Löwenstein–Jensen medium explained

Löwenstein–Jensen medium
Löwenstein-Jensen agar
Acronym:LJ medium
Uses:Culturing
Related:Petri dish
Growth medium

Löwenstein–Jensen medium, more commonly known as LJ medium, is a growth medium[1] specially used for culture of Mycobacterium species, notably Mycobacterium tuberculosis.

When grown on LJ medium, M. tuberculosis appears as brown, granular colonies (sometimes called "buff, rough and tough"). The medium must be incubated for a significant length of time, usually four weeks, due to the slow doubling time of M. tuberculosis (15–20 hours) compared with other bacteria.

The medium is named after the Austrian pathologist Ernst Löwenstein (1878–1950) and the Danish medical doctor Kai Adolf Jensen (16.7.1894-2.5.1971).[2]

Composition

The usual composition[3] as applicable to M. tuberculosis is:

The original formulation included starch, which was later found to be unnecessary, so omitted.

Low levels of penicillin and nalidixic acid are also present in LJ medium to inhibit growth of Gram-positive and Gram-negative bacteria, to limit growth to Mycobacterium species only. Presence of malachite green in the medium inhibits most other bacteria. It is disinfected and solidified by a process of inspissation. Presence of glycerol enhances the growth of M. tuberculosis.

If the slopes are made on test tubes, they must be stored in cold and used within a month.

For cultivation of M. bovis, glycerol is omitted and sodium pyruvate is added.

The medium appears green, opaque, and opalescent.

Uses

Mycobacterium tuberculosisMycobacterium bovis
Eugonic, rough tough and buffDysgonic
AerobicMicroaerophillic
Glycerol enhancement +Glycerol enhancement -
Pyruvate enhancement +Pyruvate enhancement -
Niacin production +Niacin production -

Alternatives

Alternative culture media

While LJ medium is the most popular means of culturing mycobacteria, as recommended by the International Union against Tuberculosis, several alternative media have been investigated.[4]

Solid media

Liquid media

Rapid detection techniques

The chief limitation of culture-based techniques is the time it takes to culture positivity, which can be several months. Several new molecular technologies have emerged in recent years to secure more speedy confirmation of diagnosis.

See also

Notes and References

  1. Elbir H, Abdel-Muhsin AM, Babiker A . A one-step DNA PCR-based method for the detection of Mycobacterium tuberculosis complex grown on Löwenstein–Jensen media . Am. J. Trop. Med. Hyg. . 78 . 2 . 316–7 . February 2008 . 18256436 . 10.4269/ajtmh.2008.78.316. free .
  2. Web site: Smith . Kenneth . How TB Diagnostics Have Evolved Since the Second Century . American Society for Microbiology . June 8, 2021 . March 22, 2021.
  3. https://web.archive.org/web/20160314101809/http://www.bd.com/ds/technicalCenter/inserts/L007464(11).pdf#page=3&view=Fit
  4. https://books.google.com/books?id=qCqBAYajT1EC&pg=PA352 Textbook of Microbiology by Ananthanarayan and Panicker, Sixth Edition
  5. Martin. R. S.. Sumarah. R. K.. Robart. E. M.. November 1975. Comparison of Four Culture Media for the Isolation of Mycobacterium Tuberculosis: a 2-Year Study. Journal of Clinical Microbiology. 2. 5. 438–440. 10.1128/jcm.2.5.438-440.1975 . 811686 . 274204 .