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On-line version ISSN 1678-4405
Braz. J. Microbiol. vol.39 no.1 São Paulo Jan./Mar. 2008
Molecular characterization of Rhodococcus equi isolates of horse breeding farms from an endemic region in South of Brazil by multiplex PCR
PCR multiplex para caracterização molecular de isolados de Rhodococcus equi provenientes de haras de uma região endêmica no Sul do Brasil
Cristina da Costa KrewerI; Dênis Augusto SpricigoI; Sônia de Avila BottonI; Mateus Matiuzzi da CostaII; Irene SchrankIII; Agueda Castagna de VargasI*
IUniversidade Federal de Santa Maria, Departamento de Medicina Veterinária Preventiva, Laboratório de Bacteriologia, Santa Maria, RS, Brasil
IIFundação Universidade do Vale do São Francisco, Zootecnia, Petrolina, PE, Brasil
IIIUniversidade Federal do Rio Grande do Sul, Centro de Biotecnologia, Porto Alegre, RS, Brasil
Rhodococcus equi is a gram-positive coco-bacillus and an intracellular opportunistic pathogen which causes pneumonia in foals. It is widely detected in environment and has been isolated from several sources, as soil, feces and gut from health and sick foals. The goal of this study was to characterize the epidemiological status (endemic, sporadic or no infection) of horse breeding farms from Bage County in South of Brazil, using a multiplex PCR. One hundred and eighteen R. equi isolates were identified by biochemical tests and submitted to a specie-specific and vapA multiplex PCR. These isolates were obtained from: three farms where the R. equi infection has been noticed, two farms where the disease has been not reported and one farm where the disease is frequent. All clinical isolates from horse breeding farms where the disease is endemic and/or sporadic were vapA-positive. None environmental isolates were vapA-positive. In three horse breeding farms with sporadic R. equi infection, 11.54% of the isolates from adult horse feces were vapA-positive. The multiplex PCR technique has proven to be effective for the molecular and epidemiological characterization of the R. equi isolates in horse breeding farms. An important finding in this study was the isolation of vapA-positive R. equi from adult horse feces, which is an evidence for other routes of dissemination of this pathogen in the farms.
Key-words: Rhodococcus equi, Multiplex PCR, bronchopneumonia, epidemiology.
Rhodococcus equi é um coco-bacilo gram positivo que causa pneumonia em potros. Trata-se de um patógeno oportunista amplamente detectado no ambiente e isolado de várias fontes, como solo, fezes e intestino de potros doentes e sadios. O presente estudo visa caracterizar a situação epidemiológica de criatórios eqüinos da região de Bagé, RS, Brasil, pela técnica de PCR multiplex. Cento e dezoito isolados de R. equi foram identificados por testes bioquímicos e, posteriormente, submetidos a um PCR multiplex para caracterização da espécie e da presença do gene vapA. Estes isolados eram provenientes de três haras com histórico da doença, dois haras onde não havia casos da doença e uma propriedade onde a infecção por R. equi é relatada frequentemente. Todos os isolados clínicos provenientes de haras onde a doença é endêmica e/ou esporádica foram vapA positivos. Nenhum isolado ambiental foi vapA positivo. Nos três haras onde a doença é esporádica, 11,54% dos isolados de fezes de eqüinos adultos foram positivos para o gene vapA. A técnica de PCR multiplex mostrou-se efetiva para caracterização epidemiológica e molecular dos criatórios equinos, estando de acordo com o histórico da propriedade. Um fato relevante demonstrado pela aplicação desta técnica foi a detecção de R. equi vapA positivo nas fezes de eqüinos adultos. Esta observação pode pressupor que haja outras vias de disseminação da bactéria dentro de uma propriedade.
Palavras-chave: Rhodococcus equi, PCR multiplex, broncopneumonia, epidemiologia.
Rhodococcus equicauses a very important disease in horses around the world. Virulent Rhodococcus equi strains are associated to bronchopneumonia, ulcerative lymphangitis, internal abscess, diarrhea and pleurisy in foals (23). The bacterium is a gram-positive intracellular opportunistic pathogen. It is widely spread in the environment and commonly isolated from soil, feces and gut from healthy and sick animals (8,15,24).
Rhodococcosis is endemic in some farms, sporadic in others and not reported in most of them. The epidemiologic status depends on farm management, foal population density and use of dusty floors in foaling stalls (3). Additionally, environmental issues such as temperature, humidity, dust, and soil pH can influence the development of this infection (12,13). Furthermore, the virulence of R. equi strains in a farm, especially those found in the soil and foal feces is the most important concern of this disease (14).
R. equi virulence is associated to the bacterium ability to prevent the phagosome-lysosome fusion and multiplication in macrophages, resisting to clearance by the organism defenses (8). The virulence factor associated to R. equi infection in foals is a thermorregulated virulence-associated antigen (VapA), encoded by vapA gene, located in the 85-90Kb virulence plasmid (2). According to many researchers the 15 - 17kDa VapA antigen is found in all clinical R. equi isolates from foals, as well in some environmental samples (4,20). The importance of vapA gene in the pathogenesis of R. equi infection and its use as an epidemiological marker of bacterium virulence are well established since all strains carrying the vapA gene are lethal to mice and foals (4,11,19,21).
The goal of this study was to perform the genotypic characterization of R. equi isolates and determine the epidemiological status (endemic, sporadic or no infection) of horse breeding farms from Bage County, RS, Brazil.
MATERIAL AND METHODS
This study was conducted with 118 bacterial isolates previously classified as R. equi by biochemical tests (9), collected in six horse breeding farms (Table 1). The strains have been isolated from horse feces (41 from adults and 33 from foals), soil (21), foaling stalls (10) and other domestic animals (3). Other 10 clinical isolates were cultivated from lungs of sick foals. R. equi ATCC 33701P+ (vapA positive) and R. equi ATCC 33701P- (vapA negative) were used as controls. The specificity of the PCR technique was evaluated using three R. equi related bacterial isolates (Streptococcus sp., Nocardia asteroides and Pasteurella multocida) related to R. equi. All isolates were kept lyophilized until submitted to DNA extraction.
Each isolate was, cultured in 5% ovine blood agar (DIFCO), and transferred to Mueller-Hinton agar (DIFCO) and incubated at 37ºC for 24 hours. The colonies were suspended in 500 µl of milli-Q water and boiled for 10 minutes. The suspension was centrifuged at 13.500 rpm for 3 minutes and 2 µl of the supernatant were used as DNA template for multiplex PCR (16).
The primers used in this study for amplification of 16S ribosomal RNA and vapA genes fragments were respectively: RG-Forward (CGT CTA ATA CCG GAT ATG AGC TCC TGT C); RG-Reverse (CGC AAG CTT GGG GTT GAG CCC CAA) (1) and vapA-Forward (GAC TCT TCA CAA GAC GGT); vapA-Reverse (TAG GCG TTG TGC CAG CTA) (19). The conditions tested for multiplex PCR standardization were adapted from Takai et al. (19), with adjustments on primers and magnesium chloride concentrations, as well as temperature for amplification. All conditions were tested three times. Samples were submitted to 35 cycles (30 s at 94ºC, 30 s at 56ºC and 90 s at 72ºC) followed by 10 minutes at 72ºC. The products (7 µl) were applied to a 1.5% agarosis gel and submitted to electrophoresis per 30 minutes at 100 V. After stained with ethidium bromide, the bands were visualized in ultraviolet light.
The vapA and 16S ribosomal RNA amplified fragments were purified from agarosis gel with polietileneglicol (16) and submitted to sequencing in an automatic DNA sequencer (MEGABACE 1000) at the Molecular Biology Laboratory, Federal University of Santa Maria.
In this study, the best PCR amplifying condition was achieved using 30 pmol of RG primers, 90 pmol of vapA primers and 2.5 mM of MgCl2, showing both for 16S ribosomal RNA (468 pb) and vapA (564 pb) genes fragments amplification (Fig. 1). The length of the DNA fragments amplified by multiplex PCR were in accordance with previous results (2,18). The identity of the PCR products was sustained by DNA sequencing analysis. N. asteroides, Streptococcus sp. and P. multocida, tested by the PCR assay presented no amplification, validating the multiplex PCR specificity.
The multiplex PCR results are shown in Table 1 and Fig. 1. Ten (100%) isolates obtained from sick foals and seven (6.54%) from adults and foals feces were positive for both vapA and 16S ribosomal RNA, denoting the virulence potential of these strains to susceptible foals. Most pathogenic isolates were obtained from the same endemic horse breeding farm (Fig. 2): Virulent R. equi were isolated from nine (90%) sick foals and from four (66.6%) samples of faecal matter from healthy adults and foals. Other two virulent isolates (one from sick foal and one from adult animal feces) were obtained in two other farms (1 and 2), which report sporadic occurrence of Rhodococosis. Virulent R. equi strains were isolated in adult horses feces from farms 1, 2, 3 and 4 (Fig. 2).
The multiplex PCR technique described in this study has proven to be effective for the R. equi molecular characterization. Additionally, the epidemiological status (endemic, sporadic or no infection) of horse breeding farms from Bage County, RS, Brazil (Table 1 and Fig. 2) could be confirmed using both environment (soil and foaling stalls) and horse samples (from sick and healthy animals).
The virulence-associated antigens (VapA) and plasmids are widely used as epidemiological markers of R. equi virulence for foal and experimentally infected mice (6,22). The relationship between the presence of vapA gene and the lethality of R. equi to susceptible foals and mice was reported by many researchers (19,21,25). In the present study, most virulent R. equi isolates were from the endemic horse breeding farm. This can be explained by the higher soil contamination, coming mainly from diarrheic feces from ill animals (12,18).
The R. equi isolation from horse breeding farms, where occurrence of disease, is sporadic indicate that adoption of prophylactic measures to decrease the incidence of this infection is required (12,19). The multiplex PCR was also important to determine the sources of infection and the importance of virulent isolates on epidemiological aspects of Rodococosis in horse breeding farms from Bage, RS, Brazil. The usefulness of vapA gene or virulence plasmid to determine the risk of R. equi infection was demonstrated by Takai et al. (21).
The molecular characterization of R. equi in this study indicated the occurrence of vapA-positive isolates in stools of animals, with no clinical signs associated to R. equi infection. In this way virulent R. equi were found in adult horse feces, confirming that the prevalence of R. equi infection is associated with the presence and number of virulent microorganisms in the environment and animal feces (12,17). Takai et al. (21) reported that sick foals are the major source of virulent bacteria for the environment, since R. equi is a teluric bacterium that can multiply both in soil and gastrointestinal tract, supporting a cycle involving horses and their environment (9, 14). Halbert et al. (7) demonstrated that 97% of R. equi isolates from foals were vapA-positive, suggesting that these animals are important for the transmission of this infection. In contrast, this study demonstrates that not only foals, but healthy adult horses can carry virulent R. equi in their feces and spread them in their environment, indicating that these animals play an important role as a source of contamination of susceptible foals. Future studies are needed to evaluate the potential of multiplication of R. equi in the intestinal tract of adult horses.
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Submitted: August 14, 2007; Returned to authors for corrections: October 17, 2007; Approved: January 23, 2008.
*Corresponding Author. Mailing address: Universidade Federal de Santa Maria. Departamento de Medicina Veterinária Preventiva, Laboratório de Bacteriologia. Av. Roraima, Campus Universitário. Prédio 44, Sala 5137, Santa Maria, RS, Brasil; Fone (55) 3220 8107. E-mail: firstname.lastname@example.org