BioMed Research International

Volume 2014 (2014), Article ID 702072, 3 pages

http://dx.doi.org/10.1155/2014/702072

Research Article

Evaluation of Three Formulations of Culture Media for Isolation of Brucella spp. regarding Their Ability to Inhibit the Growth of Contaminating Organisms

Acácia F. Vicente, João M. A. P. Antunes, Gustavo H. B. Lara, Mateus S. R. Mioni, Susan D. Allendorf, Marina G. Peres, Camila M. Appolinário, Fernando J. P. Listoni, Marcio G. Ribeiro, and Jane Megid

Departamento de Higiene Veterinária e Saúde Pública (DHVSP), Faculdade de Medicina Veterinária e Zootecnia (FMVZ), Universidade Estadual Paulista (UNESP), 18618-970 Botucatu, SP , Brazil

Received 14 October 2013; Revised 14 January 2014; Accepted 27 January 2014; Published 10 April 2014

Academic Editor: Klaus P. Hunfeld

Copyright © 2014 Acácia F. Vicente et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Three culture media (Brucella agar, Farrell medium, and CITA) were compared for their effectiveness in inhibiting contamination and for isolating Brucella spp. One hundred lymph nodes from pigs (n = 50) and wild boars (n = 50) with lymphadenitis were collected in slaughterhouses in the State of São Paulo and were assessed on these three selective media for Brucella spp. All of the samples were negative for Brucella spp. on the three culture media. On the agar medium, fungal (70 plates) and Gram-positive bacterial (59 plates) contaminants were observed; in the CITA medium, the absence of fungal and Gram-positive bacteria on 15 plates was observed; no bacterial or fungal growth was observed on the Farrell media. The results demonstrated that the CITA and Farrell media inhibited the growth of contaminants better than the Brucella agar.

1. Introduction

Brucella is a genus of Gram-negative, facultative intracellular bacteria that do not multiply in the environment and are usually transmitted directly between hosts. These microorganisms are responsible for causing diseases with variable clinical signs, depending on the host and the Brucella species. Most Brucella spp. are zoonotic and widely distributed in the world [1]. According to the International Committee on Taxonomy Bacteria [2], the genus has six classic species: B. abortus, B. melitensis, B. suis, B. canis, B. ovis, and B. neotomae. This classification is primarily based on the pathogenic differences, preference for hosts, and phenotypic characteristics. Recently, the marine species B. ceti, B. pinnipedialis, B. microti, and B. inopinata were included in the genus.

B. suis has five biovars, of which 1, 2, and 3 mainly affect swine [3]. After infecting an animal, the bacteria pass through the respiratory, digestive, or genital mucosa, undergo phagocytosis, and reach local lymph nodes [1]. In swine, bacteremia occurs intermittently for several weeks. The bacteria settle mainly in the mandibular, gastrohepatic, internal iliac, and retropharyngeal ganglia as well as in the liver, kidneys, joints, and reproductive organs [4]. Among the clinical signs are abortion and infertility in females and orchitis in males. Occasionally, arthritis, laminitis, and abscesses of different sizes in organs and tissues may occur [5].

Lymphadenitis is one of the main diseases of swine in Brazil and causes significant economic loss due to the condemnation of affected organs and carcasses [6].

B. abortus and B. melitensis may infect swine, although B. suis is the most common pathogenic species in swine [7].

In affected swine, Brucella spp. may be isolated from vaginal discharge, placenta, fetus, and semen. After a necropsy, Brucella may be isolated from lymph nodes, liver, spleen, mammary glands, epididymis, and prostate [8].

The “gold standard” for the diagnosis of brucellosis is bacterial isolation. The OIE (Office International des Epizooties) [7] recommends the simultaneous use of selective media, including Farrell and modified Thayer-Martin media, for the primary isolation of Brucella species from animal samples. The Farrell selective medium inhibits the growth of most contaminants and is probably the most selective medium used for bacteriological diagnosis in laboratories worldwide. However, some antimicrobials present in this formulation inhibit the growth of some Brucella species. Modified Thayer-Martin medium shows greater sensitivity than Farrell medium; however, it does not inhibit contaminating microorganisms as well. For this reason, CITA medium was developed based on modified Thayer-Martin medium with different concentrations of antimicrobials and with the addition of Amphotericin B to inhibit contaminants without inhibiting the growth of Brucella spp. [8]. Brucella agar medium is widely used in laboratories to diagnose brucellosis in Brazil and was used for the isolation of B. suis during an outbreak [9].

This study aimed to evaluate three selective culture media for Brucella spp. (Brucella agar, Farrell media, and CITA) to investigate the presence of Brucella spp. in the lymph nodes of pigs and wild boar, from slaughterhouses of the São Paulo state, Brazil, with lymphadenitis.

2. Materials and Methods

Brucella agar medium was prepared using Brucella medium base (OXOID) supplemented with 5% fetal bovine serum (Invitrogen). The same Brucella medium base was also supplemented with Farrell antimicrobials (OXOID) and 5% fetal bovine serum (Farrell medium). CITA medium was prepared using Blood Agar Base No. 2 (OXOID) supplemented with the following antimicrobials: vancomycin, colistin, nystatin, nitrofurantoin, and Amphotericin B (Sigma) and 5% fetal bovine serum. The proportions of the antimicrobials used were followed according to [8].

Lymph nodes from Brucella-negative pigs were macerated in a 1 : 10 dilution with buffered saline solution and subsequently used as negative controls. As a positive microbiological control to evaluate the culture media, these negative lymph nodes were macerated and contaminated with B. canis, B. ovis, B. abortus, B. abortus B19, and B. abortus Rb51. For the contaminations, Brucella canis, Brucella ovis, and Brucella abortus species were diluted to scale 1 of the McFarland standards, and the initial concentrations of B. abortus B19 (Biovet) and B. abortus Rb51 (Intervet-Shering-Plough Animal Health) were the recommended dilutions for the vaccines used. The initial bacterial suspensions were diluted 1 : 10 with TE buffer and used for lymph node contamination. A total of 180 μL of the macerated lymph node with 20 μL of each bacterial suspension was uniformly distributed on each plate using a Drigalski spatula.

In addition, 100 lymph nodes, 50 from pigs and 50 from wild boar with lymphadenitis, were collected in slaughterhouses in the state of São Paulo, Brazil. In the laboratory, these lymph nodes were macerated in a 1 : 10 dilution with sterile saline solution for microbiological analysis.

For this analysis, three different culture media were used: Brucella agar, Farrell medium, and CITA medium. For the controls and for the samples, two plates of each medium were used; one plate was maintained at 37°C in a normal atmosphere and another plate was maintained at 37°C with 10% CO₂ and high humidity. The plates were observed daily and considered negative if there was no bacterial growth by the 14th day. Colonies that grew on the plates were evaluated by morphology, growth period, and Gram staining [10].

3. Results and Discussion

The growth of B. canis, B. ovis, B. abortus, B. abortus B19, and B. abortus Rb51 was observed in the 10 plates of Brucella agar medium plated with lymph nodes contaminated with the different Brucella spp. (controls). In 6 of these plates, fungal growth was observed, demonstrating a lack of inhibition of fungal contamination. The results of the analyzed lymph nodes (100 lymph nodes corresponding to 200 plates) showed 70 plates with fungal growth on Brucella agar medium, 39 from pigs and 31 from wild boar. The growth of these microorganisms is due to the absence of the antimycotic cycloheximide, which is present in the Farrell supplement and inhibits the translation of mRNA by ribosomes, preventing fungal protein synthesis [8]. Fungal growth may also inhibit bacterial growth, leading to a reduction in the sensitivity of the bacteriological diagnosis [11]. Therefore, selective culture medium is recommended for the isolation of Brucella spp. from contaminated materials. On the same medium, there was bacterial growth from 29 swine lymph nodes (6 with CO₂, 6 without CO₂ and 17 in both conditions of culture) and in 30 plates of wild boar samples (5 with CO₂, 7 without CO₂, and 18 in both conditions of culture). For these cultured bacteria, Gram staining and biochemical differentiation tests were performed. All of the samples contained Gram-positive bacteria, including Mycobacterium spp., Rhodococcus equi, and Streptococcus spp. [12].

The controls of Brucella spp. also grew properly in CITA medium. However, in this medium no fungal growth was observed. The same result was also observed in the field samples. This result is due to the addition of the antimicrobial amphotericin B, which interacts with a steroid present in the membrane of the fungus and causes the loss of selective permeability of the membrane and cytoplasmic components [8]. On 11 plates of pig lymph nodes (2 with CO₂, 3 without CO₂, and 6 in both conditions of culture) and on 4 plates of wild boar lymph nodes (3 with CO₂ and 1 without CO₂), Gram-positive bacteria were observed on this medium because the antimicrobials present did not inhibit bacterial growth, with the exception of Mycoplasma species [8].

In the control material contaminated with Brucella spp., only the growth of B. ovis was inhibited on Farrell medium. The growth of the other species of Brucella and the absence of contaminants on the plates were verified. There was no bacterial or fungal growth on any of the plates cultured with material from the lymph nodes of pigs or wild boar. Farrell medium prevents the growth of fungal and commensal bacteria that commonly contaminate samples during collection and the Gram-positive bacteria that grow on Brucella agar and CITA medium. This is the best medium for inhibiting the growth of contaminants. However, some antimicrobials present in its formulation also inhibit the growth of B. ovis and make it difficult to grow B. melitensis, B. suis, and some strains of B. abortus [13]. In the case of B. melitensis, B. abortus, and B. suis, the inhibition is most likely due to high concentrations of nalidixic acid and bacitracin [11, 13].

Although Brucella strains were not isolated from the lymph nodes of pigs and wild boars evaluated here, there are many reports of pigs being seropositive for brucellosis in Brazil [14–16] and reports of brucellosis outbreaks [9]. The presence of positive animals is a concern; therefore, it is extremely important to use appropriate culture media for Brucella spp. to allow accurate detection at different stages of the production chain, from the raising and slaughtering of animals, where there is a risk of infection of humans through contact with animals and carcasses, to the sale and use of meat, which poses a risk for humans from inadequate food preparation.

4. Conclusion

The combined use of CITA and Farrell media showed good results, inhibiting contaminants in pig and wild boar lymph nodes collected from slaughterhouses and enabling the isolation of Brucella species from lymph nodes that were experimentally contaminated. Our results support the associated use of these media for Brucella spp. isolation.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

References

K. von Bargen, J.-P. Gorvel, and S. P. Salcedo, “Internal affairs: investigating the Brucella intracellular lifestyle,” FEMS Microbiology Reviews, vol. 36, no. 3, pp. 533–562, 2012.

“International Committee on Bacterial Taxonomy. Subcommittee on the Taxonomy of Brucella,” 2013, http://www.the-icsp.org/subcoms/Brucella.htm

T. di Febo, M. Luciani, O. Portanti, B. Bonfini, R. Lelli, and M. Tittarelli, “Development and evaluation of diagnostic tests for the serological diagnosis of Brucellosis in swine,” Veterinaria Italiana, vol. 48, no. 2, pp. 133–156, 2012.

B. L. Deyoe and C. A. Manthei, “Sits of location of Brucella suis in swine,” in Proceedings of the Annual Meeting of the United States Animal Health Association, vol. 71, pp. 102–108, 1967.

J. Megid, L. A. Mathias, and C. A. Robles, “Clinical manifestations of brucellosis in domestic animals and humans,” The Open Veterinary Science Journal, vol. 4, pp. 119–126, 2010.

A. L. Amaral, N. Morés, W. J. Barioni, L. Ventura, R. A. M. Silva, and V. S. Silva, “Fatores de risco associados à ocorrência de linfadenite em suínos na fase de crescimento-terminação,” Pesquisa Veterinária Brasileira, vol. 24, no. 3, pp. 120–122, 2004.

OIE, Porcine Brucellosis. NB: Version adapted by the World Assembly of Delegates of the Office International des epizooties, Paris, France, 2009

M. J. De Miguel, C. M. Marín, P. M. Muñoz, L. Dieste, M. J. Grilló, and J. M. Blasco, “Development of a selective culture medium for primary isolation of the main Brucella Species,” Journal of Clinical Microbiology, vol. 49, no. 4, pp. 1458–1463, 2011.

R. B. Meirelles-Bartoli, L. A. Mathias, and L. E. Samartino, “Brucellosis due to Brucella suis in a swine herd associated with a human clinical case in the State of São Paulo,” Tropical Animal Health and Production, vol. 44, no. 7, pp. 1575–1579, 2012.

P. J. Quinn, M. E. Carter, and B. Markey, Clinical Veterinary Microbiology, Wolfe, London, UK, 1994.

C. M. Marín, J. L. Alabart, and J. M. Blasco, “Effect of antibiotics contained in two Brucella selective media on growth of Brucella abortus, B. melitensis, and B. ovis,” Journal of Clinical Microbiology, vol. 34, no. 2, pp. 426–428, 1996.

G. H. B. Lara, M. G. Ribeiro, C. Q. F. Leite et al., “Occurrence of Mycobacterium spp. and other pathogens in lymph nodes of slaughtered swine and wild boars (Sus scrofa),” Research in Veterinary Science, vol. 90, no. 2, pp. 185–188, 2011.

L. Ferrão-Beck, R. Cardoso, P. M. Muñoz et al., “Development of a multiplex PCR assay for polymorphism analysis of Brucella suis biovars causing brucellosis in swine,” Veterinary Microbiology, vol. 115, no. 1–3, pp. 269–277, 2006.

V. L. T. Jesus, R. C. G. Pereira, G. S. Meirelles, J. S. Rodrigues, J. L. B. P. Jorge, and W. Flausino, “Brucelose suína no estado do Rio de Janeiro,” Revista Brasileira de Medicina Veterinária, vol. 32, pp. 101–104, 2010.

S. R. T. Borges, L. C. Souza, R. C. Silva, and E. Almeida, “Avaliação dos níveis de biosseguridade das granjas de reprodutores suínos certificadas no estado de São Paulo,” Veterinária e Zootecnia, vol. 18, pp. 417–431, 2011.

D. C. Rosa, K. C. O. Garcia D, and J. Megid, “Soropositividade para brucelose em suínos em abatedouros,” Pesquisa Veterinária Brasileira, vol. 32, pp. 623–626, 2012.