar fermentation test (e) Indole test (f) Citrate test (g) Urease test (a) Catalase test Purpose The catalase test facilitates the detection of the enzyme catalase in bacteria. It is essential for differentiating catalase-positive Micrococcaceae from catalase negative Streptococcaceae. While it is primarily useful in differentiating between genera, it is also valuable in speciation of certain gram positives such as Aerococcus urinae (positive) from Aerococcus viridians (negative) and gram negative organisms such as Campylobacter fetus, Campylobacter jejuni, and Campylobacter coli (all positive) from other Campylobacter species. Procedure: Place a microscope slide inside a petri dish. Keep the petri dish cover available. Using a sterile inoculating loop or wooden applicator stick, collect a small amount of organism from a well-isolated 18- to 24-hour colony and place it onto the microscope slide. Be careful not to pick up any agar. This is particularly important if the colony isolate was grown on agar containing red blood cells. Carryover of red blood cells into the test may result in a false-positive reaction. Using a dropper or Pasteur pipette, place 1 drop of 3% H2O2 onto the organism on the microscope slide. Do not mix. Immediately cover the petri dish with a MICROBIOLOGY Bacterial Identification Tests lid to limit aerosols and observe for immediate bubble formation (O2 + water = bubbles). Observing for the formation of bubbles against a dark background enhances readability. Fig. 11.1 Catalase positive bacteria: Staphylococcus spp Catalase negative bacteria: Streptococcus spp b. Coagulase test Purpose The coagulase test differentiates strains of Staphylococcus aureus from other coagulase-negative species. S. aureus strains are capable of coagulating plasma in the tube test and will produce clumps of cells in the slide test. The coagulase test can be performed using two different procedures - Slide test and tube test. The slide test is simple, giving results within 10 seconds, but it can give false negatives. The tube test is the definitive test, however, it can take up to 24 hours to complete. For both tests, clumping or clots of any size indicate a positive response. While S. aureus is the most commonly isolated coagulase positive organism, there are several other species of Staphylococcus which are positive for coagulase activity. S. schleiferi and S. lugdunensis may give positive results in the slide test for bound coagulase, and S. schleiferi and S. intermedius may give positive results in the tube coagulase test . Procedure: The slide test is performed by preparing a suspension of bacterial cells mixed into a drop of rabbit plasma on a microscope slide. If bound coagulase is present on the bacterial cells, then the presence of plasma will cause the bacterial cells to clump. The clumping will occur because the clumping factor is an adhesin, which causes the cells to bind to fibrinogen in the plasma. This will result in visible clumping of bacterial cells on the microscope slide. Figure given below illustrates the visible clumping of cells on the microscope slide.