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Juniper and Immortelle Essential Oils Synergistically Inhibit Adhesion of Nontuberculous Mycobacteria To Acanthamoeba Castellanii
Acanthamoeba is an opportunistic protozoon, widespread in the aquatic environment, where it can be in endosymbiosis with over 30 pathogenic bacteria, including nontuberculous mycobacteria (NTM). Protozoa play a crucial role in mycobacterial pathogenesis and serve as a reservoir of infection. Since t...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Sciendo
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7968501/ https://www.ncbi.nlm.nih.gov/pubmed/33074171 http://dx.doi.org/10.2478/aiht-2020-71-3442 |
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author | Peruč, Dolores Tićac, Brigita Broznić, Dalibor Gobin, Ivana |
author_facet | Peruč, Dolores Tićac, Brigita Broznić, Dalibor Gobin, Ivana |
author_sort | Peruč, Dolores |
collection | PubMed |
description | Acanthamoeba is an opportunistic protozoon, widespread in the aquatic environment, where it can be in endosymbiosis with over 30 pathogenic bacteria, including nontuberculous mycobacteria (NTM). Protozoa play a crucial role in mycobacterial pathogenesis and serve as a reservoir of infection. Since the first step in bacteria making contact with amoebae is adhesion, we were interested in investigating whether essential oils (EOs) can affect it. To that end we investigated the effects of juniper (Juniperus communis) and immortelle (Helichrysum italicum) EOs against Mycobacterium avium, M. intracellulare, and M. gordonae in tap water and against their adhesion to Acanthamoeba castellanii by combining them in synergistic EO concentrations. M. avium and M. intracellulare adhered to A. castellanii to a greater extent than M. gordonae. The adhesion of all NTMs was prevented by the subinhibitory concentrations of EOs. When comparing the effect of synergistic combinations of EOs and the effect of a single concentration from a combination, a higher percentage of adhesion inhibition in all synergistic combinations observed, except against M. gordonae. Neither oil was cytotoxic to A. castellanii. Our findings suggest that the EOs or their components weaken the contact of environmental NTMs and free-living amoebae and indirectly diminish their pathogenic potential, which could be of value in developing strategies for maintenance of water supply systems. |
format | Online Article Text |
id | pubmed-7968501 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Sciendo |
record_format | MEDLINE/PubMed |
spelling | pubmed-79685012021-05-25 Juniper and Immortelle Essential Oils Synergistically Inhibit Adhesion of Nontuberculous Mycobacteria To Acanthamoeba Castellanii Peruč, Dolores Tićac, Brigita Broznić, Dalibor Gobin, Ivana Arh Hig Rada Toksikol Original Article Acanthamoeba is an opportunistic protozoon, widespread in the aquatic environment, where it can be in endosymbiosis with over 30 pathogenic bacteria, including nontuberculous mycobacteria (NTM). Protozoa play a crucial role in mycobacterial pathogenesis and serve as a reservoir of infection. Since the first step in bacteria making contact with amoebae is adhesion, we were interested in investigating whether essential oils (EOs) can affect it. To that end we investigated the effects of juniper (Juniperus communis) and immortelle (Helichrysum italicum) EOs against Mycobacterium avium, M. intracellulare, and M. gordonae in tap water and against their adhesion to Acanthamoeba castellanii by combining them in synergistic EO concentrations. M. avium and M. intracellulare adhered to A. castellanii to a greater extent than M. gordonae. The adhesion of all NTMs was prevented by the subinhibitory concentrations of EOs. When comparing the effect of synergistic combinations of EOs and the effect of a single concentration from a combination, a higher percentage of adhesion inhibition in all synergistic combinations observed, except against M. gordonae. Neither oil was cytotoxic to A. castellanii. Our findings suggest that the EOs or their components weaken the contact of environmental NTMs and free-living amoebae and indirectly diminish their pathogenic potential, which could be of value in developing strategies for maintenance of water supply systems. Sciendo 2020-10-06 /pmc/articles/PMC7968501/ /pubmed/33074171 http://dx.doi.org/10.2478/aiht-2020-71-3442 Text en © 2020 Dolores Peruč et al., published by Sciendo http://creativecommons.org/licenses/by-nc-nd/4.0 This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. |
spellingShingle | Original Article Peruč, Dolores Tićac, Brigita Broznić, Dalibor Gobin, Ivana Juniper and Immortelle Essential Oils Synergistically Inhibit Adhesion of Nontuberculous Mycobacteria To Acanthamoeba Castellanii |
title | Juniper and Immortelle Essential Oils Synergistically Inhibit Adhesion of Nontuberculous Mycobacteria To Acanthamoeba Castellanii |
title_full | Juniper and Immortelle Essential Oils Synergistically Inhibit Adhesion of Nontuberculous Mycobacteria To Acanthamoeba Castellanii |
title_fullStr | Juniper and Immortelle Essential Oils Synergistically Inhibit Adhesion of Nontuberculous Mycobacteria To Acanthamoeba Castellanii |
title_full_unstemmed | Juniper and Immortelle Essential Oils Synergistically Inhibit Adhesion of Nontuberculous Mycobacteria To Acanthamoeba Castellanii |
title_short | Juniper and Immortelle Essential Oils Synergistically Inhibit Adhesion of Nontuberculous Mycobacteria To Acanthamoeba Castellanii |
title_sort | juniper and immortelle essential oils synergistically inhibit adhesion of nontuberculous mycobacteria to acanthamoeba castellanii |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7968501/ https://www.ncbi.nlm.nih.gov/pubmed/33074171 http://dx.doi.org/10.2478/aiht-2020-71-3442 |
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