Antimicrobial and antibiofilm activity of highly soluble polypyrrole against methicillin-resistant Staphylococcus aureus

Author:

Rosa Danillo Sales1ORCID,Oliveira Samily Aquino de Sá1ORCID,Souza Renata de Faria Silva1ORCID,de França Chirles Araujo1ORCID,Pires Isabelle Caroline1ORCID,Tavares Márcio Rennan Santos1ORCID,de Oliveira Helinando Pequeno1ORCID,da Silva Júnior Fernando Antônio Gomes1ORCID,Moreira Maria Aparecida Scatamburlo2ORCID,de Barros Mariana2ORCID,de Menezes Gustavo Batista3ORCID,Antunes Maísa Mota3ORCID,Azevedo Vasco Ariston de Carvalho3ORCID,Naue Carine Rosa4ORCID,da Costa Mateus Matiuzzi1ORCID

Affiliation:

1. Universidade Federal do Vale do São Francisco , Petrolina, Pernambuco 56300-000 , Brazil

2. Universidade Federal de Viçosa , Viçosa, Minas Gerais 36570-900 , Brazil

3. Universidade Federal de Minas Gerais , Belo Horizonte, Minas Gerais 31270-901 , Brazil

4. Hospital Universitário da Universidade Federal do Vale do São Francisco , Petrolina, Pernambuco 56304-205 , Brazil

Abstract

Abstract Aims The purpose was to evaluate the antimicrobial activity of highly soluble polypyrrole (Hs-PPy), alone or combined with oxacillin, as well as its antibiofilm potential against methicillin-resistant Staphylococcus aureus strains. Furthermore, the in silico inhibitory mechanism in efflux pumps was also investigated. Methods and results Ten clinical isolates of methicillin-resistant Staphylococcus aureus (MRSA) and two reference strains were used. Antimicrobial activity was determined by broth microdilution, and the combination effect with oxacillin was evaluated by the checkerboard assay. The biofilm formation capacity of MRSA and the interference of Hs-PPy were evaluated. The inhibitory action of Hs-PPy on the efflux pump was evaluated in silico through molecular docking. Hs-PPy showed activity against the isolates, with inhibitory action between 62.5 and 125 µg ml−1 and bactericidal action at 62.5 µg ml−1, as well as synergism in association with oxacillin. The isolates ranged from moderate to strong biofilm producers, and Hs-PPy interfered with the formation of this structure, but not with mature biofilm. There was no in silico interaction with the efflux protein EmrD, the closest homolog to NorA. Conclusions Hs-PPy interferes with biofilm formation by MRSA, has synergistic potential, and is an efflux pump inhibitor.

Funder

CAPES

FACEPE

National Council for Scientific and Technological Development

Publisher

Oxford University Press (OUP)

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5. Simulations of substrate transport in the multidrug transporter EmrD;Baker;Proteins,2012

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