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Myrrh Oil in Vitro Inhibitory Growth on Bovine and Equine Piroplasm Parasites and Babesia microti of Mice
The present experimental study was conducted for the assessment of the efficacy of in vitro inhibition of myrrh oil on the propagation of Babesia bovis, B. divergens, B. bigemina, Theileria equi, and B. caballi and in vivo efficacy on B. microti in mice through fluorescence assay based on SYBR green...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7157210/ https://www.ncbi.nlm.nih.gov/pubmed/32121352 http://dx.doi.org/10.3390/pathogens9030173 |
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author | AbouLaila, Mahmoud El-Sayed, Shimaa Abd El-Salam Omar, Mosaab A. Al-Aboody, Mohammad Saleh Abdel Aziz, Amer R. Abdel-Daim, Mohamed M. Rizk, Mohamed Abdo Igarashi, Ikuo |
author_facet | AbouLaila, Mahmoud El-Sayed, Shimaa Abd El-Salam Omar, Mosaab A. Al-Aboody, Mohammad Saleh Abdel Aziz, Amer R. Abdel-Daim, Mohamed M. Rizk, Mohamed Abdo Igarashi, Ikuo |
author_sort | AbouLaila, Mahmoud |
collection | PubMed |
description | The present experimental study was conducted for the assessment of the efficacy of in vitro inhibition of myrrh oil on the propagation of Babesia bovis, B. divergens, B. bigemina, Theileria equi, and B. caballi and in vivo efficacy on B. microti in mice through fluorescence assay based on SYBR green I. The culture of B. divergens B. bovis and was used to evaluate the in vitro possible interaction between myrrh oil and other commercial compound, such as pyronaridine tetraphosphate (PYR), diminazene aceturate (DA), or luteolin. Nested-polymerase chain reaction protocol using primers of the small-subunit rRNA of B. microti was employed to detect any remnants of DNA for studied parasitic species either in blood or tissues. Results elucidated that; Myrrh oil significantly inhibit the growth at 1% of parasitic blood level for all bovine and equine piroplasm under the study. Parasitic regrowth was inhibited subsequently by viability test at 2 µg/mL for B. bigemina and B. bovis, and there was a significant improvement in the in vitro growth inhibition by myrrh oil when combined with DA, PYR, and luteolin. At the same time; mice treated with a combination of myrrh oil/DA showed a higher inhibition in emitted fluorescence signals than the group that challenged with 25 mg/kg of diminazene aceturate at 10 and 12 days post-infection. In conclusion, this study has recommended the myrrh oil to treat animal piroplasmosis, especially in combination with low doses of DA. |
format | Online Article Text |
id | pubmed-7157210 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-71572102020-05-01 Myrrh Oil in Vitro Inhibitory Growth on Bovine and Equine Piroplasm Parasites and Babesia microti of Mice AbouLaila, Mahmoud El-Sayed, Shimaa Abd El-Salam Omar, Mosaab A. Al-Aboody, Mohammad Saleh Abdel Aziz, Amer R. Abdel-Daim, Mohamed M. Rizk, Mohamed Abdo Igarashi, Ikuo Pathogens Article The present experimental study was conducted for the assessment of the efficacy of in vitro inhibition of myrrh oil on the propagation of Babesia bovis, B. divergens, B. bigemina, Theileria equi, and B. caballi and in vivo efficacy on B. microti in mice through fluorescence assay based on SYBR green I. The culture of B. divergens B. bovis and was used to evaluate the in vitro possible interaction between myrrh oil and other commercial compound, such as pyronaridine tetraphosphate (PYR), diminazene aceturate (DA), or luteolin. Nested-polymerase chain reaction protocol using primers of the small-subunit rRNA of B. microti was employed to detect any remnants of DNA for studied parasitic species either in blood or tissues. Results elucidated that; Myrrh oil significantly inhibit the growth at 1% of parasitic blood level for all bovine and equine piroplasm under the study. Parasitic regrowth was inhibited subsequently by viability test at 2 µg/mL for B. bigemina and B. bovis, and there was a significant improvement in the in vitro growth inhibition by myrrh oil when combined with DA, PYR, and luteolin. At the same time; mice treated with a combination of myrrh oil/DA showed a higher inhibition in emitted fluorescence signals than the group that challenged with 25 mg/kg of diminazene aceturate at 10 and 12 days post-infection. In conclusion, this study has recommended the myrrh oil to treat animal piroplasmosis, especially in combination with low doses of DA. MDPI 2020-02-29 /pmc/articles/PMC7157210/ /pubmed/32121352 http://dx.doi.org/10.3390/pathogens9030173 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article AbouLaila, Mahmoud El-Sayed, Shimaa Abd El-Salam Omar, Mosaab A. Al-Aboody, Mohammad Saleh Abdel Aziz, Amer R. Abdel-Daim, Mohamed M. Rizk, Mohamed Abdo Igarashi, Ikuo Myrrh Oil in Vitro Inhibitory Growth on Bovine and Equine Piroplasm Parasites and Babesia microti of Mice |
title | Myrrh Oil in Vitro Inhibitory Growth on Bovine and Equine Piroplasm Parasites and Babesia microti of Mice |
title_full | Myrrh Oil in Vitro Inhibitory Growth on Bovine and Equine Piroplasm Parasites and Babesia microti of Mice |
title_fullStr | Myrrh Oil in Vitro Inhibitory Growth on Bovine and Equine Piroplasm Parasites and Babesia microti of Mice |
title_full_unstemmed | Myrrh Oil in Vitro Inhibitory Growth on Bovine and Equine Piroplasm Parasites and Babesia microti of Mice |
title_short | Myrrh Oil in Vitro Inhibitory Growth on Bovine and Equine Piroplasm Parasites and Babesia microti of Mice |
title_sort | myrrh oil in vitro inhibitory growth on bovine and equine piroplasm parasites and babesia microti of mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7157210/ https://www.ncbi.nlm.nih.gov/pubmed/32121352 http://dx.doi.org/10.3390/pathogens9030173 |
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