2Criteria of specimen rejection Aim of the testDetect bacterial pathogenic organisms in the stool; diagnose typhoid fever, enteric fever, bacillary dysentery.Types of specimenStool or rectal swab or stool (fresh random) in fecal transport system.Criteria of specimen rejectionspecimen contaminated with urine.residual soap, or disinfectants.Specimens received in grossly leaking transport containers.dry specimens.specimens submitted in fixative or additives.
3Pre specimen processing Patient preparingInstruct the patient on how the specimen should be collected and transferred to the container; provide him/her with sticks and containers.Specimen collectionA single stool specimen cannot be used to rule out bacteria as a cause of diarrhea.More than two specimens should only be submitted from patients for whom there is a high degree of suspicion.
4Who will collect the specimen The patient. If stool is unobtainable, nursing staff or physician will collect fecal swab.Quantity of specimenThe specimen should contain at least 5 g of faecesTime relapse before processing the sampleStool samples should be examined and cultured as soon as possible after collection. As the stool specimen cools, the drop in pH will inhibit the growth of most Shigella spp. and some Salmonella spp.
5Routine Stool Culture, Salmonella & Shigella MediaSelenite-F broth or tetrathionate.SSA, XLD and HEA.ReagentsAPI 20 E Kit.Salmonella and Shigella antiserum (polyvalent and monovalent).
7Selenite-F brothSelenite Broth (Selenite-F Broth) is used as an enrichment medium for the isolation of Salmonella from feces, urine, water, foods and other materials.Sodium selenite inhibits the growth of gram-positive and many gram-negative bacteria including Eenterococci and Coliforms, whereas the salmonellae are not affected.Sodium selenite is highly toxic at near-neutral pH.
8Buffer salts are present to help maintain the pH which may rise as the toxicity decreases . A rise in pH decreases selective activity of Selenite.A fermentable carbohydrate (lactose) is also present to provide acid to neutralise the alkali produced when the selenite is reduced by bacteria.Tetrathionate BrothTetrathionate Broth base, with added iodine-iodide solution, is used as a selective enrichment medium for the isolation of Salmonella from feces, urine, foods and other materials.
9component of (XLD) Agar XyloseLysineLactoseSucroseSodium chloridePhenol redSodium desoxycholate inhibits contaminating Gram-positive floraSodium thiosulphateFerric ammonium sulphateAgar
10Xylose Lysine Desoxycholate (XLD) Agar A selective and differential medium for the recovery of Salmonella and Shigella species.It has a pH of approximately 7.4, leaving it with a bright pink or red appearance due to the indicator phenol red.Sugar fermentation lowers the pH and the phenol red indicator registers this by changing to yellow.Most enteric organisms except Shigella ferment xylose to produce acid.Salmonella also decarboxylate lysine which keeps the pH neutral or slightly alkaline.
11At this pH Salmonella species can produce hydrogen sulphide from the reduction of thiosulphate. This is indicated by ferric ammonium citrate producing black or black-centred colonies.Other Enterobacteria such as E. coli will ferment the lactose and sucrose present in the medium to an extent that will prevent pH reversion by decarboxylation and acidify the medium turning it yellow.
12Red colonies, black centre ResultsColor of colonyOrganismRed colonies, black centreSalmonellaRed coloniesShigellaYellowE. coliProteus
14Salmonella Shigella Agar (SSA) SS Agar and Salmonella Shigella Agar are moderately selective and differential media for the isolation of pathogenic enteric bacilli, especially those belonging to the genus Salmonella and Shigella.
15Component of SSABile salts, brilliant green and Sodium citrates: inhibit Gram-positive bacteria, most coliform bacteria. Differentiation of enteric organisms is achieved by the incorporation of lactose in the medium.Sodium thiosulfate and Ferric citrate allow the detection of the H2S producing bacteria such as Proteus and some strains of Salmonella, as they produce colonies with black centersNeutral Red is the pH indicator.
16Organisms that ferment lactose produce acid which, in the presence of the neutral red indicator, results in the formation of red colonies. Lactose nonfermenters form colorless colonies.The sodium thiosulfate and ferric citrate enable the detection of hydrogen sulfide production as evidenced by colonies with black centers.
17A. Klebsiella pneumoniae B A. Klebsiella pneumoniae B. Escherichia coli Klebsiella pneumoniae & Escherichia coli are positive for acid production from fermentation of the carbohydrate(s) present. C: Salmonella sp. D: Proteus mirabilis Both Salmonella sp. & Proteus mirabilis product hydrogen sulfide. E: Pseudomona aeruginosa The Pseudomonas colonies are nearly colorless.
18Hektoen Enteric AgarBile salts and Acid Fuchsin : These substances inhibit gram-positive organisms but also can be toxic for some gram-negative strains.lactose, sucrose as carbohydrates.Sodium Chloride: maintains the osmotic balance of the mediumFerric ammonium citrate and sodium thiosulfate in the medium enable the detection of hydrogen sulfide production.Bromothymol Blue and Acid Fuchsin are added as the pH indicator. The indicator bromothymol blue changes its color to yellow and acid fuchsin would changes color from yellow to orange- red when acid is formed.
19Results Colony Color Organisms Blue to green-blue Salmonella & ShigellaYellow to salmonEscherichia coli
20Additional Information Indications for stool culture include:Bloody diarrheaFeverTenesmus (is the constant feeling of the need to empty the bowel, accompanied by pain, and cramping)Severe or persistent symptomsRecent travel to a third world countryKnown exposure to a bacterial agentPresence of fecal leukocytes
22Specimen processing Media Sorbitol MacConkey Agar (SMAC). Bile salts mixture and crystal violet largely inhibit the growth of the Gram-positive microbial floraThe addition of Cefixime Potassium tellurite (CT) Supplement increases the selectivity for E. coli 0157:H7 and suppresses the remaining accompanying flora.Sorbitol, together with the pH indicator neutral red, is used to detect sorbitol-positive colonies and turning them red in color. Sorbitol-negative strains, on the other hand, form colorless colonies.
23Culturing procedureA loopful of stool is streaked on Sorbitol MacConkey. Incubate at 37oC. Under aerobic conditions. Examine plates for non-sorbitol fermenting colonies(NSF).NSF colonies may be taken from SMAC plates or alternatively NSF isolates may be inoculated onto non-selective agar media for testing. It is necessary to test up to 10 separate NSF colonies to ensure a high probability of detection from mixed cultures.
25Interpretationa) Positive result - Agglutination of the Test latex occurs within 1 minute.No agglutination of the Control latex. Perform biochemical tests to confirm thatthe organism is an E. coli strain.b) Negative result - no agglutination of the Test latex.c) Non-interpretable result - clumping of the Control latex.
27Media Alkaline peptone water TCBS (Thiosulfate Citrate Bile salt Sucrose Agar)Alkaline Peptone Water is an enrichment medium used for the cultivation of Vibrio species from feces and other infected materials.Peptones provide nitrogen, vitamins, minerals and amino acids essential for growth.Sodium chloride supplies essential electrolytes for transport and osmotic balance and encourages the growth of Vibrio cholerae.
28Formulation of Thiosulfate Citrate Bile salt Sucrose Agar (TCBS) Nutritional component (eg: peptone)Sodium thiosulphateSodium citrateBile saltsSucroseSodium chlorideFerric citrateBromothymol blueAgar
29Thiosulfate Citrate Bile salt Sucrose Agar A selective isolation medium for pathogenic Vibrio species.Most Enterobacteriaceae other than Vibrio species are suppressed for at least 24h.Bile salts inhibit Gram-positive organisms.Sodium thiosulphate serves as a source of sulphur which, in combination with ferric citrate, detects hydrogen sulphide production.When sucrose is fermented it produces acid which changes the pH.This is indicated by bromothymol blue and thymol blue.The medium is alkaline which enhances the recovery of Vibrio cholerae.