SciELO - Scientific Electronic Library Online

 
vol.44 issue1Identification and assessment of kefir yeast potential for sugar/ethanol-resistanceZoonoses in humans from small rural properties in Jataizinho, Parana, Brazil author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

  • English (pdf)
  • Article in xml format
  • Article references
  • How to cite this article
  • SciELO Analytics
  • Curriculum ScienTI
  • Automatic translation

Indicators

Related links

Share


Brazilian Journal of Microbiology

Print version ISSN 1517-8382

Braz. J. Microbiol. vol.44 no.1 São Paulo  2013  Epub May 17, 2013

http://dx.doi.org/10.1590/S1517-83822013005000031 

Comparison of methods for the detection of biofilm formation by Staphylococcus aureus isolated from bovine subclinical mastitis

 

 

Poliana de Castro MeloI; Luciano Menezes FerreiraI; Antônio Nader FilhoI; Luiz Francisco ZafalonII; Hinig Isa Godoy VicenteIII; Viviane de SouzaIV

IDepartamento de Medicina Veterinária Preventiva, Universidade Estadual Paulista "Júlio de Mesquita Filho", Jaboticabal, SP, Brazil

IIEmbrapa  Pecuária Sudeste, São Carlos, SP, Brazil.

IIISecretaria da Agricultura do Estado de São Paulo, Jaboticabal, SP, Brazil

IVEmbrapa Caprinos e Ovinos, Sobral, CE, Brazil

Correspondence

 

 


ABSTRACT

Biofilm formation is considered to be a selective advantage for Staphylococcus aureus mastitis isolates by facilitating bacterial persistence in the udder. It requires attachment to mammary epithelium, proliferation and accumulation of cells in multilayers. The objective of this study was to determine the sensitivity and specificity of three techniques for the detection of S. aureus biofilm-positive strains. Two phenotypic tests, including growth on microtitre plates and Congo red agar, were compared with a PCR technique using 94 S. aureus strains obtained from cows with subclinical mastitis from two farms in the state of São Paulo. These strains were characterised by in vitro slime production on Congo red agar, biofilm formation on microtitre plates and the presence of the icaA and icaD genes. The results revealed that 85% of the isolates tested produced slime on the Congo red agar, 98.9% of the isolates produced biofilms in vitro by adhering to sterile 96-well "U" bottom polystyrene tissue culture plates, and 95.7% of the isolates carried the icaA and icaD genes. The results of the phenotypic tests for biofilm formation were compared with those of the molecular analysis, and the sensitivity and specificity of the Congo red agar test were 88.9% and 100%, respectively, while those of the microtitre plate test were 100% and 25%, respectively. When the phenotypic methods for the detection of biofilm producers, namely growth on microtitre plates and Congo red agar, were compared, the sensitivity and specificity were 86% and 100%, respectively. Therefore, growth on Congo red agar and the microtitre plate test are methods that could be used to determine whether an isolate has the potential for biofilm production.

Key words: biofilms, bovine mastitis, phenotypic and molecular analysis, Staphylococcus aureus.


 

 

Introduction

Staphylococcus aureus is an important etiologic agent of intramammary infections in ruminants and, most S. aureus strains associated with mastitis are found surrounded by a layer of slime. This layer allows the pathogen to adhere to and colonise the host mammary gland epithelium (Baselga et al., 1993; Bergey & Holt, 1994; Aguilar & Iturralde, 2001).

The two methods broadly used for the phenotypic identification of biofilm-producing strains are the microtitre-plate test (MtP) (Christensen et al., 1985; Christensen, 1989) and the Congo red agar (CRA) test (Freeman et al., 1989). The MtP was developed to replace the test tube method, which was the first method used for macroscopic estimation of bacterial biofilm on the surface of plastic tubes. The microtitre-plate technique uses a 96-well-plate spectrophotometer to measure the optical density (O.D.) of stained bacterial biofilms found on the bottom of tissue culture plates and produces quantitative results (Stepanovic et al., 2000; Arciola et al., 2005).

The CRA plate test uses a solid medium, namely Congo red agar. This method allows for the direct analysis of the colonies and the identification of slime-forming strains (which appear as black colonies on the red agar) and non-slime-forming strains (red-coloured colonies). This is not a quantitative assay because it is based on a subjective chromatic evaluation. The strains that score positive during the test have black spikes on red colonies which remain unchanged in colour (Freeman et al., 1989).

The implications of biofilm formation for infections and drug resistance have triggered an increased interest in the characterisation of the genes involved in biofilm formation. The intercellular adhesion (ica) locus consists of the genes icaADBC, and among the ica genes, icaA and icaD have been reported to play a significant role in biofilm formation in S. aureus and S. epidermidis (Cramton et al., 1999).

Molecular techniques have recently been used for detecting the genes responsible for the slime exopolysaccharide component of biofilms, also known as polysaccharide intercellular adhesin (PIA). PIA is made up of a linear 1,6-linked glycosaminoglycan and synthesised in vitro from UDP-N-acetylglucosamine by N-acetylglucosaminyltransferase, which is encoded by the intercellular adhesion (ica) locus, specifically by the icaA gene. Coexpression of icaA and icaD genes leads to the full phenotypic expression of the capsular polysaccharide (Vasudevan et al., 2003).

Early detection and management of potentially pathogenic staphylococci is an essential step towards prevention and management of bovine mastitis. Therefore, there is a need to evaluate a simple and cheap method for the detection of biofilm producers. Biofilm production can be a marker of virulence and, can be detected by phenotypic assays (Baselga et al., 1993; Dhanawade et al., 2010).

Herein, we evaluated strains of S. aureus isolated from cows with subclinical mastitis by the CRA, MtP and PCR analysis. Our aim was to determine the efficacy of each of the phenotypic tests using the PCR test as the gold standard. We also compared the two phenotypic tests (MtP and CRA) each other using the MtP as the standard. The results obtained were used to review and compare the efficacy of three different detection assays for the diagnosis of biofilm staphylococci mastitis.

 

Materials and Methods

Bacterial strains and storage

Ninety-four S. aureus strains were isolated from milk samples collected from dairy cows with subclinical mastitis in two herds in the state of São Paulo. The strains were collected monthly during 12 months, from 2001 until 2002 for the first dairy herd and from 2005 until 2006 for the second dairy herd. The staphylococcal species was identified by biochemical test (Bergey & Holt, 1994; MacFaddin, 1976) and confirmed by PCR analysis (Martineau et al., 1998). The biofilm-producer ATCC 25923 and the biofilm negative ATCC 12228 were used as reference strains.

Phenotypic characterization of biofilm formation by microtitre plate test

Microtitre-plate test was modified (Cucarella et al., 2001). The modification was related with the dilution that according to the author was 1:40 (Cucarella et al., 2001) and in this research the dilution was 1:200. Overnight cultures were diluted 1:200 with Trypticase Soy Broth (TSB, BD,NJ Franklin Lakes) containing 0.25% glucose, and 200 αL per well were seeded in sterile 96-well polystyrene tissue culture plates at 37 °C for 18 h. After three washes in phosphate buffered saline solution (pH 7.2), wells were dried for 1 h at 60 °C and the adherent biofilms were stained with 1% crystal violet for one minute. After rinsing three times with distilled water and subsequent drying at room temperature, the absorbance of the adherent biofilm was measured at 490 nm in a microplate reader (Thermoplate reader, Brasil). Uninoculated wells containing TSB with glucose served as blanks. The blank corrected absorbance values of S. aureus strains were used for reporting biofilm production. Strains producing a blank corrected mean absorbance value of > 0.1 were considered as weak biofilm producers, and if the value was higher than 1.0 its was considered a higher biofilm producer. (Mack et al., 2000). Each strain was tested for biofilm production in duplicates and the assay was repeated three times.

Phenotypic characterization of biofilm production in CRA

The strains were cultured on CRA plates, prepared by adding 0.8 g of Congo red and 36 g of saccharose (both from Sigma, Missouri, EUA) to 1 L of BHI (Oxoid, Basingstoke, Hampshire, England). The plates were subsequently incubated for 24 h at 37 °C and overnight at room temperature. The production of rough black colonies by slime producing strains was used to differentiate them from non-slime producing S. aureus strains (red smooth colonies) (Freeman et al., 1989).

PCR method for the identification of icaA and icaD genes responsible for PIA synthesis

Isolation of genomic DNA

S. aureus chromosomal DNA isolates were extracted with GFX kit genomic blood (Amersham Biosciences, England).

PCR

The primers for the amplification of icaA and icaD genes were designed from the published sequence of the ica locus described by Cramton et al. (1999). For the detection of icaA, primers ICAAF (TCT CTT GCA GGA GCA ATC AA) and ICAAR (TCA GGC ACT AAC ATC CAG CA) were used to amplify a 188 bp fragment. Similarly for amplifying icaD, primers ICADF (ATG GTC AAG CCC AGA CAG AG) and ICADR (CGT GTT TTC AAC ATT TAA TGC AA) were used for a 198 bp fragment. A 20 αL reaction volume consisted of 2.5 mM MgCl2, 200 mM of each nucleotide, 1 mM of each primer, 1.25 U of Taq polymerase and 100 ng of template DNA. Thirty cycles of amplification, each consisting of denaturation at 92 °C for 45 s, annealing at 49 °C for 45 s and elongation at 72 °C for 1 min, along with a final extension at 72 °C for 7 min were performed in a thermocycler (Eppendorf, USA). The presence and size of the amplified products were confirmed by electrophoresis on 1.5% agarose gel.

Statistical analysis

Statistical analysis was performed using SAS software 2002 (SAS, 2001). The test was used for comparison of sensitivity, specificity, kappa, positive predictive value (PPV) and negative predictive value (NPV) of CRA and MtP method calculated by using Test Diag (Godoy, 1999) (analysis of 22 table). MtP method was used as standard. And for the analysis of CRA and icaAD genes and MtP and icaAD genes, the molecular analysis (presence of icaAD genes) was used as gold standard.

 

Results

Detection of biofilm production phenotype by microtitre plate test

The microtitre plate test correctly identify both the positive and the negative reference bacterial strains. Ninety-three out of 94 strains (98.9%) were found to be biofilm producers. Only 1 strain was found to be negative by both the microtitre plate test and CRA test, and this strain lacked the icaAD genes indicating, it was a biofilm non-producer.

Detection of the biofilm-producing phenotype by the Congo Red Agar test (CRA)

A total of 85% of the strains (n = 80) were producers of rough black colonies, and 15% strains (Freeman et al., 1989) were classified as non-producers (smooth red colonies). The two reference strains, ATCC 25923 and ATCC 12228, were found to be positive and negative, as expected.

PCR detection of icaA and icaD

Ninety strains (95%) were positive by PCR for both icaA and icaD genes, as indicated by the sizes of the PCR bands observed (188 bp for icaA and 198 bp for icaD), whereas four strains were negative by PCR. All of the slime-producing strains were positive for both genes. Among non slime producers, 10 were positive for ica genes, which may indicate that these strains actually have the ability to produce slime. All samples that were PCR negative were also negative in the CRA test. Eighty-nine strains (94.6%) were biofilm-producers in the microtitre plate test, which were also positive by PCR. Three isolates tested positive as biofilm-producers in the microtitre plate test but were negative by PCR (Table 1).

 

Discussion

The ability of S. aureus to form biofilms helps the bacterium to survive in hostile environments within the host and is considered to be responsible for chronic or persistent infections (Christensen et al., 1985; Bernardi et al., 2007). Several studies have shown that the formation of slime and biofilms by S. aureus and S. epidermidis strains causing catheter-associated and nosocomial infections is associated with the presence of the icaA and icaD genes (Ziebuhr et al., 1997; Arciola et al., 2001, 2002). In this research, the results of a PCR test for the icaA and icaD genes and phenotypic tests were important to foment studies on mastitis and develop diagnostic tests for biofilm-producing microorganisms.

The Microtitre plate test is a convenient and economical quantitative technique for the identification of critical factors and optimal culture conditions for biofilm formation. This technique is used for direct detection of polysaccharide production because spectrophotometric measurements provide quantitative information on the ability of bacterial strains to rapidly grow while adhering to the substratum. However, it can be less accurate in determining their specific ability to secrete PIA because, while it is a very sensitive test, it has low specificity (Stepanovic et al., 2000).

Previously, the results of CRA test and the adherence to microplates test (MtP) were compared with the presence of the icaA and icaD genes for strains of Staphylococcus epidermidis isolated from medical implants, and the genotypic test was used as the gold standard (Baselga et al., 1993; Arciola et al., 2005). The authors found that 57% of the strains were positive for the icaA and icaD genes, and three of these strains were negative by the CRA test. It was also verified that 16% of the 66% strains that produced biofilms in the MtP test were negative for icaA and icaD by PCR. In total, 10% of the 16% of biofilm-positive strains that were icaA and icaD negative were classified as weak producers of biofilms (weak adherence). The presence of the genes was best correlated with a positive CRA test (Baselga et al., 1993; Arciola et al., 2005; Jain & Agarwal, 2009).

In this study, the microtitre test allowed an easy and quantitative classification of the staphylococcal isolates. Matching results from both CRA and Microtitre plate test were obtained with 81 (87%) of the strains screened. Among the 94 strains tested, a low correlation was found between the results of the PCR-based analysis and the CRA test. This finding indicates that the CRA test produces a high number of false negatives.

The CRA test identified 100% of the negative biofilm producer strains, and 28.6% of the strains identified as negative by the CRA test were actually negative, based on a negative predictive value (NPV) calculation. In total, 88.9% of the strains were positive for the production of biofilm, and the probability that they were actually positive was 100%, based on a positive predictive value (PPV) calculation. Due to the number of false negative results, the negative predictive value was low which indicates reduced sensitivity. However, this test was very specific, even thought it had a low NPV (Table 2). According to the author who developed the CRA test, polysaccharides are the target of the dye. In his article, he described the use of the Congo red dye to verify the presence of polysaccharides on gram negative bacteria of aquatic origin under a light microscope. Using the dye, he was able to verify that the polysaccharides on the bacilli and the staphylococci had a similar staining pattern (Freeman et al., 1989).

 

 

In this study, the colour scale for the CRA test, which has been reported previously, was not changed (Ziebuhr et al., 2001). Therefore, plates that had colonies of indeterminate colour (e.g., those that were dark red but were tending towards black) were repeated. Another variable that was tested was the use of sucrose. In some articles, the authors used glucose instead of sucrose, but in the present research, the results were similar for glucose and sucrose (Freeman et al., 1989; Jain & Agarwal, 2009).

The results of the microtitre plate test were compared with those of the CRA test, and the results of the microtitre plate test indicate that it was better than the CRA test in the detection of biofilms in vitro, because of it's a higher sensitivity (100%), in detecting the positive strains. Therefore, the microtitre plate test is recommended for routine analysis of strains of S. aureus isolated from samples of milk. This test also had a better correlation with the presence of icaAD by PCR, which is correlated with the detection of the intercellular polysaccharide that is the major component of biofilm (Table 3).

 

 

In a previous study, the microtitre plate test (MtP) and CRA assay were used to identify Staphylococci biofilm-producing strains, using the MtP as the gold standard, and it was determined that the sensitivity and specificity of the Congo red agar assay were 90.63% and 90.6%, respectively, for the detection of S. aureus biofilm producers (Jain & Agarwal, 2009). In the present research, the samples were placed on the same microplate in duplicate, and the test was repeated three times. All of the results were very similar; therefore, there was no need to perform the test in triplicate or quadruplicate. We did not test different concentrations of sugars because 98% of the samples produced biofilms in the microtitre plate test.

In this study, we also compared the results from the CRA and MtP tests using the MtP test as the gold standard, and the results revealed that the sensitivity and the specificity of the CRA test were 86% and 100%, respectively. These results suggest that the CRA test could be successfully used to detect S. aureus biofilm-producing strains, but when the CRA and MtP tests were compared with the molecular analysis, the results indicated that the MtP test should be the first choice because this test was more sensitive than the CRA test, identifying all of the biofilm positive strains (Table 4). The Congo red agar test has been previously compared to the microtitre plate test, which was considered to be the gold standard, in a report by Jain and colleagues (2009) published in the Journal of Microbiological Methods (Stepanovic et al., 2000; Jain & Agarwal, 2009).

 

 

The presence of the ica locus in 95% of the mastitis S. aureus isolates confirms its potential role as a virulence factor in the pathogenesis of mastitis in ruminants. Several studies have reported a higher frequency of distribution of the ica locus in clinical isolates of S. epidermidis than in saprophytic strains, emphasising its utility as a virulence marker (Christensen, 1989; Costerton et al., 1999; Ziebuhr et al., 2001; Arciola et al., 2001, 2002). The biofilm formation by strains that did not have the ica genes in this study could be explained by the presence of other genes, such as bap, which can compensate for a deficiency of ica genes. According to other studies, the bap gene in strains isolated from the bovine intramammary gland facilitated biofilm formation and the persistence of S. aureus (Cucarella et al., 2001). In the present research, the bap gene was not studied.

In a previous study detecting S. aureus biofilm producers associated with bovine mastitis, the authors verified that the PCR technique reliably identified the biofilm-producing potential of S. aureus strains, which may help in the rapid detection of biofilm-producing Staphylococci. The best correlation of the PCR test with phenotypic tests occurred with the CRA assay and the microtitre plate test (MtP). In this research, the CRA and microtitre plate tests showed results that were significantly correlated with the molecular analysis (Dhanawade et al., 2010).

The ability of Staphylococcus aureus to produce biofilm is an important factor affecting the long-term persistence of the bacteria in the mammary gland and can result in chronic mastitis and decreased efficacy of antibiotic therapy. Virulent S. aureus strains can be identified by the presence of genes participating in biofilm formation. However, PCR analysis only reveals the genetic predisposition for biofilm formation and expression of ica genes thus, the real biofilm formation must be confirmed by additional phenotypic methods.

 

Conclusion

The MtP method presents higher sensitivity when compared with molecular analysis to identify S. aureus biofilm producers. The CRA method should be used as a complementary test because of the higher specificity relative to the MtP method. All of the methods were effective at detecting S. aureus biofilm-producing strains, and the two classic phenotypic tests can be reliably used to detect biofilm-producing strains because they are acceptably sensitive and specific.

 

Acknowledgments

The authors thank the Foundation of Research Support of the State of São Paulo (FAPESP), which financed this project, and the National Council of Research Development (CNPq) for the fellowship they provided. The authors also thank the Oswaldo Cruz Foundation (Fiocruz) for providing the ATCC 29213 and 25923 strains of S. aureus.

 

References

Aguilar B, Iturralde M (2001) Binding of a surface protein of Staphylococcus aureus to cultured ovine mammary gland epithelial cells. Vet Microbiol 82:165-175.         [ Links ]

Arciola CR, Baldassarri L, Montanaro L (2001) Presence of icaA and icaD and slime production in a collection of staphylococcal strains from catheter-associated infections. J Clin Microbiol 39:2151-2156.         [ Links ]

Arciola CR, Campoccia D, Baldassarri L, Donati ME, Pirini V, Gamberini S, Montanaro L (2005) Detection of biofilm formation in Staphylococcus epidermidis from implant infections. Comparison of a PCR - method that recognizes the presence of ica genes with two classic phenotypic methods. J Biomed Mat Res 76:425-430.         [ Links ]

Arciola CR, Campoccia D, Gamberini S, Cernellati M, Donati E, Montanaro L (2002) Detection of slime production by means of an optimized congo red agar plate based on a colorimetric scale in Staphylococcus epidermidis clinical isolates genotyped for ica locus. Biomaterials 23:4233-4239.         [ Links ]

Bannerman TL (2003) Staphylococcus, Micrococcus, and other catalase-positive cocci grow aerobically. In: Murray PR, Baron EJ, Pfaller MA, Tenover FC, Yolken RH.(eds). Manual of Clinical Microbiology. Washington DC: American Society for Microbiology, p.384-404.         [ Links ]

Baselga R, Albizu I, De La Cruz M, Del Cacho E, Barberan M, Amorena B (1993) Phase variation of slime production in Staphylococcus aureus: implications in colonization and virulence. Infect Immun 61:4857-4862.         [ Links ]

Bergey DH, Holt JG (1994) Bergey's Manual of Determinative Bacteriology. Baltimore, Maryland, 350 pp.         [ Links ]

Bernardi ACA, Pizzolitto EL, Pizzolitto AC (2007) Detection of slime production by coagulase-negative staphylococci isolated from central venous catheter. Rev Cien Farm Apl 28:57-66.         [ Links ]

Christensen GD, Simpsonv WA, Yonger JJ, Baddor LM, Barrett FF, Melton DM, Beachey EH (1985) Adherence of coagulase-negative Staphylococci to plastic tissue culture plates: a quantitative model for the adherence of Staphylococci to medical devices. J Clin Microbiol 22:996-1006.         [ Links ]

Christensen BE (1989) The role of extracellular polysaccharides in biofilms. J Biotechnol 10:181-202.         [ Links ]

Costerton JW, Stewart PS, Grenberg EP (1999) Bacterial Biofilms: A Common Cause of Persistent Infections. Science 284:1318-1322.         [ Links ]

Cramton SE, Gerke C, Schnell NF, Nichols WW, Gotz F (1999) The intercellular adhesion (ica) locus is present in Staphylococcus aureus and is required for biofilm formation. Infec Immun 67:5427-5433.         [ Links ]

Cucarella C, Solano C, Valle J, Amorena B, Lasa I, Penadés JR (2001) Bap a Staphylococcus aureus surface protein involved in biofilm formation. J Bacteriol 183:2888-2896.         [ Links ]

Dhanawade NB, Kalorey DR, Srinivasan R, Barbuddhe SB, Kurkure NV (2010) Detection of intercellular adhesion genes and biofilm production in Staphylococcus aureus isolated from bovine subclinical mastitis. Vet Res Commun 34:81-89.         [ Links ]

Freeman DJ, Falkiner FR, Keane CT (1989) New method for detecting slime production by coagulase negative staphylococci. J Clin Pathol 42:872-874.         [ Links ]

Godoy MF (1999) Cálculos Estatísticos Básicos para Testes Diagnósticos, Available at: http://www.braile.com.br/DOWNLOAD/TestDiag.xs, Acessed 10 August 2007.         [ Links ]

Hensen SM, Pavis MJAMP, Lohuis JACM, Hoog JAM, Poutrel B (2000) Location of Staphylococcus aureus within the experimentally infected bovine udder and the expression of capsular polysaccharide type 5 in situ. J Dairy Sci 83:1966-1975.         [ Links ]

Holmberg O (1973) Staphylococcus epidermidis isolated from bovine milk. Acta Vet Scand 45:1-144.         [ Links ]

Jain A, Agarwal A (2009) Biofilm production, a marker of pathogenic potential of colonizing and commensal staphylococci. J Microbiol Methods 76:88-92.         [ Links ]

MacFaddin JF (1976) Biochemical Tests for Identification of Medical Bacteria. The Williams & Wilkins, Baltimore, 312 pp.         [ Links ]

Mack D, Rohde H, Dobinsky S, Riedewald J, Nedelmann M, Knoblock JKM, Elsner HA, Feucht HH (2000) Identification of three essential regulatory gene loci governing expression of Staphylococcus epidermidis polysaccharide intercellular adhesin and biofilm formation. Infect Immun 68:3799-3807.         [ Links ]

Martineau F, Picard FJ, Roy PH, Ouellette M, Bergeron MG (1998) Species-specif and ubiquitous DNA based assays for rapid identification of Staphylococcus aureus. J Clin Microbiol 36:618-623.         [ Links ]

SAS INSTITUTE INC. SAS/STAT. User's Guide: stat. Release 8.1 Edition. Cary, 2001, 1292 pp.         [ Links ]

Stepanovic S, Vukovic D, Daki I, Savic B, Vlahovic-Svabic M (2000) A modified microtiter-plate test for quantification of staphylococcal biofilm formation. J Microbiol Methods 40:175-179.         [ Links ]

Vasudevan P, Nair MKM, Annamalai T, Venkitanarayanan KS (2003) Phenotypic and Genotypic characterization of bovine mastitis isolates of Staphylococcus aureus for biofilm formation. Vet Microbiol 92:179-185.         [ Links ]

Ziebuhr W, Heilmann C, Gotz F, Meyer P, Wilms K, Straube E, Hacker J (1997) Detection of the intercellular adhesion gene cluster (ica) and phase variation in S. epidermidis blood culture strain and mucosal isolates. Infect Immun 65:890-896.         [ Links ]

Ziebuhr W, Lossner I, Krimmer V, Hacker J (2001) Methods to detect and analyze phenotypic variation in biofilm-forming staphylococci. Met Enzymol 336:195-205.         [ Links ]

 

 

Correspondence:
P.C. Melo
Departamento de Medicina Veterinária Preventiva
Universidade Estadual Paulista "Júlio de Mesquita Filho"
Jaboticabal, SP, Brazil
E-mail: policame@yahoo.com.br

Submitted: April 21, 2011
Approved: July 2, 2012

Creative Commons License All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License