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Immunogenicity and cross reactivity indices of Streptococcus equi subsp. equi strains isolated from cases of Strangles and commercial vaccines/Imunogenicidade e indices de reatividade cruzada de cepas de Streptococcus equi subsp. Equi isoladas de casos de Adenite Equina e vacinas comerciais.

INTRODUCTION

Horse Strangles is a highly transmissible infectious disease of horses caused by Streptococcus equi subsp. equi (S. equi subsp. equi), a Gram-positive streptococcus belonging to Lancefield group C (FARROW & COLLINS, 1984). It affects horses of all ages, although is more frequent among young animals (TIMONEY et al., 1997), producing mucopurulent nasal discharges, lymphadenitis and guttural pouch empyema (SWEENEY, 1993). The disease has very high morbidity and low mortality, and its economic impact is due to veterinarian expenses and to the necessity to restrain the animals from their activities during several weeks. Outbreaks may last months or even years, mainly in large horse populations where animals are frequently introduced (CHANTER, 1997).

The clinical diagnosis of the disease is easy, but the recovery of S. equi subsp. equi is hampered by opportunistic bacteria such as S. equi subsp. zooepidemicus and S. dysgalactiae subsp. equisimilis (KUWAMOTO et al., 2001), that are frequently isolated from typical cases of the disease. Typical strains of S. equi subsp. equi do not ferment lactose, sorbitol and trehalose, while lactose and sorbitol are fermented by S. equi subsp. zooepidemicus and lactose and trehalose by S. dysgalactiae subsp. equisimilis, (EUZEBY, 2005). In addition, S. equi subsp. equi carbohydrate-fermenting strains, known as atypical strains, add confusion to the bacteriologic diagnosis (GRANT et al., 1993), demanding supplementary tests for their accurate identification.

S. equi subsp. equi produces two antigenically different proteins M (HARRINGTON et al., 2002), as well as other structural or secreted antigens that may participate in its pathogenicity and immunogenicity (FLOCK et al., 2004). The inappropriate selection or manipulation of vaccinal strains may be involved in the low protection conferred by some commercial vaccines, making the study of the antigenic relationships among strains useful when candidate strains for vaccines are being chosen.

The strains isolated from field cases of Strangles and two commercial vaccines were studied through Western Blot and ELISA using recombinant S. equi protein M as antigen, and the bilateral cross reactivity index (CRI) among them was estimated. CRI, that estimates the level of cross protection induced by strains of the same antigen (PEREIRA, 1977), was profusely used to subtype Foot and Mouth Disease Virus. It was considered that a CRI of 70 is the threshold to classify strains as identical (BROOKSBY, 1968). CRIs were also used to estimate antigenic relationships of different antigenic groups of Bordetella bronchiseptica (OLIVEIRA & GIL-TURNES, 1988) and Moraxella bovis (CONCEICAO et al., 2003), the etiological agents of Atrophic Rhinitis of swine and Bovine Infectious Keratoconjunctivitis, respectively.

The objective of this research was to study the immunogenicity and the antigenic relationships among strains recovered from clinical cases of Strangles and two strains used in commercial vaccines widely used in Brazil.

MATERIAL AND METHODS

Samples

Nasal discharges were collected from 35 horses with initial signs of Strangles, that belonged to 10 herds of three municipalities of Rio Grande do Sul, Brazil. The samples were sown on 10% sheep blood agar and incubated for 48 h at 37[degrees]C. Colonies of Gram positive, catalase negative cocci, were suspended in sterile saline and grown in Phenol Red Broth base (Difco, Detroit, MI, USA) containing 1% trehalose, sorbitol or lactose, with or without 10% sterile horse serum devoid of antibodies against streptococci. The isolates were also tested by the API 20 STREP (BioMerieux Brasil S.A., Sao Paulo, SP), following manufacturer's instructions. Fermentation of carbohydrates was read up to 48h of culture at 37[degrees]C, and the API STREP reactions at 4 and 24h of culture. The strains were classified following EUZEBY (2005).

Vaccines

Ten out of 13 strains of S. equi subsp. equi isolated from field cases, were used to prepare monovalent vaccines. Each strain was grown in Brain Heart Infusion (Difco, Detroit, MI, USA) containing 2% Peptone, and incubated at 37[degrees]C overnight. The cultures were then centrifuged at 332g, the pellets suspended in sterile saline and their bacterial concentration determined by plating serial dilutions on blood agar. Suspensions containing 2.5x108 CFU in 5 ml were inactivated with 1:5000 formaldehyde during 24 h at 37[degrees]C, and Aluminum hydroxide gel to a final concentration of 2.0mg of Al mL-1 of vaccine was added. Tests for safety, sterility and purity were performed following CFR 9, [section] 113.100 (CFR 9, 1996).

Mice

Isogenic Balb-c two months-old mice were randomly divided in 13 groups with four mice each. The animals of each group were inoculated subcutaneously with 1/20th of a horse dose (CFR 9, 1996) of the respective vaccine, on days 0 and 14 of the experiment. Two groups were vaccinated with commercial vaccines, following the same protocol. Blood samples were collected from each animal at 0, 14, 28, 56 and 70 days after the application of the first dose of vaccine (dpi). One group remained as unvaccinated control.

Antibody titration

Antibodies were titrated by ELISA. Briefly, polystyrene ELISA plates (Greiner Labortechnik, Germany) were sensitized at 4[degrees]C overnight with 50[micro]L of inactivated bacterial suspensions containing 0.5 x 108 cells [ml.sup.-1] or with the commercial vaccines, suspended in carbonate-bicarbonate buffer pH 9.6. For the estimatation of CRIs, pools of sera of each group of mice collected 56dpi were added and tested with homologous and heterologous antigens. To evaluate the immunogenicity of the vaccines, individual serum samples collected 0, 14, 28, 56 and 70dpi were tested with the homologous antigen. Peroxidase conjugated rabbit anti mouse immunoglobulins (Dako Co., Carpinteria, CA, USA) and ortho-phenyl dyamine were used as reagents. Optical densities were read at 450 nm in a MR 700 ELISA reader (Dynatech Labs. Inc., Chantilly, VA, USA). Optical densities of each antiserum were transformed to seroconversions dividing [OD.sub.450] values by that of the same animal at day 0 (GIL-TURNES et al., 1999), and the means of each group calculated.

Cross reactivity indices

The Bilateral Cross Reactivity Indices (CRIs) among ten strains recovered from field cases and the two commercial vaccines were estimated using sera collected 56dpi by the equation CRI = 100 [square root of r] x r', where r is the quotient of the [OD.sub.450] of serum A with antigen B and that of serum A with antigen A, and r' the quotient of the [OD.sub.450] of serum B with antigen A and that of serum B with antigen B (ARROWSMITH, 1977). Isolates whose CRIs were [greater than or equal to] 70 were considered of the same serogroup.

Western Blots.

Western blots were done using recombinant S. equi protein M (rSEM) produced in our laboratory and sera from mice vaccinated with experimental and commercial bacterins. Briefly, rSEM was submited to SDS-PAGE and transferred to a 0,45m[micro] membrane (Hybond-C Extra, Amersham Biosciences UK Ltd., Buckinghamshire, UK). The membranes were blocked for one hour with 5% non fat dry milk, and then 1:50 dilutions of sera from each vaccinated group were added and incubated for another hour. Peroxidase conjugated rabbit anti mouse immunoglobulins diluted 1:1000 (Dako Co., Carpinteria, CA, USA) was added and incubated for one hour. Anti-6XHis alkaline phosphatase conjugated MAb (Sigma-Aldrich) was used as positive control. Following, DAB-chromogen substrate (9mL Tris-HCl 50mM, 1mL nickel sulphate 0.3%, 10iL of 30% hydrogen peroxide and 6mg 3.3- diaminobenzidine tetrahydrochloride) was placed over the membranes and the reactions recorded.

RESULTS AND DISCUSSION

S. equi subsp. equi was isolated from only thirteen (37.1%) out of thirty-five animals with typical signs of Strangles, stressing the difficulty to reach an etiological diagnosis of the disease. Atypical strains (GRANT et al., 1993), that represented 38.5% of the isolates, were recovered from three foals and two young horses belonging to three herds distanced more than 180km from one another. They fermented at least one carbohydrate, and were classified by the API 20 STREP system. Four of the five atypical strains fermented carbohydrates only in media containing serum, in agreement with previous results of TIMONEY & MUKHATAR (1993).

With the exception of strains 2 and 25, that had CRIs lower than 70 with strains 7 and 14, and 8, 26, 31 and 61, respectively, all of them from different herds, the others were antigenically homogeneous. CRIs of seven of the ten isolates tested were higher than 70 among them (Table 1), the threshold to consider strains as belonging to the same serogroup (ARROWSMITH, 1977). CRIs of 61, the lowest among field strains, were estimated for strains 2 and 14, and strains 25 and 35 (Table 1). Strains 2 and 7, and 25 with 8 and 26, had CRIs of 66 and 67, respectively. The CRI of the two commercial vaccines was 83, also showing antigenic identity, but CRIs among them and the field strains varied between 23 and 46, showing very low antigenic relationships, suggesting that the vaccines would not be able to induce acceptable immunity against field strains (Table 1).

All the vaccines were immunogenic, although those prepared with strains 14 and 35, both typical strains, induced very low seroconversions. The highest seroconversion, 9.4, was induced by strain 26, an atypical strain, 70dpi (Figure 1). The commercial vaccines and four experimental vaccines did not induce seroconversions until the animals were boosted 14dpi. The vaccines showed maximal seroconversions 70 dpi, with the exception of vaccines 14 and 35, and three experimental vaccines (2, 25 and 29), that showed maximal seroconversions 56dpi (Figure 1). Western blots (Figure 2) showed that all the experimental and one commercial vaccine induced the production of antibodies against the recombinant S. equi M protein (rSeM).

Although the protection induced by inactivated vaccines, using subunits or whole cells as antigens, is generally poor and does not resist to a challenge with pathogenic strains (JACOBS et al., 2000), bacterins are produced in Brazil and other countries using strains recovered from spontaneous cases of Strangles. In our experiment we showed that some vaccines were more immunogenic than others, although they were prepared with recently isolated field strains, following the same technology and with similar antigenic concentration to the commercial vaccines. Strain 26, recovered from a foal with guttural pouch empyema, induced seroconversions that were at least twice those of the strain that followed, and more than ten times higher than the least immunogenic strain (Figure1). On the other hand, two experimental vaccines were poorly immunogenic. The commercial vaccines were also poorly immunogenic, inducing lower seroconversions than five and four experimental vaccines, respectively. Although potency tests of commercial vaccines for Strangles are not routinely done in Brazil, the mice immunogenicity test used in our experiment could be useful to select candidate strains for vaccine production and in the quality control of bacterins.

[FIGURE 1 OMITTED]

Our results suggested that the rates of protection found in the herds studied could be related with the low immunogenicity of the commercial vaccines and with the low antigenic relationships among vaccinal and field strains.

ACKNOWLEDGEMENTS

The authors acknowledge Cleonice Rodrigues Pereira and Otavio Brod Storch for technical assistance. C.M.M. had a grant from CAPES (Ministry of Education) and C.G.T. has a CNPq (National Research Council) research productivity grant.

[FIGURE 2 OMITTED]

BIOETHICS AND BIOSSECURITY COMMITTEE APPROVAL

The animals used in this work were managed according to the requirements of the national Experimental Animals Protection Law, and with bioethics and biossecurity committee approval .

Received 07.14.08 Approved 01.09.09

REFERENCES

ARROWSMITH, A.E.M. A survey of foot and mouth disease virus type O strains from Far East. Development in Biological Standardization , v.35, p.221-230, 1977.

BROOKSBY, J. B. Variants in immunity: definitions for serological investigations. Simposia series in immunological standardization, v.8, p.1-10, 1968.

CFR 9, Code of Federal Regulations 9. Animals and animal products. Standards requirements, part 1, section 113, 1996. Washington: United States Government Printing Office,1996. 1550p.

CHANTER, N. Streptococci and enterococci as animal pathogens. Journal of Applied Microbiology, v.83 (suppl), p.1005-1095, 1997

CONCEICAO, F.R., et al. Antigenic relationships of Moraxella bovis isolates recovered from outbreaks of Infectious Bovine Keratoconjunctivitis in Argentine, Brazil and Uruguay between 1983 and 2000. Canadian Journal of Veterinary Research. v.67, p.315-318, 2003

EUZEBY, J.P. Dictionnaire de bacteriologie veterinaire. Capturado em 28 jan. 2007. On line. Disponivel na internet: http://www.bacterio.cict.fr/bacdico/ss/equi.html

FARROW, J.A.E., COLLINS, M.D. Taxonomic studies on streptococci serological group C, G and L and possible related taxa. Systematic and Applied Microbiology , v.5, p.483-493, 1984.

FLOCK, M., et al. Recombinant Streptococcus equi proteins protect mice in challenge experiments and induce immune response in horses. Infection and Immunity. v.72, n.6, p. 3228-3236, 2004. Disponivel em: http://iai.asm.org/cgi/ content/abstract/72/6/3228. Doi: 10.1128/IAI.72.6.3228-3236.2004.

GRANT, S.T. et al. Laboratory diagnosis of strangles and the isolation of atypical Streptococcus equi. Veterinary Record, v.133, p.215-216, 1993.

GIL TURNES, C., et al. DNA inoculation with a plasmid vector carrying the faeG adhesin gene of Escherichia coli K88ab induced immune response in mice and pigs. Vaccine. v.17, p.2089-2095, 1999. Disonivel em: http;//dx.doi.org/10.1016/S0264-410X(98)00384-3. Doi : 10.1016/S0264-410X(98)00384-3.

HARRINGTON, D.J. et al. The molecular basis of Streptococcus equi infection and disease. Microbes and Infection. n.4, p. 501-510, 2002. Disponivel em: http://www.sciencedirect.com/ science?_ob=ArticleURL&_udi=B6VPN-45CW9F8- D&_user=687358&_rdoc=1&_fmt=&_orig=search&_sort=d&vie w=c&_acct=C000037899&_version=1&_url Version=0&_userid=687358&md5=78c2fac5ab8d0936186abf9951d1637c. Doi: 10.1016/ S1286-4579(02)01565-4.

JACOBS, A.A., et al. Investigations towards an efficacious and safe strangles vaccine: submucosal vaccination with a live attenuated Streptococcusequi. Veterinary Record, v.20, n.147, p.563-567, 2000.

KUWAMOTO, Y. et al. Microplate sugar-fermentation assay distinguishes Streptococcus equi from other streptococci of Lancefield's group C. Equine Veterinary Science, v.12, n. 2, p.47-49, 2001.

OLIVEIRA, A.O.; GIL-TURNES, C. Studies on the antigenic relationships of six adherent isolates of Bordetella bronchiseptica. Veterinary. Microbiology, v.18, p.327-333, 1988.

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TIMONEY, J.F.; MUKHATAR, M.M. The protective M proteins of the equine group C streptococci. Veterinary Microbiology, n.37, p.389-395, 1993.

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Carina Martins de Moraes (I,IV) Mariana Sa e Silva (II) Agueda Palmira Castagna de Vargas (II) Carlos Eduardo Wayne Nogueira (I) Fabio Pereira Leivas Leite (III,IV) Carlos Gil-Turnes (I,IV) *

(I) Faculdade de Veterinaria, Universidade Federal de Pelotas (UFPel), Pelotas, RS, Brasil.

(II) Laboratorio de Doencas Infectocontagiosas, Centro de Ciencias Rurais (CCR), Universidade Federal de Santa Maria (UFSM), Santa Maria, RS, Brasil.

(III) Instituto de Biologia, UFPel, Pelotas, RS, Brasil.

(IV) Centro de Biotecnologia, UFPel, Campus Universitario, CP 354, 96010900, Pelotas, RS, Brasil. E-mail: gil@ufpel.edu.br.
Table 1--Cross reactivity indices of ten field strains of
Streptococcus equi subsp. equi and two commercial vaccines.

Strains   2      6      25 *   30 *   31     26 *

2         100    93     75     111    80     83
6                100    83     88     103    75
25 *                    100    76     69     67
30 *                           100    96     104
31                                    100    88
26 *                                         100
7
8 *
35
14
VC A
VC B

Strains   7      8 *    35     14     VC A   VC B

2         67     77     76     61     44     27
6         83     75     71     113    41     32
25 *      74     66     61     98     40     31
30 *      120    105    94     134    43     33
31        123    90     99     92     39     23
26 *      116    72     224    87     34     35
7         100    117    115    131    46     40
8 *              100    100    103    30     29
35                      100    97     41     27
14                             100    33     43
VC A                                  100    83
VC B                                         100

*, atypical strains; VC A, commercial vaccine A; VC B, commercial
vaccine B.
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Title Annotation:Texto en Portuguese
Author:de Moraes, Carina Martins; Sa e Silva, Mariana; Castagna de Vargas, Agueda Palmira; Wayne Nogueira,
Publication:Ciencia Rural
Date:Aug 1, 2009
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