Antimicrobial Activity the Essential Oil from Croton pluriglandulosus Carn. Leaves against Microorganisms of Clinical Interest

Author:

Carvalho Rayara J. P.1,Souza Pedro F. N.12ORCID,Malveira Ellen A.1,Neto Nilton A. S.1,Silva Romério R. S.1ORCID,Melo Gabriel L. C.3,Silva Ayrles F. B.1,Lima Leandro B.4,de Albuquerque Cynthia C.5,Bastos Rafael W.6,Goldman Gustavo H.7,de Freitas Cleverson D. T.1ORCID

Affiliation:

1. Department of Biochemistry and Molecular Biology, Federal University of Ceará, Fortaleza 60020-181, Brazil

2. Drug Research and Development Center, Department of Physiology and Pharmacology, Federal University of Ceará, Fortaleza 60430-160, Brazil

3. Department of Fishery Engineering, Federal University of Ceará, Fortaleza 60356-000, Brazil

4. Department of Chemistry, Faculty of Exact and Natural Sciences, State University of Rio Grande do Norte, Mossoró 59650-000, Brazil

5. Department of Biological Sciences, Faculty of Exact and Natural Sciences, State University of Rio Grande do Norte, Mossoró 59650-000, Brazil

6. Department of Microbiology and Parasitology, Biosciences Center, Federal University of Rio Grande do Norte, Natal 59078-970, Brazil

7. Faculty of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, São Paulo 14040-903, Brazil

Abstract

Multiresistant pathogens pose a serious threat to human health. The genus Candida is one class of human pathogenic yeasts responsible for infections affecting healthy and immunocompromised patients. In this context, plant essential oils emerged as a future natural alternative to control the diseases caused by these pathogens. Based on that, the present study aimed to evaluate the antimicrobial potential of essential oil from C. pluriglandulosus and understand the mechanism of action. Here, it highlighted antimicrobial activity and the mechanisms of action of the essential oil extracted from C. pluriglandulosus Carn.-Torres & Riina (CpEO) leaves on human pathogenic microorganisms in planktonic and biofilm lifestyles. In addition, for the first time, the oil composition was revealed by GC-MS analysis and the toxicity to human red blood cells (HRBC). Twenty-six chemical compounds were identified in CpEO, elemicin, bicyclogermacrene, caryophyllene, brevifolin, and 2,4,6-trimethoxy-styrene. Through hemolytic assay, it was shown that CpEO has no toxicity to human RBCs. At the concentration of 50 μg mL−1, CpEO did not show great antibacterial potential. However, promising data were found for C. krusei and C. parapsilosis inhibiting by 89.3% and 80.7% of planktonic cell growth and 83.5% and 77.9% the biofilm formation, respectively. Furthermore, the mechanisms of action CpEO were elucidated by fluorescence. Scanning electron microscopy revealed damage to the cell membrane and pore formation, ROS overproduction, and induction of apoptosis in candida cells. Our results reinforce the potential of CpEO as an effective alternative molecule of pharmaceutical interest.

Funder

CNPq

Publisher

MDPI AG

Subject

Plant Science,Ecology, Evolution, Behavior and Systematics,Microbiology (medical)

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