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Increased Expression of a MicroRNA Correlates with Anthelmintic Resistance in Parasitic Nematodes

Resistance to anthelmintic drugs is a major problem in the global fight against parasitic nematodes infecting humans and animals. While previous studies have identified mutations in drug target genes in resistant parasites, changes in the expression levels of both targets and transporters have also...

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Autores principales: Gillan, Victoria, Maitland, Kirsty, Laing, Roz, Gu, Henry, Marks, Neil D., Winter, Alan D., Bartley, David, Morrison, Alison, Skuce, Philip J., Rezansoff, Andrew M., Gilleard, John S., Martinelli, Axel, Britton, Collette, Devaney, Eileen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5701612/
https://www.ncbi.nlm.nih.gov/pubmed/29209592
http://dx.doi.org/10.3389/fcimb.2017.00452
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author Gillan, Victoria
Maitland, Kirsty
Laing, Roz
Gu, Henry
Marks, Neil D.
Winter, Alan D.
Bartley, David
Morrison, Alison
Skuce, Philip J.
Rezansoff, Andrew M.
Gilleard, John S.
Martinelli, Axel
Britton, Collette
Devaney, Eileen
author_facet Gillan, Victoria
Maitland, Kirsty
Laing, Roz
Gu, Henry
Marks, Neil D.
Winter, Alan D.
Bartley, David
Morrison, Alison
Skuce, Philip J.
Rezansoff, Andrew M.
Gilleard, John S.
Martinelli, Axel
Britton, Collette
Devaney, Eileen
author_sort Gillan, Victoria
collection PubMed
description Resistance to anthelmintic drugs is a major problem in the global fight against parasitic nematodes infecting humans and animals. While previous studies have identified mutations in drug target genes in resistant parasites, changes in the expression levels of both targets and transporters have also been reported. The mechanisms underlying these changes in gene expression are unresolved. Here, we take a novel approach to this problem by investigating the role of small regulatory RNAs in drug resistant strains of the important parasite Haemonchus contortus. microRNAs (miRNAs) are small (22 nt) non-coding RNAs that regulate gene expression by binding predominantly to the 3′ UTR of mRNAs. Changes in miRNA expression have been implicated in drug resistance in a variety of tumor cells. In this study, we focused on two geographically distinct ivermectin resistant strains of H. contortus and two lines generated by multiple rounds of backcrossing between susceptible and resistant parents, with ivermectin selection. All four resistant strains showed significantly increased expression of a single miRNA, hco-miR-9551, compared to the susceptible strain. This same miRNA is also upregulated in a multi-drug-resistant strain of the related nematode Teladorsagia circumcincta. hco-miR-9551 is enriched in female worms, is likely to be located on the X chromosome and is restricted to clade V parasitic nematodes. Genes containing predicted binding sites for hco-miR-9551 were identified computationally and refined based on differential expression in a transcriptomic dataset prepared from the same drug resistant and susceptible strains. This analysis identified three putative target mRNAs, one of which, a CHAC domain containing protein, is located in a region of the H. contortus genome introgressed from the resistant parent. hco-miR-9551 was shown to interact with the 3′ UTR of this gene by dual luciferase assay. This study is the first to suggest a role for miRNAs and the genes they regulate in drug resistant parasitic nematodes. miR-9551 also has potential as a biomarker of resistance in different nematode species.
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spelling pubmed-57016122017-12-05 Increased Expression of a MicroRNA Correlates with Anthelmintic Resistance in Parasitic Nematodes Gillan, Victoria Maitland, Kirsty Laing, Roz Gu, Henry Marks, Neil D. Winter, Alan D. Bartley, David Morrison, Alison Skuce, Philip J. Rezansoff, Andrew M. Gilleard, John S. Martinelli, Axel Britton, Collette Devaney, Eileen Front Cell Infect Microbiol Microbiology Resistance to anthelmintic drugs is a major problem in the global fight against parasitic nematodes infecting humans and animals. While previous studies have identified mutations in drug target genes in resistant parasites, changes in the expression levels of both targets and transporters have also been reported. The mechanisms underlying these changes in gene expression are unresolved. Here, we take a novel approach to this problem by investigating the role of small regulatory RNAs in drug resistant strains of the important parasite Haemonchus contortus. microRNAs (miRNAs) are small (22 nt) non-coding RNAs that regulate gene expression by binding predominantly to the 3′ UTR of mRNAs. Changes in miRNA expression have been implicated in drug resistance in a variety of tumor cells. In this study, we focused on two geographically distinct ivermectin resistant strains of H. contortus and two lines generated by multiple rounds of backcrossing between susceptible and resistant parents, with ivermectin selection. All four resistant strains showed significantly increased expression of a single miRNA, hco-miR-9551, compared to the susceptible strain. This same miRNA is also upregulated in a multi-drug-resistant strain of the related nematode Teladorsagia circumcincta. hco-miR-9551 is enriched in female worms, is likely to be located on the X chromosome and is restricted to clade V parasitic nematodes. Genes containing predicted binding sites for hco-miR-9551 were identified computationally and refined based on differential expression in a transcriptomic dataset prepared from the same drug resistant and susceptible strains. This analysis identified three putative target mRNAs, one of which, a CHAC domain containing protein, is located in a region of the H. contortus genome introgressed from the resistant parent. hco-miR-9551 was shown to interact with the 3′ UTR of this gene by dual luciferase assay. This study is the first to suggest a role for miRNAs and the genes they regulate in drug resistant parasitic nematodes. miR-9551 also has potential as a biomarker of resistance in different nematode species. Frontiers Media S.A. 2017-11-06 /pmc/articles/PMC5701612/ /pubmed/29209592 http://dx.doi.org/10.3389/fcimb.2017.00452 Text en Copyright © 2017 Gillan, Maitland, Laing, Gu, Marks, Winter, Bartley, Morrison, Skuce, Rezansoff, Gilleard, Martinelli, Britton and Devaney. http://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) or licensor 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
Gillan, Victoria
Maitland, Kirsty
Laing, Roz
Gu, Henry
Marks, Neil D.
Winter, Alan D.
Bartley, David
Morrison, Alison
Skuce, Philip J.
Rezansoff, Andrew M.
Gilleard, John S.
Martinelli, Axel
Britton, Collette
Devaney, Eileen
Increased Expression of a MicroRNA Correlates with Anthelmintic Resistance in Parasitic Nematodes
title Increased Expression of a MicroRNA Correlates with Anthelmintic Resistance in Parasitic Nematodes
title_full Increased Expression of a MicroRNA Correlates with Anthelmintic Resistance in Parasitic Nematodes
title_fullStr Increased Expression of a MicroRNA Correlates with Anthelmintic Resistance in Parasitic Nematodes
title_full_unstemmed Increased Expression of a MicroRNA Correlates with Anthelmintic Resistance in Parasitic Nematodes
title_short Increased Expression of a MicroRNA Correlates with Anthelmintic Resistance in Parasitic Nematodes
title_sort increased expression of a microrna correlates with anthelmintic resistance in parasitic nematodes
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5701612/
https://www.ncbi.nlm.nih.gov/pubmed/29209592
http://dx.doi.org/10.3389/fcimb.2017.00452
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