Pomegranate sarcotesta lectin (PgTeL) inhibits planktonic growth and disrupts biofilm formed by Cryptococcus neoformans

Author:

Ferreira Gustavo Ramos Salles1,da Silva Pollyanna Michelle1,Lopes William23,Feitosa Ana Paula Sampaio45,Coelho Luana Cassandra Breitenbach Barroso1,Brayner Fábio André45,Alves Luiz Carlos45,Paiva Patrícia Maria Guedes1,de Moura Maiara Celine1,Vainstein Marilene Henning2,Napoleão Thiago Henrique1

Affiliation:

1. Departamento de Bioquímica, Centro de Biociências, Universidade Federal de Pernambuco , 50670-901, Recife , Brazil

2. Laboratório de Biologia de Fungos de Importância Médica e Biotecnológica, Centro de Biotecnologia, Universidade Federal do Rio Grande do Sul , 91501-970, Porto Alegre , Brazil

3. Physics of Living Systems, Department of Physics, Massachusetts Institute of Technology , 02139, Cambridge, MA , USA

4. Instituto Aggeu Magalhães, Fundação Oswaldo Cruz , Recife, 50670-901 , Brazil

5. Instituto Keizo Asami, Universidade Federal de Pernambuco , 50670-901, Recife , Brazil

Abstract

Abstract Aims We investigated the putative fungistatic and fungicidal activities of pomegranate sarcotesta lectin (PgTeL) against Cryptococcus neoformans B3501 (serotype D), specifically the ability of PgTeL to inhibit yeast capsule and biofilm formation in this strain. Methods and results PgTeL showed a minimum inhibitory concentration of 172.0 μg ml−1, at which it did not exhibit a fungicidal effect. PgTeL concentrations of 4.0–256.0 μg ml−1 reduced biofilm biomass by 31.0%–64.0%. Furthermore, 32.0–256.0 μg ml−1 PgTeL decreased the metabolic activity of the biofilm by 32.0%–93.0%. Scanning electron microscopy images clearly revealed disruption of the biofilm matrix. Moreover, PgTeL disrupted preformed biofilms. At concentrations of 8.0–256.0 μg ml−1, PgTeL reduced metabolic activity in C. neoformans by 36.0%–92.0%. However, PgTeL did not inhibit the ability of B3501 cells to form capsules under stress conditions. Conclusions PgTeL inhibited biofilm formation and disrupted preformed biofilms, demonstrating its potential for use as an anticryptococcal agent.

Funder

CNPq

FACEPE

Publisher

Oxford University Press (OUP)

Subject

Applied Microbiology and Biotechnology,General Medicine,Biotechnology

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