Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2011 Apr;49(4):1458-63.
doi: 10.1128/JCM.02301-10. Epub 2011 Jan 26.

Development of a selective culture medium for primary isolation of the main Brucella species

Affiliations

Development of a selective culture medium for primary isolation of the main Brucella species

M J De Miguel et al. J Clin Microbiol. 2011 Apr.

Abstract

Bacteriological diagnosis of brucellosis is performed by culturing animal samples directly on both Farrell medium (FM) and modified Thayer-Martin medium (mTM). However, despite inhibiting most contaminating microorganisms, FM also inhibits the growth of Brucella ovis and some B. melitensis and B. abortus strains. In contrast, mTM is adequate for growth of all Brucella species but only partially inhibitory for contaminants. Moreover, the performance of both culture media for isolating B. suis has never been established properly. We first determined the performance of both media for B. suis isolation, proving that FM significantly inhibits B. suis growth. We also determined the susceptibility of B. suis to the antibiotics contained in both selective media, proving that nalidixic acid and bacitracin are highly inhibitory, thus explaining the reduced performance of FM for B. suis isolation. Based on these results, a new selective medium (CITA) containing vancomycin, colistin, nystatin, nitrofurantoin, and amphotericin B was tested for isolation of the main Brucella species, including B. suis. CITA's performance was evaluated using reference contaminant strains but also field samples taken from brucella-infected animals or animals suspected of infection. CITA inhibited most contaminant microorganisms but allowed the growth of all Brucella species, to levels similar to those for both the control medium without antibiotics and mTM. Moreover, CITA medium was more sensitive than both mTM and FM for isolating all Brucella species from field samples. Altogether, these results demonstrate the adequate performance of CITA medium for the primary isolation of the main Brucella species, including B. suis.

PubMed Disclaimer

Figures

Fig. 1.
Fig. 1.
Growth (number of CFU/plate) of representative Brucella species (see Table 1 for descriptions) on BAB-CS and three selective culture media: mTM (15), FM (15), and CITA (the new selective medium developed in this work). Statistical comparisons of means (numbers of CFU/plate) obtained for a given Brucella sp. for the different culture media were performed by Fisher's PLSD test. *, P < 0.0001 between FM and any other culture medium.

References

    1. Alton G. G., Jones L. M., Angus R. D., Verger J. M. 1988. Techniques for the brucellosis laboratory. INRA, Paris, France
    1. Barrio M. B., et al. 2009. Rough mutants defective in core and O-polysaccharide synthesis and export induce antibodies reacting in an indirect ELISA with smooth lipopolysaccharide and are less effective than Rev 1 vaccine against Brucella melitensis infection of sheep. Vaccine 27:1741–1749 - PubMed
    1. Brown G. M., Ranger C. R., Kelley D. J. 1971. Selective media for the isolation of Brucella ovis. Cornell Vet. 61:265–280 - PubMed
    1. Drancourt M., Raoult D. 2007. Cost-effectiveness of blood agar for isolation of Mycobacteria. PLoS Negl. Trop. Dis. 1:e83. - PMC - PubMed
    1. Ewalt D. R., Packer R. A., Harris S. K. 1983. An improved selective medium for isolating Brucella sp. from bovine milk, p. 577–589 In Proceedings of the Third International Symposium of the World Association of Veterinary Laboratory Diagnosticians College of Veterinary Medicine, Iowa State University, Ames, IA

Publication types

LinkOut - more resources