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.
2Phenol 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.
3Mannitol 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.
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.
5Sauton’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.
6Sula’s MediumA liquid medium containing glycerol, asparagine, and a variety of salts. The growth of M. tuberculosis results in turbidity.
7Middlebrook 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.
8Dubos’ 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.
9Pawlowsky MediumA potato-based medium. Growth of M. tuberculosis may be similar to that seen on the LJ Medium.
10Dorset 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.
11Middlebrook 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.
12Middlebrook 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.
13Petragnini 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.
14Liquid 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.
15Brilliant Green Agar (BGA)A selective medium that is used to isolate Salmonella species, but E. coli can grow on it, albeit not as well.
16Sorbitol-MacConkey agarA variant of MacConkey agar, used in detecting E. coli O157:H7, which does not ferment sorbitol, unlike most strains of E. coli.
17Urea Agar/BrothE. coli is typically urease negative, so no color change would be expected in this medium.
18Simmons 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.
19Tryptic Soy Agar (TSA)A general purpose medium. E. coli colonies are medium to large, with a shiny moist appearance.
20Cystine Lactose Electrolyte-Deficient (CLED) AgarE. coli will give lactose-positive yellow colonies.
21Violet Red Bile Agar (VRBA)E. coli colonies are red (pink to red) and may show bluish fluorescence under UV light.
22Eosin Methylene Blue (EMB) AgarA selective and differential medium where E. coli forms distinctive metallic green sheen colonies due to vigorous lactose fermentation.
23Mueller Hinton Agar (MHA)Typically used for antibiotic susceptibility testing. E. coli colonies appear pale straw colored.
24MacConkey Agar (MAC)This selective and differential medium distinguishes lactose fermenters from non-fermenters. E. coli colonies are circular, moist, smooth, and pink.
25Blood Agar (BA)E. coli colonies on this differential medium are large, circular, gray, moist, and can show β-hemolysis.
26Nutrient Agar (NA)A non-selective medium. E. coli colonies are usually large, circular, grayish-white, moist, and smooth.
27Nickerson’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.
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.
29CHROMagar 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.
30RPMI 1640 MediumIt is a rich medium that contains inorganic salts, glucose, amino acids, vitamins, and other nutrients that promote the growth of yeast cells.
31MacConkey 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.
32Azide 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.
33Todd-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.
34Enterococcosel 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.
35Bile 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
36Tryptic 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.
2DNase 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.
3Mannitol 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.
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.
5Sauton’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.
6BACTECThis 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.
7Sula’s MediumA liquid medium containing glycerol, asparagine, and a variety of salts. The growth of M. tuberculosis results in turbidity.
8Dubos’ 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.
9Loeffler MediumA serum-based medium. M. tuberculosis colonies on Loeffler medium are small, dry, wrinkled, and off-white to yellow.
10Dorset 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.
11Middlebrook 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.
12Middlebrook 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.
13Lowenstein-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.
14Lysine 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.
15Brilliant Green Agar (BGA)A selective medium that is used to isolate Salmonella species, but E. coli can grow on it, albeit not as well.
16Sorbitol-MacConkey agarA variant of MacConkey agar, used in detecting E. coli O157:H7, which does not ferment sorbitol, unlike most strains of E. coli.
17Triple 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.
18Simmons 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.
19Tryptic Soy Agar (TSA)A general purpose medium. E. coli colonies are medium to large, with a shiny moist appearance.
20Cystine Lactose Electrolyte-Deficient (CLED) AgarE. coli will give lactose-positive yellow colonies.
21Violet Red Bile Agar (VRBA)E. coli colonies are red (pink to red) and may show bluish fluorescence under UV light.
22m-ENDO AgarE. coli colonies appear as green with a metallic sheen, indicating lactose fermentation.
23Eosin Methylene Blue (EMB) AgarA selective and differential medium where E. coli forms distinctive metallic green sheen colonies due to vigorous lactose fermentation.
24Mueller Hinton Agar (MHA)Typically used for antibiotic susceptibility testing. E. coli colonies appear pale straw colored.
25MacConkey Agar (MAC)This selective and differential medium distinguishes lactose fermenters from non-fermenters. E. coli colonies are circular, moist, smooth, and pink.
26Blood Agar (BA)E. coli colonies on this differential medium are large, circular, gray, moist, and can show β-hemolysis.
27Nickerson’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.
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.
29CHROMagar 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.
30RPMI 1640 MediumIt is a rich medium that contains inorganic salts, glucose, amino acids, vitamins, and other nutrients that promote the growth of yeast cells.
31Potato 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.
32Sabouraud 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.
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.
34Blood 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.
35MacConkey 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.
36Azide 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.
37Todd-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.
38Enterococcosel 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.
39Bile 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
40Brain-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.
41Tryptic 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.
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.
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.
11Dubos’ 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.
12Pawlowsky MediumA potato-based medium. Growth of M. tuberculosis may be similar to that seen on the LJ Medium.
13Loeffler MediumA serum-based medium. M. tuberculosis colonies on Loeffler medium are small, dry, wrinkled, and off-white to yellow.
14Tarshis MediumA blood-based medium that can promote the growth of M. tuberculosis. The colonies appear similar to those on the LJ Medium.
15Dorset 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.
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.
27Cystine Lactose Electrolyte-Deficient (CLED) AgarE. coli will give lactose-positive yellow colonies.
28Violet Red Bile Agar (VRBA)E. coli colonies are red (pink to red) and may show bluish fluorescence under UV light.
29m-ENDO AgarE. coli colonies appear as green with a metallic sheen, indicating lactose fermentation.
30Eosin Methylene Blue (EMB) AgarA selective and differential medium where E. coli forms distinctive metallic green sheen colonies due to vigorous lactose fermentation.
31Mueller Hinton Agar (MHA)Typically used for antibiotic susceptibility testing. E. coli colonies appear pale straw colored.
32MacConkey Agar (MAC)This selective and differential medium distinguishes lactose fermenters from non-fermenters. E. coli colonies are circular, moist, smooth, and pink.
33Blood Agar (BA)E. coli colonies on this differential medium are large, circular, gray, moist, and can show β-hemolysis.
34Nutrient Agar (NA)A non-selective medium. E. coli colonies are usually large, circular, grayish-white, moist, and smooth.
35Nickerson’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.
36Cornmeal 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.
37CHROMagar 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.
38RPMI 1640 MediumIt is a rich medium that contains inorganic salts, glucose, amino acids, vitamins, and other nutrients that promote the growth of yeast cells.
39Potato 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.
40Sabouraud 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.
41Nutrient 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.
42Blood 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.
43MacConkey 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.
44Azide 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.
45Todd-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.
46Enterococcosel 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.
47Bile 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
48Brain-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.
49Tryptic 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.
2Mannitol 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.
3Blood 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.
4Sauton’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.
5BACTECThis 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.
6Sula’s MediumA liquid medium containing glycerol, asparagine, and a variety of salts. The growth of M. tuberculosis results in turbidity.
7Proskauer and Beck’s MediumA liquid medium. The growth of M. tuberculosis causes turbidity.
8Middlebrook 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.
9Pawlowsky MediumA potato-based medium. Growth of M. tuberculosis may be similar to that seen on the LJ Medium.
10Tarshis MediumA blood-based medium that can promote the growth of M. tuberculosis. The colonies appear similar to those on the LJ Medium.
11Dorset 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.
12Middlebrook 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.
13Petragnini 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.
14Lowenstein-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.
15Liquid 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.
16Lysine 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.
17Brilliant Green Agar (BGA)A selective medium that is used to isolate Salmonella species, but E. coli can grow on it, albeit not as well.
18Sorbitol-MacConkey agarA variant of MacConkey agar, used in detecting E. coli O157:H7, which does not ferment sorbitol, unlike most strains of E. coli.
19Urea Agar/BrothE. coli is typically urease negative, so no color change would be expected in this medium.
20Triple 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.
21Simmons 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.
22Tryptic Soy Agar (TSA)A general purpose medium. E. coli colonies are medium to large, with a shiny moist appearance.
23Cystine Lactose Electrolyte-Deficient (CLED) AgarE. coli will give lactose-positive yellow colonies.
24Violet Red Bile Agar (VRBA)E. coli colonies are red (pink to red) and may show bluish fluorescence under UV light.
25Eosin Methylene Blue (EMB) AgarA selective and differential medium where E. coli forms distinctive metallic green sheen colonies due to vigorous lactose fermentation.
26Mueller Hinton Agar (MHA)Typically used for antibiotic susceptibility testing. E. coli colonies appear pale straw colored.
27MacConkey Agar (MAC)This selective and differential medium distinguishes lactose fermenters from non-fermenters. E. coli colonies are circular, moist, smooth, and pink.
28Blood Agar (BA)E. coli colonies on this differential medium are large, circular, gray, moist, and can show β-hemolysis.
29Nutrient Agar (NA)A non-selective medium. E. coli colonies are usually large, circular, grayish-white, moist, and smooth.
30Nickerson’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.
31Cornmeal 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.
32CHROMagar 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.
33RPMI 1640 MediumIt is a rich medium that contains inorganic salts, glucose, amino acids, vitamins, and other nutrients that promote the growth of yeast cells.
34Potato 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.
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.
36Nutrient 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.
37Blood 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.
38MacConkey 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.
39Azide 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.
40Todd-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.
41Enterococcosel 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.
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.
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.
2Phenol 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.
3DNase 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.
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.
5BACTECThis 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.
6Sula’s MediumA liquid medium containing glycerol, asparagine, and a variety of salts. The growth of M. tuberculosis results in turbidity.
7Proskauer and Beck’s MediumA liquid medium. The growth of M. tuberculosis causes turbidity.
8Dubos’ 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.
9Loeffler MediumA serum-based medium. M. tuberculosis colonies on Loeffler medium are small, dry, wrinkled, and off-white to yellow.
10Dorset 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.
11Middlebrook 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.
12Petragnini 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.
13Liquid 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.
14Brilliant Green Agar (BGA)A selective medium that is used to isolate Salmonella species, but E. coli can grow on it, albeit not as well.
15Urea Agar/BrothE. coli is typically urease negative, so no color change would be expected in this medium.
16Tryptic Soy Agar (TSA)A general purpose medium. E. coli colonies are medium to large, with a shiny moist appearance.
17Cystine Lactose Electrolyte-Deficient (CLED) AgarE. coli will give lactose-positive yellow colonies.
18m-ENDO AgarE. coli colonies appear as green with a metallic sheen, indicating lactose fermentation.
19Eosin Methylene Blue (EMB) AgarA selective and differential medium where E. coli forms distinctive metallic green sheen colonies due to vigorous lactose fermentation.
20Mueller Hinton Agar (MHA)Typically used for antibiotic susceptibility testing. E. coli colonies appear pale straw colored.
21Cornmeal 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.
22CHROMagar 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.
23RPMI 1640 MediumIt is a rich medium that contains inorganic salts, glucose, amino acids, vitamins, and other nutrients that promote the growth of yeast cells.
24Potato 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.
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.
27MacConkey 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.
28Azide 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.
29Todd-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.
30Enterococcosel 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.
31Bile 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
32Tryptic 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.
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.
2Phenol 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.
3DNase 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.
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.
5Blood 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.
6BACTECThis 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.
7Sula’s MediumA liquid medium containing glycerol, asparagine, and a variety of salts. The growth of M. tuberculosis results in turbidity.
8Dubos’ 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.
9Pawlowsky MediumA potato-based medium. Growth of M. tuberculosis may be similar to that seen on the LJ Medium.
10Loeffler MediumA serum-based medium. M. tuberculosis colonies on Loeffler medium are small, dry, wrinkled, and off-white to yellow.
11Tarshis MediumA blood-based medium that can promote the growth of M. tuberculosis. The colonies appear similar to those on the LJ Medium.
12Dorset 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.
13Middlebrook 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.
14Middlebrook 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.
15Liquid 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.
16Brilliant Green Agar (BGA)A selective medium that is used to isolate Salmonella species, but E. coli can grow on it, albeit not as well.
17Sorbitol-MacConkey agarA variant of MacConkey agar, used in detecting E. coli O157:H7, which does not ferment sorbitol, unlike most strains of E. coli.
18Urea Agar/BrothE. coli is typically urease negative, so no color change would be expected in this medium.
19Triple 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.
20Tryptic Soy Agar (TSA)A general purpose medium. E. coli colonies are medium to large, with a shiny moist appearance.
21Cystine Lactose Electrolyte-Deficient (CLED) AgarE. coli will give lactose-positive yellow colonies.
22Violet Red Bile Agar (VRBA)E. coli colonies are red (pink to red) and may show bluish fluorescence under UV light.
23Mueller Hinton Agar (MHA)Typically used for antibiotic susceptibility testing. E. coli colonies appear pale straw colored.
24MacConkey Agar (MAC)This selective and differential medium distinguishes lactose fermenters from non-fermenters. E. coli colonies are circular, moist, smooth, and pink.
25Nutrient Agar (NA)A non-selective medium. E. coli colonies are usually large, circular, grayish-white, moist, and smooth.
26Cornmeal 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.
27CHROMagar 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.
28RPMI 1640 MediumIt is a rich medium that contains inorganic salts, glucose, amino acids, vitamins, and other nutrients that promote the growth of yeast cells.
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.
30Sabouraud 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.
31Nutrient 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.
32Blood 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.
33MacConkey 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.
34Azide 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.
35Todd-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.
36Enterococcosel 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.
37Bile 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
38Brain-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.
39Tryptic 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.
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.
14Tarshis MediumA blood-based medium that can promote the growth of M. tuberculosis. The colonies appear similar to those on the LJ Medium.
15Dorset 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.
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.
25Tryptic Soy Agar (TSA)A general purpose medium. E. coli colonies are medium to large, with a shiny moist appearance.
26Cystine Lactose Electrolyte-Deficient (CLED) AgarE. coli will give lactose-positive yellow colonies.
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.
30Mueller Hinton Agar (MHA)Typically used for antibiotic susceptibility testing. E. coli colonies appear pale straw colored.
31MacConkey Agar (MAC)This selective and differential medium distinguishes lactose fermenters from non-fermenters. E. coli colonies are circular, moist, smooth, and pink.
32Blood Agar (BA)E. coli colonies on this differential medium are large, circular, gray, moist, and can show β-hemolysis.
33Nutrient Agar (NA)A non-selective medium. E. coli colonies are usually large, circular, grayish-white, moist, and smooth.
34Nickerson’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.
35Cornmeal 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.
36CHROMagar 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.
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.
39Nutrient 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.
40Blood 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.
41MacConkey 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.
42Azide 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.
43Todd-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.
44Enterococcosel 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.
45Bile 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
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.