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Clinical Microbiology and Infection 23 (2017) 941e942

Contents lists available at ScienceDirect

Clinical Microbiology and Infection


journal homepage: www.clinicalmicrobiologyandinfection.com

Picture of a microorganism

Biofilm formation by Microsporum canis


L.J. Danielli 1, W. Lopes 2, M.H. Vainstein 2, A.M. Fuentefria 1, M.A. Apel 1, *
1)
Programa de Pos-Graduaça ~o em Ci^
encias Farmac^euticas, Universidade Federal do Rio Grande do Sul, Brazil
2)
Centro de Biotecnologia, Universidade Federal do Rio Grande do Sul, Brazil

a r t i c l e i n f o

Article history:
Received 23 March 2017
Received in revised form
5 June 2017
Accepted 6 June 2017
Available online 19 June 2017

Editor: Professor L Leibovici

Keywords:
Biofilm
Dermatophytes
Microsporum canis
Scanning electron microscoy
Tinea capitis

Biofilm formation is an important cause of failures in anti- The images obtained by SEM demonstrate the presence of a
microbial therapy usually associated with the increasing of highly structured three-dimensional mycelium characteristic of
resistance to antimicrobial agents and with the host immune biofilm (Fig. 1a,b) with expansion in the form of a network of
response. The ability to form such structures has been hyphae growing in all directions (Fig. 1c,d). Moreover, poly-
described for several fungal species; however, biofilm forma- saccharide extracellular matrix that links one hypha to another is
tion by dermatophytes was reported only for Trichophyton spp. observed surrounding some areas of this mycelial structure. The
[1]. In this study, we described for the first time the biofilm presence of polysaccharide was confirmed by reaction with Peri-
formation by Microsporum canis, considered as one of the main odic Acid-Schiff (PAS) (Fig. 1e,f). The extracellular matrix presents
aetiological agents of tinea capitis and characterized by a poor compact regions, but usually with a porous and thin consistency,
therapeutic response. Biofilm was formed in glass coverslips concentrated in the superficial region of the mycelium. Formation
after 120 hours of culture and observed by scanning electron of biofilm by dermatophytes can be considered an important fac-
microscopy (SEM) from a clinical sample of M. canis. tor of fungal virulence, which may be involved in the persistence

* Corresponding author. M.A. Apel, Faculdade de Farmacia, Universidade Federal do Rio Grande do Sul, Av. Ipiranga, 2752, 90610-000, Porto Alegre, Brazil.
E-mail address: miriam.apel@gmail.com (M.A. Apel).

http://dx.doi.org/10.1016/j.cmi.2017.06.006
1198-743X/© 2017 European Society of Clinical Microbiology and Infectious Diseases. Published by Elsevier Ltd. All rights reserved.
942 L.J. Danielli et al. / Clinical Microbiology and Infection 23 (2017) 941e942

Fig. 1. Scanning electron micrographs of Microsporum canis biofilm illustrating biofilm characteristics. (a,b) General view of hyphal layering networks covered by extracellular
matrix (ECM) at the top of the mycelium. (c,d) Higher magnification showing hyphae (red arrows) associated with thin layers of ECM (yellow arrows). (e,f) Presence of poly-
saccharides in the extracellular matrix confirmed by periodic acid Schiff techniques.

of infection. So, this finding contributes perspectives for effective Tecnologico (CNPq). A. M. Fuentefria, M. A. Apel and M. H. Vainstein
therapy to eradicate infections related to biofilm formation by are grateful to CNPq for the PQ fellowships.
dermatophytes.
Author's contribution
Transparency declaration
LJD and WL contributed to drafting the manuscript, literature
The authors report no conflicts of interest. review and laboratory work. MHV, AMFe and MAA contributed to
drafting the manuscript and literature review.

Financial support
Reference
This work was supported by Brazilian organizations: Coor-
[1] Costa-Orlandi CB, Sardi JCO, Santos CT, Fusco-Almeida AM, Mendes-
~o de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
denaça Giannini MJS. In vitro characterization of Trichophyton rubrum and
and Conselho Nacional de Desenvolvimento Científico e T. mentagrophytes biofilms. Biofouling 2014;30:719e27.

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