Abstract
With antimicrobial resistance reaching critical levels worldwide, the development of new compounds that are effective against resistant bacterial pathogens or that can potentiate the effect of known antibiotics is an urgent need. The formation of biofilms and the overexpression of efflux pumps are some of the most common causes of drug resistance. Previous work from our group has shown that alkaloids related to the fumiquinazolines have antibacterial potential. Herein we aimed to synthesize a small library of fumiquinazoline-related alkaloids and to study their antibacterial and anti-biofilm activities as well as their capacity to inhibit bacterial efflux pumps. To achieve these goals, two naturally occurring alkaloids, as well as several new derivatives, were synthesized through a multi-step synthetic pathway. The screening of their antibacterial activities was achieved by determination of the minimum inhibitory concentration of each compound against a panel of clinically relevant bacterial species. Several compounds exhibited promising activities against Gram-positive bacteria. Then, using the ethidium bromide accumulation assay, it was possible to identify some compounds with capacity to inhibit efflux pumps. Some of the synthesized alkaloids also showed anti-biofilm potential, reinforcing the idea that fumiquinazoline-related alkaloids can constitute a key strategy for fighting antimicrobial resistance.
Supplementary Materials
The following are available online at https://www.mdpi.com/article/10.3390/ECMC2022-13440/s1.
Author Contributions
Conceptualization, E.S. and G.S.; methodology, M.C.A., F.D. and N.S.; software, M.C.A. and F.D.; validation, D.I.S.P.R., M.P., E.S., G.S. and P.M.d.C.; formal analysis, M.C.A., F.D., M.P., D.I.S.P.R., E.S., G.S. and P.M.d.C.; investigation, M.C.A., F.D., and N.S.; resources, G.S.; P.M.d.C. and M.P.; data curation, M.C.A. and F.D.; writing—original draft preparation, M.C.A. and F.D.; writing—review and editing, M.P., E.S., G.S., P.M.d.C. and D.I.S.P.R.; visualization, E.S., G.S., P.M.d.C., M.P. and D.I.S.P.R.; supervision, M.P., P.M.d.C. and D.I.S.P.R.; project administration, E.S.; funding acquisition, E.S. All authors have read and agreed to the published version of the manuscript.
Funding
This research was supported by national funds through FCT (Foundation for Science and Technology) within the scope of Base Funding UIDB/04423/2020 and UIDP/04423/2020 (CIIMAR, Group of Natural Products and Medicinal Chemistry), projects EXPL/CTA-AMB/0810/2021, PTDC/CTA-AMB/0853/2021 and CHIRALBIO ACTIVE-PI-3RL-IINFACTS-2019 and by the Norte Portugal Regional Operational Programme (NORTE 2020), under the PORTUGAL 2020 Partnership Agreement and through the ERDF, as a result of the project ATLANTIDA (reference NORTE-01-0145-FEDER-000040). Mariana C. Almeida acknowledges the BYT+ 2020/2021 scholarship to CIIMAR and the PhD grant (2021.05224.BD) to FCT. Fernando Durães acknowledges his PhD grant (SFRH/BD/144681/2019) to FCT.
Institutional Review Board Statement
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Informed Consent Statement
Not applicable.
Conflicts of Interest
The authors declare no conflict of interest.
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