1Sf1Ep mediumCulturing Treponema pallidum, the bacteria that causes syphilis, in vitro is a challenge. T. pallidum is not routinely cultured in the laboratory for diagnostic purposes, in part because it cannot be grown on artificial media. However, a breakthrough in culturing T. pallidum was reported in 2018 when researchers managed to grow the bacterium in a rabbit epithelial cell line (Sf1Ep) using a medium called 'Sf1Ep medium'. It's not used for routine diagnostic purposes, but for research only. The diagnosis involves direct microscopic examination, serologic tests, molecular tests and histopathology.
2Baird-Parker Agar (BPA)his is a selective medium for the isolation of Staphylococcus species. It has lithium chloride and glycine to inhibit the growth of Gram-negative bacteria and most Gram-positive bacteria except Staphylococcus. Egg yolk emulsion is added to detect lecithinase production and tellurite reduction. S. aureus colonies on BPA are black due to reduction of tellurite, and they exhibit a clear zone due to lecithinase activity on egg yolk.
3Phenol Red Mannitol BrothThis is a differential medium, used to determine an organism's ability to ferment mannitol. S. aureus, which can ferment mannitol, will change the medium from red to yellow due to acid production.
4DNase Test AgarS. aureus produces the enzyme DNase which hydrolyses DNA. When S. aureus grows on this medium, the DNA is broken down, which can be visualised using a hydrochloric acid (HCl) solution: clear zones around the colonies indicate DNA breakdown.
5Mannitol Salt Agar (MSA), or Chapman AgarThis is a selective and differential medium. The high concentration of NaCl (~7.5%) selects for halophiles, organisms that can tolerate high salt concentrations, thereby favouring the growth of Staphylococcus species. Mannitol is the differential component: S. aureus ferments mannitol, lowering the pH of the medium, which results in a color change of the pH indicator from red to yellow. Thus, growth of S. aureus is indicated by yellow colonies.
6Blood Agar (BA)This is a nutrient-rich, differential medium that supports the growth of many organisms. S. aureus forms colonies that are round, smooth, and golden-yellow. This bacterium typically demonstrates β-hemolysis, which is complete lysis of red blood cells, resulting in a clear zone around the colonies. This hemolysis is due to the production of hemolysins by S. aureus.
7Sauton’s MediumA liquid medium that lacks detergents, which helps in the formation of corded colonies. When M. tuberculosis grows in this medium, it results in turbidity.
8BACTECThis is not a traditional medium but a system for detecting the growth of M. tuberculosis by monitoring the release of C14O2 from C14 palmitic acid, which the bacteria metabolize. An increase in radioactive counts in the BACTEC instrument indicates the growth of bacteria.
9Sula’s MediumA liquid medium containing glycerol, asparagine, and a variety of salts. The growth of M. tuberculosis results in turbidity.
10Proskauer and Beck’s MediumA liquid medium. The growth of M. tuberculosis causes turbidity.
11Middlebrook 7H9 BrothThis is a liquid medium that contains glycerol and Tween 80, which prevent clumping of mycobacteria. The growth of M. tuberculosis results in turbidity.
12Dubos’ MediumA liquid medium that contains a mixture of salts, fatty acids, and polysorbate. When M. tuberculosis grows in this medium, it causes the medium to become turbid.
13Pawlowsky MediumA potato-based medium. Growth of M. tuberculosis may be similar to that seen on the LJ Medium.
14Loeffler MediumA serum-based medium. M. tuberculosis colonies on Loeffler medium are small, dry, wrinkled, and off-white to yellow.
15Tarshis MediumA blood-based medium that can promote the growth of M. tuberculosis. The colonies appear similar to those on the LJ Medium.
16Middlebrook 7H11 AgarThis is a nutrient-rich medium similar to 7H10 but includes additional pyruvate for energy source, promoting more luxurious growth. The colonies of M. tuberculosis appear small, slightly domed, and rough with a butyrous consistency.
17Middlebrook 7H10 AgarA selective medium that contains oleic acid, albumin, dextrose, and catalase. The colonies of M. tuberculosis appear small, rough, and buff to white-colored, taking less time to appear compared to egg-based media.
18Petragnini MediumAn egg-based medium enriched with additional nutrients to promote the growth of Mycobacterium tuberculosis. Colonies of M. tuberculosis are small, round, buff-colored, and typically take 3-4 weeks to appear.
19Lowenstein-Jensen (LJ) MediumAn egg-based medium that uses malachite green to suppress the growth of other bacteria and glycerol to stimulate the growth of Mycobacterium tuberculosis. The colonies of M. tuberculosis on LJ are non-pigmented, dry, rough, raised, irregular with a wrinkled surface, initially creamy-white, turning yellowish or buff-colored on further incubation.
20Liquid Media (such as Nutrient Broth)E. coli exhibits homogenous turbid growth within 12-18 hours. After prolonged incubation, pellicles may form on the surface of the media.
21Lysine Iron Agar (LIA)Used to determine the ability of an organism to decarboxylate or deaminate lysine and to form hydrogen sulfide. E. coli is typically lysine decarboxylase positive and H2S negative, so you would see a reaction of red/purple slant and purple/red butt with no black precipitate.
22Brilliant Green Agar (BGA)A selective medium that is used to isolate Salmonella species, but E. coli can grow on it, albeit not as well.
23Sorbitol-MacConkey agarA variant of MacConkey agar, used in detecting E. coli O157:H7, which does not ferment sorbitol, unlike most strains of E. coli.
24Urea Agar/BrothE. coli is typically urease negative, so no color change would be expected in this medium.
25Triple Sugar Iron (TSI) AgarE. coli typically produces an acid butt, acid slant, and gas, with no H2S production, indicating it ferments lactose, sucrose, and glucose.
26Simmons Citrate AgarUsed for citrate utilization testing. E. coli usually can't utilize citrate as a sole carbon source, so no growth or color change would be expected.
27Tryptic Soy Agar (TSA)A general purpose medium. E. coli colonies are medium to large, with a shiny moist appearance.
28Cystine Lactose Electrolyte-Deficient (CLED) AgarE. coli will give lactose-positive yellow colonies.
29Violet Red Bile Agar (VRBA)E. coli colonies are red (pink to red) and may show bluish fluorescence under UV light.
30m-ENDO AgarE. coli colonies appear as green with a metallic sheen, indicating lactose fermentation.
31Eosin Methylene Blue (EMB) AgarA selective and differential medium where E. coli forms distinctive metallic green sheen colonies due to vigorous lactose fermentation.
32Mueller Hinton Agar (MHA)Typically used for antibiotic susceptibility testing. E. coli colonies appear pale straw colored.
33MacConkey Agar (MAC)This selective and differential medium distinguishes lactose fermenters from non-fermenters. E. coli colonies are circular, moist, smooth, and pink.
34Blood Agar (BA)E. coli colonies on this differential medium are large, circular, gray, moist, and can show β-hemolysis.
35Nutrient Agar (NA)A non-selective medium. E. coli colonies are usually large, circular, grayish-white, moist, and smooth.
36Nickerson’s Medium or Bismuth Sulfite Glucose Glycine Yeast (BSGG)This medium is used to stimulate the production of germ tubes, a characteristic of Candida albicans.
37RPMI 1640 MediumIt is a rich medium that contains inorganic salts, glucose, amino acids, vitamins, and other nutrients that promote the growth of yeast cells.
38Potato Dextrose Agar (PDA)Potato Dextrose Agar (PDA) consists of a nutrient-rich substrate, made from dehydrated Potato Infusion and Dextrose, ideal for robust mycological propagation. Agar provides the solidifying medium. Acidification, typically using sterile tartaric acid, adjusts the pH to 3.5 +/- 0.1 to create a more selective environment by inhibiting bacterial proliferation. Additionally, Chloramphenicol is incorporated as an antimicrobial agent to further suppress bacterial contamination, thereby facilitating the selective isolation of fungi.
39Sabouraud Dextrose Agar (SDA)It is composed of peptone, dextrose (glucose), and agar. The high dextrose concentration promotes fungal growth, while the acidic pH inhibits bacterial growth.
40Nutrient AgarIt is a general-purpose medium. However, E. faecalis grows poorly on nutrient agar, which means it does not proliferate as well on this medium compared to the others listed, indicating a negative or poor growth.
41Blood AgarA differential medium used to identify bacteria based on their hemolytic properties. E. faecalis typically shows gamma-hemolysis on this medium, i.e., no hemolysis or change in the color of the medium.
42MacConkey AgarTraditionally used to isolate and differentiate Gram-negative bacilli, E. faecalis can grow on this medium, producing small, round, magenta pink colonies due to lactose fermentation, indicating a positive result.
43Azide Dextrose BrothA selective medium inhibiting Gram-negative bacteria, used for the isolation of streptococci and staphylococci from mixed samples. E. faecalis will show a positive growth resulting in a turbid appearance of the broth.
44Todd-Hewitt BrothA liquid enrichment medium used for the cultivation of fastidious organisms such as streptococci and enterococci. E. faecalis will lead to a turbid broth due to microbial growth.
45Enterococcosel AgarA selective and differential medium that inhibits the growth of Gram-negative bacteria and distinguishes enterococci based on their ability to grow in the presence of bile and hydrolyze esculin. E. faecalis will form small, black colonies on this medium due to esculin hydrolysis.
46Brain-Heart Infusion (BHI) Broth or AgarThis is a nutrient-rich medium that supports the growth of a variety of fastidious organisms, including E. faecalis. The typical phenotype of E. faecalis on BHI is small, round, and white colonies.
47Tryptic Soy Broth or Agar (TSB/TSA)A general-purpose medium that supports the growth of a broad spectrum of bacteria. E. faecalis on TSA will typically form small, round, and white colonies, indicating a positive growth.
1Phenol Red Mannitol BrothThis is a differential medium, used to determine an organism's ability to ferment mannitol. S. aureus, which can ferment mannitol, will change the medium from red to yellow due to acid production.
2Sauton’s MediumA liquid medium that lacks detergents, which helps in the formation of corded colonies. When M. tuberculosis grows in this medium, it results in turbidity.
3Middlebrook 7H11 AgarThis is a nutrient-rich medium similar to 7H10 but includes additional pyruvate for energy source, promoting more luxurious growth. The colonies of M. tuberculosis appear small, slightly domed, and rough with a butyrous consistency.
4Blood Agar (BA)This is a nutrient-rich, differential medium that supports the growth of many organisms. S. aureus forms colonies that are round, smooth, and golden-yellow. This bacterium typically demonstrates β-hemolysis, which is complete lysis of red blood cells, resulting in a clear zone around the colonies. This hemolysis is due to the production of hemolysins by S. aureus.
5CHROMagar CandidaThis differential medium allows for the isolation and identification of Candida species based on colony color. Candida albicans usually forms green colonies on this medium.
6MacConkey AgarTraditionally used to isolate and differentiate Gram-negative bacilli, E. faecalis can grow on this medium, producing small, round, magenta pink colonies due to lactose fermentation, indicating a positive result.
7Sf1Ep mediumCulturing Treponema pallidum, the bacteria that causes syphilis, in vitro is a challenge. T. pallidum is not routinely cultured in the laboratory for diagnostic purposes, in part because it cannot be grown on artificial media. However, a breakthrough in culturing T. pallidum was reported in 2018 when researchers managed to grow the bacterium in a rabbit epithelial cell line (Sf1Ep) using a medium called 'Sf1Ep medium'. It's not used for routine diagnostic purposes, but for research only. The diagnosis involves direct microscopic examination, serologic tests, molecular tests and histopathology.
8Tryptic Soy Agar (TSA)A general purpose medium. E. coli colonies are medium to large, with a shiny moist appearance.
9Sula’s MediumA liquid medium containing glycerol, asparagine, and a variety of salts. The growth of M. tuberculosis results in turbidity.
10Middlebrook 7H9 BrothThis is a liquid medium that contains glycerol and Tween 80, which prevent clumping of mycobacteria. The growth of M. tuberculosis results in turbidity.
11Lysine Iron Agar (LIA)Used to determine the ability of an organism to decarboxylate or deaminate lysine and to form hydrogen sulfide. E. coli is typically lysine decarboxylase positive and H2S negative, so you would see a reaction of red/purple slant and purple/red butt with no black precipitate.
12Azide Dextrose BrothA selective medium inhibiting Gram-negative bacteria, used for the isolation of streptococci and staphylococci from mixed samples. E. faecalis will show a positive growth resulting in a turbid appearance of the broth.
13Mueller Hinton Agar (MHA)Typically used for antibiotic susceptibility testing. E. coli colonies appear pale straw colored.
14Loeffler MediumA serum-based medium. M. tuberculosis colonies on Loeffler medium are small, dry, wrinkled, and off-white to yellow.
15BACTECThis is not a traditional medium but a system for detecting the growth of M. tuberculosis by monitoring the release of C14O2 from C14 palmitic acid, which the bacteria metabolize. An increase in radioactive counts in the BACTEC instrument indicates the growth of bacteria.
16Mannitol Salt Agar (MSA), or Chapman AgarThis is a selective and differential medium. The high concentration of NaCl (~7.5%) selects for halophiles, organisms that can tolerate high salt concentrations, thereby favouring the growth of Staphylococcus species. Mannitol is the differential component: S. aureus ferments mannitol, lowering the pH of the medium, which results in a color change of the pH indicator from red to yellow. Thus, growth of S. aureus is indicated by yellow colonies.
17Blood AgarA differential medium used to identify bacteria based on their hemolytic properties. E. faecalis typically shows gamma-hemolysis on this medium, i.e., no hemolysis or change in the color of the medium.
18Eosin Methylene Blue (EMB) AgarA selective and differential medium where E. coli forms distinctive metallic green sheen colonies due to vigorous lactose fermentation.
19DNase Test AgarS. aureus produces the enzyme DNase which hydrolyses DNA. When S. aureus grows on this medium, the DNA is broken down, which can be visualised using a hydrochloric acid (HCl) solution: clear zones around the colonies indicate DNA breakdown.
20Lowenstein-Jensen (LJ) MediumAn egg-based medium that uses malachite green to suppress the growth of other bacteria and glycerol to stimulate the growth of Mycobacterium tuberculosis. The colonies of M. tuberculosis on LJ are non-pigmented, dry, rough, raised, irregular with a wrinkled surface, initially creamy-white, turning yellowish or buff-colored on further incubation.
21Middlebrook 7H10 AgarA selective medium that contains oleic acid, albumin, dextrose, and catalase. The colonies of M. tuberculosis appear small, rough, and buff to white-colored, taking less time to appear compared to egg-based media.
22Liquid Media (such as Nutrient Broth)E. coli exhibits homogenous turbid growth within 12-18 hours. After prolonged incubation, pellicles may form on the surface of the media.
23Simmons Citrate AgarUsed for citrate utilization testing. E. coli usually can't utilize citrate as a sole carbon source, so no growth or color change would be expected.
24Urea Agar/BrothE. coli is typically urease negative, so no color change would be expected in this medium.
25Dubos’ MediumA liquid medium that contains a mixture of salts, fatty acids, and polysorbate. When M. tuberculosis grows in this medium, it causes the medium to become turbid.
26Sorbitol-MacConkey agarA variant of MacConkey agar, used in detecting E. coli O157:H7, which does not ferment sorbitol, unlike most strains of E. coli.
27Proskauer and Beck’s MediumA liquid medium. The growth of M. tuberculosis causes turbidity.
28Nickerson’s Medium or Bismuth Sulfite Glucose Glycine Yeast (BSGG)This medium is used to stimulate the production of germ tubes, a characteristic of Candida albicans.
29Violet Red Bile Agar (VRBA)E. coli colonies are red (pink to red) and may show bluish fluorescence under UV light.
30Bile Esculin Agar (BEA)A selective and differential medium that differentiates group D Streptococci and Enterococci based on the ability to hydrolyze esculin in the presence of bile. E. faecalis hydrolyzes esculin, leading to the formation of a dark brown or black precipita
31Todd-Hewitt BrothA liquid enrichment medium used for the cultivation of fastidious organisms such as streptococci and enterococci. E. faecalis will lead to a turbid broth due to microbial growth.
32Enterococcosel AgarA selective and differential medium that inhibits the growth of Gram-negative bacteria and distinguishes enterococci based on their ability to grow in the presence of bile and hydrolyze esculin. E. faecalis will form small, black colonies on this medium due to esculin hydrolysis.
33Cystine Lactose Electrolyte-Deficient (CLED) AgarE. coli will give lactose-positive yellow colonies.
34Tryptic Soy Broth or Agar (TSB/TSA)A general-purpose medium that supports the growth of a broad spectrum of bacteria. E. faecalis on TSA will typically form small, round, and white colonies, indicating a positive growth.
35Sabouraud Dextrose Agar (SDA)It is composed of peptone, dextrose (glucose), and agar. The high dextrose concentration promotes fungal growth, while the acidic pH inhibits bacterial growth.
36Blood Agar (BA)E. coli colonies on this differential medium are large, circular, gray, moist, and can show β-hemolysis.
37RPMI 1640 MediumIt is a rich medium that contains inorganic salts, glucose, amino acids, vitamins, and other nutrients that promote the growth of yeast cells.
38Petragnini MediumAn egg-based medium enriched with additional nutrients to promote the growth of Mycobacterium tuberculosis. Colonies of M. tuberculosis are small, round, buff-colored, and typically take 3-4 weeks to appear.
39Pawlowsky MediumA potato-based medium. Growth of M. tuberculosis may be similar to that seen on the LJ Medium.
40Nutrient AgarIt is a general-purpose medium. However, E. faecalis grows poorly on nutrient agar, which means it does not proliferate as well on this medium compared to the others listed, indicating a negative or poor growth.
41Cornmeal Agar with Tween 80It is used for the identification of Candida species by promoting the formation of chlamydospores, which is a characteristic of Candida albicans.
42MacConkey Agar (MAC)This selective and differential medium distinguishes lactose fermenters from non-fermenters. E. coli colonies are circular, moist, smooth, and pink.
43m-ENDO AgarE. coli colonies appear as green with a metallic sheen, indicating lactose fermentation.
44Brilliant Green Agar (BGA)A selective medium that is used to isolate Salmonella species, but E. coli can grow on it, albeit not as well.
45Dorset MediumAn egg-based medium. M. tuberculosis colonies appear similar to those on Petragnini Medium: small, round, buff-colored, and taking 3-4 weeks to develop.
46Nutrient Agar (NA)A non-selective medium. E. coli colonies are usually large, circular, grayish-white, moist, and smooth.
47Baird-Parker Agar (BPA)his is a selective medium for the isolation of Staphylococcus species. It has lithium chloride and glycine to inhibit the growth of Gram-negative bacteria and most Gram-positive bacteria except Staphylococcus. Egg yolk emulsion is added to detect lecithinase production and tellurite reduction. S. aureus colonies on BPA are black due to reduction of tellurite, and they exhibit a clear zone due to lecithinase activity on egg yolk.
48Tarshis MediumA blood-based medium that can promote the growth of M. tuberculosis. The colonies appear similar to those on the LJ Medium.
49Potato Dextrose Agar (PDA)Potato Dextrose Agar (PDA) consists of a nutrient-rich substrate, made from dehydrated Potato Infusion and Dextrose, ideal for robust mycological propagation. Agar provides the solidifying medium. Acidification, typically using sterile tartaric acid, adjusts the pH to 3.5 +/- 0.1 to create a more selective environment by inhibiting bacterial proliferation. Additionally, Chloramphenicol is incorporated as an antimicrobial agent to further suppress bacterial contamination, thereby facilitating the selective isolation of fungi.
1Baird-Parker Agar (BPA)his is a selective medium for the isolation of Staphylococcus species. It has lithium chloride and glycine to inhibit the growth of Gram-negative bacteria and most Gram-positive bacteria except Staphylococcus. Egg yolk emulsion is added to detect lecithinase production and tellurite reduction. S. aureus colonies on BPA are black due to reduction of tellurite, and they exhibit a clear zone due to lecithinase activity on egg yolk.
2CHROMagar CandidaThis differential medium allows for the isolation and identification of Candida species based on colony color. Candida albicans usually forms green colonies on this medium.
3MacConkey AgarTraditionally used to isolate and differentiate Gram-negative bacilli, E. faecalis can grow on this medium, producing small, round, magenta pink colonies due to lactose fermentation, indicating a positive result.
4Lysine Iron Agar (LIA)Used to determine the ability of an organism to decarboxylate or deaminate lysine and to form hydrogen sulfide. E. coli is typically lysine decarboxylase positive and H2S negative, so you would see a reaction of red/purple slant and purple/red butt with no black precipitate.
5Azide Dextrose BrothA selective medium inhibiting Gram-negative bacteria, used for the isolation of streptococci and staphylococci from mixed samples. E. faecalis will show a positive growth resulting in a turbid appearance of the broth.
6Sf1Ep mediumCulturing Treponema pallidum, the bacteria that causes syphilis, in vitro is a challenge. T. pallidum is not routinely cultured in the laboratory for diagnostic purposes, in part because it cannot be grown on artificial media. However, a breakthrough in culturing T. pallidum was reported in 2018 when researchers managed to grow the bacterium in a rabbit epithelial cell line (Sf1Ep) using a medium called 'Sf1Ep medium'. It's not used for routine diagnostic purposes, but for research only. The diagnosis involves direct microscopic examination, serologic tests, molecular tests and histopathology.
7BACTECThis is not a traditional medium but a system for detecting the growth of M. tuberculosis by monitoring the release of C14O2 from C14 palmitic acid, which the bacteria metabolize. An increase in radioactive counts in the BACTEC instrument indicates the growth of bacteria.
8Sauton’s MediumA liquid medium that lacks detergents, which helps in the formation of corded colonies. When M. tuberculosis grows in this medium, it results in turbidity.
9Mueller Hinton Agar (MHA)Typically used for antibiotic susceptibility testing. E. coli colonies appear pale straw colored.
10Sula’s MediumA liquid medium containing glycerol, asparagine, and a variety of salts. The growth of M. tuberculosis results in turbidity.
11Blood Agar (BA)E. coli colonies on this differential medium are large, circular, gray, moist, and can show β-hemolysis.
12Mannitol Salt Agar (MSA), or Chapman AgarThis is a selective and differential medium. The high concentration of NaCl (~7.5%) selects for halophiles, organisms that can tolerate high salt concentrations, thereby favouring the growth of Staphylococcus species. Mannitol is the differential component: S. aureus ferments mannitol, lowering the pH of the medium, which results in a color change of the pH indicator from red to yellow. Thus, growth of S. aureus is indicated by yellow colonies.
13RPMI 1640 MediumIt is a rich medium that contains inorganic salts, glucose, amino acids, vitamins, and other nutrients that promote the growth of yeast cells.
14Potato Dextrose Agar (PDA)Potato Dextrose Agar (PDA) consists of a nutrient-rich substrate, made from dehydrated Potato Infusion and Dextrose, ideal for robust mycological propagation. Agar provides the solidifying medium. Acidification, typically using sterile tartaric acid, adjusts the pH to 3.5 +/- 0.1 to create a more selective environment by inhibiting bacterial proliferation. Additionally, Chloramphenicol is incorporated as an antimicrobial agent to further suppress bacterial contamination, thereby facilitating the selective isolation of fungi.
15Bile Esculin Agar (BEA)A selective and differential medium that differentiates group D Streptococci and Enterococci based on the ability to hydrolyze esculin in the presence of bile. E. faecalis hydrolyzes esculin, leading to the formation of a dark brown or black precipita
16Todd-Hewitt BrothA liquid enrichment medium used for the cultivation of fastidious organisms such as streptococci and enterococci. E. faecalis will lead to a turbid broth due to microbial growth.
17Enterococcosel AgarA selective and differential medium that inhibits the growth of Gram-negative bacteria and distinguishes enterococci based on their ability to grow in the presence of bile and hydrolyze esculin. E. faecalis will form small, black colonies on this medium due to esculin hydrolysis.
18Cystine Lactose Electrolyte-Deficient (CLED) AgarE. coli will give lactose-positive yellow colonies.
19Blood AgarA differential medium used to identify bacteria based on their hemolytic properties. E. faecalis typically shows gamma-hemolysis on this medium, i.e., no hemolysis or change in the color of the medium.
20Eosin Methylene Blue (EMB) AgarA selective and differential medium where E. coli forms distinctive metallic green sheen colonies due to vigorous lactose fermentation.
21DNase Test AgarS. aureus produces the enzyme DNase which hydrolyses DNA. When S. aureus grows on this medium, the DNA is broken down, which can be visualised using a hydrochloric acid (HCl) solution: clear zones around the colonies indicate DNA breakdown.
22Tryptic Soy Agar (TSA)A general purpose medium. E. coli colonies are medium to large, with a shiny moist appearance.
23Brilliant Green Agar (BGA)A selective medium that is used to isolate Salmonella species, but E. coli can grow on it, albeit not as well.
24Dorset MediumAn egg-based medium. M. tuberculosis colonies appear similar to those on Petragnini Medium: small, round, buff-colored, and taking 3-4 weeks to develop.
25Nickerson’s Medium or Bismuth Sulfite Glucose Glycine Yeast (BSGG)This medium is used to stimulate the production of germ tubes, a characteristic of Candida albicans.
26Petragnini MediumAn egg-based medium enriched with additional nutrients to promote the growth of Mycobacterium tuberculosis. Colonies of M. tuberculosis are small, round, buff-colored, and typically take 3-4 weeks to appear.
27Nutrient AgarIt is a general-purpose medium. However, E. faecalis grows poorly on nutrient agar, which means it does not proliferate as well on this medium compared to the others listed, indicating a negative or poor growth.
28Cornmeal Agar with Tween 80It is used for the identification of Candida species by promoting the formation of chlamydospores, which is a characteristic of Candida albicans.
29Blood Agar (BA)This is a nutrient-rich, differential medium that supports the growth of many organisms. S. aureus forms colonies that are round, smooth, and golden-yellow. This bacterium typically demonstrates β-hemolysis, which is complete lysis of red blood cells, resulting in a clear zone around the colonies. This hemolysis is due to the production of hemolysins by S. aureus.
30m-ENDO AgarE. coli colonies appear as green with a metallic sheen, indicating lactose fermentation.
31Nutrient Agar (NA)A non-selective medium. E. coli colonies are usually large, circular, grayish-white, moist, and smooth.
32MacConkey Agar (MAC)This selective and differential medium distinguishes lactose fermenters from non-fermenters. E. coli colonies are circular, moist, smooth, and pink.
33Phenol Red Mannitol BrothThis is a differential medium, used to determine an organism's ability to ferment mannitol. S. aureus, which can ferment mannitol, will change the medium from red to yellow due to acid production.
34Sorbitol-MacConkey agarA variant of MacConkey agar, used in detecting E. coli O157:H7, which does not ferment sorbitol, unlike most strains of E. coli.
35Brain-Heart Infusion (BHI) Broth or AgarThis is a nutrient-rich medium that supports the growth of a variety of fastidious organisms, including E. faecalis. The typical phenotype of E. faecalis on BHI is small, round, and white colonies.
36Tarshis MediumA blood-based medium that can promote the growth of M. tuberculosis. The colonies appear similar to those on the LJ Medium.
37Proskauer and Beck’s MediumA liquid medium. The growth of M. tuberculosis causes turbidity.
38Lowenstein-Jensen (LJ) MediumAn egg-based medium that uses malachite green to suppress the growth of other bacteria and glycerol to stimulate the growth of Mycobacterium tuberculosis. The colonies of M. tuberculosis on LJ are non-pigmented, dry, rough, raised, irregular with a wrinkled surface, initially creamy-white, turning yellowish or buff-colored on further incubation.
39Middlebrook 7H10 AgarA selective medium that contains oleic acid, albumin, dextrose, and catalase. The colonies of M. tuberculosis appear small, rough, and buff to white-colored, taking less time to appear compared to egg-based media.
40Simmons Citrate AgarUsed for citrate utilization testing. E. coli usually can't utilize citrate as a sole carbon source, so no growth or color change would be expected.
41Loeffler MediumA serum-based medium. M. tuberculosis colonies on Loeffler medium are small, dry, wrinkled, and off-white to yellow.
42Tryptic Soy Broth or Agar (TSB/TSA)A general-purpose medium that supports the growth of a broad spectrum of bacteria. E. faecalis on TSA will typically form small, round, and white colonies, indicating a positive growth.
43Sabouraud Dextrose Agar (SDA)It is composed of peptone, dextrose (glucose), and agar. The high dextrose concentration promotes fungal growth, while the acidic pH inhibits bacterial growth.
44Middlebrook 7H9 BrothThis is a liquid medium that contains glycerol and Tween 80, which prevent clumping of mycobacteria. The growth of M. tuberculosis results in turbidity.
1MacConkey AgarTraditionally used to isolate and differentiate Gram-negative bacilli, E. faecalis can grow on this medium, producing small, round, magenta pink colonies due to lactose fermentation, indicating a positive result.
2Lysine Iron Agar (LIA)Used to determine the ability of an organism to decarboxylate or deaminate lysine and to form hydrogen sulfide. E. coli is typically lysine decarboxylase positive and H2S negative, so you would see a reaction of red/purple slant and purple/red butt with no black precipitate.
3Azide Dextrose BrothA selective medium inhibiting Gram-negative bacteria, used for the isolation of streptococci and staphylococci from mixed samples. E. faecalis will show a positive growth resulting in a turbid appearance of the broth.
4Mueller Hinton Agar (MHA)Typically used for antibiotic susceptibility testing. E. coli colonies appear pale straw colored.
5Sf1Ep mediumCulturing Treponema pallidum, the bacteria that causes syphilis, in vitro is a challenge. T. pallidum is not routinely cultured in the laboratory for diagnostic purposes, in part because it cannot be grown on artificial media. However, a breakthrough in culturing T. pallidum was reported in 2018 when researchers managed to grow the bacterium in a rabbit epithelial cell line (Sf1Ep) using a medium called 'Sf1Ep medium'. It's not used for routine diagnostic purposes, but for research only. The diagnosis involves direct microscopic examination, serologic tests, molecular tests and histopathology.
6Baird-Parker Agar (BPA)his is a selective medium for the isolation of Staphylococcus species. It has lithium chloride and glycine to inhibit the growth of Gram-negative bacteria and most Gram-positive bacteria except Staphylococcus. Egg yolk emulsion is added to detect lecithinase production and tellurite reduction. S. aureus colonies on BPA are black due to reduction of tellurite, and they exhibit a clear zone due to lecithinase activity on egg yolk.
7Sauton’s MediumA liquid medium that lacks detergents, which helps in the formation of corded colonies. When M. tuberculosis grows in this medium, it results in turbidity.
8Blood Agar (BA)E. coli colonies on this differential medium are large, circular, gray, moist, and can show β-hemolysis.
9RPMI 1640 MediumIt is a rich medium that contains inorganic salts, glucose, amino acids, vitamins, and other nutrients that promote the growth of yeast cells.
10Middlebrook 7H11 AgarThis is a nutrient-rich medium similar to 7H10 but includes additional pyruvate for energy source, promoting more luxurious growth. The colonies of M. tuberculosis appear small, slightly domed, and rough with a butyrous consistency.
11Mannitol Salt Agar (MSA), or Chapman AgarThis is a selective and differential medium. The high concentration of NaCl (~7.5%) selects for halophiles, organisms that can tolerate high salt concentrations, thereby favouring the growth of Staphylococcus species. Mannitol is the differential component: S. aureus ferments mannitol, lowering the pH of the medium, which results in a color change of the pH indicator from red to yellow. Thus, growth of S. aureus is indicated by yellow colonies.
12CHROMagar CandidaThis differential medium allows for the isolation and identification of Candida species based on colony color. Candida albicans usually forms green colonies on this medium.
13Blood Agar (BA)This is a nutrient-rich, differential medium that supports the growth of many organisms. S. aureus forms colonies that are round, smooth, and golden-yellow. This bacterium typically demonstrates β-hemolysis, which is complete lysis of red blood cells, resulting in a clear zone around the colonies. This hemolysis is due to the production of hemolysins by S. aureus.
14Todd-Hewitt BrothA liquid enrichment medium used for the cultivation of fastidious organisms such as streptococci and enterococci. E. faecalis will lead to a turbid broth due to microbial growth.
15Enterococcosel AgarA selective and differential medium that inhibits the growth of Gram-negative bacteria and distinguishes enterococci based on their ability to grow in the presence of bile and hydrolyze esculin. E. faecalis will form small, black colonies on this medium due to esculin hydrolysis.
16Cystine Lactose Electrolyte-Deficient (CLED) AgarE. coli will give lactose-positive yellow colonies.
17Eosin Methylene Blue (EMB) AgarA selective and differential medium where E. coli forms distinctive metallic green sheen colonies due to vigorous lactose fermentation.
18Tryptic Soy Agar (TSA)A general purpose medium. E. coli colonies are medium to large, with a shiny moist appearance.
19Lowenstein-Jensen (LJ) MediumAn egg-based medium that uses malachite green to suppress the growth of other bacteria and glycerol to stimulate the growth of Mycobacterium tuberculosis. The colonies of M. tuberculosis on LJ are non-pigmented, dry, rough, raised, irregular with a wrinkled surface, initially creamy-white, turning yellowish or buff-colored on further incubation.
20Sula’s MediumA liquid medium containing glycerol, asparagine, and a variety of salts. The growth of M. tuberculosis results in turbidity.
21Nutrient Agar (NA)A non-selective medium. E. coli colonies are usually large, circular, grayish-white, moist, and smooth.
22Triple Sugar Iron (TSI) AgarE. coli typically produces an acid butt, acid slant, and gas, with no H2S production, indicating it ferments lactose, sucrose, and glucose.
23Nickerson’s Medium or Bismuth Sulfite Glucose Glycine Yeast (BSGG)This medium is used to stimulate the production of germ tubes, a characteristic of Candida albicans.
24Pawlowsky MediumA potato-based medium. Growth of M. tuberculosis may be similar to that seen on the LJ Medium.
25Nutrient AgarIt is a general-purpose medium. However, E. faecalis grows poorly on nutrient agar, which means it does not proliferate as well on this medium compared to the others listed, indicating a negative or poor growth.
26Blood AgarA differential medium used to identify bacteria based on their hemolytic properties. E. faecalis typically shows gamma-hemolysis on this medium, i.e., no hemolysis or change in the color of the medium.
27Cornmeal Agar with Tween 80It is used for the identification of Candida species by promoting the formation of chlamydospores, which is a characteristic of Candida albicans.
28Liquid Media (such as Nutrient Broth)E. coli exhibits homogenous turbid growth within 12-18 hours. After prolonged incubation, pellicles may form on the surface of the media.
29Potato Dextrose Agar (PDA)Potato Dextrose Agar (PDA) consists of a nutrient-rich substrate, made from dehydrated Potato Infusion and Dextrose, ideal for robust mycological propagation. Agar provides the solidifying medium. Acidification, typically using sterile tartaric acid, adjusts the pH to 3.5 +/- 0.1 to create a more selective environment by inhibiting bacterial proliferation. Additionally, Chloramphenicol is incorporated as an antimicrobial agent to further suppress bacterial contamination, thereby facilitating the selective isolation of fungi.
30MacConkey Agar (MAC)This selective and differential medium distinguishes lactose fermenters from non-fermenters. E. coli colonies are circular, moist, smooth, and pink.
31m-ENDO AgarE. coli colonies appear as green with a metallic sheen, indicating lactose fermentation.
32Dorset MediumAn egg-based medium. M. tuberculosis colonies appear similar to those on Petragnini Medium: small, round, buff-colored, and taking 3-4 weeks to develop.
33Brain-Heart Infusion (BHI) Broth or AgarThis is a nutrient-rich medium that supports the growth of a variety of fastidious organisms, including E. faecalis. The typical phenotype of E. faecalis on BHI is small, round, and white colonies.
34Bile Esculin Agar (BEA)A selective and differential medium that differentiates group D Streptococci and Enterococci based on the ability to hydrolyze esculin in the presence of bile. E. faecalis hydrolyzes esculin, leading to the formation of a dark brown or black precipita
35Brilliant Green Agar (BGA)A selective medium that is used to isolate Salmonella species, but E. coli can grow on it, albeit not as well.
36DNase Test AgarS. aureus produces the enzyme DNase which hydrolyses DNA. When S. aureus grows on this medium, the DNA is broken down, which can be visualised using a hydrochloric acid (HCl) solution: clear zones around the colonies indicate DNA breakdown.
37Simmons Citrate AgarUsed for citrate utilization testing. E. coli usually can't utilize citrate as a sole carbon source, so no growth or color change would be expected.
38Sabouraud Dextrose Agar (SDA)It is composed of peptone, dextrose (glucose), and agar. The high dextrose concentration promotes fungal growth, while the acidic pH inhibits bacterial growth.
39Sorbitol-MacConkey agarA variant of MacConkey agar, used in detecting E. coli O157:H7, which does not ferment sorbitol, unlike most strains of E. coli.
40Tarshis MediumA blood-based medium that can promote the growth of M. tuberculosis. The colonies appear similar to those on the LJ Medium.
41Proskauer and Beck’s MediumA liquid medium. The growth of M. tuberculosis causes turbidity.
42Middlebrook 7H10 AgarA selective medium that contains oleic acid, albumin, dextrose, and catalase. The colonies of M. tuberculosis appear small, rough, and buff to white-colored, taking less time to appear compared to egg-based media.
43Petragnini MediumAn egg-based medium enriched with additional nutrients to promote the growth of Mycobacterium tuberculosis. Colonies of M. tuberculosis are small, round, buff-colored, and typically take 3-4 weeks to appear.
44Loeffler MediumA serum-based medium. M. tuberculosis colonies on Loeffler medium are small, dry, wrinkled, and off-white to yellow.
45Tryptic Soy Broth or Agar (TSB/TSA)A general-purpose medium that supports the growth of a broad spectrum of bacteria. E. faecalis on TSA will typically form small, round, and white colonies, indicating a positive growth.
1Sf1Ep mediumCulturing Treponema pallidum, the bacteria that causes syphilis, in vitro is a challenge. T. pallidum is not routinely cultured in the laboratory for diagnostic purposes, in part because it cannot be grown on artificial media. However, a breakthrough in culturing T. pallidum was reported in 2018 when researchers managed to grow the bacterium in a rabbit epithelial cell line (Sf1Ep) using a medium called 'Sf1Ep medium'. It's not used for routine diagnostic purposes, but for research only. The diagnosis involves direct microscopic examination, serologic tests, molecular tests and histopathology.
2Baird-Parker Agar (BPA)his is a selective medium for the isolation of Staphylococcus species. It has lithium chloride and glycine to inhibit the growth of Gram-negative bacteria and most Gram-positive bacteria except Staphylococcus. Egg yolk emulsion is added to detect lecithinase production and tellurite reduction. S. aureus colonies on BPA are black due to reduction of tellurite, and they exhibit a clear zone due to lecithinase activity on egg yolk.
3Phenol Red Mannitol BrothThis is a differential medium, used to determine an organism's ability to ferment mannitol. S. aureus, which can ferment mannitol, will change the medium from red to yellow due to acid production.
4DNase Test AgarS. aureus produces the enzyme DNase which hydrolyses DNA. When S. aureus grows on this medium, the DNA is broken down, which can be visualised using a hydrochloric acid (HCl) solution: clear zones around the colonies indicate DNA breakdown.
5Mannitol Salt Agar (MSA), or Chapman AgarThis is a selective and differential medium. The high concentration of NaCl (~7.5%) selects for halophiles, organisms that can tolerate high salt concentrations, thereby favouring the growth of Staphylococcus species. Mannitol is the differential component: S. aureus ferments mannitol, lowering the pH of the medium, which results in a color change of the pH indicator from red to yellow. Thus, growth of S. aureus is indicated by yellow colonies.
6Blood Agar (BA)This is a nutrient-rich, differential medium that supports the growth of many organisms. S. aureus forms colonies that are round, smooth, and golden-yellow. This bacterium typically demonstrates β-hemolysis, which is complete lysis of red blood cells, resulting in a clear zone around the colonies. This hemolysis is due to the production of hemolysins by S. aureus.
7Sula’s MediumA liquid medium containing glycerol, asparagine, and a variety of salts. The growth of M. tuberculosis results in turbidity.
8Proskauer and Beck’s MediumA liquid medium. The growth of M. tuberculosis causes turbidity.
9Middlebrook 7H9 BrothThis is a liquid medium that contains glycerol and Tween 80, which prevent clumping of mycobacteria. The growth of M. tuberculosis results in turbidity.
10Dubos’ MediumA liquid medium that contains a mixture of salts, fatty acids, and polysorbate. When M. tuberculosis grows in this medium, it causes the medium to become turbid.
11Pawlowsky MediumA potato-based medium. Growth of M. tuberculosis may be similar to that seen on the LJ Medium.
12Loeffler MediumA serum-based medium. M. tuberculosis colonies on Loeffler medium are small, dry, wrinkled, and off-white to yellow.
13Tarshis MediumA blood-based medium that can promote the growth of M. tuberculosis. The colonies appear similar to those on the LJ Medium.
14Dorset MediumAn egg-based medium. M. tuberculosis colonies appear similar to those on Petragnini Medium: small, round, buff-colored, and taking 3-4 weeks to develop.
15Middlebrook 7H11 AgarThis is a nutrient-rich medium similar to 7H10 but includes additional pyruvate for energy source, promoting more luxurious growth. The colonies of M. tuberculosis appear small, slightly domed, and rough with a butyrous consistency.
16Middlebrook 7H10 AgarA selective medium that contains oleic acid, albumin, dextrose, and catalase. The colonies of M. tuberculosis appear small, rough, and buff to white-colored, taking less time to appear compared to egg-based media.
17Petragnini MediumAn egg-based medium enriched with additional nutrients to promote the growth of Mycobacterium tuberculosis. Colonies of M. tuberculosis are small, round, buff-colored, and typically take 3-4 weeks to appear.
18Lowenstein-Jensen (LJ) MediumAn egg-based medium that uses malachite green to suppress the growth of other bacteria and glycerol to stimulate the growth of Mycobacterium tuberculosis. The colonies of M. tuberculosis on LJ are non-pigmented, dry, rough, raised, irregular with a wrinkled surface, initially creamy-white, turning yellowish or buff-colored on further incubation.
19Liquid Media (such as Nutrient Broth)E. coli exhibits homogenous turbid growth within 12-18 hours. After prolonged incubation, pellicles may form on the surface of the media.
20Lysine Iron Agar (LIA)Used to determine the ability of an organism to decarboxylate or deaminate lysine and to form hydrogen sulfide. E. coli is typically lysine decarboxylase positive and H2S negative, so you would see a reaction of red/purple slant and purple/red butt with no black precipitate.
21Brilliant Green Agar (BGA)A selective medium that is used to isolate Salmonella species, but E. coli can grow on it, albeit not as well.
22Sorbitol-MacConkey agarA variant of MacConkey agar, used in detecting E. coli O157:H7, which does not ferment sorbitol, unlike most strains of E. coli.
23Urea Agar/BrothE. coli is typically urease negative, so no color change would be expected in this medium.
24Triple Sugar Iron (TSI) AgarE. coli typically produces an acid butt, acid slant, and gas, with no H2S production, indicating it ferments lactose, sucrose, and glucose.
25Simmons Citrate AgarUsed for citrate utilization testing. E. coli usually can't utilize citrate as a sole carbon source, so no growth or color change would be expected.
26Tryptic Soy Agar (TSA)A general purpose medium. E. coli colonies are medium to large, with a shiny moist appearance.
27Violet Red Bile Agar (VRBA)E. coli colonies are red (pink to red) and may show bluish fluorescence under UV light.
28m-ENDO AgarE. coli colonies appear as green with a metallic sheen, indicating lactose fermentation.
29Eosin Methylene Blue (EMB) AgarA selective and differential medium where E. coli forms distinctive metallic green sheen colonies due to vigorous lactose fermentation.
30MacConkey Agar (MAC)This selective and differential medium distinguishes lactose fermenters from non-fermenters. E. coli colonies are circular, moist, smooth, and pink.
31Blood Agar (BA)E. coli colonies on this differential medium are large, circular, gray, moist, and can show β-hemolysis.
32Nickerson’s Medium or Bismuth Sulfite Glucose Glycine Yeast (BSGG)This medium is used to stimulate the production of germ tubes, a characteristic of Candida albicans.
33Cornmeal Agar with Tween 80It is used for the identification of Candida species by promoting the formation of chlamydospores, which is a characteristic of Candida albicans.
34CHROMagar CandidaThis differential medium allows for the isolation and identification of Candida species based on colony color. Candida albicans usually forms green colonies on this medium.
35RPMI 1640 MediumIt is a rich medium that contains inorganic salts, glucose, amino acids, vitamins, and other nutrients that promote the growth of yeast cells.
36Potato Dextrose Agar (PDA)Potato Dextrose Agar (PDA) consists of a nutrient-rich substrate, made from dehydrated Potato Infusion and Dextrose, ideal for robust mycological propagation. Agar provides the solidifying medium. Acidification, typically using sterile tartaric acid, adjusts the pH to 3.5 +/- 0.1 to create a more selective environment by inhibiting bacterial proliferation. Additionally, Chloramphenicol is incorporated as an antimicrobial agent to further suppress bacterial contamination, thereby facilitating the selective isolation of fungi.
37Sabouraud Dextrose Agar (SDA)It is composed of peptone, dextrose (glucose), and agar. The high dextrose concentration promotes fungal growth, while the acidic pH inhibits bacterial growth.
38Nutrient AgarIt is a general-purpose medium. However, E. faecalis grows poorly on nutrient agar, which means it does not proliferate as well on this medium compared to the others listed, indicating a negative or poor growth.
39Blood AgarA differential medium used to identify bacteria based on their hemolytic properties. E. faecalis typically shows gamma-hemolysis on this medium, i.e., no hemolysis or change in the color of the medium.
40MacConkey AgarTraditionally used to isolate and differentiate Gram-negative bacilli, E. faecalis can grow on this medium, producing small, round, magenta pink colonies due to lactose fermentation, indicating a positive result.
41Azide Dextrose BrothA selective medium inhibiting Gram-negative bacteria, used for the isolation of streptococci and staphylococci from mixed samples. E. faecalis will show a positive growth resulting in a turbid appearance of the broth.
42Todd-Hewitt BrothA liquid enrichment medium used for the cultivation of fastidious organisms such as streptococci and enterococci. E. faecalis will lead to a turbid broth due to microbial growth.
43Enterococcosel AgarA selective and differential medium that inhibits the growth of Gram-negative bacteria and distinguishes enterococci based on their ability to grow in the presence of bile and hydrolyze esculin. E. faecalis will form small, black colonies on this medium due to esculin hydrolysis.
44Bile Esculin Agar (BEA)A selective and differential medium that differentiates group D Streptococci and Enterococci based on the ability to hydrolyze esculin in the presence of bile. E. faecalis hydrolyzes esculin, leading to the formation of a dark brown or black precipita
45Brain-Heart Infusion (BHI) Broth or AgarThis is a nutrient-rich medium that supports the growth of a variety of fastidious organisms, including E. faecalis. The typical phenotype of E. faecalis on BHI is small, round, and white colonies.
1Sf1Ep mediumCulturing Treponema pallidum, the bacteria that causes syphilis, in vitro is a challenge. T. pallidum is not routinely cultured in the laboratory for diagnostic purposes, in part because it cannot be grown on artificial media. However, a breakthrough in culturing T. pallidum was reported in 2018 when researchers managed to grow the bacterium in a rabbit epithelial cell line (Sf1Ep) using a medium called 'Sf1Ep medium'. It's not used for routine diagnostic purposes, but for research only. The diagnosis involves direct microscopic examination, serologic tests, molecular tests and histopathology.
2Baird-Parker Agar (BPA)his is a selective medium for the isolation of Staphylococcus species. It has lithium chloride and glycine to inhibit the growth of Gram-negative bacteria and most Gram-positive bacteria except Staphylococcus. Egg yolk emulsion is added to detect lecithinase production and tellurite reduction. S. aureus colonies on BPA are black due to reduction of tellurite, and they exhibit a clear zone due to lecithinase activity on egg yolk.
3Phenol Red Mannitol BrothThis is a differential medium, used to determine an organism's ability to ferment mannitol. S. aureus, which can ferment mannitol, will change the medium from red to yellow due to acid production.
4DNase Test AgarS. aureus produces the enzyme DNase which hydrolyses DNA. When S. aureus grows on this medium, the DNA is broken down, which can be visualised using a hydrochloric acid (HCl) solution: clear zones around the colonies indicate DNA breakdown.
5Mannitol Salt Agar (MSA), or Chapman AgarThis is a selective and differential medium. The high concentration of NaCl (~7.5%) selects for halophiles, organisms that can tolerate high salt concentrations, thereby favouring the growth of Staphylococcus species. Mannitol is the differential component: S. aureus ferments mannitol, lowering the pH of the medium, which results in a color change of the pH indicator from red to yellow. Thus, growth of S. aureus is indicated by yellow colonies.
6Blood Agar (BA)This is a nutrient-rich, differential medium that supports the growth of many organisms. S. aureus forms colonies that are round, smooth, and golden-yellow. This bacterium typically demonstrates β-hemolysis, which is complete lysis of red blood cells, resulting in a clear zone around the colonies. This hemolysis is due to the production of hemolysins by S. aureus.
7Sauton’s MediumA liquid medium that lacks detergents, which helps in the formation of corded colonies. When M. tuberculosis grows in this medium, it results in turbidity.
8BACTECThis is not a traditional medium but a system for detecting the growth of M. tuberculosis by monitoring the release of C14O2 from C14 palmitic acid, which the bacteria metabolize. An increase in radioactive counts in the BACTEC instrument indicates the growth of bacteria.
9Sula’s MediumA liquid medium containing glycerol, asparagine, and a variety of salts. The growth of M. tuberculosis results in turbidity.
10Proskauer and Beck’s MediumA liquid medium. The growth of M. tuberculosis causes turbidity.
11Middlebrook 7H9 BrothThis is a liquid medium that contains glycerol and Tween 80, which prevent clumping of mycobacteria. The growth of M. tuberculosis results in turbidity.
12Dubos’ MediumA liquid medium that contains a mixture of salts, fatty acids, and polysorbate. When M. tuberculosis grows in this medium, it causes the medium to become turbid.
13Pawlowsky MediumA potato-based medium. Growth of M. tuberculosis may be similar to that seen on the LJ Medium.
14Loeffler MediumA serum-based medium. M. tuberculosis colonies on Loeffler medium are small, dry, wrinkled, and off-white to yellow.
15Tarshis MediumA blood-based medium that can promote the growth of M. tuberculosis. The colonies appear similar to those on the LJ Medium.
16Dorset MediumAn egg-based medium. M. tuberculosis colonies appear similar to those on Petragnini Medium: small, round, buff-colored, and taking 3-4 weeks to develop.
17Middlebrook 7H11 AgarThis is a nutrient-rich medium similar to 7H10 but includes additional pyruvate for energy source, promoting more luxurious growth. The colonies of M. tuberculosis appear small, slightly domed, and rough with a butyrous consistency.
18Middlebrook 7H10 AgarA selective medium that contains oleic acid, albumin, dextrose, and catalase. The colonies of M. tuberculosis appear small, rough, and buff to white-colored, taking less time to appear compared to egg-based media.
19Petragnini MediumAn egg-based medium enriched with additional nutrients to promote the growth of Mycobacterium tuberculosis. Colonies of M. tuberculosis are small, round, buff-colored, and typically take 3-4 weeks to appear.
20Lowenstein-Jensen (LJ) MediumAn egg-based medium that uses malachite green to suppress the growth of other bacteria and glycerol to stimulate the growth of Mycobacterium tuberculosis. The colonies of M. tuberculosis on LJ are non-pigmented, dry, rough, raised, irregular with a wrinkled surface, initially creamy-white, turning yellowish or buff-colored on further incubation.
21Liquid Media (such as Nutrient Broth)E. coli exhibits homogenous turbid growth within 12-18 hours. After prolonged incubation, pellicles may form on the surface of the media.
22Lysine Iron Agar (LIA)Used to determine the ability of an organism to decarboxylate or deaminate lysine and to form hydrogen sulfide. E. coli is typically lysine decarboxylase positive and H2S negative, so you would see a reaction of red/purple slant and purple/red butt with no black precipitate.
23Brilliant Green Agar (BGA)A selective medium that is used to isolate Salmonella species, but E. coli can grow on it, albeit not as well.
24Sorbitol-MacConkey agarA variant of MacConkey agar, used in detecting E. coli O157:H7, which does not ferment sorbitol, unlike most strains of E. coli.
25Urea Agar/BrothE. coli is typically urease negative, so no color change would be expected in this medium.
26Triple Sugar Iron (TSI) AgarE. coli typically produces an acid butt, acid slant, and gas, with no H2S production, indicating it ferments lactose, sucrose, and glucose.
27Simmons Citrate AgarUsed for citrate utilization testing. E. coli usually can't utilize citrate as a sole carbon source, so no growth or color change would be expected.
28Tryptic Soy Agar (TSA)A general purpose medium. E. coli colonies are medium to large, with a shiny moist appearance.
29Cystine Lactose Electrolyte-Deficient (CLED) AgarE. coli will give lactose-positive yellow colonies.
30Violet Red Bile Agar (VRBA)E. coli colonies are red (pink to red) and may show bluish fluorescence under UV light.
31m-ENDO AgarE. coli colonies appear as green with a metallic sheen, indicating lactose fermentation.
32Eosin Methylene Blue (EMB) AgarA selective and differential medium where E. coli forms distinctive metallic green sheen colonies due to vigorous lactose fermentation.
33Mueller Hinton Agar (MHA)Typically used for antibiotic susceptibility testing. E. coli colonies appear pale straw colored.
34MacConkey Agar (MAC)This selective and differential medium distinguishes lactose fermenters from non-fermenters. E. coli colonies are circular, moist, smooth, and pink.
35Blood Agar (BA)E. coli colonies on this differential medium are large, circular, gray, moist, and can show β-hemolysis.
36Nutrient Agar (NA)A non-selective medium. E. coli colonies are usually large, circular, grayish-white, moist, and smooth.
37Nickerson’s Medium or Bismuth Sulfite Glucose Glycine Yeast (BSGG)This medium is used to stimulate the production of germ tubes, a characteristic of Candida albicans.
38Cornmeal Agar with Tween 80It is used for the identification of Candida species by promoting the formation of chlamydospores, which is a characteristic of Candida albicans.
39CHROMagar CandidaThis differential medium allows for the isolation and identification of Candida species based on colony color. Candida albicans usually forms green colonies on this medium.
40RPMI 1640 MediumIt is a rich medium that contains inorganic salts, glucose, amino acids, vitamins, and other nutrients that promote the growth of yeast cells.
41Potato Dextrose Agar (PDA)Potato Dextrose Agar (PDA) consists of a nutrient-rich substrate, made from dehydrated Potato Infusion and Dextrose, ideal for robust mycological propagation. Agar provides the solidifying medium. Acidification, typically using sterile tartaric acid, adjusts the pH to 3.5 +/- 0.1 to create a more selective environment by inhibiting bacterial proliferation. Additionally, Chloramphenicol is incorporated as an antimicrobial agent to further suppress bacterial contamination, thereby facilitating the selective isolation of fungi.
42Sabouraud Dextrose Agar (SDA)It is composed of peptone, dextrose (glucose), and agar. The high dextrose concentration promotes fungal growth, while the acidic pH inhibits bacterial growth.
43Nutrient AgarIt is a general-purpose medium. However, E. faecalis grows poorly on nutrient agar, which means it does not proliferate as well on this medium compared to the others listed, indicating a negative or poor growth.
44Blood AgarA differential medium used to identify bacteria based on their hemolytic properties. E. faecalis typically shows gamma-hemolysis on this medium, i.e., no hemolysis or change in the color of the medium.
45MacConkey AgarTraditionally used to isolate and differentiate Gram-negative bacilli, E. faecalis can grow on this medium, producing small, round, magenta pink colonies due to lactose fermentation, indicating a positive result.
46Azide Dextrose BrothA selective medium inhibiting Gram-negative bacteria, used for the isolation of streptococci and staphylococci from mixed samples. E. faecalis will show a positive growth resulting in a turbid appearance of the broth.
47Todd-Hewitt BrothA liquid enrichment medium used for the cultivation of fastidious organisms such as streptococci and enterococci. E. faecalis will lead to a turbid broth due to microbial growth.
48Enterococcosel AgarA selective and differential medium that inhibits the growth of Gram-negative bacteria and distinguishes enterococci based on their ability to grow in the presence of bile and hydrolyze esculin. E. faecalis will form small, black colonies on this medium due to esculin hydrolysis.
49Brain-Heart Infusion (BHI) Broth or AgarThis is a nutrient-rich medium that supports the growth of a variety of fastidious organisms, including E. faecalis. The typical phenotype of E. faecalis on BHI is small, round, and white colonies.
50Tryptic Soy Broth or Agar (TSB/TSA)A general-purpose medium that supports the growth of a broad spectrum of bacteria. E. faecalis on TSA will typically form small, round, and white colonies, indicating a positive growth.
1Sf1Ep mediumCulturing Treponema pallidum, the bacteria that causes syphilis, in vitro is a challenge. T. pallidum is not routinely cultured in the laboratory for diagnostic purposes, in part because it cannot be grown on artificial media. However, a breakthrough in culturing T. pallidum was reported in 2018 when researchers managed to grow the bacterium in a rabbit epithelial cell line (Sf1Ep) using a medium called 'Sf1Ep medium'. It's not used for routine diagnostic purposes, but for research only. The diagnosis involves direct microscopic examination, serologic tests, molecular tests and histopathology.
2Baird-Parker Agar (BPA)his is a selective medium for the isolation of Staphylococcus species. It has lithium chloride and glycine to inhibit the growth of Gram-negative bacteria and most Gram-positive bacteria except Staphylococcus. Egg yolk emulsion is added to detect lecithinase production and tellurite reduction. S. aureus colonies on BPA are black due to reduction of tellurite, and they exhibit a clear zone due to lecithinase activity on egg yolk.
3Phenol Red Mannitol BrothThis is a differential medium, used to determine an organism's ability to ferment mannitol. S. aureus, which can ferment mannitol, will change the medium from red to yellow due to acid production.
4Mannitol Salt Agar (MSA), or Chapman AgarThis is a selective and differential medium. The high concentration of NaCl (~7.5%) selects for halophiles, organisms that can tolerate high salt concentrations, thereby favouring the growth of Staphylococcus species. Mannitol is the differential component: S. aureus ferments mannitol, lowering the pH of the medium, which results in a color change of the pH indicator from red to yellow. Thus, growth of S. aureus is indicated by yellow colonies.
5Potato Dextrose Agar (PDA)Potato Dextrose Agar (PDA) consists of a nutrient-rich substrate, made from dehydrated Potato Infusion and Dextrose, ideal for robust mycological propagation. Agar provides the solidifying medium. Acidification, typically using sterile tartaric acid, adjusts the pH to 3.5 +/- 0.1 to create a more selective environment by inhibiting bacterial proliferation. Additionally, Chloramphenicol is incorporated as an antimicrobial agent to further suppress bacterial contamination, thereby facilitating the selective isolation of fungi.
6Blood Agar (BA)This is a nutrient-rich, differential medium that supports the growth of many organisms. S. aureus forms colonies that are round, smooth, and golden-yellow. This bacterium typically demonstrates β-hemolysis, which is complete lysis of red blood cells, resulting in a clear zone around the colonies. This hemolysis is due to the production of hemolysins by S. aureus.
7Blood AgarA differential medium used to identify bacteria based on their hemolytic properties. E. faecalis typically shows gamma-hemolysis on this medium, i.e., no hemolysis or change in the color of the medium.
8Lysine Iron Agar (LIA)Used to determine the ability of an organism to decarboxylate or deaminate lysine and to form hydrogen sulfide. E. coli is typically lysine decarboxylase positive and H2S negative, so you would see a reaction of red/purple slant and purple/red butt with no black precipitate.
9CHROMagar CandidaThis differential medium allows for the isolation and identification of Candida species based on colony color. Candida albicans usually forms green colonies on this medium.
10Azide Dextrose BrothA selective medium inhibiting Gram-negative bacteria, used for the isolation of streptococci and staphylococci from mixed samples. E. faecalis will show a positive growth resulting in a turbid appearance of the broth.
11Mueller Hinton Agar (MHA)Typically used for antibiotic susceptibility testing. E. coli colonies appear pale straw colored.
12BACTECThis is not a traditional medium but a system for detecting the growth of M. tuberculosis by monitoring the release of C14O2 from C14 palmitic acid, which the bacteria metabolize. An increase in radioactive counts in the BACTEC instrument indicates the growth of bacteria.
13MacConkey AgarTraditionally used to isolate and differentiate Gram-negative bacilli, E. faecalis can grow on this medium, producing small, round, magenta pink colonies due to lactose fermentation, indicating a positive result.
14Eosin Methylene Blue (EMB) AgarA selective and differential medium where E. coli forms distinctive metallic green sheen colonies due to vigorous lactose fermentation.
15Sula’s MediumA liquid medium containing glycerol, asparagine, and a variety of salts. The growth of M. tuberculosis results in turbidity.
16DNase Test AgarS. aureus produces the enzyme DNase which hydrolyses DNA. When S. aureus grows on this medium, the DNA is broken down, which can be visualised using a hydrochloric acid (HCl) solution: clear zones around the colonies indicate DNA breakdown.
17Blood Agar (BA)E. coli colonies on this differential medium are large, circular, gray, moist, and can show β-hemolysis.
18Middlebrook 7H11 AgarThis is a nutrient-rich medium similar to 7H10 but includes additional pyruvate for energy source, promoting more luxurious growth. The colonies of M. tuberculosis appear small, slightly domed, and rough with a butyrous consistency.
19Violet Red Bile Agar (VRBA)E. coli colonies are red (pink to red) and may show bluish fluorescence under UV light.
20Todd-Hewitt BrothA liquid enrichment medium used for the cultivation of fastidious organisms such as streptococci and enterococci. E. faecalis will lead to a turbid broth due to microbial growth.
21Enterococcosel AgarA selective and differential medium that inhibits the growth of Gram-negative bacteria and distinguishes enterococci based on their ability to grow in the presence of bile and hydrolyze esculin. E. faecalis will form small, black colonies on this medium due to esculin hydrolysis.
22Sauton’s MediumA liquid medium that lacks detergents, which helps in the formation of corded colonies. When M. tuberculosis grows in this medium, it results in turbidity.
23Cystine Lactose Electrolyte-Deficient (CLED) AgarE. coli will give lactose-positive yellow colonies.
24Tryptic Soy Agar (TSA)A general purpose medium. E. coli colonies are medium to large, with a shiny moist appearance.
25Nutrient Agar (NA)A non-selective medium. E. coli colonies are usually large, circular, grayish-white, moist, and smooth.
26Tryptic Soy Broth or Agar (TSB/TSA)A general-purpose medium that supports the growth of a broad spectrum of bacteria. E. faecalis on TSA will typically form small, round, and white colonies, indicating a positive growth.
27Brain-Heart Infusion (BHI) Broth or AgarThis is a nutrient-rich medium that supports the growth of a variety of fastidious organisms, including E. faecalis. The typical phenotype of E. faecalis on BHI is small, round, and white colonies.
28Tarshis MediumA blood-based medium that can promote the growth of M. tuberculosis. The colonies appear similar to those on the LJ Medium.
29m-ENDO AgarE. coli colonies appear as green with a metallic sheen, indicating lactose fermentation.
30Proskauer and Beck’s MediumA liquid medium. The growth of M. tuberculosis causes turbidity.
31Lowenstein-Jensen (LJ) MediumAn egg-based medium that uses malachite green to suppress the growth of other bacteria and glycerol to stimulate the growth of Mycobacterium tuberculosis. The colonies of M. tuberculosis on LJ are non-pigmented, dry, rough, raised, irregular with a wrinkled surface, initially creamy-white, turning yellowish or buff-colored on further incubation.
32Middlebrook 7H10 AgarA selective medium that contains oleic acid, albumin, dextrose, and catalase. The colonies of M. tuberculosis appear small, rough, and buff to white-colored, taking less time to appear compared to egg-based media.
33Nutrient AgarIt is a general-purpose medium. However, E. faecalis grows poorly on nutrient agar, which means it does not proliferate as well on this medium compared to the others listed, indicating a negative or poor growth.
34Loeffler MediumA serum-based medium. M. tuberculosis colonies on Loeffler medium are small, dry, wrinkled, and off-white to yellow.
35MacConkey Agar (MAC)This selective and differential medium distinguishes lactose fermenters from non-fermenters. E. coli colonies are circular, moist, smooth, and pink.
36Brilliant Green Agar (BGA)A selective medium that is used to isolate Salmonella species, but E. coli can grow on it, albeit not as well.
37Dorset MediumAn egg-based medium. M. tuberculosis colonies appear similar to those on Petragnini Medium: small, round, buff-colored, and taking 3-4 weeks to develop.
38Cornmeal Agar with Tween 80It is used for the identification of Candida species by promoting the formation of chlamydospores, which is a characteristic of Candida albicans.
39Liquid Media (such as Nutrient Broth)E. coli exhibits homogenous turbid growth within 12-18 hours. After prolonged incubation, pellicles may form on the surface of the media.
40Simmons Citrate AgarUsed for citrate utilization testing. E. coli usually can't utilize citrate as a sole carbon source, so no growth or color change would be expected.
41Urea Agar/BrothE. coli is typically urease negative, so no color change would be expected in this medium.
42Dubos’ MediumA liquid medium that contains a mixture of salts, fatty acids, and polysorbate. When M. tuberculosis grows in this medium, it causes the medium to become turbid.
43Sorbitol-MacConkey agarA variant of MacConkey agar, used in detecting E. coli O157:H7, which does not ferment sorbitol, unlike most strains of E. coli.
44Sabouraud Dextrose Agar (SDA)It is composed of peptone, dextrose (glucose), and agar. The high dextrose concentration promotes fungal growth, while the acidic pH inhibits bacterial growth.
45Middlebrook 7H9 BrothThis is a liquid medium that contains glycerol and Tween 80, which prevent clumping of mycobacteria. The growth of M. tuberculosis results in turbidity.
46Triple Sugar Iron (TSI) AgarE. coli typically produces an acid butt, acid slant, and gas, with no H2S production, indicating it ferments lactose, sucrose, and glucose.