Pseudomonas Media and Tests

Jvo Siegrist

Analytix Volume 2007 Article 5

ivo.siegrist@sial.com

Detection, Identification, Differentiation, and Cultivation of Pseudomonas Species

HiFluoro Pseudomonas Agar under UV light

Figure 1.HiFluoro Pseudomonas Agar under UV light

Pseudomonas are motile (one or more polar flagella), rod shaped, and aerobe Gram-negative bacteria. They are found almost everywhere: in soil, water, plants, and animals. In most cases, it is not pathogenic and, in fact, can be beneficial. For example, P. putida is used as a bio-scrubber to aid in the biodegradation of diverse organic compounds in polluted air and waste water. However, P. aeruginosa is an infamous opportunistic human pathogen most commonly affecting immuno-compromised patients. Along with P. maltophilia, it accounts for the majority of human infections. Pathogenic Pseudomonas are found throughout the body, most commonly in the urinary tract, respiratory tract, blood, and wounds.

Rugged and opportunistic, Pseudomonas use a wide range of nutritional sources, even very simple nutritional environments without any organic compounds. They can remain viable for long periods of time in many different habitats and under very adverse conditions. They are also widespread, being found in water, saline solutions, utensils and even in cosmetics, pharmaceuticals, and disinfectants as well as many natural and manufactured foods. Psychrotrophic (cold-tolerant) Pseudomonas species are a significant food spoilage problem in refrigerated meat, fish, shell fish and dairy products. Because Pseudomonas thrive in water systems, they can be the source of contamination in the food and beverage industry.

Pseudomonas are not generally fastidious microorganisms. They can grow on very simple media like Kind Agar, for example, which contains a protein hydrolysate, magnesium chloride, potassium sulphate, and agar. Analytical microbiology leverages a microbe's unique biochemistry to aid in its identification. For example, selective Pseudomonas media use cetrimide, nalidixic acid, cephaloridine, penicillin G, pimaricin, malachite green, and other inhibitory agents. The proteolytic activity, lipolytic activity, fluorescent pigment formation, nitrate utilisation, glutamate utilisation, hemolytic reaction, and other biochemical reactions are used in the media for the identification and differentiation of Pseudomonas species.

Pseudomonas gives negative Voges Proskauer, indole and methyl red tests, but a positive catalase test. While some species show a negative reaction in the oxidase test, most species, including P. fluorescens, give a positive result (Figure 2). Another feature associated with Pseudomonas is the secretion of pyoverdin (fluorescein, a siderophore), a fluorescent yellow-green pigment under iron-limiting conditions. Certain Pseudomonas species may also produce additional pigments, such as pyocyanin (blue pigment, a siderophore) by P. aeruginosa, quinolobactin (yellow, dark green in presence of iron, a siderophore) by P. fluorescens, a reddish pigment called pyorubrin and pyomelanin (brown pigment). On blood agar a hemolytic reaction can be observed.

Oxidase test

Figure 2.Oxidase test

Pseudomonas utilizes sugars as an energy source by using the Entner-Doudoroff pathway with pyruvate as the end product (dissimilation). The reaction utilizes a different set of enzymes from those used in glycolysis and the pentose phosphate pathway. Fermentation catabolism is not observed in Pseudomonas, but some species, like P. aeruginosa, P. stutzeri and P. denitrificans, are able to use nitrate as an electron acceptor instead of oxygen. Growth can also occur under anaerobic conditions when the denitrification pathway is used. We supply a wide array of products for the detection, identification, differentiation, enumeration and cultivation of Pseudomonas, using its biochemical characteristics, including Gram staining kit, and many types of selective growth media and diagnostic tests.

Non-selective broths
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Table 1Media for Pseudomonas
Table 2Test for identification and differentiation of Pseudomonas

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