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Transcriptomic Responses of Mycoplasma bovis Upon Treatments of trans-Cinnamaldehyde, Carvacrol, and Eugenol
Mycoplasma bovis (M. bovis) is an insidious, wall-less primary bacterial pathogen that causes bovine pneumonia, mid-ear infection, mastitis, and arthritis. The economic losses caused by M. bovis due to culling, diminished milk production, and feed conversion are underestimated because of poor diagno...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9207385/ https://www.ncbi.nlm.nih.gov/pubmed/35733968 http://dx.doi.org/10.3389/fmicb.2022.888433 |
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author | Ranjitkar, Saurav Duan, Jingyue Ellie Srirattana, Kanokwan Alqahtani, Fahad Tulman, Edan R. Mandoiu, Ion Venkitanarayanan, Kumar Tian, Xiuchun |
author_facet | Ranjitkar, Saurav Duan, Jingyue Ellie Srirattana, Kanokwan Alqahtani, Fahad Tulman, Edan R. Mandoiu, Ion Venkitanarayanan, Kumar Tian, Xiuchun |
author_sort | Ranjitkar, Saurav |
collection | PubMed |
description | Mycoplasma bovis (M. bovis) is an insidious, wall-less primary bacterial pathogen that causes bovine pneumonia, mid-ear infection, mastitis, and arthritis. The economic losses caused by M. bovis due to culling, diminished milk production, and feed conversion are underestimated because of poor diagnosis/recognition. Treatment with common antibiotics targeting the cell wall is ineffective. Plant-derived antimicrobials (PDAs) such as food-grade trans-cinnamaldehyde (TC), eugenol (EU), and carvacrol (CAR) are inexpensive and generally regarded as safe for humans and animals yet possess strong anti-bacterial properties. In preliminary studies, we found that all three PDAs inhibited the growth of M. bovis in vitro. Through RNA sequencing, we report here that CAR affected the expression of 153 genes which included the downregulation of energy generation-related proteins, pentose phosphate pathway, and upregulation of ribosomes and translation-related proteins. Few differentially expressed genes were found when M. bovis was treated with TC, EU, or when the three PDAs were double or triple combined. Our results suggest that, as opposed to the effect of CAR, the growth-inhibitory effects of TC and EU at levels tested may be exerted through mechanisms other than gene expression regulations. |
format | Online Article Text |
id | pubmed-9207385 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92073852022-06-21 Transcriptomic Responses of Mycoplasma bovis Upon Treatments of trans-Cinnamaldehyde, Carvacrol, and Eugenol Ranjitkar, Saurav Duan, Jingyue Ellie Srirattana, Kanokwan Alqahtani, Fahad Tulman, Edan R. Mandoiu, Ion Venkitanarayanan, Kumar Tian, Xiuchun Front Microbiol Microbiology Mycoplasma bovis (M. bovis) is an insidious, wall-less primary bacterial pathogen that causes bovine pneumonia, mid-ear infection, mastitis, and arthritis. The economic losses caused by M. bovis due to culling, diminished milk production, and feed conversion are underestimated because of poor diagnosis/recognition. Treatment with common antibiotics targeting the cell wall is ineffective. Plant-derived antimicrobials (PDAs) such as food-grade trans-cinnamaldehyde (TC), eugenol (EU), and carvacrol (CAR) are inexpensive and generally regarded as safe for humans and animals yet possess strong anti-bacterial properties. In preliminary studies, we found that all three PDAs inhibited the growth of M. bovis in vitro. Through RNA sequencing, we report here that CAR affected the expression of 153 genes which included the downregulation of energy generation-related proteins, pentose phosphate pathway, and upregulation of ribosomes and translation-related proteins. Few differentially expressed genes were found when M. bovis was treated with TC, EU, or when the three PDAs were double or triple combined. Our results suggest that, as opposed to the effect of CAR, the growth-inhibitory effects of TC and EU at levels tested may be exerted through mechanisms other than gene expression regulations. Frontiers Media S.A. 2022-06-06 /pmc/articles/PMC9207385/ /pubmed/35733968 http://dx.doi.org/10.3389/fmicb.2022.888433 Text en Copyright © 2022 Ranjitkar, Duan, Srirattana, Alqahtani, Tulman, Mandoiu, Venkitanarayanan and Tian. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Ranjitkar, Saurav Duan, Jingyue Ellie Srirattana, Kanokwan Alqahtani, Fahad Tulman, Edan R. Mandoiu, Ion Venkitanarayanan, Kumar Tian, Xiuchun Transcriptomic Responses of Mycoplasma bovis Upon Treatments of trans-Cinnamaldehyde, Carvacrol, and Eugenol |
title | Transcriptomic Responses of Mycoplasma bovis Upon Treatments of trans-Cinnamaldehyde, Carvacrol, and Eugenol |
title_full | Transcriptomic Responses of Mycoplasma bovis Upon Treatments of trans-Cinnamaldehyde, Carvacrol, and Eugenol |
title_fullStr | Transcriptomic Responses of Mycoplasma bovis Upon Treatments of trans-Cinnamaldehyde, Carvacrol, and Eugenol |
title_full_unstemmed | Transcriptomic Responses of Mycoplasma bovis Upon Treatments of trans-Cinnamaldehyde, Carvacrol, and Eugenol |
title_short | Transcriptomic Responses of Mycoplasma bovis Upon Treatments of trans-Cinnamaldehyde, Carvacrol, and Eugenol |
title_sort | transcriptomic responses of mycoplasma bovis upon treatments of trans-cinnamaldehyde, carvacrol, and eugenol |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9207385/ https://www.ncbi.nlm.nih.gov/pubmed/35733968 http://dx.doi.org/10.3389/fmicb.2022.888433 |
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