MICROBIOLOGICAL IMAGE

http://dx.doi.org/10.1016/j.ram.2015.07.005

Capsule expression in isolates of Streptococcus equi subsp. equi

Expresión de la cápsula en aislamientos de Streptococcus equi subsp. equi

 

Carla P. Bustos^*, Alejandra J. Muñoz, Nora Guida

Cátedra de Enfermedades Infecciosas de la Facultad de Ciencias Veterinarias de la Universidad de Buenos Aires, Av. Chorroarín 280, C1427CWO Ciudad Autónoma de Buenos Aires, Argentina

 

Received 13 May 2015; accepted 27 July 2015
Available online 11 November 2015

*Corresponding author.
E-mail address: carlabustos@fvet.uba.ar (C.P. Bustos).

© 2015 Asociación Argentina de Microbiología. Published by Elsevier España, S.L.U. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

 

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Streptococcus equi subsp. equi (S. equi) of Lancefield group C and beta-hemolytic streptococci (Fig. 1) causes strangles, an acute and contagious lymphadenopathy of young horses.^1-3S. equi is host-adapted to equine but, unlike Streptococcus equi subsp. zooepidemicus, does not colonize the nasopharynx in healthy horses.^2,3

Figure 1 Beta-hemolytic colonies of Streptococcus equi subsp. equi in blood equine agar.

The hyaluronic acid capsule is an important virulence factor for many streptococci^1-4 and it is a high molecular weight polymer consisting of alternating residues of N-acetylglucosamine and glucuronic acid. The capsule reduces the phagocytic function of neutrophils and is required for the activity of proteases, toxins and the SeM protein.³ Furthermore, this capsule mimics the molecule in animal tissue and protects the bacterium from immune recognition.³

Virulent isolates of S. equi are usually highly encapsulated^1,3 and nonencapsulated mutants are not able to progress from tonsillar tissue to the lymph nodes.² However, the high levels of capsule may reduce adhesion to the mucosal surface.²

S. equi isolates (Fig. 1) were obtained from horses suffering from clinical strangles and guttural pouch empyema in Buenos Aires. The isolates were cultured for 24 h at 37 °C in 5 ml of Todd Hewitt broth supplemented with 0.2 % yeast extract and 10 % adult horse serum. Then, capsules were observed with phosphotungstic acid (PTA) using a JEOL 1200EX II transmission electronic microscope at 50,000 magnification. The photographs were taken at 80 KV (Figs. 2 and 3).

Figure 2 Capsule observation by transmission electronic microscope of Streptococcus equi subsp. equi showing high levels of capsule expression.

Figure 3 Capsule observation by transmission electronic microscope of Streptococcus equi subsp. equi showing low levels of capsule expression.

High (Fig. 2) and low (Fig. 3) levels of capsule expression were observed, even in isolates from the same sample.

Ethical responsibilities

Protection of human and animal subjects

The authors declare that no experiments were performed on humans or animals for this study.

Confidentiality of data

The authors declare that no patient data appear in this article.

Right to privacy and informed consent

The authors declare that no patient data appear in this article.

Acknowledgements

This work was supported by Secretaría de Ciencia y Técnica, Universidad de Buenos Aires (Research Project UBA CyT 20020100100149).

References

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3. Timoney JF, Kumar P, Muthupalani S. Interaction of Streptococcus equi with the equine nasopharynx. Int Congr Ser. 2006:267-70.         [ Links ]

4. Waller AS, Paillot R, Timoney JF. Streptococcus equi: a pathogen restricted to one host. J Med Microbiol. 2011;60:1231-40.         [ Links ]